Cyclic reactions-mediated self-supply of H2O2 and O2 for cooperative chemodynamic/starvation cancer therapy

被引:90
|
作者
Zhang, Xiaojuan [1 ]
He, Chuanchuan [1 ]
Chen, Yan [1 ]
Chen, Chen [1 ]
Yan, Ruicong [1 ]
Fan, Ting [1 ]
Gai, Yongkang [2 ,3 ]
Yang, Tan [1 ]
Lu, Yao [1 ]
Xiang, Guangya [1 ]
机构
[1] Huazhong Univ Sci & Technol, Sch Pharm, Tongji Med Coll, Wuhan 430030, Peoples R China
[2] Huazhong Univ Sci & Technol, Union Hosp, Dept Nucl Med, Tongji Med Coll, Wuhan 430022, Peoples R China
[3] Hubei Prov Key Lab Mol Imaging, Wuhan 430022, Peoples R China
基金
中国国家自然科学基金;
关键词
Glucose oxidase; Starvation therapy; Chemodynamic therapy; Hypoxia; CALCIUM PEROXIDE; HYDROGEN-PEROXIDE; IN-SITU; OXYGEN; GLUCOSE; NANOPARTICLES; GENERATION;
D O I
10.1016/j.biomaterials.2021.120987
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Hydroxyl radical (center dot OH)-mediated chemodynamic therapy (CDT) and glucose oxidase (GOx)-based starvation therapy (ST) are two emerging antitumor strategies, limited by acid/H2O2 deficiency and tumor hypoxia, respectively. Herein, we developed a liposomal nanoplatform co-delivering Fe(OH)3-doped CaO2 nanocomposites and GOx molecules for synergistic CDT/ST with a complementary effect. Based on Fenton reactions initiated by iron ions, CaO2-supplied H2O2 could not only generate center dot OH for H2O2-sufficient CDT, but also produce O2 to promote the catalytic efficiency of GOx under hypoxia. In return, the enhanced ST generated gluconic acid and H2O2, further amplifying CDT. Through in vitro and in vivo experiments, we demonstrated that such a mutually reinforced modality based on the cyclic Fenton/starvation reactions provided a novel and potent anticancer mechanism for the effective treatment of hypoxic cancers.
引用
收藏
页数:11
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