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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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Published in: | Biosensors & bioelectronics 2007-06, Vol.22 (12), p.3064-3071 |
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creator | Limbut, Warakorn Loyprasert, Suchera Thammakhet, Chongdee Thavarungkul, Panote Tuantranont, Adisorn Asawatreratanakul, Punnee Limsakul, Chusak Wongkittisuksa, Booncharoen Kanatharana, Proespichaya |
description | 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 |
doi_str_mv | 10.1016/j.bios.2007.01.001 |
format | article |
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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<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.</description><identifier>ISSN: 0956-5663</identifier><identifier>EISSN: 1873-4235</identifier><identifier>DOI: 10.1016/j.bios.2007.01.001</identifier><identifier>PMID: 17289366</identifier><language>eng</language><publisher>Lausanne: Elsevier B.V</publisher><subject>Biological and medical sciences ; Bioreactor ; Bioreactors ; Biotechnology ; Conductimetric ; Enzymes, Immobilized - chemistry ; Fundamental and applied biological sciences. 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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<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.</description><subject>Biological and medical sciences</subject><subject>Bioreactor</subject><subject>Bioreactors</subject><subject>Biotechnology</subject><subject>Conductimetric</subject><subject>Enzymes, Immobilized - chemistry</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Humans</subject><subject>Immobilization</subject><subject>Microfluidic</subject><subject>Microfluidic Analytical Techniques - instrumentation</subject><subject>Microfluidic Analytical Techniques - methods</subject><subject>Urea</subject><subject>Urea - blood</subject><subject>Urease</subject><subject>Urease - chemistry</subject><issn>0956-5663</issn><issn>1873-4235</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNqFkE1LxDAQhoMo7rr6BzyIF_fWmqT5aMGLLH7Bihc9h2k6hSz9WJNW8N-bsgVvehoGnvdl5iHkktGUUaZud2np-pBySnVKWUopOyJLlussETyTx2RJC6kSqVS2IGch7GgEWUFPyYJpnheZUkuyfnXW93UzusrZa9t31WgH1-Lg4xrrPYIden9OTmpoAl7Mc0U-Hh_eN8_J9u3pZXO_TayQfEhAQkYlVxIAdS6VLXOORV0KJWydl0JaDVIBglZWSigF41gpwUsNQigmsxVZH3r3vv8cMQymdcFi00CH_RiMju06E-pfkBWaM1FMID-A8c0QPNZm710L_tswaiaNZmcmjWbSaCgzUWMMXc3tY9li9RuZvUXgZgYgWGhqD5114ZfLc6ZVUUTu7sBhlPbl0JtgHXYWK-fRDqbq3V93_AAvpo-Q</recordid><startdate>20070615</startdate><enddate>20070615</enddate><creator>Limbut, Warakorn</creator><creator>Loyprasert, Suchera</creator><creator>Thammakhet, Chongdee</creator><creator>Thavarungkul, Panote</creator><creator>Tuantranont, Adisorn</creator><creator>Asawatreratanakul, Punnee</creator><creator>Limsakul, Chusak</creator><creator>Wongkittisuksa, Booncharoen</creator><creator>Kanatharana, Proespichaya</creator><general>Elsevier B.V</general><general>Elsevier Science</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20070615</creationdate><title>Microfluidic conductimetric bioreactor</title><author>Limbut, Warakorn ; Loyprasert, Suchera ; Thammakhet, Chongdee ; Thavarungkul, Panote ; Tuantranont, Adisorn ; Asawatreratanakul, Punnee ; Limsakul, Chusak ; Wongkittisuksa, Booncharoen ; Kanatharana, Proespichaya</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c452t-a5a305265aae7856cb82e9fb464cf8b45c7a56aea76c55ab412ed642b7a446153</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Biological and medical sciences</topic><topic>Bioreactor</topic><topic>Bioreactors</topic><topic>Biotechnology</topic><topic>Conductimetric</topic><topic>Enzymes, Immobilized - chemistry</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Humans</topic><topic>Immobilization</topic><topic>Microfluidic</topic><topic>Microfluidic Analytical Techniques - instrumentation</topic><topic>Microfluidic Analytical Techniques - methods</topic><topic>Urea</topic><topic>Urea - blood</topic><topic>Urease</topic><topic>Urease - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Limbut, Warakorn</creatorcontrib><creatorcontrib>Loyprasert, Suchera</creatorcontrib><creatorcontrib>Thammakhet, Chongdee</creatorcontrib><creatorcontrib>Thavarungkul, Panote</creatorcontrib><creatorcontrib>Tuantranont, Adisorn</creatorcontrib><creatorcontrib>Asawatreratanakul, Punnee</creatorcontrib><creatorcontrib>Limsakul, Chusak</creatorcontrib><creatorcontrib>Wongkittisuksa, Booncharoen</creatorcontrib><creatorcontrib>Kanatharana, Proespichaya</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Biosensors & bioelectronics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Limbut, Warakorn</au><au>Loyprasert, Suchera</au><au>Thammakhet, Chongdee</au><au>Thavarungkul, Panote</au><au>Tuantranont, Adisorn</au><au>Asawatreratanakul, Punnee</au><au>Limsakul, Chusak</au><au>Wongkittisuksa, Booncharoen</au><au>Kanatharana, Proespichaya</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Microfluidic conductimetric bioreactor</atitle><jtitle>Biosensors & bioelectronics</jtitle><addtitle>Biosens Bioelectron</addtitle><date>2007-06-15</date><risdate>2007</risdate><volume>22</volume><issue>12</issue><spage>3064</spage><epage>3071</epage><pages>3064-3071</pages><issn>0956-5663</issn><eissn>1873-4235</eissn><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 0.09mM 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<0.05). 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subjects | Biological and medical sciences Bioreactor Bioreactors Biotechnology Conductimetric Enzymes, Immobilized - chemistry Fundamental and applied biological sciences. Psychology Humans Immobilization Microfluidic Microfluidic Analytical Techniques - instrumentation Microfluidic Analytical Techniques - methods Urea Urea - blood Urease Urease - chemistry |
title | Microfluidic conductimetric bioreactor |
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