Enantiomer separation of denopamine by capillary electrophoresis with charged and uncharged cyclodextrins

被引:18
作者
Ishibuchi, K [1 ]
Izumoto, S [1 ]
Nishi, H [1 ]
Sato, T [1 ]
机构
[1] TANABE SEIYAKU CO LTD,ANALYT RES LAB,YODOGAWA KU,OSAKA 532,JAPAN
关键词
enantiomer separation; denopamine; capillary electrophoresis; charged cyclodextrins;
D O I
10.1002/elps.1150180624
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Direct separation of enantiomers of denopamine was investigated by capillary electrophoresis employing charged and uncharged cyclodextrin (CD) derivatives. Uncharged beta-type CDs, having hydrophobic groups, were essential for the enantioseparation of denopamine; of these, especially dimethyl-beta-CD was effective. Among charged CDs, gamma-type as well as beta-type CDs were found effective for the enantioseparation of denopamine. Reversal of migration order of R-form (active) and S-form enantiomers was investigated by using two types of coated capillaries: (i) an amine capillary with an inner wall coated with dimethylamino groups, and (ii) a polyacrylamide-coated capillary. Manipulation of migration order could be easily performed by selecting suitable capillaries, buffer pH, and CDs.
引用
收藏
页码:1007 / 1012
页数:6
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