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首页> 外文期刊>Journal of Polymer Science, Part A. Polymer Chemistry >Redox-Responsive Core Cross-Linked Micelles of Poly(Ethylene Oxide)-b-Poly(Furfuryl Methacrylate) by Diels-Alder Reaction for Doxorubicin Release
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Redox-Responsive Core Cross-Linked Micelles of Poly(Ethylene Oxide)-b-Poly(Furfuryl Methacrylate) by Diels-Alder Reaction for Doxorubicin Release

机译:Diels-Alder反应对聚环氧乙烷-b-聚甲基丙烯酸糠酯的氧化还原响应性核交联胶束释放阿霉素

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摘要

Redox-responsive core cross-linked (CCL) micelles of poly(ethylene oxide)-b-poly(furfuryl methacrylate) (PEO-b-PFMA) block copolymers were prepared by the Diels-Alder click-type reaction. First, the PEO-b-PFMA amphiphilic block copolymer was synthesized by the reversible addition-fragmentation chain transfer polymerization. The hydrophobic blocks of PFMA were employed to encapsulate the doxorubicin (DOX) drug, and they were cross-linked using dithiobismaleimidoethane at 60 degrees C without any catalyst. Under physiological circumstance, the CCL micelles demonstrated the enhanced structural stability of the micelles, whereas dissociation of the micelles took place rapidly through the breaking of disulfide bonds in the cross-linking linkages under reduction environment. The core-cross-linked micelles showed fine spherical distribution with hydrodynamic diameter of 68 +/- 2.9 nm. The in vitro drug release profiles presented a slight release of DOX at pH 7.4, while a significant release of DOX was observed at pH 5.0 in the presence of 1,4-dithiothreitol. MTT assays demonstrated that the block copolymer did not have any practically cytotoxicity against the normal HEK293 cell line while DOX-loaded CCL micelles exhibited a high antitumor activity towards HepG2 cells. (C) 2016 Wiley Periodicals, Inc.
机译:聚(环氧乙烷)-b-聚(甲基丙烯酸糠基酯)(PEO-b-PFMA)嵌段共聚物的氧化还原反应性核交联(CCL)胶束是通过Diels-Alder点击型反应制备的。首先,通过可逆加成-断裂链转移聚合反应合成PEO-b-PFMA两亲嵌段共聚物。 PFMA的疏水嵌段用于包裹阿霉素(DOX)药物,并使用二硫代双马来酰亚胺基乙烷在60°C下不使用任何催化剂进行交联。在生理条件下,CCL胶束表现出增强的胶束结构稳定性,而胶束的离解通过还原环境下交联键中二硫键的断裂而迅速发生。核心交联的胶束表现出良好的球形分布,流体动力学直径为68 +/- 2.9 nm。体外药物释放曲线显示在pH 7.4时DOX略有释放,而在存在1,4-二硫苏糖醇的情况下在pH 5.0时观察到DOX明显释放。 MTT分析表明,该嵌段共聚物对正常的HEK293细胞系没有任何实际的细胞毒性,而DOX加载的CCL胶束对HepG2细胞具有很高的抗肿瘤活性。 (C)2016威利期刊公司

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