Ligand-Binding Assays

Development, Validation, and Implementation in the Drug Development Arena
Herausgegeben:Khan, Masood N.; Findlay, John W.

• Gebundenes Buch

Produktbeschreibung

A consolidated and comprehensive reference on ligand-binding assays

Ligand-binding assays (LBAs) stand as the cornerstone of support for definition of the pharmaco-kinetics and toxicokinetics of macromolecules, an area of burgeoning interest in the pharmaceutical industry. Yet, outside of the Crystal City Conference proceedings, little guidance has been available for LBA validation, particularly for assays used to support macromolecule drug development. Ligand-Binding Assays: Development, Validation, and Implementation in the Drug Development Arena answers that growing need, serving as a reference text discussing critical aspects of the development, validation, and implementation of ligand-binding assays in the drug development field.

Ligand-Binding Assays covers essential topics related to ligand-binding assays, from pharmacokinetic studies, the development of LBAs, assay validation, statistical LBA aspects, and regulatory aspects, to software for LBAs and robotics and other emerging methodologies for LBAs. Highlights include:
_ A general discussion of challenges and proven approaches in the development of ligand-binding assays
_ More detailed examination of characteristics of these assays when applied to support of pharmacokinetic and toxicokinetic studies of compounds at different stages in the discovery or development timeline
_ A concise, but detailed, discussion of validation of ligand-binding assays for macromolecules
_ A practical approach to "fit-for-purpose" validation of assays for biomarkers, those molecules receiving increased attention as potentially demonstrating that the target chosen in discovery is being modulated by the candidate therapeutic, both in nonclinical and clinical studies

Written by a team of world-recognized authorities in the field, Ligand-Binding Assays provides key information to a broad range of practitioners, both in the pharmaceutical and allied industries and in related contract research organizations and academic laboratories and, perhaps, even in the field of diagnostics and clinical chemistry.

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Produktdetails

• Verlag: Wiley / Wiley & Sons
• Artikelnr. des Verlages: 14504138000
• 1. Auflage
• Seitenzahl: 432
• Erscheinungstermin: 1. November 2009
• Englisch
• Abmessung: 241mm x 162mm x 29mm
• Gewicht: 683g
• ISBN-13: 9780470041383
• ISBN-10: 0470041382
• Artikelnr.: 27492564

Autorenporträt

Masood 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.

Inhaltsangabe

Preface.

Contributors.

1 Ligand-Binding Assays in Drug Development: Introduction and Historical Perspective (John W.A. Findlay and Masood N. Khan).

1.1 General.

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.

References.

2 Ligand-Binding Assays to Support Disposition Studies of Macromolecular Therapeutics (Marian M. Kelley, Marjorie A. Mohler, and John W.A. Findlay).

2.1 Introduction.

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.

2.5 Conclusions.

References.

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).

3.1 Introduction.

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.

3.7. Conclusions.

Acknowledgments.

References.

4 Validation of Ligand-Binding Assays to Support Pharmacokinetic Assessments of Biotherapeutics (Binodh S. DeSilva and Ronald R. Bowsher).

4.1 Introduction.

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.

4.7 Documentation.

4.8 Conclusions.

References.

5 Statistical Considerations in the Validation of Ligand-Binding Assays (Bruno Boulanger, Viswanath Devanarayan, and Walthère Dewé).

5.1 Introduction.

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.

5.8 Conclusions.

References.

6 Development and Validation of Ligand-Binding Assays for Biomarkers (Jean W. Lee, Yang Pan, Peter J. O'Brien, and Ren Xu).

6.1 Introduction.

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.

6.9 Conclusions.

Acknowledgments.

References.

7 The Use of Commercial Assay Kits for PK/PD Analysis in Drug Development (John L. Allinson and John D. Chappell).

7.1 Introduction.

7.2 Validation Definitions That May be Interpreted Inconsistently.

7.3 Validation Experiments.

7.4 Stability.

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.

7.9 Conclusions.

References.

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