Improved assay sensitivity for LC–MS bioanalysis of proteins using new SPE workflow.
Employed post-pellet-digestion precipitation to overcome sample clogging during SPE.
Validated an LC–MS/MS assay for a monoclonal antibody in serum with LLOQ at 50 ng/mL.
The method was 100-fold more sensitive than a previously reported method without SPE.
This SPE methodology is applicable to LC–MS/MS bioanalysis of other proteins.