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- Posts: 2
- Joined: Fri Feb 18, 2005 10:51 pm
I am running a reversed phase HPLC procedure for a drug in animal feed using 85% CH3CN:15% 125 mM aqueous acetate buffer as the mobile phase, with a typical C18 column and fluorescence detection. The sample extract is methanol acidified with 0.5% HCl. I note what appear to be significant carrover peaks in blank feeds at a residue testing level. I do not see such peaks when injecting the extractant or the mobile phase. Is this likely to come from the autosampler (Waters WISP 712) or is something happening on the column? I would appreciate advice on how to identify the source and suggestions to eliminate the problem.
Thanks very much,
CF at NDA
