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Recent Developments in Ocular Nanotherapy: An Editorial

Raj Bawa, Gerald F. Audette, Brian Reese

2016

Abstract

Glaucoma is the second most leading cause of blindness [6]. It is a progressive optic neuropathy and has been commonly associated with elevated intraocular pressure (IOP) [7]. The conventional drug delivery system for treatment of glaucoma comprises of ocular drops and has been linked with numerous disadvantages such as natural anatomical barrier (low residence time), poor patient compliance, and local and systemic side effects [8]. Several sustained release drug delivery systems for anti-glaucoma drugs have been proposed that include intraocular implants [9], ophthalmic inserts [10], nano-and microparticles [11], liposomes [12], nanoemulsions [13], and contact lenses [14]. However, due to potential benefits of nanoparticles (NPs) over other delivery systems, further research is focused on finding new drugs and developing better nanoformulations. One such study introduced latanoprost (an ester prodrug of prostaglandin F2a with an efficiency to lower the IOP). Latanoprost acid (LA) is the pharmacologically active component of latanoprost. LA was entrapped in biocompatible and biodegradable nanoparticles formed using polylactide-poly(ethylene glycol) (PLA-PEG) copolymers. The in vivo studies revealed that LA-loaded NPs proved to be a promising system for curing glaucoma without inducing any side effects [15].Topical drug delivery is considered as the easiest method for ophthalmic drug delivery and has gained patient compliance over time. Once a drug is topically applied, due…

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