Abstract
A simple and reliable high-performance liquid chromatographic (HPLC) method was developed for the determination of belotecan in the plasma, urine, and bile samples of rats. Belotecan was analyzed with HPLC using a C18 column with fluorescence detector. A mixture of acetonitrile–0.1 M potassium phosphate buffer at pH 2.4 (25:75, v/v) and 0.2% trifluoroacetic acid was used as the mobile phase. The lower limits of quantitation (LOQ) were 5 ng mL−1 for the plasma and 5 µg mL−1 for the urine and bile samples. The method has been readily applied for the routine pharmacokinetic study of belotecan in small laboratory animals.
This study was supported by a grant from the Korean Ministry of Science and Technology through the National Research Laboratory Program (ROA-2006-000-10290-0).
Notes
a SD, standard deviation.
a SD, standard deviation.
a SD, standard deviation.
a AUC: area under the plasma concentration time curve; CL: clearance; Vss: apparent volume of distribution at a steady state; CLb: biliary clearance; CLr: renal clearance.