Yang Qiao, Li Jianfeng, Meng Hongfang, Wang Yongdi, Hu Lanlan, Su Weiwei, Xu Jie, Hou Juedong, Zhao Rui, Wang Zihan, Zhang Kairui, Wu Yaobin, Wang Ling
Biomaterials Research Center, School of Biomedical Engineering, Southern Medical University, Guangzhou, 510515, China.
Guangdong Provincial Key Laboratory of Digital Medicine and Biomechanics, Department of Human Anatomy, School of Basic Medical Sciences, Southern Medical University, Guangzhou, 510515, China.
Adv Healthc Mater. 2025 Jan;14(1):e2402074. doi: 10.1002/adhm.202402074. Epub 2024 Nov 26.
Tendon injuries often exhibit limited healing capacity, frequently complicated by peritendinous adhesion, posing a substantial challenge in clinical tendon repair. Although present biomaterial-based membranes offer a promising strategy for tendon treatment, their clinical application is hindered by inflammation-induced adhesion. Herein, this study presents a dual-functional biomimetic tendon sheath based on a coaxial electrospun nanofibrous membrane for enhancing tendon repair and simultaneously preventing peritendinous adhesion. This nanofibrous membrane is fabricated using a coaxial electrospinning method, encapsulating celecoxib-loaded polycaprolactone (PCL) within gelatin methacryloyl (GelMA) shell. Both in vitro and in vivo analysis results demonstrated that such coaxial biomimetic tendon sheath enhanced tenogenic differentiation of tendon stem/progenitor cells (TSPCs) due to nanofibrous GelMA shell providing a suitable microenvironment surface. Simultaneously, the sustained release of celecoxib (CEL) from the core is able to significantly decrease the expression of inflammatory cytokines. Notably, in vivo assessments in animal models with patellar tendon defects revealed significant reductions in peritendinous adhesion, leading to further enhancement in tendon repair. These results underscore the potential of the coaxial nanofibrous membrane as a dual-functional biomimetic tendon sheath, offering a promising avenue for the long-term management of tendon injuries.
肌腱损伤通常表现出有限的愈合能力,常因腱周粘连而复杂化,这给临床肌腱修复带来了巨大挑战。尽管目前基于生物材料的膜为肌腱治疗提供了一种有前景的策略,但其临床应用受到炎症诱导粘连的阻碍。在此,本研究提出了一种基于同轴电纺纳米纤维膜的双功能仿生腱鞘,用于增强肌腱修复并同时预防腱周粘连。这种纳米纤维膜采用同轴电纺方法制备,将负载塞来昔布的聚己内酯(PCL)包裹在甲基丙烯酰化明胶(GelMA)壳内。体外和体内分析结果均表明,这种同轴仿生腱鞘由于纳米纤维GelMA壳提供了合适的微环境表面,增强了肌腱干/祖细胞(TSPCs)的腱向分化。同时,塞来昔布(CEL)从核心的持续释放能够显著降低炎性细胞因子的表达。值得注意的是,在髌腱缺损动物模型中的体内评估显示腱周粘连显著减少,从而进一步增强了肌腱修复。这些结果强调了同轴纳米纤维膜作为双功能仿生腱鞘的潜力,为肌腱损伤的长期管理提供了一条有前景的途径。