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Novel Amphiphilic Biodegradable Biocompatible Thermo-Responsive ABA Triblock Copolymers Based on PCL and PEG Analogues via a Combination of ROP and RAFT: Synthesis Characterization and Sustained Drug Release from Self-Assembled Micelles

机译:基于ROP和RAFT的PCL和PEG类似物的新型两亲性可生物降解生物相容性热响应性ABA Triblock共聚物:自组装胶束的合成表征和持续释放药物

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摘要

Well-defined novel, linear, biodegradable, amphiphilic thermo-responsive ABA-type triblock copolymers, poly[2-(2-methoxyethoxy) ethyl methacrylate-co-oligo(ethylene glycol) methacrylate]-b-poly(ε-caprolactone)-b-poly[2-(2-methoxyethoxy) ethyl methacrylate-co-oligo(ethylene glycol) methacrylate] [P(MEO2MA-co-OEGMA)-b-PCL-b-P(MEO2MA-co-OEGMA)] (tBPs), were synthesized via a combination of ring-opening polymerization (ROP) of ε-caprolactone (εCL) and reversible addition-fragmentation chain transfer polymerization (RAFT) of MEO2MA and OEGMA comonomers. The chemical structures and compositions of these copolymers were characterized using Fourier transform infrared spectroscopy (FT-IR) and proton nuclear magnetic resonance (1H NMR). The molecular weights of the copolymers were obtained using gel permeation chromatography (GPC) measurements. Thermo-responsive micelles were obtained by self-assembly of copolymers in aqueous medium. The temperature sensitivity and micelllization behavior of amphiphilic triblock copolymers solutions were studied by transmittance, fluorescence probe, surface tension, dynamic light scattering (DLS) and transmission electron microscopy (TEM). A hydrophobic drug, anethole, was encapsulated in micelles by using the dialysis method. The average particle sizes of drug-loaded micelles were determined by dynamic light scattering measurement. In vitro, the sustained release of the anethole was performed in pH 7.4 phosphate-buffered saline (PBS) at different temperatures. Results showed that the triblock copolymer’s micelles were quite effective in the encapsulation and controlled release of anethole. The vial inversion test demonstrated that the triblock copolymers could trigger the sol-gel transition which also depended on the temperature, and its sol-gel transition temperature gradually decreased with increasing concentration. The hydrogel system could also be used as a carrier of hydrophobic drugs in medicine.
机译:定义明确,新颖,线性,可生物降解的两亲热响应ABA型三嵌段共聚物,聚[2-(2-甲氧基乙氧基)甲基丙烯酸乙酯-低聚(乙二醇)甲基丙烯酸乙二醇酯] -b-聚(ε-己内酯)- b-聚[2-(2-(2-甲氧基乙氧基)甲基丙烯酸乙酯-共-低聚(乙二醇)甲基丙烯酸甲酯] [P(MEO2MA-co-OEGMA)-b-PCL-bP(MEO2MA-co-OEGMA)](tBPs),通过ε-己内酯(εCL)的开环聚合(ROP)和MEO2MA和OEGMA共聚单体的可逆加成-断裂链转移聚合(RAFT)的组合合成。使用傅里叶变换红外光谱(FT-IR)和质子核磁共振( 1 H NMR)表征了这些共聚物的化学结构和组成。使用凝胶渗透色谱法(GPC)测量获得共聚物的分子量。通过在水性介质中自组装共聚物获得热响应性胶束。通过透射率,荧光探针,表面张力,动态光散射(DLS)和透射电子显微镜(TEM)研究了两亲三嵌段共聚物溶液的温度敏感性和胶束化行为。通过透析方法将疏水性药物茴香脑包封在胶束中。通过动态光散射测量来确定载药胶束的平均粒径。在体外,在不同温度下在pH 7.4磷酸盐缓冲盐水(PBS)中进行茴香脑的缓释。结果表明,三嵌段共聚物的胶束在茴香脑的包封和控制释放方面非常有效。样品瓶转化试验表明,三嵌段共聚物可以触发溶胶-凝胶转变,温度也随温度的升高而变化,并且随着浓度的增加,其溶胶-凝胶转变温度逐渐降低。水凝胶系统还可以用作医学中疏水性药物的载体。

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