Signal Amplification in Enzyme-Based Amperometric Biosensors
A unique mode of current amplification was investigated in reagentless biosensors based on the clinically significant enzymes including alcohol dehydrogenase, glucose 6-phosphate dehydrogenase, glycerol 3-phosphate dehydrogenase, and glucose oxidase. The biosensors were designed by sandwiching the e...
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Veröffentlicht in: | Analytical chemistry (Washington) 2013-11, Vol.85 (21), p.10573-10580 |
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description | A unique mode of current amplification was investigated in reagentless biosensors based on the clinically significant enzymes including alcohol dehydrogenase, glucose 6-phosphate dehydrogenase, glycerol 3-phosphate dehydrogenase, and glucose oxidase. The biosensors were designed by sandwiching the enzyme–polymer film between an electrode and Nafion film. In particular, each enzyme and its cofactor were covalently attached to the chains of polysaccharide chitosan and mixed with carbon nanotubes on the electrode surface. The coating of such biosensors with Nafion resulted in the current increase by up to 1000%, depending on the enzyme. The results were analyzed considering the interplay between the enzyme activity–pH profiles and the Nafion-induced pH increase in the underlying chitosan film. The data were collected by using the rapid ( |
doi_str_mv | 10.1021/ac4026994 |
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The biosensors were designed by sandwiching the enzyme–polymer film between an electrode and Nafion film. In particular, each enzyme and its cofactor were covalently attached to the chains of polysaccharide chitosan and mixed with carbon nanotubes on the electrode surface. The coating of such biosensors with Nafion resulted in the current increase by up to 1000%, depending on the enzyme. The results were analyzed considering the interplay between the enzyme activity–pH profiles and the Nafion-induced pH increase in the underlying chitosan film. The data were collected by using the rapid (<5 min) amperometric enzyme assays and pH-sensitive iridium oxide films. The increase in the biosensor current was attributed to the pH-driven increase in the enzyme activity inside the two-film interface. Such signal amplification should also be feasible in other biosensors based on the polyelectrolytes and sandwiched enzymes providing that a proper match is made between the enzyme activity–pH profiles and the pH of buffer solutions.</description><identifier>ISSN: 0003-2700</identifier><identifier>EISSN: 1520-6882</identifier><identifier>DOI: 10.1021/ac4026994</identifier><identifier>PMID: 24099638</identifier><identifier>CODEN: ANCHAM</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Amplification ; Analytical chemistry ; Biosensing Techniques ; Biosensors ; Chitosan ; Electrical measurements ; Electrochemistry - instrumentation ; Electrodes ; Enzymes ; Hydrogen-Ion Concentration ; Indicators and Reagents ; Nanotubes</subject><ispartof>Analytical chemistry (Washington), 2013-11, Vol.85 (21), p.10573-10580</ispartof><rights>Copyright © 2013 American Chemical Society</rights><rights>Copyright American Chemical Society Nov 5, 2013</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a475t-663e9a808eb3672c20a840c1104ed7939d55f57d79cc6c7e3529f9c603e2df463</citedby><cites>FETCH-LOGICAL-a475t-663e9a808eb3672c20a840c1104ed7939d55f57d79cc6c7e3529f9c603e2df463</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/ac4026994$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/ac4026994$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,776,780,2752,27053,27901,27902,56713,56763</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24099638$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Karra, Sushma</creatorcontrib><creatorcontrib>Gorski, Waldemar</creatorcontrib><title>Signal Amplification in Enzyme-Based Amperometric Biosensors</title><title>Analytical chemistry (Washington)</title><addtitle>Anal. 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The increase in the biosensor current was attributed to the pH-driven increase in the enzyme activity inside the two-film interface. Such signal amplification should also be feasible in other biosensors based on the polyelectrolytes and sandwiched enzymes providing that a proper match is made between the enzyme activity–pH profiles and the pH of buffer solutions.</description><subject>Amplification</subject><subject>Analytical chemistry</subject><subject>Biosensing Techniques</subject><subject>Biosensors</subject><subject>Chitosan</subject><subject>Electrical measurements</subject><subject>Electrochemistry - instrumentation</subject><subject>Electrodes</subject><subject>Enzymes</subject><subject>Hydrogen-Ion Concentration</subject><subject>Indicators and Reagents</subject><subject>Nanotubes</subject><issn>0003-2700</issn><issn>1520-6882</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqN0ctKAzEUBuAgiq2XhS8gBRF0MXpynQm4aUu9QMGFuh7STEZSZiY1mVnUpze1tYgudJVAPv4czo_QCYYrDARfK82ACCnZDupjTiARWUZ2UR8AaEJSgB46CGEOgDFgsY96hIGUgmZ9dPNkXxtVDYb1orKl1aq1rhnYZjBp3pe1SUYqmGL1aryrTeutHoysC6YJzocjtFeqKpjjzXmIXm4nz-P7ZPp49zAeThPFUt4mQlAjVQaZmVGREk1AZQx0HIaZIpVUFpyXPI1XrYVODeVEllILoIYUJRP0EF2scxfevXUmtHltgzZVpRrjupBjIQmlnFPyN2WSCEwI_UcqizalcZWRnv2gc9f5uLeV4hkVjHyOeblW2rsQvCnzhbe18sscQ74qKt8WFe3pJrGb1abYyq9mIjhfA6XDt99-BX0AZ4KVeA</recordid><startdate>20131105</startdate><enddate>20131105</enddate><creator>Karra, Sushma</creator><creator>Gorski, Waldemar</creator><general>American Chemical Society</general><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>7QF</scope><scope>7QO</scope><scope>7QQ</scope><scope>7SC</scope><scope>7SE</scope><scope>7SP</scope><scope>7SR</scope><scope>7TA</scope><scope>7TB</scope><scope>7TM</scope><scope>7U5</scope><scope>7U7</scope><scope>7U9</scope><scope>8BQ</scope><scope>8FD</scope><scope>C1K</scope><scope>F28</scope><scope>FR3</scope><scope>H8D</scope><scope>H8G</scope><scope>H94</scope><scope>JG9</scope><scope>JQ2</scope><scope>KR7</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20131105</creationdate><title>Signal Amplification in Enzyme-Based Amperometric Biosensors</title><author>Karra, Sushma ; Gorski, Waldemar</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a475t-663e9a808eb3672c20a840c1104ed7939d55f57d79cc6c7e3529f9c603e2df463</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Amplification</topic><topic>Analytical chemistry</topic><topic>Biosensing Techniques</topic><topic>Biosensors</topic><topic>Chitosan</topic><topic>Electrical measurements</topic><topic>Electrochemistry - instrumentation</topic><topic>Electrodes</topic><topic>Enzymes</topic><topic>Hydrogen-Ion Concentration</topic><topic>Indicators and Reagents</topic><topic>Nanotubes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Karra, Sushma</creatorcontrib><creatorcontrib>Gorski, Waldemar</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Aluminium Industry Abstracts</collection><collection>Biotechnology Research Abstracts</collection><collection>Ceramic Abstracts</collection><collection>Computer and Information Systems Abstracts</collection><collection>Corrosion Abstracts</collection><collection>Electronics & Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Materials Business File</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><collection>Aerospace Database</collection><collection>Copper Technical Reference Library</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Materials Research Database</collection><collection>ProQuest Computer Science Collection</collection><collection>Civil Engineering Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Computer and Information Systems Abstracts Academic</collection><collection>Computer and Information Systems Abstracts Professional</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Analytical chemistry (Washington)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Karra, Sushma</au><au>Gorski, Waldemar</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Signal Amplification in Enzyme-Based Amperometric Biosensors</atitle><jtitle>Analytical chemistry (Washington)</jtitle><addtitle>Anal. 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The results were analyzed considering the interplay between the enzyme activity–pH profiles and the Nafion-induced pH increase in the underlying chitosan film. The data were collected by using the rapid (<5 min) amperometric enzyme assays and pH-sensitive iridium oxide films. The increase in the biosensor current was attributed to the pH-driven increase in the enzyme activity inside the two-film interface. Such signal amplification should also be feasible in other biosensors based on the polyelectrolytes and sandwiched enzymes providing that a proper match is made between the enzyme activity–pH profiles and the pH of buffer solutions.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>24099638</pmid><doi>10.1021/ac4026994</doi><tpages>8</tpages></addata></record> |
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subjects | Amplification Analytical chemistry Biosensing Techniques Biosensors Chitosan Electrical measurements Electrochemistry - instrumentation Electrodes Enzymes Hydrogen-Ion Concentration Indicators and Reagents Nanotubes |
title | Signal Amplification in Enzyme-Based Amperometric Biosensors |
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