Integrated Pharmaceutics - Applied Preformulation, Product Design, and Regulatory Science (2nd Edition)
Pharmaceutics refers to the subfield of pharmaceutical sciences that develops drug delivery products or devices to optimize the drug's performance once administered. This multidisciplinary field draws on physical chemistry, organic chemistry, and biophysics to generate and refine these crucial...
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Main Authors | , , |
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Format | eBook Book |
Language | English |
Published |
Hoboken, NJ
John Wiley & Sons
2023
Wiley John Wiley & Sons, Incorporated Wiley-Blackwell |
Edition | 2nd ed |
Subjects | |
Online Access | Get full text |
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Abstract | Pharmaceutics refers to the subfield of pharmaceutical sciences that develops drug delivery products or devices to optimize the drug's performance once administered. This multidisciplinary field draws on physical chemistry, organic chemistry, and biophysics to generate and refine these crucial elements of medical care. Moreover, incorporating such disparate dimensions of drug product design as material properties and legal regulation bridges the gap between effective chemicals and viable medical treatments. Integrated Pharmaceutics provides a comprehensive introduction to the creation and manufacture of effective dosage forms for drug delivery. It presents its subject following the principles of physical pharmacy, product design, and drug regulations. This tripartite structure allows readers to move from theory to practice, beginning from a firm foundation of physical pharmacy principles, including drug solubility and stability estimation, rheology, and interfacial properties. From there, it proceeds to discussions of drug product design and of harmonizing pharmaceutical design with the regulatory regimens and technological standards of the United States, European Union, and Japan. Readers of the second edition of this book will also find: A glossary defining key terms, extensive informative appendices, and a list of references leading to the primary literature in the field for each chapter; Earlier chapters are expanded, with additional new chapters including one entitled "Biotechnology Products"; Supplementary instructor guide with questions and solutions available online for registered professors; Updated regulatory guidelines including quality by design, design space analysis, process analytical technology, polymorphism characterization, blend sample uniformity, and stability protocols. This book is a useful textbook for graduate students in pharmaceutical sciences, drug formulation and design, and biomedical engineering. In addition, professionals in the pharmaceutical industry, including regulatory bodies, will find it a helpful reference guide. |
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AbstractList | This work is an examination of all aspects of the science in developing effective dosage form for drug delivery Pharmaceutics refers to the subfield of pharmaceutical sciences that develops drug delivery products or devices to optimize the drug's performance once administered. This multidisciplinary field draws on physical chemistry, organic chemistry, and biophysics to generate and refine these crucial elements of medical care. Moreover, incorporating such disparate dimensions of drug product design as material properties and legal regulation bridges the gap between effective chemicals and viable medical treatments. Integrated Pharmaceutics provides a comprehensive introduction to the creation and manufacture of effective dosage forms for drug delivery. It presents its subject following the principles of physical pharmacy, product design, and drug regulations. This tripartite structure allows readers to move from theory to practice, beginning from a firm foundation of physical pharmacy principles, including drug solubility and stability estimation, rheology, and interfacial properties. From there, it proceeds to discussions of drug product design and of harmonizing pharmaceutical design with the regulatory regimens and technological standards of the United States, European Union, and Japan. Readers of the second edition of Integrated Pharmaceutics will also find: * A glossary defining key terms, extensive informative appendices, and a list of references leading to the primary literature in the field for each chapter * Earlier chapters are expanded, with additional new chapters including one entitled "Biotechnology Products" * Supplementary instructor guide with questions and solutions available online for registered professors * Updated regulatory guidelines including quality by design, design space analysis, process analytical technology, polymorphism characterization, blend sample uniformity, and stability protocols Integrated Pharmaceutics is a useful textbook for graduate students in pharmaceutical sciences, drug formulation and design, and biomedical engineering. In addition, professionals in the pharmaceutical industry, including regulatory bodies, will find it a helpful reference guide. Pharmaceutics refers to the subfield of pharmaceutical sciences that develops drug delivery products or devices to optimize the drug's performance once administered. This multidisciplinary field draws on physical chemistry, organic chemistry, and biophysics to generate and refine these crucial elements of medical care. Moreover, incorporating such disparate dimensions of drug product design as material properties and legal regulation bridges the gap between effective chemicals and viable medical treatments. Integrated Pharmaceutics provides a comprehensive introduction to the creation and manufacture of effective dosage forms for drug delivery. It presents its subject following the principles of physical pharmacy, product design, and drug regulations. This tripartite structure allows readers to move from theory to practice, beginning from a firm foundation of physical pharmacy principles, including drug solubility and stability estimation, rheology, and interfacial properties. From there, it proceeds to discussions of drug product design and of harmonizing pharmaceutical design with the regulatory regimens and technological standards of the United States, European Union, and Japan. Readers of the second edition of this book will also find: A glossary defining key terms, extensive informative appendices, and a list of references leading to the primary literature in the field for each chapter; Earlier chapters are expanded, with additional new chapters including one entitled "Biotechnology Products"; Supplementary instructor guide with questions and solutions available online for registered professors; Updated regulatory guidelines including quality by design, design space analysis, process analytical technology, polymorphism characterization, blend sample uniformity, and stability protocols. This book is a useful textbook for graduate students in pharmaceutical sciences, drug formulation and design, and biomedical engineering. In addition, professionals in the pharmaceutical industry, including regulatory bodies, will find it a helpful reference guide. This work is an examination of all aspects of the science in developing effective dosage form for drug delivery Pharmaceutics refers to the subfield of pharmaceutical sciences that develops drug delivery products or devices to optimize the drug's performance once administered. This multidisciplinary field draws on physical chemistry, organic chemistry, and biophysics to generate and refine these crucial elements of medical care. Moreover, incorporating such disparate dimensions of drug product design as material properties and legal regulation bridges the gap between effective chemicals and viable medical treatments. Integrated Pharmaceutics provides a comprehensive introduction to the creation and manufacture of effective dosage forms for drug delivery. It presents its subject following the principles of physical pharmacy, product design, and drug regulations. This tripartite structure allows readers to move from theory to practice, beginning from a firm foundation of physical pharmacy principles, including drug solubility and stability estimation, rheology, and interfacial properties. From there, it proceeds to discussions of drug product design and of harmonizing pharmaceutical design with the regulatory regimens and technological standards of the United States, European Union, and Japan. Readers of the second edition of Integrated Pharmaceutics will also find: A glossary defining key terms, extensive informative appendices, and a list of references leading to the primary literature in the field for each chapter Earlier chapters are expanded, with additional new chapters including one entitled "Biotechnology Products" Supplementary instructor guide with questions and solutions available online for registered professors Updated regulatory guidelines including quality by design, design space analysis, process analytical technology, polymorphism characterization, blend sample uniformity, and stability protocolsIntegrated Pharmaceutics is a useful textbook for graduate students in pharmaceutical sciences, drug formulation and design, and biomedical engineering. In addition, professionals in the pharmaceutical industry, including regulatory bodies, will find it a helpful reference guide. |
Author | Al-Achi, Antoine Gupta, Mali Ram Stagner, William Craig |
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Notes | Includes bibliographical references and index |
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Snippet | Pharmaceutics refers to the subfield of pharmaceutical sciences that develops drug delivery products or devices to optimize the drug's performance once... This work is an examination of all aspects of the science in developing effective dosage form for drug delivery Pharmaceutics refers to the subfield of... |
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SubjectTerms | Biopharmaceutics Chemistry, Pharmaceutical Dosage Forms -- standards Drug and Narcotic Control Drug Design Drugs Drugs-Dosage forms Pharmaceutical chemistry Pharmaceuticals Pharmaceuticals, Cosmetics & Toiletries |
TableOfContents | Title Page
Prefaces
Table of Contents
1. Mathematical Concepts
2. Thermodynamics
3. Solubility and Dissolution
4. Biological Aspects of Formulations
5. Interfacial Properties
6. Adsorption Phenomenon
7. Rheological Principles
8. Chemical Stability and Shelf-Life Determination
9. Particle Science
10. Basic Statistics and Design of Experimental Concepts
11. Formulation Development Concepts
12. The Product Design Process
13. Tablet Product Design
14. Capsule Product Design
15. Dispersed System Product Design
16. Aerosol Product Design
17. Sterile Injectable Product Design
18. Ophthalmic Product Design
19. Transdermal Product Design
20. Oral Modified-Release Product Design
21. Regulatory Practices and Guidelines
22. Regulations for Compounding Pharmacies
23. IND and NDA Phase-Appropriate New Drug Development Process
24. Biological, Biosimilar, Generic, and OTC Products
25. Accelerated New Drug Approval and Expedited Access of New Therapies
26. Post-Drug Approval Activities
27. Drug Master Files, EU Dossiers, and API GMP Guidance
28. Commissioning and Qualification
29. Quality Systems and Controls
30. Safety, Toxicology, and Pharmacogenomics
31. Regulatory Science Initiatives for Advancing Public Health
32. Medical Devices
33. Combination Products
34. Dietary Supplements
35. Animal Drugs and Devices
Index |
Title | Integrated Pharmaceutics - Applied Preformulation, Product Design, and Regulatory Science (2nd Edition) |
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