pharmacokinetic studies. Clebopride was used as internal standard. Plasma samples were
extracted at alkaline pH with tert-butyl methyl ether. The organic phase was then extracted
with sulphuric acid to eliminate endogenous interferences, and cisapride and the internal
standard were then extracted at alkaline pH into tert-butyl methyl ether. After evaporation of
tert-butyl methyl ether, the residue was analysed by HPLC. Chromatography was performed …
BD Kiss, KB Nemes, I Klebovich - Chromatographia, 2003 - Springer
Summary A new sensitive HPLC-FLD method has been developed and validated for the
determination of cisapride in human plasma for a bioequivalence study. A gradient method
was used to remove late-eluting plasma components of no interest. The separation was
performed on a Li-ChroCART 250-4 Purospher RP-18 (5 μm particle) analytical column
fitted with a LiChroCART 4-4 Purospher RP-18 endcapped (5 μm particle) guard column.
The excitation and emission wavelengths were 295 and 350 nm during fluorescence …