Self-Assembled Redox System for Bioelectrocatalytic Assay of L-Ascorbylphosphate and Alkaline Phosphatase Activity
Ferrocene‐terminated self‐assembled monolayer (Fc‐SAM) on gold was used as an electron‐transfer mediator in the electrochemical assay of L‐ascorbic acid 2‐phosphate (AAP). The assay is based on the enzymatic action of alkaline phosphatase (ALP), which triggers the release of vitamin C (L‐ascorbic ac...
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Veröffentlicht in: | Electroanalysis (New York, N.Y.) N.Y.), 2008-10, Vol.20 (20), p.2235-2240 |
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creator | Kazakevičienė, Birutė Valinčius, Gintaras Kažemėkaitė, Marytė Razumas, Valdemaras |
description | Ferrocene‐terminated self‐assembled monolayer (Fc‐SAM) on gold was used as an electron‐transfer mediator in the electrochemical assay of L‐ascorbic acid 2‐phosphate (AAP). The assay is based on the enzymatic action of alkaline phosphatase (ALP), which triggers the release of vitamin C (L‐ascorbic acid, AA) from AAP. The latter is easily oxidized on the Fc‐SAM under the diffusion limiting conditions that favors quantitative measurement of the AA concentration on a rotating disk electrode. We demonstrate the utility of the electrochemically active Fc‐SAM to probe the mechanism and to determine the kinetic parameters of an enzymatic reaction. The electrochemical technique was compared to a conventional spectrophotometric method of ALP activity detection using p‐nitrophenylphosphate (p‐NPP) as a substrate. We demonstrate that our new technique is also suitable for the analytical determination of ALP activity. The detection limits for both AAP and ALP were found to be 13 μM and 2 pM, respectively. |
doi_str_mv | 10.1002/elan.200804316 |
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The assay is based on the enzymatic action of alkaline phosphatase (ALP), which triggers the release of vitamin C (L‐ascorbic acid, AA) from AAP. The latter is easily oxidized on the Fc‐SAM under the diffusion limiting conditions that favors quantitative measurement of the AA concentration on a rotating disk electrode. We demonstrate the utility of the electrochemically active Fc‐SAM to probe the mechanism and to determine the kinetic parameters of an enzymatic reaction. The electrochemical technique was compared to a conventional spectrophotometric method of ALP activity detection using p‐nitrophenylphosphate (p‐NPP) as a substrate. We demonstrate that our new technique is also suitable for the analytical determination of ALP activity. 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The detection limits for both AAP and ALP were found to be 13 μM and 2 pM, respectively.</description><subject>Alkaline phosphatase</subject><subject>Ascorbic acid</subject><subject>Ascorbylphosphate</subject><subject>Ferrocene</subject><subject>Self-assembled monolayer</subject><issn>1040-0397</issn><issn>1521-4109</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNqFkMlOwzAQQCMEEuuVs0_cUiZx4trHsC8RIAriaDnOWBjcuthhyd-TqlXFjZNH1nuj0UuSwwxGGUB-jE7NRjkAh4JmbCPZyco8S4sMxOYwQwEpUDHeTnZjfAMAwQqxk4QJOpNWMeK0cdiSR2z9D5n0scMpMT6QE-vRoe6C16pTru-sJgOueuINqQdT-9D0bv7q4_xVdUjUrCWVe1fOzpA8rL5VRFLpzn7Zrt9PtoxyEQ9W717yfHH-dHqV1veX16dVneqcc5Y2gAZa3rDhUqqKVmghIC-4bhC5LhnHRhtajtEYEAXNUTQFZ1QYwTXkLaN7ydFy7zz4j0-MnZzaqNENmdB_RknLktEMFuBoCergYwxo5DzYqQq9zEAu0spFWrlOOwhiKXxbh_0_tDyvq7u_brp07ZD4Z-2q8C7ZmI5L-XJ3KScvMDmDm1tZ01_4847N</recordid><startdate>200810</startdate><enddate>200810</enddate><creator>Kazakevičienė, Birutė</creator><creator>Valinčius, Gintaras</creator><creator>Kažemėkaitė, Marytė</creator><creator>Razumas, Valdemaras</creator><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7U5</scope><scope>8FD</scope><scope>L7M</scope></search><sort><creationdate>200810</creationdate><title>Self-Assembled Redox System for Bioelectrocatalytic Assay of L-Ascorbylphosphate and Alkaline Phosphatase Activity</title><author>Kazakevičienė, Birutė ; Valinčius, Gintaras ; Kažemėkaitė, Marytė ; Razumas, Valdemaras</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2886-b0ef0d8b60963a4d9c990248cbee8c568ebcf357eff09432e9b48639f98c02d63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Alkaline phosphatase</topic><topic>Ascorbic acid</topic><topic>Ascorbylphosphate</topic><topic>Ferrocene</topic><topic>Self-assembled monolayer</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kazakevičienė, Birutė</creatorcontrib><creatorcontrib>Valinčius, Gintaras</creatorcontrib><creatorcontrib>Kažemėkaitė, Marytė</creatorcontrib><creatorcontrib>Razumas, Valdemaras</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Electroanalysis (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kazakevičienė, Birutė</au><au>Valinčius, Gintaras</au><au>Kažemėkaitė, Marytė</au><au>Razumas, Valdemaras</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Self-Assembled Redox System for Bioelectrocatalytic Assay of L-Ascorbylphosphate and Alkaline Phosphatase Activity</atitle><jtitle>Electroanalysis (New York, N.Y.)</jtitle><addtitle>Electroanalysis</addtitle><date>2008-10</date><risdate>2008</risdate><volume>20</volume><issue>20</issue><spage>2235</spage><epage>2240</epage><pages>2235-2240</pages><issn>1040-0397</issn><eissn>1521-4109</eissn><abstract>Ferrocene‐terminated self‐assembled monolayer (Fc‐SAM) on gold was used as an electron‐transfer mediator in the electrochemical assay of L‐ascorbic acid 2‐phosphate (AAP). The assay is based on the enzymatic action of alkaline phosphatase (ALP), which triggers the release of vitamin C (L‐ascorbic acid, AA) from AAP. The latter is easily oxidized on the Fc‐SAM under the diffusion limiting conditions that favors quantitative measurement of the AA concentration on a rotating disk electrode. We demonstrate the utility of the electrochemically active Fc‐SAM to probe the mechanism and to determine the kinetic parameters of an enzymatic reaction. The electrochemical technique was compared to a conventional spectrophotometric method of ALP activity detection using p‐nitrophenylphosphate (p‐NPP) as a substrate. We demonstrate that our new technique is also suitable for the analytical determination of ALP activity. The detection limits for both AAP and ALP were found to be 13 μM and 2 pM, respectively.</abstract><cop>Weinheim</cop><pub>WILEY-VCH Verlag</pub><doi>10.1002/elan.200804316</doi><tpages>6</tpages></addata></record> |
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subjects | Alkaline phosphatase Ascorbic acid Ascorbylphosphate Ferrocene Self-assembled monolayer |
title | Self-Assembled Redox System for Bioelectrocatalytic Assay of L-Ascorbylphosphate and Alkaline Phosphatase Activity |
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