MALTOOLIGOSACCHARIDES AS CHIRAL SELECTORS FOR THE SEPARATION OF PHARMACEUTICALS BY CAPILLARY ELECTROPHORESIS

被引:150
作者
SOINI, H
STEFANSSON, M
RIEKKOLA, ML
NOVOTNY, MV
机构
[1] INDIANA UNIV,DEPT CHEM,BLOOMINGTON,IN 47405
[2] UNIV UPPSALA,DEPT ANALYT CHEM,S-75121 UPPSALA,SWEDEN
[3] UNIV HELSINKI,DEPT ANALYT CHEM,SF-00014 HELSINKI,FINLAND
关键词
D O I
10.1021/ac00092a028
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Complexation between the linear maltodextrin oligosaccharides and certain enantiomeric compounds of pharmaceutical interest in buffered solutions can lead to an analytically desirable chiral recognition. Different maltodextrins were assessed in their capacity to cause enantiomeric separations under various conditions of capillary electrophoresis. The mechanism of chiral recognition has been probed through electrophoretic mobility and selectivity measurements for different buffer solutions and organic solvent additives. A differential interaction of chiral solutes with the maltodextrin helical entities emerges as the basis of such enantioselectivity. This notion is further supported by H-1- and C-13-NMR experiments. Optimized separations of simendan, ibuprofen, warfarin, and ketoprofen enantiomers are demonstrated together with a chiral determination of ibuprofen in a blood serum sample at the therapeutic level.
引用
收藏
页码:3477 / 3484
页数:8
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