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羟基红花黄色素A脂质载体及水溶液在大鼠体内的代谢、排泄、生物利用度研究
引用本文:李江然,孙敏捷,平其能,陈西敬,戚建平,韩德恩. 羟基红花黄色素A脂质载体及水溶液在大鼠体内的代谢、排泄、生物利用度研究[J]. 中国天然药物, 2010, 0(3): 233-240
作者姓名:李江然  孙敏捷  平其能  陈西敬  戚建平  韩德恩
作者单位:中国药科大学药剂教研室;中国药科大学药物代谢动力学重点实验室;
基金项目:supported by the key project of the National Natural Science Foundation of China(No.30430790); the major project of the national science and technology of China for new drugs development(No.2009ZX09310-004)~~
摘    要:目的:研究不同的羟基红花黄色素A(HSYA)剂型对HSYA代谢、排泄、生物利用度的影响。方法:大鼠灌胃给予HSYA脂质制剂和水溶液,采用HPLC及LC-MS检测血浆、胆汁、粪便、尿液样品。结果:大鼠灌胃给予HSYA脂质制剂和水溶液后,在大鼠胆汁中均发现HSYA及其II相代谢产物;HSYA原药的质荷比为611,而两个II相代谢产物的质荷比分别为918和691,结合酶降解实验表明这两个代谢产物分别为HSYA的谷胱甘肽结合物和硫酸酯结合物。但是同水溶液相比,HSYA脂质制剂显著性降低了HSYA及其II相代谢产物从胆汁的排泄量。大鼠灌胃给予HSYA脂质制剂后,HSYA原药从胆汁、粪便、尿液中24h的累积排泄量分别为(0.05±0.03)%、(8.80±2.30)%、(37.99±17.50)%,其cmax、AUC0-8h分别为2.79μg·mL^-1、402.51μg·min·mL^-1;而大鼠灌胃给予HSYA水溶液后,HSYA原药从胆汁、粪便、尿液中24h的累积排泄量分别为(0.32±0.22)%、(44.66±8.00)%、(5.58±1.30)%,其cmax、AUC0-8h分别为0.08μg·mL^-1、10.73μg·min·mL^-1。结论:实验结果表明脂质制剂可能不会改变HSYA的代谢机制,但是显著性降低了HSYA从粪便和胆汁的排泄量,提高了其生物利用度。

关 键 词:羟基红花黄色素A  脂质制剂  代谢物  胆汁  排泄

Metabolism,Excretion and Bioavailability of Hydroxysafflor Yellow A after Oral Administration of Its Lipid-Based Formulation and Aqueous Solution in Rats
Affiliation:LI Jiang-Ran ,SUN Min-Jie ,Ping Qi-Neng ,CHEN Xi-Jing ,QI Jian-Ping ,HAN De-En ( 1Department of Pharmaceutics,China Pharmaceutical University,Nanjing 210009;2Key Laboratory of Drug Metabolism & Pharmacokinetics,China Pharmaceutical University,Nanjing 210009,China )
Abstract:AIM:To characterize the effect of different oral formulations on the metabolism,excretion and bioavailability of hydroxysafflor yellow A(HSYA).METHODS:HSYA lipid-based formulation and aqueous solution were prepared and orally administered to rats.A gradient HPLC and LC-MS method was performed to determine HSYA concentration in rat serum,bile,urine and feces samples.RESULTS:The bile sample digestion test combining HPLC with LC-MS proved the existence of HSYA and phase II metabolites in bile for both formulat...
Keywords:Hydroxysafflor Yellow A  Lipid-based formulation  Metabolite  Bile  Excretion  
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