首页> 外文期刊>Toxicology: An International Journal Concerned with the Effects of Chemicals on Living Systems >Multi wall carbon nanotubes induce oxidative stress and cytotoxicity in human embryonic kidney (HEK293) cells.
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Multi wall carbon nanotubes induce oxidative stress and cytotoxicity in human embryonic kidney (HEK293) cells.

机译:多壁碳纳米管在人胚胎肾脏(HEK293)细胞中诱导氧化应激和细胞毒性。

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摘要

The present study was aimed at evaluating the potential toxicity and the general mechanism involved in multi wall carbon nanotubes (MWCNT)-induced cytotoxicity using human embryonic kidney cell line (HEK293) cells. Two multi wall carbon nanotubes (coded as MWCNT1, size: 90-150nm and MWCNT2, size: 60-80nm) used in this study are MWCNT1 (produced by the electric arc method and size of the nanotubes was 90-150nm) and MWCNT2 (produced by the chemical vapor deposition method with size of 60-80nm). To elucidate the possible mechanisms of MWCNT induced cytotoxicity, cell viability, mitochondrial function (MTT assay), cell membrane damage (LDH assay), reduced glutathione (GSH), interleukin-8 (IL-8) and lipid peroxidation levels were quantitatively assessed under carbon nanotubes exposed (48h) conditions. Exposure of different sizes of two carbon nanotubes at dosage levels between 3 and 300mug/ml decreased cell viability in a concentration dependent manner. The IC(50) values (concentration of nanoparticles to induce 50% cell mortality) of two (MWCNT1, MWCNT2) nanoparticles were found as 42.10 and 36.95mug/ml. Exposure of MWCNT (10-100mug/ml) to HEK cells resulted in concentration dependent cell membrane damage (as indicated by the increased levels of LDH), increased production of IL-8, increased TBARS and decreased intracellular glutathione levels. The cytotoxicity and oxidative stress was significantly more in MWCNT2 exposed cells than MWCNT1. In summary, exposure of carbon nanotubes resulted in a concentration dependent cytotoxicity in cultured HEK293 cells that was associated with increased oxidative stress.
机译:本研究旨在评估潜在的毒性和涉及使用人胚胎肾细胞系(HEK293)的多壁碳纳米管(MWCNT)诱导的细胞毒性的一般机制。本研究中使用的两种多壁碳纳米管(编码为MWCNT1,尺寸:90-150nm和MWCNT2,尺寸:60-80nm)分别是MWCNT1(通过电弧法生产,纳米管的尺寸为90-150nm)和MWCNT2(通过化学气相沉积法生产的,尺寸为60-80nm)。为了阐明MWCNT诱导的细胞毒性,细胞活力,线粒体功能(MTT测定),细胞膜损伤(LDH测定),还原型谷胱甘肽(GSH),白介素8(IL-8)和脂质过氧化水平的可能机制,在以下条件下进行了定量评估:碳纳米管暴露(48h)的条件。剂量水平为3至300mug / ml的不同大小的两个碳纳米管的暴露以浓度依赖的方式降低了细胞活力。发现两个(MWCNT1,MWCNT2)纳米颗粒的IC(50)值(诱导50%细胞死亡的纳米颗粒浓度)为42.10和36.95mug / ml。 MWCNT(10-100ug / ml)暴露于HEK细胞会导致浓度依赖性细胞膜损伤(如LDH水平升高所指示),IL-8产量增加,TBARS升高和细胞内谷胱甘肽水平降低。暴露于MWCNT2的细胞的细胞毒性和氧化应激明显高于MWCNT1。总之,碳纳米管的暴露在培养的HEK293细胞中导致浓度依赖性的细胞毒性,这与氧化应激的增加有关。

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