活性氧
氧化应激
椎间盘
细胞生物学
细胞外基质
变性(医学)
化学
体外
细胞保护
生物物理学
体内
氧化磷酸化
退行性椎间盘病
平衡
基质金属蛋白酶
磁共振成像
细胞外
癌症研究
病理
脂质过氧化
自噬
生物医学工程
药理学
核心
病态的
作者
Linjun Yang,Zhanqiu Dai,Xuhui Fan,Jin Yao,Jianle Wang,Congcong Yu,Han Wang,Zhijun Hu
标识
DOI:10.1002/adhm.202501662
摘要
Abstract As a central driver of intervertebral disc degeneration (IVDD), oxidative stress mediates pathological changes by promoting extracellular matrix (ECM) breakdown, thereby accelerating the degenerative process. To target this pathological cascade, trimetallic nanoparticles (TriNPs) are designed and developed to modulate the oxidative microenvironment of intervertebral discs and restore ECM homeostasis through reactive oxygen species (ROS) scavenging. In vitro studies demonstrate that TriNPs provide significant cytoprotection against H 2 O 2 ‐induced oxidative damage in nucleus pulposus (NP) cells through efficient ROS elimination. For translational applications, TriNPs are encapsulated within an injectable hydrogel (termed TOH) to evaluate their therapeutic potential in a rat IVDD model. In vivo studies encompassing both radiographic and histomorphometric analyses reveal that TOH administration significantly improves the Disc Height Index (DHI) and T2‐weighted Magnetic Resonance Imaging (MRI) grading, while also reducing histological scores. Collectively, these results indicate that TOH may serve as an innovative therapeutic approach to modulate disc microenvironment and attenuate IVDD progression.
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