Fabrication of hyaluronic acid-based micelles with glutathione-responsiveness for targeted anticancer drug delivery

被引:58
作者
Yan, Ke [1 ]
Feng, Yecheng [1 ]
Gao, Ke [2 ]
Shi, Xiaojing [2 ]
Zhao, Xubo [1 ]
机构
[1] Zhengzhou Univ, Coll Chem, Green Catalysis Ctr, Zhengzhou 450001, Peoples R China
[2] Zhengzhou Univ, Acad Med Sci, Lab Anim Ctr, State Key Lab Esophageal Canc Prevent & Treatment, Zhengzhou 450052, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Hyaluronic acid; Self-assembly; GSH-responsiveness; Drug delivery system; Cancer therapy; BLOCK-COPOLYMER; POLYMERIC MICELLES; NANOPARTICLES; TUMOR; RELEASE;
D O I
10.1016/j.jcis.2021.08.129
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Hyaluronic acid (HA), a natural polymer, has gained much attention recently because of its good biocompatibility and extensive availability. Herein, a novel drug delivery system based on hyaluronic acidtetraphenyl ethylene conjugate (HA-SS-TPE) with glutathione (GSH)-responsiveness for targeted drug delivery is designed. During the self-assembly of HA-SS-TPE, doxorubicin (DOX) is loaded to form DOX-loaded polymeric micelles. These as-prepared DOX-loaded polymeric micelles not only exhibit fluorescent emission, but also fast glutathione-triggered dissociation to unload DOX by responding to tumor microenvironments. In-vitro investigations showed that the DOX-loaded polymeric micelles presented a higher intracellular release ratio in CD44-positive cells (ES2 and Hela) than in CD44-negative cells (MCF-7 and L929). Notably, in vivo investigations showed that DOX@HA-SS-TPE significantly suppressed tumor growth. As a result, such a GSH-responsive drug delivery system with fluorescent feature provides a potential treatment for CD44-overexpressing cancers. (c) 2021 Elsevier Inc. All rights reserved.
引用
收藏
页码:1586 / 1596
页数:11
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