5-氟尿嘧啶在Caco-2细胞模型中的吸收特性  

THE UPTAKE CHARACTERISTICS OF 5FLUOROURACIL IN THE CACO2 MODEL SYSTEM

作　　者：陈纪岳[1] 徐子猷[1] 李宜琪 

机构地区：[1]上海医科大学药学院

出　　处：《药学学报》1998年第3期222-225,共4页Acta Pharmaceutica Sinica

基　　金：卫生部回国人员科学研究启动基金

摘　　要：为研究５氟尿嘧啶（５ＦＵ）在Ｃａｃｏ２细胞模型中的吸收特性，用Ｃａｃｏ２细胞模型，分别测定了在各种条件下对５ＦＵ的吸收。结果显示：吸收在ｐＨ６的介质中为佳；吸收的初速随浓度的增加趋于一个饱和值，Ｍｉｃｈａｅｌｉｓ常数Ｋｍ＝２４ｍｍｏｌ·Ｌ－１；吸收可被氰化钠、哇巴因、双嘧达莫等代谢抑制剂抑制，也被同类结构的化合物尿嘧啶、胸腺嘧啶、尿核苷等抑制。由此可知，５ＦＵ的吸收可由尿嘧啶载体转运。The uptake characteristics of 5fluorouracil in the Caco2 model system were studied. The uptake of 5fluorouracil was determined at different pH and concentrations, and in the presence of various inhibitors. The results indicated that the uptake of 5fluorouracil was the best at pH 60. The rate of uptake was saturable with a Km of 24 mmol·L-1, and a Vmax of 209 nmol·min-1·mg-1 protein. The uptake was inhibited by noncompetitive inhibitors such as NaCN, ouabain, and dipyridamole. The uptake was also inhibited competitively by analogous compounds such as uracil, thymine, and uridine (but not by hypoxanthine). In conclusion, the evidence suggests that 5fluorouracil was transported by uracil carrier in Caco2 cells.

关 键 词：5-氟尿嘧啶 CACO-2细胞 吸收 

分 类 号：R979.1[医药卫生—药品]