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Aulton's Pharmaceutics 4th Edition Pdf Free 105: The Ultimate Guide to Pharmaceutics

Aultons Pharmaceutics 4th Edition Pdf Free 105: A Comprehensive Review

If you are looking for a reliable and comprehensive textbook on pharmaceutics, you might have come across Aultons Pharmaceutics. This book is one of the most popular and widely used texts on the design and manufacture of medicines. It covers all aspects of pharmaceutics, from the scientific principles to the practical applications, in a clear and accessible way.

Aultons Pharmaceutics 4th Edition Pdf Free 105

But what makes Aultons Pharmaceutics so special? And how can you get a copy of the latest edition, Aultons Pharmaceutics 4th edition pdf free 105, without breaking the law or risking your computer's security? In this article, we will answer these questions and more. We will review the history, structure, content, benefits, and features of Aultons Pharmaceutics 4th edition, and we will also show you how to access it for free online.

What is Aultons Pharmaceutics?

Aultons Pharmaceutics is a textbook that covers the science and art of pharmaceutical preparations. It encompasses the design of drugs, their manufacture, and the elimination of microorganisms from the products. It is written by experts in their fields and edited by Professors Kevin Taylor and Michael Aulton, who are both renowned authorities in pharmaceutics.

The history and evolution of Aultons Pharmaceutics

The first edition of Aultons Pharmaceutics was published in 1988 under the title "Pharmaceutics: The Science of Dosage Form Design". It was written by Professor Michael E. Aulton, who was then a lecturer at the School of Pharmacy, University of London. The book was based on his lectures and aimed to provide a comprehensive introduction to pharmaceutics for undergraduate pharmacy students.

The second edition was published in 2002, with a revised title "Pharmaceutics: The Design and Manufacture of Medicines". It reflected the changes and advances in pharmaceutics since the first edition, such as the emergence of biotechnology products, nanomedicines, and novel drug delivery systems. It also included new chapters on pharmaceutical microbiology, biopharmaceuticals, packaging, stability, and regulation.

The third edition was published in 2007, with a new co-editor, Professor Kevin M.G. Taylor, who was then a professor of clinical pharmaceutics at the School of Pharmacy, University College London. The book was updated and expanded to include more topics on pharmaceutical nanotechnology, pulmonary drug delivery, ocular drug delivery, wound dressings, plant medicines, and drug design.

The fourth edition was published in 2013, with a new publisher, Elsevier. It was further revised, updated, and extended to reflect the latest developments in formulation and drug delivery science, pharmaceutical manufacturing, and medicines regulation. It also added new chapters on solid-state properties, dissolution testing, parenteral drug delivery, nasal drug delivery, topical and transdermal drug delivery, rectal and vaginal drug delivery, design and administration of medicines for children and the elderly.

The structure and content of Aultons Pharmaceutics 4th edition

Aultons Pharmaceutics 4th edition consists of six parts:

  • Part I: Scientific Principles of Dosage Form Design (Chapters 1-8). This part covers the basic concepts and theories that underpin pharmaceutics, such as dissolution and solubility, surfaces and interfaces, disperse systems, rheology, kinetics, solid-state properties, particle size analysis, and particle size reduction and size separation.

  • Part II: Pharmaceutical Microbiology and Sterilization (Chapters 9-17). This part covers the principles and applications of microbiology and sterilization in pharmaceutics, such as fundamentals of microbiology, pharmaceutical applications of microbiological techniques, action of physical and chemical agents on microorganisms, principles of sterilization, and sterilization in practice.

  • Part III: Biopharmaceutical Principles of Drug Delivery (Chapters 18-22). This part covers the factors that affect drug absorption, distribution, metabolism, and excretion in the body, such as introduction to biopharmaceutics, gastrointestinal tract physiology and drug absorption, bioavailability physicochemical and dosage form factors, assessment of biopharmaceutical properties, and dosage regimens.

  • Part IV: Dosage Form Design and Manufacture (Chapters 23-47). This part covers the design and manufacture of various dosage forms and drug delivery systems, such as pharmaceutical preformulation, solutions, clarification, suspensions, emulsions and creams, powders granules and granulation, drying, tablets and compaction, modified-release oral drug delivery, coating of tablets and multiparticulates, hard capsules, soft capsules, dissolution testing of solid dosage forms, parenteral drug delivery, pulmonary drug delivery, nasal drug delivery, topical and transdermal drug delivery, wound dressings, ocular drug delivery, rectal and vaginal drug delivery, design and administration of medicines for children and the elderly, the formulation and manufacture of plant medicines, pharmaceutical nanotechnology and nanomedicines,

  • Part V: Packaging Stability and Pharmaceutical Regulation (Chapters 48-50). This part covers the aspects related to packaging stability and pharmaceutical regulation of medicines such as packaging materials and systems for pharmaceutical products stability testing of pharmaceutical products pharmaceutical regulation

  • Part VI: Self Assessment (Chapter 51). This part contains over 400 multiple choice questions based on the content of the book to help students test their knowledge and understanding.

The book also includes key points boxes throughout each chapter to highlight the main points and learning objectives an index a list of references at the end of each chapter


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