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Polymeric micelles for nano-scale drug delivery

机译:用于纳米级药物递送的聚合物胶束

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摘要

This review describes the design of polymeric micelles from block copolymers and their performances as nano-scale drug delivery systems, with emphasis on our recent work. The basic drug delivery system platform developed by our group consists of polymeric micelles comprising a core-shell structure with a versatile drug-loading hydrophobic core and biocompatible hydrophilic shell, and are several tens to one hundred nanometer in size. These characteristics are preferable to bypass both renal clearance and entrapment by the reticuloendothelial system, thus allowing subsequent accumulation within tumor tissues by the enhanced permeability and retention effect. Furthermore, polymeric micelles may be designed for enhanced biological performance by modification of the block copolymers to contain chemistries that can sense a specific biological environment. These "smart" micelles allow for target site-triggered drug release by reversible stabilization of the micelle structure and controlled intracellular trafficking (efficient endosomal release). Smart micelles designed with responsive features have demonstrated the utility in many cases compared to controls lacking such functionality. Additionally, the ability to control the size of polymeric micelles in the range of several tens to hundreds of nanometer significantly affects their longevity in the blood stream and efficiency of tumor tissue accumulation and penetration. In hypovascular tumor tissues, smaller polymeric micelles are more effective for tissue accumulation/penetration, bringing about stronger anti-tumor activity. All together, fine-tuning the structure of block copolymers enables preparation of polymeric micelles with versatile functions for treatment of many diseases including intractable cancer.
机译:这篇综述描述了由嵌段共聚物制成的聚合物胶束的设计及其作为纳米级药物递送系统的性能,重点是我们最近的工作。我们小组开发的基本药物输送系统平台由聚合物胶束组成,该聚合物胶束包含核壳结构,具有通用的载药疏水核和生物相容性亲水壳,尺寸为几十到一百纳米。这些特征优选绕过肾脏清除和网状内皮系统截留,从而通过增强的通透性和保留作用而使肿瘤组织随后积累。此外,可通过修饰嵌段共聚物以包含可感知特定生物学环境的化学物质,来设计聚合物胶束以增强生物学性能。这些“智能”胶束通过胶束结构的可逆稳定化和受控的细胞内运输(有效的内体释放),实现了靶位触发的药物释放。与缺少此类功能的控件相比,设计具有响应功能的智能胶束已在许多情况下证明了其实用性。另外,将聚合物胶束的尺寸控制在几十至数百纳米范围内的能力显着影响了它们在血流中的寿命以及肿瘤组织积累和渗透的效率。在血管下肿瘤组织中,较小的聚合物胶束对组织的积累/穿透更有效,从而带来更强的抗肿瘤活性。总之,对嵌段共聚物的结构进行微调可以制备具有多种功能的聚合物胶束,以治疗包括顽固性癌症在内的许多疾病。

著录项

  • 来源
    《Reactive & Functional Polymers》 |2011年第3期|p.227-234|共8页
  • 作者单位

    Center for Disease Biology and lntegmtive Medicine, Graduate School of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan;

    Department of Materials Engineering, Graduate School of Engineering, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8656, Japan;

    Center for Disease Biology and lntegmtive Medicine, Graduate School of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan, Department of Materials Engineering, Graduate School of Engineering, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8656, Japan;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    drug delivery; polymeric micelle; poly(ethylene glycol); block copolymer; polyion complex;

    机译:药物输送;聚合物胶束;聚乙二醇;嵌段共聚物;聚离子络合物;

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