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Chiral separation of the β2‐sympathomimetic fenoterol by HPLC and capillary zone electrophoresis for pharmacokinetic studies
Authors:Dirk Wesenberg  Corinna Bleuel  Gerd‐Joachim Krauss  Martin G Schmid  Michael Weiss  Gerald Gübitz
Institution:1. Faculty of Biosciences, Institute of Biochemistry and Biotechnology, Martin Luther University Halle‐Wittenberg, Kurt‐Mothes‐Str. 3, D‐06120 Halle (Saale), Germany;2. Institute of Pharmaceutical Sciences, Department of Pharmaceutical Chemistry, Karl‐Franzens University, Universit?tsplatz 1, A‐8010 Graz, Austria;3. Faculty of Medicine, Institute of Pharmacology, Martin Luther University, Magdeburger Str. 4, D‐06120 Halle (Saale), Germany
Abstract: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 © 2010 John Wiley & Sons, Ltd.
Keywords:fenoterol  precolumn derivatization  1‐naphthyl isocyanate  S‐(+)‐1‐(1‐naphthyl)‐ethylisocyanate  enantioselective HPLC  Chiracel OD‐RH  chiral CE  cyclodextrins  column switching
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