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Collection focusing and metering of DNA in microchannels using addressable electrode arrays for portable low-power bioanalysis

机译:使用可寻址的电极阵列进行便携式低功耗生物分析的微通道中的DNA收集聚焦和计量

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摘要

Although advances in microfluidic technology have enabled increasingly sophisticated biosensing and bioassay operations to be performed at the microscale, many of these applications employ such small amounts of charged biomolecules (DNA, proteins, and peptides) that they must first be preconcentrated to a detectable level. Efficient strategies for precisely handling minute quantities of biomolecules in microchannel geometries are critically needed; however, it has proven challenging to achieve simultaneous concentration, focusing, and metering capabilities with current-generation sample-injection technology. By using microfluidic chips incorporating arrays of individually addressable microfabricated electrodes, we demonstrate that DNA can be sequentially concentrated, focused into a narrow zone, metered, and injected into an analysis channel. This technique transports charged biomolecules between active electrodes upon application of a small potential difference (1 V) and is capable of achieving orders of magnitude concentration increases within a small device footprint. The collected samples are highly focused, with sample zone size and shape defined solely by electrode geometry.
机译:尽管微流体技术的进步已使越来越复杂的生物传感和生物测定操作能够在微尺度上进行,但其中许多应用使用了如此少量的带电生物分子(DNA,蛋白质和肽),因此必须首先将其预先浓缩至可检测的水平。迫切需要在微通道几何结构中精确处理微量生物分子的有效策略。然而,事实证明,利用当前的样品注射技术同时实现集中,聚焦和计量功能具有挑战性。通过使用微流控芯片并入可单独寻址的微加工电极阵列,我们证明了DNA可以顺序浓缩,聚焦到狭窄区域,计量并注入分析通道。施加小电位差(1 V)后,该技术会在有源电极之间传输带电的生物分子,并且能够在较小的设备占地面积内实现数个数量级的浓度增加。收集的样品高度集中,样品区域的大小和形状仅由电极几何形状定义。

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