材料科学
聚己内酯
生物医学工程
脚手架
聚乙二醇
生物材料
异物巨细胞
巨噬细胞极化
体内
纳米技术
巨噬细胞
化学
聚合物
体外
复合材料
病理
生物化学
医学
生物
生物技术
作者
Wenfeng Li,Fang Dai,Shan Zhang,Fancheng Xu,Zhiyong Xu,Shousheng Liao,Liangtao Zeng,Song Li,Fanrong Ai
标识
DOI:10.1021/acsami.2c02001
摘要
3D-printed porous bioactive ceramic scaffolds have been widely used in bone defect repair. However, material implantation is often accompanied by a foreign body response (FBR), which may affect host tissue regeneration. The physical properties of biomaterials, including shape, pore size, and porosity, control the relevant immune responses during tissue regeneration. To the best of our knowledge, the effect of the pore size of 3D-printed scaffolds on the immune response and bone-biomaterial integration has not been studied in vivo. Polycaprolactone/polyethylene glycol/hydroxyapatite (PCL/PEG/HA) bioactive scaffolds with different pore sizes, including 209.9 ± 77.1 μm (P200), 385.5 ± 28.6 μm (P400), and 582.1 ± 27.2 μm (P600), were prepared with a pneumatic extrusion 3D printer. Compared with other pore sizes, P600 significantly reduced the FBR and induced more M2 macrophage infiltration, vascular ingrowth, and new bone formation. Immunohistochemical staining revealed that the MyD88 protein might be involved in macrophage polarization-related signal transduction in response to the pore size. Based on these results, bone regeneration requires the active participation of the immune response, and the P600 PCL/PEG/HA scaffold is a preferable candidate for the repair of bone defects.
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