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Microfluidic conductimetric bioreactor

A microfluidic conductimetric bioreactor has been developed. Enzyme was immobilized in the microfluidic channel on poly-dimethylsiloxane (PDMS) surface via covalent binding method. The detection unit consisted of two gold electrodes and a laboratory-built conductimetric transducer to monitor the inc...

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Bibliographic Details
Published in:Biosensors & bioelectronics 2007-06, Vol.22 (12), p.3064-3071
Main Authors: Limbut, Warakorn, Loyprasert, Suchera, Thammakhet, Chongdee, Thavarungkul, Panote, Tuantranont, Adisorn, Asawatreratanakul, Punnee, Limsakul, Chusak, Wongkittisuksa, Booncharoen, Kanatharana, Proespichaya
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Language:English
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Summary:A microfluidic conductimetric bioreactor has been developed. Enzyme was immobilized in the microfluidic channel on poly-dimethylsiloxane (PDMS) surface via covalent binding method. The detection unit consisted of two gold electrodes and a laboratory-built conductimetric transducer to monitor the increase in the conductivity of the solution due to the change of the charges generated by the enzyme-substrate catalytic reaction. Urea–urease was used as a representative analyte-enzyme system. Under optimum conditions urea could be determined with a detection limit of 0.09mM and linearity in the range of 0.1–10mM (r=0.9944). The immobilized urease on the microchannel chip provided good stability (>30 days of operation time) and good repeatability with an R.S.D. lower than 2.3%. Good agreement was obtained when urea concentrations of human serum samples determined by the microfluidic flow injection conductimetric bioreactor system were compared to those obtained using the Berthelot reaction (P
ISSN:0956-5663
1873-4235
DOI:10.1016/j.bios.2007.01.001