首页> 外文OA文献 >HEPATOTOXICITY ASSESSMENT OF THE AZO DYES DISPERSE ORANGE 1 (DO1), DISPERSE RED 1 (DR1,) AND DISPERSE RED 13 (DR13) IN HEPG2 CELLS
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HEPATOTOXICITY ASSESSMENT OF THE AZO DYES DISPERSE ORANGE 1 (DO1), DISPERSE RED 1 (DR1,) AND DISPERSE RED 13 (DR13) IN HEPG2 CELLS

机译:HEPG2细胞中偶氮染料分散橙1(DO1),分散红1(DR1)和分散红13(DR13)的肝毒性评估

摘要

During the dyeing process in baths approximately 10 to 15% of the dyes used are lost and reach industrial effluents, thus polluting the environment. Studies showed that some classes of dyes, mainly azo dyes and their by-products, exert adverse effects on humans and local biota, since the wastewater treatment systems and water treatment plants were found to be ineffective in removing the color and reducing toxicity of some dyes. In the present study, the toxicity of the azo dyes disperse orange 1 (DO1), disperse red 1 (DR1), and disperse red 13 (DR13) was evaluated in HepG2 cells grown in monolayers or in three dimensional (3D) culture. Hepatotoxicity of the dyes was measured using 3-(4,5-dimethylthiazol-2yl)2,5-diphenyltetrazolium (MTT) and cell counting kit 8 (CCK-8) assays after 24, 48, and 72 h of incubation of cells with 3 different concentrations of the azo dyes. The dye DO1 only reduced the mitochondrial activity in HepG2 cells grown in a monolayer after 72 h incubation, while the dye DR1 showed this deleterious effect in both monolayer and 3D culture. In contrast, dye DR13 decreased the mitochondrial activity after 24, 48, and 72 h of exposure in both monolayer and 3D culture. With respect to dehydrogenase activity, only the dye DR13 diminished the activity of this enzyme after 72 h of exposure in both monolayer and 3D culture. Our results clearly demonstrated that exposure to the studied dyes induced cytotoxicity in HepG2 cells.
机译:在浴中染色过程中,大约10%至15%的染料会流失并进入工业废水,从而污染环境。研究表明,某些类型的染料,主要是偶氮染料及其副产物,会对人类和当地生物群产生不利影响,因为发现废水处理系统和水处理厂不能有效去除某些染料的颜色并降低其毒性。 。在本研究中,在单层或三维(3D)培养的HepG2细胞中评估了偶氮染料分散橙色1(DO1),分散红色1(DR1)和分散红色13(DR13)的毒性。使用3-(4,5-二甲基噻唑-2-基)2,5-二苯基四唑(MTT)和细胞计数试剂盒8(CCK-8)测定在24、48和72 h细胞孵育后测定染料的肝毒性3种不同浓度的偶氮染料。染料DO1在孵育72小时后仅会降低单层生长的HepG2细胞中的线粒体活性,而染料DR1在单层和3D培养中均显示出这种有害作用。相反,在单层和3D培养中,染料DR13在暴露24、48和72小时后会降低线粒体活性。关于脱氢酶活性,在单层和3D培养中,仅染料DR13暴露72 h后,该酶的活性就会降低。我们的结果清楚地表明,暴露于所研究的染料可诱导HepG2细胞的细胞毒性。

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