摘要
目的:考察芍药苷的大鼠在体肠吸收动力学性质。方法:采用大鼠在体单向灌流法,利用HPLC法测定芍药苷的含量,分别研究吸收部位、药物浓度、灌流速度对芍药苷吸收的影响。结果:各肠段间药物的吸收速率常数Ka和表观吸收系数Papp比较差异均无统计学意义(P〉0.05);芍药苷浓度在5.52~21.43 mg/L范围内,吸收速率常数Ka和表观吸收系数Papp比较差异均无统计学意义(P〉0.05);随着灌流速度的增加,吸收速率常数Ka和表观吸收系数Papp均明显增加。结论:芍药苷在全肠道均有吸收,且无特定吸收部位;吸收无高浓度饱和现象,提示芍药苷吸收主要为被动扩散机制。
Objective: To study the situ intestinal absorption kinetics of Paeoniflorin in rats.Methods: In situ single-pass perfusion model was used and the concentrations of the perfusate were determined by HPLC.Results: By the testing of the statistics,the Ka and the Papp values of the duodenum,jejunum,ileum,colonic had no significant differences(P0.05).The concentration from 5.52-21.43 mg/L had no distinctive effect on the Ka and the Papp.When the flow rate was raised,the Ka and the Papp was increased significantly(P0.05).Conclusion: Paeoniflorin could be absorbed at all segments of intestine in rats and no special absorption window is observed;The saturate absorption phenomena was not observed,and suggested that Paeoniflorin is absorbed by passive diffusion mechanism.
出处
《中国医药导报》
CAS
2011年第16期39-42,共4页
China Medical Herald
关键词
芍药苷
小肠吸收
单向灌流法
重量法
Paeoniflorin
Iintestinal absorption
Single-pass intestinal perfusion
Gravimetric method