Physico-Chemical Aspects of Dosage Forms and Biopharmaceutics

Recent and Future Trends in Pharmaceutics, Volume 2
Herausgeber: Nayak, Amit Kumar; Sen, Kalyan Kumar

• Broschiertes Buch

Produktbeschreibung

Physico-Chemical Aspects of Dosage Forms and Biopharmaceutics: Recent and Future Trends in Pharmaceutics, Volume Two explores aspects of pharmaceutics with an original approach that focuses on technology, novelties and future trends. The field of pharmaceutics is highly dynamic and rapidly expanding day-by-day, so it demands a variety of amplified efforts for designing and developing pharmaceutical processes and formulation strategies. Readers will find practical information for conducting research in pharmaceutics that is ideal for researchers in academia and industry as well as advanced graduate students in pharmaceutics. In addition, the book discusses the most recent developments in biopharmaceutics, including important and exciting areas such as solubility of drugs, pharmaceutical granulation, routes of drug administration, drug absorption, bioavailability and bioequivalence.

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Produktdetails

• Verlag: Elsevier Science
• Seitenzahl: 486
• Erscheinungstermin: 14. August 2024
• Englisch
• Gewicht: 1330g
• ISBN-13: 9780323918183
• ISBN-10: 0323918182
• Artikelnr.: 66149766

Inhaltsangabe

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