IP Library Granted Patent US 7,060,297
Granted Patent B2
US 7,060,297 · App. 10/111,520 · Granted Jun 13, 2006

Carrageenan viscoelastics for ocular surgery

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Quick Facts
Patent No.
US 7,060,297
App. No.
10/111,520
Granted
Jun 13, 2006
Kind
B2
Abstract

Disclosed are carrageenan-based transitional viscoelastics that will induce little or no IOP spike when left in the eye at the close of surgery thereon. Drug delivery systems for delivering therapeutic agents during post-operative recovery stages are also disclosed.

Claims (15)

1. A transitional viscoelastic composition for use in surgery, comprising a sterile, non-inflammatory, aqueous solution comprising kappa-carrageenan, potassium, and a second sulfated polysaccharide, such solution having a viscosity transition temperature range from 17–26° C. to 35–38° C., wherein such solution exhibits a loss of viscosity of at least 80% upon heating through such viscosity transition temperature range.

2. The composition of claim 1 , wherein the viscosity transition temperature range is from about 25° C. to about 37° C., and wherein the second sulfated polysaccharide is selected from the group consisting of: chondroitin sulfate, heparin, and combinations thereof.

3. The composition of claim 2 , wherein the second sulfated polysaccharide is chondroitin sulfate and the weight ratio of the kappa-carrageenan to the chondroitin sulfate is from about 4:5 to about 7:2.

4. The composition of claim 3 , wherein the combined concentration of the kappa-carrageenan and the chondroitin sulfate is from about 0.9 to about 1.5 wt %.

5. A transitional viscoelastic composition for delivering an ophthalmic drug to an affected eye, comprising the ophthalmic drug in a sterile, aqueous solution comprising kappa-carrageenan, potassium, and a second sulfated polysaccharide, such solution having a viscosity transition temperature range from 17–26° C. to 35–38° C., wherein such solution exhibits a loss of viscosity of at least 80% upon warming through such viscosity transition temperature range.

6. The composition of claim 5 , wherein the viscosity transition temperature range is from about 25 to about 37° C. and wherein the ophthalmic drug is selected from the group consisting of: anti-glaucoma agents; anti-infective agents; steroidal and non-steroidal anti-inflammatory agents; growth factors; immunosuppressant agents; anti-allergy agents, and combinations thereof.

7. A method of protecting, manipulating or stabilizing tissue in an eye during surgery thereon, comprising instilling in the eye a transitional viscoelastic composition comprising a sterile, non-inflammatory, aqueous solution comprising kappa-carrageenan, potassium, and a second sulfated polysaccharide, such solution having a viscosity transition temperature range from 17–26° C. to 35–38° C., wherein such solution exhibits a loss of viscosity of at least 80% upon warming through such viscosity transition temperature range.

8. The method of claim 7 , further comprising the step of allowing a protecting or stabilizing effective amount of the transitional viscoelastic to remain in the eye at the close of the surgery.

9. The method of claim 7 , wherein the second sulfated polysaccharide is selected from the group consisting of: iota-carrageenan, chondroitin sulfate, heparin, and combinations thereof.

10. The method of claim 9 wherein the second sulfated polysaccharide is iota-carrageenan and the weight ratio of the kappa-carrageenan to the iota-carrageenan and is from about 2:3 to about 9:1.

11. The method of claim 10 , wherein the weight ratio of kappa-carrageenan to iota-carrageenan is about 3:2.

12. The method of claim 11 , wherein the combined concentration of the kappa-carrageenan and the iota-carrageenan is about 0.8 wt %.

13. The method of claim 9 , wherein the second sulfated polysaccharide is chondroitin sulfate and the weight ratio of kappa-carrageenan to chondroitin sulfate is from about 4:5 to about 7:2.

14. The method of claim 13 , wherein the combined concentration of the kappa-carrageenan and the chondroitin sulfate is from about 0.9 to about 1.5 wt %.

15. The method of claim 7 , wherein the surgery is cataract surgery.