Integration of a porous coordination network and black phosphorus nanosheets for improved photodynamic therapy of tumor

被引:14
|
作者
Liu, Miao-Deng [1 ,2 ]
Yu, Yun [1 ,2 ]
Guo, Deng-Ke [1 ,2 ]
Wang, Shi-Bo [1 ,2 ]
Li, Chu-Xin [1 ,2 ]
Gao, Fan [1 ,2 ]
Cheng, Zhang [1 ,2 ]
Xie, Bo-Ru [1 ,2 ]
Zhong, Zhenlin [1 ,2 ]
Zhang, Xian-Zheng [1 ,2 ]
机构
[1] Wuhan Univ, Minist Educ, Key Lab Biomed Polymers, Wuhan 430072, Peoples R China
[2] Wuhan Univ, Dept Chem, Wuhan 430072, Peoples R China
基金
中国国家自然科学基金;
关键词
CANCER; HSP90; EXPRESSION; GENERATION; RELEASE; OXIDE;
D O I
10.1039/d0nr00956c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Selectively attenuating the protection offered by heat shock protein 90 (HSP90), which is indispensable for the stabilization of the essential regulators of cell survival and works as a cell guardian under oxidative stress conditions, is a potential approach to improve the efficiency of cancer therapy. Here, we designed a biodegradable nanoplatform (APCN/BP-FA) based on a Zr(iv)-based porphyrinic porous coordination network (PCN) and black phosphorus (BP) sheets for efficient photodynamic therapy (PDT) by enhancing the accumulation of the nanoplatforms in the tumor area and attenuating the protection of cancer cells. Owing to the favorable degradability of BP, the nanosystem exhibited accelerated the release of the HSP90 inhibitor tanespimycin (17-AAG) and an apparent promotion in the reactive oxygen species (ROS) yield of PCN as well as expedited the degradation of the PCN-laden BP nanoplatforms. Bothin vitroandin vivoresults revealed that the elevated amounts of ROS and reduced cytoprotection in tumor cells were caused by the nanoplatforms. This strategy may provide a promising method for attenuating cytoprotection to aid efficient photodynamic therapy.
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页码:8890 / 8897
页数:8
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