IP Library Granted Patent US 7,582,113
Granted Patent B2
US 7,582,113 · App. 11/538,911 · Granted Sep 1, 2009

Method in eye surgery

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Quick Facts
Patent No.
US 7,582,113
App. No.
11/538,911
Granted
Sep 1, 2009
Kind
B2
Abstract

A method for prevention of migration of epithelial cells in a capsular bag of an eye of a mammal is provided. The method comprises removing the natural lens of the eye from the capsular bag; introducing an object with at least one sharp edge into the capsular bag, in such a way that said sharp edge contacts the inside of the capsular bag to form a barrier preventing migration of epithelial cells across said barrier; and injecting a lens-forming composition into the capsular bag.

Claims (26)

1. Method for forming an intraocular lens in situ in an eye of a mammal, comprising:

removing the natural lens of the eye from the capsular bag; introducing an object with at least one sharp edge into the capsular bag and positioning the object within the capsular bag with the sharp edge contacting an inside wall of the capsular bag to form a barrier preventing migration of epithelial cells across the barrier; configuring the object to push against the inside wall of the capsular bag; injecting a lens-forming composition into the capsular bag to fill the capsular bag; and curing the lens-forming composition to form an intraocular lens in the capsular bag, wherein the formed lens completely fills the capsular bag and the sharp edge remains in contact with an inside wall of the capsular bag after lens formation to prevent migration of epithelial cells across the barrier in the capsular bag; wherein the object is a haptic of an intraocular lens, which haptic is provided with the at least one sharp edge.

2. Method according to claim 1 , wherein the object with at least one sharp edge contacts the inside of the capsular bag along an equator of the capsular bag.

3. Method according to claim 2 , wherein the object with at least one sharp edge contacts the inside wall of the capsular bag along at least 50% of the equator of the capsular bag.

4. Method according to claim 3 , wherein the object with at least one sharp edge contacts the inside wall of the capsular bag along at least 75% of the equator of the capsular bag.

5. Method according to claim 4 , wherein the object with at least one sharp edge contacts the inside wall of the capsular bag along at least 90% of the equator of the capsular bag.

6. Method according to claim 1 , wherein the object has a roughly cylindrical form, with a radius of the cylindrical form being substantially larger than a height of the cylindrical form.

7. Method according to claim 6 , wherein the at least one sharp edge of the object has a radius of less than 2 μm.

8. Method according to claim 6 , wherein the object is an intraocular lens provided with at least one sharp edge.

9. Method according to claim 8 , wherein the object is a foldable intraocular lens.

10. Method according to claim 8 , wherein the object is a non-foldable intraocular lens.

11. Method according to claim 1 , wherein the lens-forming composition comprises polysiloxane.

12. Method according to claim 11 , wherein the lens-forming composition comprising polysiloxane has a specific gravity of greater than about 1.0, a refractive index suitable for restoring the refractive power of the natural crystalline lens, and a viscosity suitable for injection of the composition through a standard cannula.

13. Method according to claim 11 , wherein the lens-forming composition comprises polysiloxane of a siloxane monomer unit —R a R b SiO—, wherein R a and R b are the same or different alkyl or phenyl groups, at least one of which is substituted with at least one fluorine atom.

14. Method according to claim 11 , wherein the lens-forming composition comprises polysiloxane that is a terpolymer or higher polymer of three or more different siloxane monomer units.

15. Method according to claim 11 , wherein the lens-forming composition comprises polysiloxane that is a terpolymer of (a) dimethylsiloxane, (b) methylphenylsiloxane or diphenylsiloxane, and (c) trifluoropropylmethylsiloxane monomers.

16. Method according to claim 11 , wherein the lens-forming composition comprises polysiloxane having crosslinkable groups, and further comprises a crosslinking agent and optionally an effective amount of a catalyst.

17. Method according to claim 1 , wherein the lens-forming composition comprises a hydrogel.

18. Method according to claim 1 , for prevention of posterior capsule opacification.

19. Method according to claim 1 , for prevention of anterior capsule opacification.

20. Method according to claim 1 , for prevention of a condition characterized by irregular growth or irregular migration of epithelial cells in the capsular bag of the eye.

21. The method of claim 1 , further comprising pressing the inside wall of the capsular bag with enough pressure to prevent migration of epithelial cells.

22. The method of claim 1 , further comprising filling the capsular bag with the lens-forming composition and, after filling the capsular bag, putting the capsular bag under tension.

23. Method for forming an intraocular lens in situ in an eye of a mammal, comprising: removing the natural lens of the eye from the capsular bag; introducing an object with at least one sharp edge having a radius of less than 2 μm into the capsular bag and positioning the object within the capsular bag, with the sharp edge contacting an inside wall of the capsular bag to form a barrier preventing migration of epithelial cells across the barrier; configuring the object to push against the inside wall of the capsular bag; injecting a lens-forming composition into the capsular bag to fill the capsular bag; and curing the lens-forming composition to form an intraocular lens, wherein the formed lens completely fills the capsular bag and the object remains in the capsular bag, the sharp edge remaining in contact with an inside wall of the capsular bag after lens formation by curing of the lens-forming composition to prevent migration of epithelial cells across the barrier in the capsular bag; wherein the object is a haptic of an intraocular lens, which haptic is provided with the at least one sharp edge.

24. The method of claim 23 , further comprising pressing the inside wall of the capsular bag with enough pressure to prevent migration of epithelial cells.

25. The method of claim 23 , further comprising filling the capsular bag with the lens-forming composition and, after filling the capsular bag, putting the capsular bag under tension.