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AuNPs amplified magnetophoretic effect for colorimetric detection of nucleic acid

机译:AuNPs扩增了磁泳效应,用于比色检测核酸

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Colorimetric assay for detection of nucleic acid offers superior simplicity for point-of-care applications. However, the limit of detection (LOD) is usually at nM level in many colorimetric assays, which is insufficient for disease diagnosis or pathogen identifications. Here we report a colorimetric detection of nucleic acids based on gold nanoparticles (AuNPs) amplified magnetophoretic effect. The assay was conducted in two steps. In the first step, the present target DNA molecules link magnetic microparticles (MMPs) and AuNPs, and the linked AuNPs can be subsequently collected after magnetic attraction and heat treatment. In the second step, the collected AuNPs linked a pair of MMPs and polymer microparticles (PMPs), forming MMPs-AuNPs-PMPs. Thus, by applying an external magnetic field that pulls the linked MMPs-AuNPs-PMPs to the sidewall, magnetophoretic effect renders a change of solution color from opaque to transparent reflecting the quantity of the target DNA molecules. Our results demonstrate the LOD reaches 45 amol (1 pM in 45 μl) by spectrometry and 2.25 fmol (50 pM in 45 μl) by naked eyes. This method is tens to hundreds times more sensitive as compared with other colorimetric detections such as AuNPs aggregation or lateral flow test strip, with great potential for applications in low resource settings.
机译:用于核酸检测的比色测定为现场护理应用提供了卓越的简便性。但是,在许多比色测定中,检出限(LOD)通常处于nM水平,不足以进行疾病诊断或病原体鉴定。在这里,我们报告基于比色法检测核酸的金纳米颗粒(AuNPs)放大了磁致热效应。该测定分两个步骤进行。在第一步中,本发明的靶DNA分子连接磁性微粒(MMP)和AuNP,并且在磁吸引和热处理之后可以随后收集连接的AuNP。在第二步中,收集的AuNP连接一对MMP和聚合物微粒(PMP),形成MMP-AuNPs-PMP。因此,通过施加将链接的MMPs-AuNPs-PMP拉到侧壁的外部磁场,磁致效应使溶液颜色从不透明变为透明,从而反映了目标DNA分子的数量。我们的结果表明,通过光谱法测得的LOD达到45 amol(45μl,1 pM),用肉眼观察到2.25 fmol(45μl,50 pM)。与其他比色检测(例如AuNPs聚合或侧向流动检测条)相比,该方法的灵敏度要高几十到几百倍,在资源匮乏的环境中具有巨大的应用潜力。

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