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Aulton's Pharmaceutics: The Design and Manufacture of Medicines

The Design and Manufacture of Medicines

9780443287824
352.75 zł
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Teaser
2026-07-01

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Description
Thoroughly revised, updated, and extended by experts in their fields, and edited by Professors Kevin Taylor and Michael Aulton, Aultons Pharmaceutics, 7th Edition, comprehensively covers the science and practice of formulation, pharmaceutical manufacturing, and drug delivery. This essential pharmaceutics textbook offers a complete course in one book for students in all years of undergraduate pharmacy and pharmaceutical sciences degrees. It is also an invaluable resource for students undertaking postgraduate studies in the pharmaceutical sciences, practitioners in the pharmaceutical and associated industries, and those working in hospital pharmacy technical services and medicines regulation. It features a clear, readily accessible writing style, extensive illustrations, and numerous tables, figures, and information boxes to assist with the understanding of this complex subject area.
Product Details
Elsevier
104465
9780443287824
9780443287824

Data sheet

Publication date
2026
Issue number
7
Cover
paperback
Pages count
720
Dimensions (mm)
216 x 276
  • 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, dosage form and formulation 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. Ointments, pastes, gels, cutaneous patches and topical sprays
    29. Powders, granules and granulation
    30. Drying
    31. Tablets and compaction
    32. Modified-release oral drug delivery
    33. Coating of tablets and multiparticulates
    34. Continuous manufacturing of tablets
    35. Hard capsules
    36. Soft capsules
    37. Dissolution testing of solid dosage forms
    38. Parenteral drug delivery
    39. Pulmonary drug delivery
    40. Nasal drug delivery
    41. Ocular drug delivery
    42. Otic drug delivery
    43. Topical and transdermal drug delivery
    44. Rectal and vaginal drug delivery
    45. Preparation and delivery of biopharmaceuticals
    46. Pharmaceutical nanotechnology and nanomedicines
    47. Radiopharmaceuticals
    48. The formulation and manufacture of plant medicines
    49. Design and administration of medicines for paediatric and geriatric patients

    Part 6 Packaging, stability and pharmaceutical regulation
    50. Packaging
    51. Chemical stability in dosage forms
    52. Microbial contamination, spoilage and preservation of medicines
    53. Product stability and stability testing
    54. Pharmaceutical quality: the application of pharmaceutics in medicines regulation Self-assessment questions
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