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酶响应性磺化环糊精/前药超分子组装用于控制释放抗癌药物苯丁酸氮芥。

Enzyme-responsive sulfatocyclodextrin/prodrug supramolecular assembly for controlled release of anti-cancer drug chlorambucil.

机构信息

College of Chemistry, State Key Laboratory of Elemento-Organic Chemistry, Nankai University, Tianjin 300071, P. R. China.

出版信息

Chem Commun (Camb). 2019 Jan 17;55(7):953-956. doi: 10.1039/c8cc09047e.

Abstract

Supramolecular drug delivery systems are becoming an increasingly important part in controlled drug release. In this work, we report a novel enzyme-responsive supramolecular assembly directly constructed using biocompatible sulfato-β-cyclodextrin (SCD) and an anti-cancer prodrug, i.e. choline modified anti-cancer drug chlorambucil (QA-Cbl). The supramolecular assembly acts as an effective drug delivery system via the controlled drug loading and enzyme-responsive drug release, because the butyrylcholinesterase (BChE) can cleave the ester bond of QA-Cbl prodrug, resulting in the release of anti-cancer drug chlorambucil (Cbl). Compared to other sophisticated drug delivery systems, the present system provides a feasible and functional approach for achievement of controlled drug release.

摘要

超分子药物输送系统在控制药物释放中变得越来越重要。在这项工作中,我们报告了一种新颖的酶响应超分子组装,该组装直接使用生物相容性的磺基-β-环糊精(SCD)和抗癌前药,即胆碱修饰的抗癌药物苯丁酸氮芥(QA-Cbl)构建。超分子组装通过控制药物负载和酶响应药物释放充当有效的药物输送系统,因为丁酰胆碱酯酶(BChE)可以切割 QA-Cbl 前药的酯键,导致抗癌药物苯丁酸氮芥(Cbl)的释放。与其他复杂的药物输送系统相比,本系统为实现控制药物释放提供了一种可行且实用的方法。

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