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Radial Flow Assay Using Gold Nanoparticles and Rolling Circle Amplification to Detect Mercuric Ions

机译:使用金纳米颗粒和滚环扩增检测汞离子的径向流分析

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摘要

A novel colorimetric assay employing oligonucleotide-conjugated gold nanoparticle (AuNP probes) and rolling circle amplification (RCA) was developed for simple detection of mercuric ions (Hg2+). The thymine-Hg2+-thymine (T-Hg2+-T) coordination chemistry makes our detection system selective for Hg2+. In the presence of Hg2+, the thymine 12-mer oligonucleotide is unable to act as a primer for RCA due to the formation of T-Hg2+-T before the RCA reaction. However, in the absence of Hg2+, DNA coils as RCA products are generated during the RCA reaction, and is further labeled with AuNP probes. Colorimetric signals that depend on the amount of DNA coil-AuNP probe complexes were generated by drop-drying the reaction solution on nitrocellulose-based paper. As the reaction solution spread radially because of capillary action, the complexes formed a concentric red spot on the paper. The colorimetric signals of the red spots were rapidly measured with a portable spectrophotometer and determined as the ΔE value, which indicates the calculated color intensity. Our assay displays great linearity (detection limit: 22.4 nM), precision, and reproducibility, thus demonstrating its utility for Hg2+ quantification in real samples. We suggest that our simple, portable, and cost-effective method could be used for on-site Hg2+ detections.
机译:为了检测汞离子(Hg 2 + ),开发了一种利用寡核苷酸结合的金纳米颗粒(AuNP探针)和滚环扩增(RCA)的比色法。胸腺嘧啶-Hg 2 + -胸腺嘧啶(T-Hg 2 + -T)配位化学使我们的检测系统对Hg 2 + 具有选择性。在Hg 2 + 存在下,胸腺嘧啶12-mer寡核苷酸由于T-Hg 2 + -T的形成而无法充当RCA的引物RCA反应。然而,在没有Hg 2 + 的情况下,在RCA反应过程中会生成DNA线圈,作为RCA产物,并用AuNP探针进一步标记。通过在基于硝酸纤维素的纸上滴干反应溶液,生成取决于DNA线圈-AuNP探针复合物数量的比色信号。由于毛细管作用,反应溶液径向扩散,络合物在纸上形成同心红点。用便携式分光光度计快速测量红色斑点的比色信号,并将其确定为ΔE值,该值表示计算出的颜色强度。我们的测定法具有很高的线性度(检测限:22.4 nM),精密度和可重复性,因此证明了其在实际样品中Hg 2 + 定量分析中的实用性。我们建议,我们的简单,便携式且经济高效的方法可用于现场检测Hg 2 +

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