Assessment of DNA Damage of Oral Mucosa due to Ceramic Bracket Using Comet Assay and Mutagenicity of Orthodontic Bonding System Using Ames Test

IF 0.2 Q4 DENTISTRY, ORAL SURGERY & MEDICINE
R. Adham, Norma Ab. Rahman, Kannan Thirumulu Ponnuraj
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Abstract

Objective: The objective of this study was to determine the DNA damage caused by ceramic bracket (Clear II, SIA Orthodontic Manufacturer Srl, Italy) on human buccal mucosal cells using comet assay and the mutagenicity of orthodontic bonding system (Transbond XT; 3M Unitek) by Ames test. Methods: In this study, twenty orthodontic patients were recruited from Specialist Orthodontic Clinic, Hospital Universiti Sains Malaysia. The Buccal mucosal cell sample was obtained from each patient at three time points-before (TO), after one month (T1) and after two months (T2) of ceramic bracket placement for performing comet assay. The spot test version of Ames test was performed using four Salmonella Typhimurium (S. Typhimurium) tester strains (TA 98, TA100, TA1535 and TA1537) for mutagenicity testing. Total comet score (TCS) and damage frequency (DF) were used to determine the DNA damage using non-parametric Friedman test followed by multiple pairwise comparison. The Ames test was analysed by a non-statistical method based on revertant growth ring formation. Results: There was no significant change of both TCS and DF between T0 and T1, but both parameters increased significantly from T0 to T1 and from T1 to T2. Non-statistical analysis was carried out to evaluate the results of Ames test based on the formation of revertant colony growth ring. None of the S. Typhimurium tester strains showed any revertant growth ring formation around the light cure adhesive primer. Conclusion: Ceramic bracket does not cause any DNA damage on human buccal mucosal cells and light cure adhesive primer is non mutagenic under the present test conditions.
彗星试验评价陶瓷托架对口腔黏膜DNA损伤及Ames试验评价正畸粘接系统致突变性
目的:本研究的目的是用彗星法测定陶瓷支架(Clear II, SIA Orthodontic Manufacturer Srl, Italy)对人颊粘膜细胞的DNA损伤和正畸结合系统(Transbond XT;3M Unitek)通过Ames测试。方法:在本研究中,从马来西亚圣士大学医院正畸专科诊所招募20例正畸患者。每个患者在放置陶瓷支架前(TO)、放置一个月后(T1)和放置两个月后(T2)三个时间点获得口腔粘膜细胞样本,进行彗星试验。采用4株鼠伤寒沙门菌(S. Typhimurium)试验菌株(ta98、TA100、TA1535和TA1537)进行Ames试验现场试验。总彗星评分(TCS)和损伤频率(DF)测定DNA损伤,采用非参数Friedman检验,并进行多两两比较。Ames试验采用基于反向生长环形成的非统计方法进行分析。结果:TCS和DF在T0和T1之间没有明显变化,但T0到T1和T1到T2这两个参数均显著升高。基于反向菌落生长环的形成,对Ames试验结果进行非统计分析。所有鼠伤寒沙门氏菌试验菌株均未在光固化胶粘剂引物周围形成任何反向生长环。结论:在本试验条件下,陶瓷支架对人口腔粘膜细胞无DNA损伤,光固化粘接引物无致突变性。
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
Journal of Dentistry Indonesia
Journal of Dentistry Indonesia DENTISTRY, ORAL SURGERY & MEDICINE-
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