Editors:
- Each chapter covers historical overview, candidate drugs, factors influencing design and development, formulation and manufacturing and delivery system design
- Provides focus on specific topics, complementing other books in the initial CRS series
- Each chapter sets the context for the inventions described and describe the latitude that the inventions allow
- Includes supplementary material: sn.pub/extras
Part of the book series: Advances in Delivery Science and Technology (ADST)
Buy it now
Buying options
Tax calculation will be finalised at checkout
Other ways to access
This is a preview of subscription content, log in via an institution to check for access.
Table of contents (18 chapters)
-
Front Matter
-
Back Matter
About this book
Editors and Affiliations
-
The John Arbuthnott Building, Strathclyde Institute of Pharmacy and Bi, Glasgow, United Kingdom
Clive G. Wilson
-
Devon, USA
Patrick J. Crowley
About the editors
Clive Wilson is the J. P. Todd Professor of Pharmaceutics at Strathclyde University in Glasgow, Scotland and the current president of the European Union Federation for Pharmaceutical Sciences. He is the Chief Scientist of Bio-Images Research Group, a Phase II imaging specialist clinical unit in Glasgow Royal Infirmary.
Major areas of research have been the study of the behaviour of drug formulations in man. With colleagues at Nottingham, he pioneered applications of scintigraphy in the study of physiological and patho-physiological effects of transit on drug absorption and began the investigations into regional drug absorption in man. This was later applied to the design and optimisation of oral dosage forms, in silico modelling of formulations in man and studies on IVIVR. He has published more than 150 papers, six books and over 130 reviews and book chapters. He was made a fellow of the Controlled Release Society in June 2010 and a Fellow of the Academy of Pharmaceutical Sciences in September 2010.
Â
Patrick Crowley has over 40 years’ experience in dosage form development in the pharmaceutical industry, in both the UK and USA. He has played key roles in the development of 16 commercial products, including fermentation products, semi synthetics, synthetic structures and a biopharmaceutical product and holds several formulation-related Patents. His interests and publications include drug and product stability, enhancing performance by dosage form design and the application of Quality by Design principles and practices in dosage form development, manufacture and control.Bibliographic Information
Book Title: Controlled Release in Oral Drug Delivery
Editors: Clive G. Wilson, Patrick J. Crowley
Series Title: Advances in Delivery Science and Technology
DOI: https://doi.org/10.1007/978-1-4614-1004-1
Publisher: Springer New York, NY
eBook Packages: Biomedical and Life Sciences, Biomedical and Life Sciences (R0)
Copyright Information: The Editor(s) (if applicable) and The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature 2011
Hardcover ISBN: 978-1-4614-1003-4Published: 21 September 2011
Softcover ISBN: 978-1-4614-3007-0Published: 24 October 2013
eBook ISBN: 978-1-4614-1004-1Published: 22 September 2011
Series ISSN: 2192-6204
Series E-ISSN: 2192-6212
Edition Number: 1
Number of Pages: XIV, 414
Industry Sectors: Biotechnology, Chemical Manufacturing, Consumer Packaged Goods, Pharma
