IP Library Granted Patent US 9,498,642
Granted Patent B2
US 9,498,642 · App. 14/507,407 · Granted Nov 22, 2016

Eye therapy system

Inventors: David Muller (Boston, MA); John Marshall (Farnborough, GB); Marc D. Friedman (Needham, MA)
Assignee: Avedro, Inc.
A61N5/062A61F9/0008A61K31/14A61F9/013
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Quick Facts
Patent No.
US 9,498,642
App. No.
14/507,407
Granted
Nov 22, 2016
Kind
B2
Abstract

Embodiments apply a cross-linking agent to a region of corneal tissue. The cross-linking agent improves the ability of the corneal tissue to resist undesired structural changes. For example, the cross-linking agent may be Riboflavin or Rose Bengal, and the initiating element may be photoactivating light, such as ultraviolet (UV) light. In these embodiments, the photoactivating light initiates cross-linking activity by irradiating the applied cross-linking agent to release reactive oxygen radicals in the corneal tissue. The cross-linking agent acts as a sensitizer to convert O 2 into singlet oxygen which causes cross-linking within the corneal tissue. The rate of cross-linking in the cornea is related to the concentration of O 2 present when the cross-linking agent is irradiated with photoactivating light. Accordingly, the embodiments control the concentration of O 2 during irradiation to increase or decrease the rate of cross-linking and achieve a desired amount of cross-linking.

Claims (28)

1. A system for controlling cross-linking in corneal tissue, comprising:

a cross-linking system configured to apply a cross-linking agent to a cornea and activate the applied cross-linking agent to cause cross-linking in corneal fibrils of the cornea;

a monitoring system configured to determine an amount of cross-linking in the cornea; and

a delivery device configured to selectively adjust an O 2 content provided to the cornea to control the rate of cross-linking in response to the amount of cross-linking in the cornea determined by the monitoring system.

2. The system according to claim 1 , wherein the delivery device is configured to provide a gas mixture that determines the O 2 content provided to the cornea.

3. The system according to claim 1 , wherein the delivery device is configured to provide an oxygenated substance to the cornea, the oxygenated substance increasing the O 2 content in the corneal tissue when the oxygenated substance is applied.

4. The system according to claim 3 , wherein the oxygenated substance includes Riboflavin.

5. The system according to claim 3 , wherein the oxygenated substance includes a gel that is saturated or supersaturated with O 2 .

6. The system according to claim 5 , wherein the oxygenated substance includes the cross-linking agent and the gel.

7. The system according to claim 1 , wherein the monitoring system is configured to determine the stiffness of the corneal tissue.

8. A system for controlling cross-linking in corneal tissue, comprising:

a vessel that stores an oxygenated substance under O 2 pressure greater than ambient increasing the equilibrium concentration of O 2 for the oxygenated substance and causing the oxygenated substance to be saturated or supersaturated with O 2 ;

a delivery device configured to apply the oxygenated substance to corneal fibrils in the corneal tissue, the oxygenated substance increasing the O 2 content in the corneal tissue when the oxygenated substance is applied; and

a cross-linking system including a light source configured to activate a cross-linking agent applied to the corneal fibrils in the corneal tissue, the activated cross-linking agent causing cross-linking in the corneal fibrils.

9. The system according to claim 8 , wherein the oxygenated substance includes a gel.

10. The system according to claim 8 , wherein the oxygenated substance is mixed with the cross-linking agent before the oxygenated substance and the cross-linking agent are applied to the cornea.

11. The system according to claim 8 , wherein the delivery device is configured to apply the oxygenated substance to the cornea before the cross-linking agent is applied to the cornea.

12. The system according to claim 11 , further comprising an applicator configured to apply the cross-linking agent to the cornea.

13. The system according to claim 12 , wherein the applicator is an eye dropper or a syringe.

14. The system according to claim 8 , wherein the cross-linking agent is the oxygenated substance, the vessel storing the cross-linking agent under O 2 pressure greater than ambient that increases the equilibrium concentration of O 2 for the cross-linking agent causing the cross-linking agent to be saturated or supersaturated with O 2 , the delivery device applying the cross-linking agent to the corneal fibrils.

15. A system for controlling cross-linking in corneal tissue, comprising:

a cross-linking system configured to activate a cross-linking agent applied to a cornea to cause cross-linking in corneal fibrils of the cornea, the cross-linking system including a light source configured to direct a photoactivating light to the cornea; and

a delivery device configured to selectively increase or decrease an O 2 content provided to the cornea to control the rate of cross-linking, wherein the delivery device is configured to selectively increase or decrease the O 2 content based on an assessment of the structure of the cornea.

16. The system according to claim 15 , further comprising an applicator configured to apply the cross-linking agent to the cornea, the delivery device being configured to separately apply a gas mixture or an oxygenated substance to the cornea to control the rate of cross-linking.

17. The system according to claim 15 , wherein the delivery device is configured to apply the cross-linking agent to the cornea, the cross-linking agent being saturated or supersaturated with O 2 such that the cross-linking agent increases the O 2 content in the cornea when the cross-linking agent is applied.

18. The system according to claim 17 , wherein the delivery device is a syringe.

19. The system according to claim 15 , wherein the delivery device is configured to apply a mixture of a cross-linking agent and an oxygenated substance to the cornea to increase the O 2 content in the cornea, the oxygenated substance being saturated or supersaturated with O 2 .

20. The system according to claim 15 , further comprising a monitoring system configured to provide the assessment of the structure of the cornea.

Assignments (4)
RELEASE OF SECURITY INTEREST Recorded Nov 21, 2019
From: ORBIMED ROYALTY OPPORTUNITIES II, LP
To: AVEDRO, INC.
Reel/Frame 051080/0756 →
CORRECTIVE ASSIGNMENT TO CORRECT THE INCORRECT SERIAL NO. 14/140,184 PREVIOUSLY RECORDED AT REEL: 042167 FRAME: 0671. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded May 1, 2017
From: AVEDRO, INC.
To: ORBIMED ROYALTY OPPORTUNITIES II, LP
Reel/Frame 042390/0659 →
SECURITY INTEREST Recorded Apr 27, 2017
From: AVEDRO, INC.
To: ORBIMED ROYALTY OPPORTUNITIES II, LP
Reel/Frame 042167/0671 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 12, 2015
From: MULLER, DAVID; MARSHALL, JOHN; FRIEDMAN, MARC D
To: AVEDRO, INC.
Reel/Frame 034681/0055 →
Continuity (4)
Continuation 14035528 · Sep 24, 2013
Continuation 12909228 · Oct 21, 2010
Provisional Application 61253736 · Oct 21, 2009
Related Publication 20150025440A1 · Jan 22, 2015