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Preparation and sustained-release testing ofchitosan/montmorillonite/acetaminophen microspheres

机译:Chitosan / montmorililililonite /乙酰氨基酚微球的制备和缓释试验

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Chitosan (CS) is an important slow-release carrier of drugs and fertilizers. The purechitosan have poor performance, it should be added to a certain amount of crosslinking agents,emulsifiers and porogenic agents to improve the performance of it. The advantage ofmontmorillonite is no pollution and no toxicity, composite material filled in montmorillonite has anexcellent mechanical properties. In this article, CS/MMT/ACAP drug-loading microsperes wasprepared with the CS, ACAP and MMT as the main raw materials by emulsification-crosslinkingmethod. Orthogonal experiment was designed to optimize the preparation process of theCS/MMT/ACAP drug-loading microspheres. FT-IR, XRD and SEM were applied to characterizethe structure and morphology of microspheres. The sustained release effect of CS/MMT/ACAPmicrosphere was measured by sustained release measurement. The results show that theCS/MMT/ACAP drug-loading micropheres were successfully prepared byemulsification-crosslinking method. The microspheres assumed a good sphericity and a uniformparticle size distribution; the drug-loading microspheres had good sustained release effect.
机译:壳聚糖(CS)是药物和肥料的重要慢速释放载体。 Purechitosan的性能差,应该加入一定量的交联剂,乳化剂和致致剂以改善其性能。 Montmorillonite的优点是没有污染,没有毒性,填充在Montmorillonite的复合材料具有多种机械性能。在本文中,CS / MMT / ACAP通过乳化 - 交叉链接方法用CS,ACAP和MMT载为主要原料。设计正交实验以优化Thecs / MMT / ACAP药物载体微球的制备方法。 FT-IR,XRD和SEM被应用于特征结构和微球的形态。通过持续释放测量测量CS / MMT / ACAPMICICROSPER的持续释放效果。结果表明,通过乳化交联方法成功制备了THECS / MMT / ACAP药物加载微球。微球呈现出良好的球形和统一的尺寸分布;药物加载微球具有良好的持续释放效果。

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