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: Hongsibsong S., Prapamontol T., Suphavilai C., Wipasa J., Pattarawarapan M., Kasinrerk W.
Format: Article
Language:English
Published: 2014
Online Access:http://www.scopus.com/inward/record.url?eid=2-s2.0-78650098765&partnerID=40&md5=d48c33d0f480a8ac2dd385ea4d21bdc7
http://www.ncbi.nlm.nih.gov/pubmed/21118018
http://cmuir.cmu.ac.th/handle/6653943832/738
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spelling th-cmuir.6653943832-7382014-08-29T09:02:02Z Production of monoclonal antibody to acaricide dicofol and its derivatives Hongsibsong S. Prapamontol T. Suphavilai C. Wipasa J. Pattarawarapan M. Kasinrerk W. 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. 2014-08-29T09:02:02Z 2014-08-29T09:02:02Z 2010 Article 15540014 10.1089/hyb.2010.0051 21118018 HYBRD http://www.scopus.com/inward/record.url?eid=2-s2.0-78650098765&partnerID=40&md5=d48c33d0f480a8ac2dd385ea4d21bdc7 http://www.ncbi.nlm.nih.gov/pubmed/21118018 http://cmuir.cmu.ac.th/handle/6653943832/738 English
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
language English
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 Article
author Hongsibsong S.
Prapamontol T.
Suphavilai C.
Wipasa J.
Pattarawarapan M.
Kasinrerk W.
spellingShingle Hongsibsong S.
Prapamontol T.
Suphavilai C.
Wipasa J.
Pattarawarapan M.
Kasinrerk W.
Production of monoclonal antibody to acaricide dicofol and its derivatives
author_facet Hongsibsong S.
Prapamontol T.
Suphavilai C.
Wipasa J.
Pattarawarapan M.
Kasinrerk W.
author_sort Hongsibsong S.
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 2014
url http://www.scopus.com/inward/record.url?eid=2-s2.0-78650098765&partnerID=40&md5=d48c33d0f480a8ac2dd385ea4d21bdc7
http://www.ncbi.nlm.nih.gov/pubmed/21118018
http://cmuir.cmu.ac.th/handle/6653943832/738
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