首页> 外文期刊>Dental and Medical Problems >Effect of photobiomodulation with 810 and 940 nm diode lasers on human gingival fibroblasts
【24h】

Effect of photobiomodulation with 810 and 940 nm diode lasers on human gingival fibroblasts

机译:用810和940nm二极管激光对人牙龈成纤维细胞的光生物调节的影响

获取原文
           

摘要

Background. The growth and proliferation of? gingival fibroblasts are important in the process of? oral wound healing, and photobiomodulation (PBM) might be able to modify this process. Objectives. The aim of?the current study was to evaluate the biomodulatory effect of?a?single session of?laser PBM by means of?810?nm and 940?nm diode lasers alone and their combined application with different fluencies on human gingival fibroblasts (HGFs). Material and methods. Cells were provided by the Pasteur Institute, the National Cell Bank of? Iran (NCBI) (C-165). Laser irradiation was carried out using 810?nm, 940?nm and 810?nm 940?nm in the continuous wave (CW) mode, 100?mW, and energy densities of?0.5, 1.5 and 2.5?J/cm2 . Cell viability was evaluated at 24?h with the MTT assay. Trypan blue staining was used to evaluate proliferation 24, 48 and 72?h after laser therapy. Propidium iodine was used to stain DNA and the cell nucleus. Results. Laser irradiation (810?nm, 0.5?J/cm2 ) increased the viability of?gingival fibroblasts, while this dose had an?inhibitory effect with 940?nm. No positive effect on cell viability was found with other settings at 24?h. The viability results were not statistically different from those of?the control in the dual wavelength group. At all single-laser irradiation doses, the cell proliferation results were lower as compared to the control at 48 and 72?h. The dual wavelength group results were significantly better than those of?the control for the 1.5?J/cm2 and 2.5?J/cm2 energy densities (p??0.001). Propidium iodine staining showed no negative effect of?laser irradiation on the cell nucleus in any of?the groups. Conclusions. Although a?single irradiation dose of?810?nm, 0.5?J/cm2 , resulted in a?positive effect on cell viability at 24?h, no statistically significant stimulatory effect on viability and proliferation was observed for the other single wavelength group. When a?combination of?the 2 wavelengths was used, better results were observed as compared to the control, which needs to be further investigated in future studies.
机译:背景。增长和增殖?牙龈成纤维细胞在该过程中是重要的?口腔伤口愈合,光生物调节(PBM)可能能够改变该过程。目标。目前的研究是评估α的生物调制效应?单一会话的α.810?NM和940?NM二极管激光器单独及其在人牙龈成纤维细胞上的不同流量的组合应用(HGFS )。材料与方法。细胞由巴斯特研究所,国家细胞库提供?伊朗(NCBI)(C-165)。在连续波(CW)模式下,使用810Ω,940·nm和810Δnm进行激光照射.NM 940Δnm,100μmw,和Δ0.5,1.5和2.5?j / cm2的能量密度。用MTT测定法在24℃下评估细胞活力。在激光治疗后,使用耳蛋白蓝染色来评估增殖24,48和72℃。碘丙氨酸碘碘用于染色DNA和细胞核。结果。激光照射(810?NM,0.5?J / CM2)增加了牙龈成纤维细胞的可行性,而该剂量具有940℃的抑制作用。在24μl的其他设置中发现了对细胞活力没有积极影响。活力结果与那些与双波长组的控制没有统计学不同。在所有单激光照射剂量时,与48和72℃的对照相比,细胞增殖结果较低。双波长组结果明显优于1.5?J / CM2和2.5?J / CM2能量密度的控制(P?<0.001)。碘染色促碘染色显示出在任何一个β上的α激光照射中的任何负效应。结论。虽然a?单次辐射剂量为?810?nm,0.5?j / cm 2导致24℃的细胞活力产生阳性作用,但对于其他单波长组没有对可生存性和增殖的统计学上显着的刺激作用。当a?组合?使用2个波长,与对照相比,观察到更好的结果,需要在未来的研究中进一步调查。

著录项

获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号