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通过胶原蛋白水凝胶实现二氧化铈和氧化铁纳米颗粒的控释以增强骨关节炎治疗

Controlled Release of Ceria and Ferric Oxide Nanoparticles via Collagen Hydrogel for Enhanced Osteoarthritis Therapy.

作者信息

Chen Xian, Wang Lili, Zhang Jingting, Yan Huiyu, Wang Shenghong, Xiao Jianxi

机构信息

State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou, 730000, P. R. China.

Gansu Engineering Research Center of Medical Collagen, Lanzhou, 730000, P. R. China.

出版信息

Adv Healthc Mater. 2024 Dec;13(32):e2401507. doi: 10.1002/adhm.202401507. Epub 2024 Jul 27.

DOI:10.1002/adhm.202401507
PMID:39073018
Abstract

Osteoarthritis (OA), characterized by chronic inflammation and cartilage degeneration, significantly affects over 500 million people globally. Nanoparticles have emerged as promising treatments for OA; however, current strategies often employ a single type of nanoparticle targeting specific disease stages, limiting sustained therapeutic efficacy. In this study, a novel collagen hydrogel is introduced, thiol crosslinked collagen-cerium oxide-poly(D,L-lactic-co-glycolic acid) microspheres encapsulating nanoparticles (CSH-CeO-pFeO), designed for the controlled release of cerium oxide (CeO) and ferric oxide (FeO) nanoparticles for comprehensive OA management. The sulfhydryl cross-linked collagen matrix embeds CeO nanoparticles and poly(D,L-lactic-co-glycolic acid) (PLGA) microspheres encapsulating FeO nanoparticles. The CSH-CeO-pFeO hydrogel exhibits enhanced mechanical strength and remarkable injectability, along with a significant promotion of cell adhesion, proliferation, and chondrogenic differentiation. Notably, the hydrogel demonstrates intelligent responsiveness to high levels of reactive oxygen species, initiating the rapid release of CeO nanoparticles to address the intense inflammatory responses of early-stage OA, followed by the sustained release of FeO nanoparticles to facilitate cartilage regeneration during the proliferative phase. In a rat model with cartilage defects, the hydrogel significantly alleviates inflammation and enhances cartilage regeneration, holding substantial potential for effectively managing the pathologically complex OA.

摘要

骨关节炎(OA)以慢性炎症和软骨退变为特征,全球有超过5亿人受到其严重影响。纳米颗粒已成为治疗OA的有前景的方法;然而,目前的策略通常采用单一类型的纳米颗粒靶向特定疾病阶段,限制了持续的治疗效果。在本研究中,引入了一种新型胶原蛋白水凝胶,即巯基交联的包裹纳米颗粒的胶原-氧化铈-聚(D,L-乳酸-共-乙醇酸)微球(CSH-CeO-pFeO),设计用于氧化铈(CeO)和氧化铁(FeO)纳米颗粒的控释,以全面管理OA。巯基交联的胶原基质嵌入CeO纳米颗粒和包裹FeO纳米颗粒的聚(D,L-乳酸-共-乙醇酸)(PLGA)微球。CSH-CeO-pFeO水凝胶具有增强的机械强度和显著的可注射性,同时显著促进细胞粘附、增殖和软骨生成分化。值得注意的是,该水凝胶对高水平的活性氧具有智能响应性,可启动CeO纳米颗粒的快速释放以应对早期OA的强烈炎症反应,随后持续释放FeO纳米颗粒以促进增殖期的软骨再生。在软骨缺损的大鼠模型中,该水凝胶显著减轻炎症并增强软骨再生,在有效管理病理复杂的OA方面具有巨大潜力。

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