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- Posts: 1
- Joined: Mon Oct 09, 2017 2:36 pm
I'm woirking on an alkaline hydrolysis method for tryptophan. I take a powder with protein and expose it to NaOH 5N and cook in an oven overnight. Then I neutralize with 12 N HCL, centrifuge, filter and finally dilute.
My moblie phase is 50 mM phosphate buffer pH around 2.58 with small amount of TEA. An Agilent application chemist had me add KCl to adjust the ionic strength.
Peak shape: excellent
Peak Area Reproducibility: excellent
But tryptophan RT moves around so much. Is this a complicated interaction or chemistry
I did accidentally use the eluant described above to make serial dilutions of my standards....and I noticed it really helped but I'm concerned that if a use it with the unknowns the pH might destroy the tryptophan because the pH is pretty low.
I started getting very good recoveries when I made sure not to expose tryptophan to pHs below 7-ish. Oh, and when things got really wacky and I noticed that changing the guard helped bring on all fronts, but RT does still move around. The ghost peaks and system peaks seems to have consistent RTs but not tryptophan. My window can be 4.3 min to 5.3 min.
Thoughts anyone?