脚手架
材料科学
溶菌酶
再生(生物学)
生物相容性
植入
生物医学工程
体外
骨组织
肽
壳聚糖
生物物理学
细胞生物学
化学
生物
医学
生物化学
外科
冶金
作者
Luxuan Shen,Shuqin Cao,Yuemin Wang,Pei Zhou,Shuaibing Wang,Yao Zhao,Lingzhuang Meng,Quan Zhang,Yanyan Li,Xinyuan Xu,Quan Yuan,Jianshu Li
标识
DOI:10.1021/acsami.2c19026
摘要
Bone defects caused by disease or trauma are often accompanied by infection, which severely disrupts the normal function of bone tissue at the defect site. Biomaterials that can simultaneously reduce inflammation and promote osteogenesis are effective tools for addressing this problem. In this study, we set up a programmed delivery platform based on a chitosan scaffold to enhance its osteogenic activity and prevent implant-related infections. In brief, the osteogenic peptide sequence (YGFGG) was modified onto the surface of cowpea chlorotic mottle virus (CCMV) to form CCMV-YGFGG nanoparticles. CCMV-YGFGG exhibited good biocompatibility and osteogenic ability in vitro. Then, CCMV-YGFGG and lysozyme were loaded on the chitosan scaffold, which exhibited a good antibacterial effect and promoted bone regeneration for infected bone defect treatment. As a delivery platform, the scaffold showed staged release of lysozyme and CCMV-YGFGG, which facilitates the regeneration of infected bone defects. Our study provides a novel and promising strategy for the treatment of infected bone defects.
科研通智能强力驱动
Strongly Powered by AbleSci AI