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从物理化学、药剂学和生物学角度设计优化和高效的疏水改性壳聚糖基聚合物胶束作为靶向递抗癌药物的纳米载体系统。

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.

机构信息

Department of Pharmaceutics, Isfahan University of Medical Sciences, Isfahan, Iran.

出版信息

J Drug Target. 2013 Sep;21(8):693-709. doi: 10.3109/1061186X.2013.824455. Epub 2013 Aug 5.

Abstract

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.

摘要

疏水改性壳聚糖基聚合物胶束(CBPMs)通过壳聚糖两亲性衍生物的自组装形成。其核壳结构、多样性以及通过调节三种主要成分(壳聚糖、亲水性链段和疏水性链段)之间的相互作用以及与外部介质的相互作用,通过改变每个成分的比例和化学结构,使它们有别于其他基于壳聚糖的药物传递系统(DDS),并为靶向传递亲脂性抗癌药物提供了这些有前途的候选药物。以前进行的大多数关于基于壳聚糖的 DDS 的综述文章仅对这些系统与通过它们传递的抗癌药物进行了简单的差异比较。在这篇综述文章中,详细讨论了 CBPMs 的所有基本性质,包括物理化学、药物和生物学性质。本文的目的是概述和讨论 CBPMs 的突出特点,为设计稳定有效的 CBPMs 的优化策略提供帮助。

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