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首页> 外文期刊>Polymer: The International Journal for the Science and Technology of Polymers >ABC block copolymer as 'smart' pH-responsive carrier for intracellular delivery of hydrophobic drugs
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ABC block copolymer as 'smart' pH-responsive carrier for intracellular delivery of hydrophobic drugs

机译:ABC嵌段共聚物作为“智能” pH响应载体,用于细胞内递送疏水性药物

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摘要

Amphiphilic triblock copolymer of poly(ethylene glycol)-block- poly(dimethylaminoethyl methacrylate)-block-poly(ε-caprolatone) (PEG-PDMA-PCL) was synthesized using a one-pot sequential oxyanionic polymerization of DMA and ε-CL, associated with a PEG-O-K ~+ macroinitiator. The pH-responsive micellization behavior of the copolymer was studied using dynamic light scattering (DLS), steady-state fluorescence and TEM techniques. The anti-cancer drug of doxorubicin (DOX) was chosen as a model drug to investigate the potential application of this triblock copolymer in drug controlled release. The results indicated the important roles of the PCL block for drug loading, the PDMA block for pH-responsive release, and PEG block for good bio-affinity. Cell cytotoxicity tests showed that the DOX-loaded PEG-PDMA-PCL micelles were pharmaceutically active to suppress the growth of SKOV-3 cells. This novel stimuli-responsive block copolymer is an attractive candidate as the "smart" pH-responsive carrier for intracellular delivery of hydrophobic drugs.
机译:使用一锅法依次进行DMA和ε-CL的氧阴离子聚合反应合成了聚(乙二醇)-嵌段-聚(甲基丙烯酸二甲氨基乙基酯)-嵌段-聚(ε-己内酯)(PEG-PDMA-PCL)的两亲三嵌段共聚物,与PEG-OK〜+大分子引发剂有关。使用动态光散射(DLS),稳态荧光和TEM技术研究了共聚物的pH响应胶束化行为。选择阿霉素(DOX)的抗癌药作为模型药物,以研究这种三嵌段共聚物在药物控释中的潜在应用。结果表明,PCL嵌段对于药物加载,PDMA嵌段对于pH响应释放以及PEG嵌段对于良好的生物亲和性具有重要作用。细胞的细胞毒性测试表明,装载DOX的PEG-PDMA-PCL胶束具有抑制SKOV-3细胞生长的药物活性。这种新颖的刺激反应性嵌段共聚物是用于疏水药物的细胞内递送的“智能” pH反应性载体,是有吸引力的候选物。

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