首页> 外文期刊>Journal of Indian Society of Periodontology >Effects of leukocyte–platelet-rich fibrin and advanced platelet-rich fibrin on the viability and migration of human gingival fibroblasts
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Effects of leukocyte–platelet-rich fibrin and advanced platelet-rich fibrin on the viability and migration of human gingival fibroblasts

机译:白细胞 - 血小板纤维蛋白和高级血小板纤维蛋白对人牙龈成纤维细胞的活力和迁移的影响

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Background: Platelet products play a fundamental role in the process of healing. The new generation of platelet-rich fibrin (PRF), namely advanced PRF (A-PRF), has different biological and mechanical properties compared to those of leukocyte-PRF (L-PRF). This study aimed to compare the effects of L-PRF and A-PRF on the viability and migration of human gingival fibroblasts (HGFs). Materials and Methods: In this in vitro study, the effects of A-PRF and L-PRF on the viability and migration of HGFs after 24 and 48 h were evaluated using the methyl thiazolyl tetrazolium assay. The viability of the negative control culture medium was considered to be 100%. The mean optical density of the test groups was divided by that of the negative control group and reported as percentage. One-way ANOVA was applied to assess the effects of time and type of PRF on the viability and migration of HGFs. Pairwise comparisons were made using the Tukey's test. Results: At 24 h, cell viability in the L-PRF group was significantly higher than that in the A-PRF group (P 0.05). However, no significant difference was noted between the two groups at 48 h. At 24 h, L-PRF caused significantly higher cell migration compared to the negative control group, whereas at 48 h, both A-PRF and L-PRF significantly increased cell migration compared to the control group. Conclusion: Within the limitations of this study, L-PRF and A-PRF had significant effects on the viability and migration of HGFs. Further studies on these platelet concentrates are warranted.
机译:背景:血小板产品在愈合过程中起着基本作用。新一代富含血小板的纤维蛋白(PRF),即高级PRF(A-PRF),与白细胞-PRF(L-PRF)相比具有不同的生物和机械性能。本研究旨在比较L-PRF和A-PRF对人牙龈成纤维细胞(HGF)的活力和迁移的影响。材料和方法:在这种体外研究中,使用甲基噻唑基四唑鎓测定法评估A-PRF和L-PRF对HGFS后的活力和迁移的影响。阴性对照培养基的可行性被认为是100%。测试基团的平均光学密度除以阴性对照组,并报告为百分比。单向ANOVA被应用于评估PRF的时间和类型对HGFS的活力和迁移的影响。配对比较使用Tukey的测试进行。结果:在24小时,L-PRF组的细胞活力明显高于A-PRF组(P <0.05)。然而,在48小时的两组之间没有发现两组之间没有显着差异。与阴性对照组相比,在24小时,L-PRF引起显着更高的细胞迁移,而在48小时,与对照组相比,A-PRF和L-PRF都显着提高了细胞迁移。结论:在本研究的局限内,L-PRF和A-PRF对HGFS的活力和迁移具有显着影响。需要进一步研究这些血小板浓缩物。

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