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首页> 外文期刊>Analytical Letters >Homogeneous Chemiluminescent Determination of Mercury(II) Using a Peroxidase-Mimicking DNAzyme Assay
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Homogeneous Chemiluminescent Determination of Mercury(II) Using a Peroxidase-Mimicking DNAzyme Assay

机译:使用过氧化物酶模拟DNAzyme测定法测定汞(II)的均匀化学发光测定

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Environmental pollution in manufacturing sectors is often accompanied by the release of diverse forms of pollutants including heavy metals. Mercury is one of the most toxic heavy metals. Here, we describe a homogeneous chemiluminescent method for Hg2+ detection based on allosteric activation of peroxidase-mimicking DNAzyme and formation of Hg2+-thymine bonds in DNA duplex with T-T mismatches in the presence of mercury. The formation of such duplex increased the activity of peroxidase-mimicking DNAzyme. The analysis conditions and structures of probes were optimized. Under the favorable conditions, the limit of detection and a linear range of the assay were 12 and 12-600nM, respectively. The values of coefficient of variation measured within the working range varied from 0.7 to 3.0%. The study of cross-reactivity of Hg2+, Ag+, Pb2+, Ca2+, Zn2+, Bi3+, Ni2+, Co2+, Ba2+, Mn2+, Cd2+, Mg2+, and Cr3+ showed that only mercury in concentration nanoscale activates peroxidase-mimicking DNAzyme that indicates high specificity of the developed Hg2+ assay. Thus, an easy-to-use, specific, rapid, and sensitive method for Hg2+ detection was developed.
机译:制造业的环境污染往往伴随着释放不同形式的污染物,包括重金属。汞是最有毒的重金属之一。这里,基于过氧化物酶 - 模拟DNAzyme的变构激活和在DNA双链体中形成HG2 + -Thymine键的均匀激活,对HG2 +检测进行均匀化学发光方法,在汞的存在下与T-T错配。这种双链体的形成增加了过氧化物酶模拟DNazyme的活性。优化了探针的分析条件和结构。在有利条件下,检测极限和测定的线性范围分别为12和12-600nm。在工作范围内测量的变化系数的值不同于0.7至3.0%。 HG2 +,Ag +,Pb2 +,Ca2 +,Zn2 +,Bi3 +,Ni2 +,CO 2 +,Ba2 +,Mn2 +,CD2 +,Mg2 +,CR3 +的研究表明,只有浓度纳米尺度的汞活化酶模拟的DNazyme,表明含有高特异性开发的HG2 +测定。因此,开发了用于HG2 +检测的易于使用,特异性,快速和敏感的方法。

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