Chiral separation of the β2-sympathomimetic fenoterol by HPLC and capillary zone electrophoresis for pharmacokinetic studies

被引:6
|
作者
Ullrich, Thomas [3 ]
Wesenberg, Dirk [3 ]
Bleuel, Corinna [3 ]
Krauss, Gerd-Joachim [3 ]
Schmid, Martin G. [1 ]
Weiss, Michael [2 ]
Guebitz, Gerald [1 ]
机构
[1] Karl Franzens Univ Graz, Inst Pharmaceut Sci, Dept Pharmaceut Chem, A-8010 Graz, Austria
[2] Univ Halle Wittenberg, Inst Pharmacol, Fac Med, D-06120 Halle, Saale, Germany
[3] Univ Halle Wittenberg, Fac Biosci, Inst Biochem & Biotechnol, D-06120 Halle, Saale, Germany
基金
日本学术振兴会;
关键词
fenoterol; precolumn derivatization; 1-naphthyl isocyanate; S-(+)-1-(1-naphthyl)-ethylisocyanate; enantioselective HPLC; Chiracel OD-RH; chiral CE; cyclodextrins; column switching; PERFORMANCE LIQUID-CHROMATOGRAPHY; FLUORESCENCE DETECTION; BLOCKING-AGENTS; ENANTIOMERS; DERIVATIZATION; DERIVATIVES; PLASMA; MEDIA;
D O I
10.1002/bmc.1415
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The development of methods for the separation of the enantiomers of fenoterol by chiral HPLC and capillary zone electrophoresis (CZE) is described. For the HPLC separation precolumn fluorescence derivatization with naphthyl isocyanate was applied. The resulting urea derivatives were resolved on a cellulose tris(3,5-dimethylphenylcarbamate)-coated silica gel column employing a column switching procedure. Detection was carried out fluorimetrically with a detection limit in the low ng/mL range. The method was adapted to the determination of fenoterol enantiomers in rat heart perfusates using liquid-liquid extraction. As an alternative a CE method was used for the direct separation of fenoterol enantiomers comparing different cyclodextrin derivatives as chiral selectors. Copyright (C) 2010 John Wiley & Sons, Ltd.
引用
收藏
页码:1125 / 1129
页数:5
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