Khademi Abbas Ali, Saei Saeed, Mohajeri Mohammad Reza, Mirkheshti Nooshin, Ghassami Fatima, Torabi nia Nakisa, Alavi Sayyed Ali
Department of Endodontics, Isfahan University, Iran.
J Contemp Dent Pract. 2008 Sep 1;9(6):25-32.
The purpose of this study is to determine the efficacy of egg white in maintaining the viability of human periodontal ligament (PDL) cells on avulsed teeth.
The experimental media were: egg white, milk, Hanks' Balanced Salt Solution (HBSS) as the positive control, and tap water as the negative control. The storage times were 1, 2, 4, 8, and 12 hours. Extracted premolar teeth of healthy individuals were rinsed in the media. After trypsinization and subsequent treatment in collagenase, cell viability was determined using trypan blue staining. The two-way analysis of variance (ANOVA) statistical test was used to compare the results among different media.
There was no difference in the cell viability between egg white and HBSS media, but there was a statistically significant difference between the viability of PDL cells in egg white medium in comparison with milk (P<0.05) and water (P<0.05).
Egg white could be suggested as a suitable storage medium. Its principle advantage is its availability.
本研究旨在确定蛋清在维持脱位牙上人牙周膜(PDL)细胞活力方面的效果。
实验培养基为:蛋清、牛奶、作为阳性对照的汉克斯平衡盐溶液(HBSS)以及作为阴性对照的自来水。储存时间为1、2、4、8和12小时。将健康个体拔除的前磨牙在培养基中冲洗。经胰蛋白酶消化并随后用胶原酶处理后,使用台盼蓝染色法测定细胞活力。采用双向方差分析(ANOVA)统计检验来比较不同培养基之间的结果。
蛋清培养基和HBSS培养基之间的细胞活力没有差异,但与牛奶(P<0.05)和水(P<0.05)相比,蛋清培养基中PDL细胞的活力存在统计学上的显著差异。
可以建议将蛋清作为一种合适的储存培养基。其主要优点是易于获得。