HANDBOOK OF LC-MS BIOANALYSIS
|
|
|
- Stephany Hensley
- 10 years ago
- Views:
Transcription
1 HANDBOOK OF LC-MS BIOANALYSIS Best Practices, Experimental Protocols, and Regulations Edited by WENKUI LI, PhD Novartis Institutes for BioMedical Research, East Hanover, NJ, USA JIE ZHANG, PhD Novartis Institutes for BioMedical Research, East Hanover, NJ, USA FRANCIS L.S. TSE, PhD Novartis Institutes for BioMedical Research, East Hanover, NJ, USA
2 CONTENTS PREFACE CONTRIBUTORS ABBREVIATIONS xi xiii xvii PART I OVERVIEW OF LC-MS BIOANALYSIS 1 Roles of LC-MS Bioanalysis in Drug Discovery, Development, and Therapeutic Drug Monitoring 3 Sieve Unger, Wenkui Li, Jimmy Fiarakos, and Francis L.S. Tse 2 Overview: Fundamentals of a Bioanalytical Laboratory 15 Slwfali Palel, Qiangtao (Mike) Huang, Wenying Jian, Richard Edom, and Naidong Weng 3 International Regulations and Quality Standards of Bioanalysis 29 Surendra K. Bansal PART II CURRENT UNDERSTANDING OF LC-MS BIOANALYSIS-RELATED REGULATIONS 4 Current Regulations for Bioanalytical Method Validations 39 Mark E. Arnold, Rafael E. Barrientos-Asiigarraga, Fabio Garofolo, Shinobu Kudoh, Shrinivas S. Savale, Daniel Tang, Philip Timmerman, and Peter van Amsterdam 5 Current Understanding of Bioanalytical Assay Reproducibility: Incurred Sample Reanalysis, Incurred Sample Stability, and Incurred Sample Accuracy 47 Manish S. Yadav, Pranav S. Slirivastav, Theo de Boer, Jaap Wieling, and Puran Singhal 6 LC-MS Bioanalytical Method Transfer 65 Zhongping (John) Lin, Wenkui Li, and Naidong Weng
3 vi CONTENTS 7 Metabolites in Safety Testing 71 Ragu Ramanathan and Dil M. Rainanathan 8 A Comparison of FDA, EMA, ANVISA, and Others on Bioanalysis in Support of Bioequivalence/ Bioavailability Studies 83 Bradley Nash 9 A Comparison of the Guidance of FDA, OECD, EPA, and Others on Good Laboratory Practice 89 J. Kirk Smith 10 Current Understanding of Bioanalysis Data Management and Trend of Regulations on Data Management 97 Zhongping (John) Lin, Michael Moyer, Jianing Zeng, Joe Rajarao, and Michael Hayes 11 Regulatory Inspection Trends and Findings of Bioanalytical Laboratories 109 Frank Chow, Martin Yau, and Leon Laclvnan PART III BEST PRACTICE IN LC-MS BIOANALYSIS 12 Assessment of Whole Blood Stability and Blood/Plasma Distribution of Drugs 129 lain Love, Graeme T. Smith, and Howard M. Hill 13 Best Practice in Biological Sample Collection, Processing, and Storage for LC-MS in Bioanalysis of Drugs 139 Maria Pawula, Glen Hawthorne, Graeme T. Smith, and Howard M. Hill 14 Best Practices in Biological Sample Preparation for LC-MS Bioanalysis 165 Guowen Liu and Anne-Franqoise Aubry 15 Best Practice in Liquid Chromatography for LC-MS Bioanalysis 185 Steve Unger and Naidong Weng 16 Best Practice in Mass Spectrometry for LC-MS 205 Richard B. van Breemen and Elizabeth M. Martinez 17 Use of Internal Standards in LC-MS Bioanalysis 217 Aimin Tan and Kayode Awaiye 18 System Suitability in LC-MS Bioanalysis 229 Chad Briscoe 19 Derivatization in LC-MS Bioanalysis 239 Tomofumi Santa 20 Evaluation and Elimination of Matrix Effects in LC-MS Bioanalysis 249 Be nut A. Bruenner and Christopher A. James 21 Evaluation and Elimination of Carryover and/or Contamination in LC-MS Bioanalysis 259 Howard M. Hill and Graeme T. Smith
4 CONTENTS 22 Automation in LC-MS Bioanalysis 275 Joseph A. Tweed 23 LC-MS Bioanalysis of Drugs in Tissue Samples 297 Hong Gao, Stacy Ho, and John Williams 24 LC-MS Bioanalysis of Drugs in Urine 307 Allena J. Ji 25 LC-MS Bioanalysis of Unbound Drugs in Plasma and Serum 317 Theo de Boer and Jaap Wieling 26 LC-MS Bioanalysis of Drugs in Bile 327 Hong Gao and John Williams 27 LC-MS Bioanalysis of Intracellular Drugs 337 Fagen Zhang and Michael J. Bartels 28 LC-MS Bioanalysis of Endogenous Compounds as Biomarkers 353 Wenying Jian, Richard Edom, and Naidong Weng 29 LC-MS Bioanalysis of Drugs in Hemolyzed and Lipemic Samples 369 Min Meng, Spencer Carter, and Patrick Bennett 30 Best Practices in LC-MS Method Development and Validation for Dried Blood Spots 379 Jie Zhang, Tapan K. Majumdai; Jimmy Flarakos, and Francis L.S. Tse 31 LC-MS Method Development Strategies for Enhancing Mass Spectrometric Detection 391 Yuan-Qing Xia and Jeffrey D. Miller 32 LC-MS Bioanalysis-Related Statistics 403 David Hoffman 33 Simultaneous LC-MS Quantitation and Metabolite Identification in Drug Metabolism and Pharmacokinetics 417 Patrick J. Rudewicz PART IV REPRESENTATIVE GUIDELINES AND/OR EXPERIMENTAL PROTOCOLS OF LC-MS BIOANALYSIS 34 LC-MS Bioanalysis of Ester Prodrugs and Other Esterase Labile Molecules 431 Wenkui Li, Yunlin Fit, Jimmy Flarakos, and Duxi Zhang 35 LC-MS Bioanalysis of Acyl Glucuronides 447 Jin Zhou, Feng (Frank) Li, and Jeffery X. Duggan 36 Regulated Bioassay of N-Oxide Metabolites Using LC-MS: Dealing with Potential Instability Issues 461 Tapan K. Majumdar
5 viii CONTENTS 37 Hydrolysis of Phase II Conjugates for LC-MS Bioanalysis of Total Parent Drugs 471 Laixin Wang, Weiwei Yuan, Scott Reuschel, and Min Meng 38 LC-MS Bioanalysis of Reactive Compounds 479 Hermes Licea-Perez, Christopher A. Evans, and Yi (Eric) Yang 39 LC-MS Bioanalysis of Photosensitive and Oxidatively Labile Compounds 491 Corey M. Ohnmacht 40 LC-MS Bioanalysis of Interconvertible Compounds 505 Nico van de Merbel 41 LC-MS Bioanalysis of Chiral Compounds 519 Naidong Weng 42 LC-MS Bioanalysis of Peptides and Polypeptides 535 Hongyan Li and Christopher A. James 43 LC-MS Bioanalysis of Nucleosides 551 Laixin Wang and Min Meng 44 LC-MS Bioanalysis of Nucleotides 559 Sabine Cohen, Marie-Claude Cagnieu, Isabelle Lefebvre, and Jerome Cuitton 45 LC-MS Bioanalysis of Steroids 573 Jie Zhang and Frank Z. Stanczyk 46 LC-MS Bioanalysis of Liposomal Drugs and Lipids 591 Troy Voelker and Roger Demers 47 LC-MS Bioanalysis of Proteins 601 Ziping Yang, Wenkui Li, Harold T. Smith, and Francis LS. Tse 48 LC-MS Bioanalysis of Oligonucleotides 607 Michael G. Bartlett, Buyun Chen, and A. Cary McGinnis 49 LC-MS Bioanalysis of Platinum Drugs 629 Troy Voelker and Min Meng 50 Microflow LC-MS for Quantitative Analysis of Drugs in Support of Microsampling 639 Heather Skor and Sadayappan V. Raluivendran 51 Quantification of Endogenous Analytes in Biofluids by a Combination of LC-MS and Construction of Calibration Curves Using Stable-Isotopes as Surrogate Analytes with True Biological Control Matrices 649 Wenlin Li, Lucinda Cohen, and Erick Kindt Appendix 1 Body and Organ Weights and Physiological Parameters in Laboratory Animals and Humans 659
6 CONTENTS ix Appendix 2 Anticoagulants Commonly Used in Blood Sample Collection 661 Appendix 3 Solvents and Reagents Commonly Used in LC-MS Bioanalysis 663 Appendix 4 Glossary of Terms Used in LC-MS Bioanalysis 665 INDEX 673
Advances in LC-MS bioanalysis for drug research and development 液 相 质 谱 生 物 样 品 分 析 技 术 在 新 药 研 发 中 的 新 进 展
Advances in LC-MS bioanalysis for drug research and development 液 相 质 谱 生 物 样 品 分 析 技 术 在 新 药 研 发 中 的 新 进 展 张 杰 DMPK, Novartis Institutes for BioMedical Research ( 诺 华 ), New Jersey 2014 南 京 国 际 药 代 会
HANDBOOK OF LC-MS BIOANALYSIS
HANDBOOK OF LC-MS BIOANALYSIS HANDBOOK OF LC-MS BIOANALYSIS Best Practices, Experimental Protocols, and Regulations Edited by WENKUI LI, PhD Novartis Institutes for BioMedical Research, East Hanover,
DMPK: Experimentation & Data
DMPK: Experimentation & Data Interpretation Mingshe Zhu, Mike S. Lee, Naidong Weng, and Mark Hayward Prerequisite: Entry-level scientists with hands on experience in LC/MS as well as advanced students
ASMS Regulated Bioanalysis Interest Group (RBIG) Workshop. Antibody-Drug Conjugates (ADC) A Complex Problem in Regulated Bioanalysis.
ASMS Regulated Bioanalysis Interest Group (RBIG) Workshop Antibody-Drug Conjugates (ADC) A Complex Problem in Regulated Bioanalysis June 17, 2014 Presiding: Dr. Keyang Xu (Genentech) and Dr. Fabio Garofolo
The Facts on Equine Drug Testing
The Facts on Equine Drug Testing CONTACT Travis Mays, MS Interim Section Head Analytical Chemistry, Drug Testing Laboratory Toxicology Laboratory 979.845.3414 tmays@ LIMITATIONS IN DRUG TESTING While advancements
Guidance for Industry
Guidance for Industry Bioanalytical Method Validation DRAFT GUIDANCE This guidance document is being distributed for comment purposes only. Comments and suggestions regarding this draft document should
Guideline on bioanalytical method validation
21 July 2011 EMEA/CHMP/EWP/192217/2009 Rev. 1 Corr. 2** Committee for Medicinal Products for Human Use (CHMP) Draft agreed by the Efficacy Working Party September 2009 Adoption by CHMP for release for
Guidance for Industry
Guidance for Industry Bioanalytical Method Validation U.S. Department of Health and Human Services Food and Drug Administration Center for Drug Evaluation and Research (CDER) Center for Veterinary Medicine
What Do We Learn about Hepatotoxicity Using Coumarin-Treated Rat Model?
What Do We Learn about Hepatotoxicity Using Coumarin-Treated Rat Model? authors M. David Ho 1, Bob Xiong 1, S. Stellar 2, J. Proctor 2, J. Silva 2, H.K. Lim 2, Patrick Bennett 1, and Lily Li 1 Tandem Labs,
Recommendations for validation of LC-MS/MS bioanalytical methods for protein biotherapeutics white paper p highlights
Recommendations for validation of LC-MS/MS bioanalytical methods for protein biotherapeutics white paper p highlights g Rand Jenkins on behalf of the AAPS Bioanalytical Focus Group Protein Bioanalysis
DRUG METABOLISM. Drug discovery & development solutions FOR DRUG METABOLISM
DRUG METABLISM Drug discovery & development solutions FR DRUG METABLISM Fast and efficient metabolite identification is critical in today s drug discovery pipeline. The goal is to achieve rapid structural
Guidance for Industry Safety Testing of Drug Metabolites
Guidance for Industry Safety Testing of Drug Metabolites U.S. Department of Health and Human Services Food and Drug Administration Center for Drug Evaluation and Research (CDER) February 2008 Pharmacology
Biological importance of metabolites. Safety and efficacy aspects
Biological importance of metabolites Safety and efficacy aspects Bernard Walther Technologie Servier Biological importance of metabolites Safety testing of drug metabolites Bioanalytical strategy Structural
SIMULTANEOUS DETERMINATION OF NALTREXONE AND 6- -NALTREXOL IN SERUM BY HPLC
SIMULTANEOUS DETERMINATION OF NALTREXONE AND 6- -NALTREXOL IN SERUM BY HPLC Katja SÄRKKÄ, Kari ARINIEMI, Pirjo LILLSUNDE Laboratory of Substance Abuse, National Public Health Institute Manerheimintie,
BIOTECHNOLOGY OPERATIONS
BIOTECHNOLOGY OPERATIONS Principles and Practices Michael J. Roy TECHNISCHE INFORMATION SBIBLIOTHEK UNIVERSITATSBIBLIOTHEK HANNOVER CRC Press TaylorStFrancis Croup Boca Raton London New York CRC Press
Contents. Abstract...i. Committee Membership... iii. Foreword... vii. 1 Scope...1
ISBN 1-56238-584-4 Volume 25 Number 27 ISSN 0273-3099 Interference Testing in Clinical Chemistry; Approved Guideline Second Edition Robert J. McEnroe, PhD Mary F. Burritt, PhD Donald M. Powers, PhD Douglas
Analytical Specifications RIVAROXABAN
Page 1 of 9 ANALYTE NAME AND STRUCTURE - RIVAROXABAN SYNONYMS Xarelto CATEGORY Anticoagulant TEST CODE PURPOSE Therapeutic Drug Monitoring GENERAL RELEVANCY BACKGROUND Xarelto (rivaroxaban) is an orally
Pharmacokinetics in Drug Development
Pharmacokinetics in Drug Development . Peter L. Bonate Danny R. Howard Editors Pharmacokinetics in Drug Development Volume 3: Advances and Applications Editors Peter L. Bonate, Ph.D. Clinical Pharmacology,
Guidance for Industry
Guidance for Industry Q2B Validation of Analytical Procedures: Methodology November 1996 ICH Guidance for Industry Q2B Validation of Analytical Procedures: Methodology Additional copies are available from:
A Generic Kit-Based Approach for Quantifying Monoclonal Antibody Drugs Through Direct Digestion of Discovery Study Samples
A Generic Kit-Based Approach for Quantifying Monoclonal Antibody Drugs Through Direct Digestion of Discovery Study Samples Mary Lame, Hua Yang, Sherri Naughton, and Erin Chambers Waters Corporation, Milford,
Contents. Contributors. 1 Quality control and regulation 1 C.J. MOORES
Contents Contributors Preface xiii xiv 1 Quality control and regulation 1 C.J. MOORES 1.1 Introduction 1 1.2 The quality of medicines 2 1.2.1 The meaning of quality 2 1.2.2 Medicines are special 3 1.2.3
Overview. Purpose. Methods. Results
A ovel Approach to Quantify Unbound Cisplatin, Carboplatin, and xaliplatin in Human Plasma Ultrafiltrate by Measuring Platinum-DDTC Complex Using LC/M/M Min Meng, Ryan Kuntz, Al Fontanet, and Patrick K.
How to develop Antibody Drug Conjugates: Bioanalysis Contribution
How to develop Antibody Drug Conjugates: Bioanalysis Contribution Recommendations and survey results Presenter: Matt Barfield on behalf of the EBF TT43 7th Open Symposium 19 th November 2014 Barcelona
8. SUMMARY AND CONCLUSION
238 8. SUMMARY AND CONCLUSION The present work aimed to assess the applicability of High Performance Liquid Chromatography with Mass Spectrometry (HPLC-MS) for analysis of different class of drugs in rat,
How To Test For Contamination In Large Volume Water
Automated Solid Phase Extraction (SPE) of EPA Method 1694 for Pharmaceuticals and Personal Care Products in Large Volume Water Samples Keywords Application Note ENV0212 This collaboration study was performed
Validation and Calibration. Definitions and Terminology
Validation and Calibration Definitions and Terminology ACCEPTANCE CRITERIA: The specifications and acceptance/rejection criteria, such as acceptable quality level and unacceptable quality level, with an
LC-MS/MS for Chromatographers
LC-MS/MS for Chromatographers An introduction to the use of LC-MS/MS, with an emphasis on the analysis of drugs in biological matrices LC-MS/MS for Chromatographers An introduction to the use of LC-MS/MS,
Biotherapeutics Drug Development
Biotherapeutics Drug Development Susan Hurst, Ph.D. University of Connecticut Bioanalytical Chemistry Spring 2011 April 19, 2011 Outline Background Therapeutic Modalities Examples of Challenges for Biotherapeutics
MultiQuant Software 2.0 for Targeted Protein / Peptide Quantification
MultiQuant Software 2.0 for Targeted Protein / Peptide Quantification Gold Standard for Quantitative Data Processing Because of the sensitivity, selectivity, speed and throughput at which MRM assays can
The 2014-2016 Board of Directors
The 2014-2016 Board of Directors President Yang, Honggang, Ph.D. 杨 红 钢 Dean, School of Humanities and Social Sciences Nova Southeastern University [email protected] Vice President Chen, Jie, Ph.D. 陈 捷 Dean,
Volume 22 Number 22. C43-A ISBN 1-56238-475-9 ISSN 0273-3099 Gas Chromatography/Mass Spectrometry (GC/MS) Confirmation of Drugs; Approved Guideline
ISBN 1-56238-475-9 ISSN 0273-3099 Gas Chromatography/Mass Spectrometry (GC/MS) Confirmation of Drugs; Approved Guideline Volume 22 Number 22 Larry D. Bowers, Ph.D., DABCC, Chairholder David A. Armbruster,
VALIDATION OF ANALYTICAL PROCEDURES: TEXT AND METHODOLOGY Q2(R1)
INTERNATIONAL CONFERENCE ON HARMONISATION OF TECHNICAL REQUIREMENTS FOR REGISTRATION OF PHARMACEUTICALS FOR HUMAN USE ICH HARMONISED TRIPARTITE GUIDELINE VALIDATION OF ANALYTICAL PROCEDURES: TEXT AND METHODOLOGY
Fit-For-Purpose Method Validation For Successful Biomarker Measurement To Support MRTP Applications
Fit-For-Purpose Method Validation For Successful Biomarker Measurement To Support MRTP Applications Rafiq Islam Senior Director, Global Bioanalytical Services Presentation Outline Definition of Modified
High sensitivity assays using online SPE-LC-MS/MS -How low can you go? Mohammed Abrar Unilabs York Bioanalytical solutions, York, UK
High sensitivity assays using online SPE-LC-MS/MS -How low can you go? Mohammed Abrar Unilabs York Bioanalytical solutions, York, UK Background Unilabs YBS are a bioanalytical CRO based in York (Uk) Copenhagen
6. ANALYTICAL METHODS
45 6.1 BIOLOGICAL MATERIALS No methods were located that are routinely used for the detection of BCEE in biological materials. Norpoth et al. (1986) reported a method for measuring thiodiglycolic acid
Careers in Chemistry. 400-Level Classes in Chemistry. Undergrad Research Opportunities
Careers in Chemistry 400-Level Classes in Chemistry Undergrad Research Opportunities Careers in Chemistry Employment & Salary Data Median salaries (means are higher) Careers in Chemistry Some Careers That
Simultaneous Qualitative and Quantitative Data Acquisition for Research of Diabetes Drugs
Liquid Chromatography Mass Spectrometry SSI-LCMS-068 Simultaneous Qualitative and Quantitative Data Acquisition for Research of Diabetes Drugs LCMS-8050 Summary By utilizing the LCMS-8050 s ultrafast scan
Future of Mass Spectrometry in Clinical Research and Forensic Toxicology. Brad Hart Market Development Director
Future of Mass Spectrometry in Clinical Research and Forensic Toxicology Brad Hart Market Development Director Agenda The Heritage of Mass Spec vendors Market Conditions Regulatory Challenges Trends/ Frontiers
How to create and interpret the predictive analysis of a compound
How to create and interpret the predictive analysis of a compound Platform with suite of tools Predict & understand biological effects of small molecules & compounds Predict targets and metabolites, potential
Human ADME and Studies with Radiolabeled Compounds: Phase I-IIa
WHITE PAPER Human ADME and Studies with Radiolabeled Compounds: Phase I-IIa AD ROFFEL, PhD Director, Global Scientific Affairs PRA Health Sciences Authors: HENK POELMAN, MSc Project Manager, Laboratory
FACT SHEET TESTETROL, A NOVEL ORALLY BIOACTIVE ANDROGEN
FACT SHEET TESTETROL, A NOVEL ORALLY BIOACTIVE ANDROGEN General Pantarhei Bioscience B.V. is an emerging specialty pharmaceutical company with a creative approach towards drug development. The Company
Quality. Now Certified to ISO 9001:2008
Quality Now Certified to ISO 90012008 Quality Policy It is Peptides International's goal is to achieve complete customer satisfaction by addressing customer needs and delivering what we promise. The company
Factors Influencing LC/MS/MS Moving into Clinical and Research Laboratories
Factors Influencing LC/MS/MS Moving into Clinical and Research Laboratories Matthew Clabaugh, Market Development AACC Workshop St. Louis, MO September 17,18 2013 Factors Influencing LCMSMS Moving into
How To Understand The Pharmacology Of The Pharmaceutical Industry
It; MM MODERN Ul NDUSTRY 77 /
Main Conference Agenda
Sponsored by: (Co-located with Bioequivalence: Intersection between Science & Regulatory Conference) Main Conference Agenda Day One Wednesday, November 5 th, 2014 7:30 Registration Opens & Continental
LC-MS/MS Solutions for the Pharmaceutical and CRO Industries TSQ Series -based Solutions for Drug Discovery and Development
m a s s s p e c t r o m e t r y LC-MS/MS Solutions for the Pharmaceutical and CRO Industries TSQ Series -based Solutions for Drug Discovery and Development Part of Thermo Fisher Scientific ACCELERATING
HRMS in Clinical Research: from Targeted Quantification to Metabolomics
A sponsored whitepaper. HRMS in Clinical Research: from Targeted Quantification to Metabolomics By: Bertrand Rochat Ph. D., Research Project Leader, Faculté de Biologie et de Médecine of the Centre Hospitalier
Thermo Scientific Prelude SPLC System FPO. Making LC/MS accessible. to clinical research and toxicology labs
Thermo Scientific Prelude SPLC System FPO Making LC/MS accessible to clinical research and toxicology labs Specifically designed to make the power of LC/MS accessible Analysis of target compounds in complex
Samsung POINT OF CARE Systems - Cardiac/Acute Care Biomarkers LABGEO IB Clinical Chemistry Analytes LABGEO PT
Samsung POINT OF CARE Systems - Cardiac/Acute Care Biomarkers LABGEO IB Clinical Chemistry Analytes LABGEO PT Alexander Belenky, PhD Director -Product Development Samsung - Nexus-Dx Edward Brennan, PhD
APPENDIX 7-B SUGGESTED OUTLINE OF A QUALITY ASSURANCE PROJECT PLAN
APPENDIX 7-B SUGGESTED OUTLINE OF A QUALITY ASSURANCE PROJECT PLAN This outline is recommended for use by UST consultants/contractors in preparing a generic Quality Assurance Project Plan (QAPP) for use
LC-MSMS - state of the art in endocrinology
LC-MSMS - state of the art in endocrinology Michael Vogeser Institute of Clinical Chemistry Hospital of the University of Munich Germany 8 June 2011, Namur Quantification of marker molecules is essential
Building innovative drug discovery alliances. Evotec Munich. Quantitative Proteomics to Support the Discovery & Development of Targeted Drugs
Building innovative drug discovery alliances Evotec Munich Quantitative Proteomics to Support the Discovery & Development of Targeted Drugs Evotec AG, Evotec Munich, June 2013 About Evotec Munich A leader
AbsoluteIDQ p180 Kit. Targeted Metabolite Identifi cation and Quantifi cation. Bringing our targeted metabolomics expertise to your lab.
AbsoluteIDQ p180 Kit Targeted Metabolite Identifi cation and Quantifi cation Bringing our targeted metabolomics expertise to your lab. The Biocrates AbsoluteIDQ p180 mass spectrometry Assay Preparation
Proteomics in Practice
Reiner Westermeier, Torn Naven Hans-Rudolf Höpker Proteomics in Practice A Guide to Successful Experimental Design 2008 Wiley-VCH Verlag- Weinheim 978-3-527-31941-1 Preface Foreword XI XIII Abbreviations,
Mass Spectrometry Signal Calibration for Protein Quantitation
Cambridge Isotope Laboratories, Inc. www.isotope.com Proteomics Mass Spectrometry Signal Calibration for Protein Quantitation Michael J. MacCoss, PhD Associate Professor of Genome Sciences University of
NUVISAN Pharma Services
NUVISAN Pharma Services CESI MS Now available! 1st CRO in Europe! At the highest levels of quality. LABORATORY SERVICES Equipment update STATE OF THE ART AT NUVISAN CESI MS Now available! 1st CRO in Europe!
A Primer of Genome Science THIRD
A Primer of Genome Science THIRD EDITION GREG GIBSON-SPENCER V. MUSE North Carolina State University Sinauer Associates, Inc. Publishers Sunderland, Massachusetts USA Contents Preface xi 1 Genome Projects:
RapidFire High-throughput MS technology. Enhancing Drug Discovery Turning Mass Specs into Plate Readers
RapidFire High-throughput MS technology Enhancing Drug Discovery Turning Mass Specs into Plate Readers 1 Drug Discovery with RapidFire Target Selection High-throughput Target Screening (HTS) Lead Optimization
Therapeutic Drug Monitoring of Antiretroviral Drugs with HPLC-MS
Therapeutic Drug Monitoring of Antiretroviral Drugs with PLC-M Ursula Gutteck-Amsler, Katharina M. Rentsch Abstract Prospective and retrospective studies have provided some evidence of the clinical and
Guideline for Industry
Guideline for Industry Quality of Biotechnological Products: Stability Testing of Biotechnological/Biological Products July 1996 ICH Q5C Table of Contents I. INTRODUCTION (1)... 1 II. SCOPE OF THE ANNEX
Good Clinical Laboratory Practice (GCLP) An international quality system for laboratories which undertake the analysis of samples from clinical trials
Good Clinical Laboratory Practice (GCLP) An international quality system for laboratories which undertake the analysis of samples from clinical trials Vanessa Grant and Tim Stiles VERSION 2 Published by
Scientific Working Group for Forensic Toxicology (SWGTOX) Standard Practices for Method Validation in Forensic Toxicology
Scientific Working Group for Forensic Toxicology (SWGTOX) Standard Practices for Method Validation in Forensic Toxicology 1. Introduction... 2 2. Definitions... 2 3. When to Validate Methods... 4 4. Method
Rapid and Reproducible Amino Acid Analysis of Physiological Fluids for Clinical Research Using LC/MS/MS with the atraq Kit
Rapid and Reproducible Amino Acid Analysis of Physiological Fluids for Clinical Research Using LC/MS/MS with the atraq Kit Fast, simple and cost effective analysis Many areas of biochemical research and
From QSAR to Big Data: Developing Mechanism-Driven Predictive Models for Animal Toxicity
From QSAR to Big Data: Developing Mechanism-Driven Predictive Models for Animal Toxicity Hao Zhu Department of Chemistry The Rutgers Center for Computational and Integrative Biology Rutgers University-Camden
Ethyl Glucuronide. Where is the Drug? Detection Windows. Urine. Blood. Absorption and Distribution. Metabolism. Excretion
Where is the Drug? Ethyl Absorption and Distribution A Biomarker for Ethanol Use Metabolism Excretion Anthony G. Costantino, Ph.D. D-ABFT NMS Labs,Willow Grove, PA John J. Treuting, Ph.D. Treuting & Assoc.
FDA Public Hearing on Clinical Accuracy Requirements for Point of Care Blood Glucose Meters (BGMs)
FDA Public Hearing on Clinical Accuracy Requirements for Point of Care Blood Glucose Meters (BGMs) Barriers to Overcoming Interferences and Limitations Alan T. Cariski, MD, JD, and Mike Flis, AdvaMed BGM
Annex 7 Guidelines for the preparation of a contract research organization master file
World Health Organization WHO Technical Report Series, No. 957, 2010 Annex 7 Guidelines for the preparation of a contract research organization master file Background 1. General information 2. Quality
INTERNATIONAL STANDARD FOR LABORATORIES
The World Anti-Doping Code INTERNATIONAL STANDARD FOR LABORATORIES Version 4.0 August 2004 PREAMBLE The World Anti-Doping Code International Standard for Laboratories is a mandatory level 2 International
PPD LABORATORIES CENTRAL LAB: SUPERIOR SERVICE, QUALITY DATA WITHOUT COMPROMISES
PPD LABORATORIES CENTRAL LAB: SUPERIOR SERVICE, QUALITY DATA WITHOUT COMPROMISES PPD Laboratories provides world-class scientific expertise with state-of-the-art technologies supported by a commitment
Development and Validation of a LC-MS/MS Method for Plasma Analysis of the Serotonin Metabolite: 5-Hydroxyindoleacetic acid (5-HIAA)
W Ward, B Begley, R Friley, M Barringer,, J Nofsinger, M Allen, D Hudson, D Witt Tandem Labs, Laboratory Corporation of America Holdings P Rosner, A Wilson, S Wason,, J Townsend, L Law, QM Yang Lexicon
Assay Qualification Template for Host Cell Protein ELISA
Assay Qualification Template for Host Cell Protein ELISA Introduction: With ever increasing importance being placed on host cell protein (HCP) removal during the purification process, it is critical to
Method Development of LC-MS/MS Analysis of Aminoglycoside Drugs: Challenges and Solutions
Method Development of LC-MS/MS Analysis of Aminoglycoside Drugs: Challenges and Solutions authors Angela (Qi) Shen, Ling Morgan, Marcele L. Barroso, and Xin Zhang; Tandem Labs Tuyen Nguyen; Sepracor Inc.
A Novel Approach to Low Volume Sample Preparation
A Novel Approach to Low Volume Sample Preparation Tony Edge, Jon Bardsley, Ken Meadows, Luisa Pereira International Symposium on Chromatography Salzburg, Austria September 2014 1 The world leader in serving
Nursing 113. Pharmacology Principles
Nursing 113 Pharmacology Principles 1. The study of how drugs enter the body, reach the site of action, and are removed from the body is called a. pharmacotherapeutics b. pharmacology c. pharmacodynamics
Advanced Database Marketing Innovative Methodologies and Applications for Managing Customer Relationships
Advanced Database Marketing Innovative Methodologies and Applications for Managing Customer Relationships Edited by KRISTOF COUSSEMENT KOEN W. DE BOCK and SCOTT A. NESLIN GOWER Contents List of Figures
Scientific Challenges for Development of Biosimilar Monoclonal Antibodies. Rafiqul Islam Director, Global Bioanalytical Services Celerion
Scientific Challenges for Development of Biosimilar Monoclonal Antibodies Rafiqul Islam Director, Global Bioanalytical Services Celerion Presentation outline Biosimilars Definitions and Concepts Regulatory
Ecology Quality Assurance Glossary
Ecology Quality Assurance Glossary Edited by William Kammin, Ecology Quality Assurance Officer Accreditation - A certification process for laboratories, designed to evaluate and document a lab s ability
Testing Services for Large Molecule Drug Development
Testing Services for Large Molecule Drug Development Our mission is to extend our clients capabilities by combining scientific knowledge, capacity, regulatory expertise and flexibility to provide the trusted,
Daniel M. Mueller, Katharina M. Rentsch Institut für Klinische Chemie, Universitätsspital Zürich, CH-8091 Zürich, Schweiz
Toxichem Krimtech 211;78(Special Issue):324 Online extraction LC-MS n method for the detection of drugs in urine, serum and heparinized plasma Daniel M. Mueller, Katharina M. Rentsch Institut für Klinische
SAMPLE. Gas Chromatography/Mass Spectrometry Confirmation of Drugs; Approved Guideline Second Edition
March 2010 Gas Chromatography/Mass Spectrometry Confirmation of Drugs; Approved Guideline Second Edition This document provides guidance on establishing uniform practices necessary to produce quality data
Global Lab Capabilities Pharma Biotech
Global Lab Capabilities Pharma Biotech NSF Health Sciences global network of laboratories delivers expert solutions to pharmaceutical, biotechnology and medical device companies in the areas of analytical
CONFIRMATION OF ZOLPIDEM BY LIQUID CHROMATOGRAPHY MASS SPECTROMETRY
CONFIRMATION OF ZOLPIDEM BY LIQUID CHROMATOGRAPHY MASS SPECTROMETRY 9.1 POLICY This test method may be used to confirm the presence of zolpidem (ZOL), with diazepam-d 5 (DZP-d 5 ) internal standard, in
Schneps, Leila; Colmez, Coralie. Math on Trial : How Numbers Get Used and Abused in the Courtroom. New York, NY, USA: Basic Books, 2013. p i.
New York, NY, USA: Basic Books, 2013. p i. http://site.ebrary.com/lib/mcgill/doc?id=10665296&ppg=2 New York, NY, USA: Basic Books, 2013. p ii. http://site.ebrary.com/lib/mcgill/doc?id=10665296&ppg=3 New
Accurate Mass Screening Workflows for the Analysis of Novel Psychoactive Substances
Accurate Mass Screening Workflows for the Analysis of Novel Psychoactive Substances TripleTOF 5600 + LC/MS/MS System with MasterView Software Adrian M. Taylor AB Sciex Concord, Ontario (Canada) Overview
Contents. Abstract... i. Committee Membership... iii. Foreword... vii. 1 Scope... 1. 2 Introduction... 1. 3 Standard Precautions...
Vol. 28 No. 20 Replaces H47-A Vol. 16 No. 3 One-Stage Prothrombin Time (PT) Test and Activated Partial Thromboplastin Time (APTT) Test; Approved Guideline Second Edition This document provides guidelines
Mouse Creatine Kinase MB isoenzyme (CKMB) ELISA
KAMIYA BIOMEDICAL COMPANY Mouse Creatine Kinase MB isoenzyme (CKMB) ELISA For the quantitative determination of mouse CKMB in serum, plasma, cell culture fluid and other biological fluids Cat. No. KT-57681
位 参 加 者 将 来 制 定 策 略 和 规 划 提 供 非 常 有 用 的 参 考. Changing Paradigm in Drug Discovery and Development: East Meets West SHANGHAI
PRELIMINARY Program AGENDA Shanghai Symposium on Chemical and Pharmaceutical Structure Analysis Revised Jan 24, Changing Paradigm in Drug Discovery and Development: East Meets West Renaissance Shanghai
Call 2014: High throughput screening of therapeutic molecules and rare diseases
Call 2014: High throughput screening of therapeutic molecules and rare diseases The second call High throughput screening of therapeutic molecules and rare diseases launched by the French Foundation for
泛 用 蛋 白 質 體 學 之 質 譜 儀 資 料 分 析 平 台 的 建 立 與 應 用 Universal Mass Spectrometry Data Analysis Platform for Quantitative and Qualitative Proteomics
泛 用 蛋 白 質 體 學 之 質 譜 儀 資 料 分 析 平 台 的 建 立 與 應 用 Universal Mass Spectrometry Data Analysis Platform for Quantitative and Qualitative Proteomics 2014 Training Course Wei-Hung Chang ( 張 瑋 宏 ) ABRC, Academia
# LCMS-35 esquire series. Application of LC/APCI Ion Trap Tandem Mass Spectrometry for the Multiresidue Analysis of Pesticides in Water
Application Notes # LCMS-35 esquire series Application of LC/APCI Ion Trap Tandem Mass Spectrometry for the Multiresidue Analysis of Pesticides in Water An LC-APCI-MS/MS method using an ion trap system
