明胶
脚手架
材料科学
微型多孔材料
生物医学工程
多孔性
复合数
细胞粘附
相容性(地球化学)
细胞外基质
纳米技术
自愈水凝胶
聚酰胺
大孔隙
细胞
粘附
骨组织
组织工程
细胞迁移
缓冲器(光纤)
细胞生长
作者
Shuang Dai,Jiaxin Hu,Yiran Li,Tingting Ma,Aolong Li,Zhengyang Qin,Yubao Li,Jidong Li
标识
DOI:10.1021/acsbiomaterials.6c00074
摘要
Three-dimensional printed porous scaffolds provide the necessary mechanical support for bone repair. However, their inherent structural design often leads to insufficient cell attachment sites within the large pores, resulting in a low-density and uneven spatial distribution of initially adhered cells, which ultimately hampers bone regeneration. To address this limitation, we developed a gradient-functionalized scaffold by incorporating an α-ketoglutarate (AKG)-loaded gelatin (Gel/AKG) network into the macropores of a 3D-printed polyamide 66/hydroxyapatite (PH) composite scaffold. This design aims to facilitate initial cell adhesion and subsequent osteogenic differentiation. Material optimization confirmed that a formulation of 5 wt % gelatin carrying 0.25 wt % AKG achieved optimal perfusion and structural stability within the scaffold. This construct establishes an integrated microporous network that significantly enhances surface properties, actively guiding and promoting dense early cell colonization. The degradation of gelatin timely creates space for bone ingrowth, while the sustained release of AKG continuously enhances cell osteogenic activity. In vivo animal studies further revealed an 110% increase in new bone volume in the experimental group compared to the control after 8 weeks implantation. In conclusion, this strategy successfully integrates robust mechanical support, guided cell adhesion, and bioactive regulation into a spatiotemporally coordinated system, offering a promising solution for bone defect repair by harmonizing structural compatibility with functional regeneration.
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