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复方右旋麻黄碱控释片的研制 被引量:6

Preparation of Compound Pseudoephedrine Controlled Release Tablets
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摘要 将右旋麻黄碱与扑尔敏配伍,添加骨架材料研制成复方右旋麻黄碱控释片,对其进行了体内外测定。结果表明控释片基本按零级速度释放药物,在兔体内血药浓度可维持16h,生物利用度是普通片的1.5倍。控释片在温湿条件下放置3个月含量无变化。 his paper reports the preparation of compound pseudoephedrine controlled release tablets. Thetest has been determined in vitro and in vivo。The dissolution of the controlled releaLse tablets was bestdescribed by zero-order release。The plasma level in rabbits could last 16 hours and its bioavailabilitywas 1.5 times as high as the ordinary tablets,The quality could keep stable in three months under con-stant temperature and humidity.
出处 《新疆医学院学报》 1994年第4期260-262,259,共4页
关键词 盐酸右旋麻黄碱 控释片 溶出度 生物利用度 pseudoephedrine controlled release tablets dissolution rate:bioavailability
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