Determination of Sophoricoside in Rat Plasma by HPLC and Its Application to Pharmacokinetic Studies

摘要

A simple, sensitive, selective and reproducible reversed-phase HPLC method was developed for the determination of sophoricoside in rat plasma after intravenous administration. Naringin was successfully used as internal standard (IS) for calibration. The chromatographic separation was accomplished on a reversed-phase C_(18) column using acetonitrile-methanol-0.08% phosphoric acid (8 : 29 : 63, v/v/v) as mobile phase with a flow rate of 1.0 ml/min, with UV detection at 260 nm. Plasma samples were injected into the HPLC system after precipitating protein directly by methanol. Good linearity was achieved in the range of 0.0240?48.0 mug/ml (R~2=0.9989). The limit of detection (LOD) and limit of quantification (LOQ) of this method were 0.0075 mug/ml and 0.0240 mug/ml, respectively. The absolute recoveries of sophoricoside from plasma were 95.8%, 93.2%, 98.0% at concentrations of 0.0240,1.92,15.0 mug/ml. The intra-day and inter-day variabilities were 3.39%~5.78% and 2.17%~4.72%, respectively. The developed method was successfully applied to the pharmacokinetic study of sophoricoside after intravenous administration of 2.5,10 and 20 mg/kg in rats.