Time-resolved fluoroimmunoassay of zearalenone in cereals with a europium chelate as label
A competitive indirect time-resolved fluoroimmunoassay (TRFIA) was developed for detection of zearalenone (ZEN) in cereals, in which ZEN conjugated to bovine serum albumin (BSA) is used as solid-phase antigen. A competitive indirect TRFIA was conducted by simultaneously incubating ZEN in standard or...
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Published in | Journal of rare earths Vol. 27; no. 6; pp. 1088 - 1091 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier B.V
01.12.2009
Jiangsu Institute of Nuclear Medicine,Key Laboratory of Nuclear Medicine,Ministry of Health,Wuxi 214063,China%Jiangsu Institute of Nuclear Medicine,Key Laboratory of Nuclear Medicine,Ministry of Health,Wuxi 214063,China Department of Pharmaceutical and Molecular Biotechnology,School of Biotechnology,Key Labor%Department of Pharmaceutical and Molecular Biotechnology,School of Biotechnology,Key Laboratory of Industrial Biotechnology,Ministry of Education,Southern Yangtze University,Wuxi 214036,China |
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Online Access | Get full text |
ISSN | 1002-0721 2509-4963 |
DOI | 10.1016/S1002-0721(08)60393-2 |
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Abstract | A competitive indirect time-resolved fluoroimmunoassay (TRFIA) was developed for detection of zearalenone (ZEN) in cereals, in which ZEN conjugated to bovine serum albumin (BSA) is used as solid-phase antigen. A competitive indirect TRFIA was conducted by simultaneously incubating ZEN in standard or extracted samples with anti-ZEN monoclonal antibody over ZEN-BSA coated plates, and then determining the bound ZEN monoclonal antibody with goat anti-mouse europium conjugate. Samples were extracted with methanol/water (70:30,
v/v), then was subject directly for TRFIA without any clean-up procedure. The sensitivity of this method was 0.2 ng/ml. The measuring range of the ZEN-TRFIA was 0.2–200 ng/ml. The mean within-assay and between-assay coefficients variation of standard curve were both less than 10%. The recoveries of spiked cereals samples ranged from 76%–132%. 10 corn and 6 wheat corn samples were tested, ZEN values obtained by this method agreed well with those obtained by commercial ELISA kit. It was concluded that this new method is suitable for rapid screening of ZEN in corn and wheat. |
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AbstractList | O6; A competitive indirect time-resolved fluoroimmunoassay (TRFIA) was developed for detection of zearalenone (ZEN) in cereals,in which ZEN conjugated to bovine serum albumin (BSA) is used as solid-phase antigen. A competitive indirect TRFIA was conducted by simultaneously incubating ZEN in standard or extracted samples with anti-ZEN monoclonal antibody over ZEN-BSA coated plates, and then determining the bound ZEN monoclonal antibody with goat anti-mouse europium conjugate. Samples were extracted with methanol/water (70:30, v/v), then was subject directly for TRFIA without any clean-up procedure. The sensitivity of this method was 0.2 ng/ml. The measur-ing range of the ZEN-TRFIA was 0.2-200 ng/ml. The mean within-assay and between-assay coefficients variation of standard curve were both less than 10%. The recoveries of spiked cereals samples ranged from 76%-132%. 10 corn and 6 wheat corn samples were tested, ZEN values obtained by this method agreed well with those obtained by commercial ELISA kit. It was concluded that this new method is suitable for rapid screening of ZEN in corn and wheat. A competitive indirect time-resolved fluoroimmunoassay (TRFIA) was developed for detection of zearalenone (ZEN) in cereals, in which ZEN conjugated to bovine serum albumin (BSA) is used as solid-phase antigen. A competitive indirect TRFIA was conducted by simultaneously incubating ZEN in standard or extracted samples with anti-ZEN monoclonal antibody over ZEN-BSA coated plates, and then determining the bound ZEN monoclonal antibody with goat anti-mouse europium conjugate. Samples were extracted with methanol/water (70:30, v/v), then was subject directly for TRFIA without any clean-up procedure. The sensitivity of this method was 0.2 ng/ml. The measuring range of the ZEN-TRFIA was 0.2-200 ng/ml. The mean within-assay and between-assay coefficients variation of standard curve were both less than 10%. The recoveries of spiked cereals samples ranged from 76%-132%. 10 corn and 6 wheat corn samples were tested, ZEN values obtained by this method agreed well with those obtained by commercial ELISA kit. It was concluded that this new method is suitable for rapid screening of ZEN in corn and wheat. A competitive indirect time-resolved fluoroimmunoassay (TRFIA) was developed for detection of zearalenone (ZEN) in cereals, in which ZEN conjugated to bovine serum albumin (BSA) is used as solid-phase antigen. A competitive indirect TRFIA was conducted by simultaneously incubating ZEN in standard or extracted samples with anti-ZEN monoclonal antibody over ZEN-BSA coated plates, and then determining the bound ZEN monoclonal antibody with goat anti-mouse europium conjugate. Samples were extracted with methanol/water (70:30, v/v), then was subject directly for TRFIA without any clean-up procedure. The sensitivity of this method was 0.2 ng/ml. The measuring range of the ZEN-TRFIA was 0.2–200 ng/ml. The mean within-assay and between-assay coefficients variation of standard curve were both less than 10%. The recoveries of spiked cereals samples ranged from 76%–132%. 10 corn and 6 wheat corn samples were tested, ZEN values obtained by this method agreed well with those obtained by commercial ELISA kit. It was concluded that this new method is suitable for rapid screening of ZEN in corn and wheat. |
Author | TU, Qiang MA, Zhihong HUANG, Biao ZHU, Lan ZHANG, Jue ZHANG, Yi |
AuthorAffiliation | Jiangsu Institute of Nuclear Medicine,Key Laboratory of Nuclear Medicine,Ministry of Health,Wuxi 214063,China%Jiangsu Institute of Nuclear Medicine,Key Laboratory of Nuclear Medicine,Ministry of Health,Wuxi 214063,China;Department of Pharmaceutical and Molecular Biotechnology,School of Biotechnology,Key Labor%Department of Pharmaceutical and Molecular Biotechnology,School of Biotechnology,Key Laboratory of Industrial Biotechnology,Ministry of Education,Southern Yangtze University,Wuxi 214036,China |
AuthorAffiliation_xml | – name: Jiangsu Institute of Nuclear Medicine,Key Laboratory of Nuclear Medicine,Ministry of Health,Wuxi 214063,China%Jiangsu Institute of Nuclear Medicine,Key Laboratory of Nuclear Medicine,Ministry of Health,Wuxi 214063,China;Department of Pharmaceutical and Molecular Biotechnology,School of Biotechnology,Key Labor%Department of Pharmaceutical and Molecular Biotechnology,School of Biotechnology,Key Laboratory of Industrial Biotechnology,Ministry of Education,Southern Yangtze University,Wuxi 214036,China |
Author_xml | – sequence: 1 givenname: Zhihong surname: MA fullname: MA, Zhihong organization: Jiangsu Institute of Nuclear Medicine, Key Laboratory of Nuclear Medicine, Ministry of Health, Wuxi 214063, China – sequence: 2 givenname: Biao surname: HUANG fullname: HUANG, Biao email: jswxhb@163.com organization: Jiangsu Institute of Nuclear Medicine, Key Laboratory of Nuclear Medicine, Ministry of Health, Wuxi 214063, China – sequence: 3 givenname: Jue surname: ZHANG fullname: ZHANG, Jue organization: Jiangsu Institute of Nuclear Medicine, Key Laboratory of Nuclear Medicine, Ministry of Health, Wuxi 214063, China – sequence: 4 givenname: Yi surname: ZHANG fullname: ZHANG, Yi organization: Jiangsu Institute of Nuclear Medicine, Key Laboratory of Nuclear Medicine, Ministry of Health, Wuxi 214063, China – sequence: 5 givenname: Lan surname: ZHU fullname: ZHU, Lan organization: Jiangsu Institute of Nuclear Medicine, Key Laboratory of Nuclear Medicine, Ministry of Health, Wuxi 214063, China – sequence: 6 givenname: Qiang surname: TU fullname: TU, Qiang organization: Department of Pharmaceutical and Molecular Biotechnology, School of Biotechnology, Key Laboratory of Industrial Biotechnology, Ministry of Education, Southern Yangtze University, Wuxi 214036, China |
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CitedBy_id | crossref_primary_10_1007_s00216_012_5981_z crossref_primary_10_1080_09540105_2020_1780418 crossref_primary_10_1002_jsfa_4151 crossref_primary_10_1007_s00217_021_03862_3 crossref_primary_10_1016_j_foodchem_2018_02_060 crossref_primary_10_3920_WMJ2014_1701 crossref_primary_10_1007_s12161_017_0850_1 crossref_primary_10_1080_09540105_2021_1886254 |
Cites_doi | 10.1093/jaoac/77.6.1500 10.1128/AEM.50.2.332-336.1985 10.1016/S0377-8401(98)00278-8 10.1016/S0021-9673(00)00063-7 10.1128/AEM.45.1.16-23.1983 10.1007/BF00310860 10.1016/S0021-9673(98)00296-9 10.1093/clinchem/32.4.637 10.1093/clinchem/29.1.65 10.1093/clinchem/33.12.2281 10.1016/0273-2300(87)90037-7 10.1080/0265203031000087968 10.1093/clinchem/29.1.60 10.1128/AEM.47.5.1161-1163.1984 |
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Keywords | food safety zearalenone europium time-resolved fluoroimmunoassay rare earths |
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Snippet | A competitive indirect time-resolved fluoroimmunoassay (TRFIA) was developed for detection of zearalenone (ZEN) in cereals, in which ZEN conjugated to bovine... O6; A competitive indirect time-resolved fluoroimmunoassay (TRFIA) was developed for detection of zearalenone (ZEN) in cereals,in which ZEN conjugated to... |
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Title | Time-resolved fluoroimmunoassay of zearalenone in cereals with a europium chelate as label |
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