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出 处:《中国医药工业杂志》2004年第4期213-215,共3页Chinese Journal of Pharmaceuticals
摘 要:采用湿法制粒压片制备吲哚美辛瓜尔胶骨架片,并测定了模拟人体胃肠道生理环境下的体外释放度。结果表明,骨架片5h内释药不超过20%;26h内不加酶组的总释药量不超过40%,加酶组为88%左右,能达到结肠靶向给药的效果。Indomethacin guar gum(GG) tablets were prepared by wet granulation technique. The drug releasebehavior from the matrix tablets were evaluated under the following conditions : 2h in 0.1 mol/L HCl and then 3h in pH7.4phosphate buffer solution(PBS), followed by 21h in pH6.8 PBS with or without galactomannanase. Less than 20% ofindomethacin was released in the first 5h.More than 88% of drug release was observed in the medium with enzymecompared to only 40% in the absence of galactomannanase after 26h. The results showed that GG used as tablet matrix wasa potential carrier for drug targeting to colon.
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