A new method for the analysis of aflatoxins in food extracts, based on
liquid chromatography/mass spectrometry interfacing, is presented. Th
e chromatographic separation was performed with a reversed phase packe
d capillary column coupled with a modified particle beam interface cap
able of handling microliter per minute flow rates. This system allows
higher overall sensitivity and easier operation procedures. The method
has proved to be particularly suitable for the analysis of the toxins
in very complex matrices. The specificity of electron impact ionizati
on allowed positive identification of the aflatoxins with an excellent
response linearity for accurate quantitation.