Assessing detergent-mediated virus inactivation, protein stability, and impurity clearance in biologics downstream processes.

Autor: Feroz H; Biologics Process Development, Global Product Development and Supply, Bristol Myers Squibb, Co., Devens, Massachusetts, USA., Chennamsetty N; Analytical Development and Attribute Sciences, Biologics Development, Bristol Myers Squibb Company, New Brunswick, New Jersey, USA., Byers S; Analytical Development and Attribute Sciences, Biologics Development, Bristol Myers Squibb Co., Devens, Massachusetts, USA., Holstein M; Biologics Process Development, Global Product Development and Supply, Bristol Myers Squibb, Co., Devens, Massachusetts, USA., Li ZJ; Biologics Process Development, Global Product Development and Supply, Bristol Myers Squibb, Co., Devens, Massachusetts, USA., Ghose S; Biologics Process Development, Global Product Development and Supply, Bristol Myers Squibb, Co., Devens, Massachusetts, USA.
Jazyk: angličtina
Zdroj: Biotechnology and bioengineering [Biotechnol Bioeng] 2022 Apr; Vol. 119 (4), pp. 1091-1104. Date of Electronic Publication: 2022 Feb 08.
DOI: 10.1002/bit.28034
Abstrakt: Detergent-mediated virus inactivation (VI) provides a valuable orthogonal strategy for viral clearance in mammalian processes, in particular for next-generation continuous manufacturing. Furthermore, there exists an industry-wide need to replace the conventionally employed detergent Triton X-100 with eco-friendly alternatives. However, given Triton X-100 has been the gold standard for VI due its minimal impact on protein stability and high inactivation efficacy, inactivation by other eco-friendly detergents and its impact on protein stability is not well understood. In this study, the sugar-based detergent commonly used in membrane protein purification, n-dodecyl-β- d-maltoside was found to be a promising alternative for VI. We investigated a panel of detergents to compare the relative VI efficacy, impact on therapeutic quality attributes, and clearance of the VI agent and other impurities through subsequent chromatographic steps. Detergent-mediated inactivation and protein stability showed comparable trends to low pH inactivation. Using experimental and modeling data, we found detergent-mediated product aggregation and its kinetics to be driven by extrinsic factors such as detergent and protein concentration. Detergent-mediated aggregation was also impacted by an initial aggregation level as well as intrinsic factors such as the protein sequence and detergent hydrophobicity, and critical micelle concentration. Knowledge gained here on factors driving product stability and VI provides valuable insight to design, standardize, and optimize conditions (concentration and duration of inactivation) for screening of detergent-mediated VI.
(© 2022 Wiley Periodicals LLC.)
Databáze: MEDLINE
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