氧化应激
二甲双胍
脊髓损伤
活性氧
炎症
自愈水凝胶
再生(生物学)
细胞生物学
脊髓
神经保护
癌症研究
程序性细胞死亡
医学
抗氧化剂
药理学
平衡
活力测定
化学
神经科学
细胞
肿瘤微环境
神经干细胞
神经毒性
RNA干扰
促炎细胞因子
细胞因子
中枢神经系统
神经系统
癌症
作者
Chenqian Feng,Qiuting Wang,Susu Xiao,Yuanli Yang,Bo Chen,Hui Li,Min Mu,Rangrang Fan,Haifeng Chen,Bo Han,Gang Guo
出处
期刊:ACS Nano
[American Chemical Society]
日期:2025-09-19
卷期号:19 (38): 33960-33980
被引量:17
标识
DOI:10.1021/acsnano.5c09794
摘要
Spinal cord injury (SCI) causes irreversible neurological damage largely due to secondary processes such as ferroptosis and inflammation response, which hinder functional recovery and lack effective targeted treatments. Ferroptosis, an iron-dependent form of cell death driven by oxidative stress, and a pro-inflammatory microenvironment contribute significantly to neuronal loss after SCI. To address these challenges, we developed MCPAD, an injectable, self-healing nanocomposite hydrogel incorporating metformin-loaded PLGA nanoparticles (Met@PLGA NPs) and phenol-derived dynamic cross-linked network (CPAD). This multifunctional platform enables targeted suppression of ferroptosis and immunomodulation. In vitro, MCPAD significantly enhanced neuronal viability by regulating iron homeostasis and upregulating antioxidant defenses. In vivo, it reduced reactive oxygen species (ROS) accumulation, glial scarring, and inflammatory cytokine expression, while promoting axonal regeneration and synaptic remodeling. Treated animals exhibited greatly improved locomotor recovery and tissue preservation. Biochemical assessments confirmed systemic biosafety. These findings demonstrate the therapeutic potential of MCPAD as a biological responsive platform that reprograms the injury microenvironment to support functional neural repair after SCI.
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