WCDG hosts monthly public meetings from September to May on the 3rd Wednesday of the month, unless otherwise noted.
May 19, 2021
Speaker: Roland F. Hirsch
Title: How Analytical Chemistry, and especially Chromatography and Mass Spectrometry, is enabling progress in understanding climate
Abstract: The Earth’s climate is a highly complex system. There is an urgent need for more accurate information about past climate and improved knowledge about the factors that influence climate today, in order to develop plausible models of future climate. Analytical chemistry, which plays a key role in studying past temperatures, rainfall, extent of ice and glaciers, and other relevant climate properties, is essential for gaining knowledge about climate-related processes that are occurring now in the atmosphere (such as formation and impact of aerosols). Mass spectrometry is the key technique for most of these studies. Chromatography, both gas and liquid, is also essential for many of these studies, usually in combination with mass spectrometry. This talk will discuss how these techniques are being used in climate research. Examples will be provided from the scientific literature.
Bio: Roland F. Hirsch lives in Overland Park, Kansas, with his wife of 49 years, Paula Jean. He received his Ph.D. in analytical chemistry from the University of Michigan. He joined the chemistry faculty of Seton Hall University, where he taught courses in general chemistry and analytical chemistry. In 1975-6 he was a Senior Visitor with Courtney Phillips at Oxford University, studying gas-solid chromatography. In 1984 he joined the Department of Energy as a program manager for analytical and separations chemistry. In 1988 he joined the civil service at NIH and in 1991 became a staff member at the DOE. He retired in 2018 and moved from Maryland to Kansas. He is a Fellow of the ACS, Honorary Fellow of the Library of America, and has been involved in ACS governance in the North Jersey Local Section and the Division of Analytical Chemistry.
April 19, 2021
Speaker: Stefani Thomas, University of Minnesota
Title: Beyond the BRCA genes: A proteome-centric view of high-grade serous ovarian cancer
Abstract: The mutational status of a solid tumor can predict the therapeutic efficacy of a specific drug in a molecularly defined subset of patients. Poly (ADP-ribose) polymerase inhibitors (PARPi) have emerged as a novel class of drugs to treat advanced ovarian cancer with mutations in BRCA1/2 genes. Unfortunately, there is considerable inter-patient heterogeneity in BRCA1/2–based determinations of PARPi treatment sensitivity. Determining proteome-level mechanisms of PARPi sensitivity could enhance our ability to select the ovarian cancer patient population that would benefit the most from PARPi therapy, consequently improving survival and overall treatment response. Our laboratory is applying mass spectrometry-based proteomics to identify protein signatures of PARPi sensitivity. This presentation will provide an overview of the experimental models and analytical approaches that we are utilizing toward a long-term goal of identifying prognostic protein biomarkers of PARPi sensitivity in patients with high-grade serous ovarian cancer.
February 17, 2021
Speaker: Nicholas Snow, Seton Hall University
Title: GC in the 21st Century: Re-thinking Basic GC Ideas and Assumptions That We Grew Up With
Abstract: Chromatography discussion groups have their origin in their name. They were formed in the 1950s and 1960s when chromatography was in its infancy and gas chromatography was dominant. Most of the theories, ideas and assumptions that we make in all chromatographic techniques have their origins in early GC work, as GC was the first instrumental chromatographic technique. The evolution of instrumentation for GC that finally takes full advantage of advances including capillary columns and selective detectors necessitates a look back at the fundamental assumptions and ideas that we all grew up with and that the book authors and short course instructors teach. This evening, we will discuss three fundamentals that we all think we know: carrier gas choice, gas hold-up time measurement and column polarity. Regarding carrier gas, we were all taught to use helium with capillary columns and if helium is not available, to use hydrogen. We suggest trying nitrogen, which we were taught not to use. The gas hold-up time is a critical measurement for nearly all calculations in GC. Back in the day, we were taught to inject methane or another supposedly non-retained substance to measure this value. With today’s automated systems, manually injecting methane is not a simple matter. We will look at alternatives to injecting methane and discuss possible impacts of variability in this measurement on further calculations. Finally, “polarity” is a broad term that is often conflated with retentiveness; a more polar column is often considered more strongly retentive. We will examine column polarity more closely and see how the classical definition and usage is often confusing.
Bio: Nicholas H. Snow is Founding Endowed Professor of Chemistry and Biochemistry at Seton Hall University and Adjunct Professor of Medical Science at Hackensack UMC Medical School in New Jersey. He is a proud alumnus of Kent Gardens Elementary School, Longfellow Middle School and McLean High School in McLean, Virginia, so this is a homecoming of sorts. Prior to moving to New Jersey in 1994, he continued his education on Virginia with a BS in Chemistry from UVA, a PhD at Virginia Tech and postdoctoral work and lecturing back at UVA. For over 25 years he has led an active research group with 80 publications and two books, mostly related to GC. He is the GC Connections Editor for LCGC Magazine and Associate Editor of the Journal of Liquid Chromatography and Related Technologies. He is co-author of the latest edition of McNair’s classic book “Basic Gas Chromatography”. He holds Seton Hall’s McQuaid Medal for exemplary service by a long-term employee and he was recently recognized for 25 years of service on the Governing Board of the Eastern Analytical Symposium.
January 20, 2021
Speaker: Camille Lombard-Banek, NIST-IBBR
Title: Building a DIA-based Proteomic Workflow for the Characterization of CAR T-cell Therapies
Abstract: CART T-cell therapies are novel cancer treatments, whereby the patient’s T-cells are engineered to express chimeric antigen receptors (CARs) on their surface. Three CAR T-cell therapies have recently received approval by the Food and Drug Administration for the treatment of refractory lymphomas, albeit as last resort solutions. To promote the broader adoption of this new therapeutic modality, innovative technologies are needed, especially ones based on mass spectrometry (MS)-based proteomic. Here, we present the development of a sensitive proteomic method using data-independent acquisition, to help better define critical quality attributes (CQAs) of the cells and final product attributes (PQAs). We evaluated multiple key steps of the data acquisition from separation to detection to enhance the sensitivity by data dependent and independent acquisition. Moreover, we developed a cell model to revise the protein extraction workflow. We also present suggestions for best practices in instrument qualifications (IQ), to facilitate the adoption of large-scale proteomics to the biopharma space. The data represent a benchmark that will be used as IQ metrics to assure instrument control for biologically relevant decision making on CAR-T proteomic samples.
Bio: Camille Lombard-Banek is a NRC postdoctoral fellow at NIST/IBBR in the laboratory of John Schiel where she is developing liquid chromatography mass spectrometry-based proteomic approaches for the analysis of emerging cell and gene therapies. She obtained her PhD from the George Washington University developing micro-analytical tools for the analysis of single embryonic cells in Peter Nemes’ laboratory.
December 16, 2020
Speaker: Kim Haynes, Waters Corporation
Title: ACQUITY PREMIER: Precision Chemistries for Particles and Surfaces
Abstract: LC-based analysis of metal sensitive analytes, such as those containing phosphate groups and deprotonated carboxylic acids, can be challenging due to their interactions with metal components within a chromatographic separation. These interactions can lead to missed analytes, quantification errors, and wasted time. In this seminar, you will learn how ACQUITY PREMIER Columns with MaxPeak High Performance Surfaces enables scientists to see compounds previously unseen, while improving sensitivity and reproducibility for all analytes. In addition, it will be shown how this technology can reduce the need for lengthy and repeated passivation.
Bio: Kim Haynes is currently a Principal Product Marketing Manager in the Chemistry Technology Center at Waters Corporation. Kim manages MaxPeak High Performance Surface Technologies as well as a variety of other programs. Prior to this position, she has worked with Waters Corporation as a chemistry sales specialist and a business development manager. During her 20 years at Waters, Kim has focused on helping customers and colleagues understand chromatographic separations and sample preparation. Before joining Waters Corporation, Kim worked as an analytical chemist at Bacardi Martini. She holds a BS in Chemistry from Ohio University. She can be contacted at email@example.com.
November 18, 2020
Joint meeting with Chemical Society of Washington (CSW)
Speaker: Geoffrey Dubrow, FDA Center for Food Safety and Applied Nutrition
Title: A Survey of Cannabinoids in Hemp-Derived Products from the United States Marketplace
Abstract: The 2018 Agricultural Improvement Act removed hemp from Schedule I control, creating a market for hemp products, including cannabidiol-containing products. Due to the market’s rapid growth, little is known about the presence and concentration of cannabinoids in commercial products. In the present study, 11 cannabinoids were quantified using liquid chromatography with diode-array detection in a non-representative sampling of 147 products labeled as containing hemp or cannabidiol. Cannabinoid content ranged from 0–143 mg/serving, with a median of 16.7 mg/serving. Fewer than half of products surveyed contained cannabidiol concentrations within 20% of their label declarations. Most products presented concentrations of ∆9-tetrahydrocannabinol below LOQ. These findings emphasize the need for further testing and representative investigation of the cannabidiol marketplace.
Bio: Dr. Geoffrey A. Dubrow is a staff fellow in the Office of Regulatory Science within FDA’s Center for Food Safety and Applied Nutrition. At CFSAN, his work focuses on the analysis of cannabinoids in hemp-containing products. Prior to his work at FDA, Geoff completed his PhD in food science and technology at the Ohio State University in 2019, focusing on the use of untargeted LC/MS and GC/MS “flavoromics” to understand chemical drivers of consumer acceptability in strawberry jams. Beyond food safety, his research interests include the application of chemometrics and metabolomics towards the understanding of food and flavor chemistry, and high-throughput sample preparation.
October 21, 2020
Speaker: Nadja B. Cech, University of North Carolina at Greensboro
Title: Challenges and Opportunities in Transitioning from Targeted to Untargeted Analysis in Small Molecule Mass Spectrometry
Abstract: Mass spectrometrists and chromatographers have spent more than 100 years developing better tools and methods to separate and identify the compounds in mixtures. Historically, much of our field was focused on identifying and quantifying specific known constituents in those mixtures. More recently, there has been a shift in interest towards “untargeted” or “nontargeted” techniques, in which the analyst seeks to capture a more comprehensive profile of the molecules present in a mixture. This talk will address some of the challenges and opportunities our fields have encountered in transitioning from targeted to untargeted approaches, particularly focusing on small molecules (metabolomics). Specific case studies will be included from ongoing research in the Cech Laboratory, where we seek to employ untargeted metabolomics to identify antimicrobial constituents in complex extracts from plants and fungi.
Bio: Dr. Nadja B. Cech is Patricia A. Sullivan Distinguished Professor of Chemistry at UNC Greensboro. She applies her expertise in mass spectrometry to solve challenging problems in natural products research, largely supported with funding from the National Institutes of Health. Work in the Cech group focuses on the application of mass spectrometry metabolomics strategies to identify biologically active constituents from complex mixtures and to understand virulence in bacterial pathogens. Dr. Cech supervises a research group of eighteen students and postdoctoral research associates and is currently schooling and feeding two children during the pandemic. She is the recipient of the 2011 Jack L. Beal Award for Best Paper in the Journal of Natural Products by a Young Investigator, and the 2017 Thomas Norwood Award for Undergraduate Research Mentorship. Dr. Cech is a member of the research team for the NCCIH-funded Center of Excellence for Natural Product Drug Interaction, and Co-Director of the Medicinal Chemistry Collaborative.
September 16, 2020
Speaker: Asif Shajahan, University of Georgia
Title: How advanced mass spectrometry can guide the therapeutic interventions against SARS-CoV-2
Abstract: The development of new therapeutic strategies against COVID-19 pandemic emergence caused by SARS-CoV-2 requires understanding of mode of viral attachment, entry, and replication. We are focused on the glycobiology of SARS-CoV-2 and on how it can help both in development of vaccine and therapeutics. The heavily glycosylated coronavirus surface spike (S) protein facilitates viral attachment, entry and membrane fusion and also plays a critical role in the elicitation of host immune response. The SARS-CoV-2 spike protein is comprised of two protein subunits (S1 and S2) and together possess 22 potential N-glycosylation sites. The S proteins of SARS-CoV-1 and SARS-CoV-2 primarily binds to human angiotensin converting enzyme 2 (hACE2) for the host cell entry. Even though hACE2 has been known for two decades and has been recognized as the entry point of several human coronaviruses, comprehensive glycosylation data of hACE2 is currently not available. Herein, we describe the quantitative N- and O- glycosylation mapping on S protein subunits S1 and S2, and also hACE2 expressed in human cells by both glycoproteomics and glycomics via high resolution LC-MSn. We have characterized the N-glycosylation profile on S protein and interestingly, observed an unexpected O-glycosylation modification on the receptor binding domain (RBD) of spike protein subunit S1. This is the first report of experimental data for both the site of O-glycosylation and identity of the O-glycans attached on the subunit S1 of SARS-CoV-2. We observed almost complete glycan occupancy at all seven possible N-glycosylation sites on hACE2 along with detection of three novel O-glycosylation sites. We have characterized the terminal sialic acid linkages, the presence of bisecting GlcNAc, and the pattern of N-glycan fucosylation to understand the detailed structure of glycan epitopes on hACE2 involved in viral binding. Understanding the site-specific glycosylation and terminal glycan epitopes on viral spike protein and its receptor hACE2 receptor can aid in the development of novel therapy.
Bio: Dr. Shajahan has about 10 years of experience in the structural characterization of glycoproteins using state-of-the-art high-resolution mass spectrometry (MS). He completed his Ph.D. in 2014 where he worked in the interface of chemistry and biology by developing glycoconjugates for the glycoengineering of brain glycans (across BBB) in mice models. He joined CCRC, University of Georgia, in 2015 and have been doing characterization of glycoproteins by both glycomics and glycoproteomics. He has contributed to over 80 projects on the structural characterization of mammalian, plant, algal, insect and bacterial origin glycoconjugates from both academic and industrial researchers. He is also performing research for the development of novel methods which enables rapid but comprehensive glycosylation profiling. He is training and mentoring undergraduate students and other junior postdoctoral trainees at CCRC and also involved as an instructor for the annual hand-on training courses held at CCRC on MS based glycomics and glycoproteomics. He is currently working as an Assistant Research Scientist faculty at CCRC.
April 20, 2020
Speaker: Ben Neely, NIST
Title: Sea lions and bats and humans, oh my! How to explore mammalian serum proteomes
Abstract: Comparative biology and biomimicry are broadly focused on understanding the underlying molecular basis of phenotypes relevant to chronic human ailments. Notably, research in hibernating mammals is improving our understanding of neurodegeneration, studies of diving mammals is identifying novel mechanisms of ischemia/reperfusion injury resistance, while studying organisms that follow Peto’s paradox is advancing longevity and cancer research. In addition to biomimetics, recent events are highlighting certain mammal’s ability to serve as reservoirs of infectious disease. Systematically characterizing the diversity of all mammalian proteomes will enable unexpected discoveries, but this presents numerous technological hurdles. In this seminar I will present results, recommendations and solutions to the issues of working in species without genomes or annotations, acquiring proteomic data in a standardized fashion, comparing proteomes between species and identifying molecular trends across clades with relevant phenotypes. Using the Atlantic bottlenose dolphin and California sea lion as examples, I will demonstrate improvements in proteomic analysis using genomic sequencing and gene annotation techniques, as well as emerging proteomic techniques such as data-independent acquisition applied to undepleted human and bat serum.
February 19, 2020
at Institute for Bioscience and Biotechnology Research (IBBR)
Presentation by 2019 Guiochon Student Award Recipient
Student Speaker: Jie Li, University of Maryland College Park
Title: LC-HRMS Based Metabolomic Analysis of Neural-Tissue Fated Cell Clones from Developing Xenopus laevis Embryos
Metabolites (small molecules <1,500 Daltons) are drivers, regulators, and products of a myriad of biological processes. However, there is limited knowledge about the role of metabolites in cell differentiation during which cells specialize to form different tissues and organs. This is, because the complexity of metabolite detection and identification is increased by several factors: metabolites occupy wide physiological concentration range and display structural diversity. Liquid chromatography-high-resolution mass spectrometry (LC-HRMS) is the benchmark technology for metabolomic analysis due to its high sensitivity and structural specificity. Moreover, coupling LC to HRMS decreases the complexity of metabolomic analysis and facilitates metabolite identification. Here, we integrate LC-HRMS with embryonic cell lineage tracing, embryonic dissociation, and fluorescence-activated cell sorting (FACS) to characterize the metabolomic state of neural-tissue fated cell clones in the early developing embryo of the Xenopus laevis frog. To tailor detection to polar metabolites, we developed a hydrophilic interaction chromatography (HILIC)-ESI-MS method that enabled <0.5 nM lower limit of detection for metabolite standards. This HILIC-ESI-MS method yielded 2,218 molecular features from the cells, of which we identified 92 cationic and 26 anionic metabolites. According to the metabolic pathway analysis for all identified metabolites using MetaboAnalyst 4.0, alanine, aspartate, and glutamate metabolism, arginine and proline metabolism, and histidine metabolism were found with high pathway impact (pathway impact > 0.4), which indicated these three metabolic pathways play important roles during embryonic development. The knowledge generated from this work will deepen the understanding of neural tissue formation from the perspective of metabolomics.
Bio: Jie Li is a Ph.D. candidate from the Department of Chemistry and Biochemistry at the University of Maryland, College Park mentored by Prof. Peter Nemes. Mr. Li has obtained a B.S. degree in Applied Chemistry from Huazhong University of Science and Technology (Wuhan, China) and an M.S. degree in Chemistry from Case Western Reserve University (Cleveland, Ohio). Mr. Li’s research focuses on developing advanced bioanalytical techniques to answer biological questions such as understanding the role of metabolites in driving cell differentiation and tissue formation. Mr. Li is a recipient of 2019 COSMOS Club Scholars Award.
Featured Speaker: Alexander Zestos, American University
Title: LC-MS/MS Method for Neurochemical Detection in Biological Samples
Abstract: We have pioneered a liquid chromatography-tandem mass spectrometry (LC-MS/MS) assay that can detect 24 neurochemicals simultaneously from microdialysate samples in freely behaving animals. The method utilizes a 4-minute gradient to detect important neurotransmitters such as dopamine, serotonin, norepinephrine, and others. This assay is immensely important in monitoring neurotransmitters in microdialysate fractions under specific behavioral and pharmacological stimuli. The method has been further developed to detect over 17 compounds at high pressures in a 2-minute gradient or over 70 compounds with a 20-minute gradient. We have applied this method to study the effects of therapeutics for cocaine abuse. Previous work has shown that protein kinase C (PKC)-β inhibitors, enzastaurin and ruboxistaurin, have attenuated amphetamine-stimulated dopamine efflux and hyperlocomotion using in vivo microdialysis and LC-MS/MS for detection. More recently, the administration of CNS permeant PKC inhibitor 6c was also shown to attenuate amphetamine-stimulated dopamine over flow and reach the brain at robust concentrations as detected by the LC-MS/MS assay. The microdialysis-LC-MS/MS experiments have also shown similar effects of the protein kinase C inhibitors on cocaine-stimulated dopamine overflow and other monoamines. Just recently, the method has been applied to measure the dynamics of glutamate and GABA (in addition to several other neurotransmitters) before, during, and after epileptic seizures to determine novel biomarkers for epileptogenesis and ictogenesis. Lastly, we have measured the release of acetylcholine from beige fat adipocytes with our LC-MS/MS assay to help understand the importance of nicotinic acetylcholine receptor signaling in thermogenesis and the adaptation to cold temperatures.
Bio: Dr. Alexander G. Zestos is a bioanalytical chemist who uses electrochemical and chromatographic techniques for neurotransmitter analysis. He received his B.S./M.S. in Chemistry at the College of William and Mary in Williamsburg, VA. He obtained a Ph.D in Chemistry at the University of Virginia in Charlottesville, VA in 2014. He was also a postdoctoral research fellow at the University of Michigan from 2014-2017 where he was mentored by Prof. Robert T. Kennedy. Since 2017, he has been an Assistant Professor of Chemistry at American University. Prof. Zestos has published over 20 papers in prestigious journals such as Nature Medicine, ACS Applied Materials and Interfaces, Analytical Chemistry, and others with his research being highlighted in several media platforms. He has won numerous accolades and awards such as the Best Paper Award at the SPE ANTEC Conference, and was named a finalist for the 2018 and 2019 Csaba Horváth Young Scientist Award at HPLC 2018 and 2019 in Washington, D.C. and Milan, Italy respectively. Recently, he was named as an Emerging Investigator by the Royal Society of Chemistry for one of his latest publications. He serves as a Manager for the Chemical Society of Washington in addition to being the Faculty Editor of the Catalyst, a student run science publication at American University. He also serves as a guest researcher at NIST in the Biophysics Group in the Microsystems and Nanotechnology Division and at the National Institute of Mental Health in the NIH. He leads an interdisciplinary bioanalytical chemistry group that uses several electrochemical and chromatographic assays to improve neurotransmitter analysis. His research is funded through the NIH BRAIN Initiative and the National Science Foundation. He serves as a reviewer for the Center for the Scientific Review at the NIH, a referee for several journals, and will be the new editor of The Chemist through the American Institute of Chemists.
January 15, 2020
at Institute for Bioscience and Biotechnology Research (IBBR)
Speaker: Ed Sisco, NIST
Title: Utilizing Trace Drug Residues in the Forensic Analysis of Opioids
Abstract: In the world of forensic chemistry, the need to rapidly and reliably detect and identify compounds of interest is becoming increasingly complex and challenging. With the increase of opioids, novel psychoactive substances (NPSs), and homemade explosives (HMEs), what were once simple analyses are now extremely difficult given current capabilities. Over the last five years, NIST has developed a forensic chemistry research program that helps practitioners combat these ever changing landscapes by addressing measurement challenges and gaps. Drug analysis, in which detection and identification of illegal substances is completed, is an area where new analytical challenges are constantly evolving. Of major interest is the opioid epidemic, which has led to dramatic increases in case backlogs and case turnaround times as well as a renewed awareness of practitioner, law enforcement, and first responder safety. To address some of these challenges, a substantial research effort has been created aimed at addressing not only the forensic analysis of opioids but the entire analysis chain, from mail interdiction through to public health. Detection of new and novel opioids and drugs in general is a main focus area within this umbrella, where utilizing new tools, such as direct analysis in real time mass spectrometry (DART-MS), is being explored alongside quantifying opioids in operational backgrounds, measuring trace drug residue stability, and development of strategies for detecting and reporting opioids using GC-MS.
Bio: Ed is a research chemist at the National Institute of Standards and Technology within the Surface and Trace Chemical Analysis Group. His areas of active research include development of advanced mass spectrometry and ambient ionization mass spectrometry systems for forensic purposes and addressing critical forensic chemistry measurement science needs. He has ongoing projects in opioid detection, developing novel approaches for drug chemistry analysis, understanding chemical backgrounds, trace narcotics and explosives detection, and development of optimized methods for ignitable liquid residue analysis. He is a member of OSAC and ASTM.
December 18, 2019
at Institute for Bioscience and Biotechnology Research (IBBR)
Speaker: Hugh Hayes, NIST
Title: Method development for the quantitation of key analytes in environmental extracts and botanical dietary supplementation reference materials
Abstract: Unambiguous determination of polycyclic aromatic hydrocarbons (PAHs) in complex environmental matrices is imperative for accurate ecotoxicological assessment due to the differences in carcinogenic and mutagenic potential of each isomer. Traditional methods for PAH quantitation utilize GC/MS and/or LC with fluorescence detection; however, similar chromatographic retention behaviors paired with nearly identical mass fragmentation patterns requires more selective techniques for accurate PAH determination. Stop-flow fluorescence detection along with stop-flow constant energy synchronous fluorescence spectroscopy is a novel technique used to collect unique spectral characteristics of PAHs during a chromatographic separation. This talk will discuss the benefits of implementing the new multidimensional identification approach and its PAH quantitation capabilities. The second half of this presentation explores the method development for ginsenoside value assignment in Panax ginseng (ginseng) candidate Standard Reference Materials. As dietary supplement consumption continuously increases worldwide, reference materials are critical for product authenticity to ensure consumer safety and prevent economic fraud. Ginseng is grown (naturally and cultivated) in various parts of the world and there are several species resulting in products of varying types and amounts of marker compounds. Therefore, the medicinal impact may change significantly from species to species. Accurate means of identifying ginsenoside compositions and concentrations in ginseng matrices is imperative for the phytochemical determination of specific Panax species for use in dietary supplement products and research.
Bio: Dr. Hugh V. Hayes is an Office of Dietary Supplements Postdoc at NIST, where he focuses on LC/MS/MS method development for SRM certification measurements of dietary supplements. Hugh earned his Ph.D. in Analytical Chemistry under Andres D. Campiglia at the University of Central Florida (UCF) in 2018. During his time as a student, he spent two summers as a guest researcher at NIST in which he focused on developing multidimensional chromatographic methods for measuring PAHs in environmental samples. While at UCF, he also focused on developing fluorescence methods for measuring PAHs in environmental samples and the forensic analysis of textile fibers exposed to various environmental conditions. He received his B.S. in Chemistry, a M.S. in Forensic Science at Stevenson University (Villa Julie College) in 2012 and 2013 respectively, and a M.S. in Chemistry at UCF in 2015.
November 14, 2019
at ACS HQ, joint meeting with Chemical Society of Washington (CSW)
Speaker: Lane C. Sander, NIST
Title: Stationary Phase Architecture and Molecular Shape Differentiation in Liquid Chromatography
Abstract: Perhaps the single most important decision made by the analyst during the development of a new chromatographic method is the selection of an appropriate column. This decision can be informed by retention theory, prior reports, or knowledge of the retention behavior of specific columns. The gamut of commercial columns provides a profusion of choices; however, an understanding of relevant molecular interactions can help to narrow column selection. If the principal interaction mechanisms can be predicted, informed choices can be made. Retention processes in LC depend on mutual interactions between the solute, the mobile phase, and the stationary phase. The morphology of the stationary phase plays a key role in retention behavior, especially for separations of compounds with constrained molecular shape. Insight into the origins of shape selectivity has been gained through chromatographic, spectroscopic, and simulation-based studies of alkyl-modified surfaces. A compelling model of surface architecture has emerged that offers an explanation of the role played by the stationary phase in promoting shape recognition. This presentation will summarize findings related to stationary phase conformational order, obtained from spectroscopic and computational studies, for correlation with chromatographic performance.
Bio: Dr. Lane C. Sander is a Senior Scientific Advisor within the Chemical Sciences Division of the National Institute of Standards and Technology (NIST), Gaithersburg, MD. He received a B.S. in Chemistry and Ph.D in Analytical Chemistry from the University of Washington. After graduation in 1982, he came to the National Bureau of Standards (NBS), now the National Institute of Standards and Technology (NIST), as a National Research Council (NRC) Postdoctoral Research Associate. His research interests include: (1) synthesis of novel stationary phases for LC; (2) characterization of LC stationary phases by spectroscopic techniques; (3) elucidation of solute retention mechanisms; and (4) chromatographic methods development in environmental, clinical, and food science applications. Dr. Sander received the U.S. Department of Commerce Bronze Medal Award in 1990 and the Stephen Dal Nogare Award in Chromatography in 2010. Dr. Sander is the recipient of the ACS 2020 National Award in Chromatography, to be presented at the ACS Spring National Meeting in Philadelphia.
October 16, 2019
Speaker: Paulina Piotrowski, NIST
Title: Characterizing the Gut Microbiome
Abstract: The microbiome constitutes of the microbial communities that live on and within our bodies. These microbes have been implicated in numerous health problems, such as cancer, depression, and autoimmune diseases. As science strives to develop diagnostics and therapeutics based on the microbiome, we at the National Institute of Standards and Technology (NIST) aim to introduce harmonization within the microbiome measurement community. As such we have engaged in efforts to develop methodologies to characterize bacterial cultures of microbes commonly found in probiotics for small molecule metabolites through solid phase microextraction (SPME) coupled to comprehensive two dimensional gas chromatography time-of-flight mass spectrometry (GCxGC-TOFMS). These efforts, in conjunction to metabolite measurements in fecal samples, are preliminary steps in the development of a microbiome reference material.
Bio: Dr. Paulina Piotrowski is a NRC postdoctoral associate at the National Institute of Standards and Technology. At NIST, Paulina develops omics-based measurement techniques for the microbiome, complex microbial systems, and endocrine disruptors. Prior to her postdoctoral studies, Paulina completed her PhD in chemistry and biogeochemistry under Frank Dorman at Penn State University studying fingerprinting mechanisms of hydraulic fracturing operations. Paulina’s research interests focus on applications of two-dimensional chromatography to omics and non-targeted analyses.
Annual Poster Session & Vendor Exhibition
September 18, 2019 at Bethesda North Marriott Conference Center, 5701 Marinelli Rd, Rockville, MD
Congratulations to Jie Li from University of Maryland for winning the Guiochon Student Award for his poster titled “Metabolic Characterization of Cell Clones in X. laevis Embryos by HPLC-MS”.
May 15, 2019 at USP
Speaker: Horacio Pappa (USP) and Fadi Alkhateeb (Waters)
Title: Method Lifecycle Management
Abstract: The pharmaceutical industry relies on data generated by analytical methods for many critical decisions. Traditional approaches consist of distinct exercises – method development, validation, transfer, verification – with limited understanding of the effect of variation on method performance.
The Method Lifecycle Management (MLCM) approach is a holistic approach encompassing all activities from method development to validation, routine use, change control and retirement of the method. This enhanced approach improves the method understanding and performance, leads to fewer out-of-specifications results (OOS), facilitates method transfer and has the potential to lessen the regulatory burden.
This seminar, presented by Dr. Horacio Pappa, Director of General Chapters, United States Pharmacopeia, and Dr. Fadi Alkhateeb, Senior Scientist, Waters Corporation will describe the method lifecycle management key concepts, its benefits to drug manufacturers and patients, and the current thinking of the USP. Case studies will showcase how software assisted analytical quality by design can be implemented to increase method robustness and minimize risk.
Horacio Pappa has been with USP since 2003. He is currently the Director of the General Chapters Department, Science division of the USP. He provides scientific leadership to a team of scientific liaisons responsible for the activities of six different expert committees that cover the majority of the USP General Chapters. Horacio earned his Ph.D. in Pharmaceutical Chemistry from the University of Buenos Aires. He has authored many publications and peer-reviewed articles and is a frequent speaker and instructor on topics related to Chromatography and Validation. Prior to joining USP, he worked in the pharmaceutical industry in QA/QC. Horacio held the position of Assistant Professor of Quality Control in the Faculty of Pharmacy at Buenos Aires University, and Executive Secretary of the Argentine Pharmacopeia in the period 1997-2001. He is a Quality Engineer certified by the American Society for Quality.
Fadi Alkhateeb joined Waters Corporation in 2017 as a senior separation scientist. He has had experience with many techniques in the field of separation and extraction science including HPLC, UPLC, SFC, GC SFE and ASE. He obtained his Ph.D. from the University of Calgary where he focused on developing novel rapid sample preparation and separation techniques for the analysis of a wide variety of analytes primarily focusing on pharmaceuticals. He strengthened his experience and gained hands on expertise with several other techniques including DSC and adsorption as a postdoctoral fellow at Alberta Sulphur Research.
Monday, April 15, 2019 at Shimadzu Training Center, Columbia, MD
Speaker: Catherine Fenselau, Univ. of Maryland
Title: Biological Mass Spectrometry: Observations on its Evolution
Abstract: Aspirations, advances in instrumentation, successful applications and Nobel prizes will be reviewed as part of the evolution of biological mass spectrometry, with illustrations from the speaker’s laboratory.
Bio: Catherine Fenselau was one of the first trained mass spectrometrists to join the faculty of an American medical school (Johns Hopkins), where she was given the job description to “exploit mass spectrometry in biomedical research.” In early work she pioneered MS investigations of intact microorganisms, novel reactivities of glucuronic acid and glutathione drug conjugates, and benchmark analyses of zinc fingers and metallothioneins. Her laboratory reported early determinations of gas phase peptide basicities including the first measurement of arginine’s proton affinity, target capture in ion molecule reactions, and the stability of α-helices and β-sheets in the gas phase. Her group introduced enzyme-catalyzed O-18 labeling, Asp-selective acid cleavage and the use of nanoparticle pellicles into proteomic workflows, and since 2000 they have exploited proteomic strategies to investigate mechanisms of tumor resistance to chemotherapy and immunotherapy.
Her contributions to mass spectrometry and its biomedical applications have been recognized by awards from the American Chemical Society, the International Mass Spectrometry Foundation, American Society for Mass Spectrometry, American Society for Pharmacology and Experimental Therapeutics, Human Proteome Organization, The Pittsburg Conference and others. She was associate editor of Analytical Chemistry for 26 years and the founding editor of Biomedical Mass Spectrometry (now Journal of Mass Spectrometry). She is a past president of ASMS, founding president of US HUPO, and was senior vice president of international HUPO. She has been an active supporter of the Washington Baltimore Mass Spectrometry Discussion Group for more than 50 years. She has published more than 400 peer reviewed research papers, book chapters and articles, and trained about one hundred and fifty undergraduates, graduate students and post-doctoral fellows in her laboratories.
Fenselau grew up in Nebraska, received her A.B. from Bryn Mawr College, and earned a Ph.D. from Stanford University. She was promoted to professor while a faculty member at the Johns Hopkins University School of Medicine, served as department chair at UMBC, and is presently a Distinguished University Professor emerita at the University of Maryland.
Wednesday, March 13, 2019 at USP
Speaker: William Craig Byrdwell, Beltsville Human Nutrition Research Center, USDA
Title: Comprehensive Multi-Dimensional Chromatography with Quadruple Parallel Mass Spectrometry for Fat-Soluble Vitamins and Triacylglycerols
Abstract: Some lipid samples are so complex that they require unusually rigorous methods for separation and analysis. Fats (solid) and oils (liquid) are composed of triacylglycerols, TAGs, and some oils include naturally-occurring trans fats and oils that require special treatment to separate them from normal (cis) fats and oils. For these samples, we have used a two-dimensional separation technique (2D-LC) in which TAGs were first separated by size and degree of unsaturation (saturated, mono-unsaturated, polyunsaturated), and then further separated by type of unsaturation (cis versus trans double bonds). We employed non-aqueous reversed-phase (NARP) HPLC as the first-dimension (1D) separation coupled to a lab-made UHPLC silver-ion column as the second-dimension (2D) separation. We used two mass spectrometers to monitor the 1D, and two more mass spectrometers to monitor the 2D, for LC1MS2 x LC1MS2 = LC2MS4. We used combinations of atmospheric pressure chemical ionization (APCI) mass spectrometry (MS), atmospheric pressure photoionization (APPI) MS, and electrospray ionization (ESI) MS. Cow’s milk is even more complex, and includes a wide range of short-chain (C4-C10) fatty acids not present in most edible oils. TAGs with those fatty acids present unique challenges for analysis, because there is extensive overlap between numerous isomers. Thus, an even more detailed analysis is required, that includes a third separation to distinguish short-chain TAG isomers. All three separations are combined into one analysis that provides a better separation than has previously been possible. A second 2D separation is performed in parallel with the silver-ion chromatography first 2D separation, both in series with NARP-HPLC as the first dimension. ESI-MS is used in parallel with APCI-MS ( for LC1MS2) to monitor the first-dimension NARP-HPLC, while APPI-MS monitored the Ag-ion UHPLC (LC1MS1) and ESI-MS monitored UHPLC using a C4 or C8 column (LC1MS1), to produce LC3MS4 = LC1MS2 x (LC1MS1 + LC1MS1).
Bio: Dr. Byrdwell is a Research Chemist at the Food Composition and Methods Development Laboratory, in the Beltsville Human Nutrition Research Center, which is part of the Agricultural Research Service, the research branch of the U.S. Department of Agriculture. Dr. Byrdwell received his undergraduate and graduate degrees from the University of Louisville, writing his dissertation on identification of the ‘Unknown Phospholipid’ in the human eye lens, and quantification of fluorophores in normal and cataractous lenses. Dr. Byrdwell took a position at the USDA’s National Center for Agricultural Utilization Research, to work on analysis of triacylglycerols (TAGs) using HPLC with APCI-MS. Then, Dr. Byrdwell took a position at Florida Atlantic University, where he routinely employed dual mass spectrometers, in parallel, using both APCI-MS and ESI-MS. He re-joined ARS in 2005, and took on quantification of Vitamin D and TAGs. Recently, Dr. Byrdwell has been analyzing fat-soluble vitamins and TAGs using triple- and quadruple- parallel mass spectrometry approaches, combining three or four mass spectrometers employing complementary ionization methods (APCI-MS, APPI-MS, and ESI-MS) coupled to one, two, or three liquid chromatographs in LCx/MSy techniques. Dr. Byrdwell has published >60 peer-reviewed articles, 10 book chapters, and been Editor/Co-Editor of three AOCS Press books. He is on the editorial advisory board of Lipids, is the Lipidomics Associate Editor for The Lipid Library (www.LipidLibrary.com), and maintains numerous websites, including http://www.LipidAcademy.com. Dr. Byrdwell received the 2012 American Oil Chemists’ Society (AOCS) Analytical Division Herbert J. Dutton Award, presented the 2013 Society of Chemical Industry Julius Lewkowitsch Award Lecture in Ghent, Belgium, and in May 2019 will receive the Fellow of the AOCS Award.
Wednesday, February 27, 2019 at USP
Speaker: Erika Portero, University of Maryland College Park
Title: Capillary Electrophoresis Mass Spectrometry for Microanalysis of Proteins and Metabolites in the Developing Vertebrate Embryo
Abstract: Chemical analysis of single-cells provides a better understanding of fundamental biological processes during cell differentiation and development. Recent advances in mass spectrometry (MS) enable exceptional sensitivity for the interrogation of metabolic activity in limited amounts of samples. However, specialized sampling techniques are required to conduct metabolomic studies at the single-cell level, where the limited sample volume and fast-changing metabolome present challenges. In this presentation, we will discuss the development and validation of single-cell mass spectrometry technologies to enable the analysis of single embryonic cells using microprobe sampling. This minimally intrusive procedure is compatible with the normal development of the live vertebrate frog embryo of Xenopus laevis, a powerful model in cell and developmental biology. Additionally, microprobe sampling and capillary electrophoresis (CE) electrospray ionization (ESI) MS have enabled the detection of metabolic activity between multiple cells from the X. laevis embryo, which are fated to give rise to distinct tissues and organs. Furthermore, this technology enabled the simultaneous cationic and anionic analysis of metabolites from a single identified cell, extending the detectable coverage of the cell’s metabolome. Altogether, this new information provides further insights into active metabolism during early development of the vertebrate embryo.
Bio: Erika Portero received her B.S. degree in Chemistry from Drew University and M.S. in Chemistry from the George Washington University. Her current research under Prof. Peter Nemes’ mentorship at University of Maryland, College Park develops next-generation mass spectrometry technologies to enable the analysis of metabolites in single differentiating cells during early embryogenesis. Ms. Portero has disseminated her research via 6 peer-reviewed publications and a number of presentations at national and international conferences. Ms. Portero is recipient of the 2017 Graduate Scholar Award by the COSMOS Club Foundation and a 2017 Helmsley Fellowship by the Cold Spring Harbor Laboratory.
Ms. Portero received an honorable mention for her poster at the 2016 WCDG Poster Session.
Wednesday, January 16, 2019 at USP
Speaker: James P. Grinias, Rowan University
Title: Increasing Throughput for Pharmaceutical and Bioanalytical Methods Using UHPLC
Abstract: One of today’s most widely used analytical tools is ultra-high pressure liquid chromatography (UHPLC). Compared to traditional HPLC techniques, UHPLC enables higher chromatographic efficiency and reduced method times, but requires two- to four-fold increases in system pressure. With this increased pressure, separation performance can suffer due to viscous friction effects across the length and radius of the column. In this presentation, the impact of thermal broadening on chromatographic performance will be described. Additionally, potential solutions for minimizing efficiency loss based on column selection and the instrument’s thermal settings will be explored. The use of these strategies was employed for two high-throughput UHPLC applications: (1) analysis of neurotransmitters in dialysate samples, and (2) content and impurity analysis in over-the-counter analgesics.
Bio: Dr. James P. Grinias is an Assistant Professor in the Department of Chemistry and Biochemistry at Rowan University. He received in B.S. in Chemistry from Eastern Michigan University, his Ph.D. in Analytical Chemistry from the University of North Carolina at Chapel Hill under the direction of Jim Jorgenson, and was an NIH NRSA Postdoctoral Research Fellow at the University of Michigan under the direction of Bob Kennedy. He is the recipient of the HPLC 2013 Csaba Horváth Young Scientist Award, was the 2017 Young Alumnus of the Year at Eastern Michigan University, and was recently named one of the Top 40 Under 40 analytical chemists in the world by The Analytical Scientist.
James’ research focuses on the fundamentals of separations in capillary and microfluidic columns. These techniques are also applied to help enhance analytical methods in the neuroscience, molecular physiology, and pharmaceutical fields. His work has led to nearly 20 peer-reviewed publications and dozens of presentations at national and international conferences.
In addition to his research interests, Dr. Grinias is also interested in improving the educational experience of students in undergraduate analytical chemistry coursework. Specifically, he focuses on finding new ways of implementing new educational technologies to help enhance the instruction of chemical instrumentation and analytical techniques.
James has previously served the professional community as the Assistant Program Chair for the 2012 Southeastern Regional Meeting of the ACS, through the HPLC 2016 & 2018 Symposium Organizing Committees, and by co-editing a special issue of the Journal of Chromatography A focused on chromatography and electrophoresis. In addition, he is a current executive committee member of the Chromatography Forum of Delaware Valley and regularly serves as a reviewer for several different separations-related journals.
Wednesday, December 12, 2018 at USP
Speaker: Perry Wang, FDA
Title: Identification and Quantitation of 16 PAHs in Tattoo Inks by UHPLC-APPI-MS/MS with Scheduled Selected Reaction Monitoring
Abstract: A method using ultrahigh performance liquid chromatography with APPI tandem mass spectrometry (UHPLC-APPI-MS/MS) with a fast sample preparation procedure was developed to determine the 16 U.S. EPA priority pollutant polycyclic aromatic hydrocarbons (PAHs) in tattoo inks. Scheduled selected reaction monitoring (sSRM) was applied to increase the sensitivity. Sixteen corresponding deuterated PAHs were used as internal standards to compensate for recovery and matrix effects. The method was validated and successfully applied to survey 78 commercial tattoo ink products. The coefficient of determination (r2) is greater than 0.99 for all sixteen analytes and the recovery ranged from 92.5% to 106% at three spiked levels. Ten PAHs were found in nine out of the fourteen black tattoo inks with concentrations ranging from 0.25 to 17 μg/g (ppm). Only three PAHs including fluoranthene, phenanthrene, and benzo[b]fluoranthene were found in twenty out of the sixty-four colored tattoo inks within a range of 0.10 to 8.5 μg/g. To date, this is the first UHPLC-APPI-MS/MS method using sSRM and stable isotopically labeled internal standards to simultaneously determine 16 PAHs in tattoo inks.
Bio: Dr. Perry G. Wang is a research chemist in the Office of Regulatory Science, CFSAN at US FDA. Prior to joining the FDA, Dr. Wang worked in the pharmaceutical and medical-device industries. His expertise in the pharmaceutical field focuses on high throughput drug analysis and validation by LC-MS/MS. His current research at the FDA includes developing analytical methods for chemical constituents and contaminants in cosmetics and personal care products by GC-MS/MS and LC-MS/MS. He received his Ph.D. degree at Oregon State University.
Wednesday, November 14, 2018 at USP
Student Speaker: 2018 Student Poster Winner, Lucas Kimerer, University of Virginia
Featured Speaker: Andre Striegel, National Institute of Standards and Technology (NIST)
Title: Multi-detector Hydrodynamic Chromatography of Colloids and Polymers
Abstract: Hydrodynamic chromatography (HDC) is a liquid chromatographic technique that separates analytes on the basis of their size in solution. HDC can be performed in an open tube (capillary) or in a packed column. In the latter case, the column packing material should be inert and either non-porous or of a pore size substantially smaller than the solution size of the analyte. The “holy grail” of particle sizing can be regarded as the accurate and precise determination of the particle size averages and distribution of a sample that is disperse in size, shape, structure, and chemistry, along with the determination of the averages, distributions, and mutual-interdependences of all these properties. While no single analytical technique will be able to provide all of these for every sample type, multi-detector HDC has demonstrated the ability to measure a number of these properties for a variety of samples. Advantages of HDC, vis-à-vis size-exclusion chromatography or flow field-flow fractionation, include its being gentler than the former (thus minimizing the possibility of on-column, flow-induced analyte degradation) and more affordable and easily implementable than the latter. Using examples from the recent literature, this talk will focus on the use of packed-column HDC for characterizing colloidal particle and ultra-high molar mass (M >> 1 million g/mol) polymer size, shape, molar mass, and structure, by combining the information obtained from detection methods such as refractometry, viscometry, and light scattering (both dynamic and static).
Bio: André Striegel received his Ph.D. in Analytical Chemistry in 1996 and his BS in Chemistry in 1991, both from the University of New Orleans. From 1996 to 1998 he performed postdoctoral research for the U.S. Department of Agriculture, at the National Center for Agricultural Utilization Research. For the next six years he worked for Solutia (now Eastman Chemical), at their Springfield, Massachusetts R&D center, first in the Physical & Analytical Sciences Center and then in Films R&D, achieving the rank of Research Specialist. From 2004 to 2011 he was Assistant Professor of both Analytical and Materials Chemistry in the Department of Chemistry & Biochemistry at Florida State University (FSU). In September 2011 he joined the National Institute of Standards & Technology (NIST), where he is a Research Chemist in the Chemical Sciences Division of the Material Measurement Laboratory. His research interests are in the area of polymer characterization, in particular applying separation science to determining structure-property relations of complex macromolecules, and in the fundamental aspects of separation and detection methods. He has received the Eli Lilly Analytical Chemistry Grantee Award, the inaugural ACS-DAC Award for Young Investigators in Separation Science, and an FSU First Year Assistant Professor Award. He also received a Solutia Technical Achievement Award for his research in private industry, and served as inaugural Professor in Residence for Preservation Research and Testing at the U.S. Library of Congress. He is the author of 80 peer-reviewed publications, lead co-author of the second edition of “Modern Size-Exclusion Liquid Chromatography” and editor of the book “Multiple Detection in Size-Exclusion Chromatography.” From 2010 to 2015, he was associate editor of the Encyclopedia of Analytical Chemistry, and is a member of the editorial board of various polymer science and analytical chemistry journals. In 2015, he became editor of Chromatographia.
Thursday, October 11, 2018 at Marvel Hall at ACS HQ
Joint meeting with Chemical Society of Washington (CSW)
Speaker: Melissa Phillips, National Institute of Standards and Technology (NIST)
Title: Application of Chromatography in the Development of Reference Materials for Foods and Dietary Supplements
Abstract: Since 1990, the National Institute of Standards and Technology (NIST) has provided matrix-based food reference materials intended to support measurements for nutrition labelling. These reference materials are used in method validation and quality control, which requires NIST to utilize higher order approaches for obtaining true results. The characterization of these reference materials was enabled through the development and use of novel separations of organic nutrients, such as fatty acids, water- and fat-soluble vitamins, and carotenoids. NIST also has a long-standing collaboration with the National Institutes of Health (NIH) Office of Dietary Supplements’ (ODS) Analytical Methods and Reference Materials (AMRM) Program. NIST supports the goals of the AMRM program by characterizing matrix-based dietary supplement reference materials for use in quality control, which often relies on development of unique extraction and separation approaches for each class of marker compounds in numerous botanical matrices. Most recently, NIST began expanding efforts in food safety beyond toxic metal measurements to include development of reference materials for arsenic speciation and mycotoxins and research into harmonization materials for protein food allergens and material authenticity. Each of these new areas requires development of new extraction, separation, and detection approaches. This presentation will highlight the use of separations to characterize various reference materials for dietary supplements, food nutrition, and food safety at NIST.
Bio: Melissa M. Phillips has been a research chemist in the Chemical Sciences Division at the National Institute of Standards and Technology (NIST) since 2008. She is involved in the certification efforts for food and dietary supplement Standard Reference Materials (SRMs) and is a coordinator of the Dietary Supplement Laboratory Quality Assurance Program (DSQAP), the Health Assessment Measurements Quality Assurance Program (HAMQAP), the Total Nutrients Quality Assurance Program (TNQAP), and the Food Reference Materials Program. Her interests include development of new analytical methods for the determination of marker compounds, vitamins, and contaminants in foods and dietary supplements, and improving the measurement capabilities of the food and dietary supplement communities using reference materials and quality assurance programs. Melissa obtained a B.S. in Chemistry, an M.S. in Forensic Chemistry, and a Ph.D. in Analytical Chemistry from Michigan State University. Melissa is a member of the AOAC INTERNATIONAL Official Methods Board and is a fellow of AOAC INTERNATIONAL.
Annual Poster Session & Vendor Exhibition
September 19, 2018 6:00PM-8:00PM
Bethesda North Marriott Conference Center
5701 Marinelli Road, North Bethesda, MD 20852
Congratulations to our student poster winner Lucas Kimerer (University of Virginia). He will receive a travel award to attend HPLC 2019 in Milan, Italy, and he will give short oral presentation at a future WCDG meeting.
May 29 to August 2, 2018 at Marriott Wardman Park, Washington, DC
WCDG sponsored the musical entertainment for the opening ceremony and reception. During the opening ceremony, The Conservatory Classic Jazz Band delighted conference attendees with jazz numbers inspired by various regions around the world to celebrate the international community of separation scientists gathered for HPLC 2018. During the evening reception, attendees were serenaded with a vocalist and guitarist. WCDG also congratulates Associate Professor Peter Nemes of UMD for receiving the Georges Guiochon Faculty Award.
Wednesday, May 16, 2018 at USP
Speaker: Ira Lurie, George Washington University
Title: Recent Developments in the Analysis of Emerging Drugs
Abstract: The use of emerging drugs created to circumvent the controlled substances laws has greatly increased over the last few years. “Designer drugs” are created by slightly modifying the chemical structure of a controlled substance. The use of these drugs has led to many deaths in the USA, especially for the abuse of fentanyl related compounds. GC-MS with electron ionization is the method of choice employed for the screening and confirmation of these solutes. LC-MS with electrospray ionization, is most commonly employed by some laboratories as an additional confirmatory method. The analysis of positional and stereoisomers can be particularly difficult using the above techniques, due to similarity in MS fragmentation, and scarcity of information in EI fragmentation for certain classes. The analysis of emerging drugs is complicated because many of them do not give a molecular ion using GC-MS with electron ionization. Therefore a chromatographic separation and additional detection techniques become of upmost importance for the identification of emerging drug. This presentation will demonstrate the utility of UHPSFC for the analysis of emerging drugs, especially for positional isomers and diastereomers. The use of two UHPSFC columns in tandem to increase overall resolution will be presented. In addition the utility of UV detection in both the liquid and gas phase and cold EI to aid in the identification of emerging drugs will be discussed. Finally the use of multi-dimensional chromatography to reduce uncertainty of retention time measurements will be detailed.
Bio: Ira Lurie a research professor at George Washington University received his BA in chemistry from Queens College, his MS in chemistry from Rutgers University and his PhD. in chemistry from University of Amsterdam under the guidance of Professor Peter Schoenmakers. Dr. Lurie served almost 40 years as both a forensic chemist and senior research chemist with the Drug Enforcement Administration, where he last served as the agency’s expert in liquid phase separations. He is the author of over 70 publications including several book chapters and a co-edited book entitled HPLC in Forensic Chemistry. Professor Lurie is the winner of the 2015 Paul Kirk award, the highest form of recognition one could receive from the criminalistics section of the American Academy of Forensic Sciences.
Monday, April 16, 2018 at Shimadzu Training Center
Speaker: Melanie Downs, University of Nebraska-Lincoln
Title: MS Analysis of Food Allergens: Just Another Proteomics Application or a Whole New Kettle of Fis
Abstract: Undeclared food allergens in packaged foods represent a significant health risk for food-allergic individuals and are the leading cause of food recalls. Food manufacturers are required to label ingredients derived from food allergens and to have controls in place to prevent allergen cross-contact. Allergen control validations and risk assessments for effective allergen management plans often require supporting analytical data. As food allergens are proteins, mass spectrometry seems like an obvious analytical tool to use for detection and quantification. The capabilities of MS instruments, combined with the established track record of protein detection and quantification in clinical systems, make quantifying proteins in foods using proteomics techniques seem like a natural fit. However, the unique challenges that come along with the analysis food proteins make the path towards validated analytical methods far from smooth. In comparison to clinical samples, food proteins are exposed to a wide array of harsh conditions during various stages of processing, which leads to a number of analytical hurdles. If these challenges can be overcome, however, MS methods have the potential to fill critical gaps in our ability to analyze food allergens and ultimately protect food-allergic consumers.
Bio: Melanie Downs is an Assistant Professor affiliated with the Food Allergy Research & Resource Program in the Department of Food Science and Technology at the University of Nebraska-Lincoln. Her research primarily focuses on the proteomics of allergenic foods, including the identification, characterization, and analytical detection of food allergens using mass spectrometry. In addition to research, Dr. Downs also works with the food industry on a number of aspects of food allergen management, including development of allergen control programs, validation of allergen preventive controls, and application of food allergen detection methods.
March 14, 2018 at USP
Student Speaker: Sarah Gao, 2017 Student Poster Winner
Featured Speaker: Mark R. Schure, Kroungold Analytical, Inc., Blue Bell, PA
Title: Multidimensional separations in three and higher dimensions
Abstract: Two-dimensional liquid chromatography is fast becoming an accepted technique in the analysis of complex molecules from biological, environmental, pharmaceutical and industrial sources. As these techniques mature we have been asking questions which look into higher dimensionality separations. These include three and higher dimensions. To discuss these types of separations, one has to have a measure of how well these separations work. Orthogonality metrics (OMs) for three and higher dimensional separations are proposed as extensions of previously developed OMs, which were used to evaluate the zone utilization of two-dimensional (2D) separations. These OMs include correlation coefficients, (fractal) dimensionality, information theory metrics and convex-hull metrics. In a number of these cases, lower dimensional subspace metrics exist and can be readily calculated. The metrics are used to interpret previously generated experimental data. Experimental datasets are derived from Gilar’s peptide data, now modified to be three dimensional (3D), and a comprehensive 3D chromatogram from Moore and Jorgenson. The Moore and Jorgenson chromatogram, which has 25 identifiable 3D volume elements or peaks, displayed good orthogonality values over all dimensions. However, OMs based on discretization of the 3D space changed substantially with changes in binning parameters. The Gilar data, which in a previous study produced 21 2D datasets by the pairing of 7 one-dimensional separations, was reinterpreted to produce 35 3D datasets. These datasets show a number of interesting properties, one of which is that geometric and harmonic means of lower dimensional subspace (i.e., 2D) OMs correlate well with the higher dimensional (i.e., 3D) OMs. This talk will use a minimum number of equations and will highlight the experimental difficulties which crop up with higher dimensional separations. We will discuss the extent to which 3D separations will yield better results than 2D separations and how simple separations in the first dimension, such as trapping, can perform critical fractionation (class separations) in a small amount of time.
Bio: Mark Schure has worked in separation science for over 35 years in industry and academics. Over a 28 year period he has worked for Digital Equipment Corporation, the Rohm and Haas Company and The Dow Chemical Company. Dr. Schure has been an Adjunct Professor in the Department of Chemical and Biomolecular Engineering at the University of Delaware for over 20 years. He has published over 115 papers, has 4 patents and recently edited the book “Multidimensional Liquid Chromatography.” His scientific interests include the fundamental separation science of complex molecules, polymers and colloids, colloid chemistry and materials science and all aspects of solving large-scale chemical and physical problems with computers. His contributions to separation science include detailed theory, simulations and experimental investigations in the areas of 2D chromatography, chromatographic stationary phase calculations and mechanism, capillary electrophoresis, electrochromatography and field-flow fractionation. He has received many awards including the Arthur Doolittle award from the American Chemical Society, the Northeastern University Distinguished Alumni Lecture award, the Douglas Leng award from The Dow Chemical Company, the Eastern Analytical Symposium award in separation science and the L. S. Palmer award from the Minnesota Chromatography Forum. In 2015 he received the Stephen Dal Nogare award and the Uwe D. Neue award.
February 15, 2018 at USP
Student Speaker: Hangu Nam, 2017 Student Poster Winner
Featured Speaker: Chunlei Wang, MedImmune
Title: Efficient peak identification for hydrophobic interaction chromatographic separations by 2DLC/MS
Abstract: With the recent advances of 2DLC hardware, software and column technologies, there is a fast growth in 2DLC applications reported in literature. In addition to combining two separation modes to fully resolve complex mixtures, 2DLC can also be used as a desalting technique to hyphen separations that use non-volatile additives to MS detectors. In this presentation, we will focus on peak identification by 2DLC/MS for hydrophobic interaction chromatography separations of antibody drug conjugates and bispecific IgGs. In addition to simple de-salting, we will demonstrate how additional structure details can be revealed by introducing an online reduction step between two dimensions.
Bio: Dr. Chunlei Wang earned his PhD from the University of Texas at Arlington in 2009 in the lab of Professor Daniel Armstrong. He has eight years-experience in developing and applying analytical solutions to support the development of small molecular drugs, peptides, and biologics in Eli Lilly, Bristol-Myers Squibb, and currently Medimmune. His research interests include chiral separation, supercritical fluid chromatography, chemometrics, protein chromatography, 2D HPLC, and automation.
January 17, 2018 at USP
Speaker: David Muddiman, North Carolina State University
Title: Innovations in Mass Spectrometry Platform Technologies for Epithelial Ovarian Cancer Research and High Throughput Screening
Abstract: Mass spectrometry offers the most robust platform to discover and characterize new diagnostic, prognostic, and therapeutic biomarkers for ovarian cancer across all molecular classes. Moreover, a systems biology approach will allow the underlying biology of ovarian cancer to be understood. This presentation will discuss the challenges specific to the study of epithelial ovarian cancer (EOC) in humans and how these challenges have directed our thinking, in terms of the development of model organisms and mass spectrometry-based bioanalytical strategies. First, to augment the human model, we developed the domestic hen model of spontaneous EOC, which allowed us to longitudinally sample the rapid onset and progression of the disease in a controlled environment. Second, we developed bioanalytical tools to characterize structurally challenging analytes that are critical to a systems-level analysis. To increase the electrospray response of N-linked glycans, perform stable-isotope relative quantification, and semi-automated data analysis, we synthesized novel hydrophobic tagging reagents (INLIGHTTM). Furthermore, we developed a novel ionization technique for tissue imaging of lipids and metabolites. This unique model organism has and continues to provide new insights into the biology of ovarian cancer; combined with other –OMICS data obtained through these novel bioanalytical approaches, we will understand the origin of ovarian cancer and ultimately translate that knowledge to humans. Novel HTS strategies will also will also be presented.
Bio: David C. Muddiman is the Jacob and Betty Belin Distinguished Professor of Chemistry and Founder and Director of the W.M. Keck FTMS Laboratory for Human Health Research at North Carolina State University in Raleigh, NC. Prior to moving his research group to North Carolina State University in 2006, David was a Professor of Biochemistry and Molecular Biology and Founder and Director of the Proteomics Research Center at the Mayo Clinic College of Medicine in Rochester, MN. Prior to this appointment, David was an Associate Professor of Chemistry at Virginia Commonwealth University. It was there that he began his professional career as an assistant professor with an adjunct appointment in the Department of Biochemistry and Molecular Biophysics and as a member of the Massey Cancer Center in 1997. These academic appointments followed a postdoctoral fellowship at Pacific Northwest National Laboratory in the Environmental Molecular Sciences Laboratory under Richard D. Smith from 1995-1997. David was born in Long Beach, CA in 1967 but spent most of his formative years in a small town in Pennsylvania. David received his B.S. in chemistry from Gannon University (Erie, PA) in 1990 and his Ph.D. in Analytical Chemistry from the University of Pittsburgh in 1995 under the auspices of David M. Hercules. Dr. Muddiman is Editor of Analytical and Biological Chemistry and Associate Editor of the Encyclopedia of Analytical Chemistry as well as on the Editorial Advisory Board of Mass Spectrometry Reviews, Molecular and Cellular Proteomics, Rapid Communications in Mass Spectrometry, and the Journal of Chromatography B. He also serves on the advisory board of the NIH Funded Complex Carbohydrate Research Center, University of Georgia and the Yale/NIDA Neuroproteomics Center, Yale University. Dr. Muddiman has served as a member of the ASMS Board of Directors and Treasurer of US-HUPO; he is currently the President of US HUPO. His group has presented over 500 invited lectures and presentations at national and international meetings including 20 plenary/keynote lectures. His group has published over 250 peer-reviewed papers and has received four US patents. He is the recipient of the 2015 ACS Award in Chemical Instrumentation, 2010 Biemann Medal (American Society for Mass Spectrometry), 2009 NCSU Alumni Outstanding Research Award, the 2004 ACS Arthur F. Findeis Award, the 1999 American Society for Mass Spectrometry Research Award, and the 1990-1991 Safford Award for Excellence in Teaching (University of Pittsburgh). Dr. Muddiman’s research is at the intersection of innovative mass spectrometry technologies, systems biology, and model organisms for diseases and bioenergy, and is funded by National Institutes of Health, National Science Foundation, Department of Energy, and US Department of Agriculture.
December 6, 2017 at USP
Speaker: Joseph Zaia, Boston University
Title: How to assign protein site-specific glycosylation
Abstract: Glycosylation modulates protein physico-chemical properties central to folding and binding partner interactions. Protein site-specific glycosylation that occurs in in the endoplasmic reticulum and Golgi apparatus is heterogeneous as a rule. In addition, the glycans present at a given protein site vary spatially and temporally. Thus, glycosylation depends on the cell growth environment. For glycosylated biologic drugs, this means that the glycosylation structure of the active molecular form is often not known. Further, it means that glycosylation must analyzed carefully to insure that drug molecules meet release criteria for function and stability. Because the masses of complex glycopeptides cannot be predicted from genomic information, standard proteomics database search workflows do not suffice for defining the glycan structures that exist at a given protein site. In fact, glycan heterogeneity multiplies the number molecular forms at each glycosylation site by more than 10-fold. In order to assign protein site-specific glycosylation, it is necessary to use tailored separations, MS-based data acquisition, and bioinformatics methods. This presentation will summarize the state-of-the art for assignment of protein site-specific glycosylation and the impacts of (i) separation method for reversed phase chromatography versus capillary electrophoresis for on-line analysis of glycoproteins, (ii) analyzer speed and resolution and (iii) sample complexity. The presentation will demonstrate analyses of glycoprotein samples of increasing complexity. Examples will include influenza A virus hemagglutinin, proteoglycans and glycoproteins from mammalian organ tissue.
November 15, 2017 at USP
Speaker: Gary Mallard, NIST
Title: Automating GC/MS Analysis – Or at least making it a little easier
Abstract: AMDIS (Automated Mass spectral Deconvolution and Identification System) is a powerful tool that was originally developed for analysis of GC/MS data files for a set of target compounds without the user needing to see the data. To do this the program makes use of the inherent multichannel data that is extracted by the GC/MS. The talk will discuss the methodology of AMDIS operation – both in the mode of finding target compounds and in the broader context of aiding in the analysis of complex data files where non-target analysis is desired. Emphasis will be place on the ability of AMDIS to provide not only spectral matching, but also quality parameters that allow the user to better assess the uncertainty associated with the GC/MS data. Examples will be taken from the area of chemical weapons, opioid analysis and essential oil analysis.
Bio: Gary was at the National Institute of Standards and Technology (NIST) for 31 years, working in fire and chemical kinetics research, chemical kinetics, mass spectrometric and retention index databases. He was the first editor of the NIST Chemistry Webbook and the group leader for the Chemical Reference Data Group which produced both the NIST Chemistry Webbook and the NIST Mass Spectral Database. He was one of the team lead by Steve Stein who worked on the development of AMDIS and developed extensive training material for AMDIS. After retiring from NIST he went to the Organization for the Prohibition of Chemical Weapons (OPCW) as head of the OPCW laboratory. After three and a half years at the OPCW he again retired and is now a consultant working with NIST on methods to improve AMDIS, the NIST Mass Spectral Database and tools for forensic analysis as well as other clients on GC/MS analysis.
October 18, 2017
6:00 pm – 8:00 pm at ACS Headquarters, Joint meeting with CSW
Speaker: John Hanover, Chief, Laboratory of Cell and Molecular Biology, NIDDK, NIH, Bethesda, MD
Title: A Little Sugar goes a Long Way: O-GlcNAc in human disease
Abstract: O-GlcNAc is a single monosaccharide modification of nuclear and cytoplasmic proteins. O-GlcNAcylation is driven by the nutrient-sensing hexosamine biosynthetic pathway and may rival protein phosphorylation in its abundant and impact on cellular signaling. Emerging evidence suggests that this modification may also have far-reaching consequences for chronic human diseases including cancer, diabetes and neurodegeneration. Findings in C. elegans, Drosophila and mouse model systems have demonstrated that the dynamic turnover of O-GlcNAc is critical for maintaining levels of key transcriptional regulators responsible for neurodevelopment fate decisions. In addition, pathways of autophagy and proteasomal degradation depend upon a transcriptional network dependent upon O-GlcNAc cycling. Like the quality control system in the endoplasmic reticulum which uses a “mannose-timer” to monitor protein folding, we propose that cytoplasmic proteostasis uses an “O-GlcNAc timer” that helps to regulate the lifetime and fate of cytosolic proteins. Worm, fly and mouse models harboring O-GlcNAc transferase and O-GlcNAcase knockout alleles have helped define the role O-GlcNAc plays in development and age-associated neurodegenerative disease. We anticipate that brain-selective knockout mouse models will be an important tool for understanding the role of O-GlcNAc in the physiology of the brain and its susceptibility to neurodegenerative injury. Blocking O-GlcNAc cycling is detrimental to mammalian brain development and interferes with neurogenesis, neural migration, and proteostasis. O-GlcNAc-dependent developmental alterations impact metabolism and growth of the developing mouse embryo and persist into adulthood. Thus, O-GlcNAcase is both a promising diagnostic and therapeutic target for human neurodegenerative disease. O-GlcNAc may also trigger a global reprograming of metabolism in cancer and metabolic disease.
Bio: Dr. Hanover carried out his doctoral research with Dr. William J. Lennarz at Johns Hopkins University School of Medicine detailing the early steps in the transmembrane assembly of membrane and secretory proteins. He then did a Jane Coffin Childs postdoctoral fellowship with Dr. Ira H. Pastan focused on growth factor signaling, endocytosis and the molecular basis of drug resistance. In his independent work, Dr. Hanover first identified the nuclear pore proteins and then cloned the first of these proteins, NUP62. He showed that many components of the nuclear pore are modified by a novel modification: O-linked N-acetylglucosamine (O-linked GlcNAc). In 1997, he cloned and sequenced C. elegans and human OGT, published back-to-back with Gerald Hart’s identification of rat OGT. These early papers by the Hart and Hanover labs have led to an explosion of research on O-GlcNAc and its many targets. Based on its substrate specificity and molecular features, the Hanover lab proposed that O-linked GlcNAc transferase is the terminal step in a glucose-responsive pathway that becomes dysregulated in diabetes, neurodegenerative disease and diabetes mellitus (NIDDM). The enzyme catalyzing O-GlcNAc removal, O-GlcNAcase, has also been identified, expressed and shown to exist as differentially targeted isoforms in man. Dr. Hanover was an early pioneer in the use of biorthogonal sugars and continues to develop probes to explore the Chemical Biology of surface and intracellular glycans. He also exploits genetically amenable Mouse, C. elegans and Drosophila models to examine the physiological impact of the enzymes of O-GlcNAc cycling. Using reverse genetics, knockout, and other transgenic models he is currently exploring the role of these essential genes in signal transduction and epigenetic regulation. O-GlcNAc has emerged as a key epigenetic regulator that may function in the intrauterine environment to influence disease susceptibility in the offspring. The enzymes of O-GlcNAc cycling also interact with key components of the machinery influencing DNA methylation associated with Genomic imprinting.
Dr. Hanover has long been a strong advocate for the field of Glycobiology. He has mentored over 20 active independent glycoscientists in such fields as carbohydrate chemistry, cancer biology, infectious diseases and immunology. He served as the leader for the glycans in the Disease and Development Subgroup of the Consortium for Functional Glycomics since the inception of the consortium subgroups, and was reelected for that role upon reorganization in 2013. Along with Kelly Ten Hagen, he serves as the Society for Glycobiology’s representative to the International Glycoconjugate Organization (IGO). He has also been involved in helping to organize Glycobiology Gordon Conferences, Glycobiology Society meetings and IGO Glycoscience meetings over many years of participation in those conferences. More generally, he has participated numerous review panels for the NIH, NSF and FDA. Most recently, he chaired the “Common Fund” Review panel in efforts to establish “Novel and Innovative tools”, and “Adapt Novel tools” to advance Glycoscience. He has been an active member of the Society for Glycobiology since its inception and was previously a member of the Society for Complex Carbohydrates.
Annual Poster Session & Vendor Exhibition
September 20, 2017 5:30PM-8:30PM
Bethesda North Marriott Hotel & Conference Center
5701 Marinelli Road, North Bethesda, MD 20852
Congratulations to our student poster winners Sarah Gao (IBBR) and Hangu Nam (Virginia Tech). They will receive travel awards to attend HPLC 2018, and they will give short oral presentations at a future WCDG meeting.
Short Course: Capillary Electrophoresis Workshop
August 22 & 23, 2017
IBBR, 9600 Gudelsky Drive, Rockville, MD 20850
Instructor: Brandon Bates (Manager, Field Application Support for Sciex)
May 17, 2017 at US Pharmacopeia
Speaker: Christian Wolf, Dept. of Chemistry, Georgetown University, Washington, DC
Title: Chromatographic and Spectroscopic Analysis of Chiral Compounds
Abstract: The ever-increasing demand for biologically active chiral compounds, in particular pharmaceuticals and agrochemicals, continues to nurture tremendous interest in asymmetric synthesis. At the same time, the development of time-efficient methods for the analysis of chiral compounds is vigorously pursued at numerous academic and industrial research laboratories. In recent years, the practicality of combinatorial and parallel synthesis has been matched with significant advances in enantioselective analytical techniques. The usefulness of enantioselective chromatography and optical chemosensing for the determination of enantiomeric composition of chiral compounds in complex mixtures and for the determination of racemization kinetics will be discussed with several case studies.
Bio: Dr. Christian Wolf earned his doctorate from the University of Hamburg, Germany in 1995 in the lab of Wilfried Konig. He was awarded a Alexander von Humboldt Feodor Lynen Postdoctoral Fellowship under William Pirkle at the University of Illinois at Urbana-Champaign, IL. In 1997, he became a senior scientist at SmithKline Beecham Pharmaceuticals in King of Prussia, PA. Dr. Wolf joined the Department of Chemistry at Georgetown University in 2000 and was promoted to full professor in 2011. His research interests include synthetic methodology, chiral recognition and chemosensing, dynamic stereochemistry of chiral compounds, transition metal catalysis, and medicinal chemistry. Dr. Wolf had been awarded the Distinguished Georgetown University Investigator, the President’s Award for Distinguished Scholars-Teachers, the Georgetown University Patent Award, the NSF CAREER Award, and the Gold Impact Award from SmithKline Beecham.
April 19, 2017 at US Pharmacopeia
Student Speaker: Rosemary Onjiko & Erika Portero, 2016 Student Poster Honorable Mentions
Featured Speaker: Walter B Wilson, Research Chemist, NIST, Gaithersburg, MD
Title: Liquid and gas chromatographic retention behavior of polycyclic aromatic compounds on stationary phases of different selectivities
Abstract: One of the most widely studied groups of environmental contaminants today is polycyclic aromatic compounds (PACs), which are comprised of a complex class of condensed multi-ring benzoid compounds. The majority of the research with PACs has focused on polycyclic aromatic hydrocarbons (PAHs). Along with PAHs, heterocyclic compounds containing at least one heteroatom such as polycyclic aromatic sulfur heterocycles (PASHs) are largely present in the same environmental samples. The total number of possible isomeric structures for PASH is greatly increased compared with the corresponding PAH because both ring arrangement and position of the sulfur atom substitution within the rings give rise to unique isomers. In the current study, the retention behavior for many key isomeric groups of PACs and their alkyl-substituted derivatives were evaluated by gas chromatography (GC) and reverse-phase liquid chromatography (RPLC). In the GC studies, three stationary phases of different selectivities were studied: a ~50% (mole fraction) phenyl-substituted methylpolysiloxane phase, smectic liquid crystalline phase, and an ionic liquid phase. In the RPLC studies, multiple LC columns consisting of C18, C30, phenyl-hexyl, and penta-fluoro-phenyl stationary phases are evaluated.
Bio: Dr. Wilson completed his PhD in chemistry in 2014 from the University of Central Florida under the mentorship of Prof. Andres Campiglia. During his time in Campiglia’s lab, his work focused on the development of new analytical extraction methods for PACs in conjunction with liquid chromatography, gas chromatography, and low temperature fluorescence spectroscopy techniques. Dr. Wilson was awarded a two-year appointment as a National Research Council post-doctoral research associate at the National Institute of Standards and Technology (NIST) under advisement of Dr. Stephen Wise and Dr. Lane Sander, where he specialized in the development of new liquid and gas chromatographic separation techniques for PACs in complex sample matrices. Currently Dr. Wilson is a research chemist at NIST, where he focuses on the development of new dietary supplements and environmental reference materials.
March 27, 2017 Joint meeting with WBMSDG
6:15 pm – 8:00 pm at Shimadzu Training Center, Columbia, MD
Speaker: Robert N. Cole, Assistant Professor Dept. Biological Chemistry, Johns Hopkins School of Medicine
Title: Adventures of Capillary Electrophoresis in Proteomics from Top-down to Bottom-up
Abstract: Capillary zone electrophoresis (CE)-MS has become more accessible with robust electrospray interfaces, presenting a potential alternative to LC-MS. CE achieves rapid and high resolution analyte separation based on net charge and hydrodynamic volume. CE is orthogonal to reversed phase LC with additional benefits of low carryover, low (nanogram) sample injection, and rapid sample loading. CE-MS analysis of complex peptide mixtures is challenging due to the seconds-wide elution peaks produced during the rapid separations. However, increases in MS data acquisition speeds warrant re-examination of the role of CE in proteomics. We are evaluating a microfluidic chip-based CE interface (ZipChip, 908 Devices Inc) for top-down analysis of intact proteins, analysis of high charge/high pI peptides, and bottom-up quantification of proteins. Even with major challenges of sample concentration, protein complexity and automation, CEMS has a bright future in protein analysis.
Bio: Dr. Robert Cole is an assistant professor of biological chemistry at the Johns Hopkins School of Medicine. His research focuses on mass spectrometry strategies to characterize proteins and their modifications in malnutrition, neurological diseases and cancer. Dr. Cole serves as the director of the Mass Spectrometry and Proteomics Facility for the Johns Hopkins University School of Medicine and director of the Mass Spectrometry Core for the Johns Hopkins Kimmel Cancer Center. Dr. Cole received his undergraduate degree in zoology/physiology from the University of Massachusetts, Amherst. He earned his M.S. in biology/physiological ecology from the University of South Carolina and his Ph.D. in physiology/neuroscience from Michigan State University. He completed postdoctoral training in glycobiology/neuroscience at the University of Alabama at Birmingham and the Johns Hopkins School of Medicine. He joined the Johns Hopkins faculty in 1998. He is a member of the American Society for Mass Spectrometry, and his work has been recognized with a National Research Service Award from the National Institutes of Health.
February 15, 2017 at US Pharmacopeia
Student Speaker: Sam Choi, 2016 Georges Guiochon Poster & Travel Award recepient
Featured Speaker: Peter Nemes, Assistant Professor, Dept. of Chemistry, George Washington University
Title: Capillary Electrophoresis Mass Spectrometry for Understanding Early Vertebrate Embryonic Development One Cell at a Time
Abstract: A critical step during normal embryonic development is differentiation of pluripotent stem cells into all the different types of tissues of the vertebrate body. By unbiased and label-free detection, high-resolution mass spectrometry (HRMS) provides a direct window to follow molecular changes during cell differentiation, especially at the level of the metabolome that responds dynamically to intrinsic/extrinsic events. To enhance detection sensitivity, traditional HRMS pools large cell populations, albeit at the expense of potentially averaging out cell-characteristic processes such as a cell’s commitment to a specific tissue fate. In this presentation, we will discuss the development and utilization of single-cell capillary electrophoresis electrospray ionization HRMS platforms and protocols that we have developed and validated to enable the ultrasensitive detection of metabolites and proteins in single embryonic cells. Last, we will demonstrate how discovery metabolomics and proteomics data by single-cell MS opens new investigative potentials in basic cell and developmental biology, including the discovery of small molecules with previously unknown impact on cell fate specification in the vertebrate embryo of the South African clawed frog (Xenopus laevis), a powerful model of embryonic development and health studies.
Bio: Peter Nemes is an Assistant Professor of Chemistry (2013–present) at the George Washington University (GWU), whence he obtained a PhD in chemistry in 2009 (advisor: Prof. Akos Vertes). He completed postdoctoral training in analytical neuroscience at the University of Illinois—Urbana-Champaign (mentor: Prof. Jonathan V. Sweedler). After serving as a Laboratory Leader and Staff Fellow at the US Food and Drug Administration between 2011–2013, Dr. Nemes joined the faculty of the GWU Department of Chemistry. Research in the Nemes Laboratory develops ultrasensitive and microanalytical platforms for high-resolution mass spectrometry to study how metabolic and proteomic processes orchestrate normal cell heterogeneity during early development of the vertebrate embryo and the central nervous system. Prof. Nemes has authored 34 peer-reviewed publications, 6 book chapters, and 100+ presentations. He is co-inventor of the patented and licensed LAESI mass spectrometry technology. In 2015, Prof. Nemes was named a Beckman Young Investigator by the Arnold and Mabel Beckman Foundation and received the Arthur F. Findeis Award for Achievements by a Young Analytical Chemist by the Division of Analytical Chemistry of the American Chemical Society. In 2016, Prof. Nemes received the DuPont Young Professor Award and the US-HUPO Robert J. Cotter New Investigator Award.
January 18, 2017 at US Pharmacopeia
Speaker: Abigail Turner, National Institute of Standards and Technology
Title: The NISTmAb: Capillary Electrophoresis-based Characterization and Life Cycle Management
Abstract: The National Institute of Standards and Technology (NIST) has recently developed the NISTmAb Reference Material (RM 8671), an IgG1κ class-representative monoclonal antibody. The NISTmAb is intended to serve as a platform for harmonization and open innovation in the biopharmaceutical analysis community. It is a widely and longitudinally available test material that will support novel technology and method development, serve as an external system suitability control, and provide a medium for open access information sharing. Here, we describe NIST’s approach to characterization and lifecycle management of the reference material. We discuss, by way of example, the role of capillary electrophoresis-based assays in NISTmAb quality assurance, including CE-SDS, cIEF, CZE, and CE-ESI-MS/MS.
Bio: Dr. Turner completed her doctoral degree in Chemistry in 2015 at the University of North Carolina at Chapel Hill under the mentorship of Prof. Nancy Allbritton. In the Allbritton lab, Dr. Turner developed capillary electrophoresis-based measurement tools for quantifying enzyme activity in single human cells. Dr. Turner is currently a National Research Council post-doctoral research associate at the National Institute of Standards and Technology and the Institute for Bioscience and Biotechnology Research, where she specializes in leveraging capillary electrophoresis and mass spectrometry for detailed structural characterization of proteins including the NISTmAb RM 8671.
Thursday, November 17, 2016
ACS Headquarters, 1155 16th St NW, Washington, DC
Joint meeting with Chemical Society of Washington (CSW)
6:00PM social hour, 6:30PM dinner, 7:15PM presentation
Free event. RSVP by November 14 to firstname.lastname@example.org
Speaker: Mark L. Miller, FBI Counterterrorism and Forensic Science Research Unit, Quantico, VA
Title: Challenges in Forensic Separations
Abstract: The popularity of forensic science on TV shows and movies has glamorized forensic scientists and their work for the last couple of decades. But can you really inject a DNA sample in your GC and instantly obtain the name and address for the criminal? Can your arsenal of instruments perform an analysis and find a chemical database for every reference material related to the evidence? While practicing chemists recognize that this is not the case in real life, we can be thankful that these TV shows inspire many young people to seek careers in science. Research in forensics manifests many challenges as new and unusual samples present themselves in casework. One of the first tasks of a researcher is to determine what is the relevant target molecule(s) and what is the matrix one must analyze? Often in casework these are common matrices such as biological material (e.g. blood, urine, etc.) or an environmental sample (e.g. soil, water, etc.). But many times there is a twist to the complexities of getting the right results. For example, who could have foreseen that one day we would need to or be able to detect drugs in bugs or hair? Forensic chemistry research deals with these challenges by developing new methods that require both a separation of a complex mixture and a detection technique. The evolving threats mean that both small and large, organic and inorganic chemicals must be separated and analyzed for evidence examinations. GC and LC are the most useful tools for the separation of complex mixtures for everything from hydrogen peroxide to ricin. One of the tricks to effective use of chromatography is to have adequate retention of your analyte on the separation column, which from review of the literature is not always present in forensic practice. This talk will provide real examples of improved and new methods developed for different types of evidence for application in toxicology and explosives casework.
Bio: Mark L. Miller is a Research Chemist at the FBI Laboratory’s Counterterrorism and Forensic Science Research Unit in Quantico, Virginia. He has been working on various chromatographic and mass spectrometric applications in forensic science since joining the FBI in 1992. His research interests include trace analysis in toxicology, drugs, explosives, chemicals and materials. Prior to working at the FBI, he was a Senior Research Chemist for Monsanto Chemical Company in the R&D group. Dr. Miller received a Ph.D. in Analytical Chemistry from the University of North Carolina in Chapel Hill where he was under the direction of Professors Richard Linton and James Jorgenson. He has a B.S. in Chemistry from Indiana University in Bloomington and did research in Professor Milos Novotny’s lab. He is an avid Tarheel fan and from a family of UNC graduates or impending graduates.
Parking: Parking is available in nearby commercial parking garages. Please be aware that garage closing times vary. Parking is also available on the street after 6:30 pm, but be aware that most parking meters are in effect until 10:00 pm and may be limited to 2 hours. You should check the individual meters for details and payment methods as some are no longer coin-operated.
Metro: Blue/Orange/Silver Line: McPherson Square or Farragut West; Red Line: Farragut North.
October 19, 2016 at US Pharmacopeia
Speaker: Trina Formolo, National Institute of Standards and Technology
Title: Considerations for Optimization of Multi-Attribute Peptide Mapping Protocols
Abstract: Peptide mapping is a widely used methodological platform in the biopharmaceutical industry. This analytical tool uses the chromatographic profile of enzymatically generated peptides to establish protein identity, evaluate stability and monitor new drug lots for variation. The use of peptide mapping for multi-attribute method (MAM) applications is becoming more widespread in the industry. These platforms have been developed to streamline the quality control process by replacing multiple analytical methods with one comprehensive peptide mapping analysis. While a powerful, streamlined data analysis workflow is important in building a successful multi-attribute method (MAM) platform, the platform must also incorporate optimized sample preparation and analysis protocols. The generation of reliable, meaningful results from any MAM platform begins with quality sample preparation and analysis. This includes developing robust, reproducible tryptic digestion protocols and optimizing chromatographic separation methods to facilitate the detection and quantitation of critical quality attributes (CQA).
Bio: Dr. Formolo received her BS in biology from the University of Dallas and her PhD in molecular medicine from the Institute for Biomedical Sciences at The George Washington University. As a research chemist in the Biomolecular Measurement Division within the Material Measurement Laboratory of the National Institute for Standards and Technology (NIST) she focuses on the development of reference materials, methods and data relevant to the biopharmaceutical industry. Her interests include the mass spectrometry characterization of biotherapeutic proteins. She recently completed the LC-UV-MS/MS peptide mapping characterization of a recombinant IgG1κ monoclonal antibody (NISTmAb RM 8671) which was recently released as a Reference Material.
Open House & Poster Session
Wednesday,September 21, 2016
6:00 pm – 8:00 pm at North Bethesda Marriott Hotel and Conference Center
Congratulations to Sam Choi, our 2016 winner of the Georges Guiochon travel award for best student poster at the WCDG Open House & Poster Session on September 21!
Sam Choi from George Washington University won the award for his outstanding poster on “CE-nanoESI-MS for Untargeted Proteomic Characterization of Single Embryonic Cells and Small Neuron Populations”. He will receive complementary travel to a separations-related conference of his choice. Congratulations, Sam!.
We also want to acknowledge our Honorable Mentions, Erika Portero and Rosemary Onjiko from George Washington University, and thank all of our poster presenters, vendors, and attendees for making this year’s event a success! Download 2016 Program
Wednesday, May 18, 2016
6:00 pm – 8:00 pm at US Pharmacopeia
Speaker: Milton L. Lee, Professor Dept. Chemistry and Biochemistry, Brigham Young University, UT
Title: Compact Capillary LC Separations
Abstract: Compact, easy-to-use capillary LC systems are desirable for applications that require (or at least would benefit from) instrument mobility, such as for analyses on location (e.g., first responder applications). Furthermore, coupling to mass spectrometry would benefit from mobile instrumentation because the LC system could be located close to the ion source for improved performance, and easily removed when not in use. Portable LC systems are not common due to difficulties encountered in engineering LC pumping and detection systems that provide acceptable weight, robustness, power usage, and mobile phase consumption. We have developed a gradient nano-flow LC system with stop-flow injector that can be easily coupled to miniaturized light-emitting diode (LED) UV-absorption detection or mass spectrometry. The pumping system is comprised of two approximately 30-uL volume syringe pumps that deliver accurate nL flow rates under gradient conditions. The extra-column dead volume of the system is much lower than commercial capillary LC systems. Detection limits have been considerably improved by paying specific attention to improved light focusing, low stray light, low noise, and novel signal averaging routines. Signals down to the ppb level are easily detected. While the system can accommodate small particle packed columns (>15,000 psi), monolithic capillary columns can be used to minimize the pressure drop needed for rapid LC analysis. Fabricated polymeric monolithic columns produce efficiencies approaching 200,000 plates/m (non-retained uracil).
Bio: Milton Lee is Professor of Chemistry in the Department of Chemistry and Biochemistry at Brigham Young University. He received his Ph.D. in Analytical Chemistry from Indiana University in 1975. Dr. Lee’s area of specialization is in microseparation techniques and instrumentation for capillary separation and mass spectrometry. Dr. Lee was involved in the commercialization of the capillary supercritical fluid chromatograph, the atmospheric pressure ionization TOF mass spectrometer, and the hand-portable gas chromatograph toroidal ion trap mass spectrometer. He has over 570 publications, 20 patents, and has mentored 63 doctoral students. He is the recipient of the 2016 LCGC North America Lifetime Achievement Award and the 2012 ACS Award in Separations Science and Technology, among many others. Dr. Lee has also been named on the Analytical Scientist Power List in 2013 and 2015.
Joint with Washington Baltimore Mass Spectrometry Discussion Group
Monday, April 11, 2016
6:15 PM – 8:00 PM at Shimadzu Training Center, 7100 Riverwood Drive, Columbia, MD 21046
Speaker: Stephen E. Stein, NIST Fellow, Director of NIST Mass Spectrometry Data Center in Biomolecular Measurement Division, Gaithersburg, MD
Title: Mass Spectral Libraries of Everything
Abstract: Libraries of mass spectra of known compounds have long been used for identifying compounds in GC/MS experiments and are finding increased use in tandem LC/MS experiments, especially in metabolomics and proteomics studies. Even given the substantial coverage of current libraries, a large fraction of the spectra remain unidentified. In some areas only a small fraction of components can be identified and even for well-developed areas (GC/MS of urine, for example), the origin of many spectra is unknown and likely to remain so for some time. To characterize these unknowns, we have been involved in building annotated libraries of good quality, but unidentified spectra in GC/MS and LC/MS experiments. Progress in three areas will be discussed: 1) GC/MS – multiple occurrences of spectra at fixed retention indices have been collected, clustered and annotated for a range of materials including urine, essential oils and various NIST reference materials; 2) LC/MS proteomics – we have constructed extensive libraries of unidentified peptide from proteomics analysis and developed special methods for their annotation and identification; 3) LC/MS metabolomics – we have built an collection of unidentified spectra from NIST urine reference materials and developed tools for organizing and identifying them. Illustration of the use of these libraries alongside more conventional libraries of reference spectra of identified compounds will be presented.
Bio: Dr. Stein is a NIST Fellow, Group Leader and Director of the NIST Mass Spectrometry Data Center in the Biomolecular Measurement Division, Material Measurement Laboratory, National Institute of Standards and Technology. He conceives, plans, directs and personally conducts advanced research and development in the area of chemical data analysis, with emphasis on mass spectral data and search algorithms, deconvolution algorithms, quality measurement and new approaches for chemical identification in proteomics and metabolomics, methods for automated chemical data analysis, algorithms for spectra and property prediction from chemical structural data. He received his undergraduate degree in Chemistry at the University of Rochester and did his graduate work at the University of Washington as a NSF pre-doctoral trainee. He then did his post-doctoral training at SRI International in Menlo Park, CA. Over the years his research has culminated in over 120 peer-reviewed publications and numerous awards including the Gold Medal from the Department of Commerce (2015), the Mike Lynch Award from the Chemical Structure Association (2014), and the Presidential Rank Award (2011).
Wednesday, March 16, 2016
6:00 pm – 8:00 pm at US Pharmacopeia
Speaker: Nicholas H. Snow, Department of Chemistry and Biochemistry, Center for Academic Industry Partnership, Seton Hall University, South Orange, NJ
Title: Six Dimensions of Separations: Are we holding ourselves back with packed column thinking?
Abstract: The advent of readily available high-resolution and sensitivity multidimensional separation and detection techniques such as GCxGC-ToFMS and GC-MS-MS has provided chromatographers with unprecedented separation and detection capability. When combined with on-line sample preparation techniques such as SPME and static headspace extraction, there are now numerous avenues for chromatographers to improve separation selectivity and ultimately resolution. These additional dimensions also provide opportunities to compromise selectivity, especially when combined with historical lessons originally applied to packed columns. Considered holistically, an SPME-GCxGC-ToFMS method actually has up to six dimensions of separation: sampling, extraction, injection, two dimensions of GC and MS detection. Each can generate both desired and undesired selectivity that impacts the ultimate resolution and sensitivity generated by the full method. Using examples from forensic, pharmaceutical and organic contaminant analysis, each of the multiple dimensions of analyses involving SPME, GCxGC-MS and GC-MS-MS will be examined in terms of selectivity (both desired and undesired) selectivity generation and whether they still suffer from packed column thinking. For example, in environmental analysis, it will be shown that, if desired selectivity is maximized and undesired selectivity minimized, the sensitivity of SPME-GC-MS-MS is easily competitive with LC-MS-MS for the analysis of emerging contaminants in water. In pharmaceutical analysis, the six “non-volatile” compounds not included in the standard USP and ICH headspace methods can, in fact, be determined by headspace extraction. To maximize the potential of GC, all of the six dimensions must be understood and optimized.
Speaker Bio: Nicholas H. Snow is Professor of Chemistry and Biochemistry and Director of the Center for Academic Industry Partnership at Seton Hall University. He is currently teaching advanced undergraduate and graduate courses in analytical chemistry and separation science. He has been recognized twice by the Seton Hall University Board of Regents for outstanding teaching and service to students. He maintains an active research group with projects involving rapid separations of complex mixtures, multidimensional separations, sampling techniques for chromatography, gas chromatography and gas chromatography/mass spectrometry. He is especially interested in working with industrial and private partners in solving difficult analytical problems. He earned his PhD in 1992 from Virginia Tech.
Wednesday, February 17, 2016
6:00 pm – 8:00 pm at US Pharmacopeia
Speaker: Robert diTargiani, U.S. Army Medical Research Institute of Chemical Defense, Aberdeen Proving Ground, MD
Title: Analytical Methods for the Verification of Human Exposure to the Chemical Warfare Agents
Abstract: While chemical warfare agents (CWAs) have generally been regarded as a threat to the military, events in Japan and more recently Syria have demonstrated that the civilian population is also at risk. The two main CWA threats are organophosphorus nerve agents and sulfur mustard and unfortunately humans have been exposed to both. It is important to have analytic methods available to identify those that have been exposed to CWAs and to verify the CWA used. Verification of exposure to CWAs typically involves determinations of urinary metabolites or adducted proteins in blood. While the intact CWA might last for just a few minutes, a biomarker can last for weeks or months (We have detected a CWA up to 42 days after exposure). Methods have been developed at USAMRICD to detect CWAs and its metabolites in blood or urine samples using both LC-MS and GC-MS.
Speaker Bio: Dr. Robert diTargiani received his PhD in chemistry from the Johns Hopkins University in 2004. He currently works at US Army Medical Research Institute of Chemical Defense (USAMRICD) as a research chemist. He is a member of the Medical Diagnostics team and ADME core at the institute. Recently, he has developed a proteomic method to verify exposure of chemical warfare agents and agent fate with high-resolution mass spectrometers. He has also collaborated with other government agencies to adopt liquid chromatography electrospray ionization tandem mass spectrometry (LC-MS/MS) techniques for analysis of organophosphate nerve agent urinary hydrolysis products and assay of protein adducts of butyrylcholinesterase and human serum albumin.
January 20, 2016 at USP
Speaker: Steve J. Lehotay, USDA-ARS Eastern Regional Research Center (ERRC), Wyndmoor, PA
Title: Improving the quality of chromatographic peak integration and analytical results without human review in multi-analyte high-throughput methods
Wednesday, December 16, 2015
6:00 pm – 8:00 pm at US Pharmacopeia
Speaker: Ronald E. Majors, LCGC North America, West Chester, PA
Title: Top Ten HPLC/UPLC Column Myths
Abstract: In any field there are often “misconceptions” or “myths” that are perpetuated and passed on to the next generation. These myths are often driven by a lack of understanding by practitioners of the real issues. And these myths can change as time moves on. Since HPLC is approaching its 50th year, many column myths have already been passed down to 2 generations of liquid chromatographers. Recently, ultrahigh pressure liquid chromatography (UHPLC) has come into its own and a new set of myths are arising. The purpose of this tutorial is to try to dispel some of these myths before they get further perpetuated. Some of the myths to be discussed are: “all C18 columns are the same”; “it takes a minimum of 10 column volumes to re-equilibrate an LC column”; “you can’t reverse an HPLC column to flush out particulates”; “UHPLC packed columns plug easier than conventional HPLC packed columns” and the list goes on. With help of a team of myth-busters, notables in the chromatography field, I will provide proof statements and literature references that showed that these myths are unjustified. There are many myths that are still around but didn’t make the top ten. However, most likely old myths will continue, some will fade away, and new myths will arise as more practitioners enter the chromatography community. Those new arrivals to this community may have to discover these myths on their own (since they don’t necessarily listen to the old timers anyway). Perhaps new myth-busters will take on the next generation of myths.
Bio: In November, 2013, Ron Majors retired from Hewlett-Packard/Agilent Technologies after 45 years of working in the area of sample preparation and chromatography column and instrumentation technology. He currently serves as a consultant. Ron received his B.S. in chemistry at California State University, Fresno, in 1963 and his Analytical Chemistry Ph.D. degree in 1968 from Purdue University under the direction of L.B. Rogers. His Ph.D. thesis was in the area of molecular-imprinted phases for chromatography and sample preparation. He is the author of over 150 publications in HPLC, GC, sample preparation and surface chemistry. Among his current activities, he has been editor for the monthly feature, “Column Watch” in LC/GC Magazine (33 years) for which he is also serves on the Editorial Board. Dr. Majors has served as Chairman of HPLC ’86 and Anabiotec ’90 and as a member of the Instrumentation Advisory Board of Analytical Chemistry. His current interests include sample preparation especially solid-phase extraction and automation, and HPLC and GC column technology. Ron is a lifetime member of The Chromatography Forum of Delaware Valley, a member of the American Chemical Society, and The Chromatography and Separations Chemistry Sub-division of the Analytical Division of the ACS where he had served as Chairman and Secretary. He has also been a member of the Chromatographic Society (U.K.) and Board of Directors for the California Separations Society (CaSSS). Ron has been an invited lecturer, session organizer, and session chairman at many national and international symposia. Dr. Majors has received many awards from chromatography societies, the most recent being the Chromatographic Society’s 2007 Martin Gold Medal from the United Kingdom, named for the Nobel Prize winner, A.J.P. Martin. Ron and his wife Carol are avid birdwatchers and travel all over the world in search of these feathered creatures.
Wednesday, November 18, 2015
6:00 pm – 8:00 pm at US Pharmacopeia
Speaker: Claude R Mallet, Waters Corporation, Workflow Integration, Milford, MA
Title: Optimized Workflow for Metabolite Identification using 3D LC/MS/MS
Abstract: The ‘holy grail’ for a biotransformation group is the irrefutable isolation and identification of a putative metabolite. When achieved, it requires several hours of patient incubation or in vivo sample collection to generate the raw starting material. This is followed by multiple chromatographic steps, manual fraction collection with concomitant lengthy evaporative steps and compromised losses in yield for gains in purity. Even with meticulous planning and sample handling, the definitive NMR spectrum is elusive. It is not uncommon for a purification to absorb 3-6 weeks of dedicated instrument and analyst time with the futile result of a complicated, un-interpretable NMR spectrum. A reasonable compromise of this fit-for-purpose process would be to automate the isolation and purification steps.As new technology emerges, new options become available thus bringing effective performance for difficult applications. The concept of hyphenated systems or multi-dimension chromatography was designed for solving complex analyses. The peak capacity or separation power can be increased by combining several separation dimensions (most instances utilize two) each using optimized conditions for maximum resolution. The main challenge is the transfer of closely resolved analytes from the primary resolving dimension (PRD) to the secondary resolving dimension (SRD). The concept of multi-dimensional-chromatography is a well established technique for the analysis of complex mixtures. However, since its beginning, the technique is also perceived as highly complex in term of hardware and also difficult to gain in depth insight for practical usage. In recent years, advances in software control and automation, are enabling hyphenated instrumentation platforms to offer enhance performances. The use of multi-fluidic circuits can decrease sample handing in term of time, resources and consumable. In this application, an intermediate API entity from a reputable pharmaceutical will be use to demonstrate the 3D LC/MS/MS workflow process.
Speaker Bio: Dr. Mallet received his Ph.D. in analytical chemistry from the University of Montreal, Montreal, Canada (1997). His thesis was entitled “Time-Coupled-timed-Resolved Chromatography or TCRC”. This new hyphenated system was based on an experimental GC/GC/MS/MS orthogonal chromatograph using a mobile heated pulse. In 1997, Dr. Mallet was hired as a senior application chemist in several biotech, contract research organization (CRO’s) and life-science firms, before accepting a senior scientist’s position at Waters Corporation in 2000. From his doctoral work with Time Decoupled Chromatography concept, the technique was extended to Waters Liquid Chromatography portfolio. Since 2013, Dr. Mallet is currently a senior scientist with the Separation Technology Division and pursuing research interest in automated 2D & 3D LC/MS/MS technologies.
2015 George Guiochon Student Poster Award recipient, Jason Reck from University of Virginia, will present his work 6:45 pm – 7:00 pm.
Wednesday, October 21, 2015
6:00 pm – 8:00 pm at US Pharmacopeia
Speaker: Irving W. Wainer, PhD, DHC, Chief Scientific Officer, Mitchell Woods Pharmaceuticals
Title: The adventures of a bioanalytical chemist in the never-never land of antidepressants: Finding a way out of the “ketamine paradigm”
Abstract: (R,S)-Ketamine is a chiral phencyclidine derivative that produces rapid and short-lived anesthesia via inhibition of the N-methyl-D-aspartate (NMDA) receptor. The anesthetic activity of this drug has been associated with the parent compound and to a lesser degree with the N-demethylated metabolite (R,S)-norketamine, while other (R,S)-ketamine metabolites were designated as “inactive”, the “Ketamine Paradigm”. Recent studies demonstrated that a single sub-anesthetic dose of (R,S)-ketamine produces rapid and profound antidepressant response. As part of our studies of this effect in patients with treatment-resistant and bipolar depression, we developed a stereoselective lc/ms/ms assay capable of quantifying all of the major (R,S)-ketamine metabolites. The analysis of plasma samples demonstrated that (R,S)-ketamine was rapidly transformed in to multiple metabolites including (R,S)-dehydronorketamine and (2S,6S;2R,6R)-hydroxynorketamine and that these metabolites were associated with clinical response. The dehydro and hydroxy metabolites of (R,S)-ketamine are weak NMDA inhibitors, raising the question of the viability of the “Ketamine Paradigm” as an explanation (R,S)-ketamine’s antidepressant effects. In addition, pharmacometabolomics analysis identified a positive relationship between reduced D-serine plasma levels and response and a second study demonstrated that basal D-serine plasma levels predict antidepressant response. This talk will address how our ability to accurately measure chemical and biological changes led us to a new “Ketamine Paradigm” and new antidepressant drugs.
Speaker Bio: Professor Irving W Wainer is Chief Scientific Office for Mitchell Woods Pharmaceuticals. He received his PhD degree in chemistry from Cornell University and did postdoctoral doctoral studies in molecular biology (University of Oregon) and clinical pharmacology (Thomas Jefferson Medical School). He worked for the FDA as a Research Chemist, at St. Jude’s Children’s Research Hospital (Associate Member), McGill University (Professor, Department of Oncology), Georgetown University (Professor, Department of Pharmacology) and until March 31, 2014 as Senior Investigator, National Institute on Aging/NIH. Professor Wainer has published 375 scientific papers, 10 books, holds 11 patents, and was founding editor of the journal Chirality and Senior Editor of the Journal of Chromatography B. His awards include: the “A.J.P. Martin Medal” presented by The Chromatographic Society; Elected Fellow of the American Academy of Pharmaceutical Sciences; Doctor Honoris Causa degrees awarded by the Medical University of Gdansk and University of Liege, the 2013 Dal Nogare Award and the 2013 Eastern Analytical Symposium Award for Outstanding Contributions to the Fields of Analytical Chemistry. Professor Wainer’s research in chromatographic science is centered on the development of new chromatographic methods for the online study of ligand-receptor interaction and drug screening. Professor Wainer’s laboratory is also engaged in the development of new therapeutic agents for the treatment of oncologic and CNS diseases.
Thursday, September 17, 2015
6:00 pm – 8:00 pm
Bethesda North Marriott Hotel
5701 Marinelli Road, North Bethesda, MD 20852If you have presented a separations related poster at a scientific meeting recently, submit your abstract and present the poster at our event. There is no cost to attend, and there will be plenty of oppSave & Closeortunities to network with other local scientists and begin or strengthen collaboration in our area.This will be the inaugural year for the Georges Guiochon Student Travel Award, which will provide for travel expenses and registration to HPLC 2016 in San Francisco, CA, as well as the opportunity to present the winning student’s work at an upcoming WCDG meeting. Student posters (undergraduate & graduate students) will be judged at the poster session, and we encourage our members (and their students) to submit poster titles and abstracts as soon as possible. Posters which have been recently presented at other meetings are both allowed and encouraged.
Camille Lombard-Banek (George Washington Univeristy) received Honorable Mention and a $500 award for travel. Contact: email@example.com
Wednesday, May 20, 2015
6:00 pm – 8:00 pm at US Pharmacopeia
Speaker: Dr. Jianghao Sun, Research Associate, Food Composition and Method Development Lab Beltsville Human Nutrition Center, USDA-ARS
Title: Fingerprinting and Metabolomics for Botanical Authentication and Identification of Dietary Biomarkers
Abstract: Metabolomics is a rapidly developing area which aims to profile small-molecules to support research on complex biological systems. The strategy used in metabolomics has shown great potential for food and nutrition sciences. In this presentation, the qualitative evaluation of botanical and related dietary supplements, identification of dietary biomarkers under different dietary patterns, and chemical changes during food storage/processing will be discussed using HPLC/UHPLC-MS fingerprinting and metabolomic approaches based on the work in this lab.
Speaker Bio: Dr. Jianghao Sun obtained his Ph.D from the Peking University (Top 1 in China) in 2007 majoring in Phamacognosy. He moved to the U.S. in the late 2009 and joined Food Composition and Method Development Lab (FCMDL) at Beltsville Human Nutrition Center (BHNRC) of USDA-ARS as a post-doctoral fellow under cooperative agreements with Johns Hopkins University and University of Maryland. Then he was promoted as a research associate of FCMDL in 2014. Dr. Sun has 8 years of research and working experience primarily as a mass spectrometrist and food chemist. The training and work experience at FCMDL made him an expert of food constituents analysis, food composition and nutritional research. He had been worked on developing the liquid chromatography tandem mass spectrometry based fingerprinting and metabolomics approaches for food/botanical authentication, food component and dietary biomarker analysis. Dr. Sun has authored and/or co-authored more than 40 peer-reviewed papers. Many of his papers were published in the top peer-reviewed journals such as Journal of Agricultural and Food Chemistry, Food Chemistry, Anal and Biochemical Chromatography and Journal of Chromatography A. Furthermore, he presented his research findings at many professional conferences, and has served as a reviewer for 11 peer-reviewed journals in the area.
Joint with Washington-Baltimore Mass Spectrometry Discussion Group (MSDG)
Wednesday, April 15, 2015
6:00 pm – 8:00 pm at US Pharmacopeia
Speaker: Dr. Matthew C. Crowe, The Dow Chemical Company, Philadelphia, PA
Title: Multidimensional Liquid Separations Coupled to Electrospray Ionization Mass Spectrometry for the Analysis of Complex Polymers
Co-Authors: Lu Bai, Miroslav Janco
Abstract: In an effort to comprehensively characterize the molecular structure of complex tetrapolymers up to 10,000 u, multidimensional separations coupled to electrospray ionization mass spectrometry (ESI/MS) were developed. Polymers composed of four different monomers were characterized to determine if performance differences could be correlated with differences in molecular structure. The polymers were analyzed with negative polarity ESI/MS, taking advantage of the presence of a permanent negative charge on one of the monomers. Direct infusion ESI/MS experiments did not provide full molecular weight coverage, so ultrahigh performance liquid chromatography (UHPLC) ESI/MS methods were developed which allowed separation of polymer components by molecular structure and the observation of a wider polymer molecular weight range with mass spectrometry. The UHPLC/ESI/MS results were dominated by low molecular weight polymer signals, making sample-to-sample comparisons difficult. To combat this, a size exclusion chromatography (SEC) fractionation technique was developed to separate polymer components by molecular weight prior to UHPLC/ESI/MS analysis. SEC fractionation followed by UHPLC/ELSD and UHPLC/ESI/MS of collected fractions was used to analyze complex tetrapolymers, increasing the mass range observable with ESI/MS over what was seen with direct infusion ESI/MS and UHPLC/ESI/MS. The results of these experiments will be presented, along with what was learned about the strengths and limitations of this analytical approach. Data analysis allowing statistical differentiation of complex polymer samples will also be discussed.
Speaker Bio: Matthew (Matt) C. Crowe received his Ph.D. in Chemistry from the University of Texas at Austin (2005) and a B.S. in Chemistry from the University of North Carolina at Chapel Hill (2000). Following graduate school, Matt served as the director of the mass spectrometry facility in UNC-Chapel Hill’s chemistry department. In 2008, Matt began work as a post-doctoral researcher at the University of Washington in Seattle doing UHV adsorption microcalorimetry. In 2010, Matt left Seattle to begin work as a Senior Analytical Chemist-Mass Spectrometrist at The Dow Chemical Company in 2010. In 2014, Matt was promoted to his current position of Associate Research Scientist at Dow, with technical focus on liquid separations and mass spectrometry. Matt has been a member of several scientific societies over the years, including the American Chemical Society (ACS), the American Society for Mass Spectrometry (ASMS), and the American Vacuum Society (AVS). He has served as a manuscript reviewer for Langmuir (2007), on the ASMS program review committee (2007 & 2008), and as a career panelist for the Center for Enabling New Technologies Through Catalysis (CENTC) (2009-2010). Matt has served on several awards committees and regularly organizes and chairs symposia for the ACS and ASMS. Matt has served as a director (2012-2013), Chair (2014), and is currently Past Chair and Councilor for the Trenton local section of the ACS.
Chromatography Community Mixer at PittCon
Tuesday, March 10, 2015
5:30 pm – 8:30 pm
Generations Hall, 310 Andrew Higgins Dr.
New Orleans, LA
Wednesday, Feburary 11, 2015
6:00 pm – 8:00 pm at US Pharmacopeia
Speaker: Dr. Rabih Jabbour, Edgewood Chemical Biological Center, Edgewood, MD
Title: Utilization of a Mass Spectrometry Proteomics Method for Detection of Biological Agents and Toxins in Complex Matrices
Abstract: Food safety and bio-surveillance are growing fields of interest to government and private sectors, as a necessary action to protect ourselves from threats disseminated through the food system. Nefarious individuals can and have intentionally contaminated food sources using biological warfare agents and other pathogens. Methods to detect the causative agent can be laborious and often require enrichment of the sample as well as a reasonable assumption of what the pathogen may be. A mass spectrometry based proteomics method (MSPM) has been developed for identification and classification of pathogens including bacteria, viruses, and toxins. The MSPM and does not require prior knowledge of microbes in the sample or an enrichment step. Utilization of MSPM in the detection and identification of food borne toxins is advantageous over genomic based methods because those toxins are proteinaceous substances with no genomic complimentary compounds.
Speaker Bio: Dr. Jabbour holds a Ph.D. in bioanalytical chemistry with more than 15 years of research experience in academia and industry in the field of chemistry and biology of microorganisms that are of vital interest to the Department of Defense. He is leading the development of the automated sample processing system for extraction and preconcentration of biological biomarkers for the detection and identification biological warfare agents down to strain level using mass spectrometry technology. His instrumentation expertise is in the area of bioseparation techniques, preconcentration of biological biomarkers method and engineering development, optical spectroscopy, chromatography and mass spectrometry. He has contributed to various DOD and DHS projects such as water monitoring and microbial fate using Raman imaging for JSAWM, toxin fate by LC-MS, Biowatch-DHS, and microbial mapping by MALDI-MS for EPA projects. He was awarded the DTRA “Best Basic Research Award” and SAIC as ” Excellence in Science Award”. He serves as a reviewer of articles with J. Analytical Chemistry in the area of microbial proteomics and genomics; acted as a volunteer for the ASTM committee on Raman Imaging standard operation procedure. He has published over 25 peer-review articles and proceedings in the field of chemistry, biochemistry, spectroscopy, molecular biology, bacteriology, and protein chemistry.
Wednesday, January 21, 2015
6:00 pm – 8:00 pm
Speaker: Dr. Jeffrey W. Hudgens, NIST, Gaithersburg, MD
Title: Hydrogen-Deuterium Exchange Mass Spectrometry: A Valuable Tool for the Biopharmaceutical Industry
Abstract: In recent years many biopharmaceutical companies have established hydrogen-deuterium exchange mass spectrometry (HDX-MS) laboratories. Such facilities contribute to the research of drug mechanisms, of protein-ligand and protein-protein interactions, and of determinations of protein functional changes induced by environment and post-translational modifications. HDX-MS measurements involve immersion of protein or glycoprotein samples in a D2O solution, rapid protease digestion of the protein to peptides, separation of the peptides on a cold (1 °C) UPLC, and mass measurements by high resolution mass spectrometry. Evaluation of HDX-MS data can determine the hydrogen exchange rates of amide hydrogens along protein chains. These H/D exchange rates are substantially governed by three-dimensional protein structure. HDX-MS quality could be substantially improved if the UPLC can be operated at lower temperature, e.g., 20 °C. To develop a HDX-MS program that is responsive to the needs of the biopharmaceutical industry, our NIST laboratory has conducted research to gain experience with problems similar to those encountered by the biopharmaceutical industry. First, we developed a new mass spectrometry method involving electron transfer dissociation (ETD) that enables determinations of the deuterium uptake by glycans within glycoproteins. The resulting increase in D-uptake measurement accuracy allowed us to demonstrate that changes in the glycan structure within glycoproteins can cause measurable changes in the HDX-MS patterns. This result is important for evaluation of similarity among biosimilars. Secondly, we present a case study where HDX-MS accelerated elucidation of a mechanism by which a small regulating protein induces the unclamping of the homotrimer, proliferating cell nuclear antigen (PCNA), from DNA. The approach is important for epitope characterization.
Speaker Bio: Dr. Jeffrey Hudgens researches methods that enable H/D exchange mass spectrometry (HDX-MS) to measure the similarity among an innovator drug, its subsequent production lots, and its competing biosimilars. His HDX-MS studies also include ligand interactions with proteins and transmembrane proteins. Dr Hudgens received his BS in Chemistry from Miami University (Ohio) and his PhD in Physical Chemistry from the University of Illinois at Urbana. He was awarded a National Research Council Postdoctoral Associateship at the Naval Research Laboratory. He remained at NRL for another seven years as a staff scientist, where he pioneered applications of laser spectroscopy and mass spectrometry. In 1984 he moved to the National Bureau of Standards (now NIST). His 125+ scientific publications and two patents span many disciplines including biochemistry, optical spectroscopy, mass spectrometry, chemical kinetics, thermochemstry, and nanochemistry. His awards for metrology include the Chemical Science Technology Laboratory’s Technical Achievement Award and a Bronze Medal. Dr. Hudgens is a Fellow of the American Physical Society.
Wednesday, December 17, 2014
6:00 pm – 8:00 pm
Speaker: Dr. Bill LaCourse, University of Maryland Baltimore County, Baltimore, MD
Title: Adventures in Analysis: New Approaches to Old Problems
Abstract: The University of Maryland, Baltimore County (UMBC) has been at the forefront of new and innovative ways to promote student success. Motivation is a key ingredient of persistence. One approach is to provide opportunities for undergraduate and graduate students to work on real-world problems using high-end analytical instrumentation (e.g., mass spectrometers, NMR, HPLC, GC and spectroscopy). In doing so, students learn to collaborate, critically think, communicate, and learn marketable skills. We are achieving this goal by reinventing the typical “core” facility at a university into an active teaching and learning environment, which is operated by a facility manager under the College of Natural and Mathematical Sciences. This presentation will visit an array of analytical applications being investigated in the Molecular Characterization and Analysis Complex (MCAC), which in itself is a new approach for an old problem. One of the oldest analytical techniques in separation science is thin layer chromatography (TLC). This technique has always suffered from lack of ability to rapidly identify separated compounds. In the MCAC, we have developed an ambient ionization source for mass spectrometry that functions as a surface analysis reader. In a matter of minutes, it can non-destructively scan an entire TLC plate and get mass spectra of each of the spots. This novel approach solves the age old problem of inconclusive information from TLC analysis. The separation and direct detection of carbohydrates and glycans has been successfully accomplished using high performance anion-exchange chromatography followed by pulsed amperometric detection (HPAEC-PAD). A continuing analytical challenge has been the selective identification of carbohydrates versus other compounds, especially for complex samples. Typically, this problem is overcome by offline clean up and isolation. We have been working on the development of multiplex-pulsed amperometric detection (MPAD), which allows the analyst to confirm the presence of glycans/sugars from peptides and other interferences without the need for offline prep or multiple runs. Another issue that has plagued us all is sensitivity, or how low can one go! Since the human olfactory system can sense off flavor compounds (OFCs), such as geosmin, as low as 10 ppt, it is imperative that analytical methods be able to quantitate below these levels. The MCAC has been working on the development of a method for OFCs using gas chromatography with mass spectrometry. Through the use of an improved chromatographic separation, optimized mass spectroscopy parameters, and a novel online trap and purge for a head space sampler, we have been able to achieve parts per quadrillion limits of quantitation and detection for water samples. In conclusion, the MCAC has developed into an active learning facility, which supports internal and external researchers and scientists, for inspiring students to persist in STEM. This presentation will highlight several of their achievements.
Speaker Bio: William R. LaCourse is the Dean of the College of Natural and Mathematical Sciences and Professor of the Department of Chemistry and Biochemistry at the University of Maryland, Baltimore County (UMBC). He is also a Kauffman Fellow of Entrepreneurship, and past CEO/cofounder of Aurora Analytics, LLC. He received his Ph.D. in Analytical Chemistry from Northeastern University in 1987. After completing a postdoctoral appointment at Ames Laboratory, he held the position of Scientists at Iowa State University/Ames Laboratory until he joined the faculty at UMBC in 1992. In 2005, he founded UMBC’s Chemistry Discovery Center, which has dramatically improved student performance in introductory chemistry courses and now oversees the College’s Active Science Teaching & Learning Environment (CASTLE), which is designed to study active-learning pedagogies across the STEM disciplines. In addition to his administrative experience at the University level, Dr. LaCourse has five years of industrial experience in the pharmaceutical industry on the development of product assays of both human and veterinarian formulations. His research interests include basic and applied research on hydrodynamic electroanalytical techniques in chromatographic and electrophoretic systems. He has 111 publications, including 20 chapters and a sole-authored book entitled Pulsed Electrochemical Detection in High Performance Liquid Chromatography, and two issued patents. He has made over 250 presentations at national and international meetings. Dr. LaCourse is the recipient of several chemistry and research awards, an Editorial Advisor for Analytica Chimica Acta, an Associate Director of the California Separation Science Society (CASSS), and an active member of local and national professional societies and groups.
Wednesday, November 12, 2014
6:00 pm – 8:00 pm
Speaker: Dr. Abul Hussam, George Mason University, Fairfax, VA
Title: Measurement of Noncovalent Association and Partitioning of Volatile Solutes by Equilibrium Headspace Gas Chromatography: Applications in Solvent Extraction, Surfactants, and Nanoparticles
Abstract: An equilibrium headspace gas chromatographic technique (eHSGC) was developed to measure noncovalent association and partitioning of n-alkylbenzenes in water with substrates such as immiscible solvents for liquid-liquid extraction (LLE), natural (fulvic and humic acids) and synthetic surfactants, and nanoparticles. A general theory based on two step reactions and the experimental methodology were developed to obtain solute-substrate association constant (K11), critical substrate association concentration (cac), and solute-aggregate association constant (Kn1). These parameters were used to calculate the vapor/liquid partition coefficients, infinite dilution activity coefficients inside the aggregate pseudophase, and transfer free energies of alkyl chain – ΔG◦CH2. These values were obtained without the solute concentration, and without a calibration. The existence of a water rich substrate pseudophase is inferred from ΔG◦CH2 values in various phases. In water-fulvic acid system the inter-aggregate transfer free energies indicate that the aggregate pseudo-phase is more polarizable benzene-like and less n-alkane aliphatic-like. The problem of defining association and partition constants with nanoparticles is discussed.
Speaker Bio: Abul Hussam is a Professor of Chemistry and the Director for the Center for Clean Water and Sustainable Technologies (CCWST) in the Department of Chemistry and Biochemistry at George Mason University. Dr. Hussam earned his Ph.D. in Analytical Chemistry from University of Pittsburgh in 1982. His research and teaching areas include analytical chemistry, environmental chemistry, and chemistry in organized media. He has published and presented over 100 scientific papers. Professor Hussam was awarded the 2007 Grainger Challenge Prize for Sustainability from the US National Academy of Engineering (NAE) for the SONO arsenic filter, which is now used by hundreds of thousands of people in the affected areas of Bangladesh, Nepal, India, and Pakistan.
One of our most prestigious members has passed away. Georges Guiochon, a previous WCDG President, after defeating pneumonia finally succumbed to neuromuscular failure due to Post Polio Syndrome on October 21, 2014. He was 83 years old and still working at UT Knoxville until the day before he entered intensive care on October 7.
Arrangements are underway for Memorials to be held in Paris, Buffalo, and UT Knoxville.
With warmest regards from another previous WCDG President, Lois Ann Beaver, surviving spouse of Georges Guiochon.
A remembrance from Journal of Chromatography A: www.journals.elsevier.com/journal-of-chromatography-a/news/professor-georges-guiochon-1931-2014-passed-away-on-october/
Wednesday, October 15, 2014
6:00 pm – 8:00 pm
Speaker: Dr. Peter Nemes, The George Washington University, Washington, DC
Title: Metabolic Analysis of Single Cells in Embryos by Mass Spectrometry
Abstract: Measurement of small-molecule changes during embryo development raises a potential to aid the understanding of basic processes underlying states of health and disease, but this requires specialized analytical tools. Particularly needed are technologies that are able to address diverse types of small molecules with single-cell resolution. Although mass spectrometry is the modern method of choice for the measurement of metabolites, typical workflows in the field combine a large cohort, often millions, of cells to improve detection performance. Because pooling inherently averages out the analytical signal among components of the sample, chemical information specific to each cell is lost in this approach. It would be transformative for cell and developmental biology to extend mass spectrometry to metabolites in developing embryos, but this depends on the development of high-sensitivity mass spectrometry platforms. In this talk, we will explore a single-cell mass spectrometry technology we have recently developed to decipher the metabolic composition of single cells in early-stage embryos of the South African clawed frog (Xenopus laevis), the favorite model in cell and developmental biology. Our approach relies on dissection of single cells from 2- to 16-cell embryos. Extracts are measured using a custom-built single-cell capillary electrophoresis electrospray ionization system that is coupled to a commercial time-of-flight mass spectrometer. High-efficiency separation, accurate mass measurements, and tandem mass spectrometry have enabled us to confidently identify an appreciable set of metabolites in the metabolome of embryonic cells. Based on this information, we found that certain cell types exhibit metabolic heterogeneity in 16-cell Xenopus embryos. We anticipate that the adaptation of mass spectrometry to single embryonic cells holds exciting, new opportunities for cell and developmental biology as well as other fields where samples are limited in volume or mass.
Speaker Bio: Peter Nemes, Ph.D., is an Assistant Professor of Chemistry (2013–Present) at the George Washington University, Washington DC, whence he obtained his Ph.D. in Chemistry in 2009. He completed his postdoctoral research in Bioanalytical Chemistry for Neurobiology at the University of Illinois—Urbana-Champaign, IL. In 2011, he assumed a Laboratory Leader position with the US Food and Drug Administration (Silver Spring, MD), where he established a mass spectrometry facility and regulatory research program with the US Public Health Emergency Medical Countermeasures Enterprise to develop a scientific framework permitting to combat present and future threats (chemicals and biologics) to the public. Prof. Nemes’ current research at the George Washington University is focused on the development of next-generation mass spectrometry platforms to assess the metabolome and proteome of volume-limited samples including single cells. Prof. Nemes has authored and co-authored 3 book chapters and 24 peer-reviewed publications, and has presented or co-presented the results at 30+ national or international conferences. He has received the 2008 International Research Fellowship Award by the Dimitris N. Chorafas Foundation (Switzerland), the 2009 The American Institute of Chemists prize in Chemistry by The American Institute of Chemists (Washington, DC), the 2010 Science and Technology Innovation Award by Baxter Healthcare Corporation (Chicago, IL), and the 2011 Special Recognition Award by the US Food and Drug Administration. Prof. Nemes is the co-inventor of laser ablation electrospray ionization (LAESI) mass spectrometry and holds four shared patents for the technology.
Wednesday, May 21, 2014
6:00 pm – 8:00 pm
Speaker: Theodore Juarez, MSPH, Uniformed Services University, Bethesda, MD
Title: Inter-variability of INFICON HAPSITE ER Instruments (man-portable Gas Chromatograph/Mass Spectrometer) operated with Manufacturer Provided Calibration Curves
Objective: Determine if the person-portable gas chromatograph/mass spectrometer (INFICON® HAPSITE ER) has comparable inter-instrument accuracy when using the same manufacturer-provided calibration curves.
Results: HAPSITE sample volumes ranged from 95% – 118% of manufacturer designed flow rate. Concentration accuracy ranged between 44% – 218% average agreement with certified concentrations over 34 TO-15 chemicals. ANOVA analysis demonstrated the instruments differed in their estimate of concentrations (α = 0.05).
Conclusions: A means of manually adjusting the flow rate would increase the concentration estimate confidence. A single calibration curve used on multiple instruments does not achieve equivalent accuracy. Additional internal standards could potentially increase confidence and accuracy. At 1 ppm, compared with typical 8-hour time-weighted average occupational exposure limits, there is not a significant uncertainty concern. However, if the instrument were used to assess ceiling, immediately dangerous to life or health or peak exposure limits, the observed uncertainty is potentially a significant concern for human health risk assessment.
Speaker Bio: Theodore Juarez is a Lieutenant Commander and an Industrial Hygienist in the United States Navy. He has a Bachelors of Science degree in Chemistry from California Polytechnic State University, San Luis Obispo where he did research in the synthesis of beta-lactam antibiotics. He has a Masters of Science degree in Public Health with a concentration in Industrial Hygiene from San Diego State University, where he conducted GC/MS analysis of nicotine, cotinine and polycyclic aromatic hydrocarbon content in household dust and analysis of their distribution among smoking, non-smoking households and their relation to traffic exposure. While deployed in support of Operation Iraqi Freedom, he conducted numerous Occupational and Environmental Health Site Assessments using person-portable chemical detection equipment, including GC/MS, and became interested in research involving development and evaluation of novel sampling and analysis methodologies for chemical compounds of military and occupational health relevance. He is currently a PhD candidate at the Uniformed Services University of the Health Sciences. He is a member of the Golden Key International Honors Society, Alpha Chi Sigma Professional in Chemistry Fraternity, past recipient of the American Industrial Hygiene Foundation Scholarship and a student member of the American Industrial Hygiene Association and the American Chemical Society.
Monday, April 14, 2014
6:15 pm – 8:15 pm
Joint Meeting with Washington-Baltimore Mass Spec Discussion Group
Shimadzu Training Center
Speaker: Maureen Kane, Ph.D., University of Maryland, School of Pharmacy
Title: The use of fast HPLC multiplexing MRM3 for retinoic acid quantitation in complex matrices
Abstract: Vitamin A is essential to numerous physiological processes including cell proliferation, differentiation, immune response, development, reproduction, cellular metabolism, and nervous system function. Metabolism activates vitamin A into an active metabolite, retinoic acid (RA), which controls gene transcription through activating nuclear receptors and can also function via non-genomic mechanisms. Because the action of RA is amplified through its signaling mechanisms and represents a key signaling node, the abundance of endogenous RA is strictly controlled. Quantification of endogenous RA is essential to understanding its biological actions and the consequences of disruption to the retinoid pathway. Additionally, there are endogenous RA isomers with distinct biological actions must be resolved to achieve accurate quantification and a full understanding of RA function. Here we describe a Fast HPLC multiplexing MRM3 assay that was developed, characterized, and applied to the detection and quantitation of RA isomers from complex matrices in order to remove interfering signal that is observed with MRM detection during some chromatographic separation systems. The combined integration of Fast HPLC using fused-core particles with an embedded polar group C18 stationary phase, LC multiplexing, and MRM3 detection is a novel combination of analysis methodology which resulted in resolution of endogenous (isobaric) RA isomers, rapid analytical throughput and enhanced specificity without compromising assay sensitivity.
Speaker Bio: Maureen A. Kane, Ph.D., is an Assistant Professor in the Department of Pharmaceutical Sciences at the University of Maryland, School of Pharmacy and Co-Director of the University of Maryland, School of Pharmacy Mass Spectrometry Center. She received a B.S. in Chemistry from Canisius College (Buffalo, NY) and a Ph.D. in Analytical Chemistry from the University at Buffalo, State University of New York. She completed postdoctoral training at the University of California, Berkeley. She has published 43 papers in peer-reviewed journals and two book chapters. The Kane Lab uses mass spectrometry to answer biological questions in a quantitative manner. Dr. Kane specializes in retinoid metabolism and quantitative analysis of active metabolites via mass spectrometry. Retinoids (compounds that exhibit vitamin A activity) regulate cell proliferation, differentiation, apoptosis, development, nervous system function, reproduction, and the immune response. Her tandem mass spectrometric methods for retinoic acid detection have been used to establish functional links between retinoid metabolism and normal physiological function, development, and various disease states. In addition to retinoid metabolism, the Kane Lab has a number of other foci including mass spectrometry imaging, biomarker discovery and validation, targeted and untargeted metabolomics/lipidomics, assay development, and PK/PD profiling.
Tuesday, March 4, 2014
5:30 – 8:30 PM
Buddy Guy’s Legends, 700 S Wabash Ave, Chicago, IL
Wednesday, March 19, 2014
6:00 pm – 8:00 pm
US PharmacopeiaSpeaker: Trina Formolo, Ph.D., NIST, Gaithersburg, MD
Title: Resolution of Sialylated Glycopeptides Using a Pentafluorophenylpropyl (PFP) Stationary PhaseAbstract: Protein-based therapeutics comprise a fast-growing class of pharmaceuticals. However, the inherent variability of these biologics poses a challenge to the industry. Protein drugs with the same primary structure can vary greatly in their glycosylation patterns, which in turn can affect many properties of the drug, including safety, efficacy and stability. Characterizing these glycan structures is therefore an essential step in the evaluation of protein biologics. For proteins that carry multiple glycosylation sites it is often necessary to not only identify each glycan structure present, but also map each structure to the individual occupied sites. This can be performed via enzymatic digestion of the protein followed by glycopeptide enrichment and LC-MS/MS analysis. This presentation will discuss the use of a pentafluorophenylpropyl (PFP) stationary phase to resolve enriched sialylated glycopeptides and compare its chromatographic properties with the commonly used C18 and bridged ethyl hybrid (BEH) phases.
Speaker Bio: Dr. Trina Formolo holds a post-doctoral position at the National Institute of Standards and Technology (NIST) and has been working with her mentor Dr. Karen Phinney in the Biomolecular Measurement Division since May 2012. Trina received her B.S. in Biology from the University of Dallas in Irving, Texas, and her Ph.D. in Molecular Medicine from The George Washington University Institute for Biomedical Sciences under the mentorship of Dr. Yetrib Hathout in the Center for Genetic Medicine Research at Children’s National Medical Center in Washington, DC. There she performed proteomic analyses of the glioblastoma secretome to elucidate the mechanisms of tumor cell aggressiveness as well as characterization of the glycoprotein chitinase-3-like protein 1 and its role in this process. Trina’s work at NIST is focused on the development of standard reference materials for the biopharmaceutical industry as well as the development of methods for glycoprotein quantitation.
Wednesday, February 12, 2014
6:00 pm – 8:00 pm
Speaker: Fabrice Gritti, Ph.D., University of Tennessee, Knoxville, TN
Title: Importance and constraints of the recent progress made in column and instrument technologies for accurate sample quantification by HPLC
Abstract: The quantitative analysis of real mixtures by high performance liquid chromatography (HPLC) requires the complete separation of the target compounds from the other sample components. Then, their accurate and precise quantification may be obtained by using highly controlled protocols if standard solutions of these target compounds are available. Excellent repeatability of the injection device, the column flow rate, the system temperature, the response of the detector, and other column and system performance are to perform reliable quantitative analysis. The increasing complexity of the samples provided by the new requirements brought by genomics, proteomics, or food analyses is constantly demanding advanced performance from the LC column and the instrumentation. High peak resolution is required for accurate quantification. As a result of recent progress, the column volume, the size of the particles with which they are packed, and the analysis times have decreased. The reproducibility of instruments improved. Yet, columns must be operated under pressures as high as 1300 bar and can no longer be run under isothermal conditions. Often, the instrument contribution to band broadening limits the column performance because instrument technology has progressed more slowly than column performance. This makes difficult the transfer of classical slow HPLC methods to advanced UPLC methods. This presentation will discuss the evolution of the performance and robustness of HPLC systems from the 1990s to today (e.g., from the 1090 HP to the 1290 Agilent) and the modern requirements of reliable sample quantifications. Then, we report on column-to-column repeatability (retention, retention, and efficiency), on the evolution of column resolution power and on our expectations for further improvements of column technology. Finally, the possible negative impacts of modern instruments on the resolution provided by highly efficient columns and of the use of very high pressures in fast gradient analyses on data reproducibility will be illustrated.
Speaker Bio: Fabrice G. Gritti received a B.S. degree in Chemistry and Physics from the University Joseph Fourier of Grenoble (France) in 1995, a graduate Engineering school degree in Chemistry and Physics from the University of Bordeaux I (France) in 1997, and a Ph.D. in Chemistry and Physics from the University of Bordeaux I (France) in 2001. He came in the U.S. in 2002 for a post-doctoral study at the University of Tennessee with Prof. Georges Guiochon. He is now a Research Scientist in the Department of Chemistry at the same university. Fabrice’s research interests involve liquid/solid adsorption thermodynamics and mass transfer in heterogeneous media for characterization and design of new HPLC column technology. He developed experimental protocols that helped refine (1) the models of adsorption isotherms used in preparative chromatography for the prediction of the band profiles of neutral and ionizable compounds and (2) the theory of band broadening along analytical columns in linear chromatography. He has published over 190 papers.
Joint Meeting with the Chemical Society of Washington
Wednesday, December 11, 2013
6:00 pm – 8:00 pm
ACS Headquarters, 1155 16th St NW, Washington, DC
Speaker: Isiah Warner, Ph.D., Louisiana State University, Baton Rouge, LA
Title: GUMBOS: Tunable Materials for Biomedical Applications
Abstract: Modern analytical methods continue to improve the ability of analysts to sensitively identify and quantify the structure and composition of complex drugs. The increased information content these technologies provide increases the level of assurance of these products’ quality. For this reason, the FDA has investigated the use of information rich analytical techniques to assess the quality of complex drug products including therapeutic proteins, monoclonal antibodies, and naturally derived small molecules. I will present examples of these techniques applied to currently marketed products.
Speaker Bio: Professor Warner is an analytical chemist with more than 300 refereed publications in a variety of journals relevant to his general area of research. He has particular expertise in the area of fluorescence spectroscopy, where his research has focused for more than 35 years. He is considered one of the world’s experts in this analytical spectroscopy. For example, he is the corresponding author in the highly cited biannual reviews on “Molecular Fluorescence, Phosphorescence, and Chemiluminescence Spectrometry“, for the journal, Analytical Chemistry. Over the past 20 years, he has also maintained a strong research effort in the areas of organized media and separation science. Professor Warner has been performing research in the more specific area of analytical measurements using ionic liquids (ILs) for several years. It is this research on ionic liquids which has lead to the recent conceptualization and implementation of a group of uniform materials based on organic salts (GUMBOS) as novel materials which can be exploited for a variety of applications. Novel nanoparticles (nanoGUMBOS) have been derived from these materials which can primarily be classified as frozen ILs. However, some GUMBOS are not ionic liquids since they do not fit the traditional definition of ILs. The utility of these materials is that they provide solid phase materials with the same tunability of ionic liquids. Several publications in key chemistry journals (e.g. JACS, Nano Letters, ACS Nano, Analytical Chemistry, Chemical Communications, and Langmuir) and pending patents have resulted from this new area of research.
Wednesday, November 13, 2013
6:00 pm – 8:00 pm
Speaker: Tony Brand, Ph.D., Agilent Technologies
Title: Do we really know what the left and right are up to? Supercritical Fluid Chromatography is now the tool to tell, with some help from an MS
Abstract: Chiral drugs are important in medicine and SFC has earned its place as a preferred chromatographic analysis tool for separating enantiomers, etc. With the new generation of instruments, SFC is now poised to take a bigger role in the laboratory. This talk will introduce the basic theory of SFC and contrast its application to reverse phase and normal phase LC and GC. A number of re-discovered SFC and SFC/MS applications will be discussed, highlighting the advantages of using liquid carbon dioxide as a chromatographic solvent.
Speaker Bio: Dr. Tony Brand obtained his Ph.D. in Physical Organic Chemistry at the University of California. He came to HP/Agilent in 1994 and hasn’t left yet. Tony started as a LIMS specialist, then joined the newly formed LC/MS team in 1997. More recently, he has been working on ultra-high throughput LC and LC/MS applications as well as process automation, as well as being a leader in the SFC team.
6:00 pm – 8:00 pm
U.S. PharmacopeiaSpeaker: Benjamin Place, Ph.D., NIST
Title: Multi-Dimensional Chromatography as a Quantitative Tool
Abstract: Comprehensive, two-dimensional liquid chromatography (LCxLC) and gas chromatography (GCxGC) are emerging techniques that increase the chromatographic peak capacity of a single analytical run through the use of orthogonal separation mechanisms. These techniques are excellent for the separation of species of interest from other compounds (e.g., isomeric separation and/or sample matrix interferences). Early studies with both GCxGC and LCxLC have mainly focused on qualitative efforts, such as increasing peak capacity. Quantitative efforts have been made with both techniques, although the methods are less developed due to a lack of data processing tools. This presentation will focus on the efforts at the National Institute of Standards and Technology (NIST) to better understand GCxGC-TOF-MS and LCxLC-UV/Vis analyses, as well as determine the quantitative performance of these tools. Quantitative analysis by LCxLC-UV/Vis is still in its infant stage and multiple studies were performed to understand the data-processing. A program was developed in-house using R statistical software, an open-source program, for the transparent examination of various peak description and integration approaches and its impact on the quantitative performance of LCxLC-UV/Vis determination of four polycyclic aromatic hydrocarbons (PAHs). Also, various commercially-available software programs were evaluated for quantitative performance by the same LCxLC-UV/Vis analysis. Quantitative GCxGC-TOF-MS analysis has been much more rigorously studied, although analytical method development for specific analytes is still being studied. At NIST, multiple analytical methods were developed for GCxGC-TOF-MS for the detection of PAHs in available NIST Standard Reference Materials (SRMs). The quantitative performance of these GCxGC methods will be presented, along with future goals of NIST multidimensional chromatography program.Speaker Bio: Dr. Benjamin Place is currently an NRC Postdoctoral Fellow at the National Institute of Standards and Technology (NIST) and has been working with his mentor Dr. Catherine Rimmer in the Chemical Sciences Division since October 2012. Ben received his B.S. in Chemistry from Alma College, Alma, MI in 2008 and his Ph.D. in Analytical Chemistry from Oregon State University while working with Dr. Jennifer Field developing analytical methods for the identification, detection, and quantification of emerging contaminants in environmentally-relevant matrices. His Ph.D. work covered a wide range of compounds, including carbon nanomaterials, per- and polyfluorinated surfactants, and oil dispersant surfactants. Ben’s NRC fellowship work at NIST is focused on the development of LCxLC-MS methods for the non-targeted screening of Standard Reference Materials (SRMs) for novel environmental compounds.
Open House and Poster Session
Wednesday, September 18, 2013
6:00 pm – 8:00 pm
Bethesda North Marriott Hotel & Conference Center
5701 Marinelli RdNorth Bethesda, MD 20852
Wednesday, May 22, 2013
6:00 pm – 8:00 pm
Speaker: Dr. Christopher Okunji, USP
Title: High Speed Counter-Current Chromatography: An Efficient Technique for Large-Scale Isolation of Pharmacopeia Reference Standards
Abstract: High-speed counter-current chromatography (HSCCC) is an all-liquid chromatographic system that uses a support-free liquid stationary phase. HSCCC is winning wide applications in the preparative separation of various natural and synthetic products. Compared to preparative HPLC, HCCCC offers several advantages including significantly higher sample load requiring only cheap solvents instead of expensive solid phase columns for the separation. Many medicinal plants have been studied and more than 1000 compounds have been successfully prepared by HSCCC for both commercial and research purposes. HPLC purities of separated compounds are all above 90-98%. The major classes of natural products that have been separated using HSCCC include alkaloids, flavonoids, phenolics, terpenoids, saponins, phenylpropanoids, quinones, stilbenes, sterols, peptides, anthraquinones and organic acids. Among these constituents the more noteworthy representatives of dietary supplement reference standards are tanshinones from Salvia miltiorrhiza, monoterpene glycosides (Rosavin) from Rhodiola rosea, cichoric acid from Echinacea purpurea root, ganoderic acids from Ganoderma lucidum fungus, ginsenosides from ginseng, capsaicin and dihydrocapsaicin from Capsicum frutescens, bilobalide and ginkgolides from Ginkgo biloba leaves, lycopene from crude extract of tomato paste, etc. Recent advances in instrument development as well as application of this technique to scale-up isolation of USP reference standards will be discussed. The strengths and versatility of HSCCC separations and their ability to increase resolution and throughput and overcome traditional drawbacks of adsorption chromatography will be highlighted.
Speaker Bio: Dr. Chris Okunji is a Scientific Liaison for the Dietary Supplements group at United States Pharmacopeia (USP), Headquarter, Rockville MD., responsible for Dietary Supplement General Chapters and works closely with the USP Dietary Supplements and General Chapters Expert Committee’s where appropriate. Before joining USP in 2011, Dr.Okunji has been an NIH Special Volunteer working with countercurrent chromatography (CCC) to isolate large quantities of natural product constituents, Scientific Review Administrator NIAID-NIH (Contractor) and Senior Research Associate at Walter Reed Army Institute of Research (WRAIR) all in Maryland. Dr.Okunji’s teaching and research experience in the field of natural products/pharmacognosy includes scale-up isolation of natural product compounds using CCC, screening African medicinal plants for biological activities such as antimalarial, antileishmanial, antifungal, anticancer, antimicrobial, antitrypanosomiasis and antitrichomonas and Anti-HIV. Dr. Okunji also has Dietary Supplement manufacturing experience and a former Associate Professor of Pharmacognosy, University of Nigeria. Dr. Okunji holds a M.Sc. and Ph.D. degrees in Pharmacognosy from University of Nigeria. He has more than 30 years of experience in academic, industrial and government settings. Dr. Okunji is a recipient of U.S. National Research Council Fellowship in 1993.
Monday, April 15, 2013
Co-sponsored with the Washington-Baltimore Mass Spectrometry Discussion Group
6:00 pm – 8:15 pm (Speaker at 7:15 pm)
Shimadzu Training Center
Speaker: Dr. Michael Boyne, FDA
Title: Modern Analytics for the Analysis of Complex Drug Products: Physicochemical Characterization using MS
Abstract: Modern analytical methods continue to improve the ability of analysts to sensitively identify and quantify the structure and composition of complex drugs. The increased information content these technologies provide increases the level of assurance of these products’ quality. For this reason, the FDA has investigated the use of information rich analytical techniques to assess the quality of complex drug products including therapeutic proteins, monoclonal antibodies, and naturally derived small molecules. I will present examples of these techniques applied to currently marketed products.
Wednesday, February 20, 2013
6:00 pm – 8:00 pm
Speaker: Andrew Alpert, PolyLC
Title: Advantages of HILIC and ERLIC for Proteomics
Abstract: Hydrophilic interaction chromatography (HILIC) can accomplish some separations that are not easy or possible with alternative modes:
Top-down proteomics: If a set of proteins can be maintained in the predominantly organic solutions, then top-down analysis of intact proteins can be done with volatile solvents. This then permits their separation on the basis of differences as minor as a single carbohydrate residue.
Bottom-up proteomics: A HILIC-RP sequence compares favorably with the widely-used SCX-RP sequence for fractionation of complex tryptic digests. The new ERLIC mode (electrostatic repulsion-hydrophilic interaction chromatography) is even better. Using volatile solvents, an ERLIC-RP sequence identifies 30-40% more peptides and proteins than does a SCX-RP sequence, with appreciably less effort. ERLIC separates tryptic peptides in order of decreasing pI value, without ampholines. ERLIC also affords selective isolation and separation of phosphopeptides and glycopeptides from unmodified peptides. Finally, a RP-ERLIC sequence permits the identification of proteins that were deamidated in vivo. This may be a new mechanism for biological control. The motifs for sites susceptible to deamidation of asparagine matched those in the literature, but sites for deamidation of glutamine were quite different.
Speaker Bio: Andrew Alpert received his B.S. degree in chemistry from Yale College in 1973 and a M.S. in biochemistry from the University of Nebraska Medical Center. His Ph.D. work was with Fred Regnier at Purdue University, developing the first HPLC packing materials and techniques for protein applications. Following two post-doctoral fellowships at Baylor College of Medicine (Arthur Beaudet’s group and H. F. Gilbert’s group), he started PolyLC in 1985. The company manufactures chromatography columns and materials for difficult protein and peptide separations. Dr. Alpert introduced the technique of Hydrophilic Interaction Chromatography (HILIC) in 1990. Current interests include: 1) Development of techniques for analysis of particularly difficult proteins, including histone variants and proteomics analysis of both membrane and nonmembrane proteins; 2) Mixed-bed ion-exchange columns for proteins; 3) Multidimensional fractionation of peptides for proteomics applications (e.g., the SCX-RP sequence); 4) HILIC of solutes on columns of the same charge (a variant called ERLIC), which permits isocratic separations of solutes differing greatly in composition such as amino acids and nucleotides. It also affords selective isolation and resolution of phosphopeptides, glycopeptides, and deamidated peptides for proteomics analyses.
Wednesday, January 16, 2013
6:00 pm – 8:00 pm
Speaker: Kevin Siek, LECO Corporation
Title: “Sharpening Chromatographic and Spectral Resolution to Reveal More in Metabolomic, Food Safety, Environmental, and Pharmaceutical Sciences”
Abstract: The analysis of complex mixtures and characterization of the analytes therein is of fundamental significance to numerous disciplines of study. In modern analytical sciences this requires separation followed by analysis using a diagnostic spectroscopic technique. This is most often achieved using liquid chromatography or gas chromatography interfaced to mass spectrometry. The degree of separation required is related inversely to the “power” (resolution and mass accuracy) of the mass spectrometric technique. An ultra-high resolution mass spectrometer (R > 25,000) requires less chromatographic resolution than a unit mass system and a high capacity (resolution) separation (two dimensional gas chromatography or capillary electrophoresis) does not necessarily require an ultra-high resolution mass spectrometer. In this presentation, examples are provided from numerous fields of analytical study including metabolomics, environmental sciences and food safety, and petroleum analysis which demonstrate utility of high mass resolving power, as well as the utility of GCxGC separation to achieve analyte identification by separation from interfering substances. The capability of ultra high performance mass spectrometry using comprehensive time of flight to provide high-confidence formula and structural identification is leveraged in a variety of matrices and to address numerous analytical issues. Mass resolving powers at 25000 or 50000 or higher and mass errors of approx. 1 ppm provide confident identifications and selective detection. Two dimensional GC in combination with library-searchable EI spectra provide an ability to complement what is detected using the high performance MS analyses.
Speaker Bio: Kevin Siek is the Technical Product Specialist for High Resolution TOFMS Technology for LECO Corporation, a position he has held for three years. Prior to his position at LECO, Kevin was in pharmaceutical research and development at Sanofi-Aventis for about fifteen years, where he gained experience in molecular characterization, quantitative method development for putatively genotoxic impurities and other assays, metabolite identification, finished product characterization, and other duties as needed, including but not limited to improvisatorial plumbing and sweeping up much shattered glassware. His greatest single accomplishment has been persuading his wife to stay married to him through all this. Anyone living with someone who finds chemistry jokes funny deserves admiration. Kevin received his BS in Chemistry from Valparaiso Univeristy.
Wednesday, December 12, 2012
6:00 pm – 8:00 pm
Speaker: Jeff Rohrer, Ph.D., Director, Applications Development, Dionex Products, Thermo Fisher Scientific
Title: Ion Chromatography for Pharmaceuticals
Abstract: The last decade has witnessed a significant increase in the number of ion chromatography (IC) based methods in the United States Pharmacopeia National Formulary (USP-NF). The methods include assays of drug substances and drug products, and the determination of related substances and impurities in drug substances and drug products. IC is also commonly used in the pharmaceutical industry to assay for excipients and active pharmaceutical ingredient (API) counterions. Compared to reversed-phase HPLC, IC offers a different and often superior approach to determining ionic compounds, especially those lacking a strong chromophore. Most IC assays feature an ion-exchange separation followed by suppressed conductivity detection, but there are IC methods for pharmaceuticals that use other detection techniques. This talk will review the general principles of IC including separation and detection strategies, as well as briefly discuss newer develops including capillary IC and the charge detector. The majority of the presentation will describe the development of IC assays for drug substances and products, related substances and impurities in drug substances and products, and API counterions. The assays presented will demonstrate the different IC separation and detection strategies that can be employed to meet the specificity and sensitivity needs of the application.
Speaker Bio: Dr. Jeffrey S. Rohrer is the Director of Applications Development, Dionex Products for Thermo Fisher Scientific. In this position he directs the work of three corporate applications laboratories in California, China, and Thailand. These labs develop HPLC, IC, HPAE-PAD, and other LC-based assays. Dr. Rohrer is an author of over 50 peer-reviewed publications and is a member of the United States Pharmacopeia (USP) Expert Committee on Monograph Development for Small Molecules #1, a member of the USP Expert Panel on Glycoprotein and Glycan Analysis, and a member of the USP Expert Panel on Modernization of Identification Tests. Between 2005 and 2010 he was a member of the USP Expert Committee for Antibiotics Monograph Development. He is also the coeditor or a recently published book: Applications of Ion Chromatography for Pharmaceutical and Biological Products (Wiley). Dr. Rohrer joined Thermo Fisher (then Dionex) in 1989 and has held positions that include, Marketing Field Chemist, Senior Biochemist in R&D, Sales Support Manager, and Applications Lab Manager. Prior to joining Thermo Fisher Scientific he spent two years as a post-doctoral associate in Dr. Elizabeth Theil’s lab at North Carolina State University studying the mechanism of iron deposition into the protein ferritin. Jeff received his BS in Chemistry from Franklin and Marshall College in 1981 and his Ph.D. in Chemistry from the University of Delaware working with Dr. Harold White III studying the role of glycosylation in the transport of chicken serum riboflavin-binding protein across the oocyte membrane.
Tuesday, November 13, 2012
6:00 pm – 8:00 pm
Speaker: Len Sidisky, R&D Manager, Gas Separations, Supelco
Title: Advances in Ionic Liquid Stationary Phases for Capillary Gas Chromatography
Abstract: Ionic liquids have received considerable interest as new green solvent systems in the areas of organic reactions and separation technologies along with a number of other areas. These materials are a class of non-molecular solvents that consist of essentially organic cations and anions. They have been found to possess negligible volatility, non-flammability, high thermal stability, and low melting points. There are numerous combinations of cations and anions possible, so tailoring the material to a specific application or function is a potential benefit of these materials.
Recently, a series of geminal dicationic and polyionic ionic liquids have been prepared for use as stationary phases in capillary gas chromatography. These materials are known to provide higher thermal stability for gas chromatography, broader liquid working ranges and broader selectivity ranges than monocationic ionic liquids. This study will examine the selectivity of newly developed ionic liquid phases along with comparing their thermal stability and durability. A variety of Petrochemical, Food & Beverage and Environmental samples will be evaluated for the comparisons.
Speaker Bio: Leonard M. Sidisky is Research & Development Manager for Gas Separations at Supelco, Division of Sigma-Aldrich. He received his B.S. degree in Biology (1980) and an M.S. in Food Science (1997) from The Pennsylvania State University. He has been working at Supelco since 1982 and is responsible for the research and development of new novel technologies related to gas chromatography, sample preparation, air sampling, solid phase microextraction and high performance carbon adsorbents. His analytical background includes expertise in Gas Chromatography, Liquid Chromatography, Sample Preparation devices such as Solid Phase Extraction (SPE), and Solid Phase Microextraction (SPME). He is a member of the American Oil Chemist’s Society (AOCS), AOCS Analytical Division, AOCS Northeast Section, AOCS Chromatography Committee Chairperson 2000-2009, AOCS Governing Board Technical Steering Committee Chairperson 2010-present, AOCS Northeast Section president 2000-2001, vice president 1998-1999, Hans Kaunitz Award Chairman 2000-2001, Supelco/Nicholas Pelick AOCS Lipid Award Representative 1994-present, 1992 Ralph H. Potts Memorial Fellowship Award Winner. He is also a member of the Institute of Food Technologists (IFT) professional member 1992-present, American Chemical Society (ACS) member 1982-present; ASTM D16 (Aromatic Hydrocarbons) 1990-present, D16.OE.09 Task Group (Capillary Applications) chairman 1995-present and ASTM E13 Committee His research interests are in the development of Gas Chromatographic products for wide range of industrial applications, capillary columns for lipid sample analyses, theory and practical application of Capillary Gas Chromatography and Solid Phase Micro Extraction (SPME) product development and applications. He has presented numerous papers and seminars worldwide and has published over 25 journals articles.
Thursday, October 11, 2012
Chemical Society of Washington Dinner Meeting
6:00 pm – 9:00 pm
Far East Restaurant, Rockville, MD
6:00 pm – Social Hour and Poster Session by Project SEED Students
7:00 pm – Dinner
8:00 pm – Speaker Presentation
Speaker: Jessica Reiner, Ph.D., National Institute of Standards and Technology
Title: Temporal and Spatial Trends of Current-use and Legacy Persistent Organic Pollutants in Marine Mammals
Abstract: The Arctic is considered a major sink for persistent organic pollutants (POPs) that are capable of long range atmospheric or oceanic transport. Once in the arctic biosphere, cold temperatures reduce their degradation and facilitate transport from air to water, enhancing bioconcentration into aquatic food webs. Consequently there have been numerous studies assessing time and location trends of POPs in arctic regions including regions in Canada, Greenland, and northern Europe. There are comparatively fewer time trend descriptions of POPs in arctic fauna from other locations particularly from the northern Bering Sea and Chukchi Sea regions of the Arctic.
The Alaska Marine Mammal Tissue Archival Project (AMMTAP) was established in 1987 through an agreement between the National Oceanic and Atmospheric Administration (NOAA), the National Institute of Standards and Technology (NIST), and the Minerals Management Service (MMS) to help determine contaminant levels in marine mammal samples that were taken primarily during native subsistence hunts in Alaska. Tissues were collected and banked at the National Marine Mammal Tissue Bank (NMMTB) for long-term archival using NIST standardized protocols. Archived samples from the NMMTB were provided for this retrospective analysis of contaminants.
From 1989 to 2006 liver (n=68) and blubber samples (n=72) were collected from beluga whales (Delphinapterus leucas) from both the Cook Inlet and the eastern Chukchi Sea beluga whale stocks and analyzed for a variety of current-use and legacy POPs, in order to provide more information on the status of POPs in the Alaskan region. From 1987 to 2007, liver (n=49) and blubber samples (n=50) were collected from northern fur seals (Callorhinus ursinus) from St. Paul Island in the Bering Sea and analyzed for the POPs. This presentation will discuss measurements of POPs from these two arctic species and demonstrate the importance of a long term archival program as a source of samples for monitoring time trends.
Speaker Bio: Dr. Jessica Reiner received a B.S. degree in Chemistry and Chemical Oceanography at the University of Rhode Island in 2001 and a Ph.D. degree in Environmental Chemistry at University at Albany, State University of New York in 2007. Dr. Reiner’s research interests are focused in the area of chemicals of emerging concern in environmental and human samples. She has worked in determining contaminant concentrations in sediment, water, food, biota, and humans, as well as establishing baseline information on potential exposure pathways. Presently, her research goals are to improve analytical measurements of chemicals of emerging concern, mainly perfluorinated alky acids, through the certification of reference materials, methods development, and other quality assurance activities. She has worked as part of the NIST staff at the Hollings Marine Laboratory in Charleston, SC; a multidisciplinary research location that focuses on solving marine and human health problems. She has authored and co-authored several peer-reviewed publications and presented at many national and international conferences.
Open House & Poster Session
Wednesday, September 12, 2012
Click here to download a PDF of the program.
Wednesday, May 16, 2012
6:00 pm – 8:00 pm
US Pharmacopeia, Rockville, MD
Speaker: Pierluigi DelMonte, Ph.D., Office of Regulatory Science Center for Food Safety and Applied Nutrition, FDA
Title: Investigation of comprehensive LCxLC for the separation of phytochemicals in dietary supplements
Abstract: Botanical dietary supplements are most often complex mixtures of phytochemicals characterized by markedly different chemical properties. Often a single dimension liquid chromatographic separation does not provide the theoretical plates or the selectivity needed for the separation of such complex mixtures. While reversed phase chromatography (RP) is the most widely applied approach for the separation of phytochemicals, normal phase and HILIC chromatography are often used to separate compounds containing sugar moieties. The combination of these separation mechanisms in a comprehensive LCxLC system using a HILIC column for the first dimension separation (D1) and an RP column for the second dimension (D2) proved to be a suitable platform for the separation of phytochemicals in dietary supplements.
Comprehensive LCxLC was tested for the separation of the polyphenolic compounds and steviol glycosides in extracts of Stevia rebaudiana. The tested platform consisted of a capillary WAX column for D1 separation and a C18 UHPLC column (2.1 mm x 30 mm, 1.8 micron) maintained at 60 °C for the D2 separation, with a modulation time of 15 sec.
Speaker Bio: Pierluigi Delmonte received his Master Degree in Chemistry from the University of Parma (Parma, Italy) in 1996 and the Doctorate Degree in Food Biotechnology from the University of Bologna (Bologna, Italy) in 2001. His Ph.D. research focused on the analysis of conjugated linoleic acid (CLA) in dairy products. In 2001, Dr. Delmonte joined the Center for Food Safety and Applied Nutrition of the U.S. Food and Drug Administration. His research focuses primarily on the development of HPLC and gas chromatography methods for the analysis of CLA and trans fatty acids in foods, and of active components in dietary supplements.
Wednesday, April 18, 2012
6:00 pm – 8:00 pm
US Pharmacopeia, Rockville, MD
Speaker: Mark Lowenthal, Ph.D., National Institute of Standards and Technology
Title: Developing LC-MS methods for qualitative characterization of NIST Standard Reference Materials
Abstract: Standard Reference Materials (SRMs) offer the scientific community a stable source of biomaterials boasting broad application possibilities. Traditionally, SRMs provide quantitative information for only a few targeted analytes in buffered solutions, or complex matrices. Current efforts attempt to broaden the scope of how and what information is offered to the SRM community by providing qualitative information about biomaterials, such as chromatographic profiles and untargeted identifications. In order to more fully characterize these biomaterials, metabolomic and proteomic profiles were applied to a suite of Vaccinium berry dietary supplement SRMs. An unbounded set of qualitative data about a biomaterial is a valuable resource intended to complement quantitative information traditionally provided in NIST Certificates of Analysis. Metabolites and proteins were separately enriched from a suite of Vaccinium-based biomaterials. Untargeted metabolite discovery was performed using mass spectral matching of tandem MS data to the NIST MS/MS library. Validation of metabolite IDs was achieved using multiple reaction monitoring MS analysis on a triple quadrupole MS with authentic standards. The use of prior probabilities for metabolite identification is discussed. Proteins were analyzed using typical bottom-up proteomics approaches. A protein database was created from Vaccinium and citrus-based expressed sequence tags (ESTs) and used for novel protein identifications. Definitive IDs are reported for metabolites and novel protein identifications. Over 50 putative identifications were determined among the biomaterials based on reporting guidelines set forth by the Metabolomics Standards Initiative. A large subset of identifications consisted of anthocyanins, organic acids, flavan-3-ols, and other flavanoids typically found from fruit extracts. Chromatographic profiling of these berry materials will provide valuable qualitative information for users of an SRM material. Using MS library matching to discriminate biomolecules or biomolecular classes in complex materials is discussed in regards to the structural similarity among many small organic molecules.
Speaker Bio: Mark Lowenthal is a research chemist at the National Institute of Standards and Technology in the Material Measurement Lab (Analytical Chemistry Division). He has been at NIST for over four years working on qualitative and quantitative measurements of metabolites and proteins in biomaterials and SRMs. Prior to joining NIST, Mark worked on molecular profiles of cellular lipid droplets at the University of Colorado Health Sciences Center, and for three years in a proteomics lab at NIH (NCI). Mark got a PhD from the University of Maryland in Analytical Chemistry.
Wednesday, March 21, 2012
6:00 pm – 8:00 pm
US Pharmacopeia, Rockville, MD
Speaker: John Van Antwerp, Waters Corporation
Title: Fundamentals and Advancements in Analytical SFC
Abstract: In the past decade, Supercritical Fluid Chromatography (SFC) has demonstrated great promise as the choice of chromatography for chiral compounds, and as a general replacement technique for normal phase liquid chromatography (NPLC). Compared to traditional normal phase HPLC, SFC is on average 3 to 10 times faster. Using inexpensive CO2 and a polar modifier such as methanol, SFC is more cost-effective and environmentally friendly by reducing the consumption and disposal of organic solvents. Widespread adoption of analytical SFC has been hampered by instrumentation which does not perform to the standards established by modern HPLC systems. Poor signal to noise ratio, poor retention time and injector reproducibility, and overall lower reliability, as compared to HPLC, are often described as major limitations. In order to bring this separation technique to a performance level desired by today’s modern laboratory, a holistic system must be designed from the ground up. The majority of system components of an analytical SFC system are the same as any LC system, pump, autosampler, detector, software solutions, along with some components unique to SFC. Although similar to LC, the design challenges for each component must be considered and each component must be designed so that the system as a whole performs at a high level. We present here some of the design challenges along with their solutions and a basic evaluation of instrument performance, at a system level. This talk will describe the advances made to the hardware and chemistries and will have examples of increases in efficiencies and throughput as well as return on investment.
Speaker Bio: John Van Antwerp is the Waters Corporation Americas Business Manager for quadrupole MS products and SFC/SFE. He has been at Waters for 24 years in various roles from regional technical support up through his current role as business manager. Over the past 15 years he has been involved in new technologies at waters including LC/MS, SFC, SFE and SFC/MS. Prior to joining Waters , John spent 15 years developing analytical HPLC methods for a major Pharmaceutical Company.
Wednesday, February 15, 2012
6:00 pm – 8:00 pm
US Pharmacopeia, Rockville, MD
Speaker: Rick Lake and Ty Kahler, Restek Corporation
Title: Characterizing Stationary Phase Selectivity – A Practical Look at Column Selection
Abstract: In this presentation, we will review the popular Hydrophobic Subtraction Model and present an extended characterization for modern non-alkyl phases. We will then discuss the dominant reversed phase separation mechanisms involved with common stationary phase types. Lastly, we will provide a practical approach to stationary phase selection, including a brief discussion on applying scouting gradients.
Speaker Bios: As a Product Line Manager, Rick Lake oversees the development and application of Restek’s LC products. He previously served as our Pharmaceutical Market Development Manager and Pharmaceutical Innovations Chemist, developing GC and LC applications and assisting in new product development. Before coming on board in 2005, he worked for 7 years as a study director and principal investigator for a contract research lab, where he developed and validated GC and LC methods while also managing the stability testing department. Prior to shifting his focus to pharmaceuticals, he spent 4 years performing pesticide residue and volatile/semivolatile analysis.
Ty Kahler joined Restek as a Senior Innovations Chemist in 2008 where his responsibilities include liquid chromatographic methods development, standard methods testing, and phase design/research. Prior to joining Restek, he worked as a manager, study director, and principal investigator for a contract pharmaceutical research laboratory conducting method development, validation, and analysis of pre-clinical and clinical pharmaceuticals. He has been in the fields of pharmaceuticals and liquid chromatography development and analysis for over 14 years, including time as a quality chemist and instrumentation metrologist. In addition to time spent in the pharmaceutical industry, he has worked as the lead chemist on studies involving agrochemicals and pesticide manufacturing.
Wednesday, January 18, 2012
6:00 pm – 8:00 pm
US Pharmacopeia, Rockville, MD
Speaker: Ruin Moaddel, Ph.D., National Institute on Aging, National Institutes of Health
Title: Bioaffinity Chromatography: The Study of Drug-Protein and Protein-Protein Interactions
Abstract: Protein-based liquid chromatography stationary phases are used in bioaffinity chromatography for studying drug-protein interactions including the determination of binding affinities and competitive and allosteric interactions, as well as for studying protein-protein interactions. The development and characterization of protein-based stationary phase, and the application of these phases using frontal and zonal chromatography techniques will be discussed. More recently, the use of the protein-coated magnetic beads for ligand and protein fishing has also been carried out, demonstrating the versatility of protein-based stationary phases for the identification of unknown ligands from cellular or botanical extracts.
Speaker Bio: Ruin Moaddel earned his Ph.D. from Northeastern University in 1999, followed by post-doctoral studies at Georgetown University. He is currently a Staff Scientist at the National Institute on Aging, NIH. Currently at the NIA, Ruin’s main research interests are in the creation of cellular membrane affinity chromatography columns on multiple formats and their use in online drug screening in complex matrices and ligand binding studies for multiple proteins. This is carried out by frontal affinity chromatography, non-linear chromatography, missing peak chromatography and/or ligand fishing in complex matrices.
Wednesday, November 16, 2011
6:00 pm – 8:00 pm
Shimadzu Scientific Instruments, Inc. Training Center
7100 Riverwood Drive, Columbia, MD 21046
Speaker: Cynthia Tyburczy, Ph.D., FDA-CFSAN
Title: Covalent Adduct Chemical Ionization Mass Spectrometry for the Identification of Fatty Acid Methyl Ester Double Bond Configuration
Abstract: Covalent adduct chemical ionization (CACI) mass spectrometry (MS) was developed as a convenient and rapid tool for the unequivocal identification of double bond configuration in most fatty acid methyl esters (FAME). Acetonitrile maintained under CI conditions yields ions at m/z 40 and 42, and an ion at m/z 54 which was identified as 1-methyleneimino-1-ethenylium, the decomposition product of the reaction of acetonitrile with itself. The m/z 54 ion selectively reacts with the double bonds of FAME, resulting in predictable fragmentation about the double bonds. Single-stage CACI-MS provides structural information related to FAME chain length, degree of unsaturation and, in some cases, double bond geometry. In CACI MS/MS, fragmentation of the preselected parent ions yields a small number of predictable peaks that are indicative of FAME double bond location. Key practical advantages of CACI MS and MS/MS over re-derivatization methods involving 4,4 dimethyloxazoline (DMOX) or picolinyl esters include the fact that FAME are analyzed directly with no additional chemical treatment and that similar gas chromatography (GC) conditions (column, temperature program, sample concentration) are used, thus enabling direct comparisons between GC and GC-MS chromatograms. This method is applicable to the identification of homoallylic and conjugated linoleic acid FAME and to the quantitation of cis and trans monoenoic FAME through selected ion monitoring. In recent years, CACI-MS and MS/MS have been used for the identification of unique partially conjugated and non methylene interrupted polyenoic FAME.
Speaker Bio: Cynthia Tyburczy earned her B.S. (2006) and M.S. (2008) degrees in Animal Science from Cornell University working with Dr. Dale E. Bauman. Her M.S. research focused on the biological activity of individual trans 18:1 fatty acids with regard to milk fat synthesis and as biomarkers for coronary heart disease risk. She earned her Ph.D. (2011) in Molecular Nutrition from the Division of Nutritional Sciences at Cornell University working with Dr. J. Thomas Brenna. Cynthia’s Ph.D. research focused on the effect of dietary arachidonic acid level and source on neonatal piglet development. She joined the U.S. Food and Drug Administration’s Center for Food Safety and Applied Nutrition in April 2011 as a postdoctoral research fellow. She currently investigates gas chromatography and infrared spectroscopy methods for quantifying trans fat in food.