脚手架
抗菌剂
间充质干细胞
血管生成
材料科学
拮抗剂
体内
小RNA
生物医学工程
癌症研究
细胞生物学
医学
生物
微生物学
生物技术
生物化学
基因
作者
Joanna M. Sadowska,Rachael N. Power,Katelyn J. Genoud,Austyn Matheson,Arlyng González‐Vázquez,Lara S. Costard,Kian F. Eichholz,Pierluca Pitacco,Tanguy Hallegouet,Gang Chen,Caroline M. Curtin,Ciara M. Murphy,Brenton Cavanagh,Huijun Zhang,Daniel J. Kelly,Aldo R. Boccaccını,Fergal J. O’Brien
标识
DOI:10.1002/adma.202307639
摘要
Treating bone infections and ensuring bone repair is one of the greatest global challenges of modern orthopedics, made complex by antimicrobial resistance (AMR) risks due to long-term antibiotic treatment and debilitating large bone defects following infected tissue removal. An ideal multi-faceted solution would will eradicate bacterial infection without long-term antibiotic use, simultaneously stimulating osteogenesis and angiogenesis. Here, a multifunctional collagen-based scaffold that addresses these needs by leveraging the potential of antibiotic-free antimicrobial nanoparticles (copper-doped bioactive glass, CuBG) to combat infection without contributing to AMR in conjunction with microRNA-based gene therapy (utilizing an inhibitor of microRNA-138) to stimulate both osteogenesis and angiogenesis, is developed. CuBG scaffolds reduce the attachment of gram-positive bacteria by over 80%, showcasing antimicrobial functionality. The antagomiR-138 nanoparticles induce osteogenesis of human mesenchymal stem cells in vitro and heal a large load-bearing defect in a rat femur when delivered on the scaffold. Combining both promising technologies results in a multifunctional antagomiR-138-activated CuBG scaffold inducing hMSC-mediated osteogenesis and stimulating vasculogenesis in an in vivo chick chorioallantoic membrane model. Overall, this multifunctional scaffold catalyzes killing mechanisms in bacteria while inducing bone repair through osteogenic and angiogenic coupling, making this platform a promising multi-functional strategy for treating and repairing complex bone infections.
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