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• W2032476510 abstract "Antibodies are complex macromolecules and their phase behavior as well as interactions within different solvents and precipitants are still not understood. To shed some light into the processes on a molecular dimension, the occurring self-interactions between antibody molecules were analyzed by means of the osmotic second virial coefficient (B22). The determined B22 follows qualitatively the phenomenological Hofmeister series describing the aggregation probability of antibodies for the various solvent compositions. However, a direct correlation between crystallization probability and B22 in form of a crystallization slot does not seem to be feasible for antibodies since the phase behavior is strongly dependent on their anisotropy. Kinetic parameters have to be taken into account due to the molecular size and complexity of the molecules. This is confirmed by a comparison of experimental data with a theoretical phase diagram. On the other hand the solubility is thermodynamically driven and therefore the B22 could be used to establish a universal solubility line for the monoclonal antibody mAb04c and different solvent compositions by using thermodynamic models. © 2015 American Institute of Chemical Engineers Biotechnol. Prog., 31:438–451, 2015" @default.
• W2032476510 created "2016-06-24" @default.
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• W2032476510 date "2015-03-01" @default.
• W2032476510 modified "2023-10-18" @default.
• W2032476510 title "From osmotic second virial coefficient (<i>B</i>₂₂) to phase behavior of a monoclonal antibody" @default.
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• W2032476510 doi "https://doi.org/10.1002/btpr.2065" @default.
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