Speciation analysis of organoarsenical compounds in biological matrices by coupling ion chromatography to atomic fluorescence spectrometry with on-line photooxidation and hydride generation

Simon, S.; Lobos, G; Pannier, F; De Gregori, I; Pinochet, H.; Potin-Gautier, M

Abstract

The optimisation of an on-line decomposition based on UV photooxidation for the analysis of organoarsenic species by coupling cation-exchange chromatography and atomic fluorescence spectrometry with hydride generation, is described. In this study, special consideration is given to the compatibility of mobile phases with post-column treatments. Results show that the most commonly used mobile phase, aqueous pyridine solutions, decreases species conversion efficiency, leading to a significant loss of sensitivity. New fully-compatible chromatographic conditions are proposed to separate arsenobetaine, arsenocholine, trimethylarsine oxide and tetramethylarsonium ion within 20 min. The very low absolute limits of detection, 4-12 pg(As), allow speciation at trace levels. Analysis of a certified reference fish tissue (DORM-2) and other seafood samples (French and Chilean oysters and mussel) highlights the robustness and the accuracy of the optimised system. © 2004 Elsevier B.V. All rights reserved.

Más información

Título según WOS: Speciation analysis of organoarsenical compounds in biological matrices by coupling ion chromatography to atomic fluorescence spectrometry with on-line photooxidation and hydride generation
Título según SCOPUS: Speciation analysis of organoarsenical compounds in biological matrices by coupling ion chromatography to atomic fluorescence spectrometry with on-line photooxidation and hydride generation
Título de la Revista: ANALYTICA CHIMICA ACTA
Volumen: 521
Número: 1
Editorial: Elsevier
Fecha de publicación: 2004
Página de inicio: 99
Página final: 108
Idioma: English
URL: http://linkinghub.elsevier.com/retrieve/pii/S0003267004006403
DOI:

10.1016/j.aca.2004.05.032

Notas: ISI, SCOPUS