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Updated: Oct 10, 2025

Safety Precautions and Operating Procedures in an ABSL-4 Laboratory: 2. General Practices
Published on: October 3, 2016
Proceedings of the 2019 Viral Clearance Symposium, Session 5: Viral Inactivation
1Genomic Medicine Purification Process Development, Sanofi Inc, 153 2 Avenue, Waltham, MA 02451 junfen.ma@sanofi.com.
Abstract:
Viral inactivation has been demonstrated to be an effective viral clearance step in the biologics purification processes. In the 2019 Viral Clearance Symposium, the topics were focused on alternative eco-friendly and cost-effective detergents, validation of on-column viral inactivation, and further understanding of low pH and solvent/detergent viral inactivation. Sugar-based surfactants and a synthetized replacement of Triton X-100 were evaluated to be effective and robust in inactivating enveloped viruses. For low pH viral inactivation, consistent pH measurement, through alignment of pH meters and probes across different labs and manufacturing facilities, was confirmed to be critical to ensure both product quality and safety. For the well-established solvent/detergent inactivation, an approach of adding premixed solvent/detergent stock significantly improved operation. Different viral clearance approaches were discussed for on-column viral inactivation using a detergent-containing wash buffer.
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