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储存于哈姆氏F-10溶液中的脱位牙牙周膜细胞的活力和可重复性

Viability and Reproducibility of Periodontal Ligament Cells on Avulsed Teeth Stored in Ham's F-10 Solution.

作者信息

Talebi Maryam, Parisay Iman, Afshari Jalil Tavakol, Shajiei Arezoo, Ghadim Mostafa Sofiani

出版信息

J Clin Pediatr Dent. 2018;42(3):203-207. doi: 10.17796/1053-4628-42.3.6. Epub 2018 Apr 26.

Abstract

OBJECTIVES

The purpose of the present study was to evaluate the efficacy of Ham's F-10 in maintaining the viability and reproducibility of PDL cells on avulsed teeth.

STUDY DESIGN

Sixty mature, healthy extracted premolars were used. The experimental media used were Ham's F-10, Hank's balanced salt solution (HBSS), skim milk, and tap water (n = 15 specimens each). Cell viability was tested after 1, 3, 6, and 24 h storage in medium. Cell reproducibility was assessed by methyl-thiazol-tetrazolium (MTT) assay after1, 3, and 6 h storage in Ham's F-10, HBSS, and tap water.

RESULTS

The viability of PDL cells stored in Ham's F-10 and HBSS was significantly greater than that of samples stored in milk and tap water at all-time points (P<0.001). A significant difference in cell viability between samples stored in Ham's F-10 and HBSS (favoring the former) was observed only at 6h (P=0.04). MTT assay results were significantly better for samples stored in Ham's F-10 and HBSS than for those stored in tap water (P<0.001), with a significant difference between Ham's F-10 and HBSS observed only at 3h (P<0.001).

CONCLUSIONS

Ham's F-10 is capable of preserving PDL cells viable and reproducible better than milk and tap water and similar to HBSS.

摘要

目的

本研究旨在评估哈姆氏F-10培养基在维持脱位牙牙周膜细胞活力和增殖能力方面的效果。

研究设计

使用60颗成熟、健康的拔除前磨牙。所用的实验培养基为哈姆氏F-10培养基、汉克斯平衡盐溶液(HBSS)、脱脂牛奶和自来水(每组n = 15个样本)。在培养基中储存1、3、6和24小时后检测细胞活力。在哈姆氏F-10培养基、HBSS和自来水中储存1、3和6小时后,通过甲基噻唑四氮唑(MTT)法评估细胞增殖能力。

结果

在所有时间点,储存在哈姆氏F-10培养基和HBSS中的牙周膜细胞活力显著高于储存在牛奶和自来水中的样本(P<0.001)。仅在6小时时观察到储存在哈姆氏F-10培养基和HBSS中的样本之间细胞活力存在显著差异(前者更优,P = 0.04)。MTT分析结果显示,储存在哈姆氏F-10培养基和HBSS中的样本明显优于储存在自来水中的样本(P<0.001),仅在3小时时观察到哈姆氏F-10培养基和HBSS之间存在显著差异(P<0.001)。

结论

哈姆氏F-10培养基能够比牛奶和自来水更好地保持牙周膜细胞的活力和增殖能力,与HBSS相似。

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