Find a copy in the library
Finding libraries that hold this item...
Details
| Document Type: | Book |
|---|---|
| All Authors / Contributors: |
Satinder Ahuja; Henrik Rasmussen |
| ISBN: | 9780123705402 0123705401 |
| OCLC Number: | 144220768 |
| Description: | xvii, 513 p. : ill. ; 25 cm. |
| Contents: | 1. Overview (Satinder Ahuja). 2. HPLC Theory (Y.V. Kazakevich). 3. HPLC Columns and Packings (U.D. Neue et al.). 4. Column Characterization and Selection (D. Visky). 5. Chiral Separations (Xiande Wang et al.). 6. Contemporary Liquid Chromatographic Systems for Method Development (M. Swartz). 7. Hyphenated Techniques (D.L. Norwood et al.). 8. HPLC Sample Preparation (G. Slack, N.H. Snow). 9. Instrument and Software Qualification and Validation (D. Van Geel). 10. Pharmaceutical Development: From Pre-clinical to Post Approval (K. Bynum). 11. HPLC Method Development for Drug Discovery LC-MS Assays in Rapid PK Applications (Xiaoying Xu, W. Korfmacher). 12. HPLC Method Development in Early Phase Pharmaceutical Development (H.T. Rasmussen et al.). 13. HPLC Method Development in Late Phase Pharmaceutical Development (M. Ilias Jimidar). 14. Use of HPLC for In-process Testing (C. Richardson). 15. Method Development for Biomolecules (D.E. Raynie, J.L. Driver). 16. Method Validation (M. Ilias Jimidar et al.). 17. Troubleshooting HPLC Methods (H. McNair). 18. Molecularly Imprinted Polymers as Sorbents for Separations and Extractions (M.T. Koesdjojo et al.). |
| Series Title: | Separation science and technology (San Diego, Calif.), v. 8. |
| Responsibility: | edited by Satinder Ahuja, Henrik Rasmussen. |
Reviews
Publisher Synopsis
Review in Doody's 2008, by Joseph Boullata, PharmD(University of Pennsylvania College of Nursing):
"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.
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 and9
Read more...
Tags
Similar Items
Related Subjects:(11)
- Pharmaceutical Preparations -- analysis.
- Chemistry, Pharmaceutical -- methods.
- Chromatography, High Pressure Liquid -- methods.
- High performance liquid chromatography -- Methodology.
- Drugs -- Analysis.
- Drug development.
- Chromatographie en phase liquide à hautes performances -- Méthodologie.
- Médicaments -- Analyse.
- Médicaments -- Développement.
- Chromatographie.
- Trennverfahren.
