2011
DOI: 10.1016/s1773-2247(11)50010-3
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Emulsions and microemulsions for ocular drug delivery

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Cited by 48 publications
(26 citation statements)
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“…The surfactant helps in reducing the surface tension between the two phases. In addition, the use of a co-solvent helps in further reducing the interfacial tension 24 .…”
Section: Introductionmentioning
confidence: 99%
“…The surfactant helps in reducing the surface tension between the two phases. In addition, the use of a co-solvent helps in further reducing the interfacial tension 24 .…”
Section: Introductionmentioning
confidence: 99%
“…Due to these clearance mechanisms and ocular barriers, less than 5% of the total administered drug reaches the aqueous humor 7. For example, after administration of a common eye‐drop solution containing 0.05% cyclosporine to treat dry eye syndrome, more than 95% of the drug reaches systemic circulation through transnasal or conjunctival absorption 8…”
Section: Challenges Of Conventional Ophthalmic Drug Deliverymentioning
confidence: 99%
“…Microemulsions offer a promising route for designing extended drug delivery systems due to improved drug solubilization, ease of preparation and administration, long shelf-life, improved corneal penetration and improved residence time [17,18,19,20]. Cationic emulsions increase the bioavailability of ophthalmic drugs in comparison to emulsions with no charge or negative charge [17,21,22]. The addition of cationic surfactant forms positively charged drops in microemulsions, which can bind to the negatively charged corneal epithelium, leading to increased residence time and drug permeability through the corneal epithelium [17].…”
Section: Introductionmentioning
confidence: 99%