摘要
目的 建立测定小鼠血浆中马钱素浓度的高效液相色谱法 ,并研究马钱素在小鼠体内的药代动力学。方法 色谱柱为C1 8柱 ,流动相甲醇 水 (30∶70 ) ,流速为 0 8mL·min- 1 ,检测波长 2 40nm ;血浆样品用固相萃取法预处理。结果 线性范围 0 0 1~ 5 0 0 μg·mL- 1 。日内RSD <10 % ,日间RSD <15 % ,回收率 86 0 %~ 91 5 % ,最低定量浓度为10ng·mL- 1 。ig给药 0 5h后血浆药物浓度达峰值 ,Cmax 为 6 8μg·mL- 1 ,T1 2 α为 2 6 1min ,T1 2 β为 2 9 0 1min。 结论该方法灵敏度高 ,操作方便 ,适用于马钱素的药代动力学研究 ;本品口服吸收快消除也快。
AIM To develop a method for determination of loganin in mouse plasma by using high-performance liquid chromatography. The method was employed to study pharmacokinetics of loganin. METHODS An RP-C 18 was used as the stationary phase.The mobile phase consisted of methanol-water (30∶70), at the flow-rate of 0.8 mL·min -1 . The UV absorbance detector was set at 240 nm. Plasma samples were treated with solid phase extraction. RESULTS The recovery of loganin in mouse plasma was 86.0%~91.5%. The calibration curve in plasma was linear over the range of 0.01~5.00 μg·mL -1 . The limit of quantitation was 10 ng·mL -1 . The RSDs of intra-day and inter-day (n=5) were less than 15%. The pharmacokinetic parameters were C max =6.8 μg·mL -1 , T max =30 min, T 1/2 α=26.1 min, T 1/2 β=29.01 min. CONCLUSION The method is accurate, sensitive and suitable for pharmcokinetic study of loganin. The absorption and elimination of loganin were rapid after ig in mice.
出处
《药学学报》
CAS
CSCD
北大核心
2002年第7期548-550,共3页
Acta Pharmaceutica Sinica
基金
国家重点基础研究发展规划项目 (G19990 5 440 1)