SIMULTANEOUS ENANTIOSELECTIVE DETERMINATION AND QUANTIFICATION OF DIMETHINDENE AND ITS METABOLITE N-DEMETHYL-DIMETHINDENE IN HUMAN URINE USING CYCLODEXTRINS AS CHIRAL ADDITIVES IN CAPILLARY ELECTROPHORESIS

Citation
M. Heuermann et G. Blaschke, SIMULTANEOUS ENANTIOSELECTIVE DETERMINATION AND QUANTIFICATION OF DIMETHINDENE AND ITS METABOLITE N-DEMETHYL-DIMETHINDENE IN HUMAN URINE USING CYCLODEXTRINS AS CHIRAL ADDITIVES IN CAPILLARY ELECTROPHORESIS, Journal of pharmaceutical and biomedical analysis, 12(6), 1994, pp. 753-760
Citations number
15
Categorie Soggetti
Pharmacology & Pharmacy
ISSN journal
07317085
Volume
12
Issue
6
Year of publication
1994
Pages
753 - 760
Database
ISI
SICI code
0731-7085(1994)12:6<753:SEDAQO>2.0.ZU;2-P
Abstract
Capillary electrophoresis (CE) has been used for the chiral resolution of the basic racemic drug dimethindene (Fenistil(R)) and its metaboli te N-demethyl-dimethindene. After oral administration of 4 mg dimethin dene maleate the enantioselective excretion in human urine was determi ned by capillary electrophoresis using a 50 mM phosphate run buffer (p H 3.3) containing 30 mM hydroxypropyl-beta-cyclodextrin. The determina tion of very low concentrations of dimethindene and N-demethyl-dimethi ndene in human urine was possible using sample stacking conditions to increase the amount of analyte in the capillary with good peak forms a nd resolutions. The detection limit of the method was approximately 1 ng ml(-1) urine for each compound.