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Isotope-labelling derivatisation: a broadly applicable approach to quantitation of algal toxins by isotope dilution LC-MS/MS
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NRC Publications Archive Archives des publications du CNRCThis publication could be one of several versions: author's original, accepted manuscript or the publisher's version. / La version de cette publication peut être l'une des suivantes : la version prépublication de l'auteur, la version acceptée du manuscrit ou la version de l'éditeur. The challenge of achieving co-elution in LC between deuterated a n dn o n -d e u t e r a t e dd a n s y l a t e dt o x i n sw a sa d d r e s s e db ym o d ifying separation conditions from the usual reverse phase (RP) separation to hydrophilic interaction liquid chromatography in the c a s eo fD Aa n das h o r t e n e dR Ps e p a r a t i o nw i t hh i g ho r g a n i c modifier content in the case of the ATXs. The new methods gave limits of detection between 10 and 60 mgk g À1 and allowedfor precise, accurate and fast determination of toxins in spiked control samples and matrix reference materials. This work demonstrates that isotope-labelling derivatisation is broadly applicable to the field of algal toxin analysis where derivatisation is well established but isotopically-labelled standards are not available.