Ocular and Nasal Drug Delivery
Start with the big picture
This topic introduces formulation strategies for improving ocular and nasal drug delivery. For ocular products, it explains how tear turnover, the corneal barrier, and drainage limit bioavailability, then surveys approaches to extend precorneal residence or support targeted delivery. These include in-situ gels, mucoadhesive polymers, particulate carriers, and controlled-release implants, alongside key formulation considerations such as sterility, pH, isotonicity, and absorption-enhancing excipients. The nasal section covers systemic and nose-to-brain delivery, particle-size considerations, dosage forms, formulation specifications, and absorption enhancers. It also examines nasal barriers—including mucociliary clearance and enzymatic degradation—and how targeted carriers may use olfactory pathways for central nervous system delivery.
What you'll learn
- Explain how tear turnover, corneal structure, and nasolacrimal drainage limit ocular bioavailability.
- Identify formulation strategies that extend ocular residence or support targeted delivery.
- Describe nasal delivery’s systemic and nose-to-brain pathways and their formulation implications.
- Recognize nasal absorption barriers and approaches used to address them.
Continue your study
Work through the complete notes and reinforce the topic with the study tools available in the full lesson.