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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. 

Prefiltration & Bioburden Control

Particulate and bioburden contaminants can cause premature fouling of aseptic filters and interfere with downstream purification. Prefilters remove particulate impurities such as colloids, aggregated and non-product proteins, lipids, and cellular debris. They also provide a cost-effective option for improving process efficiency by extending the capacity of costly sterilizing filters and reducing the impact of particulate contaminants in chromatographic separation.

Bioburden reduction filters remove particulate impurities and different types of bioburden. Downstream operations operate as “low bioburden” or “bioburden-controlled,” where bioburden is present but controlled and routinely monitored. Bioburden control strategies include assessing bioburden, mitigating the risk of occurrence, and monitoring to assure process control.

Our integrated offering of prefilters and bioburden reduction filters includes:

  • Millipore® Filters  
  • Millipore® Integrity Testers
  • Millipore® Equipment and Systems (housings)
  • Millipore® Sterile Sampling
  • Millipore® Services (single-use and filter validation, equipment installation, system qualification, system training, system services)
  • Millipore® Automation and Analytics Software
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