The use of analytical sciences in the discovery, development and
manufacture of pharmaceuticals is wide-ranging. From the analysis
of minute amounts of complex biological materials to the quality
control of the final dosage form, the use of analytical technology
covers an immense range of techniques and disciplines.
This book concentrates on the analytical aspects of drug
development and manufacture, focusing on the analysis of the active
ingredient or drug substance. It provides those joining the
industry or other areas of pharmaceutical research with a source of
reference to a broad range of techniques and their applications,
allowing them to choose the most appropriate analytical technique
for a particular purpose.
The volume is directed at analytical chemists, industrial
pharmacists, organic chemists, pharmaceutical chemists and
biochemists.
表中的内容
1. Quality control and regulation.
Clive Moores, Tunbridge Wells, UK.
2. Development of achiral separation methods in pharmaceutical
analysis.
George Okafo and John K. Roberts, Glaxo Smith Kline, Harlow,
UK.
3. Chiral analysis of pharmaceuticals.
W. John Lough, University of Sunderland, UK.
4. Nuclear magnetic resonance spectroscopy in pharmaceutical
analysis.
Richard J. Smith and Andrew J. Edwards, Glaxo Smith Kline, Harlow,
UK.
5. Mass spectrometry in pharmaceutical analysis.
Neville Haskins, Hampshire, UK.
6. Vibrational spectroscopy in pharmaceutical analysis.
Clare L. Anderton, Glaxo Smith Kline, Harlow, UK.
7. Solid-state analysis and polymorphism.
Professor Dr Ulrich Griesser, University of Innsbruck, Austria
and Dr Joseph G. Stowell, Purdue University, West Lafayette,
Indiana, USA.
.
8. Microscopy and imaging in pharmaceutical analysis.
Robert A. Carlton, Elan Pharmaceuticals, Pennsylvania, UK.
9. Process analysis in the pharmaceutical industry.
Martin Warman and Steve Hammond, Pfizer Ltd, Sandwich, UK.
References.
Index
关于作者
David C Lee and Michael L. Webb are the authors of Pharmaceutical Analysis, published by Wiley.