Physico-Chemical Aspects of Dosage Forms and Biopharmaceutics: Recent and Future Trends in Pharmaceutics, Volume 2
Editat de Amit Kumar Nayak, Kalyan Kumar Senen Limba Engleză Paperback – 14 aug 2024
- Provides extensive details on the most recent developments in biopharmaceutics
- Contains contributions from leading experts from academia, research, industry and regulatory agencies
- Includes high quality illustrations, flow charts and tables for easier understanding of the concepts
- Discusses practical examples and research case studies
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Specificații
ISBN-13: 9780323918183
ISBN-10: 0323918182
Pagini: 486
Dimensiuni: 216 x 276 mm
Greutate: 0.45 kg
Editura: ELSEVIER SCIENCE
ISBN-10: 0323918182
Pagini: 486
Dimensiuni: 216 x 276 mm
Greutate: 0.45 kg
Editura: ELSEVIER SCIENCE
Public țintă
Postgraduate pharmacy students, doctoral and postdoctoral research fellows, pharmaceutical formulators, scientists, researchers, and regulatory scientists; Researchers and postgraduate students in biotechnology, biomedical sciences and engineering, bioengineering sciences, chemical engineeringCuprins
Section I: Physico-chemical aspects of dosage forms 1. Physico-chemical factors influencing drug degradation 2. Stability and accelerated stability studies of dosage forms 3. Solubility of drugs 4. Drug dissolution studies of pharmaceutical formulations 5. Pharmaceutical granulation: Engineering perspective and futuristic trends 6. Tablet compression and consolidation: Theory and applications Section II: Biopharmaceutics 7. Introduction to Biopharmaceutics 8. Gastrointestinal absorption of drugs 9. Routes of drug administration and their impact in biopharmaceutics 10. Drug elimination and renal excretion of drugs 11. Membrane transport and permeation of drugs 12. Factors affecting drug absorption and disposition 13. Bioavailability and bioequivalence 14. Contribution of biopharmaceutics and pharmacokinetics to improve drug therapy 15. Dosage regimen 16. Multicompartment models 17. Nonlinear pharmacokinetics 18. Computer-aided biopharmaceutical model development 19. Computer simulations in pharmacokinetics 20. WHO and ICH Guidelines for ‘Good Manufacturing Practices’ 21. Pilot plant scale up techniques in pharmaceutical product development 22. Advances in solid dosage forms