Dosage Form Design Parameters
Volume II
Academic Press
Published on 25. July 2018
810 pages
978-0-12-814422-0 (ISBN)
Description
Dosage Form Design Parameters, Volume II, 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
€207.50
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Content
1. Levels of solid state properties: Role of different levels during pharmaceutical development2. Polymorphism and its Implications in Pharmaceutical Product Development3. Basics of crystallization process applied in drug research4. Role of amorphous state in drug delivery5. Particulate level properties and its implications on product performance and processing6. Bulk level properties and its role in formulation development and processing7. Concepts of hypothesis testing and types of errors8. Experimental design and analysis of variance9. Basic concept and application of Sampling procedures10. Statistical techniques in Pharmaceutical Product Development11. Drug-excipient interaction and incompatibilities12. Documentation protocols in product development department including clinical records13. Correlation between in-vitro and in-vivo screens: Special emphasis on high throughput screening, high throughput pharmacokinetic analysis14. Sterilization of pharmaceuticals: Technology, Equipment and Validation15. Package development of pharmaceutical products: Aspects of packaging materials used for Pharmaceutical Products16. Package types for different dosage forms17. Food and drug laws effecting pharmaceutical product design, development and commercial manufacturing18. Guiding Principles for Human and Animal Research during pharmaceutical product development19. Applications of Computer in Pharmaceutical Product Development20. Patents and other intellectual property rights in drug delivery21. Computer Aided Prediction of Pharmacokinetic (ADMET) Properties22. Ethics and Legal Protection of Uses of Computer Applications in Pharmaceutical Research
