Department of Prosthetic Dentistry and Stomatognathic Physiology, University of Turku, FI-20520, Turku, Finland.
Institute of Biomedicine and Cancer Research Laboratory FICAN West, University of Turku, FI-20520, Turku, Finland.
J Mater Sci Mater Med. 2024 Apr 18;35(1):25. doi: 10.1007/s10856-024-06792-0.
Bioactive, nanoporous TiO-coating has been shown to enhance cell attachment on titanium implant surface. The aim of this study was to evaluate, whether the saliva proteins affect the epithelial cell adhesion on TiO-coated and non-coated titanium. Grade V titanium discs were polished. Half of the discs were provided with TiO-coating produced in sol with polycondensation method. Half of the TiO-coated and non-coated discs were treated with pasteurized saliva for 30 min. After saliva treatment, the total protein amounts on surfaces were measured. Next, the hydrophilicity of discs were measured with water contact angle measurements. Further, the gingival keratinocyte adhesion strength was measured after 2 and 6 h of cultivation using serial trypsinization. In addition, cell growth and proliferation were measured after 1, 3, and 7 days of cell culture. Finally, cell morphology, spreading and adhesion protein signals were detected with high resolution confocal microscopy. As a result, in sol coated TiO-surface had significantly higher hydrophilicity when compared to non-coated titanium, meanwhile both non-coated and TiO-coated surfaces with saliva treatment had a significant increase in hydrophilicity. Importantly, the amounts of adhered saliva proteins were equal between TiO-coated and non-coated surfaces. Adhesion strength against enzymatic detachment was weakest on non-coated titanium after saliva exposure. Cell proliferation and cell spreading were highest on TiO-coated titanium, but saliva exposure significantly decreased cell proliferation and spreading on TiO-coated surface. To conclude, even though saliva exposure makes titanium surfaces more hydrophilic, it seems to neutralize the bioactive TiO-coating and decrease cell attachment to TiO-coated surface.
具有生物活性的纳米多孔 TiO2 涂层已被证明能增强钛植入物表面细胞的附着。本研究旨在评估唾液蛋白是否会影响上皮细胞在 TiO2 涂层和未涂层钛上的黏附。将 V 级钛片进行抛光。将一半的钛片用溶胶聚合法制备的 TiO2 涂层处理。将一半的 TiO2 涂层和未涂层的钛片用巴氏消毒的唾液处理 30 分钟。唾液处理后,测量表面的总蛋白量。然后,用水接触角测量法测量钛片的亲水性。进一步在培养 2 和 6 小时后使用连续胰蛋白酶消化测量牙龈角质形成细胞的黏附强度。此外,在细胞培养 1、3 和 7 天后测量细胞生长和增殖。最后,使用高分辨率共聚焦显微镜检测细胞形态、铺展和黏附蛋白信号。结果表明,与未涂层钛相比,溶胶涂层的 TiO2 表面具有更高的亲水性,而经过唾液处理的非涂层和 TiO2 涂层表面的亲水性均显著增加。重要的是,黏附的唾液蛋白量在 TiO2 涂层和非涂层表面之间相等。唾液暴露后,非涂层钛的黏附强度对酶切的抵抗力最弱。细胞增殖和细胞铺展在 TiO2 涂层钛上最高,但唾液暴露显著降低了 TiO2 涂层表面的细胞增殖和铺展。总之,尽管唾液暴露使钛表面更亲水,但似乎会中和具有生物活性的 TiO2 涂层并降低细胞对 TiO2 涂层表面的黏附。