Gold-Platinum Nanodots with High-Peroxidase-like Activity and Photothermal Conversion Efficiency for Antibacterial Therapy

被引:85
|
作者
Zhang, Shengnan [1 ]
Lu, Qiujun [1 ]
Wang, Feiying [1 ]
Xiao, Zhuyong [1 ]
He, Lidan [1 ]
He, Dinggeng [1 ,2 ]
Deng, Le [1 ,2 ]
机构
[1] Hunan Normal Univ, Coll Life Sci, Dept Microbiol, Changsha 410081, Hunan, Peoples R China
[2] Hunan Normal Univ, State Key Lab Dev Biol Freshwater Fish, Changsha 410081, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
gold-platinum; nanodots; photothermal therapy; chemodynamic therapy; bacterial infection; STRATEGIES;
D O I
10.1021/acsami.1c10600
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Combined therapeutic strategies for bacterial infection have attracted worldwide attention owing to their faster and more effective therapy with fewer side effects compared with monotherapy. In this work, goldplatinum nanodots (AuPtNDs) are simply and quickly synthesized by a onestep method. They not only exhibit powerful peroxidase-like activity but also confer a higher affinity for hydrogen peroxide (H2O2), which is 3.4 times that of horseradish peroxidase. Under 808 nm laser irradiation, AuPtNDs also have excellent photothermal conversion efficiency (50.53%) and strong photothermal stability. Excitingly, they can combat bacterial infection through the combination of chemodynamic and photothermal therapy. In vitro antibacterial results show that the combined antibacterial strategy has a broad-spectrum antibacterial property against both Escherichia coli (Gram negative, 97.1%) and Staphylococcus aureus (Gram positive, 99.3%). Animal experiments further show that nanodots can effectively promote the healing of bacterial infection wounds. In addition, owing to good biocompatibility and low toxicity, they are hardly traceable in the main organs of mice, which indicates that they can be well excreted through metabolism. These results reveal the application potential of AuPtNDs as a simple and magic multifunctional nanoparticle in antibacterial therapy and open up new applications for clinical anti-infective therapy in the near future.
引用
收藏
页码:37535 / 37544
页数:10
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