活性氧
化学
氧化应激
抗氧化剂
生物相容性材料
超氧化物歧化酶
体内分布
谷胱甘肽
谷胱甘肽过氧化物酶
急性肾损伤
催化作用
纳米技术
肾
碳纤维
生物物理学
荧光
线粒体
过氧化氢
药理学
生物化学
作者
Tianle Tang,Jun Zhang,Yan Wang,Yan Wang,Kehui Yuan,Kehui Yuan,Yuan He,Chenchen Li,Ping Zhang,Yijun Yang,Yanli Wang,Yanli Wang,Pir Muhammad
标识
DOI:10.1002/advs.202519393
摘要
ABSTRACT Overproduction of reactive oxygen species (ROS) is a key pathogenic feature in acute kidney injury (AKI), leading to rapid decline in renal function with high mortality rates that call for effective antioxidant therapies. Herein, we present triphenylphosphonium‐functionalized carbon dots supported by single‐atom silver (T‐Ag SA ‐CDs) that integrate fluorescent antioxidant nanozymes for the accurate ROS scavenging and real‐time bioimaging of AKI. By anchoring silver in single‐atom and sub‐nanocluster states on a carbon dot matrix, T‐Ag SA ‐CDs exhibit exceptional superoxide dismutase (SOD)‐ and glutathione peroxidase (GPx)‐like activities, surpassing traditional nanozymes in ROS neutralization efficiency. Density functional theory (DFT) calculations disclose a low‐energy reaction pathway common to both nitrogen‐doped carbon dots (N‐CDs) and Ag SA ‐CDs, clarifying the mechanism behind their dual SOD‐ and GPx‐mimetic activities. The biocompatible N‐CDs platform guarantees the stability, minimizes Ag + ‐associated toxicity, and enhances catalytic performance through synergistic Ag SA ‐CD interactions. Targeting mitochondria through triphenylphosphonium functionalization facilitates site‐specific antioxidant protection, demonstrating robust therapeutic efficacy in a cisplatin‐induced AKI mouse model. Additionally, the intrinsic fluorescence of T‐Ag SA ‐CDs facilitates non‐invasive monitoring of biodistribution and renal accumulation, promotes the recovery of damaged kidney tissue, alleviates oxidative stress and post‐cure assessment, and offers a self‐reported theranostic platform, while also aiming to improve its clinical application.
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