骨关节炎
软骨细胞
软骨
细胞生物学
硫酸软骨素
化学
自噬
药理学
体内
平衡
医学
细胞外基质
TRPV1型
基质(化学分析)
下调和上调
滑膜关节
转录组
伤害感受器
生物医学工程
材料科学
作者
Chao Xie,Huiwen Lu,Jingle Chen,Yucong Li,Bin Tang,Chunyi Wen,Lijun Lin
出处
期刊:ACS Nano
[American Chemical Society]
日期:2026-06-09
卷期号:20 (24): 17209-17232
标识
DOI:10.1021/acsnano.5c10942
摘要
Osteoarthritis (OA) is a complex degenerative joint disease perpetuated by a vicious cycle of biomechanical, biochemical, and chondrocyte homeostasis imbalances, ultimately leading to progressive cartilage degradation. A simultaneous approach to biomechanical disturbances, chondrocyte metabolic imbalances, and maintaining cartilage homeostasis simultaneously holds promise in tackling this challenge. Herein, we report a microfluidics-enabled nanoparticle, termed ZCMC, formed by grafting a magnesium-modified chondroitin sulfate polymer layer onto a zein core preloaded with cannabidiol (CBD), for multiscale synergistic OA therapy. ZCMC achieved enhanced lubrication, reducing OA cartilage friction to levels akin to healthy cartilage. The sustained release of CBD and magnesium ions exerted anti-inflammatory and analgesic effects alongside the regulation of autophagy and inhibition of chondrocyte aging. The in vitro and in vivo experiments highlighted ZCMC’s ability to enhance cartilage protection and matrix preservation, reduce inflammatory cytokines, improve gait function, mitigate joint damage, and prevent peripheral nerve demyelination. Transcriptome analysis revealed that ZCMC downregulates SCN9A expression in chondrocytes, inhibiting the Na v 1.7 channel to maintain cellular homeostasis and facilitate cartilage repair. Preclinical evaluation in human OA cartilage explants further demonstrated ZCMC’s efficacy in inhibiting explant degradation, restoring the mechanical properties of chondrocytes by modulating the Na v 1.7 channel, and thereby facilitating the recovery of their normal biological behavior, ultimately inhibiting OA progression. By targeting multiple pathological aspects simultaneously, ZCMC nanoparticles may offer a promising translational strategy for treating OA.
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