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Polymeric Drug Delivery Devices: Role in Cornea and External Disease
Aravind Roy1, Venkata V Krishna Venuganti, Shreya S Chauhan
1The Cornea Institute (A.R.), KVC Campus, L. V. Prasad Eye Institute, Vijayawada, India; Birla Institute of Technology and Science (BITS) Pilani (V.V.K.V., S.S.C.), Hyderabad Campus, Hyderabad, India; and The Cornea Institute (P.G.), KAR Campus, L. V. Prasad Eye Institute, Hyderabad, India.
Abstract:
The field of ophthalmic drug delivery is undergoing rapid changes not only in the evolution of pharmacologic agents but also in the novel drug delivery vehicles. The ocular surface has limitations to drug penetration because of the presence of tight junctions between basal epithelial cells, which limits the amount of drug that can be absorbed after topical instillation. In addition, nasolacrimal drainage reduces the precorneal residence time significantly. Contact lenses (CLs) have been considered as possible carriers for topical medications because they reside on the ocular surface for a sufficient length of time, and pharmacologic agents may be copolymerized with hydrogels allowing controlled drug diffusion. This strategy reduces the frequency of dosage while improving compliance. Modification of drug delivery vehicles is essential to allow sustained release of the drug from a polymeric complex, facilitate stability and residence time of the drug on the precorneal tear film, and improve penetration into biologic membranes. This review focuses on updates in CL-based and non-CL-based strategies in ophthalmic drug delivery.
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