INDICE: Preface. 1 Introduction. 1.1 Aim of This Book. 1.2 An Overview of the Drug Discovery and Development Process. 1.3 The Pharmaceutical Industry. 1.4 Economics of Drug Discovery and Development. 1.5 Trends in Drug Discovery and Development. 1.6 Case Study #1. 1.7 Summary of Important Points. 1.8 Review Questions. 1.9 Brief Answers and Explanations. 1.10 Further Reading. 2 Drug Discovery: Targets and receptors. 2.1 Drug Discovery Processes. 2.2 Medical Needs. 2.3 Target Identifi cation. 2.4 Target Validation. 2.5 Drug Interactions with Targets or Receptors. 2.6 Enzymes. 2.7 Receptors and Signal Transduction. 2.8 Assay Development. 2.9 Case Study #2. 2.10 Summary of Important Points. 2.11 Review Questions. 2.12 Brief Answers and Explanations. 2.13 Further Reading.3 Drug discovery: small molecule drugs. 3.1 Introduction. 3.2 Irrational Approach. 3.3 Rational Approach. 3.4 Antisense Approach. 3.5 RNA Interference Approach. 3.6 Chiral Drugs. 3.7 Closing Remarks. 3.8 Case Study #3. 3.9 Summary ofImportant Points. 3.10 Review Questions. 3.11 Brief Answers and Explanations.3.12 Further Reading. 4 Drug discovery: large molecule drugs. 4.1 Introduction. 4.2 Vaccines. 4.3 Antibodies. 4.4 Cytokines. 4.5 Hormones. 4.6 Gene Therapy. 4.7 Stem Cells and Cell Therapy. 4.8 Case Study #4. 4.9 Summary of ImportantPoints. 4.10 Review Questions. 4.11 Brief Answers and Explanations. 4.12 Further Reading. 5 Drug development and preclinical studies. 5.1 Introduction. 5.2Pharmacodynamics. 5.3 Pharmacokinetics. 5.4 Toxicology. 5.5 Animal Tests, In Vitro Assays, and In Silico Methods. 5.6 Formulations and Delivery Systems. 5.7 Nanotechnology. 5.8 Case Study #5. 5.9 Summary of Important Points. 5.10 Review Questions. 5.11 Brief Answers and Explanations. 5.12 Further Reading. 6 Clinical trials. 6.1 Defi nition of Clinical Trial. 6.2 Ethical Considerations. 6.3 Clinical Trials. 6.4 Regulatory Requirements for Clinical Trials. 6.5 Roleof Regulatory Authorities. 6.6 Gene Therapy Clinical Trial. 6.7 Case Study #6. 6.8 Summary of Important Points. 6.9 Review Questions. 6.10 Brief Answers and Explanations. 6.11 Further Reading. 7 Regulatory authorities. 7.1 Role of Regulatory Authorities. 7.2 US Food and Drug Administration. 7.3 European Medicines Agency. 7.4 Japans Ministry of Health, Labor and Welfare. 7.5 Chinas StateFood and Drug Administration. 7.6 Indias Central Drugs Standard Control Organization. 7.7 Australias Therapeutics Goods Administration. 7.8 Canadas Health Canada. 7.9 Other Regulatory Authorities. 7.10 Authorities Other than Drug Regulatory Agencies. 7.11 International Conference on Harmonization. 7.12 World Health Organization. 7.13 Pharmaceutical Inspection Cooperation Scheme. 7.14 Case Study #7. 7.15 Summary of Important Points. 7.16 Review Questions. 7.17 Brief Answers and Explanations. 7.18 Further Reading. 8 Regulatory applications. 8.1 Introduction. 8.2 Food and Drug Administration. 8.3 European Union. 8.4 Japan. 8.5 China. 8.6 India. 8.7 Australia. 8.8 Canada. 8.9 Case Study #8. 8.10 Summary of Important Points. 8.11 Review Questions. 8.12 Brief Answers and Explanations. 8.13 Further Reading. 9 Good manufacturing practice: regulatory requirement. 9.1 Introduction. 9.2 United States. 9.3 Europe. 9.4 International Conference on Harmonization. 9.5 Core Elements of GMP. 9.6 Selected GMP Systems. 9.7 The FDAs New cGMP Initiative. 9.8 Case Study #9. 9.9 Summary of Important Points. 9.10 Review Questions. 9.11 Brief Answers and Explanations. 9.12 Further Reading. 10 Good manufacturing practice: drug manufacturing. 10.1 Introduction. 10.2 GMP Manufacturing. 10.3 GMP Inspection. 10.4 Manufacture of Small Molecule APIs (Chemical Synthesis Methods). 10.5 Manufacture of Large MoleculeAPIs (Recombirant DNA Methods). 10.6 Finished Dosage Forms. 11 Future perspectives. 11.1 Past Advances and Future Challenges. 11.2 Small Molecule Pharmaceutical Drugs. 11.3 Large Molecule Biopharmaceutical Drugs. 11.4 Traditional Medicine. 11.5 Individualized Medicine. Appendix 1 History of drug discovery and development. A1.1 Early History of Medicine. A1.2 Drug Discovery and Development in the Middle Ages. A1.3 Foundation of Current Drug Discovery and Development. A1.4 Beginnings of Modern Pharmaceutical Industry. A1.5 Evolution of Drug Products. A1.6 Further Reading. Appendix 2 Cells, nucleic acids, genes, and proteins. A2.1 Cells. A2.2 Nucleic Acids. A2.3 Genes and Proteins. A2.4 Further Reading. Appendix 3 Selected drugs and their mechanisms of action. Appendix 4 A DHFR Plasmid vector. Appendix 5 Vaccine production methods. Appendix 6 Pharmacology/ Toxicology. Review format. Appendix 7 Examples of general biomarkers.Appendix 8 Toxicity grading. Appendix 9 Health systems in selected countries.Acronyms. Glossary. Index.
- ISBN: 978-0-470-19510-9
- Editorial: John Wiley & Sons
- Encuadernacion: Cartoné
- Páginas: 480
- Fecha Publicación: 19/12/2008
- Nº Volúmenes: 1
- Idioma: Inglés