Literature DB >> 24094935

In vivo performance of a drug-eluting contact lens to treat glaucoma for a month.

Joseph B Ciolino1, Cristina F Stefanescu, Amy E Ross, Borja Salvador-Culla, Priscila Cortez, Eden M Ford, Kate A Wymbs, Sarah L Sprague, Daniel R Mascoop, Shireen S Rudina, Sunia A Trauger, Fabiano Cade, Daniel S Kohane.   

Abstract

For nearly half a century, contact lenses have been proposed as a means of ocular drug delivery, but achieving controlled drug release has been a significant challenge. We have developed a drug-eluting contact lens designed for prolonged delivery of latanoprost for the treatment of glaucoma, the leading cause of irreversible blindness worldwide. Latanoprost-eluting contact lenses were created by encapsulating latanoprost-poly(lactic-co-glycolic acid) films in methafilcon by ultraviolet light polymerization. In vitro and in vivo studies showed an early burst of drug release followed by sustained release for one month. Contact lenses containing thicker drug-polymer films demonstrated released a greater amount of drug after the initial burst. In vivo, single contact lenses were able to achieve, for at least one month, latanoprost concentrations in the aqueous humor that were comparable to those achieved with topical latanoprost solution, the current first-line treatment for glaucoma. The lenses appeared safe in cell culture and animal studies. This contact lens design can potentially be used as a treatment for glaucoma and as a platform for other ocular drug delivery applications.
Copyright © 2013 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Contact lens; Drug delivery; Glaucoma; Latanoprost; Ocular release; Sustained release

Mesh:

Substances:

Year:  2013        PMID: 24094935      PMCID: PMC3874329          DOI: 10.1016/j.biomaterials.2013.09.032

Source DB:  PubMed          Journal:  Biomaterials        ISSN: 0142-9612            Impact factor:   12.479


  28 in total

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3.  Effect of temperature and light on the stability of latanoprost and its clinical relevance.

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4.  A double masked comparison of the intraocular pressure reducing effect of latanoprost 0.005% and 0.001% administered once daily in open angle glaucoma and ocular hypertension.

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5.  Patient administration of eyedrops: observation. Part II.

Authors:  M A Kass; E Hodapp; M Gordon; A E Kolker; I Goldberg
Journal:  Ann Ophthalmol       Date:  1982-09

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Journal:  Biomaterials       Date:  2000-12       Impact factor: 12.479

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8.  Ocular and systemic pharmacokinetics of latanoprost in humans.

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  35 in total

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3.  A novel murine model for contact lens wear reveals clandestine IL-1R dependent corneal parainflammation and susceptibility to microbial keratitis upon inoculation with Pseudomonas aeruginosa.

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Review 4.  Getting Drugs Across Biological Barriers.

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8.  Steroid-eluting contact lenses for corneal and intraocular inflammation.

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Review 10.  Extraocular, periocular, and intraocular routes for sustained drug delivery for glaucoma.

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