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具有电荷开关的光响应聚合物囊泡用于靶向药物递送。

Light-responsive polymersomes with a charge-switch for targeted drug delivery.

机构信息

Optogenetics & Synthetic Biology Interdisciplinary Research Center, State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, 130# Meilong Road, Shanghai 200237, China.

出版信息

J Mater Chem B. 2020 Jan 28;8(4):727-735. doi: 10.1039/c9tb02411e. Epub 2020 Jan 2.

Abstract

Unlike the traditional block amphiphilic polymersomes, we herein report a lipid-like amphiphilic polymer that self-assembles into photo-responsive polymersomes for drug delivery. The introduction of a quaternary ammonium moiety not only provides a hydrophilic segment of the polymersomes, but also enables electrostatic adsorption with folic acid, thus achieving the targeting of cancer cells with overexpression of folate receptor. Upon light irradiation, the photocleavage reaction of the o-nitrobenzyl moiety disintegrates polymersomes by changing the polymer structure from cationic amphiphilic state to zwitterionic hydrophilic state, thus realizing photo-triggered drug release. The data showed that anticancer drugs (doxorubicin hydrochloride, DOX·HCl) can be loaded into the hydrophilic cavity of polymersomes and controllably released by photo-induced disintegration of polymersomes. Cellular assay showed that the active targeting of folic acid and photo-triggered release endowed the DOX-loaded polymersomes with a higher cytotoxicity to HeLa cells. Such cationic polymersomes provide a novel strategy for designing effective and intelligent drug carriers, and have potential application as a novel integrated platform for targeted drug delivery.

摘要

与传统的嵌段两亲聚合物囊泡不同,我们在此报告了一种类脂质两亲聚合物,它可以自组装成光响应聚合物囊泡用于药物传递。季铵盐部分的引入不仅提供了聚合物囊泡的亲水性部分,而且还可以与叶酸进行静电吸附,从而实现对叶酸受体过表达的癌细胞的靶向。光照后,邻硝基苄基部分的光裂解反应通过将聚合物结构从阳离子两亲状态改变为两性离子亲水性状态来破坏聚合物囊泡,从而实现光触发药物释放。数据表明,抗癌药物(盐酸阿霉素,DOX·HCl)可以负载到聚合物囊泡的亲水性腔室中,并通过聚合物囊泡的光诱导破坏实现可控释放。细胞试验表明,叶酸的主动靶向和光触发释放使载 DOX 的聚合物囊泡对 HeLa 细胞具有更高的细胞毒性。这种阳离子聚合物囊泡为设计有效和智能药物载体提供了一种新策略,并有可能作为一种新型的靶向药物传递的集成平台。

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