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Disulfide-cross-linked Peg-poly(amino Acid)s Copolymer Micelles For Glutathione-mediated Intracellular Drug Delivery

机译:二硫键交联的聚-氨基酸共聚物胶束用于谷胱甘肽介导的细胞内药物传递

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摘要

We report biocompatible, cell-permeable core-shell-corona polymer micelles bearing glutathione-cleavable shell cross-links, which allow the facilitated release of entrapped anticancer drugs at cytoplasm in response to an intracellular glutathione level.rnRecent advances in stimuli-responsive self-assemblies have led to the development of smart nanocarriers that can trigger the release of bioactive agents, such as drugs, genes, and proteins, in response to specific cellular signals. In this area, one of the most desirable approaches for enhanced therapeutic efficacy is the development of nanocarriers that can meet the following requirements: (i) maintaining high structural stability in blood, (ii) eliminating undesirable drug release before reaching the target site, and (iii) releasing drugs specifically within target cells. Of many potent nanocarriers, polymer micelles assembled from amphiphilic diblock or triblock co-polymers have been a research target of great significance for targeted intracellular drug delivery.
机译:我们报道了具有谷胱甘肽可裂解的壳交联的生物相容性,细胞可渗透的核-壳-冠状聚合物胶束,其响应细胞内谷胱甘肽水平而允许被包埋的抗癌药物在细胞质中的释放。rns刺激反应性自我反应的最新进展组装导致了智能纳米载体的发展,该纳米载体可以响应特定的细胞信号触发生物活性剂的释放,例如药物,基因和蛋白质。在该领域,提高治疗效果的最理想方法之一是开发满足以下要求的纳米载体:(i)维持血液中的高结构稳定性,(ii)在到达目标部位之前消除不良的药物释放,以及(iii)专门在靶细胞内释放药物。在许多有效的纳米载体中,由两亲性二嵌段或三嵌段共聚物组装而成的聚合物胶束已经成为靶向细胞内药物递送的重要研究目标。

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