Säuberlich S, Klee D, Richter E J, Höcker H, Spiekermann H
Dental Prosthodontics Clinic, University Hospital RWTH, Aachen, Germany.
Clin Oral Implants Res. 1999 Oct;10(5):379-93. doi: 10.1034/j.1600-0501.1999.100505.x.
The aim of our research project was to achieve an improvement in the integration of enossal dental implants in the region of peri-implantary soft tissue. Improvement in the adhesion of the gingiva of the surface of enossal implants was to be achieved by modification of the titanium surface. The effect of different modifications on the biocompatibility of the modified titanium surfaces was tested: sulfur dioxide plasma treatment of titanium; acetylene plasma treatment of titanium followed by sulfur dioxide plasma etching; plasma nitration of titanium; replacement of titanium by glycidoxypropyltrimethoxy silane; coating titanium with poly[(ethene-co-vinyl acetate)-graft-vinyl chloride] and coating titanium with fibronectin. Determination of the chemical composition of the surface was carried out using X-ray photospectroscopy. The adsorption of fibronectin at the surface of the titanium was tested using an Enzyme Linked Immunosorbent Assay. In selected in vitro tests with human gingival fibroblasts, cell morphology was assessed using scanning electron microscopy and light microscopy. Cell proliferation and protein synthesis, as well as the activity of mitochondrial dehydrogenases were evaluated. By means of centrifugation and by determining initial cell adhesion, the adhesion of gingival fibroblasts was investigated. According to the kind of modification made to the titanium surfaces, it was possible to observe differences in the cellular behavior of gingiva fibroblasts on the differently modified surfaces of the implants. Coating the titanium using fibronectin produced optimization of cell growth and improvement in the adhesion of gingiva fibroblasts to the implant surface. In contrast, modification of the titanium with poly[(ethene-co-vinyl acetate)-graft-vinyl chloride] generally resulted in a deterioration of the biocompatibility of the surface. A marked correlation between the cellular compatibility of the modified titanium and the surface modification made did not become apparent. One reason for this is the large number of parameters determining the interaction between implant and tissue.
我们研究项目的目的是改善牙种植体在种植体周围软组织区域的整合情况。通过对钛表面进行改性,实现牙种植体表面牙龈附着力的提高。测试了不同改性对改性钛表面生物相容性的影响:钛的二氧化硫等离子体处理;钛的乙炔等离子体处理后进行二氧化硫等离子体蚀刻;钛的等离子体硝化;用环氧丙氧基丙基三甲氧基硅烷替代钛;用聚(乙烯 - 醋酸乙烯酯) - 接枝 - 氯乙烯涂覆钛以及用纤连蛋白涂覆钛。使用X射线光电子能谱对表面化学成分进行测定。使用酶联免疫吸附测定法测试纤连蛋白在钛表面的吸附情况。在选定的用人牙龈成纤维细胞进行的体外试验中,使用扫描电子显微镜和光学显微镜评估细胞形态。评估细胞增殖、蛋白质合成以及线粒体脱氢酶的活性。通过离心和测定初始细胞附着力,研究牙龈成纤维细胞的附着力。根据对钛表面所做的改性种类,可以观察到牙龈成纤维细胞在种植体不同改性表面上的细胞行为存在差异。用纤连蛋白涂覆钛可优化细胞生长并改善牙龈成纤维细胞与种植体表面的附着力。相比之下,用聚(乙烯 - 醋酸乙烯酯) - 接枝 - 氯乙烯对钛进行改性通常会导致表面生物相容性变差。改性钛的细胞相容性与所做的表面改性之间并未呈现出明显的相关性。造成这种情况的一个原因是决定种植体与组织之间相互作用的参数众多。