DFO-modified polydopamine sulfonated PEEK enhances osseointegration through macrophage immunomodulation and osteogenic differentiation of BMSCs†

IF 5.2 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY
Shengjie Wang, Wei Liu, Chao Yang, Xianlong Zhang and Chunming Lyu
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引用次数: 0

Abstract

This study aimed to develop a novel artificial joint prosthesis material with osteogenic properties. Deferoxamine mesylate (DFO) was immobilized on the porous surface of sulfonated polyetheretherketone (SPEEK) using polydopamine (PDA), resulting in a novel material designated as DFO-PDA@SPEEK (DFO-PS). DFO-PS induced macrophage M2 phenotype polarization, reduced inflammatory factor expression, promoted osteogenic differentiation of bone marrow mesenchymal stem cells (BMSCs), and enhanced implant osseointegration and osteogenic capacity. In vitro evaluation demonstrated that DFO-PS significantly modulated immune and inflammatory responses, promoted angiogenesis, and enhanced osteogenic differentiation. In the rat model with femoral bone defects, in comparison to the control group, the DFO-PS group exhibited a 1.22-fold increase in trabecular thickness and a 1.51-fold enhancement in maximum pull-out force. This work demonstrates that DFO-PS is a promising material for constructing multifunctional implants with biomineralization and immunomodulation properties for bone joint replacement.

dfo修饰的聚多巴胺磺化PEEK通过巨噬细胞免疫调节和BMSCs的成骨分化增强骨整合
本研究旨在开发一种具有成骨特性的新型人工关节假体材料。用聚多巴胺(PDA)将甲磺酸去铁胺(DFO)固定在磺化聚醚醚酮(SPEEK)的多孔表面,得到了一种新型材料DFO-PDA@SPEEK (DFO- ps)。DFO-PS诱导巨噬细胞M2表型极化,降低炎症因子表达,促进骨髓间充质干细胞(BMSCs)成骨分化,增强种植体骨整合和成骨能力。体外评估表明,DFO-PS显著调节免疫和炎症反应,促进血管生成,增强成骨分化。在股骨骨缺损大鼠模型中,与对照组相比,DFO-PS组骨小梁厚度增加1.22倍,最大拔出力增加1.51倍。该研究表明,DFO-PS是一种具有生物矿化和免疫调节特性的多功能骨关节置换术植入材料。
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来源期刊
Materials Advances
Materials Advances MATERIALS SCIENCE, MULTIDISCIPLINARY-
CiteScore
7.60
自引率
2.00%
发文量
665
审稿时长
5 weeks
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