DescriptionWith increasing use of ligand-binding assays (LBAs) in the pharmaceutical industry, the need to critically evaluate technical and regulatory issues related to the use of these technologies has increased greatly. This book fills that void and provides a reference text covering critical aspects of the development, validation, and implementation of LBAs in the drug development field. It includes: immunochemistry and protein chemistry, method development, validation, statistics, software, regulatory issues, and applications to immunogenicity and biomarkers. This is a key resource for bioanalytical personnel, laboratory analysts, and clinical and regulatory pharmacologists.
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About AuthorMasood N. Khan, PhD, received his PhD from Aligarh Muslim University, India, and did postdoctoral research at the National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina, in immunology and cell biology. He subsequently moved to McGill University, Montreal, Canada, and served as assistant professor in the Department of Medicine. In 1988, he established and successfully directed the Ligand-Binding Assay Bioanalytical (LBAB) Department at Phoenix International Life Sciences (currently MDS Life Sciences), Montreal. Dr. Khan is a founding member of the LBAB Focus Group at AAPS and has coauthored authoritative reviews on validation of LBA and biomarker assays. He has over 100 publications and presentations to his credit. He is currently the Chief Scientist at GLP Solutions Inc. in Rockville, Maryland. John W. A. Findlay, PhD, earned his PhD from the University of Aberdeen, Scotland, and did postdoctoral work in organic and medicinal chemistry at the University of Virginia. He has extensive experience in successful drug development with several major pharmaceutical companies, particularly in the areas of bioanalysis and drug disposition. Dr. Findlay was a participant in the first AAPS/FDA workshop on bioanalytical method validation in 1990 and in subsequent AAPS/FDA workshops on this topic, as well as a coauthor of a guiding review article in this field published in 2000. Dr. Findlay has coauthored more than 140 original papers, reviews, book chapters, patents, and abstracts. He is currently a Senior Director in Clinical Pharmacology at Gilead Sciences in Durham, North Carolina.
1 Ligand-Binding Assays in Drug Development: Introduction and Historical Perspective (John W.A. Findlay and Masood N. Khan).
1.2 Historical Review.
1.3 LBAs for Macromolecules.
1.4 Advantages and Limitations of LBAs.
1.5 Ligand-Binding Assay Bioanalytical Focus Group of AAPS.
1.6 Scope of the Present Volume.
2 Ligand-Binding Assays to Support Disposition Studies of Macromolecular Therapeutics (Marian M. Kelley, Marjorie A. Mohler, and John W.A. Findlay).
2.2 Differences Between Low Molecular Weight Molecules and Macromolecules.
2.3 LBA Assay Considerations Relative to Research and Development Stage.
2.4 Critical Future Challenges for Ligand-Binding Assays.
3 Development of Ligand-Binding Assays for Drug Development Support (Masood N. Khan, Proveen D. Dass, John H. Leete, Richard F. Schuman, Michele Gunsior, and Chanchal Sadhu).
3.2 Inherent Complexities of Immunoassay Development.
3.3 Steps in the Development of a Validatable Immunoassay.
3.4 Development and Optimization of an Immunoassay.
3.5 Optimization of Commercial Kit-Based Assays.
3.6 Troubleshooting Immunoassays.
4 Validation of Ligand-Binding Assays to Support Pharmacokinetic Assessments of Biotherapeutics (Binodh S. DeSilva and Ronald R. Bowsher).
4.2 Assay Development and Validation Paradigm.
4.3 Prestudy Validation Phase.
4.4 Analytical Performance Characteristics.
4.5 In-Study Validation Phase.
4.6 Partial Validations/Method Transfer/Cross-Validation.
5 Statistical Considerations in the Validation of Ligand-Binding Assays (Bruno Boulanger, Viswanath Devanarayan, and Walthere Dewe).
5.2 Objectives of Assay Validation.
5.3 Validation Criteria.
5.4 Estimating Assay Performance Characteristics.
5.5 Decision Rules and Risk Assessment in Prestudy Validation.
5.6 Decision Rules During In-Study Phase and Associated Risks.
5.7 Reconciling Validation and Routine Decision Rules.
6 Development and Validation of Ligand-Binding Assays for Biomarkers (Jean W. Lee, Yang Pan, Peter J. O Brien, and Ren Xu).
6.2 Preanalytical Considerations and Method Feasibility.
6.3 Method Development and Method Qualification for Exploratory Applications.
6.4 Method Development and Method Validation for Advanced Applications.
6.5 Partial Validation for Change Control.
6.6 Documentation, Record Keeping, and Reporting.
6.7 Regulatory Issues.
6.8 In-study Validation.
7 The Use of Commercial Assay Kits for PK/PD Analysis in Drug Development (John L. Allinson and John D. Chappell).
7.2 Validation Definitions That May be Interpreted Inconsistently.
7.3 Validation Experiments.
7.5 Reoptimizing Reagent Concentrations.
7.6 The Use of Commercial Kits for PK and TK Assays.
7.7 Matrix Problems.
7.8 Changing Method Protocol.
8 Development and Validation of Immunogenicity Assays for Preclinical and Clinical Studies (Thomas H. Parish, Deborah Finco, and Viswanath Devanarayan).
8.2 Immunogenicity Risk-Based Strategy.
8.3 Regulatory Guidance.
8.4 Assay Design.
8.5 Optimization and Validation: Total Binding Antibody Assays.
8.6 Optimization and Validation: Neutralizing Antibody Assays.
8.7 Assays and Risk Assessment.
8.8 Application and Interpretation of Data.
8.10 Appendix 8.A Illustration of Screening Cut Point Evaluation.
9 Macromolecular Reference Standards for Biotherapeutic Pharmacokinetic Analysis (Marie T. Rock and Stephen Keller).
9.2 United States Pharmacopeia.
9.3 Characterization of Non-USP Reference Standards.
9.4 The PK Assay.
10 Strategies for Successful Transfer of Ligand-Binding Assays for Successful Validation and Implementation in GXP Environment (Wolfgang Klump and Howard Hill).
10.2 Establishing Successful Working Relationships Between Laboratories.
10.3 Method Transfer.
10.4 Monitoring the Method Transfer Process.
10.5 Auditing CROs.
10.6 Method Troubleshooting.
10.7 Secrets of Successful Method Transfer.
11 Application of Automation in Ligand-Binding Assays (Chris Morrow).
11.2 Implementing Automated Systems.
11.3 Specific Ligand-Binding Assay Automation Systems.
11.4 Automated Sample Dilutors.
11.5 Assay Robots.
11.6 Integration: Tying It All Together.
11.7 Future Directions in Ligand-Binding Assay Automation.
12 Documentation and Regulatory Compliance (CT. Viswanathan and Jacqueline A. O Shaughnessy).
12.1 Regulatory Perspectives in the Documentation of Bioanalytical Data and Reports.
12.2 Recommendations for Development, Validation, Implementation, and Reporting Phases.
13 Alternative and Emerging Methodologies in Ligand-Binding Assays (Huifen F. Wang and John W.A. Findlay).
13.2 Dissociation-Enhanced Lanthanide Fluoroimmunoassay.
13.3 Enzyme-Linked Immunospot Assay.
13.4 Immuno-Polymerase Chain Reaction.
13.5 Electrochemiluminescence-Based Ligand-Binding Assays.
13.6 Hybridization-Based Ligand-Binding Assays.
13.7 Molecularly Imprinted Polymers (Synthetic Antibodies).
13.8 Surface Plasmon Resonance Methods.
13.9 Chromatography Ligand-Binding Assay Coupled Methods, Immunoaffinity Systems, and Online (Flow-Injection) Ligand-Binding Assay Methods.
13.10 Future Trends and Directions for LBATechnologies.
- publication date: 24/11/2009
- ISBN13: 9780470041383
- Format: Hardback
- Number Of Pages: 424
- ID: 9780470041383
- weight: 696
- ISBN10: 0470041382
- Saver Delivery: Yes
- 1st Class Delivery: Yes
- Courier Delivery: Yes
- Store Delivery: Yes