LASER ENHANCED LENS

• US 20110181835A1
• Filed: 01/20/2011
• Published: 07/28/2011
• Est. Priority Date: 12/27/2007
• Status: Abandoned Application

• Current Assignee: Johnson & Johnson Vision Care Incorporated (Johnson & Johnson)
• Original Assignee: Johnson & Johnson Vision Care Incorporated (Johnson & Johnson)
• Inventors: Rooney, Thomas R., Widman, Michael F., Mahadevan, Shivkumar
• Application Number:
  US13/010,389
• Publication Number:
  US 20110181835A1
• Time in Patent Office: Days
• US Class Current: 351/177
• CPC Class Codes: B29D 11/00125 Auxiliary operations, e.g. removing oxygen from the mould, conveying moulds from a storage to the production line in an inert atmosphere
• CPC Class Codes: B29D 11/00461 Adjusting the refractive index, e.g. after implanting
• CPC Class Codes: B29D 11/00932 Combined cutting and grinding thereof

Abstract

This invention discloses methods and apparatus for modifying a silicone contact lens via laser ablation and a resulting modified lens. In some embodiments a lens is ablated in a hydrated state. A lens may also be ablated in an environment of decreased oxygen content.

Claims

1. An ophthalmic lens produced by a method comprising the steps of:

receiving digital data into an apparatus for controlling an ablation process wherein the data relates to a modification to the ophthalmic lens;

calculating in the apparatus for controlling an ablation process, a control pattern for a laser apparatus based upon the data related to the modification;

calculating a control sequence for operating the laser apparatus;

securing the ophthalmic lens in a position to receive laser energy;

exposing the ophthalmic lens to laser energy based upon the control sequence, wherein the ophthalmic lens is hydrated with saline solution prior to and during the lens being exposed to laser energy and the ophthalmic lens is contained in an inert atmosphere during ablation; and

removing kerf from the surface of the lens.

2. The ophthalmic lens of claim 1 wherein the uncured lens formulation comprises a silicone hydrogel formulation.

3. The ophthalmic lens of claim 2, wherein the kerf is removed from the lens via a wash in a solution.

4. The ophthalmic lens of claim 2, wherein the kerf is removed from the lens via exposure to an air wash.

5. The ophthalmic lens of claim 2 wherein the data comprises eye topography data.

6. The ophthalmic lens of claim 1 wherein the data related to the modification to the ophthalmic lens comprises an intended use for the ophthalmic lens and the intended use is a factor determining the control sequence.

7. The ophthalmic lens of claim 2 additionally comprising the step of applying a coating to the lens subsequent to the step of exposing the ophthalmic lens to laser energy.

8. The ophthalmic lens of claim 6 wherein the intended use comprises facilitating far sighted visual performance.

9. The ophthalmic lens of claim 2 wherein the step of exposing the ophthalmic lens to laser energy is accomplished in an environment with an oxygen content of less than 20 percent.

10. The ophthalmic lens of claim 1 additionally comprising the steps of positioning the lens on a mandrel and aligning the mandrel to receive laser energy.

11. The ophthalmic lens of claim 1 additionally comprising the steps of positioning a cast mold to which the lens is adhered in a position for the lens to receive laser energy.

12. The ophthalmic lens of claim 2 wherein exposure of the ophthalmic lens to laser energy is sufficient to ablate a portion of the ophthalmic lens.

13. The ophthalmic lens of claim 2 wherein the data received related to a modification to the ophthalmic lens is received under the direction of an eye care practitioner.

14. The ophthalmic lens of claim 13 wherein the data received related to a modification to the ophthalmic lens is received as electronic digital data.

15. The ophthalmic lens of claim 2 additionally comprising the steps of repackaging the ophthalmic lens and sterilizing the modified lens.