谷胱甘肽
细胞内
前药
多重耐药
药理学
药品
抗氧化剂
药物输送
化学
生物化学
阿霉素
生物
酶
有机化学
化疗
抗生素
遗传学
作者
Xuan Xiao,Kewei Wang,Qingyu Zong,Yalan Tu,Yansong Dong,Youyong Yuan
出处
期刊:Biomaterials
[Elsevier]
日期:2021-03-01
卷期号:270: 120649-120649
被引量:53
标识
DOI:10.1016/j.biomaterials.2020.120649
摘要
High intracellular glutathione (GSH) levels play an important role in multidrug resistance (MDR) in cancer cells. It remains challenging to develop a drug delivery system that is simultaneously capable of GSH depletion and drug activation for multidrug resistance reversal. Herein, we designed a polyprodrug (denoted as PSSD) based on poly(disulfide) conjugated with doxorubicin (DOX) on the polymer side chains that exhibits GSH depletion and cascade DOX activation for drug resistance reversal. The poly(disulfide) backbone with a high disulfide density depletes intracellular antioxidant GSH via the disulfide-thiol exchange reaction to disrupt intracellular redox homeostasis in cells. Simultaneously, DOX can be activated through a cascade reaction, and degradation of the poly(disulfide) backbone further facilitates its drug release. Therefore, poly(disulfide) can be used as a GSH scavenger to reverse MDR as well as a prodrug backbone to target high intracellular GSH levels in cancer cells, providing a general strategy for drug resistance reversal.
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