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Capillary electrophoresis methods for pharmaceutical analysis
Title:
Capillary electrophoresis methods for pharmaceutical analysis
Author:
Ahuja, Satinder, 1933-
ISBN:
9780123725738
9780080559612
Edition:
1st ed.
Publication Information:
Amsterdam ; Boston : Elsevier/Academic Press, 2008.
Physical Description:
1 online resource (xvi, 529 pages) : illustrations.
Series:
Separation science and technology, v. 9
Separation science and technology (San Diego, Calif.) ; v. 9.
Contents:
Preface -- 1. Overview of Capillary Electrophoresis in Pharmaceutical Analysis -- 2. Theoretical Consideration in Performance of Various Modes of CE -- 3. Equipment Considerations for Capillary Electrophoresis -- 4. Method Development for Pharmaceutical Analysis -- 5. Role of CE in Drug Substance and Drug Product Development -- 6. General Considerations to Improve Performance of CE Methods -- 7. Overview of Current Regulatory Guidance -- 8. Qualification of CE Instrumentation -- 9. Robustness Testing of CE Methods -- 10. Validation of Analytical Methods -- 11. The Need for CE Methods in Pharmacopeial Monographs -- 12. CE in Impurity Profiling of Drugs -- 13. Ion Analysis -- 14. Role of CE in Biopharmaceutical Development and Quality Control -- 15. Capillary Electrophoresis and Bioanalysis -- 16. CE as Orthogonal Technique to Chromatography -- 17. Capillary Electrochromatography of Pharmaceuticals -- 18. Coupling CE and Chip-based Devices and Mass Spectrometry.
Abstract:
Capillary electrophoresis (CE) is a powerful analytical technique that is widely used in research and development and in quality control of pharmaceuticals. Many reports of highly efficient separations and methods have been published over the past 15 years. CE offers several advantages over high-pressure or high-performance liquid chromatography (HPLC). These include simplicity, rapid analysis, automation, ruggedness, different mechanisms for selectivity, and low cost. Moreover, EC requires smaller sample size and yet offers higher efficiency and thus greater resolution power over HPLC. These characteristics are very attractive in research and development, even more so in pharmaceutical quality control (QC) and stability monitoring (SM) studies. This book will provide busy pharmaceutical scientists a complete yet concise reference guide for utilizing the versatility of CE in new drug development and quality control. - Provides current status and future developments in CE analysis of pharmaceuticals. - Explains how to develop and validate methods. - Includes major pharmaceutical applications including assays and impurity testing.
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Electronic Access:
ScienceDirect http://www.sciencedirect.com/science/book/9780123725738 ScienceDirect https://www.sciencedirect.com/science/book/9780123725738 ScienceDirect https://www.sciencedirect.com/science/bookseries/18771718/9Available:*
Shelf Number | Item Barcode | Shelf Location | Status |
|---|---|---|---|
| RS189.5 .C34 C375 2008 EB | 1189640-1001 | Elsevier E-Book Collections | Searching... |
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