Ultrasmall copper-based nanoparticles for reactive oxygen species scavenging and alleviation of inflammation related diseases.

Liu, Tengfei; Xiao, Bowen; Xiang, Fei; Tan, Jianglin; Chen, Zhuo; Zhang, Xiaorong; Wu, Chengzhou; Mao, Zhengwei et al. · Nat Commun · 2020

basic_science · Level V

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Abstract

Oxidative stress is associated with many acute and chronic inflammatory diseases, yet limited treatment is currently available clinically. The development of enzyme-mimicking nanomaterials (nanozymes) with good reactive oxygen species (ROS) scavenging ability and biocompatibility is a promising way for the treatment of ROS-related inflammation. Herein we report a simple and efficient one-step development of ultrasmall Cu<sub>5.4</sub>O nanoparticles (Cu<sub>5.4</sub>O USNPs) with multiple enzyme-mimicking and broad-spectrum ROS scavenging ability for the treatment of ROS-related diseases. Cu<sub>5.4</sub>O USNPs simultaneously possessing catalase-, superoxide dismutase-, and glutathione peroxidase-mimicking enzyme properties exhibit cytoprotective effects against ROS-mediated damage at extremely low dosage and significantly improve treatment outcomes in acute kidney injury, acute liver injury and wound healing. Meanwhile, the ultrasmall size of Cu<sub>5.4</sub>O USNPs enables rapid renal clearance of the nanomaterial, guaranteeing the biocompatibility. The protective effect and good biocompatibility of Cu<sub>5.4</sub>O USNPs will facilitate clinical treatment of ROS-related diseases and enable the development of next-generation nanozymes.

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