University of Bonn, Bonn, Germany.
Int J Oral Maxillofac Implants. 2013 Jul-Aug;28(4):957-62. doi: 10.11607/jomi.2664.
This study was conducted to analyze how a cleaning treatment using plasma of argon would affect fibroblast growth on titanium disks at different time points to determine whether this treatment could enhance soft tissue healing around titanium dental implant abutments.
Sixty sterile disks made of machined grade 5 titanium were divided into two groups; 30 disks were left untreated (control) and 30 were cleaned using plasma of argon (test). To simulate clinical conditions during soft tissue healing around titanium abutments, both groups were immersed in a culture of murine fibroblasts (L929) for 2, 8, or 48 hours. After preparation, they were stained using 4',6-diamidino-2-phenylindole dihydrochloride (DAPI) to label the cellular nuclei and fluorescent phalloidin to label the cellular bodies. The nuclei were counted, and cellular bodies were analyzed with fluorescent microscopy and imaging analysis software. Analysis was performed at the three different time points.
Fibroblast adhesion for the test group was statistically significantly greater versus the control group at 2 and 8 hours but not at 48 hours. At 2 and 8 hours, the cellular bodies in the test group appeared flatter and more spread out, revealing more advanced cellular adhesion, compared to the cells observed in the control group. At 48 hours, the test and control specimens were nearly indistinguishable.
The removal of organic and inorganic contaminants from the surfaces of titanium disks using plasma of argon accelerated fibroblast adhesion in the early stages of colonization (2 to 8 hours). This effect disappeared after 48 hours as a result of saturation. Clinically, abutment cleaning using plasma of argon might positively affect soft tissue healing in early stages.
本研究旨在分析氩等离子体清洗处理在不同时间点对钛盘上成纤维细胞生长的影响,以确定该处理是否能增强钛牙种植体基台周围软组织的愈合。
将 60 个由机加工 5 级钛制成的无菌圆盘分为两组;30 个圆盘未经处理(对照),30 个用氩等离子体(试验)清洗。为了模拟钛基台周围软组织愈合过程中的临床情况,两组均浸入培养的鼠成纤维细胞(L929)中 2、8 或 48 小时。准备后,用 4',6-二脒基-2-苯基吲哚二盐酸盐(DAPI)标记细胞核,用荧光鬼笔环肽标记细胞体进行染色。计数细胞核,并通过荧光显微镜和成像分析软件分析细胞体。在三个不同的时间点进行分析。
试验组的成纤维细胞黏附在 2 小时和 8 小时时与对照组相比具有统计学显著差异,但在 48 小时时无差异。在 2 小时和 8 小时时,与对照组相比,试验组的细胞体更平坦,更伸展,显示出更先进的细胞黏附。在 48 小时时,试验组和对照组的标本几乎无法区分。
使用氩等离子体去除钛盘表面的有机和无机污染物加速了定植早期(2 至 8 小时)的成纤维细胞黏附。48 小时后,由于饱和,这种效应消失。临床上,使用氩等离子体清洁基台可能会在早期阶段对软组织愈合产生积极影响。