The concentrations of arsenobetaine (AB), tetramethylarsonium ion (TMA(+)),
and trimethylarsine oxide (TMAO) were determined in samples of sole, dory,
hake, and sardine, raw and after being subjected to cooking processes-baki
ng, frying, and grilling-at various temperatures. In all cases, the tempera
ture attained inside the product during the cooking process was measured. T
he arsenic species extracted from the samples with methanol/water were sepa
rated by means of a column switching technique between a PRP-X100 column an
d a PRP-X200 column. AE was detected by hydride generation atomic absorptio
n spectrometry, whereas TMA+ and TMAO were detected by hydride generation a
tomic fluorescence spectrometry. The results obtained showed that, in all o
f the types of seafood studied; TMA(+) appeared after cooking, possibly bec
ause heating facilitates decarboxylation of AB to TMA(+).