Method of corneal transplantation or corneal inlay implantation with cross-linking

Patent metadata

Field	Value
Publication number	US-10881503-B2
Application number	US-201916451247-A
Country	US
Kind code	B2
Filing date	Jun 25, 2019
Priority date	May 12, 2014
Publication date	Jan 5, 2021
Grant date	Jan 5, 2021

Abstract

A method of corneal implantation with cross-linking is disclosed herein. In one or more embodiments, the method includes the steps of: (i) forming a flap in a cornea of an eye so as to expose a stromal tissue of the cornea underlying the flap; (ii) pivoting the flap so as to expose the stromal tissue of the cornea underlying the flap; (iii) inserting an implant under the flap so as to overlie the stromal tissue of the cornea; (iv) applying laser energy and/or microwaves to the implant in the eye so as to modify the refractive power of the implant; (v) applying a cross-linking solution that includes a photosensitizer to the implant; (vi) covering the implant with the flap; and (vii) irradiating the implant so as to activate cross-linkers in the implant, and thereby cross-link the implant and the stromal tissue of the cornea surrounding the implant.

First claim

The invention claimed is:

1. A method of corneal implantation with cross-linking, said method comprising the steps of:
cutting a circular implant from a donor cornea;
marking the center of the circular implant;
forming a pocket in a recipient cornea of an eye of a patient, the pocket being bounded entirely by stromal tissue of the cornea, the pocket being created in the recipient corneal stroma using a femtosecond laser, the pocket having a diameter between approximately 3 millimeters and approximately 9 millimeters that is slightly larger than the diameter of the circular implant for ease of implantation of the circular implant;
separating portions of the pocket in the recipient cornea of the eye using a micro-spatula or a bent needle and hyaluronic acid;
forming a small side incision in the recipient cornea of the eye of the patient, the pocket being accessible through the small side incision in the recipient cornea, the small side incision being formed in the recipient cornea with the femtosecond laser or a knife;
inserting the circular implant with a crosslinking solution containing hyaluronic acid into the pocket of the recipient cornea via the small side incision, wherein the circular implant, tissue surrounding the pocket, and the hyaluronic acid are cross-linked so as to prevent an immune response to the circular implant, prevent rejection of the implant by the patient and prevent postoperative glare, where the hyaluronic acid is used for ease of insertion of the circular implant into the pocket in the recipient cornea of the eye, the hyaluronic acid being painted on a surface of the circular implant and a bounding wall of the pocket;
injecting riboflavin or photosensitizer nanoparticles into the pocket in the recipient cornea of the eye so as to penetrate the circular implant and a portion of the bounding wall of the pocket; and
irradiating the circular implant with ultraviolet light so as to cross-link the circular implant and the portion of the bounding wall of the pocket and the hyaluronic acid, and kill any potential pathogenic contaminants associated with the circular implant and prevent the postoperative glare.

2. The method according to claim 1 , wherein the circular implant is formed from donor corneal tissue, and wherein the step of cutting the circular implant from the donor cornea further comprises:
cutting the circular implant from the donor cornea by using a circular trephine, the circular implant having an outer diameter between approximately 3 millimeters and approximately 9 millimeters;
cutting the circular implant into two concentric circular parts, the first one of the two concentric circular parts comprising an annular disk portion and the second one of the two concentric circular parts comprising a central disk portion inside the annular disk portion, the central disk portion being cut using a femtosecond laser or a trephine having a diameter smaller than the outer diameter of the circular implant, each of the two concentric circular parts having a thickness between approximately 50 microns and approximately 100 microns; and
shaping a surface of at least one of the two concentric circular parts with an excimer laser outside the pocket to form a desired refractive power so as to correct a myopic, hyperopic, or astigmatic error of the eye;
wherein the step of inserting the circular implant into the pocket of the recipient cornea via the small side incision further comprises initially inserting the annular disk portion into the pocket via the small side incision using an injector syringe or forceps, and then subsequently inserting the central disk portion into the pocket via the small side incision using the injector syringe or forceps; and
wherein the method further comprises the step of:
joining the two concentric circular parts together inside the pocket.

3. The method according to claim 2 , wherein the central disk portion of the circular implant is organic and the annular disk portion of the circular implant is made from a synthetic transparent polymer or acrylic that is resilient or flexible.

4. The method according to claim 1 , wherein the step of forming the pocket in the recipient cornea of the eye further comprises cutting a circular or oval-shaped three-dimensional disk with a thickness of between approximately 60 microns and 100 microns using the femtosecond laser so as to form the pocket, and
wherein the method further comprises the steps of:
removing the circular or oval-shaped three-dimensional disk from the recipient corneal stroma to create more space inside the pocket; and
additionally using the hyaluronic acid to smoothen up the bounding wall of the pocket.

5. The method according to claim 4 , wherein, after the circular or oval-shaped three-dimensional disk is removed from the pocket, the method further comprises the steps of:
injecting cross-linkable molecules or monomers in a transparent biocompatible solution containing a crosslinker into the pocket so as to correct a hyperopic, hyperopic, or astigmatic refractive error of the eye; and
cross-linking the transparent biocompatible solution by externally applying ultraviolet radiation so as to cross-link the solution inside the pocket and convert the solution to a cross-linked gel, and to further cross-link the bounding wall of the pocket and kill any potential pathogens infecting the surgical area of the eye and to prevent postoperative glare.

6. The method according to claim 1 , wherein the step of forming the pocket in the recipient cornea of the eye further comprises cutting a circular or oval-shaped three-dimensional disk with a thickness of between approximately 60 microns and 100 microns using the femtosecond laser so as to form the pocket, and
wherein the method further comprises the steps of:
creating an additional small side incision opposite to the small side incision so as to gain entry into the pocket from two sides, thereby simplifying removal of stromal tissue or implantation of the circular implant after removal of the stromal tissue;
inserting two instruments inside the pocket using the two small side incisions, one of the instruments having a sharp edge to separate the stromal tissue from the underlying stroma, and the other one of the instruments holding an edge of the pocket or having two prongs to pull on the stromal tissue for ease of manipulation and removal;
removing the circular or oval-shaped three-dimensional disk with the thickness from the recipient corneal stroma to create more space inside the pocket; and
additionally using the hyaluronic acid for correcting a refractive error of the eye in the pocket in the recipient cornea of the eye, and smoothening up the bounding wall of the pocket.

7. The method according to claim 1 , wherein the method further comprises the steps of:
injecting a transparent fluid into the pocket in the recipient cornea of the eye, the transparent fluid containing inorganic or organic molecules or monomers that include hyaluronic acid and its modified derivatives, low molecular weight heparin, N-isopropylacrylamide, alginate, thiol, tyramine, collagen, elastin, chondroitin sulfate, hydrogel, photo-crosslinked hydrogel, polyethylene glycol, polyvinyl alcohol, biotin, or combinations thereof, in addition to a photosensitizer and one or more medications, the transparent fluid having a refractive index equal to 1.34 or more for correction of a hyperopic error;
increasing the corneal curvature by pushing an anterior wall of the pocket forward by injecting more of the transparent fluid, or reducing an amount of the transparent fluid to treat a hyperopic refractive error to the desired degree using wavefront technology; and
irradiating the recipient cornea with ultraviolet light to convert the transparent flui

Assignees

• Peyman Gholam A

Inventors

• Peyman Gholam A

Classifications

• A61F9/00831 Primary

  Transplantation · CPC title

• A61L2430/16

  for reconstruction of eye parts, e.g. intraocular lens, cornea · CPC title

• A61F9/0079

  using non-laser electromagnetic radiation, e.g. non-coherent light or microwaves · CPC title

• A61L27/3604

  characterised by the human or animal origin of the biological material, e.g. hair, fascia, fish scales, silk, shellac, pericardium, pleura, renal tissue, amniotic membrane, parenchymal tissue, fetal tissue, muscle tissue, fat tissue, enamel · CPC title

• A61F2009/00872

  Cornea · CPC title