by Aidan » Tue Jul 25, 2006 4:01 pm
I have been working with a method for a few years now and recently i have been getting a ghost peak appearing in my sample chromatograms.it shows at the same retention time (~17mins) everytime but not in every sample. It doesnt show in my diluent and mobile phase ever, but when it appears it shows up in my placebo blank as well as my samples and standards(rarely). The method is poor but to date has at least been consistent. The method isocratic, with a m.p. of 60:40 Buffer(0.05M K2HPO4): ACN, 210nm, @1.5ml/min, using a kromasil C18 4.6x150mm silica column. The product is an anti-biotic. Lately also we have been using HPMC solutions on these columns for trials and are suspsicious that this might be causing the peaks even though the blanks are clean. we have changed the systems, columns, filters and reagents without consistent success. we have also seen strange results with different filters and on one occasion a sample filtered with a millex 0.45um filter contained the peak on every system and column it was tried on consistently however when the same sample was refiltered with millex no peak appeared...??? we have run a sample on our PDA and the peak is 99.4% pure and shows a very different specrum to the active and its impurities....we are starting to pull our hair out here, so if any one has experienced anything such as this before your insight would be greatly appreciated.
thanks in advance
Aidan