Takamiya Aline Satie, Monteiro Douglas Roberto, Bernabé Daniel Galera, Gorup Luiz Fernando, Camargo Emerson Rodrigues, Gomes-Filho João Eduardo, Oliveira Sandra Helena Penha, Barbosa Debora Barros
Department of Pediatric Dentistry and Public Health Dental, Araçatuba Dental School, Universidade Estadual Paulista, Araçatuba, São Paulo, Brazil.
Department of Pediatric Dentistry and Public Health Dental, Araçatuba Dental School, Universidade Estadual Paulista, Araçatuba, São Paulo, Brazil.
J Endod. 2016 Jun;42(6):953-60. doi: 10.1016/j.joen.2016.03.014. Epub 2016 Apr 23.
Silver nanoparticles have been used for different purposes in dentistry, including endodontic treatments. The aim of this study was to determine the cytotoxicity of different types of silver nanoparticles on mouse fibroblast cell line L929 and the reaction of subcutaneous connective tissue of Wistar rats to these nanoparticles.
Silver nanoparticles of an average size of 5 nm were synthesized with ammonia (SNA) or polyvinylpyrrolidone (SNP). L929 was exposed to SNA and SNP (0.1-100 μg/mL), and 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide and enzyme-linked immunosorbent assays were performed after 6, 24, and 48 hours. Culture medium was used as the control. Sixteen rats received, individually, 3 polyethylene tubes filled with a fibrin sponge embedded in 100 μL SNA or SNP (1 μg/mL). A fibrin sponge with no embedding was the control. Tissue reaction was performed qualitatively and quantitatively after 7, 15, 30, and 90 days of implantation in the dorsal connective tissue of Wistar rats.
SNA and SNP were cytotoxic to L929 in higher concentrations, with SNA significantly more toxic than SNP. SNA and SNP did not induce significant interleukin-1β and interleukin-6 production. The release of stem cell factor by L929 increased 48 hours after the treatment with SNP at 5 μg/mL. Histologic examination showed that the inflammatory responses caused by SNA and SNP at 1 μg/mL were similar to the control in all experimental periods.
It was concluded that SNA and SNP were not cytotoxic at 25 μg/mL or lower concentrations. However, for safe clinical use, further studies establishing others points of its toxicologic profile are recommended.
银纳米颗粒已在牙科领域用于不同目的,包括牙髓治疗。本研究的目的是确定不同类型的银纳米颗粒对小鼠成纤维细胞系L929的细胞毒性以及Wistar大鼠皮下结缔组织对这些纳米颗粒的反应。
用氨水(SNA)或聚乙烯吡咯烷酮(SNP)合成平均粒径为5nm的银纳米颗粒。将L929暴露于SNA和SNP(0.1 - 100μg/mL),并在6、24和48小时后进行3 -(4,5 - 二甲基噻唑 - 2 - 基)- 2,5 - 二苯基四氮唑溴盐和酶联免疫吸附测定。以培养基作为对照。16只大鼠分别接受3根装有嵌入100μL SNA或SNP(1μg/mL)的纤维蛋白海绵的聚乙烯管。未嵌入任何物质的纤维蛋白海绵作为对照。在植入Wistar大鼠背部结缔组织7、15、30和90天后,对组织反应进行定性和定量分析。
SNA和SNP在较高浓度下对L929具有细胞毒性,其中SNA的毒性明显高于SNP。SNA和SNP未诱导显著的白细胞介素 - 1β和白细胞介素 - 6产生。用5μg/mL的SNP处理L929 48小时后,干细胞因子的释放增加。组织学检查表明,在所有实验阶段,1μg/mL的SNA和SNP引起的炎症反应与对照相似。
得出的结论是,SNA和SNP在25μg/mL或更低浓度下无细胞毒性。然而,为了安全临床使用,建议进一步开展研究以确定其毒理学特征的其他方面。