WO2007097221A1 - Intraocular lens inserter - Google Patents

Intraocular lens inserter Download PDF

Info

Publication number
WO2007097221A1
WO2007097221A1 PCT/JP2007/052460 JP2007052460W WO2007097221A1 WO 2007097221 A1 WO2007097221 A1 WO 2007097221A1 JP 2007052460 W JP2007052460 W JP 2007052460W WO 2007097221 A1 WO2007097221 A1 WO 2007097221A1
Authority
WO
WIPO (PCT)
Prior art keywords
plunger
intraocular lens
lens
main body
insertion device
Prior art date
Application number
PCT/JP2007/052460
Other languages
French (fr)
Japanese (ja)
Inventor
Takashi Ichinohe
Original Assignee
Hoya Corporation
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Hoya Corporation filed Critical Hoya Corporation
Publication of WO2007097221A1 publication Critical patent/WO2007097221A1/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters 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
    • A61F2/02Prostheses implantable into the body
    • A61F2/14Eye parts, e.g. lenses, corneal implants; Implanting instruments specially adapted therefor; Artificial eyes
    • A61F2/16Intraocular lenses
    • A61F2/1662Instruments for inserting intraocular lenses into the eye

Definitions

  • Intraocular lens insertion device Intraocular lens insertion device
  • the present invention relates to an intraocular lens insertion device for inserting an intraocular lens into an eyeball instead of a crystalline lens removed by cataract surgery.
  • the implanted intraocular lens has a hard intraocular lens whose optical part is made of a hard material such as polymethylmethallate (PMMA), and a soft material that is made of a soft material such as silicone elastomer, soft acrylic, and hyde mouth gel.
  • PMMA polymethylmethallate
  • a soft material that is made of a soft material such as silicone elastomer, soft acrylic, and hyde mouth gel.
  • intraocular lens When using a rigid intraocular lens, it is necessary to insert the intraocular lens into the cornea or sclera through an incision with a width approximately the same as or slightly larger than the diameter of the optical part.
  • the intraocular lens when a soft intraocular lens is used, the intraocular lens can be inserted into the eyeball from a smaller incision by folding the optical part. By performing surgery with a small incision, the risk of corneal astigmatism after surgery can be avoided. Powerful circumstances In recent years, soft intraocular lenses have been favored.
  • a method for inserting a soft intraocular lens into an eye is called an injector, in addition to a method for directly inserting an intraocular lens (hereinafter simply referred to as a lens) folded by an insulator directly into the eye.
  • a dedicated intraocular lens insertion device In general, the basic structure of an injector consists of a nozzle portion that is tapered to insert the lens into the eye, a plunger that pushes out the lens, and a cylindrical body that holds them.
  • Various types of intraocular lens insertion devices have been proposed. They are roughly classified into two-handed and one-handed.
  • a double-handed intraocular lens insertion instrument is one in which an intraocular lens is inserted into an eyeball by holding a body of the insertion instrument with one hand and pushing a plunger with the other hand.
  • a female screw and a screw provided in a part of the main body at the rear end of the plunger.
  • a matching male screw is provided, and the rear end of the plunger is rotated to move the plunger back and forth to push out the lens.
  • the one-hand operated intraocular lens insertion instrument is configured such that the index finger and the middle finger of one hand are brought into contact with a gripping piece provided in the insertion instrument body, and the thumb is brought into contact with the end face of the plunger and pressed.
  • the lens is inserted into the eyeball.
  • One-hand operated intraocular lens insertion instruments can be operated with only one hand, and have the advantages of using the other hand to grasp and stabilize eye tissue with tweezers, or to operate other surgical instruments.
  • By using such a dedicated indicator it is possible to fold the lens smaller than using a lever, and an incisional loci of 3 mm or less can be inserted into the eye.
  • a one-hand operated intraocular lens insertion device presses a lens with a plunger housed in a cylindrical body so as to be reciprocally movable, and releases it into the eye.
  • the pressing force varies greatly depending on the sliding resistance between the lens and the inner surface of the main body.
  • the sliding resistance between the lens and the inner surface of the main body is large, and it becomes difficult to control the pushing force when the folded lens is released at the tip of the main body, which is a nozzle. Risk damaging the intraocular tissue. Therefore, an injector having a structure that can gently push the plunger in any situation has been desired.
  • a rubber O-ring is disposed between the outer peripheral surface of the plunger and the inner peripheral surface of the main body, and a certain pressing force is applied to the side surface of the plunger to reduce the sliding resistance.
  • Technology to change is disclosed.
  • the O-ring is arranged in this way, the number of parts increases, so that the manufacturing cost becomes expensive.
  • the size of the sliding resistance varies depending on the individual due to the manufacturing dimension error of the O-ring body (see, for example, Patent Document 1).
  • a panel is interposed between the main body and the plunger so that a load in the opposite direction is applied to the plunger. Have been disclosed. (For example, see Patent Document 2).
  • Patent Document 1 Japanese Unexamined Patent Application Publication No. 2004-113610
  • Patent Document 2 Japanese Translation of Special Publication 2000-516487
  • the present invention is intended to solve such a problem of the conventional technology, and can insert the lens into the eyeball safely and securely by pushing the plunger gently with only one hand operation. It is an object to provide an instrument.
  • the invention according to claim 1 includes a cylindrical main body that passes through a deformable intraocular lens and guides it into the eyeball, and is reciprocally moved in the main body.
  • the eyeball is pressed by pressing the intraocular lens.
  • An intraocular lens insertion device comprising a plunger that is released into the body, and an elastic body and Z or a sliding resistance increasing mechanism between the main body and the plunger, and the pressing force (F) force of the plunger In the movement stroke (X) of the plunger after reaching the first peak value, 60% or more of the peak value can be maintained.
  • the invention according to claim 2 includes a cylindrical main body that passes through a deformable intraocular lens and guides it into the eyeball, and is reciprocally moved in the main body, and presses the intraocular lens to press the eyeball.
  • a plunger that releases into the body, and an elastic body and Z or between the main body and the plunger.
  • An intraocular lens insertion device provided with a sliding resistance increasing mechanism, wherein the value of the plunger pressing force (F) with respect to the movement stroke (X) of the plunger does not decrease It is.
  • the invention according to claim 3 is the intraocular lens insertion device according to claim 1 or 2, characterized in that the elastic body includes a plurality of elastic bodies having different elasticity values. is there
  • the invention according to claim 4 is the intraocular lens insertion device according to claim 1 or 2, characterized in that the elastic value of the elastic body has a nonlinear characteristic.
  • the intraocular lens insertion device of claim 1 since the pressing force of the plunger with respect to the movement stroke of the plunger does not significantly decrease even after the first peak has elapsed, Can also move the plunger gently. Therefore, the lens can be safely and reliably inserted into the eyeball.
  • the plunger can be loosened even with one-handed operation. Can be moved. Therefore, the lens can be inserted into the eyeball safely and reliably.
  • the panel reaction force with respect to the movement stroke of the plunger can be made to have a discontinuous characteristic by combining a plurality of elastic bodies having different elastic values. As a result, the maximum value of the plunger pressing force can be suppressed.
  • the panel reaction force with respect to the movement stroke of the plunger can be designed more precisely.
  • FIG. 1 is a cross-sectional view of an intraocular lens insertion device showing a first embodiment of the present invention.
  • FIG. 2 is a characteristic diagram showing the relationship between the plunger stroke and the pressing force of an intraocular lens insertion device without an elastic body.
  • FIG. 3 is a characteristic diagram showing the relationship between the plunger travel and the pressing force when a lens is not loaded into an intraocular lens insertion device provided with an elastic body.
  • FIG. 4 is a characteristic diagram showing the relationship between the plunger travel and the pressing force in the intraocular lens insertion device of the first embodiment.
  • FIG. 5 is a characteristic diagram showing the relationship between the plunger travel and the pressing force when elastic bodies having different elasticity values are used.
  • FIG. 8 is a cross-sectional view of an intraocular lens insertion device showing a second embodiment of the present invention.
  • FIG. 9 is a characteristic diagram showing the relationship between the travel of the plunger and the pressing force when the intraocular lens insertion device of the second embodiment is not loaded with a lens.
  • FIG. 10 is a cross-sectional view of an intraocular lens insertion device showing a third embodiment of the present invention.
  • FIG. 11 is a cross-sectional view of an intraocular lens insertion device showing a fourth embodiment of the present invention.
  • FIG. 1 is a sectional view showing a first embodiment of an intraocular lens insertion device to which the present invention is applied.
  • the intraocular lens insertion device 1 is housed in a cylindrical main body 3 that passes through a deformable intraocular lens 2 and is guided into the eyeball, and is reciprocally moved in the main body 3, and presses the intraocular lens 2.
  • a plunger 4 that is released into the eyeball, and an elastic body 5 between the main body 3 and the plunger 4.
  • the cylindrical main body 3 includes a nozzle 3a in which the tip of the incisional locus of the eyeball is inserted into the eyeball, a lens installation portion 3b in which the lens 2 is installed, and a gripping portion 3c in which the operator's finger holds the finger. Is provided. Further, the lens installation portion 3b is provided with a lid 6 that can be freely opened and closed, and the lens installation portion 3b is provided with a fixing projection 3d for restricting the movement of the lens 2.
  • the main body 3 is provided with an intermediate support portion 3e that pivotally supports the plunger 4, and a base end support member 7 that pivotally supports the plunger 4 is also provided on the base end side of the main body 3. In FIG.
  • the main body 3 and the base end support member 7 are configured as separate members, but both members have good lubrication characteristics and low frictional resistance. It is also possible to configure.
  • the main unit 3 It is possible to manufacture the nozzle 3a and the gripping part 3c separately, and then assemble them together by assembling.
  • the material of the constituent members of the device is required to be a physically stable material.
  • the materials used at the site of insertion into the eye must be biologically safe.
  • FDA Food and Drug Administration
  • ISO International Standardization Organization
  • the material is confirmed.
  • polyethylene, polypropylene, or the like can be used as the material of the cylindrical main body 3.
  • the lens 2 also has a force with an optical part 2a which is a lens body and two support members 2b for fixing the position of the optical part 2a in the eyeball.
  • the support member 2b has a thin beard shape.
  • This lens 2 is made of a flexible material such as soft acrylic and can fold the lens itself.
  • the plunger 4 includes a portion 4a having an outer diameter that is slightly smaller than the inner diameter of the proximal support member 7, and a portion 4b having an outer diameter that is slightly smaller than the inner diameter of the nozzle.
  • a portion 4 a having an outer diameter slightly smaller than the inner diameter of the base end support member 7 is slidably inserted into the base end support member 7.
  • a portion 4b having an outer diameter slightly smaller than the inner diameter of the nozzle 3a is slidably inserted into the intermediate support portion 3e of the main body.
  • a panel 5 as an elastic body is attached between the main body 3 and the plunger 4.
  • a string spring 5 is mounted between the right end surface of the intermediate support portion 3e of the main body and the step portion 4c of the plunger.
  • This string spring 5 must have an appropriate panel constant and an appropriate deformation amount! /, which will be described later.
  • the operator can insert the lens 2 into the eyeball with a single hand operation. Specifically, the grasping portion 3c of the main body is grasped by the index finger and middle finger of one hand, and the abdomen of the thumb is brought into contact with the base end 4d of the plunger and the plunger 4 is pushed into the main body 3. Then lens 2 is plunge It is pressed by the tip of the nozzle 4 and is pushed into the nozzle 3a while being folded at the tapered lens transition portion 3f. When the plunger 4 is further pushed in, the lens 2 moves in the nozzle 3a and is released into the eyeball from the opening 3g at the tip of the nozzle.
  • the movement stroke (X) itself of this plunger is the movement stroke (X) itself of this plunger.
  • the horizontal axis travels from the right side to the left side.
  • the point where the horizontal axis intersects the vertical axis indicates the position after the lens 2 that is not at the origin is released.
  • FIG. 2 is a characteristic diagram in which the relationship between the movement stroke (X) and the pressing force (F) of the plunger 4 of the intraocular lens insertion device 1 without the elastic body 5 is measured.
  • This characteristic has been measured for many actual objects, and it has been found that although there are some individual differences, it shows an almost constant relationship. Even if the same intraocular lens insertion device is used, the characteristics will be different because the lens thickness will be different if the power of the intraocular lens is different. As a matter of course, the peak value of the pressing force becomes large in the case of a thick lens having a high frequency.
  • the point (i) on the horizontal axis corresponds to the point (i) in FIG. 1, that is, the tip position of the nozzle 3a.
  • the (mouth) point on the horizontal axis corresponds to the (mouth) point in FIG. 1, that is, the boundary position between the lens transition portion 3f and the nozzle 3a.
  • the speed at which the plunger 4 is pushed may be a speed suitable for inserting the lens 2 into the eye, and generally a force of about 70 mm / min to about 20 mm / min to 200 mm / min. 130 mm / min is preferred.
  • the force required to fold the lens becomes maximum.
  • the plunger pressing force (F) reaches its peak. Thereafter, when the plunger 4 is further pressed and the lens 2 is moved to the left side, the pressing force (F) required for the plunger is rapidly reduced.
  • the reason why the pressing force (F) required to move the lens 2 in the substantially cylindrical nozzle 3a suddenly decreases is that the force required to fold the lens 2 becomes unnecessary and the nozzle opening 3g is folded. This is based on enlargement by receiving the internal pressure from the lens.
  • FIG. 3 is a characteristic diagram showing the relationship between the travel stroke (X) of the brassiere 4 and the pressing force (F) when the lens 2 is not loaded into the intraocular lens insertion device 1 provided with the elastic body 5. is there.
  • the significance of the vertical and horizontal axes is the same as in Fig. 2 (hereinafter also the same in Figs. 3 to 7 and 9).
  • O The point (c) on the horizontal axis moves the plunger 4
  • the position where the panel 5 starts to be compressed by the step 4c is shown. Since the string spring 5 having linear characteristics is used as an elastic body, the plunger pressing force (F) increases linearly after the panel starts to deform.
  • FIG. 4 is a characteristic diagram showing the relationship between the movement stroke (X) of the plunger 4 and the pressing force (F) when the lens 2 is loaded into the intraocular lens insertion device 1 of the first embodiment and pushed out. It is. This is the case where the panel constant and the panel deformation amount are set appropriately. As a result, the characteristics shown in Fig. 2 and Fig. 3 are superimposed. In other words, when the plunger 4 is moved from the right side to the left side, the plunger pressing force (F) starts to rise when the plunger travel (X) reaches the panel deformation start position (c).
  • the pressing force (F) of the plunger is such that the lens 2 contacts the nozzle inner wall force nozzle of the lens transition part 3f. It increases continuously until it reaches the field position (mouth) point.
  • the plunger pressing force (F) increases again without significantly decreasing although it slightly decreases from the peak value at the (mouth) point.
  • the plunger pressing force (F) does not decrease. Therefore, even if the nozzle 3a force is also at the position (ii) where the lens 2 is released, the plunger pressing force (F) suddenly disappears, and there is no danger of the tip of the plunger surging and jumping into the eyeball. .
  • FIG. 5 is a characteristic diagram showing the relationship between the plunger travel (X) and the pressing force (F) when an elastic body having an elastic value different from that of the injector of the first embodiment is used. is there.
  • This elastic body has an excessive panel reaction force against the force required to deform the lens, and has the advantage that the pressing force (F) of the plunger increases almost linearly.
  • the plunger pressing force (F) at the point (i) where the lens is released from the tip of the nozzle becomes too large.
  • FIG. 6 is a characteristic diagram showing the relationship between the plunger travel (X) and the pressing force (F) when an elastic body having an elastic value different from that of the elastic body shown in FIG. 5 is used.
  • This elastic body has a panel reaction force that is approximately appropriate for the force required to deform the lens.
  • the plunger pressing force (F) is discontinuous, the plunger travel (X The plunger's pressing force (F) against) does not decrease.
  • FIG. 7 further shows the relationship between the plunger travel (X) and the pressing force (F) when an elastic body having an elastic value different from that shown in FIGS. 5 and 6 is used.
  • This elastic body has an excessive panel reaction force against the force required to deform the lens, and the tip force of the nozzle
  • the plunger's pressing force (F) at the point (i) where the lens is released is large. There is an advantage that it does not become too much.
  • the rate of decrease in the plunger pressing force (F) after the (mouth) point has passed is too large with respect to the initial peak value.
  • the plunger pressing force (F) with respect to the movement stroke (X) of the plunger 4 is greatly increased even after the first peak has elapsed. Since it does not decrease, the plunger can be moved gently even with one-handed operation. Also, the plunger pressure against the plunger travel (X) Since the value of (F) does not decrease, the plunger can be moved gently even with one-handed operation. Therefore, the lens can be safely and reliably inserted into the eyeball.
  • the plunger travel (X) after the plunger pressing force (F) reaches the first peak value should hold 60% or more of the peak value. This is defined based on the value that can be operated without the operator feeling uncomfortable when actually operating with one hand. Although this value varies slightly between individuals, considering safety, 75% or more is preferable, and 90% or more is even more preferable.
  • FIG. 8 is a cross-sectional view of an intraocular lens insertion device showing a second embodiment of the present invention.
  • This intraocular lens insertion device 1 is characterized by comprising a plurality of elastic bodies 5a and 5b having different elasticity values. Since the basic configuration is the same as that of the first embodiment shown in FIG. 1, the description of the common portions is omitted, and only the portion having a configuration different from that of the first embodiment will be described.
  • one elastic body 5 is disposed between the main body 3 and the plunger 4, but in this embodiment, two panel 5a and 5b having different panel constants and deformation amounts are disposed. Yes.
  • the deformation amount of the string hook spring 5a disposed on the inner side is set large, and the deformation amount of the string hook spring 5b disposed on the outer side is set small.
  • a sliding ring 8 is slidably mounted on the plunger 4b between the right end of the string paddle panel 5a disposed on the inside and the step 4c of the plunger.
  • FIG. 9 is a characteristic diagram showing the relationship between the plunger movement stroke (X) and the pressing force (F) when the lens 2 is not loaded in the intraocular lens insertion device of the second embodiment. is there.
  • the pressing force (F) is small because only the sliding resistance between the plunger 4 and the main body 3 on which the plunger is supported is initially.
  • the movement of the plunger 4 advances, and the string spring 5a disposed inside by the plunger step 4c starts to be compressed through the sliding ring 8.
  • the panel reaction force with respect to the movement stroke (X) of the plunger can be made discontinuous by combining the panels 5a and 5b having a plurality of panel constants.
  • an intraocular lens insertion device capable of suppressing the maximum value of the plunger's pressing force (F) can be realized.
  • FIG. 10 is a cross-sectional view of an intraocular lens insertion device showing a third embodiment of the present invention.
  • This intraocular lens insertion device 1 is characterized in that the elastic value of the elastic body has a nonlinear characteristic. Descriptions of portions common to the first and second embodiments shown in FIG. 1 are omitted, and only portions having configurations different from those of the embodiments are described.
  • the elastic body 5 is disposed in the cylindrical main body 3, but in this embodiment, the elastic bodies 5c to 513 ⁇ 4 are provided between the main body 3 and the base end 4d of the plunger. It is arranged.
  • FIG. 10 is a cross-sectional view of an intraocular lens insertion device showing a third embodiment of the present invention.
  • This intraocular lens insertion device 1 is characterized in that the elastic value of the elastic body has a nonlinear characteristic. Descriptions of portions common to the first and second embodiments shown in FIG. 1 are omitted, and only portions having configurations different from those of the embodiments are described.
  • FIG. 10 (a) shows two string springs 5c and 5d having different elastic values are arranged between the main body 3 and the base end 4d of the plunger.
  • FIG. 10 (b) shows a string spring 5e in which the wire diameter gradually changes from one end to the other end between the main body 3 and the base end 4d of the plunger.
  • FIG. 10 (c) shows a string hook spring 5 in which the string hook diameter gradually changes from one end to the other end between the main body 3 and the base end 4d of the plunger.
  • a sliding ring 8 is attached to one end or both ends of each of the string springs 5c to 5f in order to ensure good seating when the panel is compressed.
  • FIG. 11 is a cross-sectional view of an intraocular lens insertion device showing a fourth embodiment of the present invention.
  • This intraocular lens insertion device 1 has an elastic body 5 disposed between a main body 3 and a plunger 4, and a sliding resistance increasing mechanism 9 is provided on an outer surface 4a of the plunger that slides with the inner surface of the cylindrical main body 3. It is prepared.
  • the basic configuration of this embodiment is the same as that of the first embodiment shown in FIG. The description of the minute is omitted, and only a portion having a configuration different from the first embodiment will be described.
  • a sliding resistance increasing mechanism 9 is provided on the outer surface 4a of the plunger that slides with the inner surface of the cylindrical main body 3.
  • one or more protrusions 9a to 9c are provided on the outer surface 4a of the plunger.
  • the axial position of the plunger 4 where the protrusions 9a to 9c are provided corresponds to the position where the pressing force of the plunger 4 starts to decrease when the deformation resistance required for folding the lens 2 is lost and the protrusions 9a to 9c are not provided. ing. With such a configuration, a sudden change in the plunger pressing force with respect to the plunger travel can be mitigated.
  • a string spring 5 as an elastic body is disposed between the main body 3 and the plunger 4, and a protrusion 9a to 9c as a sliding resistance increasing mechanism is provided on the outer surface 4a of the plunger.
  • a protrusion 9a to 9c as a sliding resistance increasing mechanism is provided on the outer surface 4a of the plunger.
  • the intraocular lens 2 is set in a cartridge different from the force body 3 described in the case where the intraocular lens 2 is directly set in the cylindrical main body 3, and the cartridge is mounted.
  • the present invention can also be applied to a cartridge-type intraocular lens insertion device used by being mounted on the main body 3.
  • the elastic body 5 is not limited to the string panel, but is a foamed foam. It may be an elastic body that uses the elasticity of the material itself!

Abstract

An intraocular lens inserter with which a lens can be inserted into an eyeball surely in safety by pushing a plunger gently even by a single hand operation. The intraocular lens inserter (1) comprises a tubular body (3) for passing a deformable intraocular lens (2) and introducing it into an eyeball, a plunger (4) contained reciprocatingly in the body (3) and pressing the intraocular lens (2) to be released into the eyeball, and a resilient body (5) and/or a sliding resistance increasing mechanism provided between the body (3) and the plunger (4). Pressing force (F) of the plunger (4) can be kept at 60% or above of a first peak value in the moving stroke (X) of the plunger (4) after the first peak value is reached.

Description

明 細 書  Specification
眼内レンズ揷入器具  Intraocular lens insertion device
技術分野  Technical field
[0001] 本発明は、白内障手術により摘出した水晶体の代わりに、眼球内に眼内レンズを挿 入するための眼内レンズ挿入器具に関する。  [0001] The present invention relates to an intraocular lens insertion device for inserting an intraocular lens into an eyeball instead of a crystalline lens removed by cataract surgery.
背景技術  Background art
[0002] 白内障手術においては、超音波乳化吸引によって混濁した水晶体を除去し、その 水晶体除去後の眼内へ人工眼内レンズを埋植する方法が広く行なわれている。埋植 される眼内レンズには、光学部がポリメチルメタタリレート(PMMA)などの硬質材料 力 なる硬質眼内レンズと、シリコーンエラストマ一、軟質アクリル、ハイド口ゲルなど の柔らかい材料力もなる軟質眼内レンズがある。硬質眼内レンズを用いる場合には、 角膜、あるいは強膜に光学部の径とほぼ同じか、それよりやや大きな幅の切開創から 眼内レンズを挿入する必要がある。一方、軟質眼内レンズを用いる場合には、光学 部を折り畳むことにより更に小さな切開創から眼内レンズを眼球内に挿入することが 可能となる。そして、小さな切開創により手術を行なうことで手術後の角膜乱視ゃ感 染症の危険性を回避することができる。力かる事情力 近年においては、軟質眼内レ ンズが好んで用いられる傾向にある。  In cataract surgery, a method is widely used in which a turbid lens is removed by ultrasonic emulsification and the artificial intraocular lens is implanted in the eye after the lens is removed. The implanted intraocular lens has a hard intraocular lens whose optical part is made of a hard material such as polymethylmethallate (PMMA), and a soft material that is made of a soft material such as silicone elastomer, soft acrylic, and hyde mouth gel. There is an intraocular lens. When using a rigid intraocular lens, it is necessary to insert the intraocular lens into the cornea or sclera through an incision with a width approximately the same as or slightly larger than the diameter of the optical part. On the other hand, when a soft intraocular lens is used, the intraocular lens can be inserted into the eyeball from a smaller incision by folding the optical part. By performing surgery with a small incision, the risk of corneal astigmatism after surgery can be avoided. Powerful circumstances In recent years, soft intraocular lenses have been favored.
[0003] 軟質眼内レンズを眼内に挿入する方法には、鑷子により折り畳んだ眼内レンズ (以 下、単にレンズともいう。)をそのまま直接眼内に挿入する方法の他に、インジェクター と呼ばれる専用の眼内レンズ挿入器具を用いる方法がある。一般的にインジェクター の基本構成は、レンズを眼内に挿入するために先細りとなっているノズル部と、レンズ を押し出すためのプランジャーと、それらを保持する筒状の本体とからなる。眼内レン ズ挿入器具には種々のタイプのものが提案されている力 大別すると両手操作式の ものと片手操作式のものに分類される。  [0003] A method for inserting a soft intraocular lens into an eye is called an injector, in addition to a method for directly inserting an intraocular lens (hereinafter simply referred to as a lens) folded by an insulator directly into the eye. There is a method using a dedicated intraocular lens insertion device. In general, the basic structure of an injector consists of a nozzle portion that is tapered to insert the lens into the eye, a plunger that pushes out the lens, and a cylindrical body that holds them. Various types of intraocular lens insertion devices have been proposed. They are roughly classified into two-handed and one-handed.
[0004] 両手操作式の眼内レンズ挿入器具は、一方の手で挿入器具本体を保持しつつ、 他方の手でプランジャーを押し込むことにより眼内レンズを眼球内へ挿入するもので ある。具体的にはプランジャーの後端において本体の一部に設けられた雌ねじと螺 合する雄ねじを設け、プランジャーの後端を回転させることによりプランジャーを前後 に移動させてレンズを押し出すものである。 [0004] A double-handed intraocular lens insertion instrument is one in which an intraocular lens is inserted into an eyeball by holding a body of the insertion instrument with one hand and pushing a plunger with the other hand. Specifically, a female screw and a screw provided in a part of the main body at the rear end of the plunger. A matching male screw is provided, and the rear end of the plunger is rotated to move the plunger back and forth to push out the lens.
[0005] また、片手操作式の眼内レンズ挿入器具は、挿入器具本体に設けられた把持片に 片手の人差し指と中指を当接するとともに、親指をプランジャーの端面に当接して押 圧することによりレンズを眼球内へ挿入するものである。片手操作式の眼内レンズ挿 入器具は片手だけで操作でき、他方の手を使ってピンセットで眼組織を把持し安定 化する、あるいは他の手術器具を操作するなどの利点があるため、術者は片手操作 式の眼内レンズ挿入器具を好む傾向にある。このような専用のインジヱクタ一を使用 することにより、鑷子を用いてレンズを折り畳むよりも小さく折り畳むことができ、 3mm 以下の切開創ロカもレンズを眼内へ挿入することも可能となる。  [0005] In addition, the one-hand operated intraocular lens insertion instrument is configured such that the index finger and the middle finger of one hand are brought into contact with a gripping piece provided in the insertion instrument body, and the thumb is brought into contact with the end face of the plunger and pressed. The lens is inserted into the eyeball. One-hand operated intraocular lens insertion instruments can be operated with only one hand, and have the advantages of using the other hand to grasp and stabilize eye tissue with tweezers, or to operate other surgical instruments. One tends to prefer single-handed intraocular lens insertion instruments. By using such a dedicated indicator, it is possible to fold the lens smaller than using a lever, and an incisional loci of 3 mm or less can be inserted into the eye.
[0006] しかし、片手操作式の眼内レンズ挿入器具は、筒状の本体の内部に往復移動可能 に収納されたプランジャーによりレンズを押圧して眼内に放出するものであり、プラン ジャーの押圧力はレンズと本体内面との摺動抵抗により大きく変化する。そして、レン ズと本体内面との摺動抵抗が大き 、と、折り畳まれたレンズがノズルたる本体の先端 で放出された際に押し出し力の制御が困難となり、勢い余ってレンズとプランジャー が急激に飛び出してしまい、眼内組織を損傷する危険がある。そのため、どのような 状況でも緩やかにプランジャーを押すことができる構造のインジェクターが切望され ていた。  [0006] However, a one-hand operated intraocular lens insertion device presses a lens with a plunger housed in a cylindrical body so as to be reciprocally movable, and releases it into the eye. The pressing force varies greatly depending on the sliding resistance between the lens and the inner surface of the main body. In addition, the sliding resistance between the lens and the inner surface of the main body is large, and it becomes difficult to control the pushing force when the folded lens is released at the tip of the main body, which is a nozzle. Risk damaging the intraocular tissue. Therefore, an injector having a structure that can gently push the plunger in any situation has been desired.
[0007] かかる状況下、レンズと本体内面との摺動抵抗を低減するため、本体の内面にコー ティングを施したものがある。このインジェクターでは確かにレンズ開放時の摺動抵抗 の変化が少なくなるため、レンズとプランジャーの急激な飛び出しの危険性は低くな る力 未だ術者の満足が得られるものではな力つた。  [0007] Under such circumstances, in order to reduce the sliding resistance between the lens and the inner surface of the main body, there is one in which the inner surface of the main body is coated. This injector certainly reduces the change in sliding resistance when the lens is opened, so the risk of sudden popping out of the lens and plunger is low.
[0008] また、プランジャーの外周面と本体の内周面との間にゴム製のオーリングを配設し て、プランジャーの側面に対して一定の押圧力を付与して摺動抵抗を変化させる技 術が開示されている。しかし、このようにオーリングを配設するものでは、部品数が増 加することから製作費用が高価となってしまう。また、オーリングゃ本体の製作寸法誤 差等のため、摺動抵抗の大きさが個体によって異なってしまう(例えば、特許文献 1 参照)。 [0009] また、レンズ放出時のレンズとプランジャーとの急激な飛び出しを防止するため、本 体とプランジャーとの間にパネを介在させて、プランジャーに反対方向の負荷をかけ るようにした技術が開示されている。(例えば、特許文献 2参照)。 [0008] Further, a rubber O-ring is disposed between the outer peripheral surface of the plunger and the inner peripheral surface of the main body, and a certain pressing force is applied to the side surface of the plunger to reduce the sliding resistance. Technology to change is disclosed. However, in the case where the O-ring is arranged in this way, the number of parts increases, so that the manufacturing cost becomes expensive. In addition, the size of the sliding resistance varies depending on the individual due to the manufacturing dimension error of the O-ring body (see, for example, Patent Document 1). [0009] Further, in order to prevent a sudden jump-out of the lens and the plunger when the lens is released, a panel is interposed between the main body and the plunger so that a load in the opposite direction is applied to the plunger. Have been disclosed. (For example, see Patent Document 2).
特許文献 1:特開 2004 - 113610号公報  Patent Document 1: Japanese Unexamined Patent Application Publication No. 2004-113610
特許文献 2:特表 2000 - 516487号公報  Patent Document 2: Japanese Translation of Special Publication 2000-516487
発明の開示  Disclosure of the invention
発明が解決しょうとする課題  Problems to be solved by the invention
[0010] し力し、本体とプランジャーとの間にパネを介在させて、プランジャーに反対方向の 負荷をかけるようにした片手操作式の眼内レンズ挿入器具においては、パネ定数と パネ変形量を最適に調整することが極めて重要になる。パネの強さが不十分な場合 、レンズが眼内に放出される際にレンズがノズルの先端カゝら急激に飛び出して眼内 組織を傷つける恐れがある。一方、パネの強さが大きすぎると、レンズを押し出すた めに必要な力も大きくなり、片手での操作が行い難くなる。したがって、パネの強さと 変形量が、プランジャーと本体との間の摺動抵抗力や、レンズの変形に要するプラン ジャーの押圧力との整合がとれていないと所期の目的を達成することができない。 [0010] In a one-hand operation type intraocular lens insertion device in which a panel is interposed between the main body and the plunger to apply a load in the opposite direction, the panel constant and the panel deformation It is extremely important to adjust the amount optimally. When the strength of the panel is insufficient, when the lens is released into the eye, the lens may jump out from the tip of the nozzle and damage the intraocular tissue. On the other hand, if the strength of the panel is too great, the force required to push out the lens also increases, making it difficult to operate with one hand. Therefore, if the strength and deformation of the panel do not match the sliding resistance between the plunger and the main body and the pressing force of the plunger required to deform the lens, the intended purpose is achieved. I can't.
[0011] 本発明はこのような従来技術が有する課題を解決しょうとするものであり、片手操作 だけで緩やかにプランジャーを押して眼球内にレンズを安全確実に挿入することが できる眼内レンズ挿入器具を提供することを課題とする。  [0011] The present invention is intended to solve such a problem of the conventional technology, and can insert the lens into the eyeball safely and securely by pushing the plunger gently with only one hand operation. It is an object to provide an instrument.
課題を解決するための手段  Means for solving the problem
[0012] 請求項 1記載の発明は、変形可能な眼内レンズを通過させて眼球内に導く筒状の 本体と、前記本体内において往復移動可能に収納され、眼内レンズを押圧して眼球 内に放出するプランジャーと、前記本体と前記プランジャー間に弾性体及び Z又は 摺動抵抗増加機構と、を備えた眼内レンズ挿入器具であって、前記プランジャーの 押圧力(F)力 最初のピーク値に達した後のプランジャーの移動行程 (X)において 前記ピーク値の 60%以上を保持可能なことを特徴とするものである。  [0012] The invention according to claim 1 includes a cylindrical main body that passes through a deformable intraocular lens and guides it into the eyeball, and is reciprocally moved in the main body. The eyeball is pressed by pressing the intraocular lens. An intraocular lens insertion device comprising a plunger that is released into the body, and an elastic body and Z or a sliding resistance increasing mechanism between the main body and the plunger, and the pressing force (F) force of the plunger In the movement stroke (X) of the plunger after reaching the first peak value, 60% or more of the peak value can be maintained.
[0013] 請求項 2記載の発明は、変形可能な眼内レンズを通過させて眼球内に導く筒状の 本体と、前記本体内において往復移動可能に収納され、眼内レンズを押圧して眼球 内に放出するプランジャーと、前記本体と前記プランジャー間に弾性体及び Z又は 摺動抵抗増加機構と、を備えた眼内レンズ挿入器具であって、前記プランジャーの 移動行程 (X)に対するプランジャーの押圧力(F)の値が減少しな 、ことを特徴とする ものである。 [0013] The invention according to claim 2 includes a cylindrical main body that passes through a deformable intraocular lens and guides it into the eyeball, and is reciprocally moved in the main body, and presses the intraocular lens to press the eyeball. A plunger that releases into the body, and an elastic body and Z or between the main body and the plunger. An intraocular lens insertion device provided with a sliding resistance increasing mechanism, wherein the value of the plunger pressing force (F) with respect to the movement stroke (X) of the plunger does not decrease It is.
[0014] 請求項 3記載の発明は、請求項 1または 2記載の眼内レンズ挿入器具において、前 記弾性体が異なる弾性値を有する複数の弾性体カゝらなることを特徴とするものである  [0014] The invention according to claim 3 is the intraocular lens insertion device according to claim 1 or 2, characterized in that the elastic body includes a plurality of elastic bodies having different elasticity values. is there
[0015] 請求項 4記載の発明は、請求項 1または 2記載の眼内レンズ挿入器具において、前 記弾性体の弾性値が非線形特性を有することを特徴とするものである。 [0015] The invention according to claim 4 is the intraocular lens insertion device according to claim 1 or 2, characterized in that the elastic value of the elastic body has a nonlinear characteristic.
発明の効果  The invention's effect
[0016] 請求項 1記載の眼内レンズ挿入器具によれば、プランジャーの移動行程に対する プランジャーの押圧力が最初のピーク経過後においても大幅に減少することがない ので、片手操作であってもプランジャーを緩やかに移動させることができる。したがつ て、眼球内にレンズを安全確実に挿入することができる。  [0016] According to the intraocular lens insertion device of claim 1, since the pressing force of the plunger with respect to the movement stroke of the plunger does not significantly decrease even after the first peak has elapsed, Can also move the plunger gently. Therefore, the lens can be safely and reliably inserted into the eyeball.
[0017] 請求項 2記載の眼内レンズ挿入器具によれば、プランジャーの移動行程に対する プランジャーの押圧力の値が減少することがな 、ので、片手操作であってもプランジ ヤーを緩やかに移動させることができる。したがって、眼球内にレンズを安全確実に 挿人することができる。  [0017] According to the intraocular lens insertion device of claim 2, since the value of the plunger pressing force with respect to the movement stroke of the plunger does not decrease, the plunger can be loosened even with one-handed operation. Can be moved. Therefore, the lens can be inserted into the eyeball safely and reliably.
[0018] 請求項 3記載の眼内レンズ挿入器具によれば、異なる弾性値を有する複数の弾性 体を組み合わせることによりプランジャーの移動行程に対するパネ反力を不連続な 特性にすることができる。その結果、プランジャーの押圧力の最大値を抑制すること ができる。  [0018] According to the intraocular lens insertion device of claim 3, the panel reaction force with respect to the movement stroke of the plunger can be made to have a discontinuous characteristic by combining a plurality of elastic bodies having different elastic values. As a result, the maximum value of the plunger pressing force can be suppressed.
[0019] 請求項 4記載の眼内レンズ挿入器具によれば、弾性体の弾性値が非線形特性を 有することから、プランジャーの移動行程に対するパネ反力をより精密に設計すること ができる。  [0019] According to the intraocular lens insertion device of claim 4, since the elastic value of the elastic body has nonlinear characteristics, the panel reaction force with respect to the movement stroke of the plunger can be designed more precisely.
図面の簡単な説明  Brief Description of Drawings
[0020] [図 1]本発明の第 1実施例を示す眼内レンズ挿入器具の断面図である。 FIG. 1 is a cross-sectional view of an intraocular lens insertion device showing a first embodiment of the present invention.
[図 2]弾性体を設けない眼内レンズ挿入器具のプランジャーの移動行程と押圧力との 関係を示す特性図である。 [図 3]弾性体を設けた眼内レンズ挿入器具にレンズを装填しない場合のプランジャー の移動行程と押圧力との関係を示す特性図である。 FIG. 2 is a characteristic diagram showing the relationship between the plunger stroke and the pressing force of an intraocular lens insertion device without an elastic body. FIG. 3 is a characteristic diagram showing the relationship between the plunger travel and the pressing force when a lens is not loaded into an intraocular lens insertion device provided with an elastic body.
[図 4]第 1実施例の眼内レンズ挿入器具におけるプランジャーの移動行程と押圧力と の関係を示す特性図である。  FIG. 4 is a characteristic diagram showing the relationship between the plunger travel and the pressing force in the intraocular lens insertion device of the first embodiment.
[図 5]異なる弾性値を有する弾性体を用いた場合のプランジャーの移動行程と押圧 力との関係を示す特性図である。  FIG. 5 is a characteristic diagram showing the relationship between the plunger travel and the pressing force when elastic bodies having different elasticity values are used.
[図 6]同上  [Figure 6] Same as above
[図 7]同上  [Figure 7] Same as above
[図 8]本発明の第 2実施例を示す眼内レンズ挿入器具の断面図である。  FIG. 8 is a cross-sectional view of an intraocular lens insertion device showing a second embodiment of the present invention.
[図 9]第 2実施例の眼内レンズ挿入器具にぉ 、て、レンズを装填しな 、場合のプラン ジャーの移動行程と押圧力との関係を示す特性図である。  FIG. 9 is a characteristic diagram showing the relationship between the travel of the plunger and the pressing force when the intraocular lens insertion device of the second embodiment is not loaded with a lens.
[図 10]本発明の第 3実施例を示す眼内レンズ挿入器具の断面図である。  FIG. 10 is a cross-sectional view of an intraocular lens insertion device showing a third embodiment of the present invention.
[図 11]本発明の第 4実施例を示す眼内レンズ挿入器具の断面図である。  FIG. 11 is a cross-sectional view of an intraocular lens insertion device showing a fourth embodiment of the present invention.
発明を実施するための最良の形態  BEST MODE FOR CARRYING OUT THE INVENTION
[0021] 以下、本発明を実施するための形態について図面を参照しながら説明する。図 1は 本発明が適用される眼内レンズ挿入器具の第 1実施例を示す断面図である。この眼 内レンズ挿入器具 1は、変形可能な眼内レンズ 2を通過させて眼球内に導く筒状の 本体 3と、前記本体 3内において往復移動可能に収納され、眼内レンズ 2を押圧して 眼球内に放出するプランジャー 4と、前記本体 3と前記プランジャー 4間に弾性体 5と を備える。 Hereinafter, embodiments for carrying out the present invention will be described with reference to the drawings. FIG. 1 is a sectional view showing a first embodiment of an intraocular lens insertion device to which the present invention is applied. The intraocular lens insertion device 1 is housed in a cylindrical main body 3 that passes through a deformable intraocular lens 2 and is guided into the eyeball, and is reciprocally moved in the main body 3, and presses the intraocular lens 2. A plunger 4 that is released into the eyeball, and an elastic body 5 between the main body 3 and the plunger 4.
[0022] 筒状の本体 3には、眼球の切開創ロカ 先端部が眼球内に挿入されるノズル 3a、レ ンズ 2を設置するレンズ設置部 3b、術者の指に把持される把持部 3cが設けられて 、る 。さらに、レンズ設置部 3bには開閉自在の蓋 6が設けられ、レンズ設置部 3b内にはレ ンズ 2の移動を制限するための固定突起 3dが設けられている。そして、本体 3にはプ ランジャー 4を軸支する中間支持部 3eが設けられ、本体 3の基端側にもプランジャー 4を軸支する基端支持部材 7が備えられている。図 1では本体 3と基端支持部材 7とを 別部材として構成して ヽるが、両部材とも潤滑特性が良好な摩擦抵抗の小さ!ヽ榭脂 材料力も製作されることから、適宜一体として構成することも可能である。また、本体 3 の製作に際してノズル 3aや把持部 3cを別体として製作後、組み立てにより一体ィ匕す ることち可會である。 [0022] The cylindrical main body 3 includes a nozzle 3a in which the tip of the incisional locus of the eyeball is inserted into the eyeball, a lens installation portion 3b in which the lens 2 is installed, and a gripping portion 3c in which the operator's finger holds the finger. Is provided. Further, the lens installation portion 3b is provided with a lid 6 that can be freely opened and closed, and the lens installation portion 3b is provided with a fixing projection 3d for restricting the movement of the lens 2. The main body 3 is provided with an intermediate support portion 3e that pivotally supports the plunger 4, and a base end support member 7 that pivotally supports the plunger 4 is also provided on the base end side of the main body 3. In FIG. 1, the main body 3 and the base end support member 7 are configured as separate members, but both members have good lubrication characteristics and low frictional resistance. It is also possible to configure. The main unit 3 It is possible to manufacture the nozzle 3a and the gripping part 3c separately, and then assemble them together by assembling.
[0023] ここで、本発明が適用される眼内レンズ挿入器具 1は、医療用器具であるため器具 の構成部材の材質は物理的'ィ匕学的に安定な材料であることが要求される。特に、 眼内に挿入される部位に使用される材料は、生物学的に安全性の保証のなされたも のでなければならない。例えば、 FDA (Food and Drug Administration)でインプラ ント材料として認定されたものや ISO (International Standardization Organization) でインプラント材料として規格化されたもの、あるいは ISO10993に従って行なわれ た試験の結果、問題のな!、材料であることが確認されたものであることが求められる。 これらの要求を満たす材料として、例えば筒状の本体 3の材料としては、ポリエチレン やポリプロピレンなどを用いることができる。  [0023] Here, since the intraocular lens insertion device 1 to which the present invention is applied is a medical device, the material of the constituent members of the device is required to be a physically stable material. The In particular, the materials used at the site of insertion into the eye must be biologically safe. For example, as a result of FDA (Food and Drug Administration) certified as an implant material, ISO (International Standardization Organization) standardized as an implant material, or a test conducted in accordance with ISO 10993, there are no problems! It is required that the material is confirmed. As a material that satisfies these requirements, for example, polyethylene, polypropylene, or the like can be used as the material of the cylindrical main body 3.
[0024] レンズ 2は、レンズ本体である光学部 2aと該光学部 2aを眼球内に位置固定するため の 2本の支持部材 2bと力もなる。支持部材 2bは細いひげ状をしている。このレンズ 2 は軟質アクリル等、可撓性を有する材料力 なり、レンズ自体を折り畳むことができる ものである。  [0024] The lens 2 also has a force with an optical part 2a which is a lens body and two support members 2b for fixing the position of the optical part 2a in the eyeball. The support member 2b has a thin beard shape. This lens 2 is made of a flexible material such as soft acrylic and can fold the lens itself.
[0025] プランジャー 4は、基端支持部材 7の内径寸法より若干小さな外径寸法を有する部 分 4aと、ノズルの内径寸法より若干小さな外径寸法を有する部分 4bとからなる。基端 支持部材 7の内径寸法より若干小さな外径寸法を有する部分 4aは、基端支持部材 7 内に摺動可能にして挿入されている。また、ノズル 3aの内径寸法より若干小さな外径 寸法を有する部分 4bは、本体の中間支持部 3e内に摺動可能にして挿入されて 、る。  The plunger 4 includes a portion 4a having an outer diameter that is slightly smaller than the inner diameter of the proximal support member 7, and a portion 4b having an outer diameter that is slightly smaller than the inner diameter of the nozzle. A portion 4 a having an outer diameter slightly smaller than the inner diameter of the base end support member 7 is slidably inserted into the base end support member 7. A portion 4b having an outer diameter slightly smaller than the inner diameter of the nozzle 3a is slidably inserted into the intermediate support portion 3e of the main body.
[0026] また、本体 3とプランジャー 4との間には弾性体としてのパネ 5が装着されている。具 体的には本体の中間支持部 3eの右端面とプランジャーの段部 4cとの間に弦卷バネ 5 が装着されている。この弦卷バネ 5は適正なパネ定数と適正な変形量を有するもので なければならな!/、が、それらにっ ヽては後述する。  A panel 5 as an elastic body is attached between the main body 3 and the plunger 4. Specifically, a string spring 5 is mounted between the right end surface of the intermediate support portion 3e of the main body and the step portion 4c of the plunger. This string spring 5 must have an appropriate panel constant and an appropriate deformation amount! /, Which will be described later.
[0027] このような眼内レンズ挿入器具 1を用いてレンズ 2を眼球内へ挿入する場合、術者 は片手操作でレンズ 2を眼球内へ挿入することができる。具体的には片手の人差し 指と中指により本体の把持部 3cを把持するとともに、親指の腹部をプランジャーの基 端 4dに当接してプランジャー 4を本体 3内に押し込む。そうすると、レンズ 2はプランジ ヤー 4の先端により押圧され、テーパ状のレンズ移行部 3fにおいて畳み込まれながら ノズル 3a内へと押し込まれる。さらに続けてプランジャー 4を押し込むとレンズ 2はノズ ル 3a内を移動してノズル先端の開口部 3gから眼球内へ放出される。 When the lens 2 is inserted into the eyeball using such an intraocular lens insertion device 1, the operator can insert the lens 2 into the eyeball with a single hand operation. Specifically, the grasping portion 3c of the main body is grasped by the index finger and middle finger of one hand, and the abdomen of the thumb is brought into contact with the base end 4d of the plunger and the plunger 4 is pushed into the main body 3. Then lens 2 is plunge It is pressed by the tip of the nozzle 4 and is pushed into the nozzle 3a while being folded at the tapered lens transition portion 3f. When the plunger 4 is further pushed in, the lens 2 moves in the nozzle 3a and is released into the eyeball from the opening 3g at the tip of the nozzle.
[0028] このレンズ設置部 3bからノズル先端の開口部 3gまでのレンズ移動行程、すなわちプ ランジャー 4の移動行程 (X)におけるプランジャー 4の押圧力(F)は一定ではなぐ特 有の傾向を示すことを本発明者は見い出した。図 2はこの様子を示すものであり、横 軸はプランジャーの移動行程 (X)を示し、縦軸はプランジャーの押圧力(F)を示して いる。ここで、横軸は図 1に示すインジェクターのプランジャーの移動行程 (X)そのも のである。すなわち、図 1においてレンズ 2をノズル開口部 3gから放出するためには、 プランジャー 4を右側力 左側へと移動させる必要がある力 図 2の横軸はこのプラン ジャーの移動行程 (X)そのものを示したものであるから、横軸は右側から左側へと進 行することになる。その結果、一般の図表とは異なり、横軸が縦軸と交わる点は原点 ではなぐレンズ 2が放出された後の位置を示すことになる。  [0028] The lens moving stroke from the lens installation portion 3b to the opening 3g of the nozzle tip, that is, the pressing force (F) of the plunger 4 in the moving stroke (X) of the plunger 4 has a characteristic tendency that is not constant. The inventor has found to show. Figure 2 shows this situation, with the horizontal axis representing the plunger travel (X) and the vertical axis representing the plunger pressing force (F). Here, the horizontal axis represents the travel of the plunger of the injector shown in Fig. 1 (X). That is, in order to release the lens 2 from the nozzle opening 3g in FIG. 1, it is necessary to move the plunger 4 to the left side of the right side force. The horizontal axis in FIG. 2 is the movement stroke (X) itself of this plunger. The horizontal axis travels from the right side to the left side. As a result, unlike a general chart, the point where the horizontal axis intersects the vertical axis indicates the position after the lens 2 that is not at the origin is released.
[0029] 図 2は、弾性体 5を設けない眼内レンズ挿入器具 1のプランジャー 4の移動行程 (X) と押圧力 (F)との関係を実測した特性図である。この特性は多くの実物に対して実測 したものであり、多少の個体差は認められるものの概ね一定の関係を示すことが判明 している。もっとも同一の眼内レンズ挿入器具を用いたとしても、眼内レンズの度数が 異なればレンズの厚さが異なることから特性は異なることになる。当然のことながら、 度数が高く厚いレンズの場合には押圧力のピーク値は大きくなる。ここで、横軸上の( ィ)点は、図 1中の (ィ)点、すなわちノズル 3aの先端位置に相当する。また、横軸上の (口)点は、図 1中の(口)点、すなわちレンズ移行部 3fとノズル 3aとの境界位置に相当 する。  FIG. 2 is a characteristic diagram in which the relationship between the movement stroke (X) and the pressing force (F) of the plunger 4 of the intraocular lens insertion device 1 without the elastic body 5 is measured. This characteristic has been measured for many actual objects, and it has been found that although there are some individual differences, it shows an almost constant relationship. Even if the same intraocular lens insertion device is used, the characteristics will be different because the lens thickness will be different if the power of the intraocular lens is different. As a matter of course, the peak value of the pressing force becomes large in the case of a thick lens having a high frequency. Here, the point (i) on the horizontal axis corresponds to the point (i) in FIG. 1, that is, the tip position of the nozzle 3a. The (mouth) point on the horizontal axis corresponds to the (mouth) point in FIG. 1, that is, the boundary position between the lens transition portion 3f and the nozzle 3a.
[0030] 尚、プランジャー 4を押す速さはレンズ 2を眼内に挿入させるのに適した速さであれ ば良く、一般的に 20mm/min〜200mm/min程度である力 70mm/min〜130mm/min が好ましい。  [0030] It should be noted that the speed at which the plunger 4 is pushed may be a speed suitable for inserting the lens 2 into the eye, and generally a force of about 70 mm / min to about 20 mm / min to 200 mm / min. 130 mm / min is preferred.
[0031] まず、レンズ 2を右側力 押して移動させると、レンズ 2の外周部がレンズ移行部 3fの テーパ内壁に接するまでの押圧力(F)は、本体 3とプランジャー 4間および本体 3とレ ンズ 2間の摺動抵抗だけであり小さい。続けてレンズ 2を移動させ、レンズ 2の外周部 力 Sレンズ移行部 3fのテーパ内壁に接すると、レンズ 2は変形させられて折り畳まれ始 める。そうすると、前記摺動抵抗に加えてレンズ 2の変形に要する力をプランジャー 4 力も与える必要があるため、プランジャー 4の押圧力(F)は急激に増加し始める。さら に続けてレンズ 2を左側に移動させ、レンズ 2がレンズ移行部 3fのテーパ内壁からノズ ル 3aに接する位置(口)点に到達すると、レンズの折り畳みに要する力が最大となるこ とから、プランジャーの押圧力(F)はピークに達する。その後、さらにプランジャー 4を 押圧してレンズ 2を左側に移動させる際には、プランジャーに必要な押圧力(F)は急 激に低下する。レンズ 2を略円筒形のノズル 3a内において移動させるのに必要な押 圧力(F)が急激に低下する原因は、レンズ 2の折り畳みに要する力が不要になること と、ノズル開口部 3gが折り畳まれたレンズからの内圧を受けて拡大すること等に基づ くものである。このようにインジェクター内に弾性体を設けない場合には、プランジャ 一の移動行程中においてプランジャーの押圧力(F)が極端に高くなるピークを示す ことになる。その結果、折り畳まれたレンズ 2がノズル先端部 3gより放出される段階 (ィ )点にお 、てプランジャーの押圧力(F)が急激に低下し、プランジャーの先端も勢 ヽ 余って眼球内に飛び出してしまう危険性があった。 [0031] First, when the lens 2 is moved by pushing the right side force, the pressing force (F) until the outer periphery of the lens 2 comes into contact with the tapered inner wall of the lens transition portion 3f is between the main body 3 and the plunger 4 and between the main body 3 and Only the sliding resistance between lenses 2 is small. Next, move lens 2 to the outer periphery of lens 2. When the lens touches the tapered inner wall of the S lens transition part 3f, the lens 2 is deformed and begins to fold. Then, in addition to the sliding resistance, the force required for the deformation of the lens 2 needs to be applied to the plunger 4 as well, so the pressing force (F) of the plunger 4 starts to increase rapidly. Then, when the lens 2 is moved to the left side and reaches the position (mouth) point where the lens 2 contacts the nozzle 3a from the tapered inner wall of the lens transition portion 3f, the force required to fold the lens becomes maximum. The plunger pressing force (F) reaches its peak. Thereafter, when the plunger 4 is further pressed and the lens 2 is moved to the left side, the pressing force (F) required for the plunger is rapidly reduced. The reason why the pressing force (F) required to move the lens 2 in the substantially cylindrical nozzle 3a suddenly decreases is that the force required to fold the lens 2 becomes unnecessary and the nozzle opening 3g is folded. This is based on enlargement by receiving the internal pressure from the lens. Thus, when the elastic body is not provided in the injector, a peak in which the plunger pressing force (F) becomes extremely high during the movement stroke of the plunger is shown. As a result, at the stage (ii) when the folded lens 2 is released from the nozzle tip 3g, the pressing force (F) of the plunger suddenly decreases, and the tip of the plunger also occupies the eyeball. There was a risk of jumping inside.
[0032] 図 3は、弾性体 5を設けた眼内レンズ挿入器具 1にレンズ 2を装填しない場合のブラ ンジャー 4の移動行程 (X)と押圧力(F)との関係を示す特性図である。縦軸および横 軸の意義は図 2と同一である(以下、図 3〜図 7および図 9においても同一である。 ) o 横軸上の(ハ)点は、プランジャー 4を移動して段部 4cによりパネ 5が圧縮され始める 位置を示して 、る。弾性体として線形特性を有する弦卷バネ 5を用いて ヽることから、 パネの変形開始後のプランジャーの押圧力(F)は直線的に増加している。  FIG. 3 is a characteristic diagram showing the relationship between the travel stroke (X) of the brassiere 4 and the pressing force (F) when the lens 2 is not loaded into the intraocular lens insertion device 1 provided with the elastic body 5. is there. The significance of the vertical and horizontal axes is the same as in Fig. 2 (hereinafter also the same in Figs. 3 to 7 and 9). O The point (c) on the horizontal axis moves the plunger 4 The position where the panel 5 starts to be compressed by the step 4c is shown. Since the string spring 5 having linear characteristics is used as an elastic body, the plunger pressing force (F) increases linearly after the panel starts to deform.
[0033] 図 4は、第 1実施例の眼内レンズ挿入器具 1にレンズ 2を装填して押し出す場合の プランジャー 4の移動行程 (X)と押圧力(F)との関係を示す特性図である。パネ定数 およびパネ変形量を適正に設定した場合であり、結果的に図 2と図 3を重畳した特性 となっている。すなわち、プランジャー 4を右側から左側に移動させる場合、プランジ ヤーの移動行程 (X)がパネの変形開始位置 (ハ)点に達すると、プランジャーの押圧 力(F)が上昇し始める。そこからプランジャー 4を左側に移動させ続けると、プランジ ヤーの押圧力(F)は、レンズ 2がレンズ移行部 3fのテーパ内壁力 ノズルに接する境 界位置 (口)点に到達するまで連続的に増加する。そして、力かる境界位置を超えて レンズ 2をノズル部 3aに移動させると、プランジャーの押圧力(F)は(口)点のピーク値 より若干は低下するものの大幅に低下することなく再び増加し始める。最終的にレン ズ 2がノズルの開口部 3gから放出された後においてもプランジャーの押圧力(F)は低 下することがない。したがって、ノズル 3a力もレンズ 2が放出された位置 (ィ)点におい ても、プランジャーの押圧力(F)が急激に無くなりプランジャーの先端が勢い余って 眼球内に飛び出してしまう危険性がなくなる。 FIG. 4 is a characteristic diagram showing the relationship between the movement stroke (X) of the plunger 4 and the pressing force (F) when the lens 2 is loaded into the intraocular lens insertion device 1 of the first embodiment and pushed out. It is. This is the case where the panel constant and the panel deformation amount are set appropriately. As a result, the characteristics shown in Fig. 2 and Fig. 3 are superimposed. In other words, when the plunger 4 is moved from the right side to the left side, the plunger pressing force (F) starts to rise when the plunger travel (X) reaches the panel deformation start position (c). If the plunger 4 is continuously moved to the left from there, the pressing force (F) of the plunger is such that the lens 2 contacts the nozzle inner wall force nozzle of the lens transition part 3f. It increases continuously until it reaches the field position (mouth) point. When the lens 2 is moved to the nozzle part 3a beyond the powerful boundary position, the plunger pressing force (F) increases again without significantly decreasing although it slightly decreases from the peak value at the (mouth) point. Begin to. Even after lens 2 is finally released from the nozzle opening 3g, the plunger pressing force (F) does not decrease. Therefore, even if the nozzle 3a force is also at the position (ii) where the lens 2 is released, the plunger pressing force (F) suddenly disappears, and there is no danger of the tip of the plunger surging and jumping into the eyeball. .
[0034] 図 5は、第 1実施例のインジェクターとは異なる弾性値を有する弾性体を用いた場 合のプランジャーの移動行程 (X)と押圧力(F)との関係を示す特性図である。この弾 性体はレンズの変形に要する力に対して過大なパネ反力を備えたものであり、プラン ジャーの押圧力(F)が略直線的に増加するという利点がある。その一方、ノズルの先 端からレンズを放出する段階 (ィ)点におけるプランジャーの押圧力(F)が大きくなり 過ぎるという欠点もある。  FIG. 5 is a characteristic diagram showing the relationship between the plunger travel (X) and the pressing force (F) when an elastic body having an elastic value different from that of the injector of the first embodiment is used. is there. This elastic body has an excessive panel reaction force against the force required to deform the lens, and has the advantage that the pressing force (F) of the plunger increases almost linearly. On the other hand, there is a drawback that the plunger pressing force (F) at the point (i) where the lens is released from the tip of the nozzle becomes too large.
[0035] 図 6は、図 5に示す弾性体とは異なる弾性値を有する弾性体を用いた場合のプラン ジャーの移動行程 (X)と押圧力(F)との関係を示す特性図である。この弾性体はレン ズの変形に要する力に対して略適正なパネ反力を備えたものであり、プランジャーの 押圧力(F)は不連続性を有するものの、プランジャーの移動行程 (X)に対するプラン ジャーの押圧力(F)が減少することはない。  [0035] FIG. 6 is a characteristic diagram showing the relationship between the plunger travel (X) and the pressing force (F) when an elastic body having an elastic value different from that of the elastic body shown in FIG. 5 is used. . This elastic body has a panel reaction force that is approximately appropriate for the force required to deform the lens. Although the plunger pressing force (F) is discontinuous, the plunger travel (X The plunger's pressing force (F) against) does not decrease.
[0036] 図 7は、さらに図 5や図 6に示す弾性体とは異なる弾性値を有する弾性体を用いた 場合のプランジャーの移動行程 (X)と押圧力(F)との関係を示す特性図である。この 弾性体はレンズの変形に要する力に対して過小なパネ反力を備えたものであり、ノズ ルの先端力 レンズを放出する段階 (ィ)点におけるプランジャーの押圧力(F)が大き くなり過ぎないという利点がある。その一方、(口)点経過後のプランジャーの押圧力( F)が、最初のピーク値に対して低下する割合が大き過ぎるという欠点がある。  FIG. 7 further shows the relationship between the plunger travel (X) and the pressing force (F) when an elastic body having an elastic value different from that shown in FIGS. 5 and 6 is used. FIG. This elastic body has an excessive panel reaction force against the force required to deform the lens, and the tip force of the nozzle The plunger's pressing force (F) at the point (i) where the lens is released is large. There is an advantage that it does not become too much. On the other hand, there is a drawback that the rate of decrease in the plunger pressing force (F) after the (mouth) point has passed is too large with respect to the initial peak value.
[0037] 以上説明したように本発明に係る眼内レンズ挿入器具 1によれば、プランジャー 4の 移動行程 (X)に対するプランジャーの押圧力(F)が最初のピーク経過後においても 大幅に減少することがな 、ので、片手操作であってもプランジャーを緩やかに移動さ せることができる。また、プランジャーの移動行程 (X)に対するプランジャーの押圧力 (F)の値が減少することがないので、片手操作であってもプランジャーを緩やかに移 動させることができる。したがって、眼球内にレンズを安全確実に挿入することができ る。なお、第 1実施例において、プランジャーの押圧力(F)が最初のピーク値に達し た後のプランジャーの移動行程 (X)にお 、て前記ピーク値の 60%以上を保持するこ ととしたのは、実際に片手操作した場合に操作者が違和感を覚えることなく操作可能 な値に基づいて規定したものである。この値には多少の個人差はあるが、安全性を 考慮すると 75%以上が好ましぐ 90%以上がより一層好ましい値である。 [0037] As described above, according to the intraocular lens insertion device 1 according to the present invention, the plunger pressing force (F) with respect to the movement stroke (X) of the plunger 4 is greatly increased even after the first peak has elapsed. Since it does not decrease, the plunger can be moved gently even with one-handed operation. Also, the plunger pressure against the plunger travel (X) Since the value of (F) does not decrease, the plunger can be moved gently even with one-handed operation. Therefore, the lens can be safely and reliably inserted into the eyeball. In the first embodiment, the plunger travel (X) after the plunger pressing force (F) reaches the first peak value should hold 60% or more of the peak value. This is defined based on the value that can be operated without the operator feeling uncomfortable when actually operating with one hand. Although this value varies slightly between individuals, considering safety, 75% or more is preferable, and 90% or more is even more preferable.
[0038] 図 8は、本発明の第 2実施例を示す眼内レンズ挿入器具の断面図である。この眼内 レンズ挿入器具 1は、異なる弾性値を有する複数の弾性体 5a, 5bからなることを特徴 とするものである。基本構成は図 1に示す第 1実施例と共通であるので、共通部分に ついての説明は省略し、第 1実施例と異なる構成を有する部分についてのみ説明す る。第 1実施例では本体 3とプランジャー 4との間に一つの弾性体 5を配設していたが 、本実施例ではパネ定数および変形量が異なる二つのパネ 5a, 5bが配設されている 。本実施例では内側に配設された弦卷バネ 5aの変形量は大きく設定され、外側に配 設された弦卷バネ 5bの変形量は小さく設定されている。また、内側に配設された弦卷 パネ 5aの右端とプランジャーの段部 4cとの間には、摺動リング 8がプランジャー 4bに 摺動可能に装着されている。  FIG. 8 is a cross-sectional view of an intraocular lens insertion device showing a second embodiment of the present invention. This intraocular lens insertion device 1 is characterized by comprising a plurality of elastic bodies 5a and 5b having different elasticity values. Since the basic configuration is the same as that of the first embodiment shown in FIG. 1, the description of the common portions is omitted, and only the portion having a configuration different from that of the first embodiment will be described. In the first embodiment, one elastic body 5 is disposed between the main body 3 and the plunger 4, but in this embodiment, two panel 5a and 5b having different panel constants and deformation amounts are disposed. Yes. In this embodiment, the deformation amount of the string hook spring 5a disposed on the inner side is set large, and the deformation amount of the string hook spring 5b disposed on the outer side is set small. A sliding ring 8 is slidably mounted on the plunger 4b between the right end of the string paddle panel 5a disposed on the inside and the step 4c of the plunger.
[0039] このような構成を有する眼内レンズ挿入器具を用いてレンズ 2を放出する場合のプ ランジャーの移動行程 (X)に対する押圧力(F)について説明する。図 9は、第 2実施 例の眼内レンズ挿入器具にぉ 、て、レンズ 2を装填しな 、場合のプランジャーの移動 行程 (X)と押圧力 (F)との関係を示す特性図である。プランジャー 4を右側から左側 に移動させると、最初はプランジャー 4とプランジャーが支持される本体 3間の摺動抵 抗だけであるので、押圧力(F)は小さい。プランジャー 4の移動が進み摺動リング 8を 介してプランジャーの段部 4cによって内側に配設された弦卷バネ 5aが圧縮され始め る (ハ)点に達すると、内側に配設された弦卷バネ 5aの反力がプランジャーの押圧力 として加わる。さらにプランジャーを左側に移動させると、外側に配設された弦卷バネ 5bも摺動リング 8を介してプランジャーの段部 4cによって圧縮され始める。そうすると、 外側に配設された弦卷バネ 5bが圧縮され始める位置(口)点以降にお 、ては、二つ の弦卷バネ 5a, 5bの反力がプランジャーの押圧力に加わることになる。ここで、外側 に配設された弦卷バネ 5bが圧縮され始める位置(口)点を、レンズの変形に要する力 が最大となる位置、すなわち図 8に示す (口)点に一致させると、プランジャーの押圧 力がピークに達した後の移動行程における押圧力の低下を少なくすることができると ともに、レンズ放出後の押圧力の増力!]も抑制できるという利点がある。したがって、こ のような複数のパネ定数を有するパネ 5a, 5bを組み合わせることによりプランジャーの 移動行程 (X)に対するパネ反力を不連続特性にすることができる。その結果、プラン ジャーの押圧力(F)の最大値を抑制することが可能な眼内レンズ挿入器具を実現で きる。 [0039] The pressing force (F) with respect to the movement stroke (X) of the plunger when the lens 2 is released using the intraocular lens insertion device having such a configuration will be described. FIG. 9 is a characteristic diagram showing the relationship between the plunger movement stroke (X) and the pressing force (F) when the lens 2 is not loaded in the intraocular lens insertion device of the second embodiment. is there. When the plunger 4 is moved from the right side to the left side, the pressing force (F) is small because only the sliding resistance between the plunger 4 and the main body 3 on which the plunger is supported is initially. The movement of the plunger 4 advances, and the string spring 5a disposed inside by the plunger step 4c starts to be compressed through the sliding ring 8. When reaching the point (c), it is disposed inside. The reaction force of string spring 5a is applied as the plunger pressing force. When the plunger is further moved to the left side, the string spring 5b disposed on the outside starts to be compressed by the plunger step 4c via the sliding ring 8. Then, after the position (mouth) point where the string spring 5b arranged outside starts to be compressed, two The reaction force of the string spring 5a, 5b is added to the plunger pressing force. Here, when the position (mouth) point at which the chord spring 5b disposed on the outside starts to be compressed coincides with the position where the force required to deform the lens is maximum, that is, the (mouth) point shown in FIG. It is possible to reduce the decrease in pressing force during the travel stroke after the plunger pressing force reaches its peak, and increase the pressing force after releasing the lens! ] Also has the advantage that it can be suppressed. Therefore, the panel reaction force with respect to the movement stroke (X) of the plunger can be made discontinuous by combining the panels 5a and 5b having a plurality of panel constants. As a result, an intraocular lens insertion device capable of suppressing the maximum value of the plunger's pressing force (F) can be realized.
[0040] 図 10は、本発明の第 3実施例を示す眼内レンズ挿入器具の断面図である。この眼 内レンズ挿入器具 1は、弾性体の弾性値が非線形特性を有することを特徴とするもの である。図 1に示す第 1実施例や第 2実施例と共通する部分についての説明は省略 し、これらの実施例と異なる構成を有する部分についてのみ説明する。第 1実施例や 第 2実施例では筒状の本体 3内に弾性体 5を配設していたが、本実施例では本体 3と プランジャーの基端 4dとの間に弾性体 5c〜51¾配設されている。図 10 (a)は本体 3と プランジャーの基端 4dとの間に、弾性値が異なる二つの弦卷バネ 5c, 5dを配設したも のである。また、図 10 (b)は本体 3とプランジャーの基端 4dとの間に、一端から他端に かけて素線径が徐々に変化する弦卷バネ 5eを配設したものである。さらに、図 10 (c) は本体 3とプランジャーの基端 4dとの間に、一端から他端にかけて弦卷径が徐々に 変化する弦卷バネ 5 配設したものである。なお、各弦卷バネ 5c〜5fの一端または両 端にはパネ圧縮時の着座を良好ならしめるために、摺動リング 8が装着されている。 これらの実施例によれば、プランジャーの移動行程に対して弾性体の弾性値は非線 形特性を示すことから、ノズル開口部カゝらレンズが放出される前後のプランジャーの 押圧力をより精密に設計することができる。  FIG. 10 is a cross-sectional view of an intraocular lens insertion device showing a third embodiment of the present invention. This intraocular lens insertion device 1 is characterized in that the elastic value of the elastic body has a nonlinear characteristic. Descriptions of portions common to the first and second embodiments shown in FIG. 1 are omitted, and only portions having configurations different from those of the embodiments are described. In the first embodiment and the second embodiment, the elastic body 5 is disposed in the cylindrical main body 3, but in this embodiment, the elastic bodies 5c to 51¾ are provided between the main body 3 and the base end 4d of the plunger. It is arranged. In FIG. 10 (a), two string springs 5c and 5d having different elastic values are arranged between the main body 3 and the base end 4d of the plunger. FIG. 10 (b) shows a string spring 5e in which the wire diameter gradually changes from one end to the other end between the main body 3 and the base end 4d of the plunger. Further, FIG. 10 (c) shows a string hook spring 5 in which the string hook diameter gradually changes from one end to the other end between the main body 3 and the base end 4d of the plunger. A sliding ring 8 is attached to one end or both ends of each of the string springs 5c to 5f in order to ensure good seating when the panel is compressed. According to these embodiments, since the elastic value of the elastic body exhibits a non-linear characteristic with respect to the movement stroke of the plunger, the pressing force of the plunger before and after the nozzle is released is reduced. It can be designed more precisely.
[0041] 図 11は、本発明の第 4実施例を示す眼内レンズ挿入器具の断面図である。この眼 内レンズ挿入器具 1は、本体 3とプランジャー 4間に弾性体 5を配設すると共に、筒状 の本体 3の内面と摺動するプランジャーの外面 4aに摺動抵抗増加機構 9を備えたも のである。本実施例の基本構成は図 1に示す第 1実施例と共通であるので、共通部 分についての説明は省略し、第 1実施例と異なる構成を有する部分についてのみ説 明する。本実施例では筒状の本体 3の内面と摺動するプランジャーの外面 4aに摺動 抵抗増加機構 9を備えている。具体的にはプランジャーの外面 4aに 1または複数の 突起 9a〜9cが設けられて!/、る。突起 9a〜9cが設けられるプランジャー 4の軸方向位 置は、レンズ 2の折り畳みに要する変形抵抗がなくなり突起 9a〜9cを設けない場合に プランジャー 4の押圧力が減少に転ずる位置に対応している。このような構成によりプ ランジャーの移動行程に対するプランジャーの押圧力の急激な変化を緩和すること ができる。 FIG. 11 is a cross-sectional view of an intraocular lens insertion device showing a fourth embodiment of the present invention. This intraocular lens insertion device 1 has an elastic body 5 disposed between a main body 3 and a plunger 4, and a sliding resistance increasing mechanism 9 is provided on an outer surface 4a of the plunger that slides with the inner surface of the cylindrical main body 3. It is prepared. The basic configuration of this embodiment is the same as that of the first embodiment shown in FIG. The description of the minute is omitted, and only a portion having a configuration different from the first embodiment will be described. In this embodiment, a sliding resistance increasing mechanism 9 is provided on the outer surface 4a of the plunger that slides with the inner surface of the cylindrical main body 3. Specifically, one or more protrusions 9a to 9c are provided on the outer surface 4a of the plunger. The axial position of the plunger 4 where the protrusions 9a to 9c are provided corresponds to the position where the pressing force of the plunger 4 starts to decrease when the deformation resistance required for folding the lens 2 is lost and the protrusions 9a to 9c are not provided. ing. With such a configuration, a sudden change in the plunger pressing force with respect to the plunger travel can be mitigated.
[0042] なお、図 11には本体 3とプランジャー 4間に弾性体たる弦卷バネ 5を配設すると共 に、プランジャーの外面 4aに摺動抵抗増加機構たる突起 9a〜9cを備え、弦卷バネ 5 の圧縮抵抗力と突起 9a〜9cの摺動抵抗力の組合せにより、プランジャーの移動行程 に対するプランジャーの押圧力の急激な変化を緩和する実施例を示したが、弦卷バ ネ 5の圧縮抵抗力と突起 9a〜9cの摺動抵抗力のいずれか一方だけを用いることとし てもよい。  [0042] In FIG. 11, a string spring 5 as an elastic body is disposed between the main body 3 and the plunger 4, and a protrusion 9a to 9c as a sliding resistance increasing mechanism is provided on the outer surface 4a of the plunger. Although an example has been shown in which a rapid change in the pressing force of the plunger with respect to the movement stroke of the plunger is mitigated by a combination of the compression resistance of the string spring 5 and the sliding resistance of the protrusions 9a to 9c. Only one of the compression resistance force of the screw 5 and the sliding resistance force of the protrusions 9a to 9c may be used.
[0043] 以上、本発明を実施例に基づいて説明したが、本発明は上記した実施例に限定さ れるものではなぐ種々の変形実施をすることができる。例えば、上記実施例におい ては、筒状の本体 3内に眼内レンズ 2を直接セットする場合について説明した力 本 体 3とは別のカートリッジ内に眼内レンズ 2をセットし、該カートリッジを本体 3に装着し て使用するカートリッジ式の眼内レンズ挿入器具についても適用できることは言うまで もない。  [0043] While the present invention has been described based on the embodiments, the present invention is not limited to the above-described embodiments, and various modifications can be made. For example, in the above embodiment, the intraocular lens 2 is set in a cartridge different from the force body 3 described in the case where the intraocular lens 2 is directly set in the cylindrical main body 3, and the cartridge is mounted. Needless to say, the present invention can also be applied to a cartridge-type intraocular lens insertion device used by being mounted on the main body 3.
[0044] また、上記実施例にお!ヽては弾性体 5として弦卷バネを用いた場合にっ 、て説明 したが、弾性体 5は弦卷パネに限られるものではなぐ榭脂発泡体のような素材の弾 性そのものを利用した弾性体であっても構わな!/、。  [0044] Also, in the above-described embodiment, the description has been given for the case where the string spring is used as the elastic body 5. However, the elastic body 5 is not limited to the string panel, but is a foamed foam. It may be an elastic body that uses the elasticity of the material itself!

Claims

請求の範囲 The scope of the claims
[1] 変形可能な眼内レンズを通過させて眼球内に導く筒状の本体と、  [1] A cylindrical main body that passes through a deformable intraocular lens and guides it into the eyeball,
前記本体内において往復移動可能に収納され、眼内レンズを押圧して眼球内に放 出するプランジャーと、  A plunger housed in a reciprocating manner in the main body, pressing a intraocular lens and releasing it into the eyeball;
前記本体と前記プランジャー間に弾性体及び Z又は摺動抵抗増加機構と、を備え た眼内レンズ挿入器具であって、  An intraocular lens insertion device comprising an elastic body and a Z or sliding resistance increasing mechanism between the main body and the plunger,
前記プランジャーの押圧力(F)力 最初のピーク値に達した後のプランジャーの移 動行程 (X)において前記ピーク値の 60%以上を保持可能なことを特徴とする眼内レ ンズ挿入器具。  Pushing force (F) force of the plunger Inserting an intraocular lens characterized in that it can hold 60% or more of the peak value in the movement stroke (X) of the plunger after reaching the first peak value Instruments.
[2] 変形可能な眼内レンズを通過させて眼球内に導く筒状の本体と、  [2] a cylindrical body that passes through a deformable intraocular lens and guides it into the eyeball;
前記本体内において往復移動可能に収納され、眼内レンズを押圧して眼球内に放 出するプランジャーと、  A plunger housed in a reciprocating manner in the main body, pressing a intraocular lens and releasing it into the eyeball;
前記本体と前記プランジャー間に弾性体及び Z又は摺動抵抗増加機構と、を備え た眼内レンズ挿入器具であって、  An intraocular lens insertion device comprising an elastic body and a Z or sliding resistance increasing mechanism between the main body and the plunger,
前記プランジャーの移動行程 (X)に対するプランジャーの押圧力(F)の値が減少し な 、ことを特徴とする眼内レンズ挿入器具。  The intraocular lens insertion device, wherein the value of the plunger pressing force (F) with respect to the plunger moving stroke (X) does not decrease.
[3] 前記弾性体が異なる弾性値を有する複数の弾性体力 なることを特徴とする請求 項 1または 2記載の眼内レンズ挿入器具。 [3] The intraocular lens insertion device according to [1] or [2], wherein the elastic body has a plurality of elastic body forces having different elasticity values.
[4] 前記弾性体の弾性値が非線形特性を有することを特徴とする請求項 1または 2記載 の眼内レンズ挿入器具。 4. The intraocular lens insertion device according to claim 1, wherein an elastic value of the elastic body has a nonlinear characteristic.
PCT/JP2007/052460 2006-02-22 2007-02-13 Intraocular lens inserter WO2007097221A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2006-045604 2006-02-22
JP2006045604A JP4947484B2 (en) 2006-02-22 2006-02-22 Intraocular lens insertion device

Publications (1)

Publication Number Publication Date
WO2007097221A1 true WO2007097221A1 (en) 2007-08-30

Family

ID=38437260

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2007/052460 WO2007097221A1 (en) 2006-02-22 2007-02-13 Intraocular lens inserter

Country Status (2)

Country Link
JP (1) JP4947484B2 (en)
WO (1) WO2007097221A1 (en)

Cited By (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2010021354A1 (en) * 2008-08-21 2010-02-25 Hoya株式会社 Intraocular lens insertion instrument
JP2010273985A (en) * 2009-05-29 2010-12-09 Nidek Co Ltd Intraocular lens inserter
WO2011079037A1 (en) * 2009-12-23 2011-06-30 Bausch & Lomb Incorporated An intraocular lens injector including a shaped spring
US8382769B2 (en) 2008-06-17 2013-02-26 Hoya Corporation Intraocular lens insertion device
US8460311B2 (en) 2004-12-27 2013-06-11 Hoya Corporation Intraocular lens implanting device
US8470032B2 (en) 2008-09-04 2013-06-25 Hoya Corporation Intraocular lens insertion device
US8475528B2 (en) 2007-05-30 2013-07-02 Hoya Corporation Intraocular lens insertion device
US8523941B2 (en) 2005-12-08 2013-09-03 Hoya Corporation Instrument for inserting intraocular lens
US8523877B2 (en) 2005-02-24 2013-09-03 Hoya Corporation Intraocular lens inserting instrument
WO2013137208A1 (en) * 2012-03-14 2013-09-19 興和株式会社 Intraocular lens insertion instrument
US8545512B2 (en) 2005-01-26 2013-10-01 Hoya Corporation Intraocular lens insertion device
US8574239B2 (en) 2005-09-28 2013-11-05 Hoya Corporation Intraocular lens insertion device
US8603103B2 (en) 2009-01-07 2013-12-10 Hoya Corporation Intraocular lens insertion device
US8647382B2 (en) 2010-06-10 2014-02-11 Hoya Corporation Ocular implant insertion apparatus and methods
US8747465B2 (en) 2007-05-30 2014-06-10 Hoya Corporation Intraocular lens insertion device
US9114006B2 (en) 2007-07-11 2015-08-25 Hoya Corporation Intraocular lens insertion device and method for controlling movement of the intraocular lens
CN105361997A (en) * 2015-11-17 2016-03-02 中山大学中山眼科中心 Pushing and injecting device for implanting artificial retina cytoskeleton into inner eye
US9326847B2 (en) 2010-04-08 2016-05-03 Hoya Corporation Ocular implant insertion apparatus and methods
US9463089B2 (en) 2012-05-21 2016-10-11 Novartis Ag Plunger system for intraocular lens surgery
US9554894B2 (en) 2008-06-05 2017-01-31 Hoya Corporation Intraocular lens insertion device and cartridge
US10568735B2 (en) 2017-01-13 2020-02-25 Alcon Inc. Intraocular lens injector
US10588780B2 (en) 2015-03-04 2020-03-17 Alcon Inc. Intraocular lens injector
US10799339B2 (en) 2015-09-16 2020-10-13 Hoya Corporation Intraocular lens injector
US10849738B2 (en) 2015-09-16 2020-12-01 Hoya Corporation Intraocular lens injector
US11000367B2 (en) 2017-01-13 2021-05-11 Alcon Inc. Intraocular lens injector
US11033382B2 (en) 2016-06-28 2021-06-15 Hoya Corporation Intraocular lens injector
DE102022105265B3 (en) 2022-03-07 2023-04-27 Carl Zeiss Meditec Ag Injector with a cushion having an expandable stem

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5255832B2 (en) * 2007-12-28 2013-08-07 興和株式会社 Intraocular lens insertion device
US10182906B2 (en) * 2014-07-15 2019-01-22 Alcon Pharmaceuticals, Ltd. Intraocular lens inserter with temperature compensation
JP6334328B2 (en) * 2014-08-29 2018-05-30 株式会社エクスプロア Contact lens mounting device
CN108272535B (en) * 2018-03-23 2020-05-15 魏捷 Intraocular lens taking and placing device for ophthalmology
KR102630856B1 (en) * 2023-08-25 2024-01-30 최원석 Intraocular lens insertion tool

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000516487A (en) * 1996-08-02 2000-12-12 スター・サージカル・カンパニー,インコーポレイテッド Spring-biased deformable intraocular lens injection device
WO2004112893A2 (en) * 2003-06-13 2004-12-29 Optobionics Corporation Implant instrument
JP2005178453A (en) * 2003-12-17 2005-07-07 Toyota Motor Corp Actuator disposed in steering system
JP2006017194A (en) * 2004-06-30 2006-01-19 Hitachi Ltd Torsion spring and stabilizer for vehicle

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3791421B2 (en) * 2002-01-23 2006-06-28 キヤノンスター株式会社 Intraocular lens insertion device
JP2005179453A (en) * 2003-12-18 2005-07-07 Sumitomo Bakelite Co Ltd Epoxy resin and method for producing the same

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000516487A (en) * 1996-08-02 2000-12-12 スター・サージカル・カンパニー,インコーポレイテッド Spring-biased deformable intraocular lens injection device
WO2004112893A2 (en) * 2003-06-13 2004-12-29 Optobionics Corporation Implant instrument
JP2005178453A (en) * 2003-12-17 2005-07-07 Toyota Motor Corp Actuator disposed in steering system
JP2006017194A (en) * 2004-06-30 2006-01-19 Hitachi Ltd Torsion spring and stabilizer for vehicle

Cited By (51)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8460311B2 (en) 2004-12-27 2013-06-11 Hoya Corporation Intraocular lens implanting device
US9220593B2 (en) 2005-01-26 2015-12-29 Hoya Corporation Intraocular lens insertion device
US8545512B2 (en) 2005-01-26 2013-10-01 Hoya Corporation Intraocular lens insertion device
US8523877B2 (en) 2005-02-24 2013-09-03 Hoya Corporation Intraocular lens inserting instrument
US9364320B2 (en) 2005-02-24 2016-06-14 Hoya Corporation Intraocular lens inserting instrument
US9114007B2 (en) 2005-09-28 2015-08-25 Hoya Corporation Intraocular lens insertion device
US8574239B2 (en) 2005-09-28 2013-11-05 Hoya Corporation Intraocular lens insertion device
US8968328B2 (en) 2005-12-08 2015-03-03 Hoya Corporation Instrument for inserting intraocular lens
US8523941B2 (en) 2005-12-08 2013-09-03 Hoya Corporation Instrument for inserting intraocular lens
US9289288B2 (en) 2007-05-30 2016-03-22 Hoya Corporation Intraocular lens insertion device
US11938019B2 (en) 2007-05-30 2024-03-26 Hoya Corporation Intraocular lens insertion device
US8475528B2 (en) 2007-05-30 2013-07-02 Hoya Corporation Intraocular lens insertion device
US11617643B2 (en) 2007-05-30 2023-04-04 Hoya Corporation Intraocular lens insertion device
US10405971B2 (en) 2007-05-30 2019-09-10 Hoya Corporation Intraocular lens insertion device
US10390940B2 (en) 2007-05-30 2019-08-27 Hoya Corporation Intraocular lens insertion device
US8747465B2 (en) 2007-05-30 2014-06-10 Hoya Corporation Intraocular lens insertion device
US8535375B2 (en) 2007-05-30 2013-09-17 Hoya Corporation Intraocular lens insertion device
US9114006B2 (en) 2007-07-11 2015-08-25 Hoya Corporation Intraocular lens insertion device and method for controlling movement of the intraocular lens
US9907647B2 (en) 2007-07-11 2018-03-06 Hoya Corporation Intraocular lens insertion device and method for controlling movement of the intraocular lens
US9554894B2 (en) 2008-06-05 2017-01-31 Hoya Corporation Intraocular lens insertion device and cartridge
US10517717B2 (en) 2008-06-05 2019-12-31 Hoya Corporation Intraocular lens insertion device and cartridge
US8382769B2 (en) 2008-06-17 2013-02-26 Hoya Corporation Intraocular lens insertion device
US9186246B2 (en) 2008-06-17 2015-11-17 Hoya Corporation Intraocular lens insertion devices and methods
US8702795B2 (en) 2008-08-21 2014-04-22 Hoya Corporation Intraocular lens inserting device
WO2010021354A1 (en) * 2008-08-21 2010-02-25 Hoya株式会社 Intraocular lens insertion instrument
JP2010046241A (en) * 2008-08-21 2010-03-04 Hoya Corp Intraocular lens insertion instrument
US8470032B2 (en) 2008-09-04 2013-06-25 Hoya Corporation Intraocular lens insertion device
US8603103B2 (en) 2009-01-07 2013-12-10 Hoya Corporation Intraocular lens insertion device
US9877826B2 (en) 2009-01-07 2018-01-30 Hoya Corporation Intraocular lens insertion device
US9901442B2 (en) 2009-01-07 2018-02-27 Hoya Corporation Intraocular lens insertion device
US9655718B2 (en) 2009-01-07 2017-05-23 Hoya Corporation Intraocular lens insertion device
JP2010273985A (en) * 2009-05-29 2010-12-09 Nidek Co Ltd Intraocular lens inserter
WO2011079037A1 (en) * 2009-12-23 2011-06-30 Bausch & Lomb Incorporated An intraocular lens injector including a shaped spring
US9326847B2 (en) 2010-04-08 2016-05-03 Hoya Corporation Ocular implant insertion apparatus and methods
US9572710B1 (en) 2010-06-10 2017-02-21 Hoya Corporation Ocular implant insertion apparatus and methods
US9980811B2 (en) 2010-06-10 2018-05-29 Hoya Corporation Ocular implant insertion apparatus and methods
US10039668B2 (en) 2010-06-10 2018-08-07 Hoya Corporation Ocular implant insertion apparatus and methods
US8647382B2 (en) 2010-06-10 2014-02-11 Hoya Corporation Ocular implant insertion apparatus and methods
US9314373B2 (en) 2010-06-10 2016-04-19 Hoya Corporation Ocular implant insertion apparatus and methods
JPWO2013137208A1 (en) * 2012-03-14 2015-08-03 興和株式会社 Intraocular lens insertion device
WO2013137208A1 (en) * 2012-03-14 2013-09-19 興和株式会社 Intraocular lens insertion instrument
US9463089B2 (en) 2012-05-21 2016-10-11 Novartis Ag Plunger system for intraocular lens surgery
US10588780B2 (en) 2015-03-04 2020-03-17 Alcon Inc. Intraocular lens injector
US10799339B2 (en) 2015-09-16 2020-10-13 Hoya Corporation Intraocular lens injector
US10849738B2 (en) 2015-09-16 2020-12-01 Hoya Corporation Intraocular lens injector
CN105361997A (en) * 2015-11-17 2016-03-02 中山大学中山眼科中心 Pushing and injecting device for implanting artificial retina cytoskeleton into inner eye
US11033382B2 (en) 2016-06-28 2021-06-15 Hoya Corporation Intraocular lens injector
US11000367B2 (en) 2017-01-13 2021-05-11 Alcon Inc. Intraocular lens injector
US10568735B2 (en) 2017-01-13 2020-02-25 Alcon Inc. Intraocular lens injector
DE102022105265B3 (en) 2022-03-07 2023-04-27 Carl Zeiss Meditec Ag Injector with a cushion having an expandable stem
WO2023169841A1 (en) 2022-03-07 2023-09-14 Carl Zeiss Meditec Ag Injector with a cushion having an extensible shaft

Also Published As

Publication number Publication date
JP4947484B2 (en) 2012-06-06
JP2007222309A (en) 2007-09-06

Similar Documents

Publication Publication Date Title
WO2007097221A1 (en) Intraocular lens inserter
JP5041322B2 (en) Intraocular lens insertion device
US7429263B2 (en) Preloaded IOL injector
EP2334259B1 (en) Pre-loaded iol insertion system
EP1659991B1 (en) Preloaded iol injector
JP3791421B2 (en) Intraocular lens insertion device
EP2062552B1 (en) Lens delivery system with independently movable sliding block
WO2007080868A1 (en) Instrument for inserting intraocular lens
US20050149057A1 (en) IOL inserter plunger and body interface
US20220192818A1 (en) Aiol delivery systems and associated devices and methods
JP5902864B2 (en) Plunger system for intraocular lens surgery

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application
NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 07708351

Country of ref document: EP

Kind code of ref document: A1