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 - Posts: 11
 - Joined: Fri Sep 21, 2007 9:58 am
 
the detection of one mycotxoin patulin with our HPLC column Purospher (250-4, RP-18e, 5 µm) at isogratic flow give the best seperation (with 95% water as mobile phase, RT at 12 min), but we need to run each sample 90 min to recondition the column, thus no peak shift happend. Are there some methods to fulfil the reconditioning and to reduce the time at the same time. Is a gradient elution maybe better? thanks!
Best regards,
Zhen
