65 - Cytotoxicity assessment of a self-etching primer and an orthodontic composite resin in L929 cells

IF 3.5 Q1 DENTISTRY, ORAL SURGERY & MEDICINE
Pedro Fróes , Ana Paula Tenório-De-Sá , Dayane Silva , Maria Romanos , Amanda Castro , Ana Maria Bolognese
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引用次数: 0

Abstract

Self-etching primers have simplified the process of direct bonding of dental resins by eliminating the rinsing step. The aim of the present study was to evaluate the cytotoxic effects of released residual substances from Transbond Plus Self-etching Primer (TSEP) (3M Unitek Ortho Prod, Monrovia, Calif) and Transbond XT (3M Unitek Ortho Prod, Monrovia, Calif). The study was approved by the Ethics Committee of UFRJ (CAAE: 13971513.0.0000.5257). Six human premolars and orthodontic stainless-steel brackets (Morelli, São Paulo, Brazil) were divided into two groups (n=3), as follows: Group I (Tooth + TSEP + Transbond + bracket + Light-curing) and Group II (Tooth + TSEP + Light-curing + Transbond + bracket + Light-curing). After samples immersion in the culture medium, supernatants aliquots were collected in triplicate and placed in contact with L929 cells for toxicity analysis after 0, 24, 48, 72 hours, 7, 14, 21 and 28 days. Cell viability was determined by "dye uptake" and was read in spectrophotometer. There were statistic significant differences between the number of the living cells present in the groups tested compared with the cell control group (P<0,05). Group I demonstrated toxicity until 7 days and Group II until 14 days (P<0,05). After 21 and 28 days, no significant toxicity was observed in either groups, suggesting that the release of toxic monomers occurs primarily in the first two weeks. The TSEP, Transbond XT composite associated to stainless steel brackets reduced cell viability in the first days, with toxicity persisting up to 14 days in the group with a two-step light curing.
自蚀刻引物和正畸复合树脂对L929细胞的细胞毒性评价
自蚀刻底漆通过消除冲洗步骤,简化了牙科树脂直接粘合的过程。本研究的目的是评估Transbond Plus自蚀刻引物(TSEP) (3M Unitek Ortho Prod,加利福尼亚州蒙罗维亚)和Transbond XT (3M Unitek Ortho Prod,加利福尼亚州蒙罗维亚)释放的残留物质的细胞毒性作用。该研究已获得UFRJ伦理委员会批准(CAAE: 13971513.000000.5257)。六个人类前臼齿和矫正不锈钢支架(Morelli,圣保罗,巴西)分为两组(n = 3),如下:集团我(牙 + TSEP + Transbond + 支架 + 光固化)和组II(牙 + TSEP + 光固化 + Transbond + 支架 + 光固化)。样品浸泡在培养基中后,收集上清等分三份,于0、24、48、72小时、7、14、21和28天后与L929细胞接触进行毒性分析。用“染料摄取法”测定细胞活力,并用分光光度计读取。与细胞对照组相比,各组活细胞数量差异有统计学意义(P< 0.05)。第1组毒性持续至第7天,第2组毒性持续至第14天(P< 0.05)。21和28天后,两组均未观察到明显的毒性,表明毒性单体的释放主要发生在前两周。与不锈钢支架相关的TSEP, Transbond XT复合材料在第一天降低了细胞活力,在两步光固化组中毒性持续长达14天。
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 the World Federation of Orthodontists
Journal of the World Federation of Orthodontists DENTISTRY, ORAL SURGERY & MEDICINE-
CiteScore
3.80
自引率
4.80%
发文量
34
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