AIM To develop a reversed phase high performance quid chromatographic method (RP HPLC) for determination of protopine (Pro) in rat plasma and to investigate the pharmacokinetics of Pro in rats. METHODS The column was ...AIM To develop a reversed phase high performance quid chromatographic method (RP HPLC) for determination of protopine (Pro) in rat plasma and to investigate the pharmacokinetics of Pro in rats. METHODS The column was packed with 5 μm C 18 . The mobile phase (pH 5 6) was a mixture of methanol water 10% acetic acid (80∶20∶2). After twice extracted with ether under basic condition, and reextracted with 0 02 mol·L -1 sulfuric acid, protopine in the plasma samples was isolated well. The content of protopine in the plasma sample was measured by UV detector at 285 nm. RESULTS The lowest limit of detection was 50 ng·mL -1 . The intraday and interday precisions were 1 5%-3 0% and 2 1%-6 2%, respectively. The mean recovery was 80 6%-97 6%. A good linear relationship between the peak height and the concentration of protopine in rat plasma was observed. The pharmacokinetics of protopine had been investigated in rats after intravenous administration 10 mg·kg -1 . The concentration time curve of protopine in rat was confirmed to two compartment open model. The T 1/2 α, T 1/2 β, K e, CL , V d were 0 05 h, 1 85 h, 1 52 h, 6 41 L·h -1 and 17 27 L, respectively. CONCLUSION This method is suitable for studies on pharmacokinetics of protopine.展开更多
文摘AIM To develop a reversed phase high performance quid chromatographic method (RP HPLC) for determination of protopine (Pro) in rat plasma and to investigate the pharmacokinetics of Pro in rats. METHODS The column was packed with 5 μm C 18 . The mobile phase (pH 5 6) was a mixture of methanol water 10% acetic acid (80∶20∶2). After twice extracted with ether under basic condition, and reextracted with 0 02 mol·L -1 sulfuric acid, protopine in the plasma samples was isolated well. The content of protopine in the plasma sample was measured by UV detector at 285 nm. RESULTS The lowest limit of detection was 50 ng·mL -1 . The intraday and interday precisions were 1 5%-3 0% and 2 1%-6 2%, respectively. The mean recovery was 80 6%-97 6%. A good linear relationship between the peak height and the concentration of protopine in rat plasma was observed. The pharmacokinetics of protopine had been investigated in rats after intravenous administration 10 mg·kg -1 . The concentration time curve of protopine in rat was confirmed to two compartment open model. The T 1/2 α, T 1/2 β, K e, CL , V d were 0 05 h, 1 85 h, 1 52 h, 6 41 L·h -1 and 17 27 L, respectively. CONCLUSION This method is suitable for studies on pharmacokinetics of protopine.
