Fast drug analysis by capillary electrophoresis.: II.: Analysis of denopamine tablets -: Effects of purity of dimethyl β-cyclodextrin as chiral selector on enantiomer separations

被引:6
作者
Kuwahara, Y [1 ]
Nishi, H [1 ]
机构
[1] Tanabe Seiyaku Co Ltd, Analyt Res Lab, Yodogawa Ku, Osaka 5328505, Japan
来源
YAKUGAKU ZASSHI-JOURNAL OF THE PHARMACEUTICAL SOCIETY OF JAPAN | 1999年 / 119卷 / 04期
关键词
capillary electrophoresis; denopamine; enantiomer separation; 2,6-di-O-methyl-beta-cyclodextrin; octopamine;
D O I
10.1248/yakushi1947.119.4_288
中图分类号
R9 [药学];
学科分类号
1007 [药学];
摘要
Capillary electrophoresis (CE) has been utilized as a tool for enantiomeric separation. It has been incorporated into both USP and EP forums as the methods for general tests and assays. In the present study, we applied CE to the assay and content uniformity of denopamine tablets (KALGUT(R), which are clinically used as a cardiotonic agent. The electrophoretic solution consisted of phosphate buffer of pH 2.5 containing 2,6-di-O-methyl-beta-cyclodextrin (DM-beta-CD) to achieve enantiomer separation, because denopamine is an optically active drug. During this study, we found that the purity of the positional isomerism of DM-beta-CD, significantly influenced the resolution of denopamine enantiomers. This effect of isomer purity was also confirmed by matrix-assisted laser desorption ionization time-of-flight mass spectrometer analysis. The results of the assay and system suitability test indicated that CE method could be useful as an alternative to the conventional HPLC method.
引用
收藏
页码:288 / 298
页数:11
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