𝔖 Bobbio Scriptorium
✦   LIBER   ✦

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

No coin nor oath required. For personal study only.

✦ 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


Enantiomeric resolution by capillary zon
✍ Salvatore Fanali; Gabriele Caponecchi; Zeineb Aturki 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 139 KB 👁 2 views

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

Use of heptakis-(2,3-O-dimethyl-6-sulfat
✍ Hong Cai; Gyula Vigh 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 173 KB 👁 1 views

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