OPHTHALMOSURGICAL INJECTOR SYSTEM

Abstract

An ophthalmosurgical injector system includes an injector, which has a handpiece, a plunger, and a dispensing device; an intraocular lens, which has an optic body and two C-shaped haptic arms protruding therefrom; and a cartridge, in which the intraocular lens is received. The dispensing device has an inlet opening at the proximal end and an outlet opening at the distal end. When the plunger is moved forward, the intraocular lens is conveyed from the cartridge through the inlet opening to the outlet opening of the dispensing device. When the intraocular lens is held in the cartridge in a compressed and preloaded state, a subregion of each of the haptic arms bears on and covers the optic body. In a plan view, the optic body of the preloaded intraocular lens has a circular surface area with a diameter of at least 4.0 mm that is not covered by the haptic arms.

Claims

1. An ophthalmosurgical injector system comprising: an injector having: a handpiece, a plunger, and a dispensing device, an intraocular lens having an optic body and two C-shaped haptic arms protruding from the optic body, and a cartridge configured to receive the intraocular lens and to be inserted in the injector, wherein the dispensing device has an inlet opening at a proximal end and an outlet opening at a distal end thereof, wherein the dispensing device is configured to convey the intraocular lens from the cartridge through the inlet opening to the outlet opening of the dispensing device when the plunger is moved forward, wherein the intraocular lens is held in the cartridge in a compressed and preloaded state in which a subregion of each of the C-shaped haptic arms bears on the optic body and covers the optic body in the subregion, and wherein the optic body of the intraocular lens in the preloaded state has, in a plan view, a circular surface area not covered by the haptic arms, which circular surface area has a diameter of at least 4.0 mm.

2. The ophthalmosurgical injector system as claimed in claim 1, wherein the injector system has a locking device for locking the plunger in a fixed position relative to at least one of the handpiece or the cartridge.

3. The ophthalmosurgical injector system as claimed in claim 1, the cartridge further comprising: wing elements coupled to hinges, wherein an insertion of the intraocular lens into the cartridge is permitted when the wing elements are in an opened position, and, wherein folding of the inserted intraocular lens is permitted when the wing elements are pivoted to a closed position.

4. The ophthalmosurgical injector system as claimed in claim 1, wherein an external diameter of the compressed and preloaded intraocular lens is at most 8 mm.

5. The ophthalmosurgical injector system as claimed in claim 1, wherein the intraocular lens is made of a hydrophobic acrylic polymer.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0024] Further advantages and features of the disclosure are explained with reference to the following drawings, in which:

[0025] FIG. 1 shows a schematic illustration of an injector system;

[0026] FIG. 2 shows a schematic illustration of an artificial intraocular lens in the unloaded state, in a plan view;

[0027] FIG. 3 shows a schematic illustration of the artificial intraocular lens in the compressed state, in a plan view;

[0028] FIG. 4 shows a schematic illustration of the artificial intraocular lens in the compressed state, in a side view; and

[0029] FIG. 5 shows a schematic perspective illustration of a cartridge with wing elements and an intraocular lens inserted into the cartridge and compressed.

DETAILED DESCRIPTION OF EXEMPLARY EMBODIMENTS

[0030] FIG. 1 shows a schematic illustration of one exemplary embodiment of an ophthalmosurgical injector system 100 according to the disclosure. The injector system 100 has an injector 1, which has a handpiece 2 and a plunger 3. In addition, the injector has a dispensing device 4 through which an artificial intraocular lens 5 can be conveyed. The intraocular lens 5 has an optic body 6 and two C-shaped haptic arms 7 which protrude therefrom and are arranged lying opposite each other (see also FIG. 2). The intraocular lens 5 is inserted in a cartridge 8, which is positioned in the injector system 100 before the dispensing device 4. By means of a forward movement (see arrow 9), the plunger 3 guided in the handpiece 2 can have its distal end 31 come into contact with one of the haptic arms 7, whereupon the haptic arms 7 deform in the direction toward the optic body 6.

[0031] The intraocular lens is, in an unloaded state at the time of production, such that the distance from one haptic arm 7 to the opposite haptic arm 7 has a length L1 (see FIG. 2). When the distal end 31 of the plunger 3 applies a force F to the haptic arms 7 perpendicular to an optical axis A of the optic body 6, the haptic arms reach in the direction of the optic body 6 on account of the elasticity of the material of the intraocular lens, which material is preferably a hydrophobic acrylic polymer.

[0032] FIG. 3 shows the intraocular lens 5 in a compressed state, in which a subregion 51 of each of the haptic arms 7 bears on the optic body 6 and partially covers the latter there. The optic body 6 of the preloaded intraocular lens 5 has, in a plan view, a circular surface area 61 not covered by the haptic arms 7, which circular surface area 61 has a diameter D1 of at least 4.0 mm. The outer circumference of the circular surface area is shown by a dotted line in FIG. 3. In this compressed state of the intraocular lens 5, the distance from one haptic arm 7 to the opposite haptic arm 7 has a length L2, which is shorter than the length L1. With a length L1 of 12 mm, such compression of the intraocular lens 5 leads to a length L2 of approximately 7.5 mm to 8 mm. The subregion 51 is a surface representing part of a circular ring which is formed between a ring with the external diameter D2 of the optic body 6 and a ring with the diameter D1 of the circular surface area 61.

[0033] FIG. 4 shows the compressed intraocular lens 5 in a side view. It can be seen from this view that a subregion of each of the haptic arms 7 bears on the optic body 6. The haptic arms 7 protrude only slightly, or indeed not at all, above the summit 62 of the optic body 6; this depends on the refractive power of the optic body.

[0034] FIG. 5 shows a perspective view of the intraocular lens 5 inserted in the cartridge 8 and compressed. The distal end 31 of the plunger 3 is in touching contact with one of the haptic arms 7. The cartridge 8 has two wing elements 81, which are shown in an opened position in FIG. 5. By pivoting the wing elements 81 about an associated hinge 82, preferably a film hinge, the intraocular lens 5 can be folded or rolled up, such that it can be pushed into an inlet portion 41 of the dispensing device 4. By continued movement of the plunger 3 in the direction of the arrow 9, the intraocular lens 5 emerges at the distal end of the dispensing device 4, i.e., at the outlet opening 42, to be introduced into the capsular bag of an eye.

[0035] The foregoing description of the exemplary embodiments of the disclosure illustrates and describes the present invention. Additionally, the disclosure shows and describes only the exemplary embodiments but, as mentioned above, it is to be understood that the disclosure is capable of use in various other combinations, modifications, and environments and is capable of changes or modifications within the scope of the concept as expressed herein, commensurate with the above teachings and/or the skill or knowledge of the relevant art.

[0036] The term comprising (and its grammatical variations) as used herein is used in the inclusive sense of having or including and not in the exclusive sense of consisting only of. The terms a and the as used herein are understood to encompass the plural as well as the singular.

[0037] All publications, patents and patent applications cited in this specification are herein incorporated by reference, and for any and all purposes, as if each individual publication, patent or patent application were specifically and individually indicated to be incorporated by reference. In the case of inconsistencies, the present disclosure will prevail.