红霉素口服控释微球的研制。

Drug design and delivery Pub Date : 1991-07-01
I Morishita, M Morishita, Y Machida, T Nagai
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引用次数: 0

摘要

介绍了以甲基丙烯酸和甲基丙烯酸甲酯为基料的共聚物乌德拉吉L100在红霉素微球制备中的应用。将Eudragit L100在乙醇溶液中固化,在液体石蜡中制备微球。当明胶加入到固化溶液中时,得到的微球更圆,表面光滑。通过改变乌龙茶L100在乙醇中的浓度可以控制微球的大小,红霉素的掺入效率为60-70%。高分子聚合物包被红霉素微球后,红霉素被酸降解的过程明显受到保护。包被工艺对红霉素微球的体外释放速度也有影响。因此,证明了制备口服红霉素制剂的可行性,该制剂以可控的速度释放药物,并保护药物免受胃酸的侵害。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Controlled release microspheres based on Eudragit L100 for the oral administration of erythromycin.

The use of Eudragit L100, a copolymer based on methacrylic acid and methacrylic acid methyl ester, in preparing erythromycin microspheres is described. The microspheres were simply prepared in liquid paraffin by solidifying an Eudragit L100 in ethanol solution. When gelatin was incorporated in the solidifying solution, the resultant microspheres were more spherical and had a smooth surface. The size of the microspheres could be controlled by varying the Eudragit L100 concentration in ethanol, and erythromycin was incorporated with 60-70% efficiency. The degradation of erythromycin by acid was markedly protected when the erythromycin microspheres were coated with the polymer. The in vitro release rate of erythromycin from the microspheres was also modified by the coating process. The feasibility of preparing formulations of erythromycin for oral administration, which release the drug at a controlled rate, and protect the drug from gastric acid, is thus demonstrated.

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