From: Nanotechnology-based ocular drug delivery systems: recent advances and future prospects
Delivery routes | Advantages | Disadvantages | Diseases Treated |
---|---|---|---|
Topical | High patient compliance, self-administration, noninvasive nature | Corneal barrier, dilution and efflux, low bioavailability, high dosing | Conjunctivitis, keratitis, uveitis, episcleritis, scleritis, blepharitis |
Subconjunctival and transscleral administration | Anterior and posterior drug delivery, ideal for depot formation | Choroidal and conjunctival circulation increase toxicity subconjunctival hemorrhage | Glaucoma, AMD cytomegalovirus retinitis, |
Intracameral administration | Reduce corneal and systemic side effects. topical steroid use; high anterior chamber drug concentration | Toxic endothelial cell destruction syndrome and toxic anterior segment syndrome | Anesthesia, inflammation, endophthalmitis, pupil dilation |
Intravitreal injection | Direct delivery to the vitreous humor and retina, BRB avoidance, high bioavailability and acute dosing | Poor patient compliance, invasiveness, drug toxicity, retinal detachment, cataract endophthalmitis, hemorrhage | AMD, central/branched retinal vein occlusion, diabetic macular edema, cytomegalovirus retinitis |
Retrobulbar injection | Selective delivery to both anterior and posterior segments, avoidance of corneal and conjunctival barriers, long duration of action, a site for depot formulations | Poor patient compliance, invasiveness, drug deposition,compliances including pain, bleeding, infection, scarring, eyeball or optic nerve damage | Anesthesia |
Systemic administration | High patient compliance | Blood ocular barriers, low bioavailability, systemic toxicity caused by high dosing | Scleritis, episcleritis, cytomegalovirus retinitis |