Application of antibiotics as chiral selectors for capillary electrophoretic enantioseparation of pharmaceuticals: a review

被引:27
作者
Dixit, Shuchi [1 ]
Park, Jung Hag [1 ]
机构
[1] Yeungnam Univ, Dept Chem, Gyongsan 712749, South Korea
基金
新加坡国家研究基金会;
关键词
antibiotics; capillary electrophoresis; enantioseparation; pharmaceuticals; review; ENANTIOMERIC SEPARATION; MACROCYCLIC ANTIBIOTICS; ZONE-ELECTROPHORESIS; RIFAMYCIN-B; BASIC DRUGS; AMINO-ACIDS; ELECTROMIGRATION TECHNIQUES; COUNTERCURRENT PROCESS; CHLORINE SUBSTITUENTS; ALPHA-HYDROXY;
D O I
10.1002/bmc.2950
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Recent years have witnessed several new trends in chiral separation, for example, the enantiorecognition ability of several new antibiotics has been explored using capillary electrophoresis (CE) prior to HPLC; antibiotics have been employed as chiral selectors (CSs) in a nonaqueous CE (NACE) mode; and several new detection techniques (namely, capacitively coupled contactless conductivity detection) have been used in combination with CE for quantification of enantiomers. On account of these emerging trends, this article aims to review the application of various classes of antibiotics for CE enantioseparation of pharmaceuticals. A detailed account of the basic factors affecting enantioseparation, certain limitations of antibiotics as CSs and strategies to mitigate them, and advantages of NACE while using antibiotics as CSs has also been presented. Copyright (c) 2013 John Wiley & Sons, Ltd.
引用
收藏
页码:10 / 26
页数:17
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