Linker-Assisted Immunoassay and Liquid Chromatography/Mass Spectrometry for the Analysis of Glyphosate
A novel, sensitive, linker-assisted enzyme-linked immunosorbent assay (L'ELISA) was compared to on-line solid-phase extraction (SPE) with high-performance liquid chromatography/mass spectrometry (HPLC/MS) for the analysis of glyphosate in surface water and groundwater samples. The L'ELISA...
Gespeichert in:
Veröffentlicht in: | Analytical chemistry (Washington) 2002-10, Vol.74 (19), p.4937-4943 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 4943 |
---|---|
container_issue | 19 |
container_start_page | 4937 |
container_title | Analytical chemistry (Washington) |
container_volume | 74 |
creator | Lee, E. A Zimmerman, L. R Bhullar, B. S Thurman, E. M |
description | A novel, sensitive, linker-assisted enzyme-linked immunosorbent assay (L'ELISA) was compared to on-line solid-phase extraction (SPE) with high-performance liquid chromatography/mass spectrometry (HPLC/MS) for the analysis of glyphosate in surface water and groundwater samples. The L'ELISA used succinic anhydride to derivatize glyphosate, which mimics the epitotic attachment of glyphosate to horseradish peroxidase hapten. Thus, L'ELISA recognized the derivatized glyphosate more effectively (detection limit of 0.1 μg/L) and with increased sensitivity (10−100 times) over conventional ELISA and showed the potential for other applications. The precision and accuracy of L'ELISA then was compared with on-line SPE/HPLC/MS, which detected glyphosate and its degradate derivatized with 9-fluorenylmethyl chloroformate using negative-ion electrospray (detection limit 0.1 μg/L, relative standard deviation ±15%). Derivatization efficiency and matrix effects were minimized by adding an isotope-labeled glyphosate (2-13C15N). The accuracy of L'ELISA gave a false positive rate of 18% between 0.1 and 1.0 μg/L and a false positive rate of only 1% above 1.0 μg/L. The relative standard deviation was ±20%. The correlation of L'ELISA and HPLC/MS for 66 surface water and groundwater samples was 0.97 with a slope of 1.28, with many detections of glyphosate and its degradate in surface water but not in groundwater. |
doi_str_mv | 10.1021/ac020208y |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_217877850</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>207816151</sourcerecordid><originalsourceid>FETCH-LOGICAL-a429t-415e7a57d77c0c1f42f9ed672fc97ac6cfbd2330c46132baf7f5d1db82a278113</originalsourceid><addsrcrecordid>eNpl0U1LHDEYB_AglrrVHvwCEgQPPUx9knlJ9rgMaoUtFbTFW3g2L-7ozmRMZsD59kZ2cQ8lh0Dy48-Tfwg5ZfCTAWeXqIGnJacDMmMlh6ySkh-SGQDkGRcAR-RbjM8AjAGrvpIjxnMJklUz4pZN92JDtoixiYM19LZtx85jjDhR7AxdNq9jY2i9Dr7FwT8F7NfT5e8E6H1v9ZCO7RAm6nygw9rSRYebKWVR7-jNZurXPuJgT8gXh5tov-_2Y_L3-uqh_pUt_9zc1otlhgWfD1nBSiuwFEYIDZq5gru5NZXgTs8F6kq7leF5DrqoWM5X6IQrDTMryZELyVh-TM63uX3wr6ONg3r2Y0gjRcWZkELIEhL6sUU6-BiDdaoPTYthUgzUR6Hqs9Bkz3aB46q1Zi93DSZwsQMYNW5cwE43ce_yeZU-oEgu27qPmt8-7zG8qErkolQPd_eKP16L-p98VPU-F3XcP-L_Ad8BCp2ZYA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>217877850</pqid></control><display><type>article</type><title>Linker-Assisted Immunoassay and Liquid Chromatography/Mass Spectrometry for the Analysis of Glyphosate</title><source>MEDLINE</source><source>American Chemical Society Journals</source><creator>Lee, E. A ; Zimmerman, L. R ; Bhullar, B. S ; Thurman, E. M</creator><creatorcontrib>Lee, E. A ; Zimmerman, L. R ; Bhullar, B. S ; Thurman, E. M</creatorcontrib><description>A novel, sensitive, linker-assisted enzyme-linked immunosorbent assay (L'ELISA) was compared to on-line solid-phase extraction (SPE) with high-performance liquid chromatography/mass spectrometry (HPLC/MS) for the analysis of glyphosate in surface water and groundwater samples. The L'ELISA used succinic anhydride to derivatize glyphosate, which mimics the epitotic attachment of glyphosate to horseradish peroxidase hapten. Thus, L'ELISA recognized the derivatized glyphosate more effectively (detection limit of 0.1 μg/L) and with increased sensitivity (10−100 times) over conventional ELISA and showed the potential for other applications. The precision and accuracy of L'ELISA then was compared with on-line SPE/HPLC/MS, which detected glyphosate and its degradate derivatized with 9-fluorenylmethyl chloroformate using negative-ion electrospray (detection limit 0.1 μg/L, relative standard deviation ±15%). Derivatization efficiency and matrix effects were minimized by adding an isotope-labeled glyphosate (2-13C15N). The accuracy of L'ELISA gave a false positive rate of 18% between 0.1 and 1.0 μg/L and a false positive rate of only 1% above 1.0 μg/L. The relative standard deviation was ±20%. The correlation of L'ELISA and HPLC/MS for 66 surface water and groundwater samples was 0.97 with a slope of 1.28, with many detections of glyphosate and its degradate in surface water but not in groundwater.</description><identifier>ISSN: 0003-2700</identifier><identifier>EISSN: 1520-6882</identifier><identifier>DOI: 10.1021/ac020208y</identifier><identifier>PMID: 12380816</identifier><identifier>CODEN: ANCHAM</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Analytical chemistry ; Chemistry ; Chromatographic methods and physical methods associated with chromatography ; Chromatography ; Chromatography, High Pressure Liquid ; Exact sciences and technology ; Glycine - analogs & derivatives ; Glycine - analysis ; Glyphosate ; Herbicides ; Herbicides - analysis ; Immunoassay ; Indicators and Reagents ; Mass Spectrometry ; Miscellaneous ; Other chromatographic methods ; Spectrometric and optical methods ; Water Pollutants, Chemical - analysis</subject><ispartof>Analytical chemistry (Washington), 2002-10, Vol.74 (19), p.4937-4943</ispartof><rights>Copyright © 2002 American Chemical Society</rights><rights>2002 INIST-CNRS</rights><rights>Copyright American Chemical Society Oct 1, 2002</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a429t-415e7a57d77c0c1f42f9ed672fc97ac6cfbd2330c46132baf7f5d1db82a278113</citedby><cites>FETCH-LOGICAL-a429t-415e7a57d77c0c1f42f9ed672fc97ac6cfbd2330c46132baf7f5d1db82a278113</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/ac020208y$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/ac020208y$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,776,780,2752,27053,27901,27902,56713,56763</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=13967004$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12380816$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lee, E. A</creatorcontrib><creatorcontrib>Zimmerman, L. R</creatorcontrib><creatorcontrib>Bhullar, B. S</creatorcontrib><creatorcontrib>Thurman, E. M</creatorcontrib><title>Linker-Assisted Immunoassay and Liquid Chromatography/Mass Spectrometry for the Analysis of Glyphosate</title><title>Analytical chemistry (Washington)</title><addtitle>Anal. Chem</addtitle><description>A novel, sensitive, linker-assisted enzyme-linked immunosorbent assay (L'ELISA) was compared to on-line solid-phase extraction (SPE) with high-performance liquid chromatography/mass spectrometry (HPLC/MS) for the analysis of glyphosate in surface water and groundwater samples. The L'ELISA used succinic anhydride to derivatize glyphosate, which mimics the epitotic attachment of glyphosate to horseradish peroxidase hapten. Thus, L'ELISA recognized the derivatized glyphosate more effectively (detection limit of 0.1 μg/L) and with increased sensitivity (10−100 times) over conventional ELISA and showed the potential for other applications. The precision and accuracy of L'ELISA then was compared with on-line SPE/HPLC/MS, which detected glyphosate and its degradate derivatized with 9-fluorenylmethyl chloroformate using negative-ion electrospray (detection limit 0.1 μg/L, relative standard deviation ±15%). Derivatization efficiency and matrix effects were minimized by adding an isotope-labeled glyphosate (2-13C15N). The accuracy of L'ELISA gave a false positive rate of 18% between 0.1 and 1.0 μg/L and a false positive rate of only 1% above 1.0 μg/L. The relative standard deviation was ±20%. The correlation of L'ELISA and HPLC/MS for 66 surface water and groundwater samples was 0.97 with a slope of 1.28, with many detections of glyphosate and its degradate in surface water but not in groundwater.</description><subject>Analytical chemistry</subject><subject>Chemistry</subject><subject>Chromatographic methods and physical methods associated with chromatography</subject><subject>Chromatography</subject><subject>Chromatography, High Pressure Liquid</subject><subject>Exact sciences and technology</subject><subject>Glycine - analogs & derivatives</subject><subject>Glycine - analysis</subject><subject>Glyphosate</subject><subject>Herbicides</subject><subject>Herbicides - analysis</subject><subject>Immunoassay</subject><subject>Indicators and Reagents</subject><subject>Mass Spectrometry</subject><subject>Miscellaneous</subject><subject>Other chromatographic methods</subject><subject>Spectrometric and optical methods</subject><subject>Water Pollutants, Chemical - analysis</subject><issn>0003-2700</issn><issn>1520-6882</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpl0U1LHDEYB_AglrrVHvwCEgQPPUx9knlJ9rgMaoUtFbTFW3g2L-7ozmRMZsD59kZ2cQ8lh0Dy48-Tfwg5ZfCTAWeXqIGnJacDMmMlh6ySkh-SGQDkGRcAR-RbjM8AjAGrvpIjxnMJklUz4pZN92JDtoixiYM19LZtx85jjDhR7AxdNq9jY2i9Dr7FwT8F7NfT5e8E6H1v9ZCO7RAm6nygw9rSRYebKWVR7-jNZurXPuJgT8gXh5tov-_2Y_L3-uqh_pUt_9zc1otlhgWfD1nBSiuwFEYIDZq5gru5NZXgTs8F6kq7leF5DrqoWM5X6IQrDTMryZELyVh-TM63uX3wr6ONg3r2Y0gjRcWZkELIEhL6sUU6-BiDdaoPTYthUgzUR6Hqs9Bkz3aB46q1Zi93DSZwsQMYNW5cwE43ce_yeZU-oEgu27qPmt8-7zG8qErkolQPd_eKP16L-p98VPU-F3XcP-L_Ad8BCp2ZYA</recordid><startdate>20021001</startdate><enddate>20021001</enddate><creator>Lee, E. A</creator><creator>Zimmerman, L. R</creator><creator>Bhullar, B. S</creator><creator>Thurman, E. M</creator><general>American Chemical Society</general><scope>BSCLL</scope><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>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></search><sort><creationdate>20021001</creationdate><title>Linker-Assisted Immunoassay and Liquid Chromatography/Mass Spectrometry for the Analysis of Glyphosate</title><author>Lee, E. A ; Zimmerman, L. R ; Bhullar, B. S ; Thurman, E. M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a429t-415e7a57d77c0c1f42f9ed672fc97ac6cfbd2330c46132baf7f5d1db82a278113</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Analytical chemistry</topic><topic>Chemistry</topic><topic>Chromatographic methods and physical methods associated with chromatography</topic><topic>Chromatography</topic><topic>Chromatography, High Pressure Liquid</topic><topic>Exact sciences and technology</topic><topic>Glycine - analogs & derivatives</topic><topic>Glycine - analysis</topic><topic>Glyphosate</topic><topic>Herbicides</topic><topic>Herbicides - analysis</topic><topic>Immunoassay</topic><topic>Indicators and Reagents</topic><topic>Mass Spectrometry</topic><topic>Miscellaneous</topic><topic>Other chromatographic methods</topic><topic>Spectrometric and optical methods</topic><topic>Water Pollutants, Chemical - analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lee, E. A</creatorcontrib><creatorcontrib>Zimmerman, L. R</creatorcontrib><creatorcontrib>Bhullar, B. S</creatorcontrib><creatorcontrib>Thurman, E. M</creatorcontrib><collection>Istex</collection><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>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><jtitle>Analytical chemistry (Washington)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lee, E. A</au><au>Zimmerman, L. R</au><au>Bhullar, B. S</au><au>Thurman, E. M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Linker-Assisted Immunoassay and Liquid Chromatography/Mass Spectrometry for the Analysis of Glyphosate</atitle><jtitle>Analytical chemistry (Washington)</jtitle><addtitle>Anal. Chem</addtitle><date>2002-10-01</date><risdate>2002</risdate><volume>74</volume><issue>19</issue><spage>4937</spage><epage>4943</epage><pages>4937-4943</pages><issn>0003-2700</issn><eissn>1520-6882</eissn><coden>ANCHAM</coden><abstract>A novel, sensitive, linker-assisted enzyme-linked immunosorbent assay (L'ELISA) was compared to on-line solid-phase extraction (SPE) with high-performance liquid chromatography/mass spectrometry (HPLC/MS) for the analysis of glyphosate in surface water and groundwater samples. The L'ELISA used succinic anhydride to derivatize glyphosate, which mimics the epitotic attachment of glyphosate to horseradish peroxidase hapten. Thus, L'ELISA recognized the derivatized glyphosate more effectively (detection limit of 0.1 μg/L) and with increased sensitivity (10−100 times) over conventional ELISA and showed the potential for other applications. The precision and accuracy of L'ELISA then was compared with on-line SPE/HPLC/MS, which detected glyphosate and its degradate derivatized with 9-fluorenylmethyl chloroformate using negative-ion electrospray (detection limit 0.1 μg/L, relative standard deviation ±15%). Derivatization efficiency and matrix effects were minimized by adding an isotope-labeled glyphosate (2-13C15N). The accuracy of L'ELISA gave a false positive rate of 18% between 0.1 and 1.0 μg/L and a false positive rate of only 1% above 1.0 μg/L. The relative standard deviation was ±20%. The correlation of L'ELISA and HPLC/MS for 66 surface water and groundwater samples was 0.97 with a slope of 1.28, with many detections of glyphosate and its degradate in surface water but not in groundwater.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>12380816</pmid><doi>10.1021/ac020208y</doi><tpages>7</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0003-2700 |
ispartof | Analytical chemistry (Washington), 2002-10, Vol.74 (19), p.4937-4943 |
issn | 0003-2700 1520-6882 |
language | eng |
recordid | cdi_proquest_journals_217877850 |
source | MEDLINE; American Chemical Society Journals |
subjects | Analytical chemistry Chemistry Chromatographic methods and physical methods associated with chromatography Chromatography Chromatography, High Pressure Liquid Exact sciences and technology Glycine - analogs & derivatives Glycine - analysis Glyphosate Herbicides Herbicides - analysis Immunoassay Indicators and Reagents Mass Spectrometry Miscellaneous Other chromatographic methods Spectrometric and optical methods Water Pollutants, Chemical - analysis |
title | Linker-Assisted Immunoassay and Liquid Chromatography/Mass Spectrometry for the Analysis of Glyphosate |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-04T07%3A54%3A54IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Linker-Assisted%20Immunoassay%20and%20Liquid%20Chromatography/Mass%20Spectrometry%20for%20the%20Analysis%20of%20Glyphosate&rft.jtitle=Analytical%20chemistry%20(Washington)&rft.au=Lee,%20E.%20A&rft.date=2002-10-01&rft.volume=74&rft.issue=19&rft.spage=4937&rft.epage=4943&rft.pages=4937-4943&rft.issn=0003-2700&rft.eissn=1520-6882&rft.coden=ANCHAM&rft_id=info:doi/10.1021/ac020208y&rft_dat=%3Cproquest_cross%3E207816151%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=217877850&rft_id=info:pmid/12380816&rfr_iscdi=true |