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Biocompatibility and antibacterial properties of zirconium nitride coating on titanium abutments: An in vitro study

机译:钛基台上氮化锆涂层的生物相容性和抗菌性能:体外研究

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摘要

Improving soft tissue attachment and reducing bacterial colonization on titanium abutments are key factors for the long-term maintenance of healthy soft and hard peri-implant tissues. This in vitro study was conducted to compare the biocompatibility and antibacterial activity of four different surfaces: uncoated Ti6Al4V, anodized, and coated with titanium nitride or zirconium nitride. Surface topography was investigated with a high-resolution system for measuring surface finishes. Human gingival fibroblast (HGF) adhesion and proliferation were examined using MTT assay, Scanning Electron Microscopy (SEM) imaging, immunofluorescence analysis and real-time PCR for selected target genes. The hemolysis and AMES tests were performed to assess the chemical compounds’ blood compatibility and mutagenic potential, respectively. Antibacterial activity was tested against five bacterial strains isolated from the oral cavity (Streptococcus salivarius, S. sanguinis, S. mutans, S. sobrinus, S. oralis), and the percentage of dead bacteria was calculated. Roughness measurements confirmed a substantial similarity between the surfaces and their compatibility with clinical applications. MTT assay, SEM analysis and immunofluorescence staining showed adhesion and proliferation of HGFs cultured on all the examined surfaces. PCR confirmed that HGFs produced extracellular matrix components efficiently on all the surfaces. No hemolytic activity was detected, and the AMES test confirmed the surfaces’ clinical safety. For all tested bacterial strains, biofilms grown on the zirconium nitride surface showed a higher percentage of dead bacteria than on the other disks. The titanium nitride surface inactivated bacterial biofilms, too, but to a lesser extent.
机译:改善软组织的附着并减少钛基台上的细菌定植是长期维护健康的软,硬种植体周围组织的关键因素。进行了这项体外研究,比较了四个不同表面的生物相容性和抗菌活性:未涂覆的Ti6Al4V,阳极氧化的和涂覆氮化钛或氮化锆的表面。使用用于测量表面光洁度的高分辨率系统研究了表面形貌。使用MTT分析,扫描电子显微镜(SEM)成像,免疫荧光分析和实时PCR检测选定的靶基因,检测人牙龈成纤维细胞(HGF)的黏附和增殖。进行了溶血和AMES测试,分别评估化合物的血液相容性和诱变潜力。测试了对从口腔中分离的五种细菌菌株(唾液链球菌,血红链球菌,变形链球菌,链球菌,口腔链球菌)的抗菌活性,并计算了死亡细菌的百分比。粗糙度测量证实了表面之间的实质相似性以及它们与临床应用的相容性。 MTT测定,SEM分析和免疫荧光染色显示在所有检查的表面上培养的HGF的粘附和增殖。 PCR证实HGF在所有表面上有效地产生细胞外基质成分。未检测到溶血活性,AMES测试确认了表面的临床安全性。对于所有测试的细菌菌株,在氮化锆表面上生长的生物膜显示出的死菌百分比高于其他磁盘。氮化钛表面也使细菌生物膜失活,但程度较小。

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