Enantioseparation of ofloxacin in urine by capillary electrokinetic chromatography using charged cyclodextrins as chiral selectors and assessment of enantioconversion

Citation
T. De Boer et al., Enantioseparation of ofloxacin in urine by capillary electrokinetic chromatography using charged cyclodextrins as chiral selectors and assessment of enantioconversion, ELECTROPHOR, 22(7), 2001, pp. 1413-1418
Citations number
39
Categorie Soggetti
Chemistry & Analysis
Journal title
ELECTROPHORESIS
ISSN journal
01730835 → ACNP
Volume
22
Issue
7
Year of publication
2001
Pages
1413 - 1418
Database
ISI
SICI code
0173-0835(200104)22:7<1413:EOOIUB>2.0.ZU;2-C
Abstract
A method was developed for the enantioseparation of ofloxacin, a member of the fluoroquinolones, using an anionic cyclodextrin-derivative with or with out combination with a neutral cyclodextrin-derivative, as the chiral selec tor (s) in an electrokinetic chromatography system. The best results were o btained with 0.35 mM sulfated beta -cyclodextrin dissolved in a 50 mM phosp hate buffer, pH 2.5, and at 15 degreesC. Under these conditions, a resoluti on of 2 was readily achieved. Furthermore, under adequate separation condit ions, studies were performed in order to assess possible in vitro and in vi vo enantioconversion of levofloxacin. The current method allows detection o f 2 mug R-(+)-ofloxacine/ml. diluted urine without the necessity of sample cleanup.