A moving-boundary model of dissolution from binary drug-excipient granules incorporating microstructure
نویسندگان
چکیده
• Mathematical model for dissolution of a polydisperse collection binary granules. Full accounts radial variation in drug and porosity distributions. Reduced when initial concentration greatly exceeds solubility. Model single granule size validated against experimental data. Accurate mechanistic vitro models can deliver insight into release behaviour guide formulation development. Drug profiles from drug-excipient granules be impacted by load within granules, which may arise inherent variability granulation processes. Here, we analyse validate recent spherical with matrix insoluble excipient, incorporating load. The is presented specialised to the case where large compared capacity granule’s pores at In this limit, reduces ordinary differential equation describing depletion shrinking, drug-saturated core. validation performed using data literature system consisting acetaminophen microcrystalline cellulose. A new extended describe derived. performance particle equivalent diameters. developed provides tool explore parameter space these systems considering impact arising manufacturing
منابع مشابه
soluplus®; a novel excipient to improve dissolution rate of poorly water soluble drug, celecoxib
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ژورنال
عنوان ژورنال: International Journal of Pharmaceutics
سال: 2021
ISSN: ['0378-5173', '1873-3476']
DOI: https://doi.org/10.1016/j.ijpharm.2021.120219