基于透明质酸的微颗粒具有润滑和抗炎作用,可用于缓解颞下颌关节骨关节炎。

IF 8.1 Q1 ENGINEERING, BIOMEDICAL
Biomaterials research Pub Date : 2024-09-06 eCollection Date: 2024-01-01 DOI:10.34133/bmr.0073
Lei Liu, Gang He, Yixi Li, Yiwen Xian, Guixian He, Yonglong Hong, Chong Zhang, Decheng Wu
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引用次数: 0

摘要

颞下颌关节骨关节炎(TMJOA)的发病机制与机械摩擦密切相关,机械摩擦会导致炎症介质上调和关节软骨退化。可注射的药物负载微颗粒通过提供润滑和促进局部给药,在颞下颌关节疼痛的关节内治疗中引起了广泛的兴趣。本文开发的透明质酸基微粒具有出色的润滑性能、载药能力、抗氧化活性和抗炎效果,可用于治疗颞下颌关节疼痛。该微粒是由 3-氨基苯硼酸改性透明质酸(HP)在水溶液中通过疏水作用自组装而制备的,它可以通过动态硼酸酯键进一步包裹含二醇的药物。由此产生的微颗粒具有出色的注射性、润滑性、自由基清除效率和抗菌活性。此外,在体外氧化应激微环境下,载药微粒对软骨细胞具有良好的细胞保护作用。体内实验验证了关节内注射药物微颗粒能有效缓解骨质疏松症样损伤,抑制炎症反应,促进基质再生,从而治疗颞下颌关节肿胀。HP 微颗粒表现出优异的可注射性和对含二醇药物的包裹能力,突显了其作为多功能给药载体在颞下颌关节损伤关节内治疗中的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hyaluronic Acid-Based Microparticles with Lubrication and Anti-Inflammation for Alleviating Temporomandibular Joint Osteoarthritis.

The pathogenesis of temporomandibular joint osteoarthritis (TMJOA) is closely associated with mechanical friction, which leads to the up-regulation of inflammatory mediators and the degradation of articular cartilage. Injectable drug-loaded microparticles have attracted widespread interest in intra-articular treatment of TMJOA by providing lubrication and facilitating localized drug delivery. Herein, a hyaluronic acid-based microparticle is developed with excellent lubrication properties, drug loading capacity, antioxidant activity, and anti-inflammatory effect for the treatment of TMJOA. The microparticles are facilely prepared by the self-assembly of 3-aminophenylboronic acid-modified hyaluronic acid (HP) through hydrophobic interaction in an aqueous solution, which can further encapsulate diol-containing drugs through dynamic boronate ester bonds. The resulting microparticles demonstrate excellent injectability, lubrication properties, radical scavenging efficiency, and antibacterial activity. Additionally, the drug-loaded microparticles exhibit a favorable cytoprotective effect on chondrocyte cells in vitro under an oxidative stress microenvironment. In vivo experiments validate that intra-articular injection of drug-loaded microparticles effectively alleviates osteoporosis-like damage, suppresses inflammatory response, and facilitates matrix regeneration in the treatment of TMJOA. The HP microparticles demonstrate excellent injectability and encapsulation capacity for diol-containing drugs, highlighting its potential as a versatile drug delivery vehicle in the intra-articular treatment of TMJOA.

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