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Integration of Multiplexed Microfluidic Electrokinetic Concentrators with a Morpholino Microarray via Reversible Surface Bonding for Enhanced DNA Hybridization

机译:通过可逆表面键合将多路微流电动浓缩器与Morpholino微阵列整合以增强DNA杂交

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We describe a microfluidic concentration device to accelerate the surface hybridization reaction between DNA and morpholinos (MOs) for enhanced detection. The microfluidic concentrator comprises a single polydimethylsiloxane (PDMS) microchannel onto which an ion-selective layer of conductive polymer poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate) (PE-DOT:PSS) was directly printed and then reversibly surface bonded onto a morpholino microarray for hybridization. Using this electrokinetic trapping concentrator, we could achieve a maximum concentration factor of similar to 800 for DNA and a limit of detection of 10 nM within 15 min. In terms of the detection speed, it enabled faster hybridization by around 10-fold when compared to conventional diffusion-based hybridization. A significant advantage of our approach is that the fabrication of the microfluidic concentrator is completely decoupled from the microarray; by eliminating the need to deposit an ion-selective layer on the microarray surface prior to device integration, interfacing between both modules, the PDMS chip for electrokinetic concentration and the substrate for DNA sensing are easier and applicable to any microarray platform. Furthermore, this fabrication strategy facilitates a multiplexing of concentrators. We have demonstrated the proof-of concept for multiplexing by building a device with 5 parallel concentrators connected to a single inlet/outlet and applying it to parallel concentration and hybridization. Such device yielded similar concentration and hybridization efficiency compared to that of a single-channel device without adding any complexity to the fabrication and setup. These results demonstrate that our concentrator concept can be applied to the development of a highly multiplexed concentrator-enhanced microarray detection system for either genetic analysis or other diagnostic assays.
机译:我们描述了一种微流体浓缩装置,以加速DNA和吗啉代(MOs)之间的表面杂交反应,以提高检测效率。微流体浓缩器包括单个聚二甲基硅氧烷(PDMS)微通道,其上直接印刷了导电聚合物聚(3,4-乙撑二氧噻吩)-聚苯乙烯磺酸盐(PE-DOT:PSS)的离子选择层,然后可逆地将其表面结合用于杂交的吗啉代微阵列。使用这种电动捕集浓缩器,我们可以在DNA中获得类似于800的最大浓缩因子,并且在15分钟内检测极限为10 nM。就检测速度而言,与传统的基于扩散的杂交相比,它可以使杂交速度加快约10倍。我们方法的一个显着优点是,微流体浓缩器的制造与微阵列完全脱钩。通过消除在设备集成之前在微阵列表面上沉积离子选择层的需要,两个模块之间的接口,用于电动浓缩的PDMS芯片和用于DNA传感的基板变得更容易并且适用于任何微阵列平台。此外,这种制造策略有利于集中器的多路复用。我们已经构建了一个设备,该设备具有5个平行浓缩器连接到单个入口/出口,并将其应用于平行浓缩和杂交,从而证明了多重验证的概念。与单通道设备相比,这种设备产生了相似的浓度和杂交效率,而没有增加制造和设置的复杂性。这些结果表明,我们的集中器概念可以应用于遗传分析或其他诊断测定的高度多重的集中器增强型微阵列检测系统的开发。

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