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

Nanomedicine (London, England) Pub Date : 2024-01-01 Epub Date: 2024-08-07 DOI:10.1080/17435889.2024.2382421
Sen Mei, Fangchao Jiang, Na Liu, Zhizi Feng, Yu Zheng, Wei Yang, Weizhong Zhang, Yingna Cui, Weiming Wang, Jin Xie, Nan Zhang
{"title":"Sol-gel synthesis of magnesium oxide nanoparticles and their evaluation as a therapeutic agent for the treatment of osteoarthritis.","authors":"Sen Mei, Fangchao Jiang, Na Liu, Zhizi Feng, Yu Zheng, Wei Yang, Weizhong Zhang, Yingna Cui, Weiming Wang, Jin Xie, Nan Zhang","doi":"10.1080/17435889.2024.2382421","DOIUrl":null,"url":null,"abstract":"<p><p><b>Aim:</b> We synthesized MgO NPs via sol-gel reaction and investigated them as carriers to deliver Mg<sup>2+</sup> to the affected joint for osteoarthritis (OA).<b>Materials & methods:</b> The physicochemical properties of samples were characterized by transmission electron microscope (TEM), dynamic light scattering (DLS) and x-ray diffraction (XRD). The release of Mg<sup>2+</sup> was monitored by ICP-MS. The potential cytotoxicity was evaluated using MTT assay. The efficacy and biosafety were evaluated in a rabbit OA model.<b>Results:</b> MgO NPs can prolong the Mg<sup>2+</sup> release time from 0.5 h to 12 h. No significant cytotoxicity was observed when concentrations below 250 μg/ml. Intra-articular samples could effectively alleviate the degeneration and destruction of the cartilage.<b>Conclusion:</b> 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.</p>","PeriodicalId":74240,"journal":{"name":"Nanomedicine (London, England)","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11457622/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nanomedicine (London, England)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/17435889.2024.2382421","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/8/7 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

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 μg/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.

氧化镁纳米粒子的溶胶凝胶合成及其作为骨关节炎治疗剂的评估。
目的:我们通过溶胶-凝胶反应合成了氧化镁 NPs,并研究了将其作为载体将 Mg2+ 输送到受影响关节以治疗骨关节炎(OA)。材料与方法:透射电子显微镜(TEM)、动态光散射(DLS)和 X 射线衍射(XRD)对样品的理化性质进行了表征。ICP-MS 监测了 Mg2+ 的释放。使用 MTT 试验评估了潜在的细胞毒性。在兔 OA 模型中评估了药效和生物安全性。研究结果当浓度低于 250 μg/ml 时,未观察到明显的细胞毒性。关节内样本可有效缓解软骨的退化和破坏。结论:本研究表明氧化镁氧化物具有安全有效治疗 OA 的潜力。同时,颗粒的大小可能会对治疗效果产生重要影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信