Catalytically Active CoFe2O4 Nanoflowers for Augmented Sonodynamic and Chemodynamic Combination Therapy with Elicitation of Robust Immune Response

被引:175
作者
Fu, Shiyan [1 ,2 ]
Yang, Ruihao [1 ]
Ren, Junjie [1 ]
Liu, Jiahui [1 ]
Zhang, Lei [3 ]
Xu, Zhigang [1 ]
Kang, Yuejun [1 ]
Xue, Peng [1 ]
机构
[1] Southwest Univ, Sch Mat & Energy, State Key Lab Silkworm Genome Biol, Chongqing 400715, Peoples R China
[2] North Sichuan Med Coll, Dept Nucl Med, Affiliated Hosp, Nanchong 637000, Sichuan, Peoples R China
[3] Southwest Univ, Canc Ctr, Med Res Inst, Chongqing 400716, Peoples R China
基金
中国国家自然科学基金;
关键词
cobalt ferrite; sonodynamic therapy; chemodynamic therapy; tumor microenvironment; immune activation; IMMUNOGENIC CELL-DEATH; FE3O4; NANOPARTICLES; METHYLENE-BLUE; CANCER; MICROENVIRONMENT; DEGRADATION; ACTIVATION; STRATEGIES; APOPTOSIS; DESIGN;
D O I
10.1021/acsnano.1c03128
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A hypoxic and acidic tumor microenvironment (TME) plays a significant role in cancer development through complex cellular signaling networks, and it is thus challenging to completely eradicate tumors via monotherapy. Here, PEGylated CoFe2O4 nanoflowers (CFP) with multiple enzymatic activities, serving as bioreactors responsive to TME cues, were synthesized via a typical solvothermal method for augmented sonodynamic therapy (SDT) and chemodynamic therapy (CDT) with elicitation of robust immune response. The CFP occupying multivalent elements (Co2+/3+, Fe2+/3+) exhibited strong Fenton-like and catalase-like activity. In another aspect, CFP itself is a brand-new sonosensitizer for highperformance SDT based on ultrasound-triggered electron (e(-))/ hole (h(+)) pair separation from the energy band with promptness and high efficiency. With efficient enrichment in tumorous tissue as revealed by magnetic resonance imaging, CPF could generate (OH)-O-center dot for CDT relying on Fenton-like reactions. Moreover, catalase-mimicking CFP could react with endogenous H2O2 to generate molecular oxygen, and high O-2 level may promote the production of O-1(2) for SDT. What's more, the reactive oxygen species obtained from combined SDT/CDT could efficiently trigger immunogenic cell death through a synergistic therapy based on the elicitation of antitumor immunity with the aid of an immune checkpoint blockade for the sake of suppressing primary and distant tumors as well as lung metastasis. Taken together, this paradigm delivers useful insights for developing in-coming nanocomposites based on cobalt ferrite for cancer theranostics.
引用
收藏
页码:11953 / 11969
页数:17
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