Dosage Form Design Considerations
Volume I
Academic Press
Published on 28. July 2018
820 pages
978-0-12-814424-4 (ISBN)
Description
Dosage Form Design Parameters, Volume I, examines the history and current state of the field within the pharmaceutical sciences, presenting key developments. Content includes drug development issues, the scale up of formulations, regulatory issues, intellectual property, solid state properties and polymorphism. Written by experts in the field, this volume in the Advances in Pharmaceutical Product Development and Research series deepens our understanding of dosage form design parameters. Chapters delve into a particular aspect of this fundamental field, covering principles, methodologies and the technologies employed by pharmaceutical scientists. In addition, the book contains a comprehensive examination suitable for researchers and advanced students working in pharmaceuticals, cosmetics, biotechnology and related industries.
- Examines the history and recent developments in drug dosage forms for pharmaceutical sciences
- Focuses on physicochemical aspects, prefomulation solid state properties and polymorphism
- Contains extensive references for further discovery and learning that are appropriate for advanced undergraduates, graduate students and those interested in drug dosage design
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07/2018
Academic Press
€184.50
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Content
1. Preformulation in drug research and pharmaceutical product development2. Physicochemical aspects to be considered in Pharmaceutical Product Development3. Role of physicochemical parameters on drug absorption and their Implications in Pharmaceutical Product Development 4. Physiologic Factors Related to Drug Absorption5. Physico-chemical, pharmaceutical and biological considerations in GIT Absorption of drugs6. Influence of Drug Properties and Routes of Drug Administration on the design of controlled release systems7. Drug stability and degradation studies8. First pass metabolism considerations in Pharmaceutical Product Development9. Dissolution profile considerations during Pharmaceutical Product Development10. Drug disposition considerations in Pharmaceutical Product Development11. Protein and tissue binding: Implication on pharmacokinetic parameters 12. Preformulation studies of drug substances, proteins and peptides: Role in drug discovery and Pharmaceutical Product Development13. Role of salt selection in drug discovery and development14. Drug Complexation: Implications in drug solubilization and oral bioavailability enhancement15. Solubility and solubilization approaches in Pharmaceutical Product Development16. Rheology and its implications on performance of liquid dosage forms17. Micromeritics in Pharmaceutical Product Development18. Four stages in Pharmaceutical Product Development - Preformulation - Prototype development - Biological aspects - Scale up studies - Commercialization 19. Scale up studies in Pharmaceutical Product Development20. Manipulation of physiological processes for Pharmaceutical Product Development21. Impact of pharmaceutical product Quality on Clinical Efficacy22. Formulation additives used in Pharmaceutical Products: Emphasis on regulatory perspectives and GRAS
