Comparability in both product quality and chromatographic process characteristics between a Protein A affinity capture membrane and a packed-bed resin reference was demonstrated using a set of proposed criteria. Product quality attributes and process impurities from a purified IgG1 monoclonal antibody cell culture harvest were comparable between Protein A resin and membrane affinity stationary phases, with the membrane demonstrating order-of-magnitude higher chromatographic productivity.

During the manufacturing process, therapeutic antibodies are exposed to a range of hydrodynamic forces and material contact surfaces that can potentially impact protein stability and propensity for aggregation. These forces can vary as fluid flow rates and component design elements scale alongside batch size.

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