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dc.contributor.authorFranco, José M.-
dc.contributor.authorFernández-Vila, Pablo-
dc.date.accessioned2012-11-16T08:26:38Z-
dc.date.available2012-11-16T08:26:38Z-
dc.date.issued1993-
dc.identifier.citationChromatographia 35(9-12): 613-620 (1993)es_ES
dc.identifier.issn0009-5893-
dc.identifier.urihttp://hdl.handle.net/10261/60389-
dc.description8 páginas, 4 figuras, 1 tablaes_ES
dc.description.abstractAn RP-HPLC method for the separation of shellfish toxins is described, employing three isocratic systems: Octanesulfonic acid in ammonium phosphate buffer plus acetonitrile for the separation of carbamate toxins (neoSTX, dcSTX and STX), octansulfonic acid in ammonium phosphate buffer for the separation of GTXs and tetrabutylammonium in the same buffer for Cs separation. These eluents perform the separation prior to postcolumn reaction and fluorimetric detection. The procedures have been applied to the determination of toxin production in dinoflagellate cultures, field samples of red tides, and toxic mussels.es_ES
dc.description.sponsorshipThis work was financed by Fondo de Investigacion de Sanidad y Seguridad Social, Project 102 of the IEO and by a grant from the Xunta de Galicia to P. Fernandez-Vila.es_ES
dc.language.isoenges_ES
dc.publisherSpringeres_ES
dc.rightsclosedAccesses_ES
dc.subjectColumn liquid chromatographyes_ES
dc.subjectIon pairinges_ES
dc.subjectParalytic shellfish toxinses_ES
dc.subjectDinoflagellate cultureses_ES
dc.subjectToxic molluscses_ES
dc.titleSeparation of paralytic shellfish toxins by reversed phase high performance liquid chromatography, with postcolumn reaction and fluorimetric detectiones_ES
dc.typeartículoes_ES
dc.identifier.doi10.1007/BF02267925-
dc.description.peerreviewedPeer reviewedes_ES
dc.relation.publisherversionhttp://dx.doi.org/10.1007/BF02267925es_ES
dc.identifier.e-issn1612-1112-
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