Aulton's Pharmaceutics

Aulton's Pharmaceutics

The Design and Manufacture of Medicines

5th Edition - June 16, 2017

Write a review

  • Editors: Kevin Taylor, Michael Aulton
  • Paperback ISBN: 9780702070051
  • eBook ISBN: 9780702070013

Purchase options

Institutional Subscription

Free Global Shipping
No minimum order

Description

From a review of the previous edition: ‘For all the pharmacy students out there part of your pharmacy degree will be to study formulation design and pharmaceutics. This is the holy grail of pharmaceutical technology books. The text reads well and introduces difficult concepts in a more easy-to-understand way, it is definitely worth the money to help you get through the module, if you’re doing a research project in pharmaceutical design then this would also be an excellent buy…This is essential for passing exams and developing professional competence.’ This is the best known text on pharmaceutics. Its strength lies mainly in being a complete course in one book. Reviewers consistently praise its comprehensiveness and its extremely high quality-quality content. Pharmaceutics is one of the most diverse subject areas in pharmaceutical science and an understanding of it is vital for all pharmacists and scientists involved in converting drugs to medicines that can be safely delivered to a patient. The editorial and author team deliver a tour de force of accessibility, coverage and currency in this new edition of a world-class textbook.

Key Features

  • Relevant chemistry covered throughout
  • Reflects current and future use of biotechnology products throughout
  • Covers ongoing changes in our understanding of biopharmaceutics, certain areas of drug delivery and the significance of the solid state
  • Includes the science of formulation and drug delivery
  • Designed and written for newcomers to the design of dosage forms
  • Key points boxes throughout
  • Summaries at the end of each chapter

Table of Contents

  • What is pharmaceutics?

    1. Design of dosage forms
    2. PART 1 Scientific principles of dosage form design

    3. Dissolution and solubility
    4. Properties of solutions
    5. Surfaces and interfaces
    6. Disperse systems
    7. Rheology
    8. Kinetics
    9. PART 2 Particle science and powder technology

    10. Solid-state properties
    11. Particle size analysis
    12. Particle size reduction and size separation
    13. Mixing
    14. Powder flow
    15. PART 3 Pharmaceutical microbiology and serialization

    16. Fundamentals of microbiology
    17. Pharmaceutical applications of microbiological techniques
    18. Action of physical and chemical agents on microorganisms
    19. Principles of sterilization
    20. Sterilization in practice
    21. PART 4 Biopharmaceutical principles of drug delivery

    22. Introduction to biopharmaceutics
    23. Gastrointestinal tract – physiology and drug absorption
    24. Bioavailability – physicochemical and dosage form factors
    25. Assessment of biopharmaceutical properties
    26. Dosage regimens
    27. PART 5 Dosage form design and manufacture

    28. Pharmaceutical preformulation
    29. Solutions
    30. Clarification
    31. Suspensions
    32. Emulsions and creams
    33. Powders, granules and granulation
    34. Drying
    35. Tablets and compaction
    36. Modified-release oral drug delivery
    37. Coating of tablets and multiparticulates
    38. Hard capsules
    39. Soft capsules
    40. Dissolution testing of solid dosage forms
    41. Parenteral drug delivery
    42. Pulmonary drug delivery
    43. Nasal drug delivery
    44. Ophthalmic drug delivery
    45. Topical and transdermal drug delivery
    46. Rectal and vaginal drug delivery
    47. The formulation and manufacture of plant medicines
    48. Delivery of biopharmaceuticals
    49. Pharmaceutical nanotechnology and nanomedicines
    50. Design and administration of medicines for children and the elderly
    51. Part 6 Packaging and stability of pharmaceutical products

    52. Packaging
    53. Chemical stability in dosage forms
    54. Microbial contamination, spoilage and preservation of medicines
    55. Product stability and stability testing

    Online self assessment

Product details

  • No. of pages: 936
  • Language: English
  • Copyright: © Elsevier 2017
  • Published: June 16, 2017
  • Imprint: Elsevier
  • Paperback ISBN: 9780702070051
  • eBook ISBN: 9780702070013

About the Editors

Kevin Taylor

Affiliations and Expertise

Professor of Clinical Pharmaceutics, UCL School of Pharmacy, London, UK

Michael Aulton

Affiliations and Expertise

Emeritus Professor, De Montfort University, Leicester, UK

Ratings and Reviews

Write a review

There are currently no reviews for "Aulton's Pharmaceutics"