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首页> 外文期刊>Mikrochimica Acta: An International Journal for Physical and Chemical Methods of Analysis >Sensitive determination of Hg(II) based on a hybridization chain recycling amplification reaction and surface-enhanced Raman scattering on gold nanoparticles
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Sensitive determination of Hg(II) based on a hybridization chain recycling amplification reaction and surface-enhanced Raman scattering on gold nanoparticles

机译:基于杂交链回收扩增反应和表面增强拉曼散射在金纳米粒子上的敏感测定

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摘要

A method was developed for the determination of mercuric ion Hg(II). It is based on hybridization chain reaction (HCR) and surface-enhanced Raman scattering (SERS). Raman signal DNA and streptavidin were self-assembled on gold nanoparticles as a novel signal nanoprobe (AuNP-sDNA). A thymine-mercury(II)-thymine structure was immobilized on magnetic beads (MBs). The HCR makes use of two hairpin probes that are initiated by the trigger DNA to form a stable nicked dsDNA structure (MB-TS-hDNAs). A large number of the binding sites is provided to connect the signal nanoprobe. The stable sandwich structure (MB-TS-hDNA/AuNP-sDNA) was isolated by applying a magnetic field and used in the amplification step. In this way, Hg(II) can be determined sensitively after multiple signal amplification. The SERS signal, measured at 1499 cm(-1), increases linearly in the 0.1 pM to 10 nM Hg(II) concentration range, and the limit of detection is 0.08 pM (at an S/N ratio of 3). The method was applied to the detection of Hg(II) in spiked environment water samples, with recoveries ranging from 96 to 119%.
机译:开发了一种用于测定汞离子HG(II)的方法。它基于杂交链反应(HCR)和表面增强拉曼散射(SERS)。拉曼信号DNA和链霉抗生物素蛋白在金纳米粒子上自组装为新的信号NaNoProbe(AUNP-SDNA)。将胸腺嘧啶 - 汞(II)固定在磁珠(MBS)上固定胸腺嘧啶结构。 HCR利用由触发DNA发起的两种发夹探针,形成稳定的切屑DSDNA结构(MB-TS-HDNA)。提供大量的绑定站以连接信号纳米孔。通过施加磁场并在扩增步骤中使用稳定的夹心结构(MB-TS-HDNA / AUNP-SDNA)。以这种方式,在多个信号放大后可以敏感地确定HG(II)。在1499cm(-1)下测量的SERs信号在0.1pm至10nm hg(ii)浓度范围内线性增加,并且检测限为0.08μm(以s / n比为3)。将该方法应用于尖刺环境水样中HG(II)的检测,回收率范围为96至119%。

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