冰片对原儿茶酸在家兔体内药动学的影响  被引量:12

Effects of borneol on pharmacokinetics of protocatechuic acid in rabbits

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作  者:杨洁[1] 王世祥[1] 兰薇[1] 刘春芝[1] 郑晓晖[1] 

机构地区:[1]西北大学生命科学学院,陕西西安710069

出  处:《中国中药杂志》2009年第9期1141-1143,共3页China Journal of Chinese Materia Medica

基  金:教育部科学研究重点项目(207151);陕西省中医管理局中医药科研项目(2005103)

摘  要:目的:研究冰片对原儿茶酸在家兔体内药动学的影响。方法:建立测定家兔血浆中原儿茶酸的高效液相色谱方法。将12只健康新西兰家兔随机分为2组,分别灌胃原儿茶酸(原儿茶酸30 mg.kg^-1)及原儿茶酸-冰片(原儿茶酸30 mg.kg^-1+冰片15 mg.kg^-1),采用RP-HPLC法测定家兔给药后不同时间血浆中原儿茶酸的浓度,DAS 2.0药动学软件拟合房室模型,计算药动学参数。结果:原儿茶酸在0.04-2.0 mg.L^-1线性良好(r=0.9983)。原儿茶酸与冰片配伍给药可使原儿茶酸的吸收半衰期(t1/2Ka)明显减小,药物达峰时间(Tmax)显著缩短,血药浓度曲线下面积(AUC(0-∞))增加,表观清除率(CL/F)降低,同时表观分布容积(V1/F)也相应的减小。结论:冰片促进原儿茶酸在家兔体内的吸收,使其吸收量增加,排泄减缓,可提高原儿茶酸的生物利用度。Objective: To study the effect of borneol on the pharmacokinetics of Protocatechuic acid (PA) in rabbits. Method: A method for determinating PA in rabbit plasma by high performance liquid chromatography (HPLC) was established. The 12 healthy New Zealand rabbits were randomly divided into 2 groups. PA concentration in plasma samples of rabbits was determined by HPLC after oral administration of PA (30 mg . kg^-1 ) and PA combined with borneol (protocatechuic acid 30 mg .kg^-1 + bomeol 15 mg .kg^-1 ). The data were processed by DAS 2.0 software to calculate the pharmaeokinetie parametes. Result: Chromatographic peaks were separated well by the HPLC method. Regression analysis of the data of PA concentration against its peak area showed a good straight line in the range of 0. 04-2. 0 mg.L^-1 (r =0. 998 3). In comparison with PA alone, the pharmacokinetics parameters of PA (t1/2K,, Tmax, V1/F, CL/F) in the PA + borneol combination group were decreased, while the AUC(0-∞) was increased. Conclusion : Borneol could significantly promote absorption, increase the dose absorption and slow elimination of PA in rabbits. Borneo1 could improve the bioavailability of PA.

关 键 词:原儿茶酸 冰片 药动学 高效液相色谱 “君-使”对药 

分 类 号:R285.5[医药卫生—中药学]

 

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