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用于特定部位释放的核/壳聚环氧乙烷/丙烯酸树脂纤维

Core/shell poly(ethylene oxide)/Eudragit fibers for site-specific release.

作者信息

Jia Dong, Gao Yanshan, Williams Gareth R

机构信息

UCL School of Pharmacy, University College London, London WC1N 1AX, UK.

UCL School of Pharmacy, University College London, London WC1N 1AX, UK.

出版信息

Int J Pharm. 2017 May 15;523(1):376-385. doi: 10.1016/j.ijpharm.2017.03.038. Epub 2017 Mar 23.

DOI:10.1016/j.ijpharm.2017.03.038
PMID:28344174
Abstract

Electrospinning was used to prepare core/shell fibers containing the active pharmaceutical ingredients indomethacin (IMC) or mebeverine hydrochloride (MB-HCl). The shell of the fibers was fabricated from the pH sensitive Eudragit S100 polymer, while the drug-loaded core was based on the mucoadhesive poly(ethylene oxide) (PEO). Three different drug loadings (from 9 to 23% (w/w) of the core mass) were prepared, and for MB-HCl two different molecular weights of PEO were explored. The resultant fibers generally comprise smooth cylinders, although in some cases defects such as surface particles or flattened or merged fibers were visible. Transmission electron microscopy showed all the systems to have clear core and shell compartments. The drugs are present in the amorphous physical form in the fibers. Dissolution tests found that the fibers can effectively prevent release in acidic conditions representative of the stomach, particularly for the acidic indomethacin. After transfer to a pH 7.4 medium, sustained release over between 6 and 22h is observed. Given the mucoadhesive nature of the PEO core, after dissolution of the shell the fibers will be able to adhere to the walls of the intestinal tract and give sustained local drug release. This renders them promising for the treatment of conditions such as irritable bowel disease and colon cancer.

摘要

采用静电纺丝法制备了含有活性药物成分吲哚美辛(IMC)或盐酸美贝维林(MB-HCl)的核/壳纤维。纤维的壳由pH敏感型尤特奇S100聚合物制成,而载药核则基于粘膜粘附性聚环氧乙烷(PEO)。制备了三种不同的药物载量(占核质量的9%至23%(w/w)),并对MB-HCl探索了两种不同分子量的PEO。所得纤维通常为光滑圆柱体,不过在某些情况下可见表面颗粒、扁平或合并纤维等缺陷。透射电子显微镜显示所有体系均有清晰的核和壳部分。药物以无定形物理形式存在于纤维中。溶出试验发现,这些纤维能有效防止在代表胃的酸性条件下释放,尤其是对于酸性的吲哚美辛。转移至pH 7.4介质后,观察到持续释放6至22小时。鉴于PEO核的粘膜粘附性,壳溶解后纤维将能够粘附于肠道壁并实现持续局部药物释放。这使得它们在治疗肠易激综合征和结肠癌等病症方面具有前景。

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