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- Posts: 3
- Joined: Thu Apr 25, 2019 2:41 pm
I am trying to optimize the detection of heme (hemin) via LC-MS. I have been running C18 with H2O/ACN and 0.1%FA. I detect 616,1766mz on Thermo QE or 616.1->556.9-557.4 on Thermo TSQ.
My main issue is that I have a very broad peak for hemin. Iron free protoporphyrin IX also runs broad, Coproporphyrin and biliverdin are reasonable. Suggestions on how to improve on this?
Furthermore, a strange thing is that on QE I see two peaks for heme (only with lower dilutions of standard, like 0.1µM) but on TSQ just one broad peak. What could those different peaks be? Finally, porphyrins often leach into my blanks.
I welcome your suggestions. Thanks!
Bory
