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Monitoring of troponin release from cardiomyocytes during exposure to toxic substances using surface plasmon resonance biosensing

机译:使用表面等离子体共振生物传感在暴露于有毒物质期间从心肌细胞中释放的肌钙蛋白释放

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摘要

Troponin T (TnT) is a useful biomarker for studying drug-induced toxicity effects on cardiac cells. We describe how a surface plasmon resonance (SPR) biosensor was applied to monitor the release of TnT from active HL-1 cardiomyocytes in vitro when exposed to cardiotoxic substances. Two monoclonal human TnT antibodies were compared in the SPR immunosensor to analyse the TnT release. The detection limit of TnT was determined to be 30 ng/ml in a direct assay set-up and to be 10 ng/ml in a sandwich assay format. Exposure of the cardiomyocytes to doxorubicin, troglitazone, quinidine and cobalt chloride for periods of 6 and 24 h gave significant SPR responses, whereas substances with low toxicity showed insignificant effects (ascorbic acid, methotrexate). The SPR results were verified with a validated immunochemiluminescence method which showed a correlation of r ~2 = 0.790.
机译:肌钙蛋白T(TNT)是一种用于研究对心脏细胞的药物诱导的毒性作用的有用生物标志物。 我们描述了如何将表面等离子体共振(SPR)生物传感器应用于在暴露于心脏毒性物质时在体外监测来自活性HL-1心肌细胞的TNT的释放。 在SPR免疫传感器中比较了两种单克隆人TNT抗体以分析TNT释放。 将TNT的检测限测定为30ng / ml,在直接测定设定中为30ng / ml,夹心测定形式为10ng / ml。 在6和24小时的时间内暴露于多柔比霉素,拓亮酮,奎尼丁和氯化钴,具有显着的SPR反应,而毒性低的物质显示出微不足道的效果(抗坏血酸,甲氨蝶呤)。 通过验证的免疫细胞发光方法验证SPR结果,该方法显示R〜2 = 0.790的相关性。

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