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3D-printed microfluidic device with in-line amperometric detection that also enables multi-modal detection

机译:3D印刷的微流体装置,具有在线安培检测,也能够实现多模态检测

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摘要

Microfluidic amperometric detectors often include a reservoir to house auxiliary and reference electrodes, making subsequent detection downstream challenging. Here, we present an in-line microfluidic device with amperometric detection that incorporates a three-electrode set-up, made possible by threading electrodes into a 3D-printed flow cell. The electrodes consist of a commercially available threaded reference electrode and electrodes fabricated in commercially available fittings. This approach centers the working electrode in the fluidic channel enabling the use of a pillar working electrode that is shown to increase sensitivity, as compared to a traditional thin-layer electrode. In addition, the working and auxiliary electrodes can be directly opposed, with this configuration leading to a more uniform potential being applied to the working electrode as well as fewer issues with any iR drop. To demonstrate the ability to incorporate a separate mode of detection downstream from the electrochemical flow cell, the device is modified to include a mixing T for introduction of reagents for chemiluminescent detection of ATP (via the luciferin-luciferase reaction), leading to a single 3D-printed device that can be used to detect norepinephrine and ATP, nearly simultaneously, by amperometry and chemiluminescence, respectively. This approach opens numerous possibilities, where microfluidics with in-line amperometry can be used in continuous circulation studies or in conjunction with other downstream detection events to study complex systems.
机译:微流体化工探测器通常包括储存器以容纳辅助和参考电极的储存器,使得随后检测下游挑战。这里,我们介绍一种具有电流检测的在线微流体装置,该检测包括三电极设置,通过将电极穿向3D印刷流动单元来实现。电极由市售的螺纹参考电极和在市售的配件中制造的电极组成。该方法在流体通道中为工作电极中心中心,使得与传统的薄层电极相比,使用示出的柱工作电极可以增加灵敏度。另外,工作和辅助电极可以直接相对,并且这种配置导致更均匀地施加到工作电极以及任何IR下降的问题较少。为了证明能够在电化学流动细胞下游掺杂下游的单独检测模式,该装置被修饰,包括混合T,用于引入ATP的化学发光检测的试剂(通过荧光素 - 荧光素酶反应),导致单个3D - 分别可以用于分别通过安培和化学发光分别检测Norepinephrine和ATP,几乎同时同时检测Norepinephrine和ATP。这种方法打开了许多可能性,其中可以在连续循环研究中或与其他下游检测事件一起使用微流体,以研究复杂系统。

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