Drug Targets and its Delivery in Glaucoma
-Current Trend and Future Prospects
Volume 1 - Issue 1
Rahul Rama Hegde*
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- Department of Pharmacy, Lupin Pharmaceuticals LIMITED, India
*Corresponding author:
Rahul Rama Hegde, Department of Pharmacy, Validation, Lupin Ltd, Verna Industrial Area, Verna, Goa, India
Received: January 16, 2018; Published: January 29, 2018
DOI: 10.32474/TOOAJ.2018.01.000102
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Abstract
Topical route of drug delivery always remained a route of
choice for delivering all glaucoma [1] medications rather than
systemic route. Upon topical instillation drug reaches interior
tissues of eye mainly through corneal route and route and
therefore epithelial and stromal layer of the cornea act as barrier
to transcorneal permeability of both hydrophilic and lipophilic
drugs respectively. Transcellular and Para cellular pathways are the
two major corneal transportation routes for the topically applied
drugs. Lipophillic drugs cross the cornea through transcellular
pathway while the hydrophilic drugs cross through para cellular
pathway. For treatment of glaucoma effective drugs are present
mainly beta blockers, cholinergic agonists, carbonic anhydrase
inhibitors, adrenergic agonists and prostaglandin derivatives but
lack effective delivery system to improve patient care and clinical
outcomes. Currently available drugs for ocular conditions need
to be administered two or more i.e. multiple times a day, as well
the poor patient adherence makes the treatment less clinically
effective. Studies suggest that <1% of topically administered drug
reaches aqueous humor. Up to 80% of systemic absorption of drug
occurs followed by topical administration of eye drop causing
systemic side effects.
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