High-performance liquid chromatography of domoic acid, a marine neurotoxin, with application to shellfish and plankton

From National Research Council Canada

DOIResolve DOI: https://doi.org/10.1080/03067318908026867
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Name affiliation
  1. National Research Council Canada
FormatText
TypeArticle
Journal titleInternational Journal of Environmental Analytical Chemistry
ISSN0306-7319
1029-0397
Volume36
Issue3
Pages139–154
Subjectdomoic acid; neurotoxin; shellfish; high-performance liquid chromatography; ultraviolet diode array detector
Abstract
A recent outbreak of poisoning resulting from the consumption of cultured blue mussels (Mytilus edulis L.) from a localized area in Eastern Canada has been attributed to the presence of domoic acid (1), a relatively rare neurotoxic amino acid, previously found only in some algae of the family Rhodomelaceae. Studies on aqueous extracts of shellfish tissue indicated that the toxin and several of its isomers could be separated (and isolated in sufficient amounts for subsequent structural identification) by reversed-phase high-performance liquid chromatography (HPLC) with ultraviolet (UV) diode array detection (DAD). Aqueous acetonitrile containing 0.1% v/v trifluoroacetic acid was used as mobile phase. As the retention time and characteristic UV absorption spectrum of 1 (λmax = 242 nm) permit unequivocal identification, the HPLC-DAD procedure was refined with a microbore column to provide a rapid (5 min), sensitive (0.3 ng detection limit) and reproducible assay method for the determination of 1 in shellfish tissue. Extraction was accomplished by boiling homogenized shellfish tissue for 5 min with distilled water. Extracts were taken through an octadecylsilica solid phase extraction clean-up prior to HPLC. This method has been applied to a variety of shellfish and phytoplankton samples.
Publication date
PublisherTaylor and Francis
LanguageEnglish
Peer reviewedYes
NPARC number23000945
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Record modified2016-11-21
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