Reconstitution of Highly Concentrated Lyophilized Proteins: Part 1 Amorphous Formulations

• Published in: Journal of pharmaceutical sciences 2020-05, Vol.109 (5), p.1681-1691
• Main Authors: Sane, Pooja, Bogner, Robin H., Bhatnagar, Bakul, Tchessalov, Serguei
• Format: Article
• Language: English
• Subjects: contact angle; dissolution; high concentration; hydration; lyophilization; protein(s); wetting
• ISSN: 0022-3549; 1520-6017
• DOI: 10.1016/j.xphs.2020.02.006

Long reconstitution times before patient administration remain an undesirable quality attribute for high concentration lyophilized protein formulations. In this study, 3 approaches were developed to study reconstitution behavior of lyophilized, amorphous cakes of a highly concentrated monoclonal antibody (mAb) by exploring their wetting, disintegration, and hydration behavior. As the mAb concentration increased from 0 to 83 mg/mL, reconstitution times were longer with poorer wetting, slower hydration, and disintegration rates. Furthermore, the effect of controlling ice nucleation temperature at −5 and −10°C during freezing followed by either conservative or aggressive drying conditions on the reconstitution times was explored in formulations containing 40 and 83 mg/mL mAb. Although no effect of either of the 2 processing conditions was noted at 40 mg/mL, aggressive drying led to faster reconstitution at both the nucleation temperatures with 83 mg/mL mAb. The present study combined with literature data suggests that below a protein-to-sugar ratio of 1, reconstitution was complete within 1 min, and when the ratio was greater than 1, the reconstitution times increased nonlinearly. Disintegration and hydration were determined to be the key mechanisms contributing to the complete reconstitution of the lyophilized, amorphous cakes of the highly concentrated mAb in vials.