光热治疗
化学
阿霉素
羟基自由基
纳米材料
纳米复合材料
催化作用
咪唑酯
谷胱甘肽
体内
组合化学
单宁酸
细胞凋亡
癌细胞
核化学
癌症研究
生物物理学
激进的
化疗
材料科学
纳米技术
生物化学
癌症
有机化学
酶
医学
外科
生物技术
内科学
生物
作者
Weiling Song,Huan Yang,Yujie Sun,Yuanming Yang,Qi Dong,Peng He,Gengjun Liu,Zhen Zhao,Lifeng Qin,Shunxiang Gao,Jing Liu,Hong Zhou,Haiyan Wang
标识
DOI:10.1021/acsanm.3c03729
摘要
Multifunctional nanomaterials have become a promising nanoplatform for anticancer treatment with tumor specific activation. Here, a cancer cell-activated nanocomposite Cu/ZIF-8@MPN@DOX@F127 (CZMDF) was constructed with a metal phenolic network (MPN)-modified Cu/ZIF-8 and loaded with doxorubicin (DOX). CZMDF was degraded to release tannic acid (TA), Fe3+, Cu2+, and DOX in cancer cells. Benefiting from the reducibility of TA, Fe3+ was converted to Fe2+, which could react with endogenous H2O2 to produce a highly toxic hydroxyl radical (•OH) by the Fenton reaction. The Fenton reaction-mediated chemodynamic therapy (CDT) was promoted by the accelerated Fe3+/Fe2+ conversion, which was also enhanced with a Cu2+-based Fenton-like reaction. In addition, endogenous glutathione (GSH) could reduce Fe3+ and Cu2+ to Fe2+ and Cu+, which led to further enhancement of CDT performance. DOX acted as a traditional drug to realize chemotherapy. Furthermore, the heat from MPN after near-infrared irradiation (NIR) could be applied to realize photothermal therapy (PTT). The multifunctional nanocomposite was designed to achieve synergistic tumor treatment with CDT/chemotherapy/PTT. In vitro experiments showed that the CZMDF caused about 70% of cell apoptosis, and the tumor growth in mice was also inhibited in vivo study. This multifunctional nanomaterial enriches the nanocatalyst types for synergistic tumor therapy, providing a nanoplatform for potential clinical transitions.
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