|Publication number||US20030105521 A1|
|Application number||US 10/317,714|
|Publication date||Jun 5, 2003|
|Filing date||Dec 11, 2002|
|Priority date||Jul 18, 2000|
|Also published as||CA2418306A1, CN1243573C, CN1458849A, EP1301223A2, US6544286, US6880558, US20030083743, US20050070942, US20050124982, WO2002006883A2, WO2002006883A3|
|Publication number||10317714, 317714, US 2003/0105521 A1, US 2003/105521 A1, US 20030105521 A1, US 20030105521A1, US 2003105521 A1, US 2003105521A1, US-A1-20030105521, US-A1-2003105521, US2003/0105521A1, US2003/105521A1, US20030105521 A1, US20030105521A1, US2003105521 A1, US2003105521A1|
|Original Assignee||Edward Perez|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (5), Referenced by (7), Classifications (25), Legal Events (1)|
|External Links: USPTO, USPTO Assignment, Espacenet|
 This invention is in the field of ophthalmology. More particularly, it relates to a living contact lens made of donor corneal tissue, to a method of preparing that lens, and to a technique of placing the lens on the eye.
 The visual system allows the eye to focus light rays into meaningful images. The most common problem an ophthalmologist or optometrist will encounter is that of spherical ammetropia, or the formation of an image by the eye which is out of focus with accommodation due to an improperly shaped globe. The ophthalmologist or optometrist determines the refractive status of the eye and corrects the optical error with contact lenses or glasses.
 Many procedures have been developed to correct spherical ammetropia by modifying the shape of the cornea. Light entering the eye is first focused by the cornea, which possesses approximately 75% of the eye's overall refractory power. The majority of refractive operations involve either decreasing or increasing the anterior curvature of the cornea.
 The procedures in early corneal refractive surgery such as keratophakia and keratomileusis were originally developed to correct myopia and involved removing a corneal disc from the patient with a microkeratome. The removed corneal disc was then frozen prior to reshaping the posterior surface with a cryolathe. After thawing, the disc was returned to the eye and secured with sutures.
 Epikeratophakia, as described in U.S. Pat. No. 4,662,881, is a procedure that involves inserting a precut donor corneal tissue lens with bevelled edges into corresponding grooves in recipient cornea. The lens is then sutured to the corneal bed. The donor lens is lyophilized and requires rehydration before placement on recipient cornea.
 These techniques and their variations were generally considered to be unsuccessful due to frequent complications involving irregular astigmatism, delayed surgical healing, corneal scarring, and instability of the refractive result. The problems were attributed to the technical complexity of the procedures as well as to the distortion in architecture of the corneal tissue secondary to lens manipulation. For example, in epikeratophakia, epithelial irregularity is induced by lyophilization of the donor lens. Freezing of the lenticule in keratophakia and keratomileusis also causes severe damage to epithelial and stromal cells and disrupts the lamellar architecture of the cornea.
 The present invention is a pre-fabricated lens made of donor corneal tissue obtained from tissue sources such as human or animal cornea. The lens is a corneal disc that is preferably shaped on the posterior surface generally to conform in shape to the eye's anterior surface. The inventive lens may be shaped by an ablative laser, e.g., by an excimer laser or other suitable laser. The corneal lenticule is living tissue that has not been frozen, lyophilized, or chemically modified, e.g., fixed with glutaraldehyde to crosslink corneal tissue. Pre-existing keratocytes are removed and then replaced with human keratocytes to decrease antigenicity. After removal of epithelium in the central zone of the recipient's cornea, the lens is placed on this zone in the same manner that a contact lens is placed on the eye.
 Ocular lenses found in the prior art do not use native cornea, but are formulated using soluble collagen such as collagen hydrogels, e.g., polyhydroxyethylmethacrylate, or other biocompatible materials. For example, in U.S. Pat. No. 5,213,720, to Civerchia, soluble collagen is gelled and crosslinked to produce an artificial lens. In addition to hydrogels, U.S. Pat. No. 4,715,858, to Lindstrom, discloses lenses made from various polymers, silicone, and cellulose acetate butyrate.
 In the cases where ocular lenses use corneal tissue, the lenses are either corneal implants or require a separate agent to adhere the lens to the corneal bed. U.S. Pat. No. 5,171,318, to Gibson et al., and U.S. Pat. No. 5,919,185, to Peyman, relate to a disc of corneal tissue that is partially or entirely embedded in stroma. The ocular lens device disclosed in U.S. Pat. No. 4,646,720, to Peyman et al., and U.S. Pat. No. 5,192,316, to Ting, is attached to recipient cornea with sutures. The corneal inlay described in U.S. Pat. No. 4,676,790, to Kern, is bonded to recipient cornea using sutures, laser welding, or application of a liquid adhesive or crosslinking solution.
 The ocular lens device of this invention does not alter the anatomical structure of corneal tissue. U.S. Pat. No. 4,346,482, to Tennant et al., discloses a “living contact lens” consisting of donor cornea that has been anteriorly curved for correction of vision. However, this lens is frozen prior to reshaping on a lathe which results in stromal keratocyte death. U.S. Pat. No. 4,793,344, to Cumming et al., also describes a donor corneal tissue lens that is modified by treatment with a gluteraldehyde fixative that preserves the tissue and prevents lens swelling. This treatment alters the basic structure of the corneal lenticule by crosslinking the tissue.
 Furthermore, the cited documents do not show any methods of lens preparation that remove native corneal tissue cells and replace them with cells cultivated from human cornea. My inventive device is devitalized of native epithelium and keratocytes to create an acellular corneal tissue, and then revitalized with human epithelium and keratocytes. An attempt to construct a so-called “corneal tissue equivalent” was shown in U.S. Pat. No. 5,374,515, to Parenteau et al. However, the collagen used in that “equivalent” is obtained from bovine tendon instead of from cornea. The added keratocytes and epithelium are also not from human sources. The tissue using these cell culturing procedures is also quite fragile.
 An excimer laser is used to reform a cornea via the “laser in situ keratomileusis” (LASIK) procedure. In this technique, an excimer laser is used to perform stromal photoablation of a corneal flap or in situ photoablation of the exposed stromal bed. Studies have shown that the inaccuracy of correction by this procedure may be as much as one diopter from the desired value. Lenses (contacts and spectacles), in contrast, are able to correct within 0.25 diopters of the desired value.
 U.S. Pat. No. 6,036,683, to Jean et al., shows the use of a laser to reshape the cornea. However, the laser changes the native structure of the cornea by irreversibly coagulating collagen. Post-laser relaxation of collagen is not possible with this treatment.
 This invention is a pre-fabricated donor contact lens that adheres to recipient cornea without sutures. The lens preserves the anatomy of normal corneal tissue. The donor lens can be obtained from human and animal sources, is devitalized of native keratocytes and epithelium to create an acellular tissue, and then revitalized with human keratocytes and epithelium to maintain lens viability and decrease antigenicity. The inventive corneal overlay technique may be completed under local anesthesia as well as general anesthesia, and the availability of a precut lens will greatly decrease procedure time, patient cost, and risk of operative complications. The duration of healing will also be reduced due to the implementation of a lens already repopulated with keratocytes.
 This invention is a pre-fabricated ocular contact lens device having a lens core made of donor corneal tissue from tissue sources such as human or animal cornea. The device has a generally convex anterior surface and a concave posterior surface. The stroma portion of the lens core may be repopulated with replaced keratocytes and the anterior surface is preferably covered with a replaced epithelium. The lens core adheres to recipient cornea without sutures.
 The lens core may be variously used to correct astigmatism, myopia, aphakia, and presbyopia. The lens core may be made of transgenic or xenogenic corneal tissue and have a clarity at least 85% of that of human corneal tissue of a corresponding thickness. The lens core is not frozen, lyophilized, or chemically treated with a fixative. However, variations of the device may contain therapeutic agents, growth factors, or immunosuppressive agents.
 Another component of the invention is a method for preparing the lens device. After sharp dissection of a lenticule from donor corneal tissue, the posterior surface is shaped using an ablative laser, such as an excimer laser or other suitable shaping lasers. Native epithelium and keratocytes are removed and then replaced with human epithelium and keratocytes.
 Another portion of the invention is a method of corneal overlay that involves de-epithelialization of a portion of the anterior surface of the recipient cornea and placement of the inventive ocular lens device upon that anterior surface.
FIG. 1 is a superior, cross-sectional view of the eye.
FIG. 2A is a side view of the focusing point in myopia.
FIG. 2B is a side view of a focusing point corrected by flattening the anterior curvature of the cornea.
FIG. 3A is a side, cross-sectional view of a pre-fabricated donor lens.
FIG. 3B is a side, cross-sectional view of a pre-fabricated donor lens suitable for correcting myopia.
FIG. 3C is a side, cross-sectional view of a pre-fabricated donor lens suitable for correcting aphakia.
FIG. 3D is a front view of a pre-fabricated donor lens suitable for bifocal use.
FIG. 3E is a side, cross-sectional view of the FIG. 3C lens positioned away from the cornea of an eye.
FIG. 4A is a side, cross-sectional view of an area of de-epithelialized recipient cornea prepared to receive the optical lens of the present invention.
FIG. 4B is a side, cross-sectional view of the donor lens after placement on recipient cornea.
 The eye is designed to focus light onto specialized receptors in the retina that turn quanta of light energy into nerve action potentials. As shown in FIG. 1, light rays are first transmitted through the cornea (100) of the eye. The cornea is transparent due to the highly organized structure of its collagen fibrils. The margins of the cornea merge with a tough fibrocollagenous sclera (102) and is referred to as the corneo-scleral layer.
 The cornea (100) is the portion of the corneo-scleral layer enclosing the anterior one-sixth of the eye. The smooth curvature of the cornea is the major focusing power of images on the retina (104) and it provides much of the eye's 60 diopters of converging power. The cornea is an avascular structure and is sustained by diffusion of nutrients and oxygen from the aqueous humor (106). Some oxygen is also derived from the external environment. The avascular nature of the cornea decreases the immunogenicity of the tissue, increasing the success rate of corneal transplants.
 The cornea consists of five layers. The outer surface is lined by stratified squamous epithelium which is about 5 cells thick. Failure of epithelialization results in necrosis of the stromal cap and potential scarring of recipient cornea. The epithelium is supported by a specialized basement membrane known as Bowman's membrane, which gives the cornea a smooth optical surface. The bulk of the cornea, the substantia propria (stroma), consists of a highly regular form of dense collagenous connective tissue forming thin lamellae. Between the lamellae are spindle-shaped keratocytes which can be stimulated to synthesize components of the connective tissue. The inner surface of the cornea is lined by a layer of flattened endothelial cells which are supported by Descemet's membrane, a very thick elastic basement membrane.
 As previously mentioned, the focusing power of the cornea is primarily dependent on the radius of curvature of its external surface. In myopia, as seen in FIG. 2A, increased curvature of the cornea (200) causes the focusing point of light rays (202) to fall short of the retina (204). In FIG. 2B, flattening the anterior curvature of the cornea (206) corrects the focal point (208).
 Inventive Lens Structure
 The inventive contact lens is of a size and configuration that upon installation on the cornea, supplements the curvature of the cornea to correct conditions such as astigmatism, myopia, hyperopia, presbyopia, and aphakia. The lens core may comprise or consist essentially of acellular donor corneal tissue which has been revitalized and then placed on a de-epithelialized host cornea; the lens core is formed to correct refraction. The donor lenticule or lens core may be obtained from other human (allogeneic) or foreign tissue (xenogenic) sources, such as from rabbit, bovine, porcine, or guinea pig corneal tissue. Ocular lenses may also come from transgenic corneal tissue or corneal tissue grown in vitro. In all instances, the architecture of the corneal layers, the normal corneal tissue matrix, e.g., the connective tissue or the stroma, is preserved. The “corneal tissue matrix” is made up of thin layers of collagen fibrils. By the term “donor corneal tissue”, as used here, is meant donor or harvested corneas or corneal tissue containing the “corneal tissue matrix”. Additionally, it is highly desirable to preserve the anterior surface of the donated corneal tissue as found beneath the native epithelium. The donor corneal tissue is not to undergo treatments such as lyophilization, freezing, or other chemical fixation.
 The ocular lens device of this invention desirably includes Bowman's membrane, where the donor tissue includes it, to maintain the native structure of human epithelium. Again, it is highly desirable to harvest from donor sources in such a way that the native anterior surface below the epithelium is preserved. I have found that these native structures have a superior ability, after the revitalization steps discussed below, to support and maintain the replaced epithelium also discussed below. Clarity of the inventive tissue lens core will be at least 85%, preferably between 75%-100%, and most preferably at least 90% of that of human corneal tissue of corresponding thickness.
 The overall diameter of the inventive lens is generally less than about 25 mm and more preferably in between 10 and 15 mm. The thickness of the resulting lens is generally less than 300 μm, more preferably between 5-100 μm.
 As shown in FIG. 3B, a lens core (316) for myopic patients is formed, preferably using the procedures discussed below, in such a way that a generally circular region (318) in the center flattens its anterior curvature. In correction of aphakia, a lens such as is shown in FIG. 3C is formed having a comparatively thicked center (322) and a thinner perimeter (324). In general, the shapes discussed here are similar to those found in the so-called “soft” contact lenses and instruction may be had from that technology relating to the overall form of the lenses selected for correcting specific ocular maladies.
 As shown in FIGS. 3D and 3E, the inventive lens may also be used to correct presbyopia. In particular, to treat presbyopia, the lens (330) is also provided with an generally opaque annular region (332) in the center. The open center (334) preferably has plano-lens characteristics and an effective diameter of less than about 1.5 mm, preferably between about 0.5-1.5 mm, and most preferably between 0.75 mm and 1.75 mm. The diameter of the central area or “pinhole” is generally formed to be less than the pupillary diameter of the eye in daylight. This creates a “pin-hole” effect, thereby lengthening the overall focal length of the eye and minimizing the need for the eye to accommodate. Other bifocal lens designs can also be incorporated, e.g., concentric, segmented, or progressive diffractive.
FIG. 3E shows a side, cross-sectional view of the inventive lens (330) adjacent the anterior surface of a cornea (344) to illustrate certain features of this variation. The outer diameter (336) of the opaque annular ring (332) is generally selected so that it is smaller than the diameter (338) of the pupil (340) in the iris (342) in low light conditions. In this way, the eye's cornea and lens and the inventive lens cooperate in such a way that incident light passes both though the center of the opaque ring (334), but more importantly, around the periphery of the opaque ring (332), to allow corrected sight during low light conditions.
 The annular ring may be situated on the lens core either by placement of a suitable dye, i.e., by “tattooing”, or by placement of an opaque biocompatible member of, e.g., Dacron mesh or the like, on the posterior surface to filter light rays.
 Shaping Step
 Returning to FIG. 3A, the donor ocular lens (300) desirably is obtained after slicing corneal tissue from the donor with a microkeratome to form a lens core. The donor lens has a structural surface, the anterior surface of the lens core being the structural surface of the donor corneal tissue. The lens core anterior surface is harvested preferably to retain the Bowman's membrane (where the donor lens contains one) and epithelium (302). The posterior surface (304) of the resulting inventive lens is generally concave in shape. It is made so by a shaping step which preferably involves the use of an ablative laser, such as an excimer laser, to obtain the necessary power of the lens. Another suitable forming step is high pressure water jet cutting.
 Sterilization, Devitalization, and Revitalization Steps
 Although the order of the process steps outlined below is typical, it should be understood that such steps may be varied as needed to produce the desired result.
 Generally, the lens will first be shaped to an appropriate shape as discussed above. The lens core may then be subjected to processes of sterilization, devitalization, and revitalization. Removal of epithelium (de-epithelialization) and keratocytes (acellularization) from the donor lens will be referred to as “devitalization”. The addition of human epithelium and keratocytes will be referred to as “revitalization”. One desirable method for accomplishing those steps is found just below. Other methods are known.
 Phosphate buffered saline (PBS) with antibiotics, epithelial cell media, and keratocyte media are solutions used during these processes. The “PBS with antibiotics” solution may contain:
 PBS with antibiotics
 1. Amphotericin B (ICN Biomedicals) 0.625 μg/ml
 2. Penicillin (Gibco BRL) 100 IU/ml
 3. Streptomycin (Gibco BRL) 100 μg/ml
 4. Phosphate buffered saline (Gibco BRL)
 The composition of the epithelial cell media may include:
 Epithelial cell media
 1. Dulbecco's Modified Eagle Media/Ham's F12 media (Gibco BRL) 3:1
 2. 10% fetal calf serum (Gibco BRL)
 3. Epidermal growth factor (ICN Biomedicals) 10 ng/ml
 4. Hydrocortisone (Sigma-Aldrich) 0.4 μg/ml
 5. Cholera toxin (ICN Biomedicals) 10−10 M
 6. Adenine (Sigma-Aldrich) 1.8×10−4 M
 7. Insulin (ICN Biomedicals) 5 μg/ml
 8. Transferrin (ICN Biomedicals) 5 μg/ml
 9. Glutamine (Sigma-Aldrich) 2×10−3 M
 10. Triiodothyronine (ICN Biomedicals) 2×10−7 M
 11. Amphotericin B (ICN Biomedicals) 0.625 μg/ml
 12. Penicillin (Gibco BRL) 100 IU/ml
 13. Streptomycin (Gibco BRL) 100 μg/ml
 The composition of the keratocyte media may include:
 Keratocyte media
 1. DMEM
 2. 10% neonatal calf serum (Gibco BRL)
 3. Glutamine (Sigma-Aldrich) 2×10−3 M
 4. Amphotericin B (ICN Biomedicals) 0.625 μg/ml
 Sterilization Step
 After harvesting the lens core from donor corneal tissue and following the shaping step, the lens may be sterilized by immersion into 98% glycerol at room temperature. Three weeks of glycerol treatment inactivates intracellular viruses and any bacteria or fungi. Ethylene oxide gas sterilization may also be used, but tends to induce variable damage to stromal tissue.
 Devitalization Step
 Following sterilization, I prefer to de-epithelialize the donor lens by placing it in sterile PBS with antibiotics for four hours and changing the solution many times. The lens core may then be kept submerged in the PBS solution at 37° C. for one week to produce a split between the epithelium and the stroma. The epithelium may then be removed, e.g., by physically scraping or washing with a liquid stream. Small numbers of lenses may be stripped of epithelium by gentle scraping with forceps.
 The de-epithelialized lens may then be immersed in sterile PBS with antibiotics for an appropriate period, e.g., several weeks, perhaps six weeks to remove native keratocytes. The solution may be changed twice weekly. In some instances, it may not be necessary to remove keratocytes from the donor lens, e.g., when the donor tissue is obtained from a transgenic source and has minimal antigenicity.
 Revitalization Step
 Preparation of Cells
 Human epithelial cells and keratocytes are used in the revitalization process. Epithelial cells may be obtained from a tissue bank, but are preferably obtained from fetal or neonatal tissue. Fetal cells are most preferable, since the properties of fetal tissue minimize scarring during the wound healing process.
 In any event, freshly isolated epithelial cells, obtained by trypsinization of corneal tissue, may be seeded onto a precoated feeder layer of lethally irradiated 3T3 fibroblasts (i.3T3) in epithelial cell media. Cells are cultured and media changed every three days until the cells are 80% confluent, about 7-9 days. Residual i.3T3 are removed with 0.02% EDTA (Sigma-Aldrich) before the epithelial cells are detached using trypsin (ICN Biomedicals). Another method of regenerating epithelium involves culturing autologous epithelial cells on human amniotic membrane as described in Tsai et al. (2000). “Reconstruction of Damaged Corneas by Transplantation of Autologous Limbal Epithelial Cells,” New England Journal of Medicine 343:86-93.
 Keratocytes may be extracted from the remaining stromal tissue. The stroma is washed in PBS, finely minced, and placed in 0.5% collagenase A (ICN Biomedicals) at 37° C. for 16 hours. Keratocytes obtained from this enzyme digest are then serially cultured in keratocyte media. The epithelial cells and keratocytes generated in the revitalization step will be referred to as “replaced” epithelium and keratocytes.
 Production of the Donor Lens
 The acellular donor lens core may then be placed on a hydophilic, polyelectrolyte gel for completion of the re-vitalization. The preferred polyelectrolytes are chondroitin sulfate, hyaluronic acid, and polyacrylamide. Most preferred is polyacrylic acid. The lens is immersed in keratocyte media and incubated with approximately 3×105 keratocytes for 48 hours at 37° C. Approximately the same amount of epithelial cells are then added to the anterior stromal surface. Tissue culture incubation continues for another 48 hours. Keratocyte media is changed every two to three days. Once the epithelium is regenerated, the polyelectrolyte gel draws water out of the lens at a pressure of about 20-30 mm Hg until the original lens dimensions are obtained.
 Replaced epithelium covers at least a portion of the anterior surface and replaced keratocytes repopulate the stroma of the lens core after revitalization. It may be beneficial in some instances to incorporate therapeutic agents, growth factors, or immunosuppressive agents into the lens core to further decrease the risk of rejection or remedy disease states.
 Placement of the Lens on the Eye
 During the procedure, the donor lens (300) is placed on a portion of recipient cornea that has been de-epithelialized (308). The result is the construct (312) shown in FIG. 4B. The lens' replaced epithelium and the host epithelium eventually grow to form a continuous, water-tight layer (310). I have found that the inventive lens bonds to recipient cornea without sutures or adhesives, but can also be removed without substantial difficulty.
 I have described the structural and physiologic properties and benefits of this donor ocular lens. This manner of describing the invention should not, however, be taken as limiting the scope of the invention in any way.
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|Citing Patent||Filing date||Publication date||Applicant||Title|
|US7497866||Jan 17, 2003||Mar 3, 2009||Tissue Engineering Refraction Inc.||Methods for producing epithelial flaps on the cornea and for placement of ocular devices and lenses beneath an epithelial flap or membrane, epithelial delaminating devices, and structures of epithelium and ocular devices and lenses|
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|US7828844 *||Sep 12, 2003||Nov 9, 2010||Forsight Labs, Llc||Inserting lenses into corneal epithelial pockets to improve vision|
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|US8858624||May 3, 2006||Oct 14, 2014||Acufocus, Inc.||Method for increasing the depth of focus of a patient|
|US20050070942 *||Oct 1, 2004||Mar 31, 2005||Edward Perez||Device for lifting an epitheleal layer and placing a corrective lens beneath it|
|US20050288696 *||Oct 22, 2004||Dec 29, 2005||Pallikaris Ioannis G||Device for separating the epithelial layer from the surface of the cornea of an eye|
|U.S. Classification||351/159.07, 623/906, 351/159.46, 351/159.51|
|International Classification||A61L27/00, A61L27/36, A61F2/16, A61F9/007, G02C7/04, A61F2/14|
|Cooperative Classification||A61F2/142, A61L2430/16, A61L27/3641, A61L27/3604, A61L27/3813, A61F2/145, A61L27/3839, A61L27/3683|
|European Classification||A61L27/38B4, A61L27/36B, A61L27/36H, A61L27/36F, A61L27/38D, A61F2/14E, A61F2/14C|
|Nov 9, 2006||AS||Assignment|
Owner name: TISSUE ENGINEERING REFRACTION, INC., CALIFORNIA
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:PEREZ, EDWARD;REEL/FRAME:018501/0411
Effective date: 20060302