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Physicochemical, pharmaceutical and biological approaches toward designing optimized and efficient hydrophobically modified chitosan-based polymeric micelles as a nanocarrier system for targeted delivery of anticancer drugs

机译:物理化学,药物和生物学方法,用于设计优化和高效的疏水改性的壳聚糖基聚合物胶束,作为用于靶向递送抗癌药物的纳米载体系统

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摘要

Hydrophobically modified chitosan-based polymeric micelles (CBPMs) are formed through self-aggregation of chitosan amphiphilic derivatives. Their core-shell structure, diversity and the fact that all of their properties are adjustable through reconciling the interactions among their three main constituents: chitosan, hydrophilic segment and hydrophobic segment as well as with the outside medium through changing the ratio and chemical structure of each component's, chemical structure distinguish them from other chitosan-based drug delivery systems (DDSs) and give rise to these promising candidates for targeted delivery of lipophilic anticancer drugs. The majority of review articles conducted previously on chitosan-based DDSs have only made simple differential comparisons between such systems and the anticancer drugs that have been delivered through them. In this review article, all the basic properties of CBPMs including physicochemical, pharmaceutical and biological properties are technically detailed and discussed. The intention of this article is to outline and discuss salient features of CBPMs to contribute to the understanding of optimized strategies for the design of stable and efficient CBPMs.
机译:疏水改性的基于壳聚糖的聚合物胶束(CBPM)是通过壳聚糖两亲衍生物的自聚集形成的。它们的核-壳结构,多样性以及通过调节其三个主要成分(壳聚糖,亲水链段和疏水链段)以及与外部介质之间的相互作用(通过改变每种比率和化学结构)可以调节其所有性质的事实成分的化学结构使其与其他基于壳聚糖的药物递送系统(DDS)区别开来,并为靶向递送亲脂性抗癌药物提供了这些有希望的候选者。先前对基于壳聚糖的DDS进行的大多数评论文章仅对此类系统与通过它们提供的抗癌药物进行了简单的差异比较。在这篇评论文章中,对CBPM的所有基本特性,包括物理化学,药物和生物学特性,都进行了技术详细的讨论。本文的目的是概述和讨论CBPM的显着特征,以有助于理解用于设计稳定有效的CBPM的优化策略。

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