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Fluorimetric Immunoassay for Multianalysis of Aflatoxins

A sensitive fluorimetric ELISA was developed for the analysis of aflatoxins. The assay was performed in a 384 microwell plate, wherein high specificity monoclonal antibody against AFM1 (mAb-AFM1) was used as capture antibody and FITC conjugated secondary antibody was used for detection and quantific...

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Autores principales: Kanungo, Lizy, Bhand, Sunil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3755385/
https://www.ncbi.nlm.nih.gov/pubmed/24000318
http://dx.doi.org/10.1155/2013/584964
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author Kanungo, Lizy
Bhand, Sunil
author_facet Kanungo, Lizy
Bhand, Sunil
author_sort Kanungo, Lizy
collection PubMed
description A sensitive fluorimetric ELISA was developed for the analysis of aflatoxins. The assay was performed in a 384 microwell plate, wherein high specificity monoclonal antibody against AFM1 (mAb-AFM1) was used as capture antibody and FITC conjugated secondary antibody was used for detection and quantification of the analyte. The linear range of the immunoassay was found to be 6.25–50 pg/mL. AFM1 as low as 1 pg/mL was detected by this method with assay volume 40 μL. The multi-analysis of different aflatoxins was also investigated in the microwell plate, based on the cross-reactivity (CR) approach. Real milk samples were tested along with certified reference material by standard addition method and recovery analysis was done. The mAb-AFM1 showed 23.2% CR with AFB1, 50% CR with respect to AFM2, and least CR towards AFG1 (<1%). Furthermore, mixture analysis of AFM2 and AFB1 was carried out at specific concentrations of AFM1. The advantages of this developed immunoassay are high sensitivity, high throughput, multianalyte detection, versatility, and ease of handling.
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spelling pubmed-37553852013-09-02 Fluorimetric Immunoassay for Multianalysis of Aflatoxins Kanungo, Lizy Bhand, Sunil J Anal Methods Chem Research Article A sensitive fluorimetric ELISA was developed for the analysis of aflatoxins. The assay was performed in a 384 microwell plate, wherein high specificity monoclonal antibody against AFM1 (mAb-AFM1) was used as capture antibody and FITC conjugated secondary antibody was used for detection and quantification of the analyte. The linear range of the immunoassay was found to be 6.25–50 pg/mL. AFM1 as low as 1 pg/mL was detected by this method with assay volume 40 μL. The multi-analysis of different aflatoxins was also investigated in the microwell plate, based on the cross-reactivity (CR) approach. Real milk samples were tested along with certified reference material by standard addition method and recovery analysis was done. The mAb-AFM1 showed 23.2% CR with AFB1, 50% CR with respect to AFM2, and least CR towards AFG1 (<1%). Furthermore, mixture analysis of AFM2 and AFB1 was carried out at specific concentrations of AFM1. The advantages of this developed immunoassay are high sensitivity, high throughput, multianalyte detection, versatility, and ease of handling. Hindawi Publishing Corporation 2013 2013-08-13 /pmc/articles/PMC3755385/ /pubmed/24000318 http://dx.doi.org/10.1155/2013/584964 Text en Copyright © 2013 L. Kanungo and S. Bhand. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Kanungo, Lizy
Bhand, Sunil
Fluorimetric Immunoassay for Multianalysis of Aflatoxins
title Fluorimetric Immunoassay for Multianalysis of Aflatoxins
title_full Fluorimetric Immunoassay for Multianalysis of Aflatoxins
title_fullStr Fluorimetric Immunoassay for Multianalysis of Aflatoxins
title_full_unstemmed Fluorimetric Immunoassay for Multianalysis of Aflatoxins
title_short Fluorimetric Immunoassay for Multianalysis of Aflatoxins
title_sort fluorimetric immunoassay for multianalysis of aflatoxins
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3755385/
https://www.ncbi.nlm.nih.gov/pubmed/24000318
http://dx.doi.org/10.1155/2013/584964
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