WO2019147901A2

WO2019147901A2 - Methods, computer-readable media, and systems for treating a cornea

Info

Publication number: WO2019147901A2
Application number: PCT/US2019/015095
Authority: WO
Inventors: Sinisa VUKELIC
Original assignee: The Trustees Of Columbia University In The City Of New York
Priority date: 2018-01-26
Filing date: 2019-01-25
Publication date: 2019-08-01
Also published as: WO2019147901A3; EP3743026A2; US20200352786A1; CN111836604A; EP3743026A4

Abstract

One aspect of the invention provides a method of treating a cornea. The method includes controlling a light source to apply light energy pulses to a single corneal layer selected from the group consisting of: an anterior corneal layer and a posterior corneal layer. The light energy pulses are below an optical breakdown threshold for the cornea and ionize water molecules within the treated corneal layer to generate reactive oxygen species that cross-link collagen within the single corneal layer. Another aspect of the invention provides a method of treating a cornea. The method includes controlling a light source to apply light energy pulses to at least a corneal stroma layer of a cornea. The light energy pulses are below an optical breakdown threshold for the cornea and ionize water molecules within the treated corneal stromal layer to generate reactive oxygen species that cross-link collagen within the cornea.

Description

METHODS, COMPUTER-READABLE MEDIA, AND SYSTEMS

FOR TREATING A CORNEA

CROSS-REFERENCE TO RELATED APPLICATION

Tills application claims the benefit of priority to U.S. Provisional Patent Application Serial No. 62/622,471 , filed January' 26, 2018. The entire content of this application is hereby incorporated by reference herein.

BACKGROUND OF THE INVENTION

Collagen is an abundant protein in animals. The mechanical properties and structural stability of collagen based tissues, such as comeal tissue, can be influenced by increasing collagen cross-links (CXL), in the form of intra- or inter-molecule chemical bonds.

SUMMARY OF THE INVENTION

One aspect of the invention provides a method of treating a cornea. The method includes controlling a light source to apply light energy pulses to a single comeal layer selected from the group consisting of: an anterior corneal layer and a posterior comeal layer. The light energy pulses: are below an optical breakdown threshold for the cornea; and ionize water molecules within the treated corneal layer to generate reactive oxygen species that cross-link collagen within the single comeal layer.

This aspect of the invention can have a variety of embodiments. The anterior comeal layer can extend between an anterior surface of the cornea and about 200 microns from the anterior surface. The posterior corneal layer can extend between a posterior surface of the cornea and about 200 microns from the posterior surface.

Another aspect of the invention provides a method of treating a cornea. Hie method includes controlling a light source to apply light energy pulses to at least a comeal stroma layer of a cornea. The light energy pulses: are below an optical breakdown threshold for the cornea; and ionize water molecules ithin the treated corneal stromal layer to generate reactive oxygen species that cross-link collagen within the cornea.

These aspects can have a variety of embodiments. Hie light source can be a laser. The laser can be a femtosecond laser.

The light energy pulses can have an average power output between about 10 mW and about 100 W. The light energy pulses can have a pulse energy between about 0.1 nJ and about 10 nJ. The light energy pulses can have a wavelength between about 600 nm and

- I - about 1600 nm . The light energy pulses can have a wavelength that is not absorbed by amino acids in collagen.

The light energy pulses can be applied in a pattern. The pattern can extend across a center of an iris posterior to the cornea. The pattern can surround, but not extend across a center of an iris posterior to the cornea.

The method can treat keratoconus or alter curvature of the cornea.

Another aspect of the invention provides a system for treating a cornea. The system includes: a light source configured to project light energy pulses onto at least a portion of a cornea; and a controller programmed to control the light source in accordance with any of the methods described herein.

Another aspect of the invention provides a system for adapting a laser system for treating a cornea. The system includes: laser modification optics adapted and configured to adjust laser output of the laser system: and a controller programmed to control the laser modification optics as the light source in accordance with any of the methods described herein.

BRIEF DESCRIPTION OF THE DRAWINGS

For a fuller understanding of the nature and desired objects of the present invention, reference is made to the following detailed description taken in conjunction with the accompanying drawing figures wherein like reference characters denote corresponding parts throughout the several views.

FIG. I illustrates a flow diagram of a cross-linking process applied to the cornea according to an embodiment of the invention.

FIGS. 2A and 2B are schematics illustrating a mechanism of action according to an embodiment of the invention.

FIGS. 3A-3D depict systems (FIG. 3A), topography controls (FIG. 3B), and multiple beam architectures (FIGS. 3C and 3D) for treating a cornea according to embodiments of the invention.

FIGS. 4A-4C depict the time course of the change in normalized effecti ve refractive power (EFR) after the laser treatment of porcine eyes ex vivo. FIG. 4A depicts a flattening treatment (e.g., for myopia). FIG 4B depicts a steepening treatment (e.g., for hyperopia). FIG. 4C depicts a control study analyzing the effects of the treatment protocol. The treatment involves applying laser pulses such that the path of the laser follows a zigzag trajectory, thus treating a planar area at a specific depth. The treatment is repeated at different depths, effectively inducing multiple '‘treatment layers^”'. Multiple treatment layers parallel to the superficial surface were created, with a distance of 50 pm between consecutive planes. The y axis corresponds to effective refractive power normalized against diopter (D) values before treatment. Changes in the refractive power of the eye relative to the measurement performed immediately before treatment are shown. The error bars indicate the standard deviation.

FIGS. 5A and 5B depict comeal topography of isolated porcine eyes (FIG. 5A) before and (FIG. 5B) after laser treatment.

FIGS. 5C and 5D depict results shown paired with virtual vision in FIG. 5C and FIG. 5D to demonstrate the effects of the refractive error correction applied. The comeal elevation maps show effective refractive powers of 45 diopters before and 43.5 diopters after treatment. The virtual vision for the comeal effective refractive powers shown corresponds to 45 diopters in FIG. 5C and 43.5 diopters FIG. 5D, assuming that 43.5 diopters corresponds to a visual acuity of 20/20 (normal vision).

FIG. 6 depicts isolated rabbit eyes in 3D-printed holders connected with an IV pressure control system.

FIG. 7A depicts an experimental set-up. FIG. 7B depicts a treatment system according to an embodiment of the invention.

FIG. 8 depicts a laser treatment pattern according to an embodiment of the invention. Five mutually independent layers were treated with 50 pm in between two layers and each layer was treated through a zigzag path.

FIGS. 9A-9C depict time-histories of the change in normalized effective refractive power (EFR) after the laser treatment of porcine eyes ex vivo for treatment from anterior surface (FIG. 9A), treatment from posterior surface (FIG. 9B), and control treatment (FIG. 9C). Treatment consists of applying laser pulses such that the laser path follows a zigzag pattern, thus treating a planar surface at the specific depth. The treatment is repeated at different depths, effectively inducing‘treatment layers”. Multiple treatment layers parallel to the superficial surface were applied with 50 pin distance between two consecutive planes.

FIGS. 10A-C illustrate two-photon fluorescence (TPF) images of (a) untreated control, (b) anterior laser treated, and (c) posterior laser treated cross sections of ex vivo rabbit eyes. The central zone of the untreated control or laser irradiated comeal tissues were imaged. The control sample and the untreated region of the laser irradiated specimen show* approximately the same properties. Three different intensity lines were drawn through the whole corneal thickness (location indicated as three arrows in FIGS. 10A-C). FIG. 11 is a chart of the average gray value for intensity lines of the three groups in FIG. 10. The chart clearly illustrated the treatment-induced intensity change. The anterior treated group showed an increased intensity from superficial surface to a depth around 200 pm, and the posterior treated group showed a similar trend from the bottom surface to a depth around 200 pin in the cornea, whereas the untreated control group presented a relatively stable signal intensity throughout the whole corneal thickness. Boxed regions in FIGS. 10A- C indicated the histogram acquirements for each group.

FIG. 12 depicts the average pixel value for all the three groups from FIG. 10.

FIGS. 13A-13C depict histological sections of H&E-stained samples of untreated control (FIG. 13 A), anterior treated (FIG. 13B), and posterior treated (FIG. 13C) rabbit corneas. The scale bar is 100 pm.

FIGS. 14A-14F provide representative CLSM (Confocal Laser Scanning Microscopy) images of the ex vivo untreated control (FIGS. 14A and 14D), anterior laser treated (FIGS. 14B and 14E) and posterior treated (FIGS. 14C and 14F) rabbit eyes. The scale bar is 100 p .

DEFINITIONS

The instant invention is most clearly understood with reference to the following definitions.

As used herein, the singular form‘a,”“an,” and“the” include plural references unless the context clearly dictates otherwise.

Unless specifically stated or obvious from context, as used herein, the term“about” is understood as within a range of normal tolerance in the art, for example within 2 standard deviations of the mean.“About” can be understood as within 10%, 9%, 8%, 7%, 6%, 5%, 4%, 3%, 2%, 1%, 0.5%, 0.1%, 0.05%, or 0.01% of the stated value. Unless otherwise clear from context, all numerical values provided herein are modified by the term about.

As used in the specification and claims, the terms“comprises,”“comprising,” “containing,”“having,” and the like can have the meaning ascribed to them in U.S. patent law and can mean“includes,”‘including,” and the like.

Unless specifically stated or obvious from context, the term“or,” as used herein, is understood to be inclusive.

Ranges provided herein are understood to be shorthand for all of the values within the range. For example, a range of 1 to 50 is understood to include any number, combination of numbers, or sub-range from the group consisting 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21 , 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, or 50 (as well as fractions thereof unless the context dearly dictates otherwise).

DETAILED DESCRIPTION OF THE INVENTION

Embodiments of the invention provide methods, computer-readable media, and systems for treating a cornea by applying light to a single comeal layer. Other embodiments of the invention provide methods, computer-readable media, and systems for treating a cornea by applying light to the comeal stroma (exclusively or in addition to other comeal layers).

Referring now to FIG. 1, an example of a method of inducing cross-linking in corneal tissue is shown. In step S 101 , the topography of the patient’s cornea can be measured. In step SI 02, the desired cornea geometry' can be computed. In some embodiments, the goal may to strengthen the cornea without changing its shape. In this case, step S102 can compute the desired locations to strengthen without changing the corneal shape. In an embodiment, a coupling mechanism can be placed over the eye to be treated in step SI 03. However, this method is not limited to such embodiments, and the cornea can be treated without a coupling mechanism. In step SI 04, a light source can be driven to emit low' energy pulses that are guided and focused as discussed herein. As shown in step S 105, the interaction of the pulse laser with the aqueous medium m and around the tissue initiates cross-linking. In step SI 06, a lens of the coupling mechanism (if one was used) is removed from the cornea.

Exemplary Therapies

The methods and systems can be used to treat various corneal disorders including keratoconus, myopia, hyperopia, stigmatism, irregular astigmatism, and other ectatic diseases {e.g., those that result from a weakened corneal stroma). The methods and systems can also be used in refractive surgery, e.g., to modify comeal curvature or correct irregular surfaces and higher-order optical aberrations.

Exemplary Irradiation Parameters

As described in International Publication No. WO 2017/070637 and U.S. Patent Application Publication Nos. 2018/0193188 and 2018/0221201, comeal cross-linking can be achieved without the need for exogenous photosensitizers such as riboflavin by ionizing water within comeal tissue to generate reactive oxygen species that cross-link collagen strands. Cross-linking can be achieved o ver a broad range of wavelengths including those that are not absorbed by amino acids within collagen strands. For example, the laser wavelength can be in the range from about 250 run to about 1600 nm. In some embodiments, the laser wavelength can be in the range from about 250 nm to about 1600 nm, but excluding wavelengths between 260-290 nm, 520-580 nm, 780-870 nm, and 1040-1160 nm.

By controlling pulse energy to be below the optical breakdown threshold of collagen (about 1.0 v 10¹³ W cm ²), the mechanical properties of the collagen can be modified without modifying the refractive index of the collagen. For example, the curvature of the cornea can be modified to change the refractive power of the cornea.

Ionization can be created within tissue using a laser emission that is absorbed by the tissue. For example, the laser emission can be based on ultrashort laser pulses. As used herein, the phrase‘ultrashort laser pulses^’’ includes emissions in the femtosecond, picosecond, and nanosecond ranges. Nonlinear absorption of laser emissions can occur, in part, due to the highly compressed nature of the light pulses, allowing treatments of the interior of a transparent dielectric, such as corneal tissue, without affecting the surface layer.

The ultrashort laser pulse can induce low-density plasma that ionizes water molecules within the tissue, while still operating below the energy level required for optical breakdown. Optical breakdown is the effect of an ultrafast laser focused in the interior of collagen-rich tissue, where photoionization triggers non-linear absorption. Continued supply of incoming photons leads to the buil dup of free electrons, further leading to avalanche ionization, which enhances the growth of free electron density resulting in formation of plasma. As contrasted from the low'-density plasma, high-density, opaque plasma strongly absorbs laser energy through free carrier absorption. The high-density plasma expands rapidly, creating a shock wave that propagates into surrounding material, creating optical breakdown.

Collagen cross-linking can be safely induced when the laser is operated below' optical breakdown level in the so-called“low-density plasma” regime. For example, the laser emission, as defined by its wavelength, temporal pulse width, and pulse energy, as well as the numerical aperture of the scanning objective and the scanning speed should be high enough to induce ionization of water molecules in the collagen rich tissue, but below optical breakdown level. Further, such ionization can be induced in the cornea without reducing the transparency of the cornea.

Without being bound by theory, the ionization can cause the formation of reactive oxygen products, such as singlet oxygen, OH , and H2O2, which, in turn, can interact with collagen and increase cross-linking in the fibrils, as shown in FIGS. 2A and 2B.

Additionally, singlet oxygen generated by the ionization can inactivate col!agenase and have a germicidal effect, increasing the utility of these methods for clinical applications. In embodiments, deuterium oxide can be introduced on to the cornea to prolong half-life of the produced singlet oxygen, thereby increasing cross-linking efficiency.

In certain aspects, the presently disclosed subject matter provides methods of inducing such ionization. The methods can be used in the treatment of various ectatic diseases or during refractive surger . The methods can include modifying the corneal curvature by inducing selective corneal cross-linking.

Exemplary Comeal Lavers

Referring now to FIGS. 10, cross-linking can be spatially resolved to particular layers of the cornea. For example, cross-linking can be limited to an anterior or posterior layer of the cornea. The layers can be defined as within a specified distance of an anterior or posterior surface of the cornea, respectively, e.g., the posterior surface of the eomea epithelium. Exemplary’ layer thicknesses include: about 50 microns, about 100 microns, about 150 microns, about 200 microns, about 250 microns, and the like. This thickness can he measured from the apex of either the anteri or or posterior comeal surfaces, both of which are curved. The posterior layer can include the comeal stroma at the center and/or the periphery’ of the treatment layer.

Exemplary Cross-Linking Patterns

Light energy pulses can be applied in a vari ety of patterns to produce a desired comeal treatment. For example, the curvature of the cornea can be modified to change the refractive power of tire cornea. The applied pattern can be a custom-generated pattern based on imaging of a particular subject’s cornea. However, and without being bound by theory, Applicant describes general principles of cross-linking patterns below.

Comeal curvature can be flattened to reduce the optical power of the cornea by cross- linking in a solid patern that extends over the center of an ins posterior to the cornea.

Corneal curvature can be steepened to increase the optical power of the cornea by cross- linking in a pattern surrounding, but not extending over the center of an iris posterior to the cornea. For example, an un-cross-linked region over the center of the iris can have a cross- sectional dimension of about 4 mm.

Although a square and an annular pattern are depicted in FIGS 4.4-B, respectively, other shapes can be utilized. For example, the cross-linked region and the un-cross-linked region (if any) can approximate a variety of shapes such as circles, ellipses, triangles, quadrilaterals, rectangles, squares, squircles, trapezoids, parallelograms, rhombuses, pentagons, hexagons, heptagons, octagons, nonagons, decagons, n-gons, and the like. Additionally, cross-linking within a pattern can be produced using various sub- patterns within the outline of the pattern. For example, cross-linking can be performed in rows and/or columns that begin and break at the borders of the pattern. In some

embodiments, cross-linking can wrap in a zigzag or serpentine manner from row-to-row. In still other embodiments, the pattern can be a matrix of cross-linked dots (e.g., in a rectangular grid or close-packed pattern). In still other embodiments, cross-linking can occur in lines that follow the pattern. For example, the pulses can form an annulus or spiral.

Also, cross-linking can be performed in multiple overlapping planes within a comeal layer. For example, a plurality of planes (e.g., 2, 3, 4, 5, and the like) can be cross-linked at a depth offset of about 25 pm, about 50 pm, and the like.

As used herein,“planes” can either include the classical geometrical definition as a flat, two-dimensional surface or can refer to a treatment surface having a defined depth from a curved surface or a treatment layer. (In some embodiments, the application of a cover slip to the cornea will flatten or substantially flatten the normally curved cornea.)

Depths can be determined by measuring thickness of the cornea with a pachymeter, then focusing the light energy pulses on desired locations within the cornea.

Exemplary Systems

As shown in FIG. 3 A, an embodiment of the cross-linking system 300 includes an objective 302. The objective can be high-magnification lens (e.g., 40x).

lire objective 302 can be a scanning objective with a large numerical aperture. The large numerical aperture (NA) allows the objective 302 to focus diffuse light to a small area.

A laser 304 supplies the light (e.g., laser light) to the objective 302. In one embodiment, the NA is 0.4. In another embodiment, the numerical aperture is 0.6, with a long working distance. However, the NA could be varied together with the pulse energy to achieve similar effect in a different control volume. Without being bound by theory, Applicant believes that NAs below 0.4, between about 0 4 and about 0.95, above 0.95, and above 1 would be capable of creating low-density plasma without causing optical breakdown.

In an embodiment, one or more optical filters 306 can be interspersed between the laser 304 and the objective 302.

The laser 304 can be a femtosecond laser that outputs laser light. In some embodiments, the laser light has a single frequency, and in other embodiments includes multiple frequencies. Embodiments can use any wavelength including multiple or continuous spectra covering a wide range of wavelengths. In embodiments, radiation at frequencies that may harm tissue or reduce the locality of the generation of reactive species are minimized or eliminated. Radiation that may he directly absorbed by the collagen can be minimized or eliminated, e.g., through filters. In an embodiment, the frequency or frequencies of the laser 304 are outside of the ultraviolet range. In embodiments, the frequency or frequencies of the laser 304 are in the infrared frequency band. The laser 304 receives control input from controls 308, which can be implemented on a stand-alone processing device, e.g., a computer executing software, or as embedded circuitry of the system.

Generation of such short pulses can be achieved with the technique of passive mode locking Tire laser 203 can be any suitable laser type, including bulk lasers, fiber lasers, dye lasers, semiconductor lasers, and oilier types of lasers. In an embodiment, the laser operates in the infrared frequency range. In other embodiments, the lasers may cover a wide range of spectra domain. In embodiments, the disclosed subject matter can be implemented as an add on system to a femtosecond laser system, such as used in certain Lasik systems.

In particular embodiments, the laser can be a Nd: Glass femtosecond laser. In embodiments, the laser wavelength can be in the range from about 250 nm to about 1600 nm. In embodiments, the fem tosecond laser can have a temporal pulse width of from about 20 fs to about 26 ps. In embodiments, the pulse energy is from about 0.1 nJ to 100 nJ, 0.1 nJ to about 50 mΐ, 0.1 nJ to about 10 pj, from about 0.5 nJ to 50 nJ, or from about I nJ to 10 nJ. In embodiments, the femtosecond laser can be a SPIRIT® femtosecond laser in combination with a SPIRIT -NOP A® amplifier (Spectra-Physics, Santa Clara, CA).

As further shown in FIG. 3 A, the objective 302 focuses incoming laser light into a focused beam 310 that irradiates a target. In the example of FIG. 3, the target is corneal tissue 392. The objective 302 may have a large numerical aperture.

Referring still to FIG. 3A, a topography system 312 includes controls 314, which can communicate with controls 308 of the cross-linking system 300. "lire topography system 312 can include a light source 316 and an imaging device 318, such as a camera. The light source 316 projects light to mirror 320 and a device, such as a mask, to produce an illumination pattern 322. The illumination pattern 322 guides the cross-linking system 300 to induce cross-linking in specified locations to produce the desired change in the treated tissue.

Referring to FIG. 3B, additional details of the controls 314 of the topography system 312 are shown. A spatial deformation map 324 spatially defines the deformation of the cornea, winch, when considered with the topography map 326 of the cornea, provides information on where to induce cross-linking.

In embodiments, multiple beams can be provided by splitting a laser beam to multiple scanning objectives. For example, a laser head can include multiple scanning objectives bundled together, as shown in FIGS. 3C and 3D. FIG. 3C illustrates an example of a linear array 328 of objectives 302. FIG. 3D illustrates a two-dimensional array 330 of objectives 302. Although the objectives 302 are illustrated as identical in the drawings, in embodiments different objectives are used at different positions in the array. A high-energy laser beam (e.g. , having a pulse energy of greater than about 10 mΐ) can be split using a beam splitter to send individual laser beams to each scanning objective. Therefore, the number of passes required to fully treat the cornea can be reduced by providing multiple laser beams simultaneously. In embodiments, an entire corneal layer could be treated simultaneously, e.g., by bundling many scanning objectives to the laser head such that only one pass is required. Beams can treat different x-y coordinates and/or can treat different treatment layers simultaneously.

Implementation in Computer-Readable Media and/or Hardware

Hie methods described herein can be readily implemented, m whole or in part, in software that can be stored in computer-readable media for execution by a computer processor. For example, the computer-readable media can be volatile memory (e.g., random access memory and the like) non-volatile memory (e.g., read-only memory, hard disks, floppy disks, magnetic tape, optical discs, paper tape, punch cards, and the like).

Additionally or alternatively, the methods described herein can be implemented in computer hardware such as an application-specific integrated circuit (ASIC).

WORKING EXAMPLES

Working Example 1 - Cross-Linking of Ex Vivo Porcine Eves

A total of 60 fresh pig eyes were used for the study. Fifteen of these eyes underwent comeal flattening, and the treated eyes were paired with 10 control eyes. Thirteen eyes underwent laser irradiation to induce post-treatment steepening; these eyes were also paired with 10 control eyes. The remaining 12 eyes were used for a separate control study, to evaluate the effects of the experimental setup.

For the flattening treatment (FIG. 4A), a square in the middle of the eye was treated. A strong change in corneal curvature, corresponding to a change in refractive pow'er of about 12% (about 5.1 1 diopters on average), was initially observed, followed by partial recovery. Most of the change in curvature occurred within eight hours of treatment, after which the cornea stabilized at a refractive power about 92% the initial level (about 3.45 diopters on average). This significant change became evident when comeal topography before and after

- 1 G - treatment was paired with the corresponding virtual vision, demonstrating the effects of the correction of refractive errors applied (FIG. 5).

The initially large change refractive power is due to a combination of the effects of the treatment itself and experimental conditions, which include temporary fl attening of the cornea with a coverslip to ensure even volumetric exposure of the stroma to laser irradiation. The coverslip has an effect analogous to that of orthokeratology (ortho-K), a temporary reshaping of the cornea used to reduce refractive errors, and the duration of the effect is similar to that of an ortho-K procedure.

Once the coverslip effect wears off, the adjusted curvature remains stable throughout the rest of the 24-hour period. By contrast, laser treatment of the peripheral zone of the cornea leads to its steepening (FIG. 4B). The effective refractive power of pig eyes is significantly increased by treatment of a ring-shaped region. In the case of corneal steepening, the effective power of tire eye increases gradually over a 12 -hour period, after which it stabilizes at a new value higher than that before treatment. This indicates that the induction of new CxLs counteracts the influence of the cover slip. For confirmation that the induced changes were photochemical in nature, with no influence of the thermal denaturation of collagen fibrils, Applicant measured the laser-induced changes in comeal temperature. The relative change in temperature at the focal volume and in its immediate vicinity was less than 7°C. The heating induced by the treatment was, therefore, well below the threshold for the thermal denaturation of collagen. Furthermore, light microscopy with a microscope equipped with Nomarski interference contrast optics revealed no difference in refractive index between the treated and untreated parts of the cornea, consistent with an absence of comeal hazing. Working Example 2 - Spatially Resolved Alterations of Rabbit Eves Ex Vivo

Ex vivo rabbit eyes for the experiments were delivered to the lab as intact rabbit heads from a local abattoir (La Granja Live Poultry Corporation, New⁷ York, NY) within an hour after being euthanized. Eyes were isolated, rinsed with Dulbecco’s phosphate-buffered saline (DPBS, 1 ^c, Sigma-Aldrich), inspected for presence of defects and gradually brought to room temperature in a humidified chamber. Defective samples were discarded. After removing excess tissue, the eye globe was mounted onto a custom-built eye holder (FIG. 6). In order to maintain tire eye pressure (-16 mm Hg), an intravenous (IV) system filled with the 0.9% sodium chloride solution (Hospira Inc.) was attached to the eyeball via 22G injection needle (BD). A customized digital pressure gauge (OMEGA™ PX154) was applied to adjust the pressure level. Comeal thickness was measured by a DGH™ PACHETTE™ 2 Pachymeter (DGH Technology, Inc.). Before treatment, the comeal surface was covered with a microscope cover glass (#1 Microscope Cover Glasses, VWR) to ensure even volumetric treatment of the cornea and reduce light scattering.

A Nd:Giass femtosecond laser oscillator system (HIGH Q LASER™, Spectra- Physics) was applied to generate laser pulses with temporal pulse width of 99 fs and 52.06 MHz repetition rate at 1060 nm wavelength. A ZEISS® PLAN-NEOFLUAR® 40x/0.6 objective lens was employed to focus the beam, and tire average pulse energy and photon energy produced by the proposed lasing system are 60 mW and 1.1696 e V respectively after the objective lens. Tire laser beam was motorized by Z825B motors (Thorlahs) through a 3- dimensional PT1 translation stage (Thorlabs). Schematic diagram shows a femtosecond laser optical system set up in FIGS. 7A and 7B. Hie laser beam as initially focused on the superficial surface of the cornea. Laser pulses were del ivered within a 25 mm² square via zigzag motion of the focused beam at 2.2 nirn/s feedrate. Multiple planes parallel to the corneal surface were treated with 50 pm distance between two consecutive planes.

Schemati c diagrams of treatment paths are shown in FIG. 8. Two treatment patterns were applied in the study to show the selective spatial treatment ability. Tire anterior treatment pattern utilized the treatment from the superficial surface to the central cornea. Hie posterior treatment pattern employed the treatment from the central cornea to the endothelium layer by applying a subtraction of the corneal. A paired control eye was placed on the same stage for every treatment. After the treatment, the cover glass was carefully removed.

Topographic refractive power measurement of an entire corneal area by an EYESYS® VISTA™ non-contact eye-topographer (EyeSys Vision Inc.) was performed before and every 3 hours during the 24 hours period after the application of the laser treatment, to assess the effect of laser light-induced corneal crosslinking and reshaping. After topographic characterization the corneal tissue was isolated form eye globe and prepared for confocal imaging and two photon autofluorescence (TPF) imaging. The cornea, retina, and lens were isolated, fixed with 10% formalin overnight and desorbed with 70% ethanol for 24 hrs prior to histology staining. Histology staining was performed by Columbia Medical Center Histology Service. Briefly, samples were embedded in paraffin wax and cut into 5 pm thickness slices through cross section and stained with hematoxylin and eosin. Histological slices were imaged by a VHX 5000 digital microscope (Keyence Corporation, NJ) and processed by IMAGE J™ software.

Confocal Laser Scanning Microscopy (CLSM)

Referring now to FIGS. 14A-14F, CLSM was employed for cellular evaluations of comeal tissues. CLSM imaging was performed with the HRT3-RCM laser scanning system (670 nm laser beam, Heidelberg Engineering) equipped with a 63^c/0.95 NA water immersion objective (Zeiss). A disposable sterile plastic cap was placed on the objective to maintain the distance between the corneal surface and the objective. GENTEAL™ water-based gel was applied as a coupling medium. Imaging was characterized before and immediately after the laser irradiation. The entire comeal volume was scanned and recorded, with optical sections through the epithelium, stroma, and endothelium.

The images show no evidence of negative effects of the applied femtosecond laser treatment on the cellular component of the rabbit cornea. In the cases of the anterior and the posterior application of the treatment, CLSM shows no significant differences in the morphology or cellular density of the stromal keratocytes and endothelium layers comparing to the untreated control. These prelim inary results could contribute to the evidence of safe application of the tested laser irradiation for vision corrections.

Two-Photon Fluorescence (TPF) Microscopy

isolated untreated control and laser treated comeal samples were cut into 2 mm² blocks by a customized sheer and mounted by 50% glycerol in PBS a 3 mm Petri dish filled with PBS solution. TPF was conducted by a two-photon microscope (Broker) with MAI TAI™ DEEPSEE™ Ti: Sapphire laser (Spectra Physics) as the excitation source. A 40x/0.8 NA water immersion objective (Olympus) was applied to collect the fluorescence signal. Tire signal was registered with two different photomultiplier tubes, one in the red (580-620 nm) and one in the green (480-570 nm) wavelength regime. Excitation wavelengths used were 826 nm to excite collagen matrix

Results and Discussion

Due to the nature of the delivery of concentrated nonlinear laser energy, the alteration of refractive power is spatially resolved and, thus, controllable. This may be particularly applied for the treatment of selective volumetric regions of comeal tissue that yields macroscopic changes in overall corneal curvature, which can be utilized for selectively treatment of myopia, hyperopia, stigmatism and irregular astigmatism. In order to show the spatial resolution of the proposed treatment, two treatment patterns were employ ed in this study. The anterior treatment pattern utilized the treatment from the superficial surface to the central cornea, and the posterior treatment pattern applied the treatment from the central cornea to the endothelium layer.

A total of 47 eyes were applied in this study. 20 eyes were subjected to anterior treatment, whereas 8 eyes were exposed to the posterior treatment. Treated samples were properly paired with untreated control eyes. The remaining 8 eyes were used as untreated control eyes to evaluate the experimental setup.

For the anterior treatment pattern, initially a steep change in corneal curvature, corresponding to an approximate 7.1% change in the overall refractive power (about 3.5 diopters on average), is followed by a partial recovery. The major curvature change occurs within 8 hours from the treatment, after which the comeal refractive power stabilizes at about 94.5% of its initial refractive power before the treatment (about 2.7 diopters on average). The relative significan t change of corneal refractive power is further evident by the paired untreated control eyes, which showed approximately no change of refractive power over the 24 hours characterization period (FIG. 9C). Initially, the major change in refractive power is attributed to the superposition of the treatment itself and the temporary fl attening of the cornea by the appearance of a cover slip. The duration of the coverslip effect is comparable to the clinical orthokeratology (ortho-K) operation. After the cover slip wears off, the adjusted curvature remains stable throughout the remainder of the 24 hours period. The NLO- HRMac imaging of three-dimensional collagen organization of the rabbit cornea showed the bulk of the rabbit cornea exhibits a parallel arrangement of collagen fibers, with collagen intertwining present only in the anterior aspect. Thus, theoretically, tire treatment of posterior region and anterior region should not be the same. However, the posterior treatment leads to a similar effect as the anterior treatment by the proposed laser irradiation (FIG. 9B). Tins may demonstrate that the newly formed CxLs are dominating the overall refractive power adjustment, and the introduction of CxLs by the proposed method may not be dependent on the orientation of comeal collagen. Initially, a steep change in comeal curvature corresponds to an approximate 12% change in refractive power (about 5.7 diopters on average), which is followed by a partial recovery. The most curvature change also occurs within 8 hours from the treatment, after which the cornea stabilizes at about 94.7% of its initial refractive power (about 2.55 diopters on average).

Two-photon autofluorescence (TPF) identifies fibrillar collagen in response to near- infrared laser light excitation. Thus, TPF imaging is employed to evaluate the laser induced CxLs in the cornea. The collagen extracellular structural differences among anterior treated, posterior treated, and untreated control eyes are presented in FIG. 10. Hie excitation of tyrosine, dityrosine oxidation products, and pyridinium-type fiuorophores are responsible for the contrast of the TPF images. TPF images showed a bright region for both untreated control and laser treated samples near the comeal posterior, which may result from the Descemet’s membrane, the basement membrane for the endothelial layer composed mostly of different types of collagen. Similar to the reported TPF images of collagen hydrogels crosslinked by glutaraldehyde and rabbit comeal tissue treated by riboflavin and UVA light to induce corneal CxLs, the treated region of laser irradiated samples showed a significantly stronger signal compared to the untreated region or control cornea, indicated that the proposed treatment introduced an increased CxLs density. Three lines were drawn on both central and peripheral zones through the whole corneal thickness indicated by the arrows in figure FIG. 10A. The averaged gray values of the three lines for the untreated control and laser treated samples were presented in FIG. 1 1. Tire average pixel values of histograms for boxed regions in FIGS. 10A-C indicated that the intensities for the laser treated eyes were much stronger than the untreated control eye and the intensities for anterior and posterior treated regions were approximately the same. Corresponding well with the treatment depth, tire average gray values showed the size of the treated region were all about 200 pm for both anterior and posterior treated corneas, together with the average pixel values of the histograms, suggesting that the crosslinking efficiency does not diminish as the focusing of the laser pulses is shifted in the cornea. As the treatment pattern goes from anterior to posterior treatment, the collagen-rich zone shifted from anterior to posterior, which revealed the proposed treatment has the spatial selectivity ability.

Histological analysis ofH&E-stained sections (FIGS. 13A-13C) reveals all main elements of comeal architecture: epithelial and endothelial layers, keratocytes and extracellular stromal matrix. There are no signs of thermal damage such as collagen di sorganization, stromal edema, disorganization of cellular components commonly observed in the cases of corneal overheating on the obtained images. Light microscopy show's no differences in corneal structure of the anterior and posterior treated samples comparing to the untreated ones.

Treatment of the posterior stroma provides similar change in corneal curvature to that seen in treatment of the anterior stroma. This is unexpected due to differences in architecture of these two corneal segments, and it goes against conventional wisdom of ophthalmologists. The ability to achieve changes in eye refractive power through treatment of the comeal stroma also allows for treatment to be extended throughout the comeal thickness to treat more severe cases of myopia.

EQUIVALENTS

Although preferred embodiments of the invention have been described using specific terms, such description is for illustrative purposes only, and it is to be understood that changes and variations may be made without departing from the spirit or scope of the following claims.

INCORPORATION BY REFERENCE

The entire contents of all patents, published patent applications, and other references cited herein are hereby expressly incorporated herein in their entireties by reference.

Claims

1. A method of treating a cornea, the method comprising:

controlling a light source to apply light energy pulses to a single corneal layer selected from the group consisting of: an anterior corneal layer and a posterior corneal layer;

w'herein the light energy pulses:

are below an optical breakdown threshold for the cornea; and

ionize water molecules within the treated corneal layer to generate reactive oxygen species that cross-link collagen within the single corneal layer.

2. The method of claim 1, wherein the anterior corneal layer extends between an anterior surface of the cornea and about 200 microns from the anterior surface.

3. The method of claim 1, wherein the posterior corneal layer extends between a posterior surface of the cornea and about 200 microns from the posterior surface.

4. A method of treating a cornea, the method comprising:

controlling a light source to apply light energy pulses to at least a corneal stroma layer of a cornea;

wherein the light energy pulses:

are below an optical breakdown threshold for the cornea; and

ionize water molecules within the treated corneal stromal layer to generate reactive oxygen species that cross-link collagen within the cornea.

The method of any one of claims 1-4, w_'herein the light source is a laser.

6. The method of claim 5, w'herein the laser is a femtosecond laser.

7. The method of any one of claims 1-4, wherein the light energy pulses have an average power output between about 10 rnW and about 100 rnW.

8. The method of any one of claims 1-4, wherein the light energy pulses have a pulse energy between about 0.1 nJ and about 10 nJ.

9. The method of any one of claims 1-4, wherein the light energy pulses have a wavelength between about 600 nrn and about 1600 run.

10. The method of any one of claims 1-4, wherein the light energy pulses have a wavelength that is not absorbed by ammo acids in collagen.

11. The method of any one of claims 1-4, wherein the light energy pulses are applied in a pattern.

12. The method of claim 11, wherein the pattern extends across a center of an ins posterior to the cornea.

13. The method of claim 11, wherein the pattern surrounds, but does not extend across a center of an iris posterior to the cornea.

14. The method of any one of claims 1-4, wherein the method treats keratoconus or alters curvature of the cornea.

15. A system for treating a cornea, the system comprising;

a light source configured to project light energy pulses onto at least a portion of a cornea; and

a controller programmed to control the light source in accordance with any of method claims 1-4.

16. A system for adapting a laser system for treating a cornea, the system comprising;

laser modification optics adapted and configured to adjust laser output of the laser system; and

a controller programmed to control the laser modification optics as the light source in accordance with anv of method claims 1 -4.