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Preparation of biodegradable microspheres and matrix devices containing naltrexone

机译:含纳曲酮的可生物降解的微球和基质装置的制备

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摘要

In this study, the use of biodegradable polymers for microencapsulation of naltrexone using solvent evaporation technique is investigated. The use of naltrexone microspheres for the preparation of matrix devices is also studied. For this purpose, poly(L-lactide) (PLA) microspheres containing naltrexone prepared by solvent evaporation technique were compressed at temperatures above the Tg of the polymer. The effect of different process parameters, such as drug/polymer ratio and stirring rate during preparation of microspheres, on the morphology, size distribution, and in vitro drug release of microspheres was studied. As expected, stirring rate influenced particle size distribution of microspheres and hence drug release profiles. By increasing the stirring speed from 400 to 1200 rpm, the mean diameter of microspheres decreased from 251 μm to 104 μm. The drug release rate from smaller microspheres was faster than from larger microspheres. However, drug release from microspheres with low drug content (20% wt/wt) was not affected by the particle size of microspheres. Increasing the drug content of microspheres from 20% to 50% wt/wt led to significantly faster drug release from microspheres. It was also shown that drug release from matrix devices prepared by compression of naltrexone microspheres is much slower than that of microspheres. No burst release was observed with matrix devices. Applying higher compression force, when compressing microspheres to produce tablets, resulted in lower drug release from matrix devices. The results suggest that by regulating different variables, desired release profiles of naltrexone can be achieved using a PLA microparticulate system or matrix devices.
机译:在这项研究中,利用溶剂蒸发技术研究了可生物降解的聚合物用于纳曲酮微囊化的应用。还研究了纳曲酮微球在制备基质装置中的用途。为此,在高于聚合物的Tg的温度下压缩含有通过溶剂蒸发技术制备的纳曲酮的聚(L-丙交酯)(PLA)微球。研究了不同工艺参数(如微球制备过程中的药物/聚合物比和搅拌速率)对微球的形态,尺寸分布和体外药物释放的影响。如预期的那样,搅拌速率影响微球的粒度分布,从而影响药物释放曲线。通过将搅拌速度从400 rpm增加到1200 rpm,微球的平均直径从251μm减小到104μm。较小的微球的药物释放速率比较大的微球的药物释放速率快。但是,药物从低药物含量(20%wt / wt)的微球中释放不会受到微球粒径的影响。将微球的药物含量从20%wt / wt增加到50%wt / wt导致从微球释放的药物明显更快。还显示了通过纳曲酮微球压缩制备的基质装置释放的药物比微球慢得多。使用矩阵设备未观察到爆发释放。在压缩微球以生产片剂时,施加较高的压缩力可降低从基质装置中释放的药物。结果表明,通过调节不同的变量,可以使用PLA微粒系统或基质设备实现所需的纳曲酮释放曲线。

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