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用于药物递送纳米系统 (DDnSs) 的嵌段共聚物。

Block copolymers for drug delivery nano systems (DDnSs).

机构信息

Theoretical and Physical Chemistry Institute, National Hellenic Research Foundation, 48 Vassileos Constantinou Avenue, 11635, Athens, Greece.

出版信息

Curr Med Chem. 2012;19(29):5088-100. doi: 10.2174/0929867311209025088.

Abstract

The application of polymers in medicine, as components of drug carriers, as well as their synthetic strategies are considered essential for producing and developing new drug formulations against human deceases. The synthesis of block copolymers is a timeconsuming process with a high cost of the final product, although several block copolymer systems have been already commercialized successfully. The biocompatibility, the biodegradability and the non toxic profile of newly synthesized polymers towards healthy tissues, should be taken into account in order to be acceptable for biomedical applications. In this review article, focus is placed on new approaches and synthetic strategies for preparing novel block copolymers and their utilization as parts of new and advanced Drug Delivery nanoSystems (aDDnSs) with a Modulatory Controlled Release profile (MCR). Such complex and advanced nanosystems can alter the pharmacokinetic properties of the encapsulated drug and consequently its effectiveness. Emphasis is given to the use of living polymerization methodologies and post polymerization chemical transformation reactions for the synthesis of mainly diblock copolymers for novel drug delivery nanosystems. Issues related to self-assembly of block copolymers in solution toward formation of colloidal functional nanostructures that can serve as nanocontainers and nanocarriers, and strategies for controlling encapsulation of specific drugs are also discussed. Specific examples are reported mainly on diblock copolymer systems, including authors' recent work.

摘要

聚合物在医学中的应用,作为药物载体的组成部分,以及它们的合成策略,对于生产和开发针对人类疾病的新药物制剂是至关重要的。嵌段共聚物的合成是一个耗时且成本高的过程,尽管已经有几个嵌段共聚物系统成功商业化。新合成聚合物对健康组织的生物相容性、可生物降解性和非毒性特征,应该在可接受用于生物医学应用的前提下加以考虑。在这篇综述文章中,重点介绍了制备新型嵌段共聚物的新方法和合成策略,以及将其用作具有调节控制释放(MCR)特性的新型先进药物输送纳米系统(aDDnS)的一部分。这种复杂而先进的纳米系统可以改变包裹药物的药代动力学特性,从而影响其疗效。重点介绍了使用活性聚合方法学和聚合后化学转化反应来合成主要的二嵌段共聚物,用于新型药物输送纳米系统。还讨论了有关嵌段共聚物在溶液中自组装形成胶体功能纳米结构(可作为纳米容器和纳米载体)以及控制特定药物包封的策略的问题。报告了主要基于二嵌段共聚物系统的具体示例,包括作者的最新工作。

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