90:10聚(D, l -丙交酯-羟基乙酸酯)含去甲睾酮微球的评价:药物释放和生物降解。

Z Zhou, M Zhou, Z Shen, W Shen
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引用次数: 5

摘要

采用溶剂蒸发法制备了含20%去甾酮(NET)的聚(D, l -丙交酯-羟基乙酸酯)(PLG, 90:10)微球。65 ~ 100微米的微球经辐照灭菌后用于进一步研究。体外释放表明,在超过90天的时间内,上述微球的NET释放相当稳定。然而,大鼠体内注射后残留NET分析的药物释放量显示出更快的释放速度。大约95%的。NET是在45天内发布的。在80 mg微球剂量下,大鼠阴道发情周期被抑制45天,而相同剂量的NET晶体则被抑制27天。通过直接测量分子量损失和扫描电镜观察微球的形态变化来检测微球的生物降解情况,微球的内部基质随着PLG分子量的降低而不断被侵蚀,直至微球完全崩溃,并且在体外37℃条件下,大鼠的生物降解速度快于人血清。90:10 PLG微球在大鼠体内总降解时间小于7个月,在体外降解时间大于9个月。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of 90:10 poly(D,L-lactide-co-glycolide) microspheres containing norethisterone: drug release and biodegradation.

Poly(D,L-lactide-co-glycolide) (PLG, 90:10) microspheres containing 20% norethisterone (NET) were prepared by solvent evaporation method. Microspheres in the size ranges of 65 to 100 microns were sterilized by irradiation and used for further study. In vitro release showed fairly constant release of NET from the above microspheres over more than 90 days. However, in vivo drug release determined by residual NET analysis after i.m. injection in rats indicated a faster release rate. About 95% of NET was released in a period of 45 days. At the dose of 80 mg of microspheres, vaginal estrus cycles were inhibited for 45 days compared to 27 days for the same dose of NET crystals in rats. Biodegradation of the microspheres was tested by direct measurement of molecular weight losses and SEM observation of morphological changes of the microspheres, which showed continuous erosion in the internal matrix of microspheres with the decrease of molecular weight of PLG until total collapse of microspheres, and biodegradation was faster in rats than in human serum at 37 degrees C in vitro. Total degradation of 90:10 PLG microspheres was less than 7 months in rats and more than 9 months in vitro.

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