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pubmed-article:12113795pubmed:abstractTextThe cornea is a major pathway for drug delivery to diseased eye structures. We have investigated the application of 1-s bursts of 20-kHz ultrasound, at I(SAPA) of 14 W/cm(2) (I(SATA) of 2 W/cm(2)), for enhancement of corneal permeability to glaucoma drugs of different lipophilicity (atenolol, carteolol, timolol and betaxolol). The permeability of rabbit cornea increased by 2.6 times for atenolol, 2.8 for carteolol, 1.9 for timolol and 4.4 times for betaxolol (all p-values < 0.05), after 60 min of ultrasound (US) exposure in vitro. The differences between the treatment and control experiments were statistically significant after 10 to 30 min of US exposure for all four drugs. US application appeared to produce epithelial disorganization and structural changes in the corneal stroma. Further studies are needed to determine the optimal US parameters for a safe and effective treatment.lld:pubmed
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pubmed-article:12113795pubmed:authorpubmed-author:MartinRoy WRWlld:pubmed
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pubmed-article:12113795pubmed:authorpubmed-author:ClarkJohn IJIlld:pubmed
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pubmed-article:12113795pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:12113795pubmed:articleTitleOcular drug delivery using 20-kHz ultrasound.lld:pubmed
pubmed-article:12113795pubmed:affiliationDepartment of Bioengineering, University of Washington, Seattle, WA, USA. vesna@u.washington.edulld:pubmed
pubmed-article:12113795pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:12113795pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed