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Low-Temperature Adaptive Single-Atom Iron Nanozymes against Viruses in the Cold Chain.

Tao QinYulian ChenXinyu MiaoMengjuan ShaoNuo XuChunxiao MouZhenhai ChenYuncong YinSujuan ChenYinyan YinLizeng GaoDaxin PengXiufan Liu
Published in: Advanced materials (Deerfield Beach, Fla.) (2024)
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 FeN 4 P 2 -single-atom nanozymes (SAzymes), exhibiting lipid oxidase (OXD)-like activity at cold chain temperatures (-20, and 4 °C). This feature enables FeN 4 P 2 -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, FeN 4 P 2 -SAzymes are successfully applied as antiviral coatings on outer packaging and personal protective equipment; Therefore, FeN 4 P 2 -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.
Keyphrases
  • sars cov
  • respiratory syndrome coronavirus
  • human health
  • infectious diseases
  • risk assessment
  • endothelial cells
  • climate change
  • deep learning