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Publication numberUS20040024454 A1
Publication typeApplication
Application numberUS 10/629,272
Publication dateFeb 5, 2004
Filing dateJul 29, 2003
Priority dateJul 30, 2002
Also published asCA2493583A1, CN1671335A, CN100404003C, EP1531755A2, EP1531755B1, US8419791, US20060276892, WO2004010895A2, WO2004010895A3
Publication number10629272, 629272, US 2004/0024454 A1, US 2004/024454 A1, US 20040024454 A1, US 20040024454A1, US 2004024454 A1, US 2004024454A1, US-A1-20040024454, US-A1-2004024454, US2004/0024454A1, US2004/024454A1, US20040024454 A1, US20040024454A1, US2004024454 A1, US2004024454A1
InventorsPeter Toop
Original AssigneePeter Toop
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Intraocular lens
US 20040024454 A1
Abstract
An intraocular lens comprises an optic and one or more haptics, wherein the or each haptic can be compressed in the plane of the lens, and which additionally comprises, around the optic, an annular rim that, in use, is in contact with the posterior capsular sac.
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Claims(8)
I claim:
1. An intraocular lens comprising an optic and one or more haptics, wherein the, or each, haptic can be compressed in the plane of the lens, and which additionally comprises, around the optic, an annular rim that, in use, is in contact with the posterior capsular sac.
2. The lens according to claim 1, wherein the lens is adapted so that, in use, the optic touches the posterior capsular sac.
3. The lens according to claim 1, which also comprises an annular rim on the anterior surface of the lens.
4. The lens according to claims 1, wherein the, or each, haptic is curved, and shaped such that, in a first stage of compression, the proximal part of the haptic can be fully compressed, and, in a second stage, the distal part of the haptic can be compressed.
5. The lens according to claim 4, wherein the, or each, haptic includes an aperture of which opposed points are brought into contact, in the first stage of compression.
6. The lens according to claim 4, wherein the, or each, stage of compression is essentially continuous, full compression being reached gradually from the proximal end towards the distal end of the haptic.
7. The lens according to, claim 1 wherein the annular rim is thicker in a region proximal to the, or each, haptic.
8. The lens according to claim 7, wherein the rim comprises a gradual change in thickness.
Description
FIELD OF THE INVENTION

[0001] This invention relates to an intraocular lens which, in use, inhibits posterior capsular opacification.

BACKGROUND TO THE INVENTION

[0002] Posterior capsular opacification (PCO) is a common long-term complication of cataract surgery. During cataract surgery, the central anterior lens capsule is removed and the natural lens replaced with an artificial intraocular lens. The posterior lens capsule remains intact. After surgery, viable epithelial cells of the natural lens may remain in the lens capsule equator. These cells can migrate across the inner surface of the posterior capsule, causing it to opacify. The effect, i.e. PCO, is similar to a cataract and for this reason is sometimes called “secondary cataract”. PCO is age-related, occurring more in children rather than adults.

[0003] The standard treatment for PCO is neodymium: yttrium-aluminium-garnet (Nd-YAG) laser posterior capsulotomy. The laser is used to create an opening in the centre of the posterior capsule, to produce a clear area for light to reach the retina. Although the procedure is non-invasive, complications such as retinal detachment and lens damage may arise.

[0004] EP-A-0962196 describes an intraocular lens wherein the haptics are shaped such that, in a first stage of compression, the proximal part of the haptic can be fully compressed; and in a second stage, the distal part of the haptic can be compressed, to provide a lens that is eventually resistant to haptic failure.

[0005] A number of lenses for the prevention of PCO have been proposed, but on the whole, little if any reduction in PCO has been achieved. There still exists the need for an intraocular lens which is effective at reducing PCO.

SUMMARY OF THE INVENTION

[0006] An intraocular lens of the present invention comprises an optic and one or more haptics, wherein the or each haptic can be compressed in the plane of the lens, and which additionally comprises, around the optic, an annular rim that, in use, is in contact with the posterior capsular sac. The annular rim is preferably present on both the posterior and anterior surfaces of the lens; this facilitates insertion of the lens since the surgeon may not need to distinguish between the two surfaces.

[0007] The thickness (i.e. the depth) of the annular rim is preferably greatest in a region proximal to the or each haptic. This allows easier folding of the lens and insertion through a smaller incision. The change in the thickness of the rim is preferably gradual.

[0008] Preferably, the or each haptic is curved and shaped such that, in a first stage of compression, the proximal part of the haptic can be fully compressed, and, in a second stage, the distal part of the haptic can be compressed. This two-stage compression has been shown to be particularly effective in maintaining contact between the rim and the sac.

[0009] Lenses of the invention are effective at inhibiting PCO. Haptic compression allows contact between the rim of the optic and the posterior chamber to be maintained, thus preventing the migration of epithelial cells into the posterior lens region.

BRIEF DESCRIPTION OF THE DRAWINGS

[0010]FIG. 1 is a plan view of an intraocular lens embodying the present invention.

[0011]FIGS. 2A to 2C are side views of intraocular lenses which, with the exception of FIG. 2C, embody the present invention.

[0012]FIGS. 3A and 3B are respectively plan and cut-away side views of a lens of the invention in which the thickness of the annular rim is greatest in the region of the optic binding the haptic.

[0013]FIGS. 4A to 4D are cut-away side views of four lenses of the invention. Each lens comprises an annular rim on the posterior and anterior faces; each lens has a rim of different geometry with respect to the others.

[0014]FIGS. 5A to 5D are similar to FIGS. 4A to 4D, except that the lenses only comprise an annular rim on the posterior face.

[0015]FIGS. 6A and 6B are “roll-out” representations of two lenses of the invention, i.e. they are views of the complete optic edge. A plan view of a lens of the invention is also shown, to clarify where a point on a “roll-out” representation corresponds to a position on the optic circumference.

DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0016] The size of the annular rim is preferably minimised to allow the optic to be as large as possible. Intraocular lenses are generally inserted into the eye using an injector; in this case, a lens of the invention must be able to withstand the forces of injection.

[0017] A lens of the invention may comprise an optic of negative and/or positive powers. Typical negative powers, but not limited thereto, are −10 to −1 Diopters. Typical positive powers but not limited thereto are +1 to +34 Diopters.

[0018] Since the shape/size of the annular rim is proportional to the power of the optic, it may be possible to express this relationship mathematically. This may allow the size of the rim to be calculated simply by determining a patient's optical power.

[0019] Embodiments of the invention will now be described by way of example with reference to the accompanying drawings.

[0020]FIG. 1 shows an intraocular lens having an optic 1, comprising convex faces (the posterior face 2 b, is shown) and haptics 3 a and 3 b. Each haptic comprises an aperture, respectively 4 a and 4 b. Opposed points of each aperture, at 5 a and 6 a, and 5 b and 6 b, are shown.

[0021] These features are such that initial compression of the haptic leads to abutment of opposite walls of the aperture, bringing the opposed points 5 a and 6 a, and 5 b and 6 b, into contact, thereby defining a proximal part that is fully compressed and a distal part that can undergo further compression. Such further compression brings the distal end of each haptic substantially into contact with the periphery of the optic, to give an essentially elliptical shape, in plan.

[0022] The lens comprises an annular rim on each of the anterior and posterior faces of the optic, respectively; the posterior rim 7 b is shown. The periphery of the posterior optic face 8 b is also shown.

[0023] The haptics hold the capsular sac tight against the posterior annular rim, such that epithelial cells are prevented from migrating to the optic region. This inhibits the onset of PCO.

[0024]FIGS. 2A and 2B show lenses of the invention, each comprising a biconvex optic 1, having an anterior face 2 a and a posterior face 2 b. The lenses comprise compressible haptics 3 a and 3 b, and annular rims 4 a and 4 b. In each case, the posterior capsular sac 5 compresses the haptics, such that the posterior annular rim 4 b is held tight against the posterior sac. The lens of FIG. 2A is of higher power than that of FIG. 2B, and requires a thicker annular rim since the biconvex optic is wider.

[0025]FIG. 2C shows a conventional planar haptic PCO retarding lens. Instead of comprising an annular rim, the edge surfaces of the optic in contact with the haptic (6 a and 6 b) are effectively tapered. These tapered edges fail to prevent cell migration since there still exists gaps between the posterior capsular sac and the lens edge. Cells may migrate through this gap, resulting in PCO.

[0026]FIGS. 3A and 3B show a lens similar to that of FIG. 1 except in that the thickness of the annular rims is greatest in the region of the optic binding the haptic.

[0027]FIGS. 4A to 4D illustrate a range of rim geometries which may be suitable for use in the present invention. The lenses are shown in relation to the posterior capsular sac. Each lens has a different rim geometry. Particular reference is made to the lens of FIG. 4D, where the rim and haptic effectively act as a single unit, pressing fast against the posterior capsular sac.

[0028]FIGS. 5A to 5D show similar rim geometries to those in FIGS. 4A to 4D, except that each lens only comprises a rim on the posterior face.

[0029]FIGS. 6A and 6B are “roll-out” representations of optic edges of two lenses of the invention. In general, it is desirable to reduce the optic width at the points 90° and 270° (as shown in FIGS. 6A and 6B) because a known adverse effect of thick optic edges is an increased risk of glare from internal reflections.

[0030]FIG. 6A shows a lens of the invention where the edge of the optic abruptly changes from thick to thin. Such an abrupt change is not ideal since slight pressure from the vitreous may be insufficient to force the posterior capsule into the “corner” regions such as that indicated by the angle B.

[0031]FIG. 6B shows a preferred embodiment of the invention, in which there is a gradual change of edge thickness, allowing a full (i.e. 360°) seal between the barrier and the capsule, substantially reducing any edge glare effects. Angle A is preferably less than 15°.

[0032] The following Example illustrates the invention.

EXAMPLE

[0033] Experiments were performed to compare the extent of PCO resulting from the use of a known intraocular lens “A” (570H Centerflex™ lens, Rayner Intraocular Lenses Ltd.,), and a lens of the invention “B” (570C). Essentially, lens B is the same as lens A except that it comprises an annular rim.

[0034] All lenses used in this study had an optic body diameter of 5.75 mm and a refractive power of +21 D. Five IOLs of each type were used. The lenses were implanted in a randomised manner by the same surgeon.

[0035] Dutch Beited pigmented rabbits weighting 2.4-3.0 kg were used. Each animal was prepared for surgery by pupil dilation with 1% cyclopentolate hydrochloride and 2.5% phenylephrine drops, applied topically every 5 minutes for 15 minutes. Anesthesia was obtained, with an intramuscular injection of ketamine hydrochloride (50 mg/kg) and xylazine (7 mg/Kg) in a mixture of 7:1, respectively. One drop of topical proparacaine hydrochloride anesthetic was also placed in each eye prior to beginning surgery. The area around the eye was draped in an aseptic manner, and a lid speculum was placed to retract the lids.

[0036] Using aseptic technique and a Zeiss surgical microscope, a fornixed-based conjunctival flap was fashioned. A 3.2-mm partial thickness limbal incision was then made using a beaver blade and the anterior chamber was entered. One ml of heparin (10,000 units/ml) was injected into the anterior chamber, followed by injection of a viscoelastic material (Amvisc Plus™, Bausch & Lomb). A capsulorhexis forceps was used to create a continuous curvilinear capsulotomy, with a diameter of around 4.5 to 5.0 mm. The phaco handpiece (Alcon Coopervision Series 10,000) was inserted into the posterior chamber for removal of lens nucleus and cortical material. 0.5 ml of epinephrine 1:1000 and 0.5 ml of heparin (10,000 USP units/ml) were added to each 500 ml of irrigation solution to facilitate pupil dilation and control inflammation. The endocapsular technique was used with the phacoemulsification to take place entirely within the capsular bag. Any residual cortex was then removed with the same handpiece. After removal of the lens, a viscoelastic was used to inflate the capsular bag. The IOLs were then inserted into the capsular bag using the manufacturer's recommended injector system (Rayner titanium injector). Wound closure was achieved with 10.0 monofilament nylon suture after aspiration of viscoelastic material.

[0037] Combination antibiotics/steroid ointment (neomycin and polimixin B sulfates, and dexamethasone) was applied to the eyes following surgery. The same ointment was placed in the rabbit eyes four times per day for the first postoperative week. This was then discontinued after one week. In the second postoperative week each animal received topical prednisolone acetate drops four times per day with discontinuation of the drops following the second postoperative week.

[0038] All eyes were evaluated by slit lamp examination and scored for ocular inflammatory response at one week, two weeks and three weeks post-operatively. A standard scoring method in different specific categories was used at each examination, including assessment of corneal edema, as well as the presence of cell and flare within the anterior chamber. PCO was evaluated under retro-illumination with the pupil fully dilated.

[0039] After the final clinical examination at three weeks, the animals were anesthetised using a 1.6 ml intramuscular injection of a 7:1 mixture of ketamine hydrochloride and xylazine, and then humanely euthanised with a 1 ml intravenous injection of pentobarbital sodium/phenytoin sodium (Euthasol®, Delmarva Laboratories). Their globes were enucleated and placed in 10% neutral buffered formalin for twenty-four hours. The globes were then bisected coronally just anterior to the equator. Gross examination and photographs from the posterior aspect (Miyake-Apple view) were performed to assess the PCO development. The intensity of central and peripheral PCO was scored from grades 0-4; see Hansen et al, J.Cataract Refract.Surg. 14:605-413 (1988), for details of the method of scoring.

[0040] Table 1 summarises the results of the PCO scoring done from a posterior (Miyake-Apple) view. In Table 1, OD (oculus dexter) refers to the right eye, OS (oculus sinister) to the left. In each eye, central and peripheral PCO scores were lower for lens B, and higher for lens A. The average central PCO scores for lenses A and B were 0.90 and 0.39 respectively. The average peripheral scores for A and B were 1.85 and 0.83 respectively. This illustrates the desirability of a lens of the invention.

TABLE 1
Central PCO Peripheral PCO
A B A B
0 0.5 3 1
1 1 2 1
1 0.5 2 1
1 0 2 0
2.5 0 3 1
0 0 2 1
1 1 2 2
1 0.5 1 0.5
1 0 1 0
0.5 0 0.5 0

Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US7226479Apr 21, 2005Jun 5, 2007Humanoptics AgIntraocular lens
US7569073Dec 29, 2004Aug 4, 2009Bausch & Lomb IncorporatedSmall incision intraocular lens with anti-PCO feature
US7615073Dec 7, 2004Nov 10, 2009Advanced Medical Optics, Inc.Foldable intraocular lens and method of making
US7621949Dec 9, 2004Nov 24, 2009Advanced Medical Optics, Inc.Foldable intraocular lens and method of making
US7862611Mar 12, 2003Jan 4, 2011Bausch & Lomb IncorporatedIntraocular lens
US7931686Jun 30, 2009Apr 26, 2011Bausch & Lomb IncorporatedSmall incision intraocular lens with anti-PCO feature
US8267996 *May 20, 2005Sep 18, 2012Kowa Company, Ltd.Intraocular lens
US8382832Sep 25, 2009Feb 26, 2013Abbott Medical Optics Inc.Foldable intraocular lens and method of making
EP1591080A1 *Apr 16, 2005Nov 2, 2005Humanoptics AGIntraocular Lens
EP1743601A1 *Jun 29, 2006Jan 17, 2007Alcon, Inc.Intraocular lens system
WO2005115278A1 *May 4, 2005Dec 8, 2005Humanoptics AgAdaptable intraocular lens
Classifications
U.S. Classification623/6.4, 623/6.49, 623/6.51
International ClassificationA61F2/16
Cooperative ClassificationA61F2/1613, A61F2002/1681
European ClassificationA61F2/16B
Legal Events
DateCodeEventDescription
Sep 22, 2003ASAssignment
Owner name: RAYNER INTRAOCULAR LENSES LIMITED, UNITED KINGDOM
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:TOOP, PETER;REEL/FRAME:014508/0494
Effective date: 20030626