I am working on puffers and I have to prove the presence of Tetrodotoxin in them through GC-MS. I processed my fish extract with a standard procedure, and in that I have to evaporate the final volume of the processed extract to dryness and derivatize the residue with derivatizing agent. I evaporated through lyophilizing and direct bunsen flame methods, but the residue I obtained is insoluble in the derivatizing agent called MSTFA. The residue remains separate from MSTFA even after vortexing and boiling. Can anyone suggest me a solution to sort out this issue?