The Impact of the Metal Interface on the Stability and Quality of a Therapeutic Fusion Protein

• Published in: Molecular pharmaceutics 2020-02, Vol.17 (2), p.569-578, Article acs.molpharmaceut.9b01000
• Main Authors: Defante, Adrian P, Kalonia, Cavan K, Keegan, Emma, Bishop, Steven M, Satish, Hasige A, Hudson, Steven D, Santacroce, Paul V
• Format: Article
• Language: English
• Subjects: Adsorption; Aluminum Oxide - chemistry; Antibodies, Monoclonal, Humanized - chemistry; Antibodies, Monoclonal, Humanized - genetics; Ceramics - chemistry; Drug Compounding - methods; Drug Stability; Immunoglobulin Fc Fragments - chemistry; Immunoglobulin Fc Fragments - genetics; Immunoglobulin G - chemistry; Immunoglobulin G - genetics; Protein Aggregates; Quartz Crystal Microbalance Techniques; Stainless Steel - chemistry; Surface Properties; Tumor Necrosis Factor-alpha - chemistry; Tumor Necrosis Factor-alpha - genetics
• ISSN: 1543-8384; 1543-8392
• DOI: 10.1021/acs.molpharmaceut.9b01000

Subvisible particle formation, which occurs after the sterile filtration step of the fill/finish process, is a challenge that may occur during the development of biotherapeutics with complex molecular structures. Here, we show that a stainless steel pump head from a rotary piston pump produces more protein aggregates, past the limit of the acceptable quality range for subvisible particle counts, in comparison to a ceramic pump head. The quartz crystal microbalance was used to quantify the primary layer, proteins irreversibly adsorbed at the solid–liquid interface, and the secondary diffuse gel-like layer interacting on top of the primary layer. The results showed that the mass of protein irreversibly adsorbed onto stainless steel sensors is greater than on an aluminum oxide surface (ceramic pump mimic). This suggests that the amount of adsorbed protein plays a role in surface-induced protein aggregation at the solid–liquid interface.