Electrochemical urea biosensor based on Proteus mirabilis urease immobilized over polyaniline PANi‐Glassy carbon electrode
In this study, a novel, sensitive electrochemical enzyme‐based biosensor for urea detection was presented. This biosensor combines a three‐electrode system consisting of a classic Glassy Carbon Electrode (GCE) as the working electrode, a platinum counter electrode, and Ag/AgCl as the reference elect...
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Veröffentlicht in: | Electroanalysis (New York, N.Y.) N.Y.), 2023-09, Vol.35 (9) |
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creator | Atailia, Sara Baraket, Abdoullatif Rabai, Selma Benounis, Messaoud Jaffrezic, Nicole Araar, Hala Naït‐Bouda, Abdelyamine Boumaza, Abdecharif Errachid, Abdelhamid Houhamdi, Moussa |
description | In this study, a novel, sensitive electrochemical enzyme‐based biosensor for urea detection was presented. This biosensor combines a three‐electrode system consisting of a classic Glassy Carbon Electrode (GCE) as the working electrode, a platinum counter electrode, and Ag/AgCl as the reference electrode. To construct this urea platform, a GCE was modified with a polyaniline (PANi) film. Then, bacterial urease from Proteus mirabilis was immobilized on the modified GCE (P m ‐Urease‐PANi‐GCE). For the characterization of surface modification, Cyclic Voltammetry (CV) and Scanning Electron Microscope (SEM) were applied, while the Square Wave Voltammetry (SWV) technique was performed for urea detection. The main analytical characteristics of the P m ‐Urease‐PANi‐GCE biosensor showed a good linear range from 0.1 to 10 mM of urea, a limit of detection (LOD) of 0.1 mM, a Michaelis‐Menten K m of 0.23 mM, and a sensitivity value 46 μA/mM/cm 2 . This biosensor allows the detection of urea in solutions, and it could be improved for further medical, environmental, or engineering applications. |
doi_str_mv | 10.1002/elan.202200502 |
format | Article |
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This biosensor combines a three‐electrode system consisting of a classic Glassy Carbon Electrode (GCE) as the working electrode, a platinum counter electrode, and Ag/AgCl as the reference electrode. To construct this urea platform, a GCE was modified with a polyaniline (PANi) film. Then, bacterial urease from Proteus mirabilis was immobilized on the modified GCE (P m ‐Urease‐PANi‐GCE). For the characterization of surface modification, Cyclic Voltammetry (CV) and Scanning Electron Microscope (SEM) were applied, while the Square Wave Voltammetry (SWV) technique was performed for urea detection. The main analytical characteristics of the P m ‐Urease‐PANi‐GCE biosensor showed a good linear range from 0.1 to 10 mM of urea, a limit of detection (LOD) of 0.1 mM, a Michaelis‐Menten K m of 0.23 mM, and a sensitivity value 46 μA/mM/cm 2 . This biosensor allows the detection of urea in solutions, and it could be improved for further medical, environmental, or engineering applications.</description><identifier>ISSN: 1040-0397</identifier><identifier>EISSN: 1521-4109</identifier><identifier>DOI: 10.1002/elan.202200502</identifier><language>eng</language><publisher>Wiley-VCH Verlag</publisher><subject>Analytical chemistry ; Chemical Sciences</subject><ispartof>Electroanalysis (New York, N.Y.), 2023-09, Vol.35 (9)</ispartof><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c273t-a9a0d023db323d406ff4358ad15c84cbae209f697f282382aa289d62a91e9c0d3</citedby><cites>FETCH-LOGICAL-c273t-a9a0d023db323d406ff4358ad15c84cbae209f697f282382aa289d62a91e9c0d3</cites><orcidid>0000-0002-1627-1353</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27915,27916</link.rule.ids><backlink>$$Uhttps://hal.science/hal-04497305$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Atailia, Sara</creatorcontrib><creatorcontrib>Baraket, Abdoullatif</creatorcontrib><creatorcontrib>Rabai, Selma</creatorcontrib><creatorcontrib>Benounis, Messaoud</creatorcontrib><creatorcontrib>Jaffrezic, Nicole</creatorcontrib><creatorcontrib>Araar, Hala</creatorcontrib><creatorcontrib>Naït‐Bouda, Abdelyamine</creatorcontrib><creatorcontrib>Boumaza, Abdecharif</creatorcontrib><creatorcontrib>Errachid, Abdelhamid</creatorcontrib><creatorcontrib>Houhamdi, Moussa</creatorcontrib><title>Electrochemical urea biosensor based on Proteus mirabilis urease immobilized over polyaniline PANi‐Glassy carbon electrode</title><title>Electroanalysis (New York, N.Y.)</title><description>In this study, a novel, sensitive electrochemical enzyme‐based biosensor for urea detection was presented. This biosensor combines a three‐electrode system consisting of a classic Glassy Carbon Electrode (GCE) as the working electrode, a platinum counter electrode, and Ag/AgCl as the reference electrode. To construct this urea platform, a GCE was modified with a polyaniline (PANi) film. Then, bacterial urease from Proteus mirabilis was immobilized on the modified GCE (P m ‐Urease‐PANi‐GCE). For the characterization of surface modification, Cyclic Voltammetry (CV) and Scanning Electron Microscope (SEM) were applied, while the Square Wave Voltammetry (SWV) technique was performed for urea detection. The main analytical characteristics of the P m ‐Urease‐PANi‐GCE biosensor showed a good linear range from 0.1 to 10 mM of urea, a limit of detection (LOD) of 0.1 mM, a Michaelis‐Menten K m of 0.23 mM, and a sensitivity value 46 μA/mM/cm 2 . 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This biosensor combines a three‐electrode system consisting of a classic Glassy Carbon Electrode (GCE) as the working electrode, a platinum counter electrode, and Ag/AgCl as the reference electrode. To construct this urea platform, a GCE was modified with a polyaniline (PANi) film. Then, bacterial urease from Proteus mirabilis was immobilized on the modified GCE (P m ‐Urease‐PANi‐GCE). For the characterization of surface modification, Cyclic Voltammetry (CV) and Scanning Electron Microscope (SEM) were applied, while the Square Wave Voltammetry (SWV) technique was performed for urea detection. The main analytical characteristics of the P m ‐Urease‐PANi‐GCE biosensor showed a good linear range from 0.1 to 10 mM of urea, a limit of detection (LOD) of 0.1 mM, a Michaelis‐Menten K m of 0.23 mM, and a sensitivity value 46 μA/mM/cm 2 . This biosensor allows the detection of urea in solutions, and it could be improved for further medical, environmental, or engineering applications.</abstract><pub>Wiley-VCH Verlag</pub><doi>10.1002/elan.202200502</doi><orcidid>https://orcid.org/0000-0002-1627-1353</orcidid></addata></record> |
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title | Electrochemical urea biosensor based on Proteus mirabilis urease immobilized over polyaniline PANi‐Glassy carbon electrode |
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