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- Posts: 5
- Joined: Wed Nov 24, 2010 8:24 pm
I have tried several things. I measured the flow rate from each line and verified that the pump and proportioning valve are delivering an accurate and consistant flow. I have tried premixing the mobile phases and running the method isocratically through one of the solvent lines. I have tried running the gradient though the other two solvent lines I typically don't use (lines C and D instead of A and B). I have measured the pH of the mobile phase to confirm that it is still 4.5. In fact, I have also tried running the method on two other preparations of the buffer. I have replaced the syringe purge and needle wash solvents. Nothing has helped. I even tried replacing the column and that hasn't helped either.
To add to the level of confusion, this instrument is used to run two other compound assays and the chromatography of those assays have not been impacted.
As I mentioned earlier, I am seeing fronting peaks. Well, because this is an LC/MS/MS method, the MS detector is in MRM mode. The internal standard is a deuterated form of methlymalonic acid (D3-MMA). We are looking at 3 transitions: 116.8>72.8 (Daugter of MMA), 116.8>116.8 (Parent of MMA), and 119.8>75.8 (Daughter of D3-MMA). The peak fronting seems to only be affecting the peaks from the two MMA transitions. The D3-MMA transition appears to have a symmetrical peak shape.
At this point, I can not tell if this is an application issue or an instrument issue, since the method has been working very consistantly up till the PM. Does anyone have experience with this column or have any ideas of what might be causing these problems??