The ability of SPEEK to promote the proliferation and osteogenic differentiation of BMSCs on PEEK surfaces

偷看 热重分析 傅里叶变换红外光谱 扫描电子显微镜 差示扫描量热法 碱性磷酸酶 化学 材料科学 染色 高分子化学 核化学 化学工程 分析化学(期刊) 复合材料 有机化学 聚合物 生物 工程类 物理 遗传学 热力学
作者
Shuang Wang,Junxiong Ma,Liang Zheng,Hong Wang,Hailong Yu,Yu Chen
出处
期刊:Heliyon [Elsevier BV]
卷期号:10 (16): e36448-e36448
标识
DOI:10.1016/j.heliyon.2024.e36448
摘要

To investigate the ability of sulfonated polyetheretherketone (SPEEK) to promote the proliferation and osteogenic differentiation of bone marrow mesenchymal stem cells (BMSCs) and compare the effects of different degrees of sulfonation (DS), SPEEK was made with two different DS. The L-SPEEK group had a lower DS, while the H-SPEEK group had a higher DS. The physicochemical properties of both species were evaluated by scanning electron microscopy (SEM), capitilize Fourier transform infrared (FTIR) spectroscopy, thermogravimetric analysis (TGA), X-ray diffraction (XRD) and differential scanning calorimetry (DSC). Then, proliferation and osteogenic differentiation between the two groups and with pure polyetheretherketone (PEEK) were compared after surface inoculation of bone marrow mesenchymal stem cells (BMSCs). Scanning electron microscopy (SEM) revealed that the surface of the PEEK substrates could be smooth or coarse, and the degree of roughness increased with increasing sulfonation. FTIR spectroscopy showed that both the L-SPEEK and H-SPEEK samples contained sulfonic acid. TGA and XRD revealed that the components in the two groups were the same, but the intensities were different. After BMSC inoculation, a CCK8 assay revealed that the cells proliferated more on the H-SPEEK surface and little on the L-SPEEK surface compared with the PEEK surface. Then, osteogenic differentiation was verified by immunofluorescence staining for OCN and Runx2, which indicated that H-SPEEK had the greatest effect on improving differentiation. The results of alizarin red staining (ARS) and alkaline phosphatase staining (APS) also revealed this trend. Sulfonation can change the microsurface of PEEK, which can improve both BMSC proliferation and osteogenic differentiation.
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