活性氧
氧化应激
生物相容性
化学
体内
抗氧化剂
心肌梗塞
先天免疫系统
炎症
体内分布
免疫系统
生物物理学
体外
纳米技术
单宁酸
催化作用
氧化磷酸化
药理学
材料科学
生物医学工程
荧光
心肌保护
促炎细胞因子
脂多糖
纳米颗粒
生物相容性材料
作者
Shuli Bi,Yì Wáng,Xue‐Hui Shi,Hui‐Ping Wen,Wei Zhao,S Liu,Zhi‐Gang Wang,Zhuhua Yao
出处
期刊:Small
[Wiley]
日期:2026-05-15
卷期号:: e13213-e13213
标识
DOI:10.1002/smll.202513213
摘要
ABSTRACT Acute myocardial infarction (AMI) involves ischemia‐driven cardiomyocyte necrosis accompanied by excessive reactive oxygen species (ROS) and innate immune activation. While reperfusion restores blood flow, it does not mitigate oxidative stress and inflammation that worsen injury, and conventional anti‐inflammatories risk systemic immunosuppression. Here, we developed manganese‐doped Ag 2 Te quantum dots (Mn: Ag 2 Te QDs) surface‐modified with tannic acid (TA) to achieve myocardial‐targeted therapy, real‐time visualization of drug distribution, and post‐treatment verification. Mn doping endows enzyme‐mimetic antioxidant activity, enabling efficient scavenging of ROS to alleviate oxidative stress and dampen inflammatory signaling, including cGAS–STING‐ and ZBP1‐associated pathways. TA confers strong cardiac affinity, enhancing selective accumulation in infarcted myocardium. The QDs emit in the NIR‐IIb window, allowing deep‐tissue, high‐contrast, real‐time fluorescence imaging for noninvasive monitoring of biodistribution and targeted delivery. In vitro and in vivo studies demonstrate robust ROS clearance, reduced inflammation, and improved cardiac function, with favorable biocompatibility and safety. This integrated platform unites myocardial targeting, ROS scavenging, and NIR‐IIb imaging, offering a promising approach for the precision treatment of AMI.
科研通智能强力驱动
Strongly Powered by AbleSci AI