Cytotoxicity and genotoxicity of orthodontic bands with or without silver soldered joints

被引:21
作者
Goncalves, Tatiana Siqueira [1 ]
de Menezes, Luciane Macedo [1 ]
Trindade, Cristiano [2 ]
Machado, Miriana da Silva [2 ]
Thomas, Philip [3 ]
Fenech, Michael [3 ]
Pegas Henriques, Joao Antonio [2 ,4 ,5 ]
机构
[1] Pontificia Univ Catolica Rio Grande do Sul, Dept Orthodont, BR-90619900 Porto Alegre, RS, Brazil
[2] Univ Fed Rio Grande do Sul, Ctr Biotecnol, Inst Educ Pesquisa Desenvolvimento & Inovacao Tec, ROYAL Unidade GENOTOX ROYAL, Porto Alegre, RS, Brazil
[3] Commonwealth Sci & Ind Res Org Anim Food & Hlth S, Adelaide, SA, Australia
[4] Univ Caxias do Sul, Inst Biotecnol, Porto Alegre, RS, Brazil
[5] Univ Fed Rio Grande do Sul, Ctr Biotecnol, Dept Biofis, Lab Reparacao DNA Eucariotos, Porto Alegre, RS, Brazil
关键词
Orthodontics; Metal ion toxicity; Cell viability; Genotoxicity; Mutagenicity; MICRONUCLEUS CYTOME ASSAY; IN-VITRO; COMET ASSAY; DNA-DAMAGE; INDIRECT MUTAGENS; OXIDATIVE STRESS; STAINLESS-STEEL; METAL RELEASE; HEPG2; CELLS; NICKEL;
D O I
10.1016/j.mrgentox.2014.01.011
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Stainless steel bands, with or without silver soldered joints, are routinely used in orthodontics. However, little is known about the toxic biological effects of these appliances. The aims of this study were to evaluate the cytotoxic, cytostatic, genotoxic and DNA damage-inducing effects of non-soldered bands (NSB) and silver soldered bands (SSB) on the HepG2 and HOK cell lines and to quantify the amount of ions released by the bands. The 24-h metallic eluates of NSBs and SSBs were quantified by atomic absorption spectrophotometry. An KIT reduction assay was performed to evaluate the cytotoxicity, alkaline and modified comet assays were employed to measure genotoxicity and oxidative DNA damage effects, and cytokinesis-block micronucleus cytome (CBMN-Cyt) assays were used to verify DNA damage, cytostasis and cytotoxicity. Ag, Cd, Cr, Cu and Zn were detected in SSB medium samples, and Fe and Ni were detected in both the SSB and NSB medium samples. The SSB group induced stronger cytotoxic effects than the NSB group in both evaluated cell lines. NSB and SSB induced genotoxicity as evaluated by comet assays; stronger effects were observed in the SSB group. Both groups induced similar increases in the number of oxidative DNA lesions, as detected by the FPG and Endo III enzymes. Nucleoplasmic bridges, biomarkers of DNA misrepair and/or telomere end fusions, were significantly elevated in the SSB group. The SSB eluates showed higher amounts of Ni and Fe than NSB, and all the quantified ions were detected in SSB eluates, including Cd. The SSB eluates were more cytotoxic and genotoxic than the NSB samples. Based on these results, we propose that other brands, materials and techniques should be further investigated for the future manufacture of orthodontic appliances. (C) 2014 Elsevier B.V. All rights reserved.
引用
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页码:1 / 8
页数:8
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