Drug Metabolism Handbook Concepts and Applications
, by Nassar, Ala F.- ISBN: 9780470118030 | 0470118032
- Cover: Hardcover
- Copyright: 2/12/2009
Ala F. Nassar, PhD, provides technical and operational leadership in characterizing in vitro and in vivo metabolites. His research focuses on understanding how structure modification can improve the ADME profile for new chemical entities as they advance towards clinical candidacy. Recently, he identified and patented pharmacologically active metabolites of Nexavar®. Dr. Nassar serves on the Editorial Board of Drug Metabolism Letters and The Open Drug Metabolism Journal and is also a reviewer for several other journals.
Paul F. Hollenberg, PhD, is Maurice H. Seevers Collegiate Professor and Chair of Pharmacologyat The University of Michigan. His current research focuses on the relationship between thestructures of the active sites of cytochrome P450s and their catalytic function. Dr. Hollenbergwas cofounder and Associate Editor of Chemical Research in Toxicology and has served onnumerous editorial boards and review panels.
Joann Scatina, PhD, has over twenty-four years of drug metabolism experience, and is currentlyVice President of the Drug Metabolism Division, Drug Safety and Metabolism, for WyethResearch. Dr. Scatina's research interests include identification of metabolites, metabolicpathways and enzymes responsible, in vitro-in vivo extrapolation, and prediction of druginteractions. She is a member of the American Society for Pharmacology and ExperimentalTherapeutics and the International Society for the Study of Xenobiotics (ISSX) and is currentlyserving on the Editorial Board of Drug Metabolism Reviews.
Preface | p. xiii |
List of Contributors | p. xv |
Introduction | p. 1 |
Historical Perspective | p. 3 |
Controversies Spanning Past, Present, and Future | p. 3 |
1800s: Discovery of Major Drug Metabolism Pathways (Conti and Bickel, 1977) | p. 4 |
1900-1950s: Confirmation of Major Pathways and Mechanistic Studies | p. 7 |
1950s-1980: Modern Drug Metabolism Emerges, with Enzymatic Basis | p. 8 |
1980-2005: Field Driven by Improved Technologies | p. 9 |
2005+: High Technology | p. 9 |
Acknowledgments | p. 10 |
References | p. 10 |
Factors Affecting Metabolism | p. 13 |
Biotransformations in Drug Metabolism | p. 17 |
Drug Metabolism in Drug Development and Drug Therapy | p. 17 |
Prediction of Metabolite and Responsible Enzyme | p. 20 |
Functional Group Biotransformations: Phase I, Phase II, Catalysis | p. 20 |
Oxidations and Cytochrome P450 | p. 23 |
Enzymology and Modifiers of CYPs | p. 34 |
References | p. 38 |
In Vivo Metabolite Kinetics | p. 41 |
Introduction | p. 41 |
In Vivo Metabolite Kinetic Concepts and Principles | p. 42 |
Effect of Inhibition and Induction on Metabolite Kinetics | p. 55 |
Determination of Formation and Elimination Clearance of Metabolite | p. 60 |
Summary | p. 62 |
Acknowledgments | p. 62 |
References | p. 62 |
Pharmacogenetics and Pharmacogenomics | p. 65 |
Introduction: Pharmacogenetics and Pharmacogenomics | p. 65 |
Pharmacogenomics of Drug-Metabolizing Enzymes (DME) | p. 66 |
Polymorphisms in Genes Encoding DME and Implications for Drug Discovery and Development | p. 67 |
Applications of Genetics and Genomics in Drug Discovery and Development | p. 75 |
References | p. 77 |
Introduction to Drug Transporters | p. 89 |
Introduction | p. 89 |
Transporter Classification, Localization, and Functions | p. 89 |
Clinical Drug-Drug Interactions | p. 99 |
Polymorphisms and Regulation of Drug Transporters | p. 106 |
In Vitro Methods in Evaluation of Drug Transporters | p. 107 |
Transporters-Drug-Metabolizing Enzymes Interplay | p. 109 |
Outlook | p. 110 |
References | p. 111 |
Technologies for in Vitro and in Vivo Studies | p. 127 |
Automated Drug Screening for ADMET Properties | p. 129 |
Introduction | p. 129 |
Background | p. 129 |
Modern Laboratory Automation: Origins in Admet | p. 132 |
Computational Chemistry 101: The Lipinski Rules | p. 134 |
Automated Methods for Determining log P/log D | p. 135 |
Drug Solubility | p. 137 |
Drug Permeability | p. 141 |
Drug Transporters in Intestinal Absorption | p. 146 |
Drug Metabolism | p. 147 |
Plasma Protein Binding | p. 158 |
QC-QA Considerations | p. 160 |
Summary | p. 161 |
References | p. 162 |
Mass Spectrometry | p. 167 |
Introduction | p. 167 |
A Brief History | p. 168 |
General Background in Mass Spectrometry | p. 170 |
Instrumentation | p. 172 |
Inlet Systems: Getting Samples In | p. 173 |
Ionization Methods: Making Ions | p. 179 |
Mass Analysis: Sorting by Size | p. 188 |
Detection: Seeing What Has Been Generated | p. 190 |
Interpretation of Mass Spectral Data | p. 192 |
References | p. 221 |
Approaches to Performing Metabolite Elucidation: One Key to Success in Drug Discovery and Development | p. 229 |
Introduction | p. 229 |
Criteria for LC-MS Methods | p. 231 |
Matrices Effect | p. 231 |
Metabolite Characterization | p. 232 |
Strategies for Identifying Unknown Metabolites | p. 235 |
"All-in-One" Radioactivity Detector, Stop Flow, and Dynamic Flow for Metabolite Identification | p. 242 |
Strategies to Screen for Reactive Metabolites | p. 247 |
Summary | p. 248 |
References | p. 249 |
Structural Modifications of Drug Candidates: How Useful Are They in Improving Metabolic Stability of New Drugs? Part I: Enhancing Metabolic Stability | p. 253 |
Background | p. 253 |
Introduction | p. 254 |
Significance of Metabolite Characterization and Structure Modification | p. 255 |
Part I: Enhance Metabolic Stability | p. 255 |
Metabolic Stability and Intrinsic Metabolic Clearance | p. 256 |
Advantages of Enhancing Metabolic Stability | p. 257 |
Strategies to Enhance Metabolic Stability | p. 257 |
Conclusions | p. 265 |
References | p. 266 |
Structural Modifications of Drug Candidates: How Useful Are They in Improving PK Parameters of New Drugs? Part II: Drug Design Strategies | p. 269 |
Introduction | p. 269 |
Active Metabolites | p. 269 |
Prodrugs | p. 273 |
Hard and Soft Drugs | p. 274 |
PK Parameters | p. 275 |
PK Analysis | p. 278 |
Conclusions | p. 278 |
References | p. 280 |
Minimizing the Potential for Drug Bioactivation of Drug Candidates to Success in Clinical Development | p. 283 |
Introduction | p. 283 |
Idiosyncratic Drug Toxicity and Molecular Mechanisms | p. 287 |
Key Tools and Strategies to Improve Drug Safetly | p. 290 |
Peroxidases | p. 295 |
Acyl Glucuronidation and S-acyl-CoA Thioesters | p. 295 |
Covalent Binding | p. 296 |
Mechanistic Studies | p. 298 |
Preclinical Development | p. 300 |
Clinical Development: Strategy | p. 301 |
Conclusion and Future Possibilities | p. 302 |
References | p. 302 |
Screening for Reactive Metabolites Using Genotoxicity Arrays and Enzyme/DNA Biocolloids | p. 307 |
Introduction | p. 307 |
Electrochemical and Electrochemiluminescent Arrays | p. 310 |
DNA/Enzyme Biocolloids for LC-MS Toxicity Screening | p. 318 |
Alternative Arrays and Other Novel Approaches | p. 325 |
Summary and Future Outlook | p. 332 |
References | p. 333 |
Drug Interactions | p. 341 |
Enzyme Inhibition | p. 343 |
Introduction | p. 343 |
Mechanisms of Enzyme Inhibition | p. 345 |
Competitive Inhibition | p. 345 |
Noncompetitive Inhibition | p. 347 |
Uncompetitive Inhibition | p. 348 |
Product Inhibition | p. 348 |
Transition-State Analogs | p. 348 |
Slow, Tight-Binding Inhibitors | p. 349 |
Mechanism-Based Inactivators | p. 349 |
Inhibitors That Are Metabolized to Reactive Products That Covalently Attach to the Enzyme | p. 352 |
Substrate Inhibition | p. 352 |
Partial Inhibition | p. 353 |
Inhibition of Cytochrome P450 Enzymes | p. 353 |
Reversible Inhibitors | p. 354 |
Quasi-Irreversible Inhibitors | p. 355 |
Mechanism-Based Inactivators | p. 356 |
References | p. 357 |
Evaluating and Predicting Human Cytochrome P450 Enzyme Induction | p. 359 |
Introduction | p. 359 |
Receptor-Based In Vitro Bioassays | p. 361 |
Immortalized Hepatocytes | p. 364 |
HepG2 and HepG2-Derived Cell Lines | p. 364 |
HBG-BC2 | p. 365 |
Hepatocarcinoma-Derived Cell Line: HepaRG | p. 366 |
Cells of Intestinal Origin: LS180 and Caco-2 | p. 366 |
Immortalized Human Hepatocyte Cell Lines: Fa2N-4 | p. 367 |
Other Immortalized Hepatocyte Cell Lines | p. 368 |
Primary Human Hepatocyte Culture Systems | p. 368 |
Interpretation and Quantitative Prediction of Enzyme Induction | p. 373 |
Clinical Drug Interaction Studies | p. 375 |
Industrial and Regulatory Perspectives | p. 377 |
Future Models | p. 378 |
Conclusions | p. 380 |
Acknowledgments | p. 381 |
References | p. 381 |
An Introduction to Metabolic Reaction Phenotyping | p. 391 |
Introduction | p. 391 |
Drug Metabolism | p. 391 |
Objectives of Reaction Phenotyping in Drug Discovery | p. 393 |
Metabolic Stability Screening | p. 393 |
Drug-Metabolizing Enzymes | p. 394 |
Assay Optimization for Metabolic Clearance and Reaction-Phenotyping Studies | p. 404 |
In Vitro to In Vivo Extrapolation of Metabolic Clearance | p. 413 |
In Vitro to In Vivo Extrapolation and Physiological Models of Hepatic Clearance | p. 419 |
Summary | p. 435 |
Acknowledgment | p. 436 |
References | p. 436 |
Further Reading | p. 446 |
Nuclear Receptor-Mediated Gene Regulation in Drug Metabolism | p. 449 |
Introduction | p. 449 |
Pregnane X Receptor | p. 451 |
Constitutive Androstane/Activated Receptor (CAR) | p. 461 |
Aryl Hydrocarbon Receptor (AhR) | p. 470 |
Closing Remarks and Perspectives | p. 470 |
Acknowledgments | p. 471 |
References | p. 471 |
Characterization of Cytochrome P450 Mechanism-Based Inhibition | p. 479 |
Introduction | p. 479 |
Inhibitors That upon Activation, Bind Covalently to the P450 Apoprotein | p. 488 |
Inhibitors That Interact in a Pseudo-Irreversible Manner with Heme Iron | p. 489 |
Inhibitors That Cause Destruction of the Prosthetic Heme Group, Oftentimes Leading to Heme-Derived Products That Covalently Modify the Apoprotein | p. 491 |
References | p. 524 |
Clinical Drug-Drug Interactions | p. 535 |
Introduction | p. 535 |
Mechanisms of DDIs | p. 537 |
Avoiding DDI | p. 543 |
References | p. 543 |
Further Reading | p. 546 |
Pharmaceutical Excipients in Drug-Drug Interaction | p. 547 |
Introduction | p. 547 |
Interaction of Pharmaceutical Excipients with Cytochrome P450s (CYPs) | p. 548 |
Interaction of Pharmaceutical Excipients with Transporters | p. 552 |
Summary | p. 554 |
References | p. 555 |
Toxicity | p. 559 |
The Role of Drug Metabolism in Toxicity | p. 561 |
Introduction | p. 561 |
Drug-Metabolizing Enzymes | p. 562 |
Classification of Toxicity | p. 581 |
Molecular Mechanisms of Toxicity | p. 582 |
Organ Systems Toxicology | p. 588 |
Carcinogenesis | p. 599 |
Teratogenesis | p. 601 |
Abrogation/Mitigation of Bioactivation-Case Examples | p. 602 |
Experimental Methods for Screening | p. 605 |
Summary | p. 606 |
Acknowledgment | p. 608 |
References | p. 608 |
Allergic Reactions to Drugs | p. 629 |
Introduction | p. 629 |
Immune System: A Brief Overview | p. 630 |
Drug Metabolism and the Hapten Hypothesis | p. 631 |
Allergic Reactions to Drugs (Examples) | p. 632 |
Conclusions | p. 644 |
Acknowledgments | p. 646 |
References | p. 646 |
Chemical Mechanisms in Toxicology | p. 655 |
Introduction | p. 655 |
Glutathione Adducts | p. 659 |
Covalent Binding | p. 662 |
Structural Alerts | p. 663 |
Examples of Metabolic Activation | p. 664 |
Conclusions | p. 685 |
Acknowledgments | p. 687 |
References | p. 687 |
Mechanisms of Reproductive Toxicity | p. 697 |
Introduction | p. 697 |
Overview-Female Reproduction | p. 698 |
Overview-Male Reproduction | p. 701 |
Sites of Targeting and Outcomes | p. 704 |
Effects of Specific Chemicals | p. 708 |
Translational Applications | p. 721 |
Conclusions and Future Directions | p. 723 |
References | p. 724 |
An Introduction to Toxicogenomics | p. 737 |
Introduction | p. 737 |
Microarrays: Genomics-Based Methods for Transcriptional Profiling | p. 737 |
Chemical Classification-Identifying Chemically Induced Signatures and Their Potential Use in Risk Assessment | p. 738 |
Experimental Designs of Microarray-Based Technologies | p. 744 |
The Interpretation and Analysis of Data Generated by Microarray Methodologies | p. 747 |
Four Basic Microarray-Based Approaches | p. 748 |
Informatics Tools Utilized by These Informatics Approaches | p. 755 |
Conclusion | p. 755 |
References | p. 756 |
Role of Bioactivation Reactions in Chemically Induced Nephrotoxicity | p. 761 |
Overview of Renal Structure and Function: Toxicological Implications | p. 761 |
Interorgan and Intra-renal Bioactivation Pathways | p. 762 |
Cytochrome P450 (CYP)-Dependent Bioactivation in Renal Proximal Tubular Cells | p. 765 |
Flavin-Containing Monooxygenase (FMO)-Dependent Bioactivation in Renal Proximal Tubular Cells | p. 767 |
Renal Bioactivation of Cysteine Conjugates: GSH Conjugation as a Bioactivation Rather Than a Detoxication Pathway | p. 768 |
Renal Bioactivation of Acetaminophen | p. 775 |
Summary and Conclusions | p. 776 |
References | p. 777 |
Regulatory Perspectives | p. 783 |
Drug Metabolism in Regulatory Guidances, Clinical Trials, and Product Labeling | p. 785 |
Introduction | p. 785 |
The Regulatory Environment | p. 786 |
Background Information in Regulatory Guidances | p. 795 |
Nonclinical Guidances and Early-Stage Drug Development | p. 798 |
Clinical Guidances and Clinical Trials | p. 858 |
Biologics | p. 948 |
Miscellaneous Topics | p. 955 |
Product Labeling | p. 959 |
Procedural Guidances | p. 974 |
Initiatives from Regulatory Agencies | p. 980 |
Summary | p. 982 |
References | p. 982 |
Index | p. 1001 |
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