Ophthalmic solution comprising diquafosol

US2018353531A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2018353531-A1
Application numberUS-201816103328-A
CountryUS
Kind codeA1
Filing dateAug 14, 2018
Priority dateMar 26, 2012
Publication dateDec 13, 2018
Grant date

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  1. Title

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  2. Abstract

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  5. First independent claim

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Abstract

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Regarding Diquafosol ophthalmic solution comprising a chelating agent at a concentration of 0.0001 to 1% (w/v), formation of insoluble precipitates found in Diquafosol ophthalmic solution during storage of the solution, as well as deterioration of the filtration performance in the course of production (course of filtration sterilization), have been inhibited. Further, in Diquafosol ophthalmic solution comprising a chelating agent, reduction of eye irritation and enhancement of the preservative effectiveness have been confirmed, in comparison to Diquafosol ophthalmic solution comprising no chelating agent. Accordingly, the present invention has been confirmed to provide physicochemical properties that are stable during the courses of production and distribution as well as the course of storage by a patient, and also reduce eye irritation and enhance preservative effectiveness.

First claim

Opening claim text (preview).

1 . A method for treating dry eye comprising applying to corneal epithelium disorder found in a dry-eye patient an aqueous ophthalmic solution consisting of diquafosol or salt thereof at a concentration of 0.1 to 10% (w/v) and a chelating agent at a concentration of 0.0001 to 1% (w/v) and optionally at least one other agent of a buffer agent, isotonizing agent, surfactant or pH adjuster, wherein the surfactant is selected from the group consisting of polyoxyl 40 stearate and polyoxyethylene hydrogenated castor oil, and wherein the chelating agent is at least one type selected from the group consisting of edetic acid, citric acid, metaphosphoric acid, pyrophosphoric acid, polyphosphoric acid, malic acid, tartaric acid, phytic acid, and salts thereof. 2 . The method according to claim 1 , wherein the chelating agent is at least one type selected from the group consisting of edetic acid, critic acid, metaphosphoric acid, polyphosphoric acid, and salts thereof. 3 . The method according to claim 1 , wherein chelating agent is a salt of edetic acid. 4 . The method according to claim 1 , wherein the chelating agent is at a concentration of 0.000 to 0.5% (w/v) in the ophthalmic solution. 5 . The method according to claim 1 , wherein the chelating agent is at a concentration of 0.001 to 0.1% (w/v) in the ophthalmic solution. 6 . The method according to claim 1 , wherein diquafosol or a salt thereof is at a concentration of 1 to 10% (w/v) in the ophthalmic solution. 7 . The method according to claim 1 , wherein diquafosol or a salt thereof is at a concentration of 3% (w/v) in the ophthalmic solution. 8 . The method according to claim 1 , wherein the chelating agent is a salt of edetic acid, the chelating agent is at a concentration of 0.001 to 0.1% (w/v) in the ophthalmic solution, and diquafosol or a salt thereof is at a concentration of 3% (w/v) in the ophthalmic solution. 9 . The method according to claim 1 , wherein the buffer agent is at least one type selected from the group consisting of sodium phosphate, sodium hydrogen phosphate, sodium dihydrogen phosphate, sodium acetate, and epsilon aminocaproic acid. 10 . The method according to claim 1 , wherein the isotonizing agent is at least one type selected from the group consisting of sodium chloride, potassium chloride, and concentrated glycerin.

Assignees

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Classifications

  • Ophthalmic agents · CPC title

  • Artificial tears; Irrigation solutions · CPC title

  • Carboxylic acids; Salts or anhydrides thereof · CPC title

  • Eye, e.g. artificial tears · CPC title

  • Compounds having two nucleosides or nucleotides, e.g. nicotinamide-adenine dinucleotide, flavine-adenine dinucleotide · CPC title

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What does patent US2018353531A1 cover?
Regarding Diquafosol ophthalmic solution comprising a chelating agent at a concentration of 0.0001 to 1% (w/v), formation of insoluble precipitates found in Diquafosol ophthalmic solution during storage of the solution, as well as deterioration of the filtration performance in the course of production (course of filtration sterilization), have been inhibited. Further, in Diquafosol ophthalmic s…
Who is the assignee on this patent?
Santen Pharmaceutical Co Ltd
What technology area does this patent fall under?
Primary CPC classification A61K31/7084. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Thu Dec 13 2018 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 1 related publication on this page (citations in our corpus or others sharing the same primary CPC).