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龙血竭中龙血素A在大鼠体内的药动学研究
引用本文:易军,金描真,孙晓博,乔淑娟.龙血竭中龙血素A在大鼠体内的药动学研究[J].广东药学院学报,2010,26(5):452-454.
作者姓名:易军  金描真  孙晓博  乔淑娟
作者单位:广东药学院,药科学院,广东广州,510006
基金项目:广东省中医药管理局项目,国家中医药管理局项目 
摘    要:目的考察龙血竭中龙血素A在大鼠体内的药动学行为。方法按100 g大鼠给予龙血竭250 mg灌胃给药,测定不同时间点的血药浓度,并以3P97软件计算其药动学参数。结果龙血素A的Ka为(1.46±0.19)h-1,t1/2(Ka)为(0.48±0.06)h,t1/2(K)为(2.59±0.67)h,tmax为(2.00±0.55)h,Cmax为(1.13±0.24)μg.mL-1,AUC为(2.84±0.68)μg.h.mL-1。结论龙血素A在大鼠体内符合线性动力学一室开放模型,吸收较快。

关 键 词:龙血竭  龙血素A  高效液相色谱法  大鼠  药动学

Study on pharmacokinetics of loureirin A in rats
YI Jun,JIN Miao-zhen,SUN Xiao-bo,QIAO Shu-juan.Study on pharmacokinetics of loureirin A in rats[J].Academic Journal of Guangdong College of Pharmacy,2010,26(5):452-454.
Authors:YI Jun  JIN Miao-zhen  SUN Xiao-bo  QIAO Shu-juan
Institution:(School of Pharmacy,Guangdong Pharmaceutical College,Guangzhou,Guangdong 510006,China)
Abstract:Objective To study on pharmacokinetics of loureirin A in rats.Methods The blood samples were collected at a series of time points after an oral administration of Dragon′s blood to rats(2.5 g·kg-1),and were analyzed by HPLC.Pharmacokinetic parameters were valuated by 3P97 software.Results Pharmacokinetic parameters of loureirin A were as follows:Ka(1.46±0.19) h-1,t1/2(Ka)(0.48±0.06) h,t1/2(K)(2.59±0.67) h,tmax(2.00±0.55) h,Cmax(1.13±0.24) μg·mL-1,AUC(2.84±0.68) μg·h·mL-1.Conclusion The results demonstrated that the pharmacokinetics of loureirin A was consistent with one-compartment model,which was absorbed and distributed rapidly in rats.
Keywords:Dragon′s blood  loureirin A  HPLC  pharmacokinetics
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