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结肠定位释药瓜尔胶/乙基纤维素包衣小丸
引用本文:季崇敏,徐惠南,孙宁云,陆燕萍,吴伟.结肠定位释药瓜尔胶/乙基纤维素包衣小丸[J].药学学报,2007,42(6):656-662.
作者姓名:季崇敏  徐惠南  孙宁云  陆燕萍  吴伟
作者单位:复旦大学,药学院,上海,200032
基金项目:Shanghai Education Bureau for Excellent Young High Education Teacher Candidates (03YQHB008); Fudan University Postgraduate Innovation Found (CQF301808).
摘    要:体外研究瓜尔胶/乙基纤维素混合包衣小丸的结肠靶向性。以5-氟尿嘧啶为模型药, 采用流化包衣技术以瓜尔胶/乙基纤维素混合物的水/醇混悬液对载药小丸进行喷液包衣。瓜尔胶/乙基纤维素混合包衣小丸的释药行为取决于包衣处方中瓜尔胶与乙基纤维素的比例和包衣厚度。分别以混合包衣液中瓜尔胶与乙基纤维素的比例及包衣增重为自变量, 以T5T90(药物释放5%和90%所需要的时间)为效应, 进行3×4析因设计/效应面优化, 筛选较优处方。结果表明随着乙基纤维素在衣层中所占比例的增大及包衣厚度的增加, 药物释放时滞增加。当瓜尔胶与乙基纤维素的比例在0.2~0.7, 并且包衣增重在250%~500%时, T5%为5.1~7.8 h, T90%为9.8~16.3 h。并且在释药时滞之后, 进入模拟结肠微菌群酶解作用的释放环境中(pH 6.5)药物释放速度加快, T90%缩短到9.0~14.5 h。由此可以看出适当的瓜尔胶/乙基纤维素混合衣层既可以保护药物顺利通过上消化道而不释放, 达到结肠后药物开始释放, 并且可在结肠微菌群的酶解作用下加速药物的释放, 实现结肠定位释药的目的。

关 键 词:结肠靶向  瓜尔胶  乙基纤维素  小丸  5-氟尿嘧啶
文章编号:0513-4870(2007)06-0656-07
收稿时间:2006-10-11
修稿时间:2006-10-11

Guar gum/ethylcellulose coated pellets for colon-specific drug delivery
JI Chong-min,XU Hui-nan,SUN Ning-yun,LU Yan-ping,WU Wei.Guar gum/ethylcellulose coated pellets for colon-specific drug delivery[J].Acta Pharmaceutica Sinica,2007,42(6):656-662.
Authors:JI Chong-min  XU Hui-nan  SUN Ning-yun  LU Yan-ping  WU Wei
Institution:School of Pharmacy, Fudan University, Shanghai 200032, China
Abstract:The aim of this work was to investigate guar gum/ethylcellulose mix coated pellets for potential colon-specific drug delivery. The coated pellets, containing 5-fluorouracil as a model drug, were prepared in a fluidized bed coater by spraying the aqueous/ethanol dispersion mixture of guar gum and ethylcellulose. The lag time of drug release and release rate were adjustable by changing the ratio of guar gum to ethylcellulose and coat weight gain. In order to find the optimal coating formulation that was able to achieve drug targeting to the colon, the effect of two independent variables (the ratio of guar gum to ethylcellulose and the coat weight gain) on drug release characteristics was studied using 3 x 4 factorial design and response surface methodology. Results indicated that drug release rate decreased as the proportion of ethylcellulose in the hybrid coat and the coat weight gain increased. When the ratio of guar gum to ethylcellulose was kept in the range of 0.2 to 0.7, and the coat weight gain in the range of 250% to 500%, the coated pellets can keep intact for about 5 h in upper gastrointestine and achieve colon-specific drug delivery. The pellets prepared under optimal conditions resulted in delayed-release sigmoidal patterns with T(5%) (time for 5% drug release) of 5.1 - 7.8 h and T(90%) (time for 90% drug release) of 9.8 - 16.3 h. Further more, drug release was accelerated and T(90%) of the optimum formulation pellets decreased to 9.0 - 14.5 h in pH 6.5 phosphate buffer with hydrolase. It is concluded that mixed coating of guar gum and ethylcellulose is able to provide protection of the drug load in the upper gastrointestinal tract, while allowing enzymatic breakdown of the hybrid coat to release the drug load in the colon.
Keywords:colon-specific  guar gum  ethylcellulose  pellet  5-fluorouracil
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