Experimental Evaluation of the Impact of Intrinsic Process Parameters on the Performance of a Continuous Chromatographic Polishing Unit (MCSGP)

Biotechnol J. 2019 Jul;14(7):e1800732. doi: 10.1002/biot.201800732. Epub 2019 May 2.

Abstract

The semicontinuous twin-column multicolumn countercurrent solvent gradient purification (MCSGP) process improves the trade-off between purity and yield encountered in traditional batch chromatography, while its complexity, in terms of hardware requirements and process design, is reduced in comparison to process variants using more columns. In this study, the MCSGP process is experimentally characterized, specifically with respect to its unique degrees of freedom, i.e., the four switching times, which alternate the columns between interconnected and batch states. By means of isolation of the main charge isoform of an antibody, it is shown that purity is determined by the selection of the product collection window with negligible influence from the recycle phases. In addition, the amount of weak and strong impurities can be specifically attributed to the start and end of the collection, respectively. Due to higher abundance of weakly adsorbing impurities, the start of product collection influences productivity and yield more than the other switching times. Furthermore, most of the encountered tendencies scale between different loadings. The found trends can be rationalized from the corresponding batch chromatogram and therefore used during process design to obtain desirable process performances without extensive trial-and-error experimentation or complete model development and calibration.

Keywords: MCSGP; charge isoforms; continuous chromatography; downstream processing; monoclonal antibody.

MeSH terms

  • Animals
  • Antibodies, Monoclonal / isolation & purification
  • Batch Cell Culture Techniques
  • Biotechnology
  • CHO Cells
  • Countercurrent Distribution / methods*
  • Cricetinae
  • Cricetulus
  • Protein Isoforms
  • Recombinant Proteins / isolation & purification*

Substances

  • Antibodies, Monoclonal
  • Protein Isoforms
  • Recombinant Proteins