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双氯芬酸钠缓释骨架微丸的评价:聚乙二醇分子量的影响

Evaluation of diclofenac sodium sustained release matrix pellets: impact of polyethylene glycols molecular weight.

作者信息

Ibrahim A, Shazly A

出版信息

Acta Pol Pharm. 2014 Sep-Oct;71(5):821-31.

Abstract

Sustained release matrix pellets loaded with 5% w/w diclofenac sodium (DS) were prepared using extrusion/spheronization technique. Different polyethylene glycols (PEGs) of different molecular weight, namely PEG 2000, PEG 4000 and PEG 6000, were mixed with avicel PH 101 in different weight ratios to manufacture the pellet formulations and water was used as a binder. Mix torque rheometer was used to characterize the pellets' wet mass. Also, the prepared pellets were characterized for their particle sizes, DS content, shape and morphology as well as the in vitro drug release. The results showed increasing PEG weight ratio resulted in a reduction of wet mass torque as well as binder ratio, especially at PEG high weight ratios (30% and 50%) and the extent of lowering wet mass peak torque was inversely proportional to PEG molecular weight. The manufactured pellets exhibited size range of 993 μm to 1085 μm with small span values. The drug release from pellets was governed by the molecular weight of PEG used, since increasing PEG molecular weight resulted in slowing the drug release rate from pellets, but increasing its level resulted in enhancing release rate. This was attributed to increasing pellet wet mass peak torque by increasing PEG molecular weight and lowering it by increasing PEG level. The prepared pellets showed non-Fickian or anomalous drug release or the coupled diffusion/polymer relaxation.

摘要

采用挤出滚圆法制备了载有5%(w/w)双氯芬酸钠(DS)的缓释骨架微丸。将不同分子量的聚乙二醇(PEG),即PEG 2000、PEG 4000和PEG 6000,与微晶纤维素PH 101按不同重量比混合,以制备微丸制剂,并用水作为粘合剂。使用混合扭矩流变仪对微丸的湿物料进行表征。此外,对制备的微丸进行了粒径、DS含量、形状和形态以及体外药物释放的表征。结果表明,PEG重量比增加导致湿物料扭矩以及粘合剂比例降低,尤其是在PEG高重量比(30%和50%)时,且湿物料峰值扭矩降低程度与PEG分子量成反比。制备的微丸粒径范围为993μm至1085μm,跨度值较小。微丸的药物释放受所用PEG分子量的控制,因为PEG分子量增加导致微丸药物释放速率减慢,但PEG水平增加导致释放速率加快。这归因于PEG分子量增加导致微丸湿物料峰值扭矩增加,而PEG水平增加导致其降低。制备的微丸表现出非菲克或异常药物释放或耦合扩散/聚合物松弛。

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