Yao J, Liu X A, Gillis K D
Department of Bioengineering, University of Missouri, Columbia, Missouri, 65201; Dalton Cardiovascular Research Center, Columbia, Missouri, USA.
Dalton Cardiovascular Research Center, Columbia, Missouri, USA.
Anal Methods. 2015 Jul 21;7(14):5760-5766. doi: 10.1039/C5AY00229J. Epub 2015 Jun 22.
Although patterning hundreds or thousands of electrochemical electrodes on lab-on-a-chip devices is straightforward and cost-effective using photolithography, easily making connections between hundreds of electrodes and external amplifiers remains a bottleneck. Here we describe two electrode addressing approaches using multiple fluid compartments that can potentially reduce the number of external connections by ~100-fold. The first approach enables all compartments on the device to be filled with solution at the same time, and then each fluid compartment is sequentially electrically activated to make the measurements. The second approach achieves lower measurement noise by sequentially filling recording chambers with solution. We propose an equivalent circuit to explain measurement noise in these recording configurations and demonstrate application of the approaches to measure quantal exocytosis from individual cells. A principle advantage of using these approaches is that they reduce the fraction of the microchip area that needs to be dedicated to making external connections and therefore reduces the cost per working electrode.
虽然使用光刻技术在芯片实验室设备上对数百或数千个电化学电极进行图案化既直接又经济高效,但要轻松实现数百个电极与外部放大器之间的连接仍然是一个瓶颈。在此,我们描述了两种使用多个流体隔室的电极寻址方法,这有可能将外部连接数量减少约100倍。第一种方法能使设备上的所有隔室同时充满溶液,然后依次对每个流体隔室进行电激活以进行测量。第二种方法通过依次向记录室填充溶液来实现更低的测量噪声。我们提出了一个等效电路来解释这些记录配置中的测量噪声,并展示了这些方法在测量单个细胞的量子分泌中的应用。使用这些方法的一个主要优点是,它们减少了芯片上需要专门用于进行外部连接的面积比例,从而降低了每个工作电极的成本。