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Design and optimization of a double-enzyme glucose assay in microfluidic lab-on-a-chip

机译:微流控芯片实验室中双酶葡萄糖测定的设计与优化

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摘要

An electrokinetic driven microfluidic lab-on-a-chip was developed for glucose quantification using double-enzyme assay. The enzymatic glucose assay involves the two-step oxidation of glucose, which was catalyzed by hexokinase and glucose-6-phosphate dehydrogenase, with the concomitant reduction of NADP+ to NADPH. A fluorescence microscopy setup was used to monitor the different processes (fluid flow and enzymatic reaction) in the microfluidic chip. A two-dimensional finite element model was applied to understand the different aspects of design and to improve the performance of the device without extensive prototyping. To our knowledge this is the first work to exploit numerical simulation for understanding a multisubstrate double-enzyme on-chip assay. The assay is very complex to implement in electrokinetically driven continuous system due to the involvement of many species, which has different transport velocity. With the help of numerical simulation, the design parameters, flow rate, enzyme concentration, and reactor length, were optimized. The results from the simulation were in close agreement with the experimental results. A linear relation exists for glucose concentrations from 0.01 to 0.10 g l−1. The reaction time and the amount of enzymes required were drastically reduced compared to off-chip microplate analysis.
机译:开发了一种电动双芯片实验室微动电用于葡萄糖定量。酶促葡萄糖测定法包括通过己糖激酶和葡萄糖-6-磷酸脱氢酶催化的葡萄糖的两步氧化,同时将NADP +还原为NADPH。荧光显微镜设置用于监测微流控芯片中的不同过程(流体流动和酶促反应)。应用二维有限元模型来了解设计的不同方面,并在不进行大量原型设计的情况下提高设备的性能。据我们所知,这是利用数值模拟来理解多底物双酶芯片检测的第一项工作。由于许多物种的参与,具有不同的传输速度,因此在电动驱动的连续系统中实施该测定非常复杂。借助数值模拟,优化了设计参数,流速,酶浓度和反应器长度。仿真结果与实验结果非常吻合。葡萄糖浓度从0.01到0.10 g l-1存在线性关系。与芯片外微孔板分析相比,反应时间和所需酶的数量大大减少。

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