The effects of mPEG proportion and LA/GA ratio on degradation and drug release behaviors of PLGA-mPEG microparticles.

Chen Shi, Ping Liu, Xianzhe Liu, Xiaobo Feng, Dehao Fu
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引用次数: 6

Abstract

The purpose of this research was to evaluate the effects of mPEG proportion and LA/GA ratio on degradation and release behavior of PLGA-mPEG microparticles prepared by the emulsion evaporation method. Mometasone furoate was employed as model drug and encapsulated into five types of PLGA-mPEG microparticles in the same molecular weight (Mw), but different in mPEG proportion or LA/GA ratio. All types of PLGA-mPEG microparticles showed similar drug encapsulation efficiency and particle mean size, but PLGA-mPEG microparticles with higher mPEG proportion showed a faster Mw reduction rate, mass loss rate and size decrease rate according to the in vitro degradation experiment, and also, a faster drug release rate according to the in vitro release experiment. On the other hand, higher LA/GA ratio in PLGA chain of PLGA-mPEG causes a slower Mw reduction rate, mass loss rate, size decrease rate, and thus, a slower drug release rate.
mPEG比例和LA/GA比对PLGA-mPEG微颗粒降解和药物释放行为的影响。
本研究的目的是评价mPEG比例和LA/GA比对乳液蒸发法制备的PLGA-mPEG微颗粒降解和释放行为的影响。以糠酸莫米松为模型药物,包被5种分子量相同(Mw),但mPEG比例或LA/GA比不同的PLGA-mPEG微粒。各类型PLGA-mPEG微颗粒的药物包封效率和颗粒平均尺寸相似,但mPEG比例越高的PLGA-mPEG微颗粒体外降解实验显示,其Mw还原速率、质量损失率和粒径减小率越快,体外释放实验显示,其药物释放速度也越快。另一方面,在PLGA- mpeg的PLGA链中,较高的LA/GA比值会导致较慢的Mw还原速率、质量损失速率、尺寸减小速率,从而导致较慢的药物释放速率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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