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|a Preclinical development handbook.
|p ADME and biopharmaceutical properties /
|c [edited by] Shayne Cox Gad.
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246 |
3 |
0 |
|a ADME and biopharmaceutical properties
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260 |
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|a Hoboken, N.J. :
|b Wiley-Interscience,
|c ©2008.
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300 |
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|a 1 online resource (xv, 1329 pages) :
|b illustrations
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336 |
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|a text
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|2 rdacontent
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|a Pharmaceutical Development Series
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504 |
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|a Includes bibliographical references and index.
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588 |
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|a Print version record.
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520 |
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|a This book gives the professional pharmaceutical scientist a basic and comprehensive tool to facilitate the preclinical development process by bringing together an overview of the preclinical process and a compendium of methods and techniques that need to.
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505 |
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|a PRECLINICAL DEVELOPMENT HANDBOOK ADME and Biopharmaceutical Properties; CONTRIBUTORS; CONTENTS; Preface; 1 Modeling and Informatics in Drug Design; 2 Computer Techniques: Identifying Similarities Between Small Molecules; 3 Protein-Protein Interactions; 4 Method Development for Preclinical Bioanalytical Support; 5 Analytical Chemistry Methods: Developments and Validation; 6 Chemical and Physical Characterizations of Potential New Chemical Entity; 7 Permeability Assessment; 8 How and Where Are Drugs Absorbed?; 9 Absorption of Drugs after Oral Administration
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|a 10 Distribution: Movement of Drugs through the Body11 The Blood-Brain Barrier and Its Effect on Absorption and Distribution; 12 Transporter Interactions in the ADME Pathway of Drugs; 13 Accumulation of Drugs in Tissues; 14 Salt and Cocrystal Form Selection; 15 Dissolution; 16 Stability: Physical and Chemical; 17 Dosage Formulation; 18 Cytochrome P450 Enzymes; 19 Metabolism Kinetics; 20 Drug Clearance; 21 In Vitro Metabolism in Preclinical Drug Development; 22 Utilization of In Vitro Cytochrome P450 Inhibition Data for Projecting Clinical Drug-Drug Interactions
|
505 |
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|a 23 In Vivo Metabolism in Preclinical Drug Development24 In Vitro Evaluation of Metabolic Drug-Drug Interactions: Scientific Concepts and Practical Considerations; 25 Mechanisms and Consequences of Drug-Drug Interactions; 26 Species Comparison of Metabolism in Microsomes and Hepatocytes; 27 Metabolite Profiling and Structural Identification; 28 Linkage between Toxicology of Drugs and Metabolism; 29 Allometric Scaling; 30 Interrelationship between Pharmacokinetics and Metabolism; 31 Experimental Design Considerations in Pharmacokinetic Studies; 32 Bioavailability and Bioequivalence Studies
|
505 |
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|a 33 Mass Balance Studies34 Pharmacodynamics; 35 Physiologically Based Pharmacokinetic Modeling; 36 Mathematical Modeling as a New Approach for Improving the Efficacy/Toxicity Profile of Drugs: The Thrombocytopenia Case Study; 37 Regulatory Requirements for INDs/FIH (First in Human) Studies; 38 Data Analysis; Index
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|a Gad, Shayne C.,
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|1 https://id.oclc.org/worldcat/entity/E39PBJtMv3dQXtdXFvrKPThPwC
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|i has work:
|a Preclinical development handbook ADME and biopharmaceutical properties (Text)
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|t Preclinical development handbook. ADME and biopharmaceutical properties.
|d Hoboken, N.J. : Wiley-Interscience, ©2008
|z 9780470248478
|z 0470248475
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|
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