Aulton's pharmaceutics : the design and manufacture of medicines

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書誌事項

Aulton's pharmaceutics : the design and manufacture of medicines

edited by Michael E. Aulton and Kevin M.G. Taylor

Churchill Livingstone/Elsevier, c2013

4th ed

タイトル別名

Pharmaceutics

大学図書館所蔵 件 / 全4件

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注記

Includes bibliographical references and index

内容説明・目次

内容説明

Pharmaceutics is one of the most diverse subject areas in all of pharmaceutical science. In brief, it is concerned with the scientific and technological aspects of the design and manufacture of dosage forms or medicines. An understanding of pharmaceutics is therefore vital for all pharmacists and those pharmaceutical scientists who are involved with converting a drug or a potential drug into a medicine that can be delivered safely, effectively and conveniently to the patient. Now in its fourth edition, this best-selling textbook in pharmaceutics has been brought completely up to date to reflect the rapid advances in delivery methodologies by eye and injection, advances in drug formulations and delivery methods for special groups (such as children and the elderly), nanomedicine, and pharmacognosy. At the same time the editors have striven to maintain the accessibility of the text for students of pharmacy, preserving the balance between being a suitably pitched introductory text and a clear reflection of the state of the art. provides a logical, comprehensive account of drug design and manufacture includes the science of formulation and drug delivery designed and written for newcomers to the design of dosage forms New to this edition New editor: Kevin Taylor, Professor of Clinical Pharmaceutics, School of Pharmacy, University of London. Twenty-two new contributors. Six new chapters covering parenteral and ocular delivery; design and administration of medicines for the children and elderly; the latest in plant medicines; nanotechnology and nanomedicines, and the delivery of biopharmaceuticals. Thoroughly revised and updated throughout.

目次

1. Design of dosage forms. PART 1: Scientific principles of dosage form design. 2. Dissolution and solubility. 3. Properties of solutions. 4. Surfaces and interfaces. 5. Disperse systems. 6. Rheology. 7. Kinetics. PART 2: Particle science and powder technology. 8. Solid-state properties. 9. Particle size analysis. 10. Particle size reduction and size separation. 11. Mixing. 12. Powder flow. PART 3: Pharmaceutical microbiology and sterilization. 13. Fundamentals of microbiology. 14. Pharmaceutical applications of microbiological techniques. 15. Action of physical and chemical agents on microorganisms. 16. Principles of sterilization. 17. Sterilization in practice. PART 4: Biopharmaceutical principles of drug delivery. 18. Introduction to biopharmaceutics. 19. Gastrointestinal tract - physiology and drug absorption. 20. Bioavailability - physicochemical and dosage form factors. 21. Assessment of biopharmaceutical properties. 22. Dosage regimens. PART 5: Dosage form design and manufacture. 23. Pharmaceutical preformulation. 24. Solutions. 25. Clarification. 26. Suspensions . 27. Emulsions and Creams. 28. Powders, granules and granulation. 29. Drying. 30. Tablets and compaction. 31. Modified-release oral drug delivery. 32. Coating of tablets and multiparticulates. 33. Hard capsules. 34. Soft capsules. 35 Dissolution testing of solid dosage forms. 36 Parenteral drug delivery. 37. Pulmonary drug delivery. 38. Nasal drug delivery. 39. Topical and transdermal drug delivery. 40. Wound dressings. 41. Ocular drug delivery. 42. Rectal and vaginal drug delivery. 43. Design and administration of medicines for children and the elderly. 44. The formulation and manufacture of plant medicines. 45. Pharmaceutical nanotechnology and nanomedicines. 46. Delivery of biopharmaceuticals. Part 6: PACKAGING AND STABILITY OF PHARMACEUTICAL PRODUCTS. 47. Packaging. 48. Chemical stability in dosage forms. 49. Product stability and stability testing. 50. Microbial contamination, spoilage and preservation of medicines.

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