Effects of Product Handling Parameters on Particle Levels in a Commercial Factor VIII Product: Impacts and Mitigation

• Published in: Journal of pharmaceutical sciences 2019-01, Vol.108 (1), p.775-786
• Main Authors: Ueda, Tsutomu, Nakamura, Koji, Abe, Yoshihiko, Carpenter, John F.
• Format: Article
• Language: English
• Subjects: Factor VIII - chemistry; freeze-drying; immunogenicity; lyophilization; microparticles; nanoparticles; Particle Size; protein aggregation; Silicone Oils - chemistry; Silicones - chemistry; Syringes
• ISSN: 0022-3549; 1520-6017
• DOI: 10.1016/j.xphs.2018.08.022

To reduce the risk of immunogenicity that may be caused by therapeutic protein products, it is important to properly characterize subvisible particles and to develop strategies to reduce the levels of particles delivered to patients. In the present study, by using state-of-the-art methods to quantify particle levels, we found that the factor VIII product, Kogenate FS, contained relatively high levels of protein particles and silicone oil droplets, the vast majority of which were submicron in size. In a test of effects of product mishandling, the Kogenate FS vial was shaken instead of swirled during reconstitution. Levels of silicone oil droplets and protein particles were increased. In contrast, these levels were greatly reduced by 2 mitigation strategies tested, using a nonsiliconized syringe for the diluent container or using submicron pore size syringe filters during simulated infusion. Thus, to avoid potential adverse effects due to mishandling-induced increases in particle levels, it is important to educate end-users about proper product handling. Furthermore, effective particle mitigation and reduction strategies should be developed for factor VIII, and other therapeutic protein products. Such efforts could lead to clinically useful approaches to reduce the levels of particles delivered to patients and to an associated reduction in adverse immunogenicity.