Synthesis of MoSe2/CoSe2 Nanosheets for NIR‐Enhanced Chemodynamic Therapy via Synergistic In‐Situ H2O2 Production and Activation

光热治疗 材料科学 异质结 光催化 电子转移 过氧化氢酶 PEG比率 纳米技术 生物物理学 核化学 光化学 催化作用 光电子学 生物 生物化学 化学 经济 财务
作者
Yang Li,Ran Jia,Huiming Lin,Xilin Sun,Fengyu Qu
出处
期刊:Advanced Functional Materials [Wiley]
卷期号:31 (8) 被引量:69
标识
DOI:10.1002/adfm.202008420
摘要

Abstract Currently, the limited intratumoral H 2 O 2 level restricts the development of chemodynamic therapy (CDT). Herein, MoSe 2 /CoSe 2 @PEG nanosheets are prepared to reveal NIR‐photocatalytic H 2 O 2 generation to insure the intracellular H 2 O 2 supplement. The formation mechanism is investigated, showing the dissolved O 2 and photo‐excited electrons to determine H 2 O 2 production via sequential single‐electron transfer process. The experimental data and density functional theory calculation further display their typical‐II heterostructure, which possesses the effective charge separation and nearly four times H 2 O 2 generation than MoSe 2 @PEG. In addition, the nanocomposites also reveal the peroxidase/catalase activity, making the in‐situ H 2 O 2 activation and ·OH generation. And, the O 2 production derived from catalase‐mimic activity not only relieves hypoxia but also offers the source for H 2 O 2 production. Because of the decreased resistance for charge transfer, MoSe 2 /CoSe 2 @PEGs also reveal more than three times enzyme‐activity for MoSe 2 @PEG. With the narrow band gap and high NIR‐harvest, MoSe 2 /CoSe 2 @PEG exhibits the great photothermal converting ability (62.5%). MoSe 2 /CoSe 2 @PEG reveals the novel biodegradation, and most of them can be eliminated via urine and feces within 2 weeks. Here, the computed tomography/magnetic resonance imaging/photothermal imaging and the synergistic photothermal therapy/CDT treatments further make sure potential application on anticancer.
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