4.5 Article

Competitive Adsorption of Monoclonal Antibodies and Nonionic Surfactants at Solid Hydrophobic Surfaces

Journal

JOURNAL OF PHARMACEUTICAL SCIENCES
Volume 104, Issue 2, Pages 593-601

Publisher

WILEY
DOI: 10.1002/jps.24265

Keywords

adsorption; protein formulation; physical stability; surfactants; protein; monoclonal antibodies; QCM-D; TIRF

Funding

  1. Amgros I/S
  2. Drug Research Academy (DRA)

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Two monoclonal antibodies from the IgG subclasses one and two were compared in their adsorption behavior with hydrophobic surfaces upon dilution to 10 mg/mL with 0.9% NaCl. These conditions simulate handling of the compounds at hospital pharmacies and surfaces encountered after preparation, such as infusion bags and i.v. lines. Total internal reflection fluorescence and quartz crystal microbalance with dissipation monitoring were used to follow and quantify this. Furthermore, the influence of the nonionic surfactant polysorbate 80 (PS80) on the adsorption process of these two antibodies was investigated. Despite belonging to two different IgG subclasses, both antibodies displayed comparable adsorption behavior. Both antibodies readily adsorbed in the absence of PS80, whereas adsorption was reduced in the presence of 30 mg/L surfactant. The sequence of exposure of the surfactant and protein to the surface was found to have a major influence on the extent of protein adsorption. Although only a fraction of adsorbed protein could be removed by rinsing with 30 mg/L surfactant solution, adsorption was entirely prevented when surfaces were pre-exposed to PS80. (c) 2014 Wiley Periodicals, Inc. and the American Pharmacists Association J Pharm Sci 104:593-601, 2015

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