Simultaneous or separate detection of heavy metal ions Hg2+ and Ag+ based on lateral flow assays

IF 5.3 2区 化学 Q1 CHEMISTRY, ANALYTICAL
Zhili Wang, Yueyang Cheng, Ting Tang, Xiaoru Zhang, Xunyi Yuan
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引用次数: 0

Abstract

A lateral flow assay (LFA) was developed for the simultaneous or separate detection of mercury ion and silver ion based on isothermal nucleic acid amplification. T-Hg2+-T and C–Ag+-C were utilized in the isothermal nucleic acid amplification strategy to form specific complementary base pairs. Under the action of KF polymerase and endonuclease Nt.BbvCl, trace amounts of Hg2+ and Ag+ were converted to Product-Hg2+ and Product-Ag+ as bridges. Biotin-labeled capture strands (Biotin-DNA1, Biotin-DNA1, and Biotin-DNA3) immobilized on the test strips could capture the Au NPs-DNA nanoprobes by hybridization with the generated bridge products for monitoring of two heavy metal ions simultaneously or separately. The assembly method of DNAs on the nanoprobes was explored, and the DNA sequences on the nanoprobes were designed so that only one kind of DNA strand was used to bind to all three capture DNA strands on the C, T1, and T2 bands. Under optimal detection conditions, the limits of detection for Hg2+ and Ag+ were 2.19 and 5.41 pM, respectively, with desired selectivity and reproducibility.

Graphical Abstract

同时或单独检测重金属离子Hg2+和Ag+基于横向流动分析
建立了一种基于等温核酸扩增技术同时或单独检测汞离子和银离子的横向流动法(LFA)。在等温核酸扩增策略中利用T-Hg2+-T和C-Ag +-C形成特异性互补碱基对。在KF聚合酶和内切酶Nt.BbvCl的作用下,微量的Hg2+和Ag+作为桥梁转化为Product-Hg2+和Product-Ag+。生物素标记的捕获链(Biotin-DNA1, Biotin-DNA1和Biotin-DNA3)固定在试纸上,通过与生成的桥接产物杂交,可以捕获Au NPs-DNA纳米探针,同时或单独监测两种重金属离子。探索了DNA在纳米探针上的组装方法,并设计了纳米探针上的DNA序列,使得只使用一种DNA链结合C、T1和T2上的三个捕获DNA链。在最佳检测条件下,Hg2+和Ag+的检出限分别为2.19和5.41 pM,具有良好的选择性和重复性。图形抽象
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来源期刊
Microchimica Acta
Microchimica Acta 化学-分析化学
CiteScore
9.80
自引率
5.30%
发文量
410
审稿时长
2.7 months
期刊介绍: As a peer-reviewed journal for analytical sciences and technologies on the micro- and nanoscale, Microchimica Acta has established itself as a premier forum for truly novel approaches in chemical and biochemical analysis. Coverage includes methods and devices that provide expedient solutions to the most contemporary demands in this area. Examples are point-of-care technologies, wearable (bio)sensors, in-vivo-monitoring, micro/nanomotors and materials based on synthetic biology as well as biomedical imaging and targeting.
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