Fundamental aspects of chiral electromigration techniques and application in pharmaceutical and biomedical analysis

被引:79
作者
Scriba, Gerhard K. E. [1 ]
机构
[1] Univ Jena, Dept Pharmaceut Chem, D-07743 Jena, Germany
关键词
Capillary electrophoresis; Enantioseparation; Pharmaceuticals; Review; CAPILLARY-ELECTROPHORESIS SEPARATION; MONOLITHIC STATIONARY PHASES; NUCLEAR-MAGNETIC-RESONANCE; LIGAND-EXCHANGE CE; BETA-CYCLODEXTRIN; DEXAMPHETAMINE SULFATE; ENANTIOSELECTIVE DETERMINATION; ELECTROKINETIC CHROMATOGRAPHY; COMPUTATIONAL CALCULATION; PROPRANOLOL ENANTIOMERS;
D O I
10.1016/j.jpba.2010.11.018
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Capillary electromigration techniques are often considered ideal methods for the analysis of chiral compounds due to the high resolution power and flexibility of the technique. Therefore, especially capillary electrophoresis using a chiral selector in the background electrolyte, also termed electrokinetic chromatography, has found widespread acceptance in analytical enantioseparations of drug compounds in pharmaceuticals and biological media. Moreover, mechanistic studies on analyte complexation by the chiral selectors have continuously been conducted in an effort to rationalize enantioseparation phenomena. These studies combined capillary electrophoresis with spectroscopic techniques such as nuclear magnetic resonance and/or molecular modeling. The present review focuses on recent examples of mechanistic aspects of capillary electromigration enantioseparations and summarizes recent applications of chiral pharmaceutical and biomedical analysis published between January 2009 and August 2010. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:688 / 701
页数:14
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