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Merck

mAbs Downstream

Products for Development and Manufacturing

 

Higher cell densities and antibody titers from increasingly advanced upstream processes result in complex downstream purification challenges. The focus of downstream bioprocessing is efficient recovery and purification while controlling bioburden and assuring viral safety to provide drug safety for patients. The downstream workflow, which includes clarification, chromatography, concentration, viral clearance, and sterile filtration steps, is essential for ensuring monoclonal antibody (mAb) product quality, yield, safety, and sterility. 

Concentration and Diafiltration (UF/DF)

Tangential flow filtration (TFF) including ultrafiltration (UF) and diafiltration (DF) are used throughout monoclonal antibody (mAb) production, to remove process chemicals, exchange buffers, reduce volumes and concentrate drug substance. These steps improve yields and enable formulation at the high concentrations necessary for subcutaneous administration of drug product.

Key considerations for any TFF operation include maximizing the capacity of filtration device and molecule recovery. Additionally, with higher molecule concentrations, strategies for managing increased aggregation and viscosity must be implemented.

Single-pass tangential flow filtration (SPTFF) is increasingly being implemented in intensified and continuous processes to reduce in-process volumes either before or after column chromatography, or before formulation.

To help you overcome your UF/DF challenges, we provide the following solutions:

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