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A label-free optical sensor based on nanoporous gold arrays for the detection of oligodeoxynucleotides

机译:基于纳米孔金阵列的无标签光学传感器,用于寡聚脱氧核苷酸的检测

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Interest in using nanoporous materials for sensing applications has increased. The present study reports a method of preparing well-ordered nanoporous gold arrays using a porous silicon (PSi) template. Gold nanolayer could be electrodeposited on the surface of the PSi template at low electrolysis currents in low concentration of chloroauric acid (HAuCl4) solution. Surface morphology characterizations and optical measurements revealed that a PSi-templated nanoporous gold (Au-PSi) array well replicated the nanoporous structure and retained the optical properties of PSi. Fourier transform reflectometric interference spectra showed that a characteristic blue-shifted effective optical thickness (EOT) was observed due to the low refractive index of the gold film. An optical DNA biosensor was then fabricated via the self-assembly of single-stranded DNA (ssDNA) with a specific sequence on the surface of Au-PSi. The attachment of ssDNA and its hybridization with target oligonucleotides (ODNs) persistently caused the blue shift of the EOT. Consequently, a relationship between the EOT shift and the ODN concentration was established. The mechanism of the optical response caused by DNA hybridization on the Au-PSi surface was qualitatively explained by the electromagnetic theory and electrochemical impedance spectroscopy (EIS). The lowest detection limit for target ODNs was estimated at around 10-14molL-1, when the baseline noise, a variation in the value of EOT is around 5nm. The fabricated Au-PSi based optical biosensor has potential use in the discovery of new ODN drugs because it will be able to detect the binding event between ODNs and the target DNA.
机译:使用纳米多孔材料进行传感应用的兴趣已经增加。本研究报告了一种使用多孔硅(PSi)模板制备有序的纳米多孔金阵列的方法。金纳米层可以在低浓度的氯金酸(HAuCl4)溶液中以低电解电流电沉积在PSi模板的表面上。表面形态表征和光学测量表明,以PSi为模板的纳米孔金(Au-PSi)阵列很好地复制了纳米孔结构,并保留了PSi的光学性质。傅里叶变换反射光谱干涉光谱表明,由于金膜的低折射率,观察到了特征性的蓝移有效光学厚度(EOT)。然后,通过在Au-PSi表面上具有特定序列的单链DNA(ssDNA)的自组装,制造出光学DNA生物传感器。 ssDNA的附着及其与靶寡核苷酸(ODN)的杂交持续引起EOT的蓝移。因此,建立了EOT偏移和ODN浓度之间的关系。通过电磁学原理和电化学阻抗谱(EIS)定性地解释了DNA杂交在Au-PSi表面上引起的光响应机理。目标ODN的最低检测限估计为10-14molL-1,当基线噪声时,EOT值的变化约为5nm。基于制造的基于Au-PSi的光学生物传感器在发现新的ODN药物方面具有潜在用途,因为它能够检测ODN与目标DNA之间的结合事件。

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