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Ocular delivery of triamcinolone acetonide phosphate and related compounds

a technology of triamcinolone acetonide and related compounds, applied in the field of ocular delivery of triamcinolone acetonide phosphate and related compounds, can solve the problems of complex treatment of intermediate and posterior uveitis, systemic toxicities, and blindness of uveitis, and achieve the effect of treating or preventing an ocular condition

Inactive Publication Date: 2008-01-10
ACIONT
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

"The present invention provides systems and methods for noninvasively delivering a triamcinolone acetonide agent to the eye for the treatment or prevention of ocular conditions. The triamcinolone acetonide agent may be administered by iontophoretic or passive diffusion techniques. The condition that can be treated or prevented includes macular edema, age-related macular degeneration, uveitis, retinitis, eye cancers, glaucoma, and others. The invention also provides a system that includes an ocular device with a drug reservoir and a triamcinolone acetonide agent, as well as an enhancer reservoir containing a vasoconstricting agent."

Problems solved by technology

If left untreated, uveitis leads to blindness.
Treatments of intermediate and posterior uveitis are complicated by the inaccessibility of the posterior eye to topically applied medications.
Therefore large systemic doses are needed to treat intermediate and posterior uveitis, which often result in systemic toxicities including immunosuppression, adrenal suppression, ulcerogenesis, fluid and electrolyte imbalances, fat redistribution and psychological disorders.
Intravitreal injections are necessary because periocular injections and systemic administration do not deliver efficacious amounts of antibiotics to the target sites in the eye.
While intravitreal and periocular injections are preferable to systemic administration, the half-life of most injected compounds in the vitreous is relatively short, usually on the scale of just a few hours.
Therefore, intravitreal injections require frequent administration.
The repeated injections can cause pain, discomfort, intraocular pressure increases, intraocular bleeding, increased chances for infection, and the possibility of retinal detachment.
The major complication of periocular injections is accidental perforation of the globe, which causes pain, retinal detachment, ocular hypertension, and intraocular hemorrhage.
Therefore, these methods of ocular drug delivery into the posterior of the eye have significant limitations and major drawbacks.
In addition, injections are very poorly accepted by patients.
These methods also involve high healthcare cost due to the involvement of skilled and experienced physicians to perform the injections.

Method used

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  • Ocular delivery of triamcinolone acetonide phosphate and related compounds
  • Ocular delivery of triamcinolone acetonide phosphate and related compounds

Examples

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example 1

[0065] This example describes the non-invasive delivery of a triamcinolone acetonide agent into the eyes of rabbits. In this study, an ocular device was placed on the eyes of rabbits. The electrode chamber of the device was positioned on the conjunctiva near the pars plana. The triamcinolone acetonide agent in the electrode chamber was 0.5 M triamcinolone acetonide phosphate. The delivery of the active agent was achieved by applying a constant direct electric current of two milliampere across the electrode chamber for 15 minutes, thus delivering the triamcinolone acetonide agent. Six groups of 2 to 3 rabbits with each group assigned to the different time point (10-min, 4-hour, or 1-day) were used. At 10 minutes, 4 hours, and 1 day after the iontophoresis applications, the animals were euthanized and the eyes were enucleated for triamcinolone acetonide and triamcinolone acetonide phosphate assays. The assay procedure involved extracting these compounds from the conjunctiva, sclera, a...

example 2

[0066] This example describes the non-invasive delivery of a sustained release triamcinolone acetonide agent into the eyes of rabbits using a depot forming agent. In this study, an ocular device of side-by-side active and depot forming agent chambers was placed on the eyes of rabbits. The electrode chambers of the device were positioned on the conjunctiva near the pars plana. The active and depot forming agents were 0.5 M triamcinolone acetonide phosphate and 1.0 M dodecyl ammonium, respectively. The delivery of the sustained release system was achieved by applying a constant direct electric current of two milliampere across the side-by-side chambers for 15 minutes, in which the active agent was delivered from the cathode and the depot forming agent was from the anode. Six groups of 2 to 3 rabbits with each group assigned to the different time point (10-min, 4-hour, or 1-day) were used. At 10 minutes, 4 hours, and 1 day after the iontophoresis applications, the animals were euthaniz...

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Abstract

The present invention provides systems and methods for ocularly delivering a triamcinolone acetonide agent to a subject. In one aspect, for example, a method is provided for treating or preventing an ocular condition in a subject for which triamcinolone acetonide is effective. Such a method may include ocularly administering a triamcinolone acetonide agent to the subject in order to treat or prevent the condition. Although any administration technique is contemplated, in some aspects a triamcinolone acetonide agent may be delivered to eye tissue via ocular iontophoresis.

Description

PRIORITY DATA [0001] This application is a continuation-in-part of U.S. patent application Ser. No. 11 / 238,144, filed on Sep. 27, 2005, which claims the benefit of U.S. Provisional Patent Application Ser. No. 60 / 623,150, filed on Oct. 27, 2004, both of which are incorporated herein by reference. This application is also a continuation-in-part of U.S. patent application Ser. No. 11 / 238,104, filed on Sep. 27, 2005, which claims the benefit of U.S. Provisional Patent Application Ser. No. 60 / 623,150, filed on Oct. 27, 2004, both of which are incorporated herein by reference.FIELD OF THE INVENTION [0002] The present invention relates to systems, methods, and devices for the minimally invasive or noninvasive delivery ocular delivery of an active agent. Accordingly, the present invention involves the fields of chemistry, pharmaceutical sciences, and medicine, particularly ophthalmology. BACKGROUND OF THE INVENTION [0003] Posterior and intermediate eye diseases that require ocular drug deli...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A61K31/56A61N1/30A61P27/02
CPCA61F9/0017A61K9/0009A61N1/327A61N1/303A61N1/044A61K9/0048A61K31/573A61K31/58A61K41/00A61K45/06A61N1/0412A61K2300/00A61P17/00A61P27/02A61P27/06A61P29/00A61P31/04A61P31/10A61P31/12A61P31/22A61P35/00A61P43/00A61P5/38A61P9/00A61P9/10A61N1/30
Inventor HIGUCHI, JOHN W.TUITUPOU, ANTHONY L.KOCHAMBILLI, RAJAN P.LI, S. KEVIN
Owner ACIONT
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