Injectable polymeric nanoparticle hydrogel system for long-term anti-inflammatory effect to treat osteoarthritis

骨关节炎 曲安奈德 水溶液 纳米颗粒 软骨 化学 药品 两亲性 药物输送 材料科学 聚合物 生物医学工程 控制释放 药理学 外科 纳米技术 医学 有机化学 病理 共聚物 替代医学 解剖
作者
Bo‐Bae Seo,Youngjoong Kwon,Jun Kim,Ki Hyun Hong,Sung Eun Kim,Hae‐Ryong Song,Young‐Min Kim,Soo‐Chang Song
出处
期刊:Bioactive Materials [Elsevier BV]
卷期号:7: 14-25 被引量:103
标识
DOI:10.1016/j.bioactmat.2021.05.028
摘要

Treatment of osteoarthritis (OA) by administration of corticosteroids is a commonly used method in clinics using anti-inflammatory medicine. Oral administration or intra-articular injection of corticosteroids can reduce the pain and progress of cartilage degeneration, but they are usually insufficient to show local and long-term anti-inflammatory effects because of their fast clearance in the body. In this study, we suggest an injectable anti-OA drug depot system for sustained drug release that provides long-term effective therapeutic advantages. Amphiphilic poly(organophosphazene), which has temperature-dependent nanoparticle forming and sol-gel transition behaviors when dissolved in aqueous solution, was synthesized for triamcinolone acetonide (TCA) delivery. Because hydrophobic parts of the polymer can interact with hydrophobic parts of the TCA, the TCA was encapsulated into the self-assembled polymeric nanoparticles. The TCA-encapsulated polymeric nanoparticles (TePNs) were well dispersed in an aqueous solution below room temperature so that they can be easily injected as a sol state into an intra-articular region. However, the TePNs solution transforms immediately to a viscose 3D hydrogel like a synovial fluid in the intra-articular region via the conducted body temperature. An in vitro TCA release study showed sustained TCA release for six weeks. One-time injection of the TePN hydrogel system in an early stage of OA-induced rat model showed a great inhibition effect against further OA progression. The OA-induced knees completely recovered as a healthy cartilage without any abnormal symptoms.
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