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Volume-amplified magnetic bioassay integrated with microfluidic sample handling and high-Tc SQUID magnetic readout

机译:体积放大的磁性生物测定法结合了微流体样品处理和高Tc SQUID磁性读数

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摘要

A bioassay based on a high-Tc superconducting quantum interference device (SQUID) reading out functionalized magnetic nanoparticles (fMNPs) in a prototype microfluidic platform is presented. The target molecule recognition is based on volume amplification using padlock-probe-ligation followed by rolling circle amplification (RCA). The MNPs are functionalized with single-stranded oligonucleotides, which give a specific binding of the MNPs to the large RCA coil product, resulting in a large change in the amplitude of the imaginary part of the ac magnetic susceptibility. The RCA products from amplification of synthetic Vibrio cholera target DNA were investigated using our SQUID ac susceptibility system in microfluidic channel with an equivalent sample volume of 3 μl. From extrapolation of the linear dependence of the SQUID signal versus concentration of the RCA coils, it is found that the projected limit of detection for our system is about 1.0 × 105 RCA coils (0.2 × 10−18 mol), which is equivalent to 66 fM in the 3 μl sample volume. This ultra-high magnetic sensitivity and integration with microfluidic sample handling are critical steps towards magnetic bioassays for rapid detection of DNA and RNA targets at the point of care.
机译:提出了一种基于高Tc超导量子干涉装置(SQUID)的生物测定方法,该装置可在原型微流体平台中读出功能化的磁性纳米颗粒(fMNP)。靶分子识别基于使用挂锁探针连接的体积扩增,然后是滚环扩增(RCA)。用单链寡核苷酸对MNP进行功能化,从而使MNP与大型RCA线圈产物产生特异性结合,从而导致交流磁化率虚部的幅度发生较大变化。使用我们的SQUID ac磁化率系统在微流体通道中以3μl的当量样品研究了合成霍乱弧菌靶DNA扩增得到的RCA产物。从SQUID信号与RCA线圈浓度的线性相关性的外推法可以发现,我们系统的检测预测极限约为1.0×10 5 RCA线圈(0.2×10 −18 mol),相当于3μl样品体积中的66 fM。这种超高的磁性灵敏度以及与微流体样品处理的集成是朝着磁性生物测定法迈出的关键步骤,以便在护理点快速检测DNA和RNA靶标。

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