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Label-free colorimetric assay for biological thiols based on ssDNA/silver nanoparticle system by salt amplification

机译:盐扩增基于ssDNA /银纳米颗粒体系的生物硫醇的无标记比色测定

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摘要

We report a novel method for biological thiols detection using ssDNA/sliver nanoparticles system. The adsorbing ssDNA supplies silver nanoparticles high density charge to rescue nanoparticles from aggregation induced by salt. However, homocysteine (cysteine or glutathione) is conjugated more powerfully than ssDNA to AgNPs via Ag–S bond, which holds back ssDNA binding to AgNPs surface. When salt is added, AgNPs aggregation occurs and the corresponding color changes from yellow to brown after these biological thiols is introduced. A high sensitivity can be achieved using salt as an amplifier to assay thiols. In our study, a favorable linear correlation between the A0/Ax ratio and homocysteine concentration was obtained in the range of 10 to 500 nM with a low detection limit of 10 nM, indicating that homocysteine could be analyzed at low concentration. A concentration as low as 300 nM homocysteine caused a visible color change. As well as, cysteine and glutathione can be detected at a detection limit of 50 nM and 100 nM, respectively. In addition, study on the selectivity of this method shows that only homocysteine , cysteine and glutathione can generate signal response.
机译:我们报告了使用ssDNA / sliver纳米粒子系统进行生物硫醇检测的新方法。吸附的ssDNA为银纳米颗粒提供高密度电荷,以拯救纳米颗粒免受盐诱导的聚集。但是,同型半胱氨酸(半胱氨酸或谷胱甘肽)比ssDNA通过Ag-S键与AgNPs的结合更牢固,这使ssDNA不能与AgNPs结合。当加入盐时,引入了这些生物硫醇后,AgNPs发生聚集,相应的颜色从黄色变为棕色。使用盐作为放大器分析硫醇可以实现高灵敏度。在我们的研究中,A0 / Ax比与高半胱氨酸浓度之间存在良好的线性相关性,检测限为10 nM,低至10 nM,这表明可以在低浓度下分析高半胱氨酸。低至300 nM高半胱氨酸的浓度会导致可见的颜色变化。同样,半胱氨酸和谷胱甘肽也可以分别以50 nM和100 nM的检测限进行检测。此外,对这种方法的选择性的研究表明,只有高半胱氨酸,半胱氨酸和谷胱甘肽可以产生信号响应。

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