Dear Karthikeyan, I think that the ideal analytical technique would be a chromatographic method. Particularly with mass spectrometry, or in the absence of that possibility, fluorescence detection has been applied successfully on multiple occasions to determine the mycotoxins of interest.
As a clean-up and extraction method, the use of specific immunoaffinity columns for AFs, OTA and ZON would be ideal; although QueChers and SPE are also options.
I share some titles of papers that may be useful.
1. Validation of the procedure for the simultaneous determination of aflatoxins ochratoxin A and zearalenone in cereals using HPLC-FLD A.
Jose Troestch Thanks, sir it is useful information, and we know about lit bit toxin extraction and quantified the toxin level in different raw materials and feed, we did TLC and HPLC analysis. but I need how long it's sustainable to use multi-toxin std. toxin std self-life.
Ok, sorry for my confusion. For the verification that you mention, the "molar absorption coefficient" is used. You can find this procedure in an AOAC manual and this article can also be useful.