Optimization of preparative electrophoretic chiral separation of ritalin enantiomers

被引:7
作者
Schneiderman, E
Gratz, SR
Stalcup, AM
机构
[1] Univ Cincinnati, Dept Chem, Cincinnati, OH 45221 USA
[2] FDA, Forens Chem Ctr, Cincinnati, OH 45237 USA
关键词
ritalin; methylphenidate; chiral; preparative; separation; continuous free flow electrophoresis; capillary electrophoresis; deflection angle;
D O I
10.1016/S0731-7085(01)00572-6
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Continuous free flow electrophoresis (CFFE) was applied to the preparative chiral separation of ritalin enantiomers. Sulfated beta-cyclodextrin (sbeta-CD) was used as the chiral additive. Liquid chromatography-mass spectrometry (LC-MS) experiments were applied to study the time averaged concentration of sbeta-CD in the separation chamber. The distribution of sbeta-CD in the separation chamber greatly influenced resolution and the angle of deflection. To optimize the separation, several parameters (methanol, concentration of sbeta-CD in the cathodic wash and in the separation buffer, and the introduction of a low conductivity zone) were investigated. The dependence of the resolution and deflection angles of ritalin enantiomers on the concentration of sbeta-CD in both the separation buffer and in the cathode wash solution appeared to be non-linear. Under close to optimal conditions, resolution of ritalin enantiomers was about 0.8 with an average processing rate of 0.5 mg/h. Overall, the enantiomeric purity of the individual isomers was similar to 83%; however, of the 20 vials containing ritalin, the presence of both enantiomers was only detected in three vials. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:639 / 650
页数:12
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