WO2010102156A1 - System for characterizing a cornea and obtaining an ophthalmic lens - Google Patents
System for characterizing a cornea and obtaining an ophthalmic lens Download PDFInfo
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- WO2010102156A1 WO2010102156A1 PCT/US2010/026281 US2010026281W WO2010102156A1 WO 2010102156 A1 WO2010102156 A1 WO 2010102156A1 US 2010026281 W US2010026281 W US 2010026281W WO 2010102156 A1 WO2010102156 A1 WO 2010102156A1
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- Prior art keywords
- cornea
- light
- eye
- illuminating
- interior region
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Classifications
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- B23—MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
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- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
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Definitions
- a difficulty with known systems for characterizing the cornea is that properties of the human cornea can be affected by the amount of water present at the time of measurement.
- an ophthalmic lens designed for a patient where the patient's cornea was characterized when the patient had a dry eye condition, may not be suitable for the patient when the patient's eye is adequately hydrated.
- Another problem with conventional systems is the internal structure of the cornea usually is not considered. It is believed that the focusing effect of the cornea is achieved by the anterior surface of the cornea, the posterior surface of the cornea, and the interior structure of the cornea, each contributing about 80%, 10%, and 10%, respectively. This failure to consider the internal structure of the cornea, and in some instances failure to consider the shape of the posterior surface of the cornea, can result in a lens that provides unsatisfactory vision.
- the invention also includes a system for determining the clarity of vision of a patient to ascertain the effectiveness of an implanted lens or other ophthalmic modification provided to a patient.
- the eye of the patient is illuminated with a scanning light of a wavelength that generates fluorescent light at the retina and clarity of the image generated by the fluorescent light is detected such as with a photodetector.
- Fluorescent light is generated by proteins in the pigment epithelial cells of the retina as well as photoreceptors of the retina.
- the path length of the scanning light is adjusted to increase the clarity of the image generated by the fluorescent light.
- the scanning light has a wavelength of from 750 to about 800 nm, and preferably about 780 nm.
- the present invention provides a system that meets this need.
- the system includes a method and apparatus for determining the shape of the cornea of an eye, where the cornea has an anterior surface, a posterior surface, and an interior region between the anterior and posterior surfaces.
- the method relies upon generation of fluorescent light by the cornea, unlike prior art techniques, where reflectance of incident light is used for determining the cornea shape.
- at least one of the anterior surface, the posterior surface and the interior region of the eye is illuminated with infrared light of a wavelength that can generate fluorescent light from the portion of the cornea illuminated.
- the generated fluorescent light is detected.
- the detected fluorescence can be used to generate a map of the anterior surface, posterior surface, and/or internal region of the cornea.
- anterior surface there is meant a surface that faces outwardly in the eye.
- a "posterior surface” faces rearwardly toward the retina.
- the optical path length at a plurality of locations in the interior region is determined.
- the presence of generated blue light from the interior region indicates the presence of collagen lamellae in the cornea.
- the step of illuminating comprises focusing the infrared light in a plurality of different planes substantially perpendicular to the optical axis of the eye.
- the planes can intersect the anterior surface of cornea, the posterior surface of cornea, and/or the interior region of the cornea.
- the present invention also includes apparatus for performing this method.
- a preferred apparatus comprises a laser for illuminating a selected portion of the cornea with infrared light of a wavelength that can generate fluorescent light from the portion of the cornea illuminated; focusing means such as focusing lenses for focusing the light in the selected portion of the cornea; and a detector, such as a photodiode detector, for detecting the generated fluorescent light.
- the invention also includes a system for determining the clarity of vision of a patient to ascertain the effectiveness of an implanted lens or other ophthalmic modification provided to a patient.
- the eye of the patient is illuminated with a scanning light of a wavelength that generates fluorescent light at the retina and the clarity of the image generated by the fluorescent light is detected such as with a photodetector.
- Fluorescent light is generated by proteins in the pigment epithelial cells as well as photoreceptors of the retina.
- the path length of the scanning light is adjusted to increase the clarity of the image generated by the fluorescent light.
- the scanning light has a wavelength of from 750 to about 800 nm, and preferably about 780 nm.
- the term "clarity of vision” refers to the ability of a subject to distinguish two images differing in brightness (white is 100% bright and black is 0% bright). The less that the two images differ in contrast (relative brightness) where the subject can perceive the difference, the higher the subject's clarity of vision.
- Fig. 1 is a schematic drawing of the method of the present invention being used with a pseudophakic eye
- Fig. 2 is a graphical presentation of the presence of spherical aberration of the crystalline lens of the human eye, and in a post-LASIK eye;
- Fig. 3 is a schematic presentation of a route of calculation to determine clarity of a retinal image
- Fig. 4 is a graphical visualization of the mathematical procedure of convolution which can be employed in a computing method to determine clarity of vision
- Fig. 5 is a side cross sectional view showing the stress strain distribution in a loaded cornea as the result of Finite Element Modeling (FEM);
- Fig. 6 is a schematic drawing depicting the physical processes of second harmonic generation imaging (SHGi) and two photon excited fluorescence imaging (TPEFi);
- Fig. 7 schematically shows the major components of a two-photon microscope/ophthalmoscope that can be employed in the present invention;
- Fig. 8 is an overview of SHG-imaging of collagen tissue structures;
- Fig. 9 sketches the micromorphometry of the cornea;
- Fig. 10 shows a schematic arrangement for generating a composite cornea map over a field of view that resembles the size of a customized intraocular lens (C-IPSM);
- Fig. 11 is a schematic view of a system for detecting the clarity of images achieved with an implanted intraocular lenses. DESCRIPTION
- a system for determining the topography of the cornea includes measurement and simulation procedures that provide values for the refractive index distribution inside the cornea. Statistical distributions and results of finite element modeling of the stress/strain relationship inside the cornea can be employed.
- the apparatus used can be a two-photon microscope to obtain a plurality of measurements with high spatial resolution. Each individual beam used in the apparatus can have a unique optical path length.
- the processes of Second Harmonic Generation imaging (SHGi) and Two Photon Excited Fluorescence imaging (TPEFi) are employed.
- SHGi Second Harmonic Generation imaging
- TPEFi Two Photon Excited Fluorescence imaging
- a detailed spatial distribution of the refractive properties of the cornea can be evaluated for the purpose of fabricating an intraocular lens that can precisely compensate for detected aberrations.
- the system also includes techniques for determining the effectiveness of a lens in the eye, i.e., a quality control technique. Characterizing the Cornea
- a system for determining the refractive properties of an implanted lens such as a customized intraocular lens
- a plurality of optical rays 40 are transmitted through a pseudophakic eye, implanted with a customized intraocular lens 20, providing local corrections to the optical path lengths of the individual optical rays with high spatial resolution. These optical rays are directed through the pseudophakic eye to form an image on the retina 30.
- the plurality of individual beams 40 are characterized by the fact that each beam has a unique optical path length. Specifically, each optical path length is indicative of the refraction that was experienced by its respective individual beam during transit of the individual beam through the eye.
- the optical path lengths of the individual beams are collectively used by a computer to create a digitized image on the retina of the eye.
- the plurality of optical rays 40 is transmitted in sequence through the anterior surface 12 of the cornea 14, the interior region 13 of the cornea 14, the posterior surface 16 of the cornea 14, and a customized intraocular lens, having an anterior surface layer 22, and is brought to a focused image on the retina 30.
- a method for forming the lens 20 is described in my co-pending Application Serial No.12/717,886, filed event date herewith, entitled “System for Forming and Modifying Lenses and Lenses Formed Thereby"(Docket 19780-1), which is incorporated herein by reference.
- three neighboring rays 42, 44, and 46 are depicted, symbolizing a local zone in the zonal approach.
- tens of millions of rays are evaluated with regard to their optical path lengths in the human eye.
- a reference plane 18, close to the natural pupil of the pseudophakic eye, is selected, towards which the optical path lengths of the individual beams are normalized.
- the propagation of an individual optical ray from the pupil plane 18 to the anterior surface 22 of the customized intraocular lens 20 can be evaluated as exp (i x (2 ⁇ / ⁇ ) x n(x,y) x z(x,y)), where exp resembles the exponential function, i denotes the imaginary unit number, % amounts to approximately 3.14, ⁇ denotes the wavelength of the optical ray, n(x,y) describes the local refractive index and z(x,y) the physical distance at the transverse location with coordinates x and y from the pupil plane 18.
- any inaccuracy of the positioning of the customized intraocular lens (C-IPSM) 20 during lens implantation with regard to axial or lateral position or tilt can be expressed by a profile of physical lengths z(x,y) and can be compensated for by in- vivo fine-tuning of the surface layer 22 with an optical technique, as described in my aforementioned copending application Serial No. 12/717,886 (Docket 19780-1), filed on even date herewith, entitled “System for Forming and Modifying Lenses and Lenses Formed Thereby," which is incorporated herein by reference.
- Fig. 2 is a graphical presentation of the presence of one particular optical aberration of the human eye, e.g. spherical aberration, in a normal eye (e.g. crystalline lens) and in a post- LASIK eye (e.g. reshaped cornea), visualizing the induction of spherical aberration in a post- LASIK eye 60.
- a normal eye e.g. crystalline lens
- a post- LASIK eye e.g. reshaped cornea
- a post-LASIK eye 60 which underwent a myopia correction procedure, the introduction of a considerable amount of spherical aberration is demonstrated.
- the eyeball 62 exhibits a cornea 66, a lens 64 and a retina 68.
- an amount of spherical aberration of approximately ten wavelengths (lO ⁇ ), corresponding to 5 ⁇ m, is encountered, mainly associated with the edges of the centrally flattened cornea.
- Fig. 3 is a schematic presentation of a route of calculation 70 for determining the necessary refractive effect of an implanted lens.
- PSF point spread function
- the point spread function (PSF) 80 and the Strehl Ratio i 86 are useful to visualize the optical quality of an eye and the clarity of a retinal image.
- Fig. 4 is a graphical visualization of the mathematical procedure of convolution which can be employed for the purpose of evaluating the clarity of the retinal image.
- the image formation process 90 can be envisaged as a mathematical operation - called convolution 94 - in which the idealized image of an object 92 is blurred by convolving each image point with the point spread function PSF 96 of the optical system resulting in an image 100.
- the PSF 96 is depicted as a pseudo-three dimensional graph 98.
- the clarity of the retinal image 100 can be ascertained by the point spread function PSF 96.
- FIG. 5 is a side cross-sectional view showing the stress and strain distribution in a loaded cornea as the result of Finite Element Modeling (FEM).
- FEM Finite Element Modeling
- FEM Finite Element Modeling
- the local density of the stromal tissue inside the cornea can be determined, from which the spatial distribution of the refractive index n (x,y) is derived, yielding a measure of the variability of the optical path lengths of the manifold of the optical rays inside the cornea.
- finite element Modeling provides the distribution of stiffness parameters in the volume elements, which are proportional to local tissue densities.
- Bowman's layer 108 is fully fixed at the limbus.
- a Cauchy stress distribution along the radial direction is depicted; the absolute values range from -2.5 kPa to +2.5 kPa.
- the maximum principle strain distribution is visualized; the relative compression resp. dilation of the stromal tissue range from -0.07 to +0.07.
- Fig. 6 is a schematic drawing depicting the physical processes of second harmonic generation imaging (SHGi) and two photon excited fluorescence imaging (TPEFi).
- SHGi second harmonic generation imaging
- TPEFi photon excited fluorescence imaging
- a wavelength of 780 nm of the illuminating femtosecond laser is used, for optimized contrast of the imaging of collagen fibrils and cell processes inside the cornea.
- Fig. 7 schematically shows a preferred apparatus 702 for characterizing a cornea for designing a customized intraocular lens.
- the apparatus 702 comprises a laser 704, preferably a two-photon laser, a control unit 706, and a scanning unit 708.
- Two-photon excitation microscopy is a fluorescence imaging technique that allows imaging living tissue up to a depth of one millimeter.
- the two-photon excitation microscope is a special variant of the multiphoton fluorescence microscope.
- Two-photon excitation can be a superior alternative to confocal microscopy due to its deeper tissue penetration, efficient light detection and reduced phototoxicity.
- the concept of two-photon excitation is based on the idea that two photons of low energy can excite a fluorophore in a quantum event, resulting in the emission of a fluorescence photon, typically at a higher energy than either of the two excitatory photons.
- the probability of the near-simultaneous absorption of two photons is extremely low. Therefore, a high flux of excitation photons is typically required, usually a femtosecond laser.
- a suitable laser is available from Calmar Laser, Inc., Sunnyvale, California.
- Each pulse emitted by the laser can have a duration of from about 50 to about 100 femtoseconds and an energy level of at least about 0.2 nJ.
- the laser 704 generates about 50 million pulses per second at a wavelength of 780 nm, a pulse length of about 50 fs, each pulse having a pulse energy of about 10 nJ, the laser being a 500 mW laser.
- An emitted laser beam 720 is directed by a turning mirror 722 through a neutral density filter 724 to select the pulse energy.
- the laser beam 720 typically has a diameter of about 2mm when emitted by the laser.
- the laser beam 720 then travels through a dichroic mirror 728 and then to the scanning unit 708 that spatially distribute the pulses into a manifold of beams.
- the scanning unit 708 is controlled by a computer control system 730 to scan a cornea 732 in an eye.
- the beam 720 emitted from the laser has a diameter from about 2 to about 2.5 mm.
- the beam 720 after exiting the scanner 708, is then focused by focusing means to a size suitable for scanning the cornea 732, typically a beam having a diameter from about 1 to about 2 ⁇ m.
- the focusing means can be any series of lenses and optical devices, such as prisms, that can be used for reducing the laser beam to a desired size.
- the focusing means can be a telescopic lens pair 742 and 744 and a microscope objective 746, where a second turning mirror 748 directs the beam from the lens pair to the microscopic objective.
- the focusing microscope objective can be a 40 x/0.8 objective with a working distance of 3.3 mm.
- the scanning and control unit are preferably a Heidelberg Spectralis HRA scanning unit available from Heidelberg Engineering located in Heidelberg, Germany.
- the optics in the scanning unit allow a region having a diameter of about 150 to about 450 ⁇ m to be scanned without having to move either the cornea 732 or the optics.
- To scan other regions of the cornea it is necessary to move the cornea in the X-, y- plane. Also, to scan in varying depths in the cornea, it is necessary to move the focal plane of the laser scanner in the z- direction.
- the control unit 706 can be any computer that includes storage memory, a processor, a display, and input means such as a mouse, and/or keyboard.
- the control unit is programmed to provide a desired pattern of laser beams from the scanning unit 708.
- the cells on the anterior surface of the cornea 732, when excited by the laser beam at a wavelength of 780 nm fluoresce, producing a green light having a wavelength of about 530 nm.
- the emitted light tracks through the path of the incident laser light, namely the emitted light passes through the microscope objective 746, to be reflected by the turning mirror 748, through the lenses 744 and 742, through the scanning unit 708 into the dichroic mirror 728 which reflects the fluorescent light to path 780, generally at a right angle to the path of the incident laser light that passed through the dichroic mirror 728.
- the emitted light passes through a filter 782 to remove light of unwanted frequencies, and then through a focusing lens 784 to a photodetector 786.
- the photodetector can be an avalanche photodiode. Data from the photodetector can be stored in the memory of the computer control unit 730, or in other memory.
- the anterior surface of the cornea is illuminated with infrared light of a wavelength that generates fluorescent light and the generated fluorescent light is detected.
- incident infrared light is focused in a plurality of different planes that are substantially perpendicular to the optical axis of the eye, where the planes intersect the anterior surface of the cornea.
- the same procedure can be used for characterizing the posterior surface, by focusing the infrared light in a plurality of different planes substantially perpendicular to the optical axis of the eye where the planes intersect the posterior surface.
- the scanning can be done in 64 separate planes, where the scanning is done with beams about three microns apart.
- a difference for scanning the interior of the cornea is that the collagen lamellae in the interior region generate blue light rather than green light.
- the blue light has a wavelength of about 390 nm.
- Fig. 8 is an overview of SHG-imaging of collagen tissue structures.
- the collagen triple helix 188 is visualized in the upper left part of Fig. 8, exhibiting the typical structure of collagen fibrils.
- the collagen fibrils are organized in a complex three dimensional layered structure inside the corneal stroma.
- the Second Harmonic Generation (SHG) laser/collagen fibril interaction process is depicted.
- a photon 194 with the frequency ⁇ polarizes the collagen fibril to an intermediate level 196, whereas a second photon 198 of the same frequency ⁇ further creates an instantaneous electronic level 192.
- the electronic excitation is immediately reradiated as a photon 200 of double energy, exhibiting the frequency 2 ⁇ .
- a SHGi-image of high contrast visualizes the three dimensional layered structure of the corneal stroma, due to the strong unidirectionality of the collagen fibrils and the ultrashort pulse length of the femtosecond laser employed in the in-vivo Two Photon Cornea Microscope/Ophthalmoscope, as described with regard to Fig. 7.
- the cornea 14 of an eye is shown in Fig. 9 to include, in order from its anterior surface 12 to its posterior surface 16, an epithelium 230, a Bowman's membrane 244, a stroma 246, a Descemet's membrane 248, and an endothelium 250.
- the epithelium 230 is comprised of several cell layers, e.g.
- the basal cell layer 242, as well as the anterior surface 12, can clearly be imaged by the two-photon excited autofluorescence mode (TPEF) of the two-photon cornea microscope, providing a spatially resolved measure of the thickness of the epithelium 230.
- the endothelium can also be imaged by the two-photon excited autofluorescence mode of the two-photon cornea microscope, resulting in a spatially resolved thickness measurement of the cornea 14.
- the stroma 246 is composed of approximately 200 collagen lamellae, e.g.
- the optical path lengths - inside the cornea - of the plurality of the optical rays in the ray-tracing calculation can be determined with high spatial resolution.
- the anterior surface, posterior surface and/or internal structure of the cornea can be mapped.
- a central imaging field 280 extends over a diameter of about 2 mm, comprising approximately 2000 x 2000 imaging pixels, which amount to 4 million imaging points or pixels, providing a resolution of approximately 1 ⁇ m (e.g. utilizing a Nikon 50x/0.45 microscope objective.).
- the composite cornea map 270 contains a three dimensional stack of two-photon microscope images, comprised of either the Two-Photon Excited Fluorescence imaging (TPEFi)- or the Second Harmonic Generation imaging (SHGi)-imaging mode.
- TPEFi Two-Photon Excited Fluorescence imaging
- SHGi Second Harmonic Generation imaging
- the alignment of the individual fields is accomplished by utilizing a run-time grey value pixel cross correlation algorithm in the overlap zones 310, 312, 314, 316, 318, and 320.
- the composite cornea map exhibits approximately 28 million data, providing a spatially resolved composite image of one transversal slice through the cornea.
- one hundred transversal slices through the cornea are employed for reconstructing the optical path lengths of the plurality of optical rays as they are transmitted through the cornea of the pseudophakic eye.
- Fig. 11 there is schematically shown a system for determining the clarity of vision experienced by a patient, and in the instance of Fig. 11, with an implanted intraocular lens 1102.
- the system used for this is substantially the same as the apparatus shown in Fig. 7 using the same laser 704 and scanner 708.
- an adaptive-optics module (AO-module) 1104 can be used for the purpose of simulating the effect of a refractive correction, with regard to image clarity and depth of focus.
- the AO-module 708 can be composed of a phase-plate compensator and an active mirror for the purpose of pre-compensating individual light beams generated by the laser 704.
- An adapted optics device to compensate for asymmetric aberrations in a beam of light useful for the invention described in my U.S. Patent No. 7,611,244.
- a method and apparatus for pre-compensating the refractive properties of the human with an adaptive optical feedback control is described in my U.S. Patent No. 6,155,684.
- Use of active mirrors is described in my U.S. Patent No. 6,220,707.
- Individual light beams 1112 pass through the cornea 1114 and then the intraocular lens 1102 to be focused on the retina to form a retinal image at 1120.
- fluorescent proteins in the pigment epithelial cells With the incoming light being at a wavelength of from about 750 to about 800 nm, preferably about 780 nm, fluorescent proteins in the pigment epithelial cells, as well as the photoreceptors, emit fluorescent light having a frequency of about 530 nm to about 550 nm.
- the emitted light is represented by lines 1122 in Fig. 11.
- the intensity of the fluorescent light emitted indicates and correlates with how well the cornea 1114 and intraocular lens 1102 focus the incoming light beams, wherein higher intensity indicates better focusing.
- the path length of the incoming scanning light can be changed, such as by adjusting the phase plate or the active mirror in the adaptive optics module 1104.
- vision stimulae 1124 such as a Snellen chart can be provided, to receive subjective feedback from the patient with regard to the clarity of vision.
- a prescription for an implanted lens such as an IOL, corneal lens, or contact lens, as well as modification for an in situ lens (cornea, IOL, natural crystalline lens) can be determined.
Abstract
Description
Claims
Priority Applications (13)
Application Number | Priority Date | Filing Date | Title |
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BRPI1006739A BRPI1006739A2 (en) | 2009-03-04 | 2010-03-04 | "Method and apparatus for generating an eye corneal map, method for determining patient vision clarity, determining tissue structure of the inner cornea and determining an optical adjustment for a custom intraocular lens for a patient". |
CA2754775A CA2754775C (en) | 2009-03-04 | 2010-03-04 | System for characterizing a cornea and obtaining an ophthalmic lens |
MX2011009197A MX2011009197A (en) | 2009-03-04 | 2010-03-04 | System for characterizing a cornea and obtaining an ophthalmic lens. |
CN201080018948.XA CN102939044B (en) | 2009-03-04 | 2010-03-04 | For characterizing cornea and manufacturing the system of eye-use lens |
JP2011553121A JP5797563B2 (en) | 2009-03-04 | 2010-03-04 | System and method for measuring ocular characteristics to obtain an ophthalmic lens |
EP10707782.8A EP2405798B1 (en) | 2009-03-04 | 2010-03-04 | System and method for characterizing a cornea |
KR1020117023183A KR101647533B1 (en) | 2009-03-04 | 2010-03-04 | System for characterizing a cornea and obtaining an ophthalmic lens |
KR1020157005682A KR101624090B1 (en) | 2009-03-04 | 2010-03-04 | System for characterizing a cornea and obtaining an ophthalmic lens |
PCT/US2010/048161 WO2011109039A1 (en) | 2010-03-04 | 2010-09-08 | System for forming and modifying lenses and lenses formed thereby |
CN201080066621XA CN102883681A (en) | 2010-03-04 | 2010-09-08 | System for forming and modifying lenses and lenses formed thereby |
US13/582,017 US20130103144A1 (en) | 2010-03-04 | 2010-09-08 | System for forming and modifying lenses and lenses formed thereby |
EP10847149.1A EP2542183A4 (en) | 2010-03-04 | 2010-09-08 | System for forming and modifying lenses and lenses formed thereby |
HK13108170.0A HK1180927A1 (en) | 2009-03-04 | 2013-07-12 | System for characterizing a cornea and obtaining an ophthalmic lens |
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