The NISTmAb is a monoclonal antibody Reference Material from the National Institute of Standards and Technology; it is a class-representative IgG1κ intended to serve as a pre-competitive platform for harmonization and technology development in the biopharmaceutical industry. The publication series of which this paper is a part describes NIST’s overall control strategy to ensure NISTmAb quality and availability over its lifecycle. In this paper, the development of a control strategy for monitoring NISTmAb size heterogeneity is described. Optimization and qualification of size heterogeneity measurement spanning a broad size range are described, including capillary electrophoresis-sodium dodecyl sulfate (CE-SDS), size exclusion chromatography (SEC), dynamic light scattering (DLS), and flow imaging analysis. This paper is intended to provide relevant details of NIST’s size heterogeneity control strategy to facilitate implementation of the NISTmAb as a test molecule in the end user’s laboratory. [Figure not available: see fulltext.].
CITATION STYLE
Turner, A., Yandrofski, K., Telikepalli, S., King, J., Heckert, A., Filliben, J., … Schiel, J. E. (2018). Development of orthogonal NISTmAb size heterogeneity control methods. Analytical and Bioanalytical Chemistry, 410(8), 2095–2110. https://doi.org/10.1007/s00216-017-0819-3
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