Author/Authors :
Zhou، نويسنده , , Joe X. and Tressel، نويسنده , , Tim and Gottschalk، نويسنده , , Uwe and Solamo، نويسنده , , Felix and Pastor، نويسنده , , Andre and Dermawan، نويسنده , , Shinta and Hong، نويسنده , , Tony and Reif، نويسنده , , Oscar and Mora، نويسنده , , Jeff and Hutchison، نويسنده , , Fred and Murphy، نويسنده , , Michael، نويسنده ,
Abstract :
Process-scale antibody production requires polishing steps with extremely high product throughput and robust operation. In this communication, the Sartobind Q membrane adsorber for process-scale antibody production is evaluated as an alternative to Q column chromatography. Although the capacity seen with large-scale membrane adsorbers is competitive with column chromatography, the same throughput is not achieved with the current scale-down models. The operational issues currently found in membrane scale-down models, including backpressure, which significantly compromises the membraneʹs capacity, were examined. A new scale-down model was designed to mimic the liquid flow path found in the large-scale capsule, and a new process capacity equivalent at both small and large scale was successfully achieved. Results of a 4-model virus study with a redesigned Sartobind Q absorber scale-down model at the new process capacity are presented.
Keywords :
Membrane chromatography , Monoclonal antibodies , Viral clearance , Product throughput , mAb purification , Q membrane