Dosage Form Design Parameters
eBook - ePub

Dosage Form Design Parameters

Volume II

,
  1. 810 pages
  2. English
  3. ePUB (mobile friendly)
  4. Available on iOS & Android
eBook - ePub

Dosage Form Design Parameters

Volume II

,
Book details
Table of contents
Citations

About This Book

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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Information

Publisher
Academic Press
Year
2018
ISBN
9780128144220
Topic
Medicine
Subtopic
Pharmacology

Table of contents

  1. Cover image
  2. Title page
  3. Table of Contents
  4. Copyright
  5. Dedication
  6. List of Contributors
  7. About the Editor
  8. Chapter 1. Levels of Solid State Properties: Role of Different Levels During Pharmaceutical Product Development
  9. Chapter 2. Polymorphism and its Implications in Pharmaceutical Product Development
  10. Chapter 3. Basics of Crystallization Process Applied in Drug Exploration
  11. Chapter 4. Role of Amorphous State in Drug Delivery
  12. Chapter 5. Particulate Level Properties and its Implications on Product Performance and Processing
  13. Chapter 6. Bulk Level Properties and its Role in Formulation Development and Processing
  14. Chapter 7. Concepts of Hypothesis Testing and Types of Errors
  15. Chapter 8. Experimental Design and Analysis of Variance
  16. Chapter 9. Basic Concept and Application of Sampling Procedures
  17. Chapter 10. Statistical Techniques in Pharmaceutical Product Development
  18. Chapter 11. Drug–Excipient Interaction and Incompatibilities
  19. Chapter 12. Documentation Protocol in Product Development Including Clinical Records
  20. Chapter 13. Correlation Between In Vitro and In Vivo Screens: Special Emphasis on High Throughput Screening and High Throughput Pharmacokinetic Analysis
  21. Chapter 14. Sterilization of Pharmaceuticals: Technology, Equipment, and Validation
  22. Chapter 15. Package Development of Pharmaceutical Products: Aspects of Packaging Materials Used for Pharmaceutical Products
  23. Chapter 16. Package Types for Different Dosage Forms
  24. Chapter 17. Food and Drug Laws Affecting Pharmaceutical Product Design, Development, and Commercial Manufacturing
  25. Chapter 18. Guiding Principles for Human and Animal Research During Pharmaceutical Product Development
  26. Chapter 19. Applications of Computers in Pharmaceutical Product Formulation
  27. Chapter 20. Patents and Other Intellectual Property Rights in Drug Delivery
  28. Chapter 21. Computer-Aided Prediction of Pharmacokinetic (ADMET) Properties
  29. Chapter 22. Ethics and Legal Protection of Uses of Computer Applications in Pharmaceutical Research
  30. Index