Contrasting the Influence of Cationic Amino Acids on the Viscosity and Stability of a Highly Concentrated Monoclonal Antibody

• Published in: Pharmaceutical research 2017, Vol.34 (1), p.193-207
• Main Authors: Dear, Barton J., Hung, Jessica J., Truskett, Thomas M., Johnston, Keith P.
• Format: Article
• Language: English
• Subjects: Amino acids; Amino Acids - chemistry; Antibodies, Monoclonal - chemistry; Biochemistry; Biomedical and Life Sciences; Biomedical Engineering and Bioengineering; Biomedicine; Cations - chemistry; Diffusion; Histidine; Hydrogen-Ion Concentration; Hydrophobic and Hydrophilic Interactions; Immunoglobulin G - chemistry; Medical Law; Monoclonal antibodies; Osmolar Concentration; Pharmacology; Pharmacology/Toxicology; Pharmacy; Protein binding; Protein Interaction Domains and Motifs; Protein Stability; Protein-protein interactions; Proteins; Research Paper; Rheology; Solutions - chemistry; Viscosity
• ISSN: 0724-8741; 1573-904X
• DOI: 10.1007/s11095-016-2055-5

Purpose To explain the effects of cationic amino acids and other co-solutes on the viscosity, stability and protein-protein interactions (PPI) of highly concentrated (≥200 mg/ml) monoclonal antibody (mAb) solutions to advance subcutaneous injection. Methods The viscosities of ≥200 mg/ml mAb1 solutions with various co-solutes and pH were measured by capillary rheometry in some cases up to 70,000 s −1 . The viscosities are analyzed in terms of dilute PPI characterized by diffusion interaction parameters ( k D ) from dynamic light scattering (DLS). MAb stability was measured by turbidity and size exclusion chromatography (SEC) after 4 weeks of 40°C storage. Results Viscosity reductions were achieved by reducing the pH, or adding histidine, arginine, imidazole or camphorsulfonic acid, each of which contains a hydrophobic moiety. The addition of inorganic electrolytes or neutral osmolytes only weakly affected viscosity. Systems with reduced viscosities also tended to be Newtonian, while more viscous systems were shear thinning. Conclusions Viscosity reduction down to 20 cP at 220 mg/ml mAb1 was achieved with co-solutes that are both charged and contain a hydrophobic interaction domain for sufficient binding to the protein surface. These reductions are related to the DLS diffusion interaction parameter, k D , only after normalization to remove the effect of charge screening. Shear rate profiles demonstrate that select co-solutes reduce protein network formation.