Macrocyclic Antibiotics as Chiral Selectors in High-Performance Liquid Chromatography and Capillary Electrophoresis

被引:15
作者
Shapovalova, E. N. [1 ]
Fedorova, I. A. [1 ]
Anan'eva, I. A. [1 ]
Shpigun, O. A. [1 ]
机构
[1] Moscow MV Lomonosov State Univ, Dept Chem, Moscow 119991, Russia
基金
俄罗斯基础研究基金会;
关键词
chiral selectors; macrocyclic antibiotics; chiral chromatography; nonaqueous capillary electrophoresis; mixed selectors; AMINO-ACID ENANTIOMERS; STATIONARY PHASES; ENANTIOSEPARATION; EREMOMYCIN; SEPARATION; VANCOMYCIN; SILICA; PHARMACEUTICALS; RECOGNITION; MECHANISM;
D O I
10.1134/S1061934818110114
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Data on the use of macrocyclic antibiotics (vancomycin, teicoplanin, teicoplanin aglycone, and eremomycin) for the enantioseparation of amino acids, various amino acid derivatives, -phenylcarboxylic acids, -blockers, and some pharmaceutical preparations in reversed-phase and polar-organic HPLC modes are summarized. It is shown that mixed chiral selectors (eremomycin-vancomycin, eremomycin-bovine serum albumin) combine the properties of two selectors. Eremomycin and macrolides (azithromycin, erythromycin, and clarithromycin) are successfully used as chiral selectors in capillary electrophoresis. Aqueous and aqueous-organic supporting electrolytes (SEs) with the addition of eremomycin or nonaqueous supporting electrolytes with the addition of a macrolide are used for enantioseparation. The use of nonaqueous supporting electrolytes decreases the adsorption of the selectors on the quartz capillary surface and enables the separation of enantiomers at a low concentration of a chiral selector. Additions of boric acid into the supporting electrolyte improve the selectivity of separation.
引用
收藏
页码:1064 / 1075
页数:12
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