活性氧
氧化应激
心肌梗塞
炎症
化学
心脏病学
心功能曲线
内科学
超氧化物歧化酶
硫化物
生物医学工程
医学
药理学
巨噬细胞极化
抗氧化剂
超氧化物
材料科学
细胞因子
预加载
缺氧(环境)
硫化氢
心室重构
体内
作者
Ying Wang,Xiaoya Duan,Chen Men,Guo Xi,Zhenduo Cui,Linfei Zhang,Wei Zhuang,Hao Ren,Jiang‐Kai Qiu,Kai Guo,Xiangxiang Zheng
标识
DOI:10.1186/s12951-025-03920-y
摘要
Myocardial infarction (MI) remains a critical global health challenge. Excessive reactive oxygen species (ROS) and intense inflammation are two primary drivers of myocardial injury, leading to cardiac dysfunction and heart failure. Herein, a multifunctional microneedle (MN) patch based on gelatin methacryloyl (GelMA) is developed to deliver a hybrid gas-nanozyme with antioxidant and anti-inflammatory activities for MI treatment. The hybrid gas-nanozyme (ZnSBS), comprising zinc sulfide (ZnS) and superoxide dismutase (SOD), is fabricated via microfluidic synthesis. It exhibits pH-responsive hydrogen sulfide (H2S) release in the acidic myocardial microenvironment, thereby synergizing with SOD to enhance ROS scavenging and mitigate oxidative damage in vitro. Furthermore, ZnSBS promotes macrophage polarization toward the M2 phenotype, suppressing inflammatory cytokine secretion. Upon implantation of the MN patch onto the infarcted myocardium in a rat MI model, the patch exhibits strong cardiac adhesion and prolonged ZnSBS retention in infarcted area. This localized delivery effectively inhibits fibrosis, reduces infarct size and improves cardiac function by attenuating ROS-induced injury and inflammation in vivo. This innovative MN patch, integrated with microfluidic-synthesized hybrid gas-nanozyme, offers a promising strategy for MI treatment by targeting oxidative stress and modulating inflammatory.
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