Handbook of Modern Pharmaceutical Analysis: Volume 3
Published on 2. August 2001
Book
Hardback
566 pages
978-0-12-045555-3 (ISBN)
Description
This book describes the role modern pharmaceutical analysis plays in the development of new drugs. Detailed information is provided as to how the quality of drug products is assured from the point of discovery until the patient uses the drug. Coverage includes state-of-the-art topics such as analytics for combinatorial chemistry and high-throughput screening, formulation development, stability studies, international regulatory aspects and documentation, and future technologies that are likely to impact the field. Emphasis is placed on current, easy-to-follow methods that readers can apply in their laboratories.
No book has effectively replaced the very popular text, Pharmaceutical Analysis, that was edited in the 1960s by Tak Higuchi. This book will fill that gap with an up-to-date treatment that is both handy and authoritative.
No book has effectively replaced the very popular text, Pharmaceutical Analysis, that was edited in the 1960s by Tak Higuchi. This book will fill that gap with an up-to-date treatment that is both handy and authoritative.
Reviews / Votes
In today's pharmaceutical industry, the analytical department plays a major role in the drug development process, providing accurate and precise data to support drug discovery, development, and market support. This handbook presents analytical research and development as a process-driven function assuring identity, safety, efficacy, purity, and quality of a product. Regulatory requirements and compliance are discussed as well as attempts to harmonize international regulatory authorities. Analytical techniques from the molecular to the bulk level, new drug discoveries, identification of impurities, various routes of administration, stability testing, and analytical documentation are all parts of the regulatory requirements during pre-approval inspections."This book is well referenced and indexed. Each of the 16 chapters is written by experts and illustrated with figures, tables, and graphs. Anyone involved with new drug development, production, and control in the pharmaceutical industry would fine this title useful as well as graduate students and faculty in these areas. This would be a good acquisition for a graduate or research chemical or pharmaceutical library." --E-Streams E-STREAMS Vol. 5, No. 6 - June 2002
"On the whole this well written and thoroughly edited volume brings the reader up to date on a wide range of subjects pertaining to analytics in pharmaceutical industry." --Alexander Nezlin, CTS Chemical Industries Ltd, Kiryat Malachi, Israel
More details
Series
Language
English
Place of publication
San Diego
United States
Publishing group
Elsevier Science Publishing Co Inc
Target group
Professional and scholarly
Pharmaceutical scientists in industry and government as well as academia. Specifically laboratory chemists in the pharmaceutical industry and their supervisors or group leaders/managers, academic researchers, postgraduate students, and regulatory chemists in government agencies.
Dimensions
Height: 254 mm
Width: 152 mm
Weight
1200 gr
ISBN-13
978-0-12-045555-3 (9780120455553)
Copyright in bibliographic data is held by Nielsen Book Services Limited or its licensors: all rights reserved.
Schweitzer Classification
Other editions
New editions
Book
11/2010
2nd Edition
Academic Press
€246.50
Shipment within 15-20 days
Persons
Satinder Ahuja is a leading expert on water quality improvement. He earned his PhD in analytical chemistry from the University of the Sciences in Philadelphia. He worked for Novartis Corp. in various leadership positions for over 25 years and taught as an adjunct professor at Pace University for over 10 years. As president of Ahuja Consulting, he advises on water quality issues relating to chemicals and pharmaceuticals. A member of the executive committee of the Rivers of the World Foundation (ROW), Dr. Ahuja has organized numerous global symposia on improving water quality, including presentations for the American Chemical Society and UNESCO. Dr. Ahuja has published numerous papers and more than 25 books. His latest books are Contaminants in Our Water (ACS, 2020); Evaluating Water Quality to Prevent Future Disasters (Elsevier, 2019); Advances in Water Purification Techniques (Elsevier, 2019); and Chemistry and Water (Elsevier, 2017). Stephen Scypinski obtained his Ph.D. in analytical chemistry from Seton Hall University. He is director of analytical chemistry research and development department at R.W. Johnson Pharmaceutical Research Institute.
Content
Modern Pharmaceutical Analysis: An Overview (S. AHUJA)
Combinatorial Chemistry and High-Throughput Screening in Drug Discovery and Development (KEN APPELL, JOHN J. BALDWIN, AND WILLIAM J. EGAN)
Solid-State Analysis (HARRY G. BRITTAIN)
Degradation and Impurity Analysis for Pharmaceutical Drug Candidates (KAREN M. ALSANTE, ROBERT C. FRIEDMANN, TODD D. HATAJIK, LINDA L. LOHR,
THOMAS R. SHARP, KIMBERLY D. SNYDER, AND EDWARD J. SZCZESNY)
Preformulation Studies (EDWARD LAU (deceased))
Solid Dosage-Form Analysis (PHILIP J. PALERMO)
Parenteral Dosage Forms (GREGORY A. BIRRER, SATYA S. MURTHY, AND JIE LIU)
New Drug Delivery Systems (DAVID C. PANG)
Compendial Testing (CHRISTINE F. RICHARDSON)
Method Development (HENRIK T. RASMUSSEN)
Setting Up Specifications (IAN E. DAVIDSON)
Validation of Pharmaceutical Test Methods (JONATHAN B. CROWTHER)
Stability Studies (JESSICA CHA, JOSEPH S. RANWEILER, PHILIP A. LANE)
Analytical Methodology Transfer (STEPHEN SCYPINSKI)
Pharmaceutical Analysis Documentation (HITESH CHOKSHI AND KATHLEEN SCHOSTACK)
An Innovative Separation Platform: Electrophoretic Microchip Technology (LIAN JI JIN, JEROME FERRANCE, ZHILI HUANG, AND JAMES P. LANDERS)
Index
Combinatorial Chemistry and High-Throughput Screening in Drug Discovery and Development (KEN APPELL, JOHN J. BALDWIN, AND WILLIAM J. EGAN)
Solid-State Analysis (HARRY G. BRITTAIN)
Degradation and Impurity Analysis for Pharmaceutical Drug Candidates (KAREN M. ALSANTE, ROBERT C. FRIEDMANN, TODD D. HATAJIK, LINDA L. LOHR,
THOMAS R. SHARP, KIMBERLY D. SNYDER, AND EDWARD J. SZCZESNY)
Preformulation Studies (EDWARD LAU (deceased))
Solid Dosage-Form Analysis (PHILIP J. PALERMO)
Parenteral Dosage Forms (GREGORY A. BIRRER, SATYA S. MURTHY, AND JIE LIU)
New Drug Delivery Systems (DAVID C. PANG)
Compendial Testing (CHRISTINE F. RICHARDSON)
Method Development (HENRIK T. RASMUSSEN)
Setting Up Specifications (IAN E. DAVIDSON)
Validation of Pharmaceutical Test Methods (JONATHAN B. CROWTHER)
Stability Studies (JESSICA CHA, JOSEPH S. RANWEILER, PHILIP A. LANE)
Analytical Methodology Transfer (STEPHEN SCYPINSKI)
Pharmaceutical Analysis Documentation (HITESH CHOKSHI AND KATHLEEN SCHOSTACK)
An Innovative Separation Platform: Electrophoretic Microchip Technology (LIAN JI JIN, JEROME FERRANCE, ZHILI HUANG, AND JAMES P. LANDERS)
Index