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

被引:22
作者
Atalay, Yegermal Tesfaw [1 ]
Witters, Daan [1 ]
Vermeir, Steven [1 ]
Vergauwe, Nicolas [1 ]
Verboven, Pieter [1 ]
Nicolai, Bart [1 ]
Lammertyn, Jeroen [1 ]
机构
[1] Katholieke Univ Leuven, BIOSYST MeBioS, Fac Biosci Engn, B-3001 Louvain, Belgium
来源
BIOMICROFLUIDICS | 2009年 / 3卷 / 04期
关键词
biochemistry; biological techniques; bioMEMS; catalysts; electrokinetic effects; enzymes; finite element analysis; fluorescence; lab-on-a-chip; microfluidics; molecular biophysics; optical microscopy; oxidation; MASS-SPECTROMETRY; YEAST HEXOKINASE; FLUID-FLOW; MICROCHIP; QUANTIFICATION; CHANNELS; SYSTEMS; DEVICE;
D O I
10.1063/1.3250304
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
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.
引用
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页数:14
相关论文
共 35 条
[1]   Design optimization of an enzymatic assay in an electrokinetically-driven microfluidic device [J].
Atalay, Y. T. ;
Verboven, P. ;
Vermeir, S. ;
Vergauwe, N. ;
Delport, F. ;
Nicolai, B. M. ;
Lammertyn, J. .
MICROFLUIDICS AND NANOFLUIDICS, 2008, 5 (06) :837-849
[2]   Modeling and optimization of a multi-enzyme electrokinetically driven multiplexed microchip for simultaneous detection of sugars [J].
Atalay, Yegermal Tesfaw ;
Verboven, Pieter ;
Vermeir, Steven ;
Vergauwe, Nicolas ;
Nicolai, Bart ;
Lammertyn, Jeroen .
MICROFLUIDICS AND NANOFLUIDICS, 2009, 7 (03) :393-406
[3]   Biochemical analysis with microfluidic systems [J].
Bilitewski, U ;
Genrich, M ;
Kadow, S ;
Mersal, G .
ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2003, 377 (03) :556-569
[4]  
Boy DA, 2008, LAB CHIP, V8, P1424, DOI [10.1039/b812596c, 10.1039/16812596c]
[5]  
Burke BJ, 2001, ELECTROPHORESIS, V22, P3744, DOI 10.1002/1522-2683(200109)22:17<3744::AID-ELPS3744>3.0.CO
[6]  
2-7
[7]   Development of an in vitro microassay for glucose quantification in submicrolitre volumes of biological fluid [J].
Ciantar, M ;
Spratt, DA ;
Newman, HN ;
Wilson, M .
JOURNAL OF PERIODONTAL RESEARCH, 2002, 37 (02) :79-85
[8]   A microfluidic-based enzymatic assay for bioactivity screening combined with capillary liquid chromatography and mass spectrometry [J].
de Boer, AR ;
Bruyneel, B ;
Krabbe, JG ;
Lingeman, H ;
Niessen, WMA ;
Irth, H .
LAB ON A CHIP, 2005, 5 (11) :1286-1292
[9]   Multiplex inhibitor screening and kinetic constant determinations for yeast hexokinase using mass spectrometry based assays [J].
Gao, H ;
Leary, JA .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 2003, 14 (03) :173-181
[10]   Multiplexed high-throughput electrokinetically-controlled immunoassay for the detection of specific bacterial antibodies in human serum [J].
Gao, Yali ;
Shermanb, Philip M. ;
Sun, Yu ;
Li, Dongqing .
ANALYTICA CHIMICA ACTA, 2008, 606 (01) :98-107