药物输送
化学
咪唑酯
骨关节炎
自愈水凝胶
纳米颗粒
细胞内
沸石咪唑盐骨架
纳米技术
氧化应激
生物物理学
金属有机骨架
材料科学
医学
生物化学
高分子化学
有机化学
病理
吸附
生物
替代医学
作者
Han Ye,Peng Ren,Xuekang Pan,Xinyu Zhang,Jun Ma,Jiayi Chen,Jian Sheng,Huanhuan Luo,Huigen Lu,Gang Chen
出处
期刊:Pharmaceutics
[Multidisciplinary Digital Publishing Institute]
日期:2023-02-22
卷期号:15 (3): 724-724
被引量:1
标识
DOI:10.3390/pharmaceutics15030724
摘要
Treatment of osteoarthritis (OA) remains a significant clinical challenge. Itaconate (IA), an emerging regulator of intracellular inflammation and oxidative stress, may potentially be harnessed to treat OA. However, the short joint residence time, inefficient drug delivery, and cell-impermeable property of IA can seriously hamper the clinical translation. Herein, IA-encapsulated zeolitic imidazolate framework-8 (IA-ZIF-8) nanoparticles were self-assembled by zinc ions, 2-methylimidazole, and IA to render them pH-responsive. Subsequently, IA-ZIF-8 nanoparticles were firmly immobilized in hydrogel microspheres via one-step microfluidic technology. It was demonstrated in vitro experiments that IA-ZIF-8-loaded hydrogel microspheres (IA-ZIF-8@HMs) exhibited good anti-inflammatory and anti-oxidative stress effects by releasing pH-responsive nanoparticles into chondrocytes. Importantly, compared with IA-ZIF-8, IA-ZIF-8@HMs showed better performance in the treatment of OA due to their superior performance in sustained release. Thus, such hydrogel microspheres not only hold enormous potential for OA therapy, but also provide a novel avenue for cell-impermeable drugs by constructing appropriate drug delivery systems.
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