首页> 外文期刊>Polymer: The International Journal for the Science and Technology of Polymers >Redox-responsive flower-like micelles of poly(L-lactic acid)-b-poly(ethylene glycol)-b-poly(L-lactic acid) for intracellular drug delivery
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Redox-responsive flower-like micelles of poly(L-lactic acid)-b-poly(ethylene glycol)-b-poly(L-lactic acid) for intracellular drug delivery

机译:聚(L-乳酸)-b-聚(乙二醇)-b-聚(L-乳酸)对细胞内药物的氧化还原反应性花状胶束

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Redox-responsive micelles self-assembled from triblock copolymers of poly(L-lactic acid)-poly(ethylene glycol)-poly(L-lactic acid) (PLA-PEG-PLA) with double-disulfide linkage in the backbone were synthesized and characterized by proton nuclear magnetic resonance (H-1 NMR) and size exclusion chromatography (SEC), in which both PEG (M-n = 1000, 2000 and 4000 g mol(-1)) and PLA (M-n = 1600 g mol(-1)) have different molecular weights respectively. The triblock copolymers PLA(3000)-PEG(2000)-PLA(3000) and PLA(3000)-PEG(4000)-PLA(3000) can self-assemble into flower-like micelles in aqueous media with average diameters 110 nm and 43 nm and lower critical micelle concentrations (CMC) 0.017 and 0.014 mg mL(-1) respectively compared with that of diblock copolymers. Moreover, in vitro drug release analyses indicated that reductive environment can result in triggered drug release profiles. 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl- 2-H-tetrazolium bromide (MTT) assay in vitro showed no significant cytotoxicity as NIH 3T3 cells incubated in the micelles even when the concentrations up to 1000 mu g/mL. Additionally fluorescence microscopy measurements and MTT assay demonstrated that the micelles exhibited a faster drug release and higher cellular proliferation inhibition due to the effect of intracellular reduction responsiveness compared with that of diblock copolymers. The above results suggest that the reduction-responsive, biodegradable and biocompatibility micelles could provide a platform to construct potential drug delivery systems for cancer therapy. (C) 2016 Elsevier Ltd. All rights reserved.
机译:合成了骨架中具有双二硫键的聚(L-乳酸)-聚(乙二醇)-聚(L-乳酸)(PLA-PEG-PLA)三嵌段共聚物自组装而成的氧化还原反应性胶束,并通过质子核磁共振(H-1 NMR)和尺寸排阻色谱(SEC)进行表征,其中PEG(Mn = 1000、2000和4000 g mol(-1))和PLA(Mn = 1600 g mol(-1) ))分别具有不同的分子量。三嵌段共聚物PLA(3000)-PEG(2000)-PLA(3000)和PLA(3000)-PEG(4000)-PLA(3000)可以在平均直径为110 nm的水性介质中自组装成花状胶束。与二嵌段共聚物相比,分别具有43 nm和更低的临界胶束浓度(CMC)0.017和0.014 mg mL(-1)。此外,体外药物释放分析表明还原性环境可导致触发的药物释放曲线。体外3-(4,5-二甲基-2-噻唑基)-2,5-二苯基-2-H-四唑溴化物(MTT)分析显示,即使NIH 3T3细胞在胶束中孵育,也没有明显的细胞毒性1000微克/毫升另外,荧光显微镜测量和MTT测定表明,与二嵌段共聚物相比,由于细胞内还原反应性的影响,胶束表现出更快的药物释放和更高的细胞增殖抑制作用。以上结果表明,还原反应性,可生物降解性和生物相容性的胶束可以为构建潜在的用于癌症治疗的药物递送系统提供平台。 (C)2016 Elsevier Ltd.保留所有权利。

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