Combined Use of Ionic Liquid and Hydroxypropyl-β-Cyclodextrin for the Enantioseparation of Ten Drugs by Capillary Electrophoresis

被引:42
作者
Cui, Yan [1 ]
Ma, Xiaowei [1 ]
Zhao, Min [1 ]
Jiang, Zhen [1 ]
Xu, Shuying [1 ]
Guo, Xingjie [1 ]
机构
[1] Shenyang Pharmaceut Univ, Sch Pharm, Shenyang 110016, Peoples R China
基金
中国国家自然科学基金;
关键词
capillary electrophoresis; enantiomeric purity determination; enantioseparation; hydroxypropyl-beta-cyclodextrin; ionic liquid; SEPARATION;
D O I
10.1002/chir.22168
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
In the present study, hydroxypropyl-beta-cyclodextrin and an ionic liquid (1-ethyl-3-methylimidazolium-L-lactate) were used as additives in capillary electrophoresis for the enantioseparation of 10 analytes, including ofloxacin, propranolol hydrochloride, dioxopromethazine hydrochloride, isoprenaline hydrochloride, chlorpheniramine maleate, liarozole, tropicamide, amlodipine benzenesulfonate, brompheniramine maleate, and homatropine methylbromide. The effects of ionic liquid concentrations, salt effect, cations, and anions of ionic liquids on enantioseparation were investigated and the results proved that there was a synergistic effect between hydroxypropyl-b-cyclodextrin and the ionic liquid, and the cationic part of the ionic liquid played an important role in the increased resolution. With the developed dual system, all the enantiomers of 10 analytes were well separated in resolutions of 5.35, 1.76, 1.85, 2.48, 2.88, 1.43, 5.45, 4.35, 2.76, and 2.98, respectively. In addition, the proposed method was applied to the determination of the enantiomeric purity of S-ofloxacin after validation of the method in terms of selectivity, repeatability, linearity range, accuracy, precision, limit of detection (LOD), and limit of quality (LOQ). (C) 2013 Wiley Periodicals, Inc.
引用
收藏
页码:409 / 414
页数:6
相关论文
共 28 条
[1]  
Aboul-Enein H. Y., 2003, CHIRAL SEPARATION LI, P69
[2]   Enantioselective analysis of ofloxacin and ornidazole in pharmaceutical formulations by capillary electrophoresis using single chiral selector and computational calculation of their inclusion complexes [J].
Al Azzam, Khaldun M. ;
Saad, Bahruddin ;
Adnan, Rohana ;
Aboul-Enein, Hassan Y. .
ANALYTICA CHIMICA ACTA, 2010, 674 (02) :249-255
[3]   Ionic liquids in analytical chemistry [J].
Anderson, Jared L. ;
Armstrong, Daniel W. ;
Wei, Guor-Tzo .
ANALYTICAL CHEMISTRY, 2006, 78 (09) :2892-2902
[4]   Quantitation of the enantiomers of ofloxacin by capillary electrophoresis in the parts per billion concentration range for in vitro drug absorption studies [J].
Awadallah, B ;
Schmidt, PC ;
Wahl, MA .
JOURNAL OF CHROMATOGRAPHY A, 2003, 988 (01) :135-143
[5]   Enantioseparation of chiral tropa alkaloids by means of cyclodextrin-modified microemulsion electrokinetic chromatography [J].
Bitar, Yaser ;
Holzgrabe, Ulrike .
ELECTROPHORESIS, 2007, 28 (15) :2693-2700
[6]  
Chen YQ, 2008, CHIN J CHROMATOGR, V26, P643
[7]  
de Boer T, 2001, ELECTROPHORESIS, V22, P1413, DOI 10.1002/1522-2683(200105)22:7<1413::AID-ELPS1413>3.3.CO
[8]  
2-L
[9]   Evaluation of chiral ionic liquids as additives to cyclodextrins for enantiomeric separations by capillary electrophoresis [J].
Francois, Yannis ;
Varenne, Anne ;
Juillerat, Emilie ;
Villemin, Didier ;
Gareil, Pierre .
JOURNAL OF CHROMATOGRAPHY A, 2007, 1155 (02) :134-141
[10]   DETERMINATION OF THE ABSOLUTE-CONFIGURATION OF THE ACTIVE AMLODIPINE ENANTIOMER AS (-)-S - A CORRECTION [J].
GOLDMANN, S ;
STOLTEFUSS, J ;
BORN, L .
JOURNAL OF MEDICINAL CHEMISTRY, 1992, 35 (18) :3341-3344