Cytotoxicity of two different intercanal medicaments on human gingival fibroblasts - A Laboratory study

Q3 Dentistry
Behnaz Barakatein, A. Farhad, E. Shadmehr, H. Sharifi, Masoud Mohamad Sharif, A. Davoudi
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引用次数: 0

Abstract

Aim: Intracanal medicaments are often recommended during endodontic sessions to eliminate the necrotic debris and microorganisms. The aim of the present study was to observe the cytotoxicity of calcium hydroxide (CH) and colchicine (COL), at different concentrations, on human gingival fibroblast cells. Materials and Methods: Human gingival fibroblasts were cultured on plastic flasks containing RPMI 1640 media and fetal calf serum 10% supplemented with antibiotic agents. Trypsin/ethylenediaminetetraacetic acid 0.2% enzyme was used to isolate the cells, and the suspension was transferred to tubes for centrifuging. Conventional CH and COL were separately mixed with sterile saline solution to prepare a stock media. By serial dilution of stock media, desired concentrations were prepared at 2, 1.75, 1.5, and 1.25 mg/ml, separately. After considering a control group, the cells were exposed to test materials. 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay was conducted at 24 h, 72 h, and 7 days later. Optical density (OD) was evaluated to attain cell viability percentage. Finally, the recorded data were analyzed by Kruskal–Wallis and Mann–Whitney tests using SPSS software version 19 at a significant level of 0.05. Results: The highest (1.40 ± 0.66) and lowest (0.15 ± 0.00) ODs were observed in CH 1.25 mg/ml and COL 1.5 mg/ml after 72 h, respectively. All of the concentrations of both CH and COL showed significant OD differences with the control group (all P = 0.001). Conclusion: Both CH and COL manifested similar cytotoxicity on human gingival fibroblast cells.
两种不同肛门间药物对人牙龈成纤维细胞的细胞毒性实验研究
目的:在牙髓治疗期间,经常建议使用肛门内药物来清除坏死的碎片和微生物。本研究的目的是观察不同浓度的氢氧化钙(CH)和秋水仙碱(COL)对人牙龈成纤维细胞的细胞毒性。材料和方法:在含有RPMI 1640培养基和添加抗生素的10%胎牛血清的塑料瓶上培养人牙龈成纤维细胞。使用0.2%胰蛋白酶/乙二胺四乙酸酶分离细胞,并将悬浮液转移到试管中进行离心。将常规CH和COL分别与无菌盐水溶液混合以制备储备培养基。通过储备培养基的连续稀释,分别以2、1.75、1.5和1.25mg/ml制备所需浓度。在考虑对照组之后,将细胞暴露于测试材料。在24小时、72小时和7天后进行3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四唑溴化测定。评估光密度(OD)以获得细胞活力百分比。最后,使用SPSS软件19版,通过Kruskal–Wallis和Mann–Whitney检验对记录的数据进行分析,显著水平为0.05。结果:72小时后,CH 1.25mg/ml和COL1.5mg/ml的ODs最高(1.40±0.66),最低(0.15±0.00)。结论:CH和COL对人牙龈成纤维细胞具有相似的细胞毒性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Endodontology
Endodontology Medicine-Anatomy
CiteScore
0.60
自引率
0.00%
发文量
0
审稿时长
28 weeks
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