L. Dalbo et al., DETERMINATION OF TICLOPIDINE IN HUMAN PLASMA BY HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY AND ULTRAVIOLET ABSORBENCY DETECTION, Journal of chromatography B. Biomedical applications, 665(2), 1995, pp. 404-409
Citations number
9
Categorie Soggetti
Chemistry Analytical
Journal title
Journal of chromatography B. Biomedical applications
A simple HPLC method has been developed for the determination of ticlo
pidine in human plasma. Plasma samples were buffered at pH 9 and extra
cted with n-heptane-isoamyl alcohol (98.5:1.5, v/v). Imipramine was us
ed as internal standard. Chromatography was performed isocratically wi
th acetonitrile-methanol-0.05 M KH2PO4 (20:25:55, v/v) at pH 3.0 conta
ining 3% triethylamine at a flow-rate of 1 ml/min. A reversed-phase co
lumn Supelcosil LC-8-DB, 15 cm x 4.6 mm I.D., 5 mu m particle size, wa
s used. The effluent was monitored by UV absorbance detection at 235 n
m. The method showed good accuracy, precision and linearity in the con
centration range 5-1200 ng/ml. The limit of quantitation was 5 ng/ml,
with a precision (C.V.) of 8.91%, which is the same as that achieved b
y other authors with a previously published GC-MS method. The procedur
e described in this paper is simple and allows the routine assessment
of ticlopidine plasma concentration in pharmacokinetic studies followi
ng therapeutic doses in human subjects.