急性肾损伤
抗氧化剂
药理学
肾
过氧化脂质
氧化应激
炎症
肾缺血
再灌注损伤
缺血
医学
脂质过氧化
免疫学
生物化学
化学
内科学
作者
Chenguang Ding,Bo Wang,Jin Zheng,Mingzhen Zhang,Yang Li,Hsin‐Hui Shen,Yingcong Guo,Bingxuan Zheng,Puxun Tian,Xiaoming Ding,Wujun Xue
标识
DOI:10.1021/acsami.3c08573
摘要
Ischemia/reperfusion (I/R) injury causes excessive oxidative events and initiates destructive inflammatory responses, and it is an important promoter to the pathology of various pathema states. Ferroptosis is an iron-dependent type of nonapoptotic cell death accompanied by the accumulation of membrane lipid peroxide and consumption of polyunsaturated fatty acid, and it plays a key role in I/R injury diseases. Moreover, the excessive production of inflammatory cytokines contributes to the development of acute kidney injury. Here, we reported neutrophil membrane-coated copper-based nanoparticles (N-Cu5.4O@DFO NPs) for I/R kidney injury treatment. The highly biocompatible and stable N-Cu5.4O@DFO NPs showed excellent antioxidant and iron ion scavenging abilities in vitro. Our finding showed that the N-Cu5.4O@DFO NPs strategy could significantly accumulate in the inflammatory kidney, reduce oxidative damage events and inflammatory response, and finally achieve synergistic therapy against renal I/R injury. This work promotes the development of nanoantioxidant agents with multiple antioxidant properties for the therapy of other I/R injury diseases.
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