Comparison of Protein A affinity resins for twin-column continuous capture processes: Process performance and resin characteristics

J Chromatogr A. 2021 Sep 27:1654:462454. doi: 10.1016/j.chroma.2021.462454. Epub 2021 Aug 9.

Abstract

Continuous chromatography is a promising technology for downstream processing of biopharmaceuticals. The operation of continuous processes is significantly different to batch-mode chromatography and needs comprehensive evaluation. In this work, the performances of four Protein A affinity resins were studied systematically for twin-column continuous capture processes. A model-based approach was used to evaluate the process performance (productivity and capacity utilization) under varying operation conditions, and the objective was to reveal the crucial resin properties for continuous capture. The trade-off between productivity and capacity utilization was found, and it is necessary to select appropriate resins for different feedstock and operation conditions. The capacity utilization heavily depends on mass transfer, and steep breakthrough curves are favorable for high capacity utilization. The productivity is determined by both equilibrium binding capacity and mass transfer, and the balance of feed amount and feed time is critical. Moreover, the influence of binding capacity and mass transfer on process productivity and parameter sensitivity with two important resin properties (equilibrium binding capacity qmax and effective pore diffusion coefficient De) were assessed by the model, and suitable resin parameter ranges for twin-column continuous capture were determined. The model-based approach is an effective and useful tool to evaluate the complex performance of different resins and guide the design of next-generation resins for continuous processes.

Keywords: Continuous chromatography; Model-based approach; Protein A affinity resin; Resin property; Twin-column continuous capture.

MeSH terms

  • Chromatography, Affinity* / instrumentation
  • Chromatography, Affinity* / standards
  • Models, Chemical
  • Staphylococcal Protein A* / metabolism

Substances

  • Staphylococcal Protein A