Sol-gel synthesis of magnesium oxide nanoparticles and their evaluation as a therapeutic agent for the treatment of osteoarthritis

被引:4
作者
Mei, Sen [1 ]
Jiang, Fangchao [2 ]
Liu, Na [1 ]
Feng, Zhizi [2 ]
Zheng, Yu [1 ]
Yang, Wei [2 ]
Zhang, Weizhong [2 ]
Cui, Yingna [3 ]
Wang, Weiming [1 ]
Xie, Jin [2 ]
Zhang, Nan [1 ]
机构
[1] Dalian Univ, Affiliated Xinhua Hosp, Dept Orthoped, Dalian 116000, Liaoning, Peoples R China
[2] Univ Georgia, Dept Chem, Athens, GA 30602 USA
[3] Dalian Univ, Dept Chem, Dalian 116000, Liaoning, Peoples R China
关键词
controlled release; magnesium oxide; nanoparticles; osteoarthritis; therapeutic agent; IN-VITRO; RELEASE; DEGRADATION; DELIVERY;
D O I
10.1080/17435889.2024.2382421
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Aim: We synthesized MgO NPs via sol-gel reaction and investigated them as carriers to deliver Mg2+ to the affected joint for osteoarthritis (OA). Materials & methods: The physicochemical properties of samples were characterized by transmission electron microscope (TEM), dynamic light scattering (DLS) and x-ray diffraction (XRD). The release of Mg2+ was monitored by ICP-MS. The potential cytotoxicity was evaluated using MTT assay. The efficacy and biosafety were evaluated in a rabbit OA model. Results: MgO NPs can prolong the Mg2+ release time from 0.5 h to 12 h. No significant cytotoxicity was observed when concentrations below 250 mu g/ml. Intra-articular samples could effectively alleviate the degeneration and destruction of the cartilage. Conclusion: this study demonstrates the potential of MgO NPs as a safe and effective treatment of OA. Simultaneously, the size of the particles may play a significant role in influencing the therapeutic outcome.
引用
收藏
页码:1867 / 1878
页数:12
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