Evaluation of Adhesion and Viability of Human Gingival Fibroblasts on Strontium-Coated Titanium Surfaces: an in vitro Study

被引:0
|
作者
Bakitian, Fahad [1 ,5 ]
Alshammari, Hatem [2 ]
Youssef, Abdel-Rahman [3 ,4 ]
Hawsawi, Rayan A. [1 ]
Alreshedi, Anwar Doufan [2 ]
Alkhashram, Mariam Abdulaziz [2 ]
机构
[1] Umm Al Qura Univ, Fac Dent, Dept Restorat Dent, Mecca, Saudi Arabia
[2] Univ Hail, Coll Dent, Dept Prevent Dent, Hail, Saudi Arabia
[3] Umm Al Qura Univ, Fac Dent, Dept Basic & Clin Oral Sci, Mecca, Saudi Arabia
[4] Suez Canal Univ, Fac Med, Dept Microbiol & Immunol, Ismailia, Egypt
[5] Umm Al Qura Univ, Fac Dent Med, Dept Restorat Dent, Mecca, Saudi Arabia
关键词
cytotoxicity; dental implant; peri-implantitis; metal ions; multifunctional coatings; titanium surfaces; DENTAL IMPLANTS; TISSUES;
D O I
10.2147/CCIDE.S462763
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Background: Applying multifunctional coatings employing strontium (Sr) ions on titanium (Ti) surfaces is a useful and biocompatible method to improve osseointegration and prevent tissue infections through antimicrobial activity. Nonetheless, the effectiveness of Sr coating on the adhesion and viability of human gingival fibroblasts (HGFs) to Ti surfaces remains unclear. Purpose: The study aimed to evaluate the effect of Sr coating on the adhesion and viability of HGFs to Ti surfaces. Materials and Methods: The Ti wafers were divided into two groups based on Sr coating: uncoated Ti (control) and Sr-coated Ti. The Magnetron sputtering technique was used for Sr coating on Ti surfaces. The HGFs were seeded onto the surfaces and cultured for 48 and 96 hours before the cell adhesion and viability of the attached HGFs were assessed. The adhesion of HGFs was analyzed using the attached cell numbers at 48 h and 96 h, and the morphology at 24 h and 72 h. The cytotoxic effect on HGFs was assessed after 24 and 72 hours of incubation using cell viability assay. Student's t -test was used for statistical analysis. Results: The number of cells attached to Sr-coated surfaces was significantly greater than those attached to uncoated Ti surfaces after 48 hours (P<0.0001) and 96 hours (P=0.0002). Sr-coated and uncoated Ti surfaces were not cytotoxic to HGFs, with the cell viability ranging from 92% to 105% of the untreated control HGFs. There were no significant differences in cell viability between Sr-coated and uncoated Ti surfaces at 24 hours (P=0.3675) and 72 hours (P=0.0982). Conclusion: Sr-coated Ti surfaces induce adhesion of HGFs compared to uncoated Ti surfaces. Further, Sr-coated and uncoated Ti surfaces show no cytotoxic effect on the attached HGFs.
引用
收藏
页码:127 / 134
页数:8
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