Gao Wenyan, Li Shaochun, Miao Ya, Yuan Guangfu, Li Gaoyang, Zhou Guoqiang, Jia Guang, Yang Xinjian, Jin Yi
College of Basic Medical Science, Key Laboratory of Pathogenesis Mechanism and Control of Inflammatory-autoimmune Diseases of Hebei Province, State Key Laboratory of New Pharmaceutical Preparations and Excipients, Key Laboratory of Medicinal Chemistry and Molecular Diagnosis of the Ministry of Education, Hebei University, Baoding 071002, PR China.
Department of Orthopedics, Affiliated Hospital of Hebei University, Baoding 071002, PR China.
J Colloid Interface Sci. 2025 Sep;693:137612. doi: 10.1016/j.jcis.2025.137612. Epub 2025 Apr 15.
Osteoarthritis (OA), a degenerative joint disease, is characterized by chondrocyte senescence, extracellular matrix (ECM) degradation, and chronic inflammation, with limited regenerative capacity. Current therapies primarily provide symptom relief, therefore highlighting the need for more effective strategies to address OA's multifactorial pathology. This study introduces an innovative selenium nanozyme-crosslinked injectable composite hydrogel (Se/PRP-OGel), which combines selenium nanoparticles (SeNPs) with platelet-rich plasma (PRP) in a biocompatible oxidized chondroitin sulfate-gelatin scaffold (OGel), to address OA through an integrated "outside-in" and "inside-out" strategy. The "outside-in" strategy utilizes SeNPs to scavenge reactive oxygen species (ROS), alleviate oxidative stress, and restore redox balance, thereby reducing extracellular damage and modulating inflammation in the OA microenvironment. Concurrently, the "inside-out" strategy utilizes PRP's bioactive growth factors (e.g., TGF-β, IGF, FGF) to rejuvenate senescent chondrocytes, stimulate proliferation, and enhance ECM synthesis, creating a regenerative microenvironment. The results showed that Se/PRP-OGel demonstrated excellent biocompatibility, reduced ROS levels, mitigated chondrocyte senescence, and balanced ECM homeostasis. Moreover, it promoted cartilage repair, pain relief, and functional restoration in an OA rat model. This dual approach interrupts OA's degenerative cycle and fosters cartilage regeneration, providing a groundbreaking solution for effective cartilage regeneration and OA treatment.
骨关节炎(OA)是一种退行性关节疾病,其特征在于软骨细胞衰老、细胞外基质(ECM)降解和慢性炎症,再生能力有限。目前的治疗主要是缓解症状,因此凸显了需要更有效的策略来解决OA的多因素病理问题。本研究引入了一种创新的硒纳米酶交联可注射复合水凝胶(Se/PRP-OGel),它将硒纳米颗粒(SeNPs)与富含血小板血浆(PRP)结合在生物相容性氧化硫酸软骨素-明胶支架(OGel)中,通过综合的“由外而内”和“由内而外”策略来解决OA问题。“由外而内”策略利用SeNPs清除活性氧(ROS)、减轻氧化应激并恢复氧化还原平衡,从而减少细胞外损伤并调节OA微环境中的炎症。同时,“由内而外”策略利用PRP的生物活性生长因子(如TGF-β、IGF、FGF)使衰老的软骨细胞恢复活力、刺激增殖并增强ECM合成,营造一个再生微环境。结果表明,Se/PRP-OGel表现出优异的生物相容性,降低了ROS水平,减轻了软骨细胞衰老,并平衡了ECM稳态。此外,它促进了OA大鼠模型中的软骨修复、疼痛缓解和功能恢复。这种双重方法中断了OA的退行性周期并促进了软骨再生,为有效的软骨再生和OA治疗提供了一种开创性的解决方案。