Capillary electrophoresis has been used for the enantiomeric resolution of several basic compounds of pharmaceutical interest employing a background electrolyte containing pepsin as chiral selector. The separations have been performed in a polyacrylamide-coated capillary to suppress or minimize the
Chiral separation of the β2-sympathomimetic fenoterol by HPLC and capillary zone electrophoresis for pharmacokinetic studies
✍ Scribed by Thomas Ullrich; Dirk Wesenberg; Corinna Bleuel; Gerd-Joachim Krauss; Martin G. Schmid; Michael Weiss; Gerald Gübitz
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 396 KB
- Volume
- 24
- Category
- Article
- ISSN
- 0269-3879
- DOI
- 10.1002/bmc.1415
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✦ Synopsis
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.
📜 SIMILAR VOLUMES
The single isomer, fully and permanently charged heptakis-2,3-di-. methyl-6-sulfato --cyclodextrin was used to study the complexation behavior of the enantiomers of noncharged analytes in capillary electrophoresis. Separation selectivities were calculated from the measured effective mobilities and