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A novel bioactive system based on surface-functionalized plasmonic nanosystems for tunable biological surfaces

机译:一种基于表面官能化等离子体纳米系统的新型生物活性系统,可调谐生物表面

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A 2D AuNRs-SH-PEG-NH_2 nanocomposite was deposited on a plastic surface via a novel technique. This structure was utilized to evaluate the use of AuNRs as a bioactive substrate, as it allows cell-substrate interaction analysis. AuNRs with an aspect ratio of around 3 and a diameter of around 12 nm were used in this study after they were functional ized with thiolated PEG; they were also supplemented with-NH_2 groups to improve cell adhesion. Cytotoxicity tests confirmed that the system does not harm cell growth. The AuNR system was analyzed for its ability to support neural differentiation of human MSCs. hMSC differentiation into neural cells was compared with and without AuNRs by examining the expression of three important target proteins: GFAP, S100β, and Vimentin. The expression outcomes and patterns of Vimentin showed that the cells kept their fibroblastic morphology and experience the changes that occur with normal neural differentiation. Additionally, the S100β and GFAP expression patterns indicated that the AuNR system accelerated neural differentiation (Fig. 1e-f).
机译:通过新颖的技术在塑料表面上沉积2D AUNRS-SH-PEG-NH_2纳米复合材料。利用该结构来评估AUNR作为生物活性底物的使用,因为它允许细胞基板相互作用分析。在本研究中使用纵横比的纵横比宽度约为3〜12nm,在用硫醇化钉功能性IzEd的情况下使用;它们还补充了-NH_2组,以改善细胞粘附。细胞毒性试验证实系统不损害细胞生长。分析AUNR系统以支持人体MSCs神经分化的能力。通过检查三个重要靶蛋白的表达:GFAP,S100β和Vimentin,将HMSC分化与神经细胞分化为神经细胞。皮瓣的表达结果和模式表明细胞保持其纤维细胞形态,并经历正常神经分化的变化。另外,S100β和GFAP表达式模式表明AUNR系统加速了神经分化(图1E-F)。

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