Production of monoclonal antibody to acaricide dicofol and its derivatives

In Thailand detection of acaricide dicofol residues has been sporadically performed due to the limitation of analytical techniques. Conventional analytical methods for detecting dicofol residues most often use chromatographic-based techniques. Our ultimate aim is to develop an alternative method for...

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Main Authors: Surat Hongsibsong, Tippawan Prapamontol, Chaisuree Suphavilai, Jiraprapa Wipasa, Mookda Pattarawarapan, Watchara Kasinrerk
Format: Journal
Published: 2018
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http://cmuir.cmu.ac.th/jspui/handle/6653943832/50910
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Institution: Chiang Mai University
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spelling th-cmuir.6653943832-509102018-09-04T04:49:59Z Production of monoclonal antibody to acaricide dicofol and its derivatives Surat Hongsibsong Tippawan Prapamontol Chaisuree Suphavilai Jiraprapa Wipasa Mookda Pattarawarapan Watchara Kasinrerk Immunology and Microbiology Medicine In Thailand detection of acaricide dicofol residues has been sporadically performed due to the limitation of analytical techniques. Conventional analytical methods for detecting dicofol residues most often use chromatographic-based techniques. Our ultimate aim is to develop an alternative method for rapidly analyzing dicofol residues in vegetables and fruit samples. Here we report the production of monoclonal antibodies specific to dicofol and its derivatives. Hapten-protein carriers were prepared by linking succinic anhydride to dichlorobenzhydrol (DCBH), which was then conjugated to bovine serum albumin (BSA) and oval albumin (OVA). DCBH-BSA conjugate was used as immunogen while DCBH-OVA conjugate was used as capture antigen for competitive inhibition assay. Female BALB/c mice were immunized with DCBH-BSA conjugate subcutaneously, and antibody (Ab) level was determined 2 weeks after the last immunization. Spleen cells producing high titer antibody were isolated and fused with myeloma cells of P3.X6.Ag8.653. After limiting dilutions, antibody produced by one clone had high affinity, which was found to be of IgG1 with κ light chain. Specificity and inhibition concentrations of the monoclonal antibody (MAb) were determined by competitive indirect ELISA with dicofol, and its 50% (IC50) was 0.28 μg/mL. Working ranges of the developed immunoassay were from 0.07 to 25 μg/mL. Hence, the prepared MAb will be able to be applied for immunoassay development for detecting dicifol residue in vegetables and fruits far below the maximum residue limit such that 5 g of fruits and berries can be detected below 0.1 mg/kg. © Copyright 2010, Mary Ann Liebert, Inc. 2010. 2018-09-04T04:47:26Z 2018-09-04T04:47:26Z 2010-12-01 Journal 15540014 2-s2.0-78650098765 10.1089/hyb.2010.0051 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=78650098765&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/50910
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
topic Immunology and Microbiology
Medicine
spellingShingle Immunology and Microbiology
Medicine
Surat Hongsibsong
Tippawan Prapamontol
Chaisuree Suphavilai
Jiraprapa Wipasa
Mookda Pattarawarapan
Watchara Kasinrerk
Production of monoclonal antibody to acaricide dicofol and its derivatives
description In Thailand detection of acaricide dicofol residues has been sporadically performed due to the limitation of analytical techniques. Conventional analytical methods for detecting dicofol residues most often use chromatographic-based techniques. Our ultimate aim is to develop an alternative method for rapidly analyzing dicofol residues in vegetables and fruit samples. Here we report the production of monoclonal antibodies specific to dicofol and its derivatives. Hapten-protein carriers were prepared by linking succinic anhydride to dichlorobenzhydrol (DCBH), which was then conjugated to bovine serum albumin (BSA) and oval albumin (OVA). DCBH-BSA conjugate was used as immunogen while DCBH-OVA conjugate was used as capture antigen for competitive inhibition assay. Female BALB/c mice were immunized with DCBH-BSA conjugate subcutaneously, and antibody (Ab) level was determined 2 weeks after the last immunization. Spleen cells producing high titer antibody were isolated and fused with myeloma cells of P3.X6.Ag8.653. After limiting dilutions, antibody produced by one clone had high affinity, which was found to be of IgG1 with κ light chain. Specificity and inhibition concentrations of the monoclonal antibody (MAb) were determined by competitive indirect ELISA with dicofol, and its 50% (IC50) was 0.28 μg/mL. Working ranges of the developed immunoassay were from 0.07 to 25 μg/mL. Hence, the prepared MAb will be able to be applied for immunoassay development for detecting dicifol residue in vegetables and fruits far below the maximum residue limit such that 5 g of fruits and berries can be detected below 0.1 mg/kg. © Copyright 2010, Mary Ann Liebert, Inc. 2010.
format Journal
author Surat Hongsibsong
Tippawan Prapamontol
Chaisuree Suphavilai
Jiraprapa Wipasa
Mookda Pattarawarapan
Watchara Kasinrerk
author_facet Surat Hongsibsong
Tippawan Prapamontol
Chaisuree Suphavilai
Jiraprapa Wipasa
Mookda Pattarawarapan
Watchara Kasinrerk
author_sort Surat Hongsibsong
title Production of monoclonal antibody to acaricide dicofol and its derivatives
title_short Production of monoclonal antibody to acaricide dicofol and its derivatives
title_full Production of monoclonal antibody to acaricide dicofol and its derivatives
title_fullStr Production of monoclonal antibody to acaricide dicofol and its derivatives
title_full_unstemmed Production of monoclonal antibody to acaricide dicofol and its derivatives
title_sort production of monoclonal antibody to acaricide dicofol and its derivatives
publishDate 2018
url https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=78650098765&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/50910
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