PhD Student Queen's University Belfast Belfast, Northern Ireland, United Kingdom
Introduction: Inflammatory eye disease is a complex condition that accounts for 15% of preventable blindness1. The first line of treatment for this disease are topical corticosteroids, which are highly hydrophobic substances. In addition, static and dynamic physiological barriers in the eye impede drug absorption resulting in only 5% bioavailability of conventional dosage forms like eyedrops or ointments2. This project aims to provide solutions by developing optimized nanocrystals (NCs) formulation of Triamcinolone acetonide and Prednisolone using a Design of Experiments (DoE) approach to increase dissolution rate and saturation solubility and providing a predictive model to control particle size.
Learning Objectives:
See nanocrystals as an elegant technology to increase dissolution rate of hydrophobic drugs.
understand that predictive models in NCs formulation identify critical quality attributes for production