HPLC Method Development for Pharmaceuticals

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Satinder Ahuja (President, Ahuja Consulting for Water Quality, Calabash, NC, USA) Henrik Rasmussen (Global Analytical Development, Johnson and Johnson Pharmaceutical Research and Development, Raritan, NJ, USA)

HPLC Method Development for Pharmaceuticals

Satinder Ahuja (President, Ahuja Consulting for Water Quality, Calabash, NC, USA), Henrik Rasmussen (Global Analytical Development, Johnson and Johnson Pharmaceutical Research and Development, Raritan, NJ, USA)

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English

Academic Press Inc
07 June 2007

Pharmaceutical industries; Chromatography

Series: Separation Science and Technology

High pressure, or high performance, liquid chromatography (HPLC) is the method of choice for checking purity of new drug candidates, monitoring changes during scale up or revision of synthetic procedures, evaluating new formulations, and running control/assurance of the final drug product. HPLC Method Development for Pharmaceuticals provides an extensive overview of modern HPLC method development that addresses these unique concerns. Includes a review and update of the current state of the art and science of HPLC, including theory, modes of HPLC, column chemistry, retention mechanisms, chiral separations, modern instrumentation (including ultrahigh-pressure systems), and sample preparation. Emphasis has been placed on implementation in a pharmaceutical setting and on providing a practical perspective.

HPLC Method Development for Pharmaceuticals is intended to be particularly useful for both novice and experienced HPLC method development chemists in the pharmaceutical industry and for managers who are seeking to update their knowledge.

Edited by: Satinder Ahuja (President Ahuja Consulting for Water Quality Calabash NC USA), Henrik Rasmussen (Global Analytical Development, Johnson and Johnson Pharmaceutical Research and Development, Raritan, NJ, USA)
Imprint: Academic Press Inc
Country of Publication: United States
Edition: 8th edition
Volume: v. 8
Dimensions: Height: 240mm, Width: 165mm, Spine: 28mm
Weight: 1.100kg
ISBN: 9780123705402
ISBN 10: 0123705401
Series: Separation Science and Technology
Pages: 532
Publication Date: 07 June 2007
Audience: Professional and scholarly , Undergraduate
Format: Hardback
Publisher's Status: Active

Satinder Ahuja obtained his Ph.D. in analytical chemistry from the Philadelphia College of Pharmacy and Science. He serves as adjunct research professor at Pace University and is a consultant to pharmaceutical companies as president of Ahuja Consulting.

Reviews for HPLC Method Development for Pharmaceuticals

Review in Doody's 2008, by Joseph Boullata, PharmD(University of Pennsylvania College of Nursing): <br> This book is written with pharmaceutical scientists in mind, regardless of their level of experience with HPLC method development. By extension, it would be valuable for managers and regulators as well. It may also be of value to those managing a lab or research program in the academic setting. <br>The 18 chapters are written by 35 contributors, mostly from the U.S., with just over half from the pharmaceutical industry. The book is divided into two major sections, one a state-of-the-science review of HPLC and one on the unique needs in a pharmaceutical setting. This latter section is what makes the book most useful to the intended audience. It addresses topics such as method development for each phase in the drug development process, strategies for software/hardware validation, and prevention/troubleshooting problems. There is lots of concern for instrument qualification andy