경구투여용 마이크로캡슐 및 이의 제조방법
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    发明公开
    경구투여용 마이크로캡슐 및 이의 제조방법 无效
    口服微胶囊及其制备方法

    公开(公告)号:KR1020120124191A

    公开(公告)日:2012-11-13

    申请号:KR1020110041930

    申请日:2011-05-03

    Abstract: PURPOSE: A microcapsule for oral administration and a method for manufacturing the same are provided to improve mucosal adhesion and durability. CONSTITUTION: A microcapsule for oral administration contains 40-85 wt% of alginate, 5-20 wt% of poly-L-lysine, 5-20 wt% of alginate with a thiol group, and 5-20 wt% of physiologically active substance. The alginate is denoted by chemical formula 1. A method for preparing the alginate with the thiol group comprises: a step of adding L-cysteine salt to a reaction mixture; a step of adjusting pH of reacted mixture; and a step of performing dialysis of the reaction mixture. The average particle diameter of the microcapsule is 5-5000 um. A method for preparing the microcapsule comprises: a step of suspending the physiologically active substance in saline solution and adding alginate to the suspension; a step of reacting the reaction mixture in a calcium salt solution; a step of reacting the reaction mixture in a poly-L-lysine solution; and a step of coating the reaction mixture with the alginate solution containing thiol groups.

    Abstract translation: 目的:提供用于口服的微胶囊及其制造方法,以改善粘膜粘附性和耐久性。 构成:用于口服给药的微胶囊包含40-85重量%的藻酸盐,5-20重量%的聚-L-赖氨酸,5-20重量%的具有硫醇基团的藻酸盐和5-20重量%的生理活性物质 。 藻酸盐由化学式1表示。用硫醇基制备藻酸盐的方法包括:向反应混合物中加入L-半胱氨酸盐的步骤; 调节反应混合物的pH的步骤; 以及进行反应混合物的透析的步骤。 微胶囊的平均粒径为5-5000μm。 制备微胶囊的方法包括:将生理活性物质悬浮在盐水溶液中并向悬浮液中加入藻酸盐的步骤; 使反应混合物在钙盐溶液中反应的步骤; 将反应混合物在聚-L-赖氨酸溶液中反应的步骤; 以及用含有硫醇基团的藻酸盐溶液涂覆反应混合物的步骤。

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