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机构地区:[1]新疆医科大学中医学院,新疆乌鲁木齐830011 [2]新疆名医名方与特色方剂学重点实验室,新疆乌鲁木齐830011 [3]新疆医科大学药学院,新疆乌鲁木齐830011
出 处:《中国中医药信息杂志》2015年第11期79-82,共4页Chinese Journal of Information on Traditional Chinese Medicine
基 金:国家自然科学基金(81260668)
摘 要:目的 研究安石榴苷在Caco-2 细胞的摄取特性.方法 采用Caco-2 细胞单层模型研究安石榴苷在不同时间、浓度、pH 值、温度、P-糖蛋白抑制剂条件下对细胞摄取的影响.采用高效液相色谱法测定安石榴苷在细胞中的含量.结果 安石榴苷在0.024 8~0.992 μg 范围内呈良好线性关系(r =0.997 9).安石榴苷在Caco-2 细胞上的摄取呈现-定的时间、浓度和pH 值依赖性,且P-糖蛋白抑制剂能显著增加安石榴苷的摄取量.结论 该方法操作简单、灵敏,安石榴苷在Caco-2 细胞上的摄取主要是被动转运,P-糖蛋白参与安石榴苷的转运过程.Objective To study the uptake property of punicalagin in Caco-2 cells. Methods Caco-2 cell monolayer model was used to research the effects of punicalagin on cell uptake in different times, concentrations, p H values, temperatures and P-gp inhibitors. HPLC was used to determine the content of punicalagin in cells. Results The linearity of punicalagin concentration curve was found in the range of 0.024 8-0.992 μg(r =0.997 9). Uptake determination of punicalagin in Caco-2 cells absorbed a certain amount of time, concentration and p H dependence and P-gp inhibitors could significantly increase the punicalagin uptake. Conclusion This method is simple and sensitive to determine the punicalagin concentration in Caco-2 cells, which is mainly passively transported. P-gp is involved in punicalagin transport process.
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