Key Laboratory of Sensor Analysis of Tumor Marker, Ministry of Education; Shandong Key Laboratory of Biochemical Analysis; Key Laboratory of Analytical Chemistry for Life Science in Universities of Shandong, College of Chemistry and Molecular Engineering, Qingdao University of Science and Technology, Qingdao, 266042, People's Republic of China.
Department of Neurology, Qingdao City Center Hospital, No.127 5 Siliu South Road, Qingdao, Shandong, 266042, People's Republic of China.
Mikrochim Acta. 2018 Jul 5;185(8):363. doi: 10.1007/s00604-018-2907-2.
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, 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%. Graphical abstract Schematic of a method based on the use of a stable T-Hg(II)-T structure and a self-assembled nanoprobe. It was applied to the trace Hg(II) detection based on hybridization chain reaction (HCR) and surface-enhanced Raman scattering (SERS).
一种测定汞离子 Hg(II) 的方法。它基于杂交链式反应 (HCR) 和表面增强拉曼散射 (SERS)。Raman 信号 DNA 和链霉亲和素自组装在金纳米粒子上作为新型信号纳米探针 (AuNP-sDNA)。胸腺嘧啶-汞 (II)-胸腺嘧啶结构固定在磁性珠 (MBs) 上。HCR 利用两个发夹探针,由触发 DNA 引发,形成稳定的缺口 dsDNA 结构 (MB-TS-hDNAs)。提供了大量的结合位点来连接信号纳米探针。通过施加磁场可以分离稳定的三明治结构 (MB-TS-hDNA/AuNP-sDNA),并用于放大步骤。通过这种方式,可以在多次信号放大后灵敏地测定 Hg(II)。在 1499 cm 处测量的 SERS 信号在 0.1 pM 至 10 nM Hg(II) 浓度范围内呈线性增加,检测限为 0.08 pM(信噪比为 3)。该方法用于测定加标环境水样中的 Hg(II),回收率在 96%至 119%之间。