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Inhalation metal-phenolic nanozyme as a novel therapeutic strategy for lung ischemia-reperfusion injury

  • Shirui Sun
  • , Kaixiang Ren
  • , Bin He
  • , Yilong Zhao
  • , Rongxuan Jiang
  • , Xingzhuo Zhu
  • , Niuniu Dong
  • , Yingcong Guo
  • , Qi He
  • , Jiahao Huang
  • , Chenguang Ding
  • , Mei Yang
  • The First Affiliated Hospital of Xi’an Jiaotong University
  • Xi'an Jiaotong University

Research output: Contribution to journalArticlepeer-review

4 Scopus citations

Abstract

Background Lung ischemia-reperfusion injury (LIRI) is a complex pathophysiological process with few existing therapeutic options. New drugs are needed to target both oxidative stress and enhanced sterile inflammation during ischemia-reperfusion. Results In this study, we developed a metal-phenolic nanozyme (Cur-Fe) that possesses significant enzyme-like activities, including superoxide dismutase (SOD)-like activity and hydroxyl radical (•OH) scavenging ability, and can effectively modulate inflammatory cytokines and maintain cellular homeostasis in vitro . In the mouse LIRI model, nebulized inhalation of Cur-Fe nanozyme significantly reduced lung inflammation and oxidative stress, improved lung tissue function, and restored alveolar structure. It is important to note that transcriptomics and metabolomics analyses demonstrated that Cur-Fe nanozyme modulated key metabolic pathways, including the cGMP-PKG signaling pathway and amino acid metabolism, thereby promoting its protective effects on lung tissue. Conclusion In this study, we present a Cur-Fe nanozyme that shows great potential in mitigating LIRI-associated lung injury by targeting oxidative stress and inflammation as well as regulating key transcriptional and metabolic pathways. This innovative approach provides a new avenue for the development of nanomedicines for the treatment of ischemia-reperfusion-related diseases with promising clinical applications.

Original languageEnglish
Article number214558
JournalBiomaterials Advances
Volume180
DOIs
StatePublished - Mar 2026

Keywords

  • Inflammation
  • Inhalation
  • Lung ischemia-reperfusion injury
  • Metal-phenolic nanozyme
  • Oxidative stress

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