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Demonstrating how and why to measure physicochemical and biomimetic properties in early stages of drug discovery for lead optimization, Physicochemical and Biomimetic Properties in Drug Discovery encourages readers to discover relationships between various measurements and develop a sense of interdisciplinary thinking that will add to new research in drug discovery. This practical guide includes detailed descriptions of state-of-the-art chromatographic techniques and uses real-life examples and models to help medicinal chemists and scientists and advanced graduate students apply measurement data for optimal drug discovery.
Auteur
KLARA VALKO is an Investigator in the Analytical Chemistry Department of Molecular Discovery Research at GlaxoSmithKline. Dr. Valko has more than thirty years of experience in HPLC, GC, and LC/MS. She also has more than ten years of experience teaching physicochemical measurements and ADME optimization tools at the UCL School of Pharmacy. Currently, Dr. Valko is an Honorary Professor, leading the Physchem/ADME module for a drug discovery MSc course.
Texte du rabat
Explains how to take full advantage of chromatography to find successful drug candidates
Based on a course taught by the author for many years, this book demonstrates how to use chromatography to measure the physicochemical and biomimetic properties of drug candidates in the early stages of drug discovery in order to fully optimize drug leads. Readers will learn how to interpret chromatographic retention data using various models in order to estimate the in vivo distribution behavior of drugs. The property data obtained by these chromatographic measurements can then be used to select and prioritize compounds for further in vitro and in vivo studies at the early stages of the drug discovery process.
Physicochemical and Biomimetic Properties in Drug Discovery provides clear explanations and guidance to facilitate reproduction of the chromatographic measurements discussed in the book in any laboratory equipped with HPLC. It begins with a quick review of the drug discovery process. Next, it covers:
Throughout the book, real-life examples demonstrate how to optimize the use of chromatography to obtain successful drug candidates. Each chapter concludes with a series of questions, with answers in the appendix, making this book ideal for students as well as researchers in drug discovery.
Contenu
Preface xi
1 The Drug Discovery Process 1
Summary 7
Question for Review 7
References 7
2 Drug-Likeness and Physicochemical Property Space of Known Drugs 9
Summary 12
Questions for Review 13
References 13
3 Basic Pharmacokinetic Properties 15
Absorption 17
Plasma Protein Binding 20
Distribution 22
Volume of Distribution 23
Unbound Volume of Distribution 29
Half-Life 30
Metabolism and Clearance 30
Free Drug Hypothesis 31
Summary 31
Questions for Review 32
References 33
4 Principles and Methods of Chromatography for the Application of Property Measurements 34
Theoretical Background of Chromatography 35
Retention Factor and Its Relation to the Distribution Constant Between the Mobile and the Stationary
Phases 37
Measure of Separation Efficiency 40
Resolution and Separation Time 42
Gradient Elution 44
Applicability of Chromatography for Measurements of Molecular Properties 47
Summary 49
Questions for Review 50
References 50
5 Molecular Physicochemical Properties that Influence Absorption and DistributionLipophilicity 52
Partition Coefficient 52
Lipophilicity Measurements by Reversed Phase Chromatography with Isocratic Elution 58
Lipophilicity Measurements by Reversed Phase Chromatography with Gradient Elution 68
Lipophilicity of Charged MoleculespH Dependence of Lipophilicity 72
Biomimetic Lipophilicity Measurements by Chromatography 78
Comparing Various Lipophilicity Measures by the Solvation Equation Model 90
Summary 102
Questions for Review 105
References 105
6 Molecular Physicochemical Properties that Influence Absorption and DistributionSolubility 112
Definition of Solubility 112
Molecular Interactions with Water 116
Various Solubility Measurements that can be Applied During the Drug Discovery Process 119
Conditions that Affect Solubility 121
SolubilitypH Profile 132
Solubility and Dissolution in Biorelevant Media 134
Composition of Fasted State Simulated Intestinal Fluid (FaSSIF) 136
Preparation of FaSSIF Solution 136
Composition of Fed State Simulated Intestinal Fluid (FeSSIF) 136
Preparation of FeSSIF solution 136
Summary 143
Questions for Review 146
References 146
7 Molecular Physicochemical Properties that Influence Absorption and DistributionPermeability 150
Biological Membranes 150
Artificial Membranes 153
Physicochemical Principles of Permeability 155
Experimental Methods to Measure Artificial Membrane Permeability 159
Relationships Between Permeability, Lipophilicity, and Solubility 166
Chromatography as a Potential Tool for Measuring the Rate of Permeation 171
Summary 175
Questions for Review 178
References 178
8 Molecular Physicochemical Properties that Influence Absorption and DistributionAcid Dissociation ConstantpKa 182
Definition of pKa 182
Methods for Determining pKa 188
Spectrophotometric Determination of pKa 192
Determination of pKa by Capillary Electrophoresis 195
Chromatographic Approaches for the Determination of pKa 197
Summary 207
Questions for Review 209
References 209
9 Models with Measured Physicochemical and Biomimetic Chromatographic DescriptorsAbsorption 213
Lipinski Rule of Five 214
Absorption Models with Lipophilicity and Size 217
Biopharmaceutics Classification System (BCS) 221
Absorption PotentialMaximum Absorbable Dose 227 Abraham Solvation Equations for Modeling Absorption 232</p...