Abstract
In recent years, monoclonal antibodies (mAb) have become one of the most important classes of therapeutic proteins. Among many of the quality attributes monitored and controlled throughout therapeutic antibody development, particulate matter is one of the critical quality attributes (CQAs) for drug products. Visible and subvisible particulates in drug products may pose safety and immunogenicity risks to patients and therefore are tightly controlled and regulated. Characterization of the particle composition in drug products is essential to understand the origin of particulates and their mechanism of formation. In this study, we developed a liquid chromatography-mass spectrometry (LC-MS) based method and integrated it into the typical particulate characterization workflow to identify and quantify the composition of proteinaceous particles isolated from a therapeutic mAb drug product. The LC-MS workflow provides a useful tool to study particle formation and monitor the protein composition of particulates during therapeutic mAb development.
| Original language | English |
|---|---|
| Pages (from-to) | 3403-3409 |
| Number of pages | 7 |
| Journal | Journal of Pharmaceutical Sciences |
| Volume | 110 |
| Issue number | 10 |
| DOIs | |
| State | Published - Oct 2021 |
| Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2021 The Authors
Keywords
- LC-MS
- Mass spectrometry
- Monoclonal antibody
- Particle characterization
ASJC Scopus subject areas
- Pharmaceutical Science