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Microfluidic conductimetric bioreactor
Authors:Limbut Warakorn  Loyprasert Suchera  Thammakhet Chongdee  Thavarungkul Panote  Tuantranont Adisorn  Asawatreratanakul Punnee  Limsakul Chusak  Wongkittisuksa Booncharoen  Kanatharana Proespichaya
Institution:

aBiophysics Research Unit of Biosensors and Biocurrents, Prince of Songkla University, Hat Yai, Songkhla 90112, Thailand

bAnalytical and Environmental Chemistry/Trace Analysis Research Unit, Prince of Songkla University, Hat Yai, Songkhla 90112, Thailand

cDepartment of Chemistry, Faculty of Science, Prince of Songkla University, Hat Yai, Songkhla 90112, Thailand

dDepartment of Physics, Faculty of Science, Prince of Songkla University, Hat Yai, Songkhla 90112, Thailand

eNanoelectronics and MEMS Laboratory, National Electronics and Computer Technology Center, Pathumthani 12120, Thailand

fDepartment of Biochemistry, Faculty of Science, Prince of Songkla University, Hat Yai, Songkhla 90112, Thailand

gDepartment of Electrical Engineering, Faculty of Engineering, Prince of Songkla University, Hat Yai, Songkhla 90112, Thailand

Abstract: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 0.09 mM and linearity in the range of 0.1–10 mM (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 < 0.05). After prolong use the immobilized enzyme could be removed from the PDMS microchannel chip enabling new active enzyme to be immobilized and the chip to be reused.
Keywords:Microfluidic  Urea  Urease  Immobilization  Conductimetric  Bioreactor
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