冷链
病毒学
冠状病毒
材料科学
2019年冠状病毒病(COVID-19)
生物
食品科学
传染病(医学专业)
医学
疾病
病理
作者
Tao Qin,Yulian Chen,Xinyu Miao,Mengjuan Shao,Nuo Xu,Chunxiao Mou,Zhenhai Chen,Yuncong Yin,Sujuan Chen,Yinyan Yin,Lizeng Gao,Daxin Peng,Xiufan Liu,Daxin Peng,Xiufan Liu
标识
DOI:10.1002/adma.202309669
摘要
Outbreaks of viral infectious diseases, such as the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and influenza A virus (IAV), pose a great threat to human health. Viral spread is accelerated worldwide by the development of cold chain logistics; Therefore, an effective antiviral approach is required. In this study, it is aimed to develop a distinct antiviral strategy using nanozymes with low-temperature adaptability, suitable for cold chain logistics. Phosphorus (P) atoms are added to the remote counter position of Fe-N-C center to prepare FeN4P2-single-atom nanozymes (SAzymes), exhibiting lipid oxidase (OXD)-like activity at cold chain temperatures (-20, and 4 °C). This feature enables FeN4P2-SAzymes to disrupt multiple enveloped viruses (human, swine, and avian coronaviruses, and H1-H11 subtypes of IAV) by catalyzing lipid peroxidation of the viral lipid envelope. Under the simulated conditions of cold chain logistics, FeN4P2-SAzymes are successfully applied as antiviral coatings on outer packaging and personal protective equipment; Therefore, FeN4P2-SAzymes with low-temperature adaptability and broad-spectrum antiviral properties may serve as key materials for developing specific antiviral approaches to interrupt viral transmission through the cold chain.
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