Du Wei, Gong Jiang-Shan, Chen Xia, Wu Yang, Yang Yu, Zhu Sheng, Zhang Yu, Chen Bei, Liu Yi-Wei, He Ze-Hui, Guan Zhe, Zhang Yan, Wang Zhen-Xing, Xie Hui
Department of Orthopaedics, Movement System Injury and Repair Research Centre, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Hunan Key Laboratory of Angmedicine, Changsha, Hunan, China.
Biomater Transl. 2025 Mar 25;6(1):85-102. doi: 10.12336/biomatertransl.2025.01.007. eCollection 2025.
Orthopedic implant-associated infections pose a significant clinical challenge, often requiring surgical intervention along with systemic antibiotic treatments. To address this issue, we developed a novel approach using Ångstrom-scale silver particles (AgÅPs) with broad-spectrum antibacterial properties. Specifically, we formulated a polyethylene glycol hydrogel infused with AgÅPs (Gel-AgÅPs) designed for treating fracture fixation infections. This novel hydrogel formulation is injectable, ensuring precise adherence to both the exposed tissue and fracture surfaces, thereby allowing the direct targeted action of AgÅPs at the infection site. The Gel-AgÅPs significantly reduced the infection caused by Escherichia coli (a model pathogen of orthopedic implant infection) in a murine femoral fracture model. Moreover, the Gel-AgÅPs-treated infected fractures healed completely within 6 weeks, exhibiting bone formation and mechanical strength comparable to those of uninfected fractures. Further analysis revealed a significant downregulation of local inflammatory response as evidenced by a lower expression of inflammatory markers in Gel-AgÅPs-treated fractures compared to untreated infected controls. Furthermore, Gel-AgÅPs exhibited a unique ability to inhibit osteoclast differentiation, a critical factor in infection-induced bone degradation, without impacting osteoblast activity. In conclusion, Gel-AgÅPs exerted a dual therapeutic effect by eradicating bacterial infection and mitigating inflammation-induced osteoclast activity, thereby expediting infected fracture healing. This innovative approach is a promising therapeutic alternative to conventional antibiotic treatments, potentially transforming the treatment landscape for orthopedic implant-associated infections.
骨科植入物相关感染带来了重大的临床挑战,通常需要手术干预以及全身性抗生素治疗。为了解决这个问题,我们开发了一种使用具有广谱抗菌特性的埃级银颗粒(AgÅPs)的新方法。具体而言,我们配制了一种注入AgÅPs的聚乙二醇水凝胶(Gel-AgÅPs),用于治疗骨折固定感染。这种新型水凝胶制剂是可注射的,可确保精确附着于暴露的组织和骨折表面,从而使AgÅPs能够在感染部位直接发挥靶向作用。在小鼠股骨骨折模型中,Gel-AgÅPs显著降低了由大肠杆菌(骨科植入物感染的模型病原体)引起的感染。此外,经Gel-AgÅPs治疗的感染性骨折在6周内完全愈合,其骨形成和机械强度与未感染的骨折相当。进一步分析显示,与未治疗的感染对照组相比,Gel-AgÅPs治疗的骨折中炎症标志物表达较低,这表明局部炎症反应显著下调。此外,Gel-AgÅPs表现出独特的抑制破骨细胞分化的能力,破骨细胞分化是感染诱导的骨降解的关键因素,而不会影响成骨细胞活性。总之,Gel-AgÅPs通过消除细菌感染和减轻炎症诱导的破骨细胞活性发挥双重治疗作用,从而加速感染性骨折的愈合。这种创新方法是传统抗生素治疗的一种有前景的替代疗法,可能会改变骨科植入物相关感染的治疗格局。