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SERS-based sandwich bioassay protocol of miRNA-21 using Au@Ag core–shell nanoparticles and a Ag/TiO2 nanowires substrate

机译:使用Au @ Ag核壳纳米粒子和Ag / TiO2纳米线底物的基于SERS的miRNA-21夹心生物测定方案

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Based on surface-enhanced Raman scattering (SERS) technology, Au@Ag@4MBA@5′-NH2-ssDNA probes and a Ag/TiO2@3′-NH2-ssDNA substrate were prepared and constructed into a sandwich structure to develop a high sensitivity bioassay of miRNA-21. The Au@Ag@4MBA@5′-NH2-ssDNA probes were prepared by immobilizing 5′-NH2-ssDNA onto the surfaces of 4MBA-labelled Au@Ag core–shell nanoparticles, and the Ag/TiO2@3′-NH2-ssDNA substrate was prepared by immobilizing 3′-NH2-ssDNA on the surface of Ag/TiO2 nanowires SERS-active substrates. The experimental results showed that the SERS-based sandwich bioassay of miRNA-21 presented a low limit of detection of 0.75 fM and a broad dynamic range from 1.0 fM to 1.0 nM. Also, the test data for the SERS-based sandwich bioassay were not only consistent with that of the real-time fluorescence quantitative polynucleotide chain reaction (RT-qPCR) method but also displayed higher detection sensitivity. It was shown that the SERS-based sandwich bioassay of miRNA-21 has importance for use in potential applications involving diagnosing clinical cancer patients.
机译:基于表面增强拉曼散射(SERS)技术,制备了Au @ Ag @ 4MBA @ 5′-NH2-ssDNA探针和Ag / TiO2 @ 3′-NH2-ssDNA底物,并构建成三明治结构以形成高miRNA-21的敏感性生物测定。 Au @ Ag @ 4MBA @ 5′-NH2-ssDNA探针是通过将5′-NH2-ssDNA固定在4MBA标记的Au @ Ag核壳纳米颗粒和Ag / TiO2 @ 3′-NH2-表面上制备的通过将3'-NH2-ssDNA固定在Ag / TiO2纳米线SERS活性底物表面上来制备ssDNA底物。实验结果表明,基于SERS的miRNA-21夹心生物测定法的检测下限为0.75 fM,动态范围为1.0 fM至1.0 nM。此外,基于SERS的夹心生物测定的测试数据不仅与实时荧光定量多核苷酸链反应(RT-qPCR)方法一致,而且显示出更高的检测灵敏度。结果表明,基于SERS的miRNA-21夹心生物测定法在涉及诊断临床癌症患者的潜在应用中具有重要意义。

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