间充质干细胞
化学
骨关节炎
炎症
干细胞
癌症研究
体内
细胞内
再生医学
移植
软骨
药理学
糖胺聚糖
细胞
体外
明胶
细胞疗法
巨噬细胞
细胞生物学
自噬
活力测定
槲皮素
细胞培养
组织工程
软骨发生
细胞生长
离体
纳米纤维
药物输送
再生(生物学)
抗氧化剂
作者
Anwesha Mukherjee,Saswata Mitra,Nilangshuk Chaudhuri,Rupinder K Sodhi,Kaushik Mukherjee,Bodhisatwa Das
出处
期刊:Small
[Wiley]
日期:2026-02-20
卷期号:22 (23): e11555-e11555
标识
DOI:10.1002/smll.202511555
摘要
Osteoarthritis (OA) is a progressive, chronic disorder of the musculoskeletal system affecting more than 500 million individuals globally. Current treatment strategies primarily provide palliative care, with limited potential to alter disease progression or reverse tissue deterioration. Stem cell transplantation holds promising results. But poor cell retention and survival due to ROS and inflammation in OA lead to subpar therapeutic outcomes. In this study, we developed a dual-network gelatin methacrylate (GelMA) and κ-carrageenan-based injectable hydrogel loaded with antioxidant quercetin-PLGA nanoparticles for stem cell delivery to treat OA. Physicochemical studies demonstrated stable gelation, controlled degradation, and self-healing properties. In vitro studies revealed that the sustained release of quercetin effectively scavenged intracellular ROS, reduced the expression of pro-inflammatory factors such as IL6, COX2, NFκβ, and TNFα, and increased the expression of TGFβ, IL4, SOX9, COL2, and ACAN, which are responsible for inflammation control and cartilage tissue regeneration. The sustained release of nanoparticles also enhanced the M1-to-M2 macrophage transition and collagen II deposition. In vivo studies demonstrated that the nanoparticle-loaded stem cell-encapsulated hydrogel increased glycosaminoglycan deposition, reduced inflammation, and improved joint mobility and cartilage repair. Thus, this antioxidant hydrogel-based cell delivery system demonstrated suitability for OA therapy.
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