脚手架
破骨细胞
骨愈合
生物医学工程
材料科学
化学
介孔二氧化硅
细胞毒性
聚乳酸
细胞生物学
骨细胞
再生(生物学)
药物输送
骨水泥
骨组织
纳米技术
复合数
骨形成
作者
Hao Zhou,D.L. Wu,Cheng Jun,Qianqi Liu,Xin Wu,Binbin Jiang,Honghui He,Jinpeng He,Renfeng Liu,Junxing Wu
摘要
Bone defect repair is a complex process governed by intricate and well-coordinated temporal regulatory mechanisms. Conventional bone scaffolds are frequently proved underperformance due to their inability to adapt to these spatio-temporal demands. In this study, we developed a 3D-printed composite bone scaffold using ordered hexagonal mesoporous silica nanoparticles (SBA-15) loaded with Akebia saponin D (ASD) and polylactic acid (PLLA) through selective laser sintering (SLS). The outcomes revealed that the scaffold possessed a favorable porous structure, degradability, and the capability of slow drug release. Simultaneously, the scaffold exhibited minimal cytotoxicity and high cell adhesion. Significantly, the scaffold demonstrated the capacity to orchestrate macrophage polarization to reduce inflammation in the early phase of bone repair, enhance osteogenesis in the intermediate phase, and impede osteoclast activity in the final stages. These properties are instrumental in promoting effective bone healing. This study introduces a novel 3D-printed composite bone scaffold system capable of temporally regulating bone healing, offering a promising approach for treating bone defects.
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