Abstract
Therapeutic monoclonal antibodies (mAbs) are rapidly taking over the treatment of many malignancies, and an astonishing number of mAbs is in development. This causes a high demand for quantification of mAbs in biomatrices both for measuring therapeutic mAb concentrations and to support pharmacokinetics and pharmacodynamics studies. Conventionally, ligand-binding assays are used for these purposes, but LC-MS is gaining popularity. Although intact (top-down) and subunit (middle-down) mAb quantification is reported, signature peptide (bottom-up) quantification is currently most advantageous. This review provides an overview of the reported bottom-up mAb quantification methods in biomatrices as well as general recommendations regarding signature peptide and internal standard selection, reagent use and optimization of digestion in bottom-up quantification methods.
Original language | English |
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Pages (from-to) | 1405-1425 |
Number of pages | 21 |
Journal | Bioanalysis |
Volume | 12 |
Issue number | 19 |
DOIs | |
Publication status | Published - Oct 2020 |
Externally published | Yes |
Keywords
- bottom-up
- mass spectrometry
- monoclonal antibodies
- oncology
- sample preparation
- signature peptide