Enantioselective analysis of the antipsychotic 9-hydroxyrisperidone, main metabolite of risperidone, by chiral capillary EKC using dual CDs

被引:19
作者
Danel, Cecile
Chaminade, Pierre
Odou, Pascal
Bartelemy, Christine
Azarzar, Dalila
Bonte, Jean-Paul
Vaccher, Claude
机构
[1] Univ Lille 2, Fac Sci Pharmaceut & Biol, EA 4034, Chim Analyt Lab, F-59006 Lille, France
[2] Univ Paris 11, Fac Pharm, Grp Chim Analyt Paris Sud, F-92290 Chatenay Malabry, France
[3] Univ Lille 2, Fac Sci Pharmaceut & Biol, Lab Biopharm & Pharm Clin, F-59006 Lille, France
关键词
central composite design; chiral capillary EKC; dual CD mode; highly sulfated cyclodextrins; 9-hydroxyrisperidone;
D O I
10.1002/elps.200600837
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
An analytical method for the enantioseparation of the 9-hydroxyrisperidone, main metabolite of the antipsychotic risperidone (Risp), was developed by CD-EKC in the dual CDs mode using anionic and neutral CDs at acidic pH 2.5. Preliminary experiments allowed us to select the more suitable couple of CDs composed of sulfated-alpha-CD and hydroxypropylated-beta-CD. The optimization of the main experimental parameters (concentrations of both CDs and concentration of the phosphate buffer) was based on a central composite design through the response surface methodology. Then, the influence of the voltage and the temperature on the enantioseparation was studied using the classical univariate approach. The final method permits to resolve the enantiomers of the 9-hydroxyrisperidone with a resolution of 3.13 and an analysis time of about 13 min. Finally, this method was successfully applied for the simultaneous determination of Risp and the enantiomers of 9-hydroxyrisperidone (9-OHRisp).
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页码:2683 / 2692
页数:10
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