IP Library Granted Patent US 9,259,472
Granted Patent B2
US 9,259,472 · App. 14/180,396 · Granted Feb 16, 2016

Polymeric artificial tear system

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Quick Facts
Patent No.
US 9,259,472
App. No.
14/180,396
Granted
Feb 16, 2016
Kind
B2
Abstract

The present invention relates to artificial tear formulations and ophthalmic formulations suitable for drug delivery. The formulations comprise galactomannans such as guar or hydroxypropyl guar and a borate source such as boric acid. The formulations further comprise a cis-diol such as sorbitol that interferes with the cross-linking of galactomannan and borate. Optionally, the formulations are substantially free of divalent cations.

Claims (24)

1. An ophthalmic formulation comprising a galactomannan, borate, and a cis-diol, wherein said formulation is substantially free of divalent cations, wherein said galactomannan is present at a concentration of about 0.1 w/v % to about 2.0 w/v % and said borate is present at a concentration of about 0.2 w/v % to about 2.0 w/v % and said cis-diol is sorbitol at a concentration of 0.5 to 5.0 w/v %, said formulation further comprising one or more pharmaceutically active compounds suitable as ophthalmic therapeutics.

2. A formulation according to claim 1 wherein said galactomannan is present at a concentration of about 0.16 w/v % to about 0.19 w/v % and said borate is present at a concentration of about 0.7 w/v %.

3. A formulation according to claim 1 wherein said galactomannan is selected from the group consisting of:

guar, hydroxylpropyl guar, and combinations thereof.

4. A formulation according to claim 1 wherein said cis-diol is present at a concentration of about 1.4 w/v %.

5. A formulation according to claim 1 wherein said borate is boric acid.

6. A formulation according to claim 1 further comprising a demulcent selected from the group consisting of:

glycerin, polyvinyl pyrrolidone, polyethylene oxide, polyethylene glycol, propylene glycol, polyacrylic acid, and combinations thereof.

7. A formulation according to claim 6 wherein said demulcent is polypropylene glycol or polyethylene glycol.

8. In an ophthalmic formulation comprising a galactomann and borate, the improvement comprising adding a cis-diol to prevent galactomann and borate cross-linking, thereby reducing the viscosity of the formulation.

9. A formulation according to claim 8 , said formulation further being substantially free of divalent cations, thereby reducing the viscosity of the formulation.

10. A method for lubricating the eye comprising administering to the eye a formulation of claim 1 .

11. A method for delivering a pharmaceutically active agent to the eye comprising:

administering to the eye a formulation of claim 1 .

12. An improved ophthalmic formulation comprising galactomannan and borate, said formulation comprising a cis-diol that is eliminated from tear film more rapidly than said galactomannan when the formulation is instilled in an eye.

13. An improved ophthalmic formulation according to claim 12 wherein said galactomannan is present at a concentration of about 0.16 w/v % to about 0.19 w/v % and said borate is present at a concentration of about 0.7 w/v %.

14. An improved ophthalmic formulation according to claim 13 wherein said galactomannan is selected from the group consisting of:

guar, hydroxylpropyl guar, and combinations thereof.

15. An improved ophthalmic formulation according to claim 12 wherein said cis-diol is selected from the group consisting of sorbitol, mannitol, polyethylene glycols, polypropylene glycols, polyethyleneoxide-polybutyleneoxide block copolymers, and combinations thereof.

16. An improved ophthalmic formulation according to claim 15 wherein said cis-diol is sorbitol or mannitol.

17. An improved ophthalmic formulation according to claim 12 , said formulation further being substantially free of divalent cations, thereby reducing the viscosity of the formulation.

18. An improved ophthalmic formulation according to claim 12 , said formulation further comprising a demulcent selected from the group consisting of:

glycerin, polyvinyl pyrrolidone, polyethylene oxide, polyethylene glycol, propylene glycol, polyacrylic acid, and combinations thereof.

19. A formulation according to claim 1 wherein said active pharmaceutical agent is selected from the group consisting of: glaucoma therapeutics, pain relievers, anti-inflammatory medications, anti-allergy medications, and anti-microbials.

Assignments (3)
CONFIRMATORY DEED OF ASSIGNMENT EFFECTIVE APRIL 8, 2019 Recorded Jul 23, 2020
From: ALCON RESEARCH, LLC
To: ALCON INC.
Reel/Frame 053293/0484 →
MERGER Recorded Jul 21, 2020
From: ALCON RESEARCH, LTD.
To: ALCON RESEARCH, LLC
Reel/Frame 053273/0022 →
CONFIRMATORY DEED OF ASSIGNMENT EFFECTIVE APRIL 8, 2019 Recorded Dec 10, 2019
From: NOVARTIS AG
To: ALCON INC.
Reel/Frame 051454/0788 →