谷胱甘肽
药物输送
活性氧
聚乙二醇
体内
材料科学
化疗
智能聚合物
药品
肿瘤微环境
药理学
癌症研究
化学
纳米技术
生物化学
医学
肿瘤细胞
生物
酶
聚合物
外科
复合材料
生物技术
作者
Ping Shen,Xinyi Zhang,Ni Ding,Yinhua Zhou,Changquan Wu,Chengyuan Xing,Ling Zeng,Lixin Du,Jianpeng Yuan,Yang Kang
标识
DOI:10.1021/acsami.3c01155
摘要
Conventional chemotherapy usually fails to achieve its intended effect because of the poor water solubility, poor tumor selectivity, and low tumor accumulation of chemotherapy drugs. The systemic toxicity of chemotherapy agents is also a problem that cannot be ignored. It is expected that smart nano-drug delivery systems that are able to respond to tumor microenvironments will provide better therapeutic outcomes with decreased side effects of chemotherapeutics. Nano-drug delivery systems capable of breaking the redox balance can also increase the sensitivity of tumor cells to chemotherapeutics. In this study, using polymer-containing disulfide bonds, ester bonds, and d-α-tocopherol polyethylene glycol succinate (TPGS), which can amplify reactive oxygen species (ROS) in tumor cells, we have successfully prepared a smart glutathione (GSH) and esterase dual-responsive nano-drug delivery system (DTX@PAMBE-SS-TPGS NPs) with the ability to deplete GSH as well as amplify ROS and effectively release an encapsulated chemotherapy drug (DTX) in tumor cells. The potential of DTX@PAMBE-SS-TPGS NPs for enhanced antitumor effects was thoroughly evaluated using in vitro as well as in vivo experiments. Our research offers a promising strategy for maximizing the efficacy of tumor therapy.
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