Self-Supply of O2 and H2O2 by a Nanocatalytic Medicine to Enhance Combined Chemo/Chemodynamic Therapy

被引:323
作者
Gao, Shutao [1 ,2 ]
Jin, Yan [1 ]
Ge, Kun [1 ]
Li, Zhenhua [1 ]
Liu, Huifang [1 ]
Dai, Xinyue [1 ]
Zhang, Yinghua [1 ]
Chen, Shizhu [3 ]
Liang, Xingjie [3 ]
Zhang, Jinchao [1 ]
机构
[1] Hebei Univ, Analyt Chem Key Lab Hebei Prov, Chem Biol Key Lab Hebei Prov,Minist Educ, Key Lab Med Chem & Mol Diag,Coll Chem & Environm, Baoding 071002, Peoples R China
[2] Hebei Agr Univ, Coll Sci, Baoding 071001, Peoples R China
[3] Natl Ctr Nanosci & Technol, CAS Key Lab Biol Effects Nanomat & Nanosafety, Beijing 100190, Peoples R China
关键词
CaO2; chemodynamic therapy; chemotherapy; doxorubicin; ZIF-67; OXYGEN; DEGRADATION; ZIF-67; IRON;
D O I
10.1002/advs.201902137
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Combined chemo/chemodynamic therapy is a promising strategy to achieve an improved anticancer effect. However, the hypoxic microenvironment and limited amount of H2O2 in most solid tumors severely restrict the efficacy of this treatment. Herein, the construction of a nanocatalytic medicine, CaO2@DOX@ZIF-67, via a bottom-up approach is described. CaO2@DOX@ZIF-67 simultaneously supplies O-2 and H2O2 to achieve improved chemo/chemodynamic therapy. In the weakly acidic environment within tumors, CaO2@DOX@ZIF-67 is broken down to rapidly release the Fenton-like catalyst Co2+ and the chemotherapy drug doxorubicin (DOX). The unprotected CaO2 reacts with H2O to generate both O-2 and H2O2. The generated O-2 relieves the hypoxia in the tumor and further improve the efficacy of DOX. Meanwhile, the generated H2O2 reacts with Co2+ ions to produce highly toxic center dot OH through a Fenton-like reaction, resulting in improved chemodynamic therapy.
引用
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页数:9
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