期刊
ELECTROPHORESIS
卷 -, 期 -, 页码 -出版社
WILEY
DOI: 10.1002/elps.202200208
关键词
capillary electrophoresis; charge variants; high-throughput; monoclonal antibodies; sequential injections
The complexity of biotherapeutic products requires monitoring and characterization of numerous product quality attributes. Capillary electrophoresis (CE) has been used in biopharmaceutical analysis but is considered low-throughput. In this study, the dead time of CE was utilized to analyze three monoclonal antibody samples, resulting in a significant reduction in analysis time and increased productivity without compromising resolution. Good method reproducibility was observed, suggesting that sequential injections can be applied for fast and robust CE analysis of biopharmaceuticals.
The complexity of biotherapeutic products implies an ever-increasing list of product quality attributes that need to be monitored and characterized. In addition, the growing interest in implementing process analytical technology in biopharmaceutical production has further increased the testing burden, together with the need for rapid testing that can facilitate real-time or near-real-time decision-making. Capillary electrophoresis (CE) has made a place in biopharmaceutical analysis but is regarded as a low-throughput method, with the instrument dead time constituting more than 80% of the total time of analysis. In this study, the dead time of CE was utilized to analyse 3 mAb samples in a single-CE run. This approach resulted in an up to 77% reduction in the total analysis time and increased the productivity by up to 300%, compared to traditional single CE-ultraviolet runs, without compromising resolution or relative peak areas. Additionally, good method reproducibility was observed. The compatibility of the method has been demonstrated with protein A eluate and cation exchange chromatography fractions. We, thus, propose that sequential injections can be applied for fast and robust CE analysis of biopharmaceuticals.
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