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槲皮素在兔体内的药代动力学
引用本文:赵维中,戴俐明.槲皮素在兔体内的药代动力学[J].中国药理学通报,1992,8(6):452-455.
作者姓名:赵维中  戴俐明
作者单位:安徽医科大学药理教研室 合肥230032 (赵维中,戴俐明,方明,马传庚,徐叔云),安徽医科大学物理教研室 合肥230032 (冯仁骏),安徽医科大学物理教研室 合肥230032(黄磊)
摘    要:槲皮素为黄酮类化合物。兔iv槲皮素10m g·kg~(-1)后.血药浓度—时间曲线符合二室模型。T_(1/2)(α)为2.91 ±1.36min,T_(1/2)(β)183.78±82.67min,V_B为0.624±0.225 L·kg~(-1),CL为3.15±2.11 ml·kg~(-1)·min~(-1).槲皮素10mg·kg~(-1)ig后,生物利用度为42.7%,药峰浓度(C_(Dk))为10.9mg·L~(-1),药峰时间(t_(pk))为60min。iv槲皮素后.药物以原型和代谢产物两种形式经尿、胆汁排泄,消除较迅速。

关 键 词:槲皮素  紫外分光光度法  药代动力学

The studies on pharmacokinetics of Quercetin in rabbits.
ZHAO Wei -Zhong,DEI Li-Ming,MA Chuan -Geng.The studies on pharmacokinetics of Quercetin in rabbits.[J].Chinese Pharmacological Bulletin,1992,8(6):452-455.
Authors:ZHAO Wei -Zhong  DEI Li-Ming  MA Chuan -Geng
Abstract:The studies on pharmacoki-netics of Quercetin in rabbits were carried out by UV-spectrophotometry. The experimental results were shown that after 10mg · kg-1 of Quercetin iv administration in rabbits, the curve of plasma concentration - time was shown to fit an open two compartment model. The pharmacokinetic parameters were as follow:T1/2 (α) = 2. 91 ± 1. 36min,T1/2(β) = 183. 78±82. 67min,Vd=0. 624±0. 225L ??? kg-1,CL = 3. 15 ±2. llml · kg-1 · min-1. The bioavailability (F) of Quercetin after 10mg · kg-1 ig in rabbits was 42.7% and Cpk was 10. 9mg · L, tpk was 60min. After 10mg · kg-1 iv administration in rabbits,Quercetin was rapidly eliminated from the blood. The compound and its metabolites were exereten by kidney and bile.
Keywords:Quercetin  UV - spec-trophotometriy  pharmacokinetics
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