IP Library Granted Patent US 9,119,827
Granted Patent B2
US 9,119,827 · App. 13/381,604 · Granted Sep 1, 2015

Ophthalmic composition

Inventors: Akito Odaka (Tokyo, JP); Chieko Inoue (Tokyo, JP); Manabu Hattori (Tokyo, JP); Nobuhito Tabuchi (Tokyo, JP)
Assignee: LION CORPORATION
A61K31/203A61K9/0048A61K31/20A61K31/22A61K31/23A61K31/232A61K47/44
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 9,119,827
App. No.
13/381,604
Granted
Sep 1, 2015
Kind
B2
Abstract

Disclosed is an ophthalmic composition which is characterized by containing (A) a vitamin A, (B) a polyoxyethylene polyoxypropylene glycol, and (C) an oil component that is selected from the group consisting of castor oil, soybean oil, sesame oil, peanut oil, olive oil, almond oil, wheat germ oil, corn oil, rapeseed oil, sunflower oil, purified lanolin and gel hydrocarbon.

Claims (31)

1. An ophthalmic composition comprising:

(A) 50,000 to 500,000 units/100 mL of vitamin A,

(B) 0.2 to 10 W/V % of a polyoxyethylene polyoxypropylene glycol selected from the group consisting of polyoxyethylene ( 200 ) polyoxypropylene ( 70 ) glycol, polyoxyethylene ( 160 ) polyoxypropylene ( 30 ) glycol, and polyoxyethylene ( 54 ) polyoxypropylene ( 39 ) glycol,

(C) 0.01 to 5 W/V % of an oil ingredient selected from the group consisting of castor oil, soybean oil, sesame oil, olive oil, almond oil, wheat germ oil, corn oil, canola oil, sunflower oil, and purified lanolin,

(D) 0.001 to 0.5 W/V % of vitamin E or dibutylhydroxytoluene,

(E) 0.001 to 1.0 W/V % of a polyoxyethylene hardened castor oil and/or a polyoxyethylene sorbitain fatty acid ester,

sodium edetate,

boric acid, and

trometamol; and

wherein a total content of the ingredients (B) and (E) is 1.1 to 20.001 W/V %; and

wherein said composition contains no antiseptic selected from the group consisting of benzalkonium chloride, benzethonium chloride, sorbic acid or a salt thereof, paraoxybenzoic acid esters, chlorhexidine gluconate, thimerosal, phenyl ethyl alcohol, alkyldiaminoethylglycine hydrochloride, polyhexanide hydrochloride, and polydronium chloride.

2. The ophthalmic composition of claim 1 , wherein the ingredient (A) is retinol palmitate, retinol acetate or retinoic acid.

3. The ophthalmic composition of claim 1 , wherein said composition is the ophthalmic composition for contact lens.

4. The ophthalmic composition of claim 1 , wherein ingredient (C) is castor oil.

5. A method for treating dry eye, which comprises the administration an ophthalmic composition according to claim 1 .

6. The method of claim 5 , wherein the ophthalmic composition is formulated with no antiseptic.

7. The method of claim 5 , wherein the ingredient (A) is retinol palmitate, retinol acetate or retinoic acid.

8. The method of claim 5 , wherein said composition is the ophthalmic composition for contact lens.

9. The method of claim 5 , wherein ingredient (C) is castor oil.

10. An ophthalmic composition consisting of:

(A) 50,000 to 500,000 units/100 mL of vitamin A,

(B) 0.2 to 10 W/V % of polyoxyethylene polyoxypropylene glycol selected from the group consisting of polyoxyethylene ( 200 ) polyoxypropylene ( 70 ) glycol, polyoxyethylene ( 160 ) polyoxypropylene ( 30 ) glycol, and polyoxyethylene ( 54 ) polyoxypropylene ( 39 ) glycol,

(C) 0.01 to 5 W/V % of an oil ingredient selected from the group consisting of castor oil, soybean oil, sesame oil, peanut oil, olive oil, almond oil, wheat germ oil, corn oil, canola oil, sunflower oil and purified lanolin,

(D) 0.001 to 0.5 W/V % of vitamin E or dibutylhydroxytoluene,

(E) 0.001 to 1.0 W/V % of a polyoxyethylene hardened castor oil and/or a polyoxyethylene sorbitan fatty acid ester,

sodium edetate,

boric acid,

trometamol, and

optionally at least one selected from the group consisting of polyhydric alcohols, surfactants other than the ingredients (B) and (E), buffering agents, thickening agents, sugars, pH adjusters, tonicity agents, stabilizing agents, cooling agents, drugs, and water; and

wherein a total content of the ingredients (B) and (E) is 1.1 to 20.001 W/V %, and

wherein said composition contains no antiseptic selected from the group consisting of benzalkonium chloride, benzethonium chloride, sorbic acid or a salt thereof, paraoxybenzoic acid esters, chlorhexidine gluconate, thimerosal, phenyl ethyl alcohol, alkyldiaminoethylglycine hydrochloride, polyhexanide hydrochloride, and polydronium chloride.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 30, 2011
From: ODAKA, AKITO; INOUE, CHIEKO; HATTORI, MANABU; TABUCHI, NOBUHITO
To: LION CORPORATION
Reel/Frame 027466/0973 →
Priority Claims (1)
JP 2009-154862 · Jun 30, 2009 · national
Continuity (1)
Related Publication 20120108658A1 · May 3, 2012