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