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Development of a novel immunobiosensor method for the rapid detection of okadaic acid contamination in shellfish extracts.

Development of a novel immunobiosensor method for the rapid detection of okadaic acid contamination in shellfish extracts. Research Abstract Details 

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  • Development of a novel immunobiosensor method for the rapid detection of okadaic acid contamination in shellfish extracts. Abstract Text:

    nuria m llamasNuria M Llamas,linda stewartLinda Stewart,terry fodeyTerry Fodey,h cowan higginsH Cowan Higgins, velasco Velasco,luis m botanaLuis M Botana,christopher t elliottChristopher T Elliott,nuria m llamasNuria M Llamas,linda stewartLinda Stewart,terry fodeyTerry Fodey,h cowan higginsH Cowan Higgins, velasco Velasco,luis m botanaLuis M Botana,christopher t elliottChristopher T Elliott,

    The mouse bioassay is the methodology that is most widely used to detect okadaic acid (OA) in shellfish samples. This is one of the best-known toxins, and it belongs to the family of marine biotoxins referred to as the diarrhetic shellfish poisons (DSP). Due to animal welfare concerns, alternative methods of toxin detection are being sought. A rapid and specific biosensor immunoassay method was developed and validated for the detection of OA. An optical sensor instrument based on the surface plasmon resonance (SPR) phenomenon was utilised. A polyclonal antibody to OA was raised against OA-bovine thyroglobulin conjugate and OA-N-hydroxy succinimide ester was immobilised onto an amine sensor chip surface. The assay parameters selected for the analysis of the samples were: antibody dilution, 1/750; ratio of antibody to standard, 1:1; volume of sample injected, 25 microl min(-1); flow rate, 25 microl min(-1). An assay action limit of 126 ng g(-1) was established by analysing of 20 shellfish samples spiked with OA at the critical concentration of 160 ng g(-1), which is the action limit established by the European Union (EU). At this concentration of OA, the assay delivered coefficient of variations (CVs) of <10%. The chip surface developed was shown to be highly stable, allowing more than 50 analyses per channel. When the concentrations of OA determined with the biosensor method were compared with the values obtained by LC-MS in contaminated shellfish samples, the correlation between the two analytical methods was found to be highly satisfactory (r(2) = 0.991).

    Development of a novel immunobiosensor method for the rapid detection of okadaic acid contamination in shellfish extracts. Publishing Authors By Initials

    nm llamasNM Llamas,l stewartL Stewart,t fodeyT Fodey,hc higginsHC Higgins,ml velascoML Velasco,lm botanaLM Botana,ct elliottCT Elliott,nm llamasNM Llamas,l stewartL Stewart,t fodeyT Fodey,hc higginsHC Higgins,ml velascoML Velasco,lm botanaLM Botana,ct elliottCT Elliott,

    For similar abstracts research abstracts see: abstracts research

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    Development of a novel immunobiosensor method for the rapid detection of okadaic acid contamination in shellfish extracts. Journal Published:

    PUBLICATION TYPE: Validation Studies

    Journal: Analytical and bioanalytical chemistry

    VOLUME: 389

    Page Numbers: 581-7

    Journal Abbreviation:

    ISSN: 1618-2642

    DAY: 24

    MONTH: 07

    YEAR: 2007

    Development of a novel immunobiosensor method for the rapid detection of okadaic acid contamination in shellfish extracts. Information

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    LANGUAGE: eng

    NlmUniqueID: 101134327

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    Grant and Affiliation Information for Development of a novel immunobiosensor method for the rapid detection of okadaic acid contamination in shellfish extracts.

    AFFILIATION: Institute of Agri-Food and Land Use, Queen's University of Belfast, Stranmillis Road, BT9 5AG Belfast, Northern Ireland, UK.

    Country: Germany

    Germany Research PublicationGermany Research Publication

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    MEDLINETA: Anal Bioanal Chem

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