Injectable Chondroitin Sulfate Microspheres with Gallic Acid-Magnesium MOF for Anti-Inflammatory and Cartilage Degeneration Alleviation in Osteoarthritis Treatment

被引:0
|
作者
He, Jiachen [1 ,2 ]
Wu, Jianjun [1 ,2 ]
Zheng, Jingcheng [1 ,2 ]
Xu, Yidan [5 ]
Li, Keyun [1 ]
Yin, Siwei [1 ,2 ]
Liu, Yanyun [1 ]
Hu, Yuelin [3 ]
Xie, Chaoming [3 ]
Cai, Limin [1 ,2 ,4 ]
Du, Yikuan [1 ,2 ,4 ]
Lu, Xiong [1 ,2 ,3 ]
机构
[1] Southern Med Univ, Affiliated Hosp 10, Dongguan Peoples Hosp, Dongguan 523059, Peoples R China
[2] Southern Med Univ, Sch Clin Med 1, Guangzhou 510515, Peoples R China
[3] Southwest Jiaotong Univ, Inst Biomed Engn, Coll Med, Chengdu 610031, Sichuan, Peoples R China
[4] Dongguan Key Lab Translat Med & Innovat Drugs, Dongguan 523059, Peoples R China
[5] Anhui Med Univ, Affiliated Hosp 1, Dept Oncol, Hefei 230022, Anhui, Peoples R China
关键词
metal-organicframeworks; microspheres; osteoarthritis; anti-inflammation; cartilage degeneration; INFLAMMATION; PROGRESSION; CHONDROCYTES; PLAY;
D O I
10.1021/acsami.4c22415
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Inflammation and cartilage degeneration are critical challenges in osteoarthritis (OA) treatment. Achieving sustained drug efficacy while mitigating the adverse effects of inflammation and reactive oxygen species remains a significant challenge. This study synthesizes a gallic acid-magnesium (GA-Mg) metal-organic framework (MOF) as a drug carrier for puerarin (PA). The PA-loaded GA-Mg MOF (pGM) is encapsulated within chondroitin sulfate methacrylate, forming monodisperse hybrid microspheres (CM@pGM) under ultraviolet light using microfluidic technology. The pGM is physically confined within the microspheres through a network of structural obstructions and noncovalent interactions. During degradation, GA and Mg2+ ions release from pGM, improving the inflammatory microenvironment of the articular cavity and mitigating oxidative stress. The sustained release of Mg2+ and PA supports chondrocyte anabolism and facilitates cartilage repair. In vitro studies confirm that injectable microspheres extend the drug release period to over 2 weeks. In vivo experiments demonstrate that CM@pGM significantly reduces osteophyte formation, alleviates degenerative changes in articular cartilage, and delays OA progression. In conclusion, CM@pGM, as a drug delivery platform that ameliorates the inflammatory microenvironment, alleviates oxidative stress, and promotes cartilage repair, holds significant potential for OA treatment.
引用
收藏
页码:11898 / 11910
页数:13
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