Osteoarthritis (OA) is a chronic joint disease characterized by degenerative changes in articular cartilage and chronic inflammation. Recent studies suggest that intra-articular (i.a.) injection of magnesium salts holds promise as a therapeutic approach for OA. However, the rapid diffusion of magnesium ions limits their efficacy, resulting in a short duration of action. To overcome this limitation, we developed a nanoparticle delivery system using MgO@SiO(2) core/shell nanoparticles, designed as a depot for the controlled release of magnesium ions. Electron microscopy confirmed the formation of the core/shell structure with silica shells of varying thickness. Release studies demonstrated that the silica coating effectively slows nanoparticle degradation, extending magnesium release to over 72 hours. In a rabbit OA model, i.a. injection of these nanocapsules significantly mitigated the pathological progression of OA within four weeks without inducing systemic toxicity. Immunohistochemical analysis further revealed that MgO@SiO(2) nanocapsules alleviate the inflammatory response in OA cartilage by inhibiting the NF-κB/p65 signaling pathway. In summary, this study confirms the potential of intra-articular magnesium supplementation as a therapeutic option for OA and introduces a novel approach to enhance the delivery and efficacy of magnesium ions in OA treatment, addressing a relatively underexplored area in the field.
MgO@SiO(2) nanocapsules: a controlled magnesium ion release system for targeted inhibition of osteoarthritis progression.
MgO@SiO(2)纳米胶囊:一种可控镁离子释放系统,用于靶向抑制骨关节炎的进展
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作者:Liu Na, Jiang Fangchao, Feng Zhizi, Mei Sen, Cui Yingna, Zheng Yu, Yang Wei, Wang Benjie, Zhang Weizhong, Xie Jin, Zhang Nan
| 期刊: | Nanoscale Advances | 影响因子: | 4.600 |
| 时间: | 2025 | 起止号: | 2025 Jan 21; 7(7):1814-1824 |
| doi: | 10.1039/d4na00900b | 研究方向: | 免疫/内分泌 |
| 疾病类型: | 关节炎 | ||
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