Signal Amplification in a Microchannel from Redox Cycling with Varied Electroactive Configurations of an Individually Addressable Microband Electrode Array

被引:37
作者
Lewis, Penny M. [1 ]
Sheridan, Leah Bullard [1 ]
Gawley, Robert E. [1 ]
Fritsch, Ingrid [1 ]
机构
[1] Univ Arkansas, Dept Chem & Biochem, Fayetteville, AR 72701 USA
基金
美国国家科学基金会;
关键词
ELECTROCHEMICAL DETECTION; FABRICATION; MICROELECTRODES; IMMUNOASSAY; RESPONSES; BEHAVIOR; COUPLES; FILM; BAND;
D O I
10.1021/ac901066p
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Amperometric detection at microelectrodes in lab-on-a-chip (LOAC) devices lose advantages in signal-to-background ratio, reduced ohmic iR drop, and steady-state signal when volumes are so small that diffusion fields reach the walls before flux becomes fully radial. Redox cycling of electroactive species between multiple, closely spaced microelectrodes offsets that limitation and provides amplification capabilities. A device that integrates it microchannel with an individually addressable microband electrode array has been used to study effects of signal amplification due to redox cycling in a confined, static solution with different configurations and numbers of active generators and collectors. The microfabricated device consists of a 22 mu m high, 600 mu m wide microchannel containing an array of 50 mu m wide, 600 mu m long gold microbands, separated by 25 mu m gaps, interspersed with an 800 mu m wide counter electrode and 400 mu m wide passive conductor, with it distant but on-chip 400 mu m wide pseudoreference electrode. Investigations involve solutions of potassium chloride electrolyte containing potassium ferrocyanide. Amplification factors were as high as 7.60, even with these microelectrodes of fairly large dimensions (which are generally less expensive, easier, and more reproducible to fabricate), because of the significant role that passive and active (instrumentally induced) redox cycling plays in confined volumes of enclosed microchannels. The studies are useful in optimizing designs for LOAC devices.
引用
收藏
页码:1659 / 1668
页数:10
相关论文
共 38 条
[1]   Self-contained microelectrochemical immunoassay for small volumes using mouse IgG as a model system [J].
Aguilar, ZP ;
Vandaveer, WR ;
Fritsch, I .
ANALYTICAL CHEMISTRY, 2002, 74 (14) :3321-3329
[2]  
Akoub I.A., 2001, J PHYS CHEM B, V105, P8694
[3]   Using electrochemical coupling between parallel microbands for in situ monitoring of flow rates in microfluidic channels [J].
Amatore, C ;
Belotti, M ;
Chen, Y ;
Roy, E ;
Sella, C ;
Thouin, L .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2004, 573 (02) :333-343
[4]   Effects of chemical environment on diffusivities within thin Nafion® films as monitored from chronoamperometric responses of generator-collector double microband assemblies [J].
Amatore, C ;
Sella, C ;
Thouin, L .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2003, 547 (02) :151-161
[5]   Diffusional cross-talk between paired microband electrodes operating within a thin film: Theory for redox couples with unequal diffusion coefficients [J].
Amatore, C ;
Sella, C ;
Thouin, L .
JOURNAL OF PHYSICAL CHEMISTRY B, 2002, 106 (44) :11565-11571
[6]  
[Anonymous], 2001, ELECTROCHEMICAL METH
[7]   QUANTITATIVE-ANALYSIS OF REVERSIBLE DIFFUSION-CONTROLLED CURRENTS OF REDOX SOLUBLE SPECIES AT INTERDIGITATED ARRAY ELECTRODES UNDER STEADY-STATE CONDITIONS [J].
AOKI, K ;
MORITA, M ;
NIWA, O ;
TABEI, H .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1988, 256 (02) :269-282
[8]   DIGITAL-SIMULATION OF THE MEASURED ELECTROCHEMICAL RESPONSE OF REVERSIBLE REDOX COUPLES AT MICROELECTRODE ARRAYS - CONSEQUENCES ARISING FROM CLOSELY SPACED ULTRAMICROELECTRODES [J].
BARD, AJ ;
CRAYSTON, JA ;
KITTLESEN, GP ;
SHEA, TV ;
WRIGHTON, MS .
ANALYTICAL CHEMISTRY, 1986, 58 (11) :2321-2331
[9]  
Björefors F, 2000, ELECTROANAL, V12, P255
[10]   Development and Characterization of Microfluidic Devices and Systems for Magnetic Bead-Based Biochemical Detection [J].
Choi, Jin-Woo ;
Oh, Kwang W. ;
Han, Arum ;
Okulan, Nihat ;
Wijayawardhana, C. Ajith ;
Lannes, Chad ;
Bhansali, Shekhar ;
Schlueter, Kevin T. ;
Heineman, William R. ;
Halsall, H. Brain ;
Nevin, Joseph H. ;
Helmicki, Arthur J. ;
Henderson, H. Thurman ;
Ahn, Chong H. .
BIOMEDICAL MICRODEVICES, 2001, 3 (03) :191-200