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Microfluidic Device Architecture for Electrochemical Patterning and Detection of Multiple DNA Sequences

机译:用于电化学模式化和检测多个DNA序列的微流体装置架构

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摘要

Electrochemical biosensors pose an attractive solution for point-of-care diagnostics because they require minimal instrumentation and they are scalable and readily integrated with microelectronics. The integration of electrochemical biosensors with microscale devices has, however, proven to be challenging due to significant incompatibilities among biomolecular stability, operation conditions of electrochemical sensors, and microfabrication techniques. Toward a solution to this problem, we have demonstrated here an electrochemical array architecture that supports the following processes in situ, within a self-enclosed microfluidic device: (a) electrode cleaning and preparation, (b) electrochemical addressing, patterning, and immobilization of sensing biomolecules at selected sensor pixels, (c) sequence-specific electrochemical detection from multiple pixels, and (d) regeneration of the sensing pixels. The architecture we have developed is general, and it should be applicable to a wide range of biosensing schemes that utilize gold–thiol self-assembled monolayer chemistry. As a proof-of-principle, we demonstrate the detection and differentiation of polymerase chain reaction (PCR) amplicons diagnostic of human (H1N1) and avian (H5N1) influenza.
机译:电化学生物传感器为即时诊断提供了一种有吸引力的解决方案,因为它们所需的仪器最少,并且具有可扩展性并且易于与微电子集成。然而,由于生物分子稳定性,电化学传感器的操作条件和微加工技术之间的显着不兼容性,电化学生物传感器与微型设备的集成已被证明具有挑战性。为了解决该问题,我们在这里展示了一种电化学阵列结构,该结构可在自封闭微流控设备中支持以下原位过程:(a)电极清洁和制备,(b)电化学寻址,图案化和固定化在选定的传感器像素处检测生物分子,(c)从多个像素进行序列特定的电化学检测,以及(d)传感像素的再生。我们开发的体系结构是通用的,应该适用于利用金-硫醇自组装单层化学的多种生物传感方案。作为原理的证明,我们证明了对人类(H1N1)和禽(H5N1)流感的诊断的聚合酶链反应(PCR)扩增子的检测和分化。

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