Nanozyme-mediated cascade reaction based on metal-organic framework for synergetic chemo-photodynamic tumor therapy

被引:63
|
作者
Sheng, Shu [1 ,2 ,3 ]
Liu, Feng [1 ,2 ,3 ]
Lin, Lin [1 ,3 ]
Yan, Nan [1 ,2 ,3 ]
Wang, Yanbing [1 ,3 ,4 ]
Xu, Caina [1 ,3 ]
Tian, Huayu [1 ,2 ,3 ,4 ]
Chen, Xuesi [1 ,2 ,3 ,4 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, Key Lab Polymer Ecomat, Changchun 130022, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Jilin Biomed Polymers Engn Lab, Changchun 130022, Peoples R China
[4] Univ Sci & Technol China, Hefei 230026, Peoples R China
基金
中国国家自然科学基金;
关键词
Nanozyme; Cascade reaction; Metal-organic framework; Chemodynamic therapy; Photodynamic therapy; NANOMATERIALS; STRATEGIES;
D O I
10.1016/j.jconrel.2020.09.029
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Numerous biological enzymes are considered promising for tumor therapy. However, the remote control of enzymatic activity in vivo to achieve a satisfactory therapeutic effect remains challenge. Herein, we loaded chlorin e6 (Ce6) to the peroxidase-mimic metal-organic framework (MOF) MIL-100 (Ce6@MIL-100) to develop cascade-reaction nanoparticles shielded with hyaluronic acid (CMH NPs). CMH NPs and the highly expressed H2O2 in the tumor site underwent Fenton reaction to generate hydroxyl radical ((OH)-O-center dot) and O-2. The produced (OH)-O-center dot and O-2 were used for chemodynamic therapy and alleviating hypoxia, respectively. Under near-infrared light irradiation, the Ce6-mediated photochemical effect not only generated cytotoxic singlet oxygen (O-1(2)) for enhanced photodynamic therapy with additional oxygen supply, but also produced H2O2 to amplify the Fenton reaction. Therefore, the CMH NPs exhibited a virtuous cycle of cascade reactions. Furthermore, comprehensive experiments demonstrated that combined therapy could effectively ablate tumors. Thus, the nanozyme based on MOF realized potent chemo-photodynamic therapeutic efficacy. Overall, the nanoplatform displayed an exciting biomedical application of MOF-derived nanozyme as a versatile therapeutic agent.
引用
收藏
页码:631 / 639
页数:9
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