Development of Enzyme-Linked Immunosorbent Assay for Analysis of Total Aflatoxins Based on Monoclonal Antibody Reactive with Aflatoxins B1, B2, G1 and G2
A direct competitive enzyme-linked immunosorbent assay (dc-ELISA) was developed for the determination of total amount of aflatoxin B1, B2, G1 and G2 (AFB1, AFB2, AFG1 and AFG2), using a mouse monoclonal antibody that shows similar reactivity to each of these AFs. The working range of the developed d...
Gespeichert in:
Veröffentlicht in: | Food Hygiene and Safety Science (Shokuhin Eiseigaku Zasshi) 2018/10/25, Vol.59(5), pp.200-205 |
---|---|
Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 205 |
---|---|
container_issue | 5 |
container_start_page | 200 |
container_title | Food Hygiene and Safety Science (Shokuhin Eiseigaku Zasshi) |
container_volume | 59 |
creator | Yamasaki, Tomomi Miyake, Shiro Sato, Natsuki Hirakawa, Yuki Iwasa, Seiji Narita, Hiroshi Watanabe, Takaho |
description | A direct competitive enzyme-linked immunosorbent assay (dc-ELISA) was developed for the determination of total amount of aflatoxin B1, B2, G1 and G2 (AFB1, AFB2, AFG1 and AFG2), using a mouse monoclonal antibody that shows similar reactivity to each of these AFs. The working range of the developed dc-ELISA was 50–230 pg/mL for AFB1, 50–270 pg/mL for AFB2, 60–390 pg/mL for AFG1 and 65–700 pg/mL for AFG2. The recovery of AFs from spiked roasted peanuts was 98%. Further, when 4 samples actually contaminated with AFB1, AFB2, AFG1 and AFG2 were examined, the results of dc-ELISA were highly correlated with the values assigned by the Food Analysis Performance Assessment Scheme. The developed dc-ELISA appears to be suitable for the determination of total AFs at concentrations around the maximum permitted level (10 μg/kg for all foods) in Japan. |
doi_str_mv | 10.3358/shokueishi.59.200 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2133825113</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2133825113</sourcerecordid><originalsourceid>FETCH-LOGICAL-c306t-7b4be59bc80f5adb8aca7c5d3fd355aeb3d73f076230233aec920fa3ab56a4f3</originalsourceid><addsrcrecordid>eNpdkU2P0zAQhi0EEqXwA7hZ4sJhU_xRJ-mx-0FZqQgJ9W5NnDF1N7GL7ewS_gn_llRdLWJPI837PCONXkLec7aQUtWf0j7cDejS3i3UaiEYe0FmvK5FwRkrX5IZY1wV5VKUr8mblA7TkklWz8ifa7zHLhx79JkGS2_877HHYuv8Hbb0tu8HH1KIzSlepwQjtSHStYduTC6djF3I0NG17SCHX84neglpUoOnX4MPpgv-FPvsmtCO9DuCye4e6YPL-_8sfkEvxQXdcAq-pRvxlryy0CV89zjnZPf5Znf1pdh-29xerbeFkazMRdUsG1SrxtTMKmibGgxURrXStlIpwEa2lbSsKoVkQkpAsxLMgoRGlbC0ck4-ns8eY_g5YMq6d8lg14HHMCQtuJS1UHwac_LhGXoIQ5zemyghVVmVTKmJ4mfKxJBSRKuP0fUQR82ZPnWl_3Wl1UpPXU3O9dk5pAw_8MmAmJ3p8JmhHrWn2OwhavTyL5LjpQg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2235676055</pqid></control><display><type>article</type><title>Development of Enzyme-Linked Immunosorbent Assay for Analysis of Total Aflatoxins Based on Monoclonal Antibody Reactive with Aflatoxins B1, B2, G1 and G2</title><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><creator>Yamasaki, Tomomi ; Miyake, Shiro ; Sato, Natsuki ; Hirakawa, Yuki ; Iwasa, Seiji ; Narita, Hiroshi ; Watanabe, Takaho</creator><creatorcontrib>Yamasaki, Tomomi ; Miyake, Shiro ; Sato, Natsuki ; Hirakawa, Yuki ; Iwasa, Seiji ; Narita, Hiroshi ; Watanabe, Takaho</creatorcontrib><description>A direct competitive enzyme-linked immunosorbent assay (dc-ELISA) was developed for the determination of total amount of aflatoxin B1, B2, G1 and G2 (AFB1, AFB2, AFG1 and AFG2), using a mouse monoclonal antibody that shows similar reactivity to each of these AFs. The working range of the developed dc-ELISA was 50–230 pg/mL for AFB1, 50–270 pg/mL for AFB2, 60–390 pg/mL for AFG1 and 65–700 pg/mL for AFG2. The recovery of AFs from spiked roasted peanuts was 98%. Further, when 4 samples actually contaminated with AFB1, AFB2, AFG1 and AFG2 were examined, the results of dc-ELISA were highly correlated with the values assigned by the Food Analysis Performance Assessment Scheme. The developed dc-ELISA appears to be suitable for the determination of total AFs at concentrations around the maximum permitted level (10 μg/kg for all foods) in Japan.</description><identifier>ISSN: 0015-6426</identifier><identifier>EISSN: 1882-1006</identifier><identifier>DOI: 10.3358/shokueishi.59.200</identifier><language>eng</language><publisher>Tokyo: Japanese Society for Food Hygiene and Safety</publisher><subject>aflatoxin ; Aflatoxins ; ELISA ; Food analysis ; immunoassay ; Monoclonal antibodies ; monoclonal antibody ; Peanuts ; Performance assessment ; total aflatoxin</subject><ispartof>Food Hygiene and Safety Science (Shokuhin Eiseigaku Zasshi), 2018/10/25, Vol.59(5), pp.200-205</ispartof><rights>2018 Japanese Society for Food Hygiene and Safety</rights><rights>Copyright Japan Science and Technology Agency 2018</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c306t-7b4be59bc80f5adb8aca7c5d3fd355aeb3d73f076230233aec920fa3ab56a4f3</citedby><cites>FETCH-LOGICAL-c306t-7b4be59bc80f5adb8aca7c5d3fd355aeb3d73f076230233aec920fa3ab56a4f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,27929,27930</link.rule.ids></links><search><creatorcontrib>Yamasaki, Tomomi</creatorcontrib><creatorcontrib>Miyake, Shiro</creatorcontrib><creatorcontrib>Sato, Natsuki</creatorcontrib><creatorcontrib>Hirakawa, Yuki</creatorcontrib><creatorcontrib>Iwasa, Seiji</creatorcontrib><creatorcontrib>Narita, Hiroshi</creatorcontrib><creatorcontrib>Watanabe, Takaho</creatorcontrib><title>Development of Enzyme-Linked Immunosorbent Assay for Analysis of Total Aflatoxins Based on Monoclonal Antibody Reactive with Aflatoxins B1, B2, G1 and G2</title><title>Food Hygiene and Safety Science (Shokuhin Eiseigaku Zasshi)</title><addtitle>Food Hyg. Saf. Sci.</addtitle><description>A direct competitive enzyme-linked immunosorbent assay (dc-ELISA) was developed for the determination of total amount of aflatoxin B1, B2, G1 and G2 (AFB1, AFB2, AFG1 and AFG2), using a mouse monoclonal antibody that shows similar reactivity to each of these AFs. The working range of the developed dc-ELISA was 50–230 pg/mL for AFB1, 50–270 pg/mL for AFB2, 60–390 pg/mL for AFG1 and 65–700 pg/mL for AFG2. The recovery of AFs from spiked roasted peanuts was 98%. Further, when 4 samples actually contaminated with AFB1, AFB2, AFG1 and AFG2 were examined, the results of dc-ELISA were highly correlated with the values assigned by the Food Analysis Performance Assessment Scheme. The developed dc-ELISA appears to be suitable for the determination of total AFs at concentrations around the maximum permitted level (10 μg/kg for all foods) in Japan.</description><subject>aflatoxin</subject><subject>Aflatoxins</subject><subject>ELISA</subject><subject>Food analysis</subject><subject>immunoassay</subject><subject>Monoclonal antibodies</subject><subject>monoclonal antibody</subject><subject>Peanuts</subject><subject>Performance assessment</subject><subject>total aflatoxin</subject><issn>0015-6426</issn><issn>1882-1006</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNpdkU2P0zAQhi0EEqXwA7hZ4sJhU_xRJ-mx-0FZqQgJ9W5NnDF1N7GL7ewS_gn_llRdLWJPI837PCONXkLec7aQUtWf0j7cDejS3i3UaiEYe0FmvK5FwRkrX5IZY1wV5VKUr8mblA7TkklWz8ifa7zHLhx79JkGS2_877HHYuv8Hbb0tu8HH1KIzSlepwQjtSHStYduTC6djF3I0NG17SCHX84neglpUoOnX4MPpgv-FPvsmtCO9DuCye4e6YPL-_8sfkEvxQXdcAq-pRvxlryy0CV89zjnZPf5Znf1pdh-29xerbeFkazMRdUsG1SrxtTMKmibGgxURrXStlIpwEa2lbSsKoVkQkpAsxLMgoRGlbC0ck4-ns8eY_g5YMq6d8lg14HHMCQtuJS1UHwac_LhGXoIQ5zemyghVVmVTKmJ4mfKxJBSRKuP0fUQR82ZPnWl_3Wl1UpPXU3O9dk5pAw_8MmAmJ3p8JmhHrWn2OwhavTyL5LjpQg</recordid><startdate>20181025</startdate><enddate>20181025</enddate><creator>Yamasaki, Tomomi</creator><creator>Miyake, Shiro</creator><creator>Sato, Natsuki</creator><creator>Hirakawa, Yuki</creator><creator>Iwasa, Seiji</creator><creator>Narita, Hiroshi</creator><creator>Watanabe, Takaho</creator><general>Japanese Society for Food Hygiene and Safety</general><general>Japan Science and Technology Agency</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7T2</scope><scope>7T7</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>F1W</scope><scope>FR3</scope><scope>H95</scope><scope>H96</scope><scope>H97</scope><scope>H98</scope><scope>H99</scope><scope>L.F</scope><scope>L.G</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20181025</creationdate><title>Development of Enzyme-Linked Immunosorbent Assay for Analysis of Total Aflatoxins Based on Monoclonal Antibody Reactive with Aflatoxins B1, B2, G1 and G2</title><author>Yamasaki, Tomomi ; Miyake, Shiro ; Sato, Natsuki ; Hirakawa, Yuki ; Iwasa, Seiji ; Narita, Hiroshi ; Watanabe, Takaho</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c306t-7b4be59bc80f5adb8aca7c5d3fd355aeb3d73f076230233aec920fa3ab56a4f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>aflatoxin</topic><topic>Aflatoxins</topic><topic>ELISA</topic><topic>Food analysis</topic><topic>immunoassay</topic><topic>Monoclonal antibodies</topic><topic>monoclonal antibody</topic><topic>Peanuts</topic><topic>Performance assessment</topic><topic>total aflatoxin</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yamasaki, Tomomi</creatorcontrib><creatorcontrib>Miyake, Shiro</creatorcontrib><creatorcontrib>Sato, Natsuki</creatorcontrib><creatorcontrib>Hirakawa, Yuki</creatorcontrib><creatorcontrib>Iwasa, Seiji</creatorcontrib><creatorcontrib>Narita, Hiroshi</creatorcontrib><creatorcontrib>Watanabe, Takaho</creatorcontrib><collection>CrossRef</collection><collection>Health and Safety Science Abstracts (Full archive)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Engineering Research Database</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 2: Ocean Technology, Policy & Non-Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 3: Aquatic Pollution & Environmental Quality</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Aquaculture Abstracts</collection><collection>ASFA: Marine Biotechnology Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Marine Biotechnology Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Food Hygiene and Safety Science (Shokuhin Eiseigaku Zasshi)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yamasaki, Tomomi</au><au>Miyake, Shiro</au><au>Sato, Natsuki</au><au>Hirakawa, Yuki</au><au>Iwasa, Seiji</au><au>Narita, Hiroshi</au><au>Watanabe, Takaho</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Development of Enzyme-Linked Immunosorbent Assay for Analysis of Total Aflatoxins Based on Monoclonal Antibody Reactive with Aflatoxins B1, B2, G1 and G2</atitle><jtitle>Food Hygiene and Safety Science (Shokuhin Eiseigaku Zasshi)</jtitle><addtitle>Food Hyg. Saf. Sci.</addtitle><date>2018-10-25</date><risdate>2018</risdate><volume>59</volume><issue>5</issue><spage>200</spage><epage>205</epage><pages>200-205</pages><issn>0015-6426</issn><eissn>1882-1006</eissn><abstract>A direct competitive enzyme-linked immunosorbent assay (dc-ELISA) was developed for the determination of total amount of aflatoxin B1, B2, G1 and G2 (AFB1, AFB2, AFG1 and AFG2), using a mouse monoclonal antibody that shows similar reactivity to each of these AFs. The working range of the developed dc-ELISA was 50–230 pg/mL for AFB1, 50–270 pg/mL for AFB2, 60–390 pg/mL for AFG1 and 65–700 pg/mL for AFG2. The recovery of AFs from spiked roasted peanuts was 98%. Further, when 4 samples actually contaminated with AFB1, AFB2, AFG1 and AFG2 were examined, the results of dc-ELISA were highly correlated with the values assigned by the Food Analysis Performance Assessment Scheme. The developed dc-ELISA appears to be suitable for the determination of total AFs at concentrations around the maximum permitted level (10 μg/kg for all foods) in Japan.</abstract><cop>Tokyo</cop><pub>Japanese Society for Food Hygiene and Safety</pub><doi>10.3358/shokueishi.59.200</doi><tpages>6</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0015-6426 |
ispartof | Food Hygiene and Safety Science (Shokuhin Eiseigaku Zasshi), 2018/10/25, Vol.59(5), pp.200-205 |
issn | 0015-6426 1882-1006 |
language | eng |
recordid | cdi_proquest_miscellaneous_2133825113 |
source | Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals |
subjects | aflatoxin Aflatoxins ELISA Food analysis immunoassay Monoclonal antibodies monoclonal antibody Peanuts Performance assessment total aflatoxin |
title | Development of Enzyme-Linked Immunosorbent Assay for Analysis of Total Aflatoxins Based on Monoclonal Antibody Reactive with Aflatoxins B1, B2, G1 and G2 |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-15T07%3A37%3A28IST&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=Development%20of%20Enzyme-Linked%20Immunosorbent%20Assay%20for%20Analysis%20of%20Total%20Aflatoxins%20Based%20on%20Monoclonal%20Antibody%20Reactive%20with%20Aflatoxins%20B1,%20B2,%20G1%20and%20G2&rft.jtitle=Food%20Hygiene%20and%20Safety%20Science%20(Shokuhin%20Eiseigaku%20Zasshi)&rft.au=Yamasaki,%20Tomomi&rft.date=2018-10-25&rft.volume=59&rft.issue=5&rft.spage=200&rft.epage=205&rft.pages=200-205&rft.issn=0015-6426&rft.eissn=1882-1006&rft_id=info:doi/10.3358/shokueishi.59.200&rft_dat=%3Cproquest_cross%3E2133825113%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=2235676055&rft_id=info:pmid/&rfr_iscdi=true |