摘要
目的:比较研究不同浓度和纯度的川续断皂苷Ⅵ在大鼠小肠的吸收情况,初步探讨川续断皂苷Ⅵ的吸收机理。方法:利用大鼠在体肠吸收实验模型,采用HPLC法测定肠循环液中川续断皂苷Ⅵ和酚红的浓度,对川续断皂苷Ⅵ大鼠在体肠吸收特性进行研究。结果:川续断皂苷Ⅵ在大鼠肠道的吸收速率常数(ka)、吸收百分率(pA)随浓度的升高无显著性差异。纯度升高时虽然ka有所降低(P>0.05);但吸收百分率(pA)显著增加(P<0.01)。结论:川续断皂苷Ⅵ提取物中的共存成分可降低其吸收;其吸收方式可能为被动扩散。
Objective :To observe the absorption of different purities and concentrations of asperosaponin Ⅵ in rat's intestine. Methods: HPLC method was used to determine the concentration of asperosaponin Ⅵ in the perfusion which outleted from the opened rat small intestine in rive. Result: No significant increase of rat intestinal absorption was found when of different concentration of asperosaponin Ⅵ were used. Although a slight decrease ( P 〉 0.05 ) on the intestinal absorption rate constant ( ka ) was observed when administration of higher purity of asperosaponin Ⅵ, the absorption rate (pA) increased significantly (P 〈0.01 ). Conclusion: The components in the extract of Dipsacus asper Wall appears to reduce the intestinal absorption of asperosaponin Ⅵ, whose transportation mechanism may due to passive diffusion.
出处
《药学与临床研究》
2008年第4期249-252,共4页
Pharmaceutical and Clinical Research
基金
国家自然科学基金重点项目(编号:30730113)