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
相关论文
共 31 条
  • [21] Sturgeon cartilage-derived chondroitin sulfate exhibited anti-inflammatory activity against dextran sulfate sodium-induced colitis via modification of gut microbiota
    Ruiyun Wu
    Zixin Han
    Zhenyu Wang
    Pinglan Li
    Nan Shang
    Food Science and Human Wellness, 2025, 14 (04) : 1239 - 1250
  • [22] Gallic acid-selenium nanoparticles with dual anti-inflammatory and antioxidant functions for synergistic treatment of acute kidney injury
    Zhou, Jie
    Guan, Min
    Ma, Huili
    Dong, Xiaomeng
    Feng, Junfen
    Zhang, Tong
    Wei, Yuxin
    NANOMEDICINE-NANOTECHNOLOGY BIOLOGY AND MEDICINE, 2024, 62
  • [23] Chondroitin sulfate-functionalized lipid nanoreservoirs: a novel cartilage-targeting approach for intra-articular delivery of cassic acid for osteoarthritis treatment
    Ebada, Heba M. K.
    Nasra, Maha M. A.
    Nassra, Rasha A.
    Abdallah, Ossama Y.
    DRUG DELIVERY, 2022, 29 (01) : 652 - 663
  • [24] An anti-inflammatory chondroitin sulfate-poly(lactic-co-glycolic acid) composite electrospinning membrane for postoperative abdominal adhesion prevention
    Gao, Rui
    Li, Fenghui
    Zhang, Yushan
    Kong, Pengxu
    Gao, Yu
    Wang, Jingrong
    Liu, Xiang
    Li, Shuangyang
    Jiang, Liqin
    Zhang, Ju
    Zhang, Chuangnian
    Feng, Zujian
    Huang, Pingsheng
    Wang, Weiwei
    BIOMATERIALS SCIENCE, 2023, 11 (19) : 6573 - 6586
  • [25] Possible synergic action of non-steroidal anti-inflammatory drugs and glucosamine sulfate for the treatment of knee osteoarthritis: a scoping review
    Nicola Veronese
    Fiona Ecarnot
    Sara Cheleschi
    Antonella Fioravanti
    Stefania Maggi
    BMC Musculoskeletal Disorders, 23
  • [26] Possible synergic action of non-steroidal anti-inflammatory drugs and glucosamine sulfate for the treatment of knee osteoarthritis: a scoping review
    Veronese, Nicola
    Ecarnot, Fiona
    Cheleschi, Sara
    Fioravanti, Antonella
    Maggi, Stefania
    BMC MUSCULOSKELETAL DISORDERS, 2022, 23 (01)
  • [27] Grafting of sinapic acid onto glucosamine nanoparticle as a potential therapeutic drug with enhanced anti-inflammatory activities in osteoarthritis treatment
    Tajik, Ehteram
    Vaezi, Zahra
    Tabarsa, Mehdi
    Hekmat, Azadeh
    Naderi-Manesh, Hossein
    INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2023, 253
  • [28] Cost-Effectiveness of Glucosamine, Chondroitin Sulfate, Their Combination, Celecoxib, Non-Selective Non-Steroidal Anti-Inflammatory Drugs, and Placebo in Treating Knee Osteoarthritis.
    Garg, Vishvas
    Raisch, Dennis
    Gu, Ning Yan
    Borrego, Matthew E.
    Clegg, Daniel O.
    ARTHRITIS & RHEUMATOLOGY, 2014, 66 : S971 - S971
  • [29] Tannic acid/Sr2+-coated silk/graphene oxide-based meniscus scaffold with anti-inflammatory and anti-ROS functions for cartilage protection and delaying osteoarthritis
    Li, Yangyang
    Chen, Mingxue
    Yan, Jianglong
    Zhou, Wenhao
    Gao, Shuang
    Liu, Shuyun
    Li, Qiyao
    Zheng, Yufeng
    Cheng, Yan
    Guo, Quanyi
    ACTA BIOMATERIALIA, 2021, 126 : 119 - 131
  • [30] Intra-articular hyaluronic acid injection versus oral non-steroidal anti-inflammatory drug for the treatment of knee osteoarthritis: a multi-center, randomized, open-label, non-inferiority trial
    Muneaki Ishijima
    Toshitaka Nakamura
    Katsuji Shimizu
    Kunihiko Hayashi
    Hiraku Kikuchi
    Satoshi Soen
    Go Omori
    Toshihiko Yamashita
    Yuji Uchio
    Junji Chiba
    Yuki Ideno
    Mitsuaki Kubota
    Hisashi Kurosawa
    Kazuo Kaneko
    Arthritis Research & Therapy, 16