Li Guangjie, He Fei, Feng Jianbao, Xu Ge, Wu Chengye, Qiao Yufei, Liu Yang, Chen Hanlin, Du Pengcheng, Wang Jizeng
The First Hospital of Lanzhou University, Lanzhou, Gansu Province, People's Republic of China.
College of Civil Engineering and Mechanics, Lanzhou University, Lanzhou, Gansu Province, People's Republic of China.
Int J Nanomedicine. 2025 Jan 29;20:1133-1145. doi: 10.2147/IJN.S496827. eCollection 2025.
Osteoarthritis (OA), a prevalent joint disease, causes immense suffering to thousands of patients, impairing their mobility and diminishing their quality of life. Current treatment methods primarily rely on analgesics or anti-inflammatory drugs to alleviate symptoms but fail to achieve the desired therapeutic outcome.
To better realize therapeutic effects of OA, procyanidins (PAs), as a type of plant flavonoids with strong antioxidant and anti-inflammatory activities, were designed to self-assembly with well-dispersible Pluronic F127 (PF127) through the hydrogen-bond interaction to present an injectable, biocompatibility PA nanospheres.
These nanospheres significantly increased the cell viability in mouse L929 fibroblasts and ADTC5 chondrocytes compared with unassembled PAs. In addition, the self-assembling PAs/PF127 nanospheres enhanced the protein expression of collagen (COL1A1 and COL3A1) in fibroblasts, and the expression of glycosaminoglycan and COL2A1 was also higher than unassembled PAs in chondrocytes, this heralded the potential to achieve OA repair strategies at the cellular level. In an enzymolysis model of rat OA, PAs/PF127 nanospheres significantly reduce joint space swelling in the early stages of cartilage destruction and accelerate the formation of subchondral bone and cartilaginous surface.
This study offers valuable insights into the preparation of novel PA nanospheres for effective repair of OA.
骨关节炎(OA)是一种常见的关节疾病,给成千上万的患者带来巨大痛苦,损害他们的行动能力并降低生活质量。目前的治疗方法主要依靠镇痛药或抗炎药来缓解症状,但未能达到理想的治疗效果。
为了更好地实现OA的治疗效果,原花青素(PAs)作为一种具有强大抗氧化和抗炎活性的植物黄酮类化合物,通过氢键相互作用与可良好分散的泊洛沙姆F127(PF127)自组装,以呈现可注射的、具有生物相容性的PA纳米球。
与未组装的PAs相比,这些纳米球显著提高了小鼠L929成纤维细胞和ADTC5软骨细胞的细胞活力。此外,自组装的PAs/PF127纳米球增强了成纤维细胞中胶原蛋白(COL1A1和COL3A1)的蛋白表达,软骨细胞中糖胺聚糖和COL2A1的表达也高于未组装的PAs,这预示着在细胞水平实现OA修复策略的潜力。在大鼠OA的酶解模型中,PAs/PF127纳米球在软骨破坏的早期显著减轻关节间隙肿胀,并加速软骨下骨和软骨表面的形成。
本研究为制备用于有效修复OA的新型PA纳米球提供了有价值的见解。