FN Archimer Export Format
PT C
TI Identification of paralytic shellfish poisons using liquid chromatography / ion mobility - high resolution mass spectrometry
BT 
AF POYER, Salomé
   LOUTELIER-BOURHIS, Corinne
   MONDEGUER, Florence
   COADOU, Gaël
   HUBERT-ROUX, Marie
   ENCHE, Julien
   BOSSEE, Anne
   HESS, Philipp
   AFONSO, Carlos
AS 1:1;2:1;3:2;4:1;5:1;6:3;7:3;8:2;9:3;
FF 1:;2:;3:PDG-ODE-LITTORAL-PHYC;4:;5:;6:;7:;8:PDG-ODE-LITTORAL-PHYC;9:;
C1 Normandie Université, COBRA, UMR 6014 et FR 3038 ; Université de Rouen ; INSA de Rouen ; CNRS, IRCOF, 1 rue Tesnière, 76821 Mont Saint Aignan Cedex, France.
   IFREMER, Laboratoire Phycotoxines, F-44311 Nantes 03, France
   DGA Maîtrise NRBC, département Analyse Chimique, F-91710 Vert Le Petit, France
C2 UNIV ROUEN, FRANCE
   IFREMER, FRANCE
   CDNBC, FRANCE
SI NANTES
SE PDG-ODE-LITTORAL-PHYC
UR https://archimer.ifremer.fr/doc/00179/29039/27475.pdf
LA English
DT Poster
AB Saxitoxin and its analogues also called paralytic shellfish poisons (PSPs) are very potent neurotoxins [1] produced by dinoflagellates and referenced as chemical weapon in the chemical warfare convention (CWC). The official detection methods for these toxins present limitations concerning their speed and reliability [2].  Due to the presence of isomers, not differentiable by mass spectrometry (MS), an upstream separation is necessary. In order to separate saxitoxin analogues, hydrophilic interaction liquid chromatography (HILIC) and ion mobility (IM) were used. Those techniques respectively developed for high polar compounds and three dimensional structure differentiation are particularly well adapted to the separation of PSPs. This HILIC/IM-MS coupling was used to develop a fast, reproducible and sensitive method for the separation and the detection of the PSPs
PY 2013
PD MAY
ID 29039
ER

EF