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 Al-Achi, Antoine, Gupta, Mali Ram, Stagner, William Craig
Format eBook Book
LanguageEnglish
Published Hoboken, NJ John Wiley & Sons 2023
Wiley
John Wiley & Sons, Incorporated
Wiley-Blackwell
Edition2nd ed
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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.
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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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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