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A quantitative enzyme-linked immunoassay for the detection of 2,6- dichlorobenzamide (BAM), a degradation product of the herbicide dichlobenil

  • Leif Bruun
  • , Claus Koch
  • , Brian Pedersen
  • , Mogens Havsteen Jakobsen
  • , Jens Aamand

Research output: Contribution to journalArticleResearchpeer-review

30 Citations (Scopus)

Abstract

2,6-Dichlorobenzamide (BAM) is the dominant degradation product in soil of the widely used herbicide dichlobenil. To detect BAM in water, a highly sensitive and specific enzyme-linked immunosorbent assay (ELISA) was developed. As an alternative to conventional coating of ELISA plates, the assay is based on direct covalent immobilisation. We achieved a surface which requires a short time for the immobilisation of ligand, is stable under dry storage, and which permits assays with a low CV. The performance of the assay was demonstrated by an inter-well CV that was generally less than 6%, a detection limit (DL15) of 0.02 μg/l and an IC50 of 0.19 μg/l. Cross- reactivity was measured against nine analytes with structural homology to BAM. The highest degree of cross-reactivity (10.8%) was seen with 2,6- dichlorothiobenzamide (Chlorthiamid). Considering an EU-limit of 0.1 μg/l as the permissible maximum for the presence of pesticides in drinking water, this ELISA-procedure is suitable for large-scale screening of water samples suspected of being contaminated with BAM. (C) 2000 Elsevier Science B.V.

Original languageEnglish
Pages (from-to)133-142
Number of pages10
JournalJournal of Immunological Methods
Volume240
Issue number1-2
DOIs
Publication statusPublished - 23 Jun 2000

Keywords

  • 2,6-Dichlorobenzamide
  • Antibody
  • BAM
  • Covalent immobilisation
  • Dichlobenil
  • Herbicide
  • Immunoassay
  • Pesticide

Programme Area

  • Programme Area 2: Water Resources

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