POD Nanozyme optimized by charge separation engineering for light/pH activated bacteria catalytic/photodynamic therapy.
POD Nanozyme optimized by charge separation engineering for light/pH activated bacteria catalytic/photodynamic therapy.
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经电荷分离工程优化的POD纳米酶用于光/pH活化细菌催化/光动力治疗。
DOI:
10.1038/s41392-022-00900-8
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发表时间:
2022-03-28
影响因子:
39.3
通讯作者:
Zhao Y
中科院分区:
文献类型:
--
作者:
Cao C;Zhang T;Yang N;Niu X;Zhou Z;Wang J;Yang D;Chen P;Zhong L;Dong X;Zhao Y
The current feasibility of nanocatalysts in clinical anti-infection therapy, especially for drug-resistant bacteria infection is extremely restrained because of the insufficient reactive oxygen generation. Herein, a novel Ag/Bi2MoO6 (Ag/BMO) nanozyme optimized by charge separation engineering with photoactivated sustainable peroxidase-mimicking activities and NIR-II photodynamic performance was synthesized by solvothermal reaction and photoreduction. The Ag/BMO nanozyme held satisfactory bactericidal performance against methicillin-resistant Staphylococcus aureus (MRSA) (~99.9%). The excellent antibacterial performance of Ag/BMO NPs was ascribed to the corporation of peroxidase-like activity, NIR-II photodynamic behavior, and acidity-enhanced release of Ag+. As revealed by theoretical calculations, the introduction of Ag to BMO made it easier to separate photo-triggered electron-hole pairs for ROS production. And the conduction and valence band potentials of Ag/BMO NPs were favorable for the reduction of O2 to ·O2−. Under 1064 nm laser irradiation, the electron transfer to BMO was beneficial to the reversible change of Mo5+/Mo6+, further improving the peroxidase-like catalytic activity and NIR-II photodynamic performance based on the Russell mechanism. In vivo, the Ag/BMO NPs exhibited promising therapeutic effects towards MRSA-infected wounds. This study enriches the nanozyme research and proves that nanozymes can be rationally optimized by charge separation engineering strategy.
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影响因子:
13.3
作者:
Cao, Changyu;Ge, Wei;Dong, Xiaochen
通讯作者:
Dong, Xiaochen
影响因子:
64.8
作者:
Seiple IB;Zhang Z;Jakubec P;Langlois-Mercier A;Wright PM;Hog DT;Yabu K;Allu SR;Fukuzaki T;Carlsen PN;Kitamura Y;Zhou X;Condakes ML;Szczypiński FT;Green WD;Myers AG
通讯作者:
Myers AG
影响因子:
3.9
作者:
Li, Shijie;Liu, Yanping;Liu, Jianshe
通讯作者:
Liu, Jianshe
影响因子:
13.3
作者:
Bi, Xuelong;Bai, Qiang;Zhu, Zhiling
通讯作者:
Zhu, Zhiling
影响因子:
64.8
作者:
Jones KE;Patel NG;Levy MA;Storeygard A;Balk D;Gittleman JL;Daszak P
通讯作者:
Daszak P