Novel Chemiluminescence Immunoassay for the Determination of Zearalenone in Food Samples Using Gold Nanoparticles Labeled with Streptavidin–Horseradish Peroxidase
A novel highly sensitive chemiluminescence immunoassay (CLIA) was developed to detect zearalenone in food samples by using both biotinylated zearalenone conjugates and gold (Au) nanoparticles labeled with streptavidin–horseradish peroxidase for signal amplification. Biotinylated zearalenone–ovalbumi...
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Veröffentlicht in: | Journal of agricultural and food chemistry 2013-05, Vol.61 (18), p.4250-4256 |
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creator | Wang, Yuan-Kai Yan, Ya-Xian Ji, Wen-Hui Wang, Heng-an Zou, Qi Sun, Jian-He |
description | A novel highly sensitive chemiluminescence immunoassay (CLIA) was developed to detect zearalenone in food samples by using both biotinylated zearalenone conjugates and gold (Au) nanoparticles labeled with streptavidin–horseradish peroxidase for signal amplification. Biotinylated zearalenone–ovalbumin conjugates and Au nanoparticles labeled with streptavidin–horseradish peroxidase were synthesized separately. The concentrations of immunoreagents and the reaction times of these immunoreagents were optimized to improve the performances of analytical methods. For the CLIA based on biotinylated zearalenone conjugates and Au nanoparticles labeled with streptavidin–horseradish peroxidase, the limit of detection was 0.008 ng/mL and the IC50 was 0.11 ng/mL. The linear working range was 0.02–0.51 ng/mL. The cross-reactivities with the zearalenone analogues (α-zearalanol, zearalanone, α-zearalenol, β-zearalanol, and β-zearalenol) were 32, 17, 12, 0.3, and 0.1%, respectively. The recovery rates in spiked food samples were 97–117%, and the intraday and interday relative standard deviations were both |
doi_str_mv | 10.1021/jf400731j |
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Biotinylated zearalenone–ovalbumin conjugates and Au nanoparticles labeled with streptavidin–horseradish peroxidase were synthesized separately. The concentrations of immunoreagents and the reaction times of these immunoreagents were optimized to improve the performances of analytical methods. For the CLIA based on biotinylated zearalenone conjugates and Au nanoparticles labeled with streptavidin–horseradish peroxidase, the limit of detection was 0.008 ng/mL and the IC50 was 0.11 ng/mL. The linear working range was 0.02–0.51 ng/mL. The cross-reactivities with the zearalenone analogues (α-zearalanol, zearalanone, α-zearalenol, β-zearalanol, and β-zearalenol) were 32, 17, 12, 0.3, and 0.1%, respectively. The recovery rates in spiked food samples were 97–117%, and the intraday and interday relative standard deviations were both <10%. Parallel analysis of natural food samples showed a good correlation between this novel CLIA and liquid chromatography–tandem mass spectrometry. This method provides a rapid, accurate, and highly sensitive method to determine levels of zearalenone in food samples.</description><identifier>ISSN: 0021-8561</identifier><identifier>EISSN: 1520-5118</identifier><identifier>DOI: 10.1021/jf400731j</identifier><identifier>PMID: 23581862</identifier><identifier>CODEN: JAFCAU</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Biological and medical sciences ; Chromatography, Liquid ; Food Analysis - methods ; Food Contamination - analysis ; Food industries ; Food toxicology ; Fundamental and applied biological sciences. Psychology ; Gold - chemistry ; Horseradish Peroxidase - chemistry ; Immunoassay - methods ; Luminescence ; Metal Nanoparticles - chemistry ; Streptavidin - analysis ; Tandem Mass Spectrometry ; Zearalenone - analogs & derivatives ; Zearalenone - analysis ; Zeranol - analogs & derivatives ; Zeranol - analysis</subject><ispartof>Journal of agricultural and food chemistry, 2013-05, Vol.61 (18), p.4250-4256</ispartof><rights>Copyright © 2013 American Chemical Society</rights><rights>2014 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a345t-be0761137267d72fedb690760b4092d72db2945ead84aac0db100aefa7bf57453</citedby><cites>FETCH-LOGICAL-a345t-be0761137267d72fedb690760b4092d72db2945ead84aac0db100aefa7bf57453</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/jf400731j$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/jf400731j$$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=27349682$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23581862$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Yuan-Kai</creatorcontrib><creatorcontrib>Yan, Ya-Xian</creatorcontrib><creatorcontrib>Ji, Wen-Hui</creatorcontrib><creatorcontrib>Wang, Heng-an</creatorcontrib><creatorcontrib>Zou, Qi</creatorcontrib><creatorcontrib>Sun, Jian-He</creatorcontrib><title>Novel Chemiluminescence Immunoassay for the Determination of Zearalenone in Food Samples Using Gold Nanoparticles Labeled with Streptavidin–Horseradish Peroxidase</title><title>Journal of agricultural and food chemistry</title><addtitle>J. Agric. Food Chem</addtitle><description>A novel highly sensitive chemiluminescence immunoassay (CLIA) was developed to detect zearalenone in food samples by using both biotinylated zearalenone conjugates and gold (Au) nanoparticles labeled with streptavidin–horseradish peroxidase for signal amplification. Biotinylated zearalenone–ovalbumin conjugates and Au nanoparticles labeled with streptavidin–horseradish peroxidase were synthesized separately. The concentrations of immunoreagents and the reaction times of these immunoreagents were optimized to improve the performances of analytical methods. For the CLIA based on biotinylated zearalenone conjugates and Au nanoparticles labeled with streptavidin–horseradish peroxidase, the limit of detection was 0.008 ng/mL and the IC50 was 0.11 ng/mL. The linear working range was 0.02–0.51 ng/mL. The cross-reactivities with the zearalenone analogues (α-zearalanol, zearalanone, α-zearalenol, β-zearalanol, and β-zearalenol) were 32, 17, 12, 0.3, and 0.1%, respectively. The recovery rates in spiked food samples were 97–117%, and the intraday and interday relative standard deviations were both <10%. Parallel analysis of natural food samples showed a good correlation between this novel CLIA and liquid chromatography–tandem mass spectrometry. This method provides a rapid, accurate, and highly sensitive method to determine levels of zearalenone in food samples.</description><subject>Biological and medical sciences</subject><subject>Chromatography, Liquid</subject><subject>Food Analysis - methods</subject><subject>Food Contamination - analysis</subject><subject>Food industries</subject><subject>Food toxicology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gold - chemistry</subject><subject>Horseradish Peroxidase - chemistry</subject><subject>Immunoassay - methods</subject><subject>Luminescence</subject><subject>Metal Nanoparticles - chemistry</subject><subject>Streptavidin - analysis</subject><subject>Tandem Mass Spectrometry</subject><subject>Zearalenone - analogs & derivatives</subject><subject>Zearalenone - analysis</subject><subject>Zeranol - analogs & derivatives</subject><subject>Zeranol - analysis</subject><issn>0021-8561</issn><issn>1520-5118</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpt0c1u1DAQB3ALUdGlcOAFkC9IcEgZ58vJES30Q1oVpNILl2gST1ivHDvYTqE33oFX4Ml4Elx1KRw4jTTz04w0f8aeCTgWkIvXu7EEkIXYPWArUeWQVUI0D9kK0jBrqlocssch7ACgqSQ8Yod5UTWiqfMV-3nhrsnw9ZYmbZZJWwoD2YH4-TQt1mEIeMNH53ncEn9LkXwyGLWz3I38E6FHQ9ZZ4tryE-cUv8RpNhT4VdD2Mz91RvELtG5GH_VwO9hgT4YU_6rjll9GT3PEa620_fX9x5nzgTwqHbb8A3n3TSsM9IQdjGgCPd3XI3Z18u7j-izbvD89X7_ZZFiUVcx6AlkLUci8lkrmI6m-blML-hLaPHVUn7dlRaiaEnEA1QsApBFlP1ayrIoj9vJu7-zdl4VC7Cad3mEMWnJL6ERRthLyFiDRV3d08C4ET2M3ez2hv-kEdLehdPehJPt8v3bpJ1L38k8KCbzYAwwDmtGjHXT462S6Wzf_OBxCt3OLt-kb_zn4GyCipK0</recordid><startdate>20130508</startdate><enddate>20130508</enddate><creator>Wang, Yuan-Kai</creator><creator>Yan, Ya-Xian</creator><creator>Ji, Wen-Hui</creator><creator>Wang, Heng-an</creator><creator>Zou, Qi</creator><creator>Sun, Jian-He</creator><general>American Chemical Society</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>7X8</scope></search><sort><creationdate>20130508</creationdate><title>Novel Chemiluminescence Immunoassay for the Determination of Zearalenone in Food Samples Using Gold Nanoparticles Labeled with Streptavidin–Horseradish Peroxidase</title><author>Wang, Yuan-Kai ; Yan, Ya-Xian ; Ji, Wen-Hui ; Wang, Heng-an ; Zou, Qi ; Sun, Jian-He</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a345t-be0761137267d72fedb690760b4092d72db2945ead84aac0db100aefa7bf57453</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Biological and medical sciences</topic><topic>Chromatography, Liquid</topic><topic>Food Analysis - methods</topic><topic>Food Contamination - analysis</topic><topic>Food industries</topic><topic>Food toxicology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gold - chemistry</topic><topic>Horseradish Peroxidase - chemistry</topic><topic>Immunoassay - methods</topic><topic>Luminescence</topic><topic>Metal Nanoparticles - chemistry</topic><topic>Streptavidin - analysis</topic><topic>Tandem Mass Spectrometry</topic><topic>Zearalenone - analogs & derivatives</topic><topic>Zearalenone - analysis</topic><topic>Zeranol - analogs & derivatives</topic><topic>Zeranol - analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Yuan-Kai</creatorcontrib><creatorcontrib>Yan, Ya-Xian</creatorcontrib><creatorcontrib>Ji, Wen-Hui</creatorcontrib><creatorcontrib>Wang, Heng-an</creatorcontrib><creatorcontrib>Zou, Qi</creatorcontrib><creatorcontrib>Sun, Jian-He</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>MEDLINE - Academic</collection><jtitle>Journal of agricultural and food chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Yuan-Kai</au><au>Yan, Ya-Xian</au><au>Ji, Wen-Hui</au><au>Wang, Heng-an</au><au>Zou, Qi</au><au>Sun, Jian-He</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Novel Chemiluminescence Immunoassay for the Determination of Zearalenone in Food Samples Using Gold Nanoparticles Labeled with Streptavidin–Horseradish Peroxidase</atitle><jtitle>Journal of agricultural and food chemistry</jtitle><addtitle>J. Agric. Food Chem</addtitle><date>2013-05-08</date><risdate>2013</risdate><volume>61</volume><issue>18</issue><spage>4250</spage><epage>4256</epage><pages>4250-4256</pages><issn>0021-8561</issn><eissn>1520-5118</eissn><coden>JAFCAU</coden><abstract>A novel highly sensitive chemiluminescence immunoassay (CLIA) was developed to detect zearalenone in food samples by using both biotinylated zearalenone conjugates and gold (Au) nanoparticles labeled with streptavidin–horseradish peroxidase for signal amplification. Biotinylated zearalenone–ovalbumin conjugates and Au nanoparticles labeled with streptavidin–horseradish peroxidase were synthesized separately. The concentrations of immunoreagents and the reaction times of these immunoreagents were optimized to improve the performances of analytical methods. For the CLIA based on biotinylated zearalenone conjugates and Au nanoparticles labeled with streptavidin–horseradish peroxidase, the limit of detection was 0.008 ng/mL and the IC50 was 0.11 ng/mL. The linear working range was 0.02–0.51 ng/mL. The cross-reactivities with the zearalenone analogues (α-zearalanol, zearalanone, α-zearalenol, β-zearalanol, and β-zearalenol) were 32, 17, 12, 0.3, and 0.1%, respectively. The recovery rates in spiked food samples were 97–117%, and the intraday and interday relative standard deviations were both <10%. Parallel analysis of natural food samples showed a good correlation between this novel CLIA and liquid chromatography–tandem mass spectrometry. This method provides a rapid, accurate, and highly sensitive method to determine levels of zearalenone in food samples.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>23581862</pmid><doi>10.1021/jf400731j</doi><tpages>7</tpages></addata></record> |
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subjects | Biological and medical sciences Chromatography, Liquid Food Analysis - methods Food Contamination - analysis Food industries Food toxicology Fundamental and applied biological sciences. Psychology Gold - chemistry Horseradish Peroxidase - chemistry Immunoassay - methods Luminescence Metal Nanoparticles - chemistry Streptavidin - analysis Tandem Mass Spectrometry Zearalenone - analogs & derivatives Zearalenone - analysis Zeranol - analogs & derivatives Zeranol - analysis |
title | Novel Chemiluminescence Immunoassay for the Determination of Zearalenone in Food Samples Using Gold Nanoparticles Labeled with Streptavidin–Horseradish Peroxidase |
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