Topical Gel/Microsphere Eyedrop for Combined Delivery of Brimonidine and Timolol: A Comparative Study With Traditional Eye Drops in Rabbits.
Fan Xin, Harding Phillip A, Ziaei Parissa, Chaudhry Ahmad B, West Raymond E, Nolin Thomas D, DiLeo Morgan V
AI Summary
A novel gel/microsphere eyedrop for glaucoma drugs showed sustained ocular delivery for 27 days, lower systemic exposure, and potential for improved patient compliance compared to traditional drops.
Abstract
Purpose
Topical eye drops combining multiple antiglaucoma agents are often required when monotherapy fails to reduce intraocular pressure (IOP). However, their effectiveness is compromised by low bioavailability and poor patient compliance. To address these issues, we developed a novel gel/microsphere eye drop (GME) containing brimonidine and timolol, aimed at enhancing ocular bioavailability, reducing dosing frequency, and improving patient compliance.
Methods
The GME system comprises separate formulations of brimonidine-loaded and timolol-loaded polymer microspheres within a thermoresponsive hydrogel, enabling simple off-the-shelf preparation. We examined the in vitro drug release, compared the biodistribution with traditional eye drops, and assessed pharmacodynamic effects in New Zealand white rabbits and Dutch Belted rabbits.
Results
Brimonidine and timolol reached high concentrations in the aqueous and vitreous humor at 1 hour following eye drop administration, declining to nearly undetectable levels by 24 hours. The GME system at a similar dose extended the drug release to 27 days with initially lower drug levels but decreasing more slowly. The GME system also resulted in significantly lower plasma drug concentrations than eye drops, suggesting a reduced risk of systemic side effects. Neither the GME nor eye drops significantly reduced IOP in normotensive rabbits.
Conclusions
The GME system presents a promising alternative to traditional eye drops for controlled drug release in ocular applications, enabling sustained drug delivery while minimizing systemic exposure and thereby potentially enhancing the safety and efficacy of ocular therapies.
Translational relevance: The GME system bridges basic research and clinical application by providing a controlled-release platform that sustains drug delivery, reduces systemic side effects, and enhances patient adherence.
MeSH Terms
Shields Classification
Key Concepts5
Brimonidine and timolol reached high concentrations in the aqueous and vitreous humor at 1 hour following traditional eye drop administration in New Zealand white rabbits and Dutch Belted rabbits, declining to nearly undetectable levels by 24 hours.
A novel gel/microsphere eye drop (GME) system containing brimonidine and timolol, at a similar dose to traditional eye drops, extended drug release to 27 days with initially lower drug levels but decreasing more slowly in New Zealand white rabbits and Dutch Belted rabbits.
The novel gel/microsphere eye drop (GME) system containing brimonidine and timolol resulted in significantly lower plasma drug concentrations than traditional eye drops in New Zealand white rabbits and Dutch Belted rabbits, suggesting a reduced risk of systemic side effects.
Neither the novel gel/microsphere eye drop (GME) system containing brimonidine and timolol nor traditional eye drops significantly reduced intraocular pressure (IOP) in normotensive New Zealand white rabbits and Dutch Belted rabbits.
The novel gel/microsphere eye drop (GME) system containing brimonidine and timolol presents a promising alternative to traditional eye drops for controlled drug release in ocular applications, enabling sustained drug delivery while minimizing systemic exposure and thereby potentially enhancing the safety and efficacy of ocular therapies.
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