Impact of Silicone Oil on Free Fatty Acid Particle Formation due to Polysorbate 20 Degradation
Autor: | Raphael Fish, Nidhi Doshi, Jasper C. Lin |
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Rok vydání: | 2020 |
Předmět: |
Drug Compounding
Polysorbates Pharmaceutical Science Myristic acid 02 engineering and technology Myristic Acid 030226 pharmacology & pharmacy Surface-Active Agents 03 medical and health sciences chemistry.chemical_compound 0302 clinical medicine Pulmonary surfactant Silicone Oils Pharmacology (medical) Drug Packaging Pharmacology chemistry.chemical_classification Aqueous solution Chromatography Glass Vial Hydrolysis Syringes Organic Chemistry Fatty acid Hydrogen-Ion Concentration 021001 nanoscience & nanotechnology Silicone oil Partition coefficient Models Chemical Solubility chemistry Molecular Medicine Polysorbate 20 0210 nano-technology Biotechnology |
Zdroj: | Pharmaceutical Research. 37 |
ISSN: | 1573-904X 0724-8741 |
DOI: | 10.1007/s11095-020-02936-3 |
Popis: | Polysorbate 20 (PS20), a commonly used surfactant in biopharmaceutical formulations, can undergo hydrolytic degradation resulting in free fatty acids (FFAs) that precipitate to form particles. This work investigates the ability for silicone oil (si-oil) coated on the interior walls of prefilled syringes (PFSs) to act as a sink for FFAs and potentially delay FFA particle formation. Myristic acid distribution coefficient was measured in a two-phase system containing si-oil and formulation buffer at a range of aqueous conditions. An empirical model was built from these data to predict distribution coefficient based on aqueous conditions. To verify the model, PS20 was degraded using model lipases side-by-side in glass vials and PFSs while monitoring sub-visible particles. The empirical model demonstrates that the partitioning of myristic acid into si-oil is maximized at low pH and low PS20 concentration. The model predicts that the presence of si-oil at levels typical in PFSs provides at most an 8.5% increase in the total carrying capacity for myristic acid compared to a non-coated glass vial. The time to onset of FFA particles was equivalent between degradations performed in two PFS models coated with differing levels of silicone oil and in non-coated glass vials. Herein, we demonstrate that FFAs partition from aqueous solution into si-oil. However, the extent of the partitioning effect is not large enough to delay PS20-related FFA particle formation at typical formulation conditions (pH 5.0–7.5, 0.01% - 0.1% w/v PS20) filled in typical PFSs ( |
Databáze: | OpenAIRE |
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