TY - JOUR
T1 - Three dimensional microelectrode array device integrating multi-channel microfluidics to realize manipulation and characterization of enzyme-immobilized polystyrene beads
AU - Kunikata, Ryouta
AU - Takahashi, Yasufumi
AU - Koide, Masahiro
AU - Itayama, Tomoaki
AU - Yasukawa, Tomoyuki
AU - Shiku, Hitoshi
AU - Matsue, Tomokazu
N1 - Funding Information:
This work was partly supported by Special Coordination Funds for Promoting Science and Technology, Formation of Innovation Center for Fusion of Advanced Technologies, from Japan Science and Technology Agency, by Grant-in-Aid for Scientific Research from the Ministry of Education, Culture, Sports, Science and Technology of Japan, and by the R&D Project for Environmental Nanotechnology from the Ministry of Environment.
PY - 2009/8/18
Y1 - 2009/8/18
N2 - We microfabricated a novel device consisting of a 4 × 4 array microchamber sandwiched with the two microband electrode array. This device allows dielectrophoretic (DEP) manipulation of microbeads to introduce into and release out a certain address of the V-shaped microchamber, by applying AC voltage (10 Vpp, 10 kHz) on the basis of DEP forces. The design and the position of the two electrodes (row and column electrodes) at each microchamber were optimized by simulation based on a finite element method. More importantly, electrochemical generation-collection measurement was possible to evaluate enzymatic activity. After microbeads immobilized with glucose oxidase (GOD) was entrapped in the V-shaped microchamber with DEP, a measuring solution containing 3 mM ferrocenemethanol (FcCH2OH) and 0.1 M glucose was introduced. The medium in the V-shaped microwell was immediately exchanged into the measuring solution whereas microbeads stayed within the microwell without applying DEP voltage, because the flow within the microchamber was isolated from that of the main channel. Then the potential of the row and column electrodes were set at 0.5 and 0.1 V vs Ag/AgCl. The GOD activity can be monitored as the decrease in the [FcCH2OH]+ reduction current.
AB - We microfabricated a novel device consisting of a 4 × 4 array microchamber sandwiched with the two microband electrode array. This device allows dielectrophoretic (DEP) manipulation of microbeads to introduce into and release out a certain address of the V-shaped microchamber, by applying AC voltage (10 Vpp, 10 kHz) on the basis of DEP forces. The design and the position of the two electrodes (row and column electrodes) at each microchamber were optimized by simulation based on a finite element method. More importantly, electrochemical generation-collection measurement was possible to evaluate enzymatic activity. After microbeads immobilized with glucose oxidase (GOD) was entrapped in the V-shaped microchamber with DEP, a measuring solution containing 3 mM ferrocenemethanol (FcCH2OH) and 0.1 M glucose was introduced. The medium in the V-shaped microwell was immediately exchanged into the measuring solution whereas microbeads stayed within the microwell without applying DEP voltage, because the flow within the microchamber was isolated from that of the main channel. Then the potential of the row and column electrodes were set at 0.5 and 0.1 V vs Ag/AgCl. The GOD activity can be monitored as the decrease in the [FcCH2OH]+ reduction current.
KW - Chronoamperometry
KW - Dielectrophoresis
KW - Enzyme-immobilized beads
KW - Microelectrode array
KW - Microfluidics
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U2 - 10.1016/j.snb.2009.05.028
DO - 10.1016/j.snb.2009.05.028
M3 - Article
AN - SCOPUS:67949120306
SN - 0925-4005
VL - 141
SP - 256
EP - 262
JO - Sensors and Actuators B: Chemical
JF - Sensors and Actuators B: Chemical
IS - 1
ER -