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A magnetic-based SERS approach for highly sensitive and reproducible detection of cancer-related serum microRNAs

机译:基于磁性的SERS方法可高度灵敏,可重现地检​​测与癌症相关的血清microRNA

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This paper describes the combination of silica-coated, analyte-tagged gold nanoparticles (SA@GNPs) and gold-coated paramagnetic nanoparticles (Au@MNPs) in a sandwich assay for the surface enhanced Raman scattering (SERS) detection of cancer-related serum microRNA, miRNA 141. The target sequence is captured by hybridization reactions with complementary oligonucleotide probes conjugated to the SA@GNPs and Au@MNPs, respectively. The resultant hybridization complexes, SA@GNP/miRNA 141/Au@MNP, are removed from solution by using an external magnet. Laser excitation of the concentrated complexes provides a SERS signature spectrum diagnostic for the analyte molecules embedded in the SA@GNPs and specific to the target sequence, miRNA 141. The limit of detection (LOD) for target sequences in serum was 1.8 pM, which is lower by a factor of ~110 than the previously reported LOD in a similar magnetic-based SERS assay using uncoated, Raman-tagged GNPs as SERS nanotags, which have been demonstrated to suffer signal loss due to the serum protein displacement of Raman analyte molecules on the surface. These results indicate that silica coating plays an essential role in preventing disassociation of Raman reporters from the GNPs, allowing more quantitative and reproducible detection of serum miRNAs than conventional uncoated SERS nanotags.
机译:本文介绍了在三明治测定中用于表面增强拉曼散射(SERS)检测癌症相关血清的夹层法中二氧化硅涂层,被分析物标记的金纳米颗粒(SA @ GNPs)和金涂层顺磁性纳米颗粒(Au @ MNPs)的组合microRNA,miRNA141。通过与分别与SA @ GNPs和Au @ MNPs偶联的互补寡核苷酸探针的杂交反应捕获靶序列。通过使用外部磁体从溶液中除去所得的杂交复合物SA @ GNP / miRNA 141 / Au @ MNP。浓缩物的激光激发为嵌入SA @ GNPs且对靶序列miRNA 141特异的分析物分子提供了SERS签名光谱诊断。血清中靶序列的检测限(LOD)为1.8 pM,为在未使用拉曼标记的GNPs作为SERS纳米标签的类似的基于磁性的SERS分析中,其比以前报道的LOD低约110倍,已经证明由于拉曼分析物分子在血清中的蛋白质位移而遭受信号损失表面。这些结果表明,二氧化硅涂层在防止拉曼报道分子与GNP分离方面起着至关重要的作用,与传统的未涂层SERS纳米标签相比,可以更定量和可重现地检​​测血清miRNA。

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