Ke Re Mu A Li Mu, Liang Zhi Lin, Chen Linlin, Tu Xun Ai Ke Bai Er, A Bu Li Ke Mu Mai Mai Ti Ai Li, Wu Yuan Quan
Orthopedics Center, First People's Hospital of Kashgar, Kashgar 844000, Xinjiang, China.
Nanjing Genebios Biotechnology Co., Ltd., Nanjing 21100, China.
Biomed Pharmacother. 2024 Mar;172:116228. doi: 10.1016/j.biopha.2024.116228. Epub 2024 Feb 5.
Linezolid has been reported to protect against chronic bone and joint infection. In this study, linezolid was loaded into the 3D printed poly (lactic-co-glycolic acid) (PLGA) scaffold with nano-hydroxyapatite (HA) to explore the effect of this composite scaffold on infected bone defect (IBD).
PLGA scaffolds were produced using the 3D printing method. Drug release of linezolid was analyzed by elution and high-performance liquid chromatography assay. PLGA, PLGA-HA, and linezolid-loaded PLGA-HA scaffolds, were implanted into the defect site of a rabbit radius defect model. Micro-CT, H&E, and Masson staining, and immunohistochemistry were performed to analyze bone infection and bone healing. Evaluation of viable bacteria was performed. The cytocompatibility of 3D-printed composite scaffolds in vitro was detected using human bone marrow mesenchymal stem cells (BMSCs). Long-term safety of the scaffolds in rabbits was evaluated.
The linezolid-loaded PLGA-HA scaffolds exhibited a sustained release of linezolid and showed significant antibacterial effects. In the IBD rabbit models implanted with the scaffolds, the linezolid-loaded PLGA-HA scaffolds promoted bone healing and attenuated bone infection. The PLGA-HA scaffolds carrying linezolid upregulated the expression of osteogenic genes including collagen I, runt-related transcription factor 2, and osteocalcin. The linezolid-loaded PLGA-HA scaffolds promoted the proliferation and osteogenesis of BMSCs in vitro via the PI3K/AKT pathway. Moreover, the rabbits implanted with the linezolid-loaded scaffolds showed normal biochemical profiles and normal histology, which suggested the safety of the linezolid-loaded scaffolds.
Overall, the linezolid-loaded PLGA-HA scaffolds fabricated by 3D printing exerts significant bone repair and anti-infection effects.
据报道,利奈唑胺可预防慢性骨与关节感染。在本研究中,将利奈唑胺负载于含纳米羟基磷灰石(HA)的3D打印聚乳酸-乙醇酸共聚物(PLGA)支架中,以探究该复合支架对感染性骨缺损(IBD)的影响。
采用3D打印方法制备PLGA支架。通过洗脱和高效液相色谱法分析利奈唑胺的药物释放情况。将PLGA、PLGA-HA和负载利奈唑胺的PLGA-HA支架植入兔桡骨缺损模型的缺损部位。进行显微CT、苏木精-伊红(H&E)染色、Masson染色和免疫组织化学分析以评估骨感染和骨愈合情况。对活菌进行评估。使用人骨髓间充质干细胞(BMSC)检测3D打印复合支架在体外的细胞相容性。评估支架在兔体内的长期安全性。
负载利奈唑胺的PLGA-HA支架表现出利奈唑胺的持续释放,并显示出显著的抗菌效果。在植入该支架的IBD兔模型中,负载利奈唑胺的PLGA-HA支架促进了骨愈合并减轻了骨感染。负载利奈唑胺的PLGA-HA支架上调了包括I型胶原蛋白、 runt相关转录因子2和骨钙素在内的成骨基因的表达。负载利奈唑胺的PLGA-HA支架在体外通过PI3K/AKT途径促进了BMSC的增殖和成骨。此外,植入负载利奈唑胺支架的兔生化指标和组织学正常,这表明负载利奈唑胺支架的安全性。
总体而言,通过3D打印制备的负载利奈唑胺的PLGA-HA支架具有显著的骨修复和抗感染作用。