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高内涵筛选分析测定螺吡喃细胞毒性及其在生物纳米传感中的安全应用

Determination of spiropyran cytotoxicity by high content screening and analysis for safe application in bionanosensing.

机构信息

Centre for Research on Adaptive Nanostructures and Nanodevices (CRANN), School of Chemistry, School of Physics, and School of Medicine, Trinity College Dublin, Dublin, Ireland.

出版信息

Chem Res Toxicol. 2010 Sep 20;23(9):1459-66. doi: 10.1021/tx100123g.

Abstract

The in vitro toxic response of spiropyrans in cellular models has not been previously addressed, despite the fact that such photoswitchable molecules have shown great potential as versatile and tunable components for bionanodevices and imaging agents. In this study, we examine the cytotoxic effects of a spiropyran, namely, 8-methoxy-6-nitro-BIPS (1',3'-dihydro-1'-ethanol-3',3'-dimethyl-8-methoxy-6-nitro-spiro(2H-1-benzopyran-2,2'-(2H)-indole) [1], in three cultured cellular models (THP-1, AGS, and A549 cell lines) by High Content Screening and Analysis (HCSA) and by enzyme-linked immunosorbent (ELISA) assays (Interleukin-6 and Tumor Necrosis Factor-alpha). The HCSA results show that low concentrations of 8-methoxy-6-nitro-BIPS (10(-6), 10(-8), and 10(-9) M) do not induce any cytotoxic response after 24 and 72 h exposure time, while at the highest concentrations (10(-3)and 10(-4) M) the exposure time becomes a critical parameter of the toxic response. The cell viability is reduced by 60% for THP-1 cells, 50% for AGS cells, and 40% for A549 cells at a spiropyran concentration of 10(-3) M after 24 h incubation, whereas at 72 h, the cell loss increases above 90%. Interestingly, at 10(-4) M no significant cytotoxic response is registered after 24 h exposure, where contrarily cytotoxicity is verified after 72 h. Our ELISA results show that consistently with the HCSA analysis a robust inflammatory response is present at 10(-3) M after 24 h exposure and at 10(-3) M and 10(-4) M after 72 h, in all three cell lines investigated.

摘要

尽管这类光致变色分子已显示出作为生物纳米器件和成像剂的多功能和可调组件的巨大潜力,但迄今为止,尚未研究过螺旋吡喃在细胞模型中的体外毒性反应。在这项研究中,我们通过高通量筛选和分析(HCSA)以及酶联免疫吸附(ELISA)测定法(白细胞介素 6 和肿瘤坏死因子-α)来检查一种螺旋吡喃,即 8-甲氧基-6-硝基-BIPS(1',3'-二氢-1'-乙醇-3',3'-二甲基-8-甲氧基-6-硝基螺[2H-1-苯并吡喃-2,2'-(2H)-吲哚] [1]在三种培养的细胞模型(THP-1、AGS 和 A549 细胞系)中的细胞毒性作用。HCSA 结果表明,在 24 和 72 h 暴露时间内,低浓度的 8-甲氧基-6-硝基-BIPS(10^-6、10^-8 和 10^-9 M)不会引起任何细胞毒性反应,而在最高浓度(10^-3 和 10^-4 M)下,暴露时间成为毒性反应的关键参数。在 10^-3 M 浓度下,THP-1 细胞的细胞活力降低了 60%,AGS 细胞的细胞活力降低了 50%,A549 细胞的细胞活力降低了 40%,孵育 24 h 后,而在 72 h 时,细胞损失超过 90%。有趣的是,在 10^-4 M 下,24 h 暴露后未检测到明显的细胞毒性反应,而相反,在 72 h 后则证实了细胞毒性。我们的 ELISA 结果表明,与 HCSA 分析一致,在所有三种研究的细胞系中,在 24 h 暴露后浓度为 10^-3 M 时存在强烈的炎症反应,并且在 72 h 后在 10^-3 M 和 10^-4 M 时存在炎症反应。

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