US20110130677A1 - System for characterizing a conrea and obtaining an ophthalmic lens - Google Patents

Abstract

A system for determining the shape of a cornea of an eye illuminates at least one of the interior surface, the posterior surface, and the interior region of the eye with infrared light of a wavelength that can generate fluorescent light from the portion of the cornea illuminated. The generated fluorescent light is then detected. A step of illuminating can comprise focusing the infrared light in a plurality of different planes substantially perpendicular to the optical axis of the eye. From the detected light it is possible to create a map of at least a portion of the interior surface, at least a portion of the posterior surface, and/or portion of the interior region of the cornea. Clarity of vision can be determined by generating autofluorescence from proteins in the pigment epithelial cells of the retina.

Description

CROSS-REFERENCES
• This application claims the benefit of the following U.S. provisional application Ser. Nos. 61/209,362 filed Mar. 4, 2009; 61/209,363 filed Mar. 4, 2009; 61/181,420 filed May 27, 2009; 61/181,519 filed May 27, 2009; and 61/181,525 filed May 27, 2009. These U.S. provisional applications are incorporated herein by reference. To the extent the following description is inconsistent with the disclosures of the provisional applications, the following description controls.
BACKGROUND
• A variety of systems are known for characterizing a cornea, and using information from the characterization to model an ophthalmic lens. See for example U.S. Pat. Nos. 6,413,276; 6,511,180; 6,626,535; and 7,241,311
• 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. Thus, for example, 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.
• Accordingly, there is a need for an improved system for characterizing a cornea for the purpose of obtaining ophthalmic lenses for placement in the human eye. It is also desirable that the system permit analysis of effectiveness of a placed lens in focusing light on the retina.
• 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. According to this method, 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. Then the path length of the scanning light is adjusted to increase the clarity of the image generated by the fluorescent light. Typically the scanning light has a wavelength of from 750 to about 800 nm, and preferably about 780 nm.
SUMMARY
• 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. According to the method, 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. By “anterior surface” there is meant a surface that faces outwardly in the eye. A “posterior surface” faces rearwardly toward the retina.
• For example, in the case of the anterior region of the cornea, 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.
• Preferably 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. According to this method, 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. Then the path length of the scanning light is adjusted to increase the clarity of the image generated by the fluorescent light. Typically 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.
DRAWINGS
• These and other features, aspects, and advantages of the present invention will become better understood with regard to the following description, appended claims, and accompanying drawings where:
• 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); and
• FIG. 11 is a schematic view of a system for detecting the clarity of images achieved with an implanted intraocular lenses.
DESCRIPTIONOverview
• A system for determining the topography of the cornea, including the topography of the anterior and posterior surfaces and interior regions 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. By using a plurality of pixelized data that are generated from these measurements, 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
• Referring initially toFIG. 1, a system for determining the refractive properties of an implanted lens, such as a customized intraocular lens, is shown in a schematic drawing, and is generally designated10. A plurality ofoptical rays40 are transmitted through a pseudophakic eye, implanted with a customizedintraocular lens20, 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 theretina30. The plurality ofindividual beams40 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. Next, 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 ofoptical rays40 is transmitted in sequence through theanterior surface12 of thecornea14, theinterior region13 of thecornea14, theposterior surface16 of thecornea14, and a customized intraocular lens, having ananterior surface layer22, and is brought to a focused image on theretina30. A method for forming thelens20 is described in my co-pending application Ser. No. __/___,___, filed event date herewith, entitled “System for Forming and Modifying Lenses and Lenses Formed Thereby” (Docket 19780-1), which is incorporated herein by reference.
• In the upper part of the plurality ofoptical rays40, three neighboringrays42,44, and46 are depicted, symbolizing a local zone in the zonal approach. Typically, in ray-tracing calculations of highest spatial resolution, tens of millions of rays are evaluated with regard to their optical path lengths in the human eye. For calculation purposes, areference plane18, close to the natural pupil of the pseudophakic eye, is selected, towards which the optical path lengths of the individual beams are normalized. In particular, the propagation of an individual optical ray from thepupil plane18 to theanterior surface22 of the customizedintraocular lens20 can be evaluated as exp (i x (2π/λ) x n(x,y) x z(x,y)), where exp resembles the exponential function, i denotes the imaginary unit number, π amounts to approximately 3.14, λ 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 thepupil plane18. 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 thesurface layer22 with an optical technique, as described in my aforementioned copending application Ser. No. __/___,___ (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 apost-LASIK eye60. In the upper part ofFIG. 2, the situation in anormal eye50 is exemplified. Theeyeball52 contains acornea56, alens54 and aretina58. Typically, for a pupil diameter of6 mm, an amount ofspherical aberration59 of approximately one wavelength λ, corresponding to 0.5 μm, is introduced, mainly associated with the peripheral shape of the crystalline lens. In the lower part ofFIG. 2, for the case of apost-LASIK eye60, which underwent a myopia correction procedure, the introduction of a considerable amount of spherical aberration is demonstrated. Theeyeball62 exhibits acornea66, alens64 and aretina68. Typically, an amount of spherical aberration of approximately ten wavelengths (10 λ), corresponding to 5 μm, is encountered, mainly associated with the edges of the centrally flattened cornea.
• FIG. 3 is a schematic presentation of a route ofcalculation70 for determining the necessary refractive effect of an implanted lens. A manifold ofoptical rays72 is transformed into apupil function74 which can be visualized as the spatial distribution of thepath lengths76 and can be expressed as the mathematical function78: P(x,y)=P(x,y) exp(ikW(x,y)), where P(x,y) is the amplitude and exp(ikW(x,y)) is the phase of the complex pupil function. The phase depends on the wave vector k=2π/λ, λ being the wavelength of the individual optical ray, W(x,y) being its path length, and i denotes the imaginary unit number. From thepupil function74 the point spread function (PSF)80 can be derived which mathematically can be expressed as a Fourier Transform82: PSF(x,y)=iFT(P(x,y))i², which is graphically represented as a pseudo-threedimensional function84, depicting a nearly diffraction-limited case, exhibiting a pseudophakic eye with only minor optical aberrations. From thecalculation70, the Strehl Ratio i86 can be derived which is defined as88: i=(max(PSF(x,y))/max(PSF_diff(x,y)), where PSF(x,y) denotes the point spread function of the aberrated optical system, and PSF_diff(x,y) resembles an idealized diffraction-limited optical system. The point spread function (PSF)80 and the Strehl Ratio i86 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. Theimage formation process90 can be envisaged as a mathematical operation—calledconvolution94—in which the idealized image of anobject92 is blurred by convolving each image point with the pointspread function PSF96 of the optical system resulting in animage100. For the ease of a human eye with a pupil of 6 mm diameter, thePSF96 is depicted as a pseudo-threedimensional graph98. Thus, the clarity of theretinal image100 can be ascertained by the pointspread function PSF96.
• 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). By employing a Finite Element Modeling (FEM)algorithm102 for simulating thestress104 and strain106 distribution throughout a loaded cornea, 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. Initially, finite element Modeling (FEM) provides the distribution of stiffness parameters in the volume elements, which are proportional to local tissue densities. The application of FEM-modeling to cornea biomechanics is described in, e.g., A. Pandolfi, et al., Biomechan. Model Mechanobiology 5237-246, 2006. An intraocular pressure of 2 kiloPascal (kPA) (15 mm Hg) is applied homogeneously to the posterior surface. Only Bowman'slayer108 is fully fixed at the limbus. On the left part ofFIG. 5, a Cauchy stress distribution along the radial direction is depicted; the absolute values range from −2.5 kPa to +2.5 kPa. On the right part ofFIG. 5, the maximum principle strain distribution is visualized; the relative compression resp. dilation of the stromal tissue range from −0.07 to +0.07.
Use of Fluorescent Emission to Characterize a Cornea
• FIG. 6 is a schematic drawing depicting the physical processes of second harmonic generation imaging (SHGi) and two photon excited fluorescence imaging (TPEFi). On the upper left side ofFIG. 6, the principle of Second Harmonic Generation imaging (SHGi)140 is shown. Twophotons146 and148 with frequency ω_pcoherently add on to generate aphoton150 with frequency 2ω_pwhich is instantaneously reradiated fromlevel144 to142. In the upper right side ofFIG. 6, the Two Photon Excited Fluorescence imaging (TPEFi) process is visualized. Twophotons156 and158 with frequency co_pexcite a molecule from theground level152 to anexcited level154. After thermal relaxation tolevel160 in about1 picosecond, the fluorescence photon ω_Fis reradiated, as the molecule is de-excited tolevel162 in about 1 nanosecond. In the lower part ofFIG. 6, the wavelength dependence of the SHGi (Second Harmonic Generation)- and TPEFi (Two Photon Excited Fluorescence)-imaging processes are exemplified. Generally, as the wavelength of the illuminating femtosecond laser beam with frequency ω_pis decreased from166 via168 to170, the intensity of the SHGi-signals174,176 and178 with frequency 2ω_pare increased, as well as the intensities of the TPEFi signals182,184 and186 with frequency ω_F. In the Two Photon Cornea Microscope/Ophthalmoscope, as described with regard toFIG. 7, 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 apreferred apparatus702 for characterizing a cornea for designing a customized intraocular lens. Theapparatus702 comprises alaser704, preferably a two-photon laser, acontrol unit706, and ascanning unit708. 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, Calif. 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. Preferably thelaser704 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 emittedlaser beam720 is directed by aturning mirror722 through aneutral density filter724 to select the pulse energy. Thelaser beam720 typically has a diameter of about 2 mm when emitted by the laser. Thelaser beam720 then travels through adichroic mirror728 and then to thescanning unit708 that spatially distribute the pulses into a manifold of beams. Thescanning unit708 is controlled by acomputer control system730 to scan acornea732 in an eye.
• Thebeam720 emitted from the laser has a diameter from about 2 to about 2.5 mm. Thebeam720, after exiting thescanner708, is then focused by focusing means to a size suitable for scanning thecornea732, typically a beam having a diameter from about 1 to about 2 μm. 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 atelescopic lens pair742 and744 and amicroscope objective746, where asecond turning mirror748 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 μm to be scanned without having to move either thecornea732 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.
• Thecontrol unit706 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 thescanning unit708.
• The cells on the anterior surface of thecornea732, 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 themicroscope objective746, to be reflected by theturning mirror748, through thelenses744 and742, through thescanning unit708 into thedichroic mirror728 which reflects the fluorescent light topath780, generally at a right angle to the path of the incident laser light that passed through thedichroic mirror728. Inpath780, the emitted light passes through a filter782 to remove light of unwanted frequencies, and then through a focusinglens784 to aphotodetector786. The photodetector can be an avalanche photodiode. Data from the photodetector can be stored in the memory of thecomputer control unit730, or in other memory.
• Thus, 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. For the anterior surface, 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 in64 separate planes, where the scanning is done with beams about three microns apart.
• A difference for scannin_gthe 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. When scanning the interior of the cornea, it is necessary to use adifferent filter732 to be certain to have the blue light pass through the filter to thephotodetector786.
• FIG. 8 is an overview of SHG-imaging of collagen tissue structures. The collagentriple helix188 is visualized in the upper left part ofFIG. 8, exhibiting the typical structure of collagen fibrils. The collagen fibrils are organized in a complex three dimensional layered structure inside the corneal stroma. On the lower left part ofFIG. 8, the Second Harmonic Generation (SHG) laser/collagen fibril interaction process is depicted. Aphoton194 with the frequency co polarizes the collagen fibril to anintermediate level196, whereas asecond photon198 of the same frequency ω further creates an instantaneouselectronic level192. The electronic excitation is immediately reradiated as aphoton200 of double energy, exhibiting the frequency 2ω. This process occurs with high yield because of the unidirectional shape of the collagen fibrils. Second Harmonic Generation imaging (SHGi) of corneal tissue was recently reported (M. Han, G. Giese, and J. F. Bille, “Second harmonic generation imaging of collagen fibrils in cornea and sclera”,Opt.Express 13, 5791-5795(2005)). The measurement was performed with the apparatus ofFIG. 7. The SHGi signal is determined according to theformulas224 from the nonlinear optical polarization226 of the collagen fibrils. The signal-strength228 is directly proportional to the second order polarization term [ω⁽²⁾]²and inversely proportional to the pulse length r of the femtosecond laser pulses. Thus, 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 toFIG. 7.
• Anatomically, thecornea14 of an eye is shown inFIG. 9 to include, in order from itsanterior surface12 to itsposterior surface16, anepithelium230, a Bowman'smembrane244, a stroma246, a Descemet'smembrane248, and anendothelium250. Theepithelium230 is comprised of several cell layers, e.g.232,234,236,238 and240, merging into thebasal cell layer242. Thebasal cell layer242, as well as theanterior surface12, 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 theepithelium230. 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 thecornea14. The stroma246 is composed of approximately200 collagen lamellae, e.g.252,254,256,258,260,262, and264, exhibiting a complex three dimensional structure, which can be evaluated utilizing the Second Harmonic Generation imaging (SHGi) mode of the two-photon cornea microscope. Based on these measurements, supported by Finite Element Modeling (FEM) of the stiffness of the collagen structure—as exemplified in FIG.5—the three-dimensional distribution of the refractive index inside the cornea can be reconstructed. Thus, 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. Thus the anterior surface, posterior surface and/or internal structure of the cornea can be mapped.
• InFIG. 10, the formation of acomposite cornea map270 from individual imaging fields is demonstrated. Typically, acentral imaging field280 extends over a diameter of about 2 mm, comprising approximately 2000×2000 imaging pixels, which amount to 4 million imaging points or pixels, providing a resolution of approximately 1 μm (e.g. utilizing a Nikon 50x/0.45 microscope objective.). Thecomposite cornea map270 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. In order to match the size of the customized intraocular lens of approximately 6 mm diameter, six peripheral imaging fields290,292,294,296,298, and300 are employed. The alignment of the individual fields is accomplished by utilizing a run-time grey value pixel cross correlation algorithm in theoverlap zones310,312,314,316,318, and320. Thus, the composite cornea map exhibits approximately 28 million data, providing a spatially resolved composite image of one transversal slice through the cornea. Typically, 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.
Designing and Forming Lenses
• Techniques for designing lenses from the data generated by the apparatus ofFIG. 7 are known in the art and include the methods described by Roffman in U.S. Pat. No. 5,050,981, which is incorporated herein by reference with regard to such methods. Techniques for manufacturing or modifying a lens are described in my aforementioned copending U.S. patent application Ser. No. __/___,___ (Docket 19780-1).
Clarity of Vision Determination
• With regard toFIG. 11 there is schematically shown a system for determining the clarity of vision experienced by a patient, and in the instance ofFIG. 11, with an implantedintraocular lens1102. The system used for this is substantially the same as the apparatus shown inFIG. 7 using thesame laser704 andscanner708. Optionally 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-module708 can be composed of a phase-plate compensator and an active mirror for the purpose of pre-compensating individual light beams generated by thelaser704. An adapted optics device to compensate for asymmetric aberrations in a beam of light useful for the invention described in my U.S. Pat. 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. Pat. No. 6,155,684. Use of active mirrors is described in my U.S. Pat. No. 6,220,707.Individual light beams1112 pass through thecornea1114 and then theintraocular lens1102 to be focused on the retina to form a retinal image at1120. 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 bylines1122 inFIG. 11. The intensity of the fluorescent light emitted indicates and correlates with how well thecornea1114 andintraocular lens1102 focus the incoming light beams, wherein higher intensity indicates better focusing. To determine if improved focusing can be obtained, to increase the clarity of the image generated by the fluorescent light, the path length of the incoming scanning light can be changed, such as by adjusting the phase plate or the active mirror in theadaptive optics module1104.
• Optionally,vision stimulae1124, such as a Snellen chart can be provided, to receive subjective feedback from the patient with regard to the clarity of vision.
• Using the method, 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.
• Although the present invention has been described in considerable detail with reference to the preferred versions thereof, other versions are possible. For example, although the present invention is described with regard to use of intraocular lenses, it is understood that the data generated characterizing the cornea can be used for forming contact lenses and other lenses implanted in an eye. Therefore the scope of the appended claims should not be limited to the description of the preferred versions contained therein.

Claims (7)

1-34. (canceled)

35. A method for determining the tissue structure of the interior region of the cornea, the method comprising the steps of:

a) illuminating a portion of the interior region of the cornea with light of a wavelength that generates second harmonic light from the portion of the cornea illuminated;

b) detecting the generated second harmonic light;

c) determining the optical path length at a plurality of locations in the portion of the interior region illuminated by detecting any generated blue light, wherein the presence of blue light indicates the presence of collagen lamellae in the cornea; and

d) generating a map of the tissue structure from the detected second harmonic light, wherein the map is of the spatial distribution of optical path lengths for the portion of the interior region of the cornea illuminated.

36. The method ofclaim 35 wherein the wavelength of the blue light is about 390 nanometers.

37. The method ofclaim 35 wherein the map comprises a three-dimensional distribution of the refractive index of the illuminated tissue structure inside of the cornea.

38. A method for determining the tissue structure of the interior region of the cornea, the method comprising the steps of:

a) illuminating a portion of the interior region of the cornea with light of a wavelength that generates autofluorescent light from the portion of the cornea illuminated;

b) detecting the generated autofluorescent light;

c) determining the optical path length at a plurality of locations in the portion of the interior region illuminated by detecting any generated green light, wherein the presence of green light indicates the presence of collagen lamellae in the cornea; and

d) generating a map of the tissue structure from the detected autofluorescent light, wherein the map is of the spatial distribution of optical path lengths for the portion of the interior region of the cornea illuminated.

39. The method ofclaim 38 wherein the wavelength of the green light is about 550 nanometers.

40. The method ofclaim 38 wherein the map comprises a three-dimensional distribution of the refractive index of the illuminated tissue structure inside of the cornea.

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