JPH01300948A - Intraocular lens - Google Patents
Intraocular lensInfo
- Publication number
- JPH01300948A JPH01300948A JP63133151A JP13315188A JPH01300948A JP H01300948 A JPH01300948 A JP H01300948A JP 63133151 A JP63133151 A JP 63133151A JP 13315188 A JP13315188 A JP 13315188A JP H01300948 A JPH01300948 A JP H01300948A
- Authority
- JP
- Japan
- Prior art keywords
- intraocular lens
- silicone rubber
- core material
- optical part
- outer layer
- Prior art date
- Legal status (The legal status 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 status listed.)
- Pending
Links
- 239000000463 material Substances 0.000 claims abstract description 31
- 239000011162 core material Substances 0.000 claims abstract description 25
- 230000003287 optical effect Effects 0.000 claims abstract description 23
- 229920002379 silicone rubber Polymers 0.000 abstract description 19
- 239000004945 silicone rubber Substances 0.000 abstract description 19
- 229920003023 plastic Polymers 0.000 abstract description 15
- -1 polypropylene Polymers 0.000 abstract description 15
- 239000004033 plastic Substances 0.000 abstract description 14
- 239000004743 Polypropylene Substances 0.000 abstract description 12
- 229920001155 polypropylene Polymers 0.000 abstract description 12
- 238000000034 method Methods 0.000 abstract description 4
- 210000000695 crystalline len Anatomy 0.000 description 32
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 6
- 238000001356 surgical procedure Methods 0.000 description 6
- 230000014759 maintenance of location Effects 0.000 description 5
- 230000002093 peripheral effect Effects 0.000 description 4
- 210000005252 bulbus oculi Anatomy 0.000 description 3
- 230000000694 effects Effects 0.000 description 2
- 208000002177 Cataract Diseases 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 239000002033 PVDF binder Substances 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 206010036346 Posterior capsule opacification Diseases 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 238000010828 elution Methods 0.000 description 1
- 210000001508 eye Anatomy 0.000 description 1
- 210000000744 eyelid Anatomy 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000005499 meniscus Effects 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 229920002981 polyvinylidene fluoride Polymers 0.000 description 1
- 229910001285 shape-memory alloy Inorganic materials 0.000 description 1
- 239000004447 silicone coating Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000002604 ultrasonography Methods 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS 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
- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/02—Prostheses implantable into the body
- A61F2/14—Eye parts, e.g. lenses, corneal implants; Implanting instruments specially adapted therefor; Artificial eyes
- A61F2/16—Intraocular lenses
- A61F2/1613—Intraocular lenses having special lens configurations, e.g. multipart lenses; having particular optical properties, e.g. pseudo-accommodative lenses, lenses having aberration corrections, diffractive lenses, lenses for variably absorbing electromagnetic radiation, lenses having variable focus
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS 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
- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/02—Prostheses implantable into the body
- A61F2/14—Eye parts, e.g. lenses, corneal implants; Implanting instruments specially adapted therefor; Artificial eyes
- A61F2/16—Intraocular lenses
- A61F2002/1681—Intraocular lenses having supporting structure for lens, e.g. haptics
- A61F2002/1683—Intraocular lenses having supporting structure for lens, e.g. haptics having filiform haptics
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は、白内障手術等により水晶体を取り去った後に
挿入して、眼の屈折矯正に用いる眼内レンズに関するも
のである。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to an intraocular lens that is inserted after removing the crystalline lens during cataract surgery or the like and is used for refractive correction of the eye.
[従来の技術]
白内障手術の後に嫡出した水晶体の代りに、近年では眼
内レンズが挿入されることが多い、この手術は超音波に
よる水晶体組織の粉砕、吸引そして眼内レンズの挿入の
順序で行われる。水晶体の摘出及び眼内レンズの挿入に
際して行う眼球組織の切開及び縫合は、できる限り小さ
な部位に留める方がより安全であり、手術後の結果も良
好となる。そのため、挿入する眼内レンズとしては、従
来のアクリル等のプラスチックレンズに代って、折り畳
み可能な柔軟な材料、例えばシリコーンゴム等で形成さ
れた眼内レンズが提案されている。[Prior art] In recent years, an intraocular lens is often inserted in place of the legitimate lens after cataract surgery.This surgery consists of crushing the crystalline lens tissue using ultrasound, suction, and inserting the intraocular lens. It will be done. It is safer to keep the incision and suture of the ocular tissues as small as possible when removing the crystalline lens and inserting the intraocular lens, and the results after surgery are also better. Therefore, as an intraocular lens to be inserted, an intraocular lens made of a foldable and flexible material, such as silicone rubber, has been proposed in place of the conventional plastic lens such as acrylic.
また、シリコーンゴムはアクリル等のプラスチック材料
と異なりオートクレーブ消毒が可能であり、人体にとっ
て有害なエチレンオキサイドガスの残留が問題になるこ
ともなく、更には虹彩、水晶体嚢、水晶体残存物質など
に対して癒着を生ずることがないため、最近ではその優
位性が注目されている。In addition, unlike plastic materials such as acrylic, silicone rubber can be sterilized in an autoclave, so there is no problem with residual ethylene oxide gas, which is harmful to the human body, and it is also effective against iris, lens capsule, and residual substances in the lens. Recently, its superiority has been attracting attention because it does not cause adhesions.
[発明が解決しようとする問題点]
しかしながら、シリコーンゴム自体の材料強度は、アク
リルやポリプロピレン等のプラスチック材料に比べて約
1/10程度しかないため、第4図に示すような支持部
の形状を持つシリコーンゴム一体型、つまり光学部lも
支持gB2もシリコーンゴムで形成された眼内レンズが
従来から提案されてさているが、それでも通常のアクリ
ル一体型、或いは第5図に示すように光学部1がアクリ
ルで、細条状の支持12がポリプロピレン等のプラスチ
ック材料で構成されている形状の眼内レンズに比べて、
支持部2のばね性が少ないことから、眼内保持性に劣り
、手術後に眼球から飛び出してしまったり、位置ずれが
生じたりするという問題点がある。[Problems to be Solved by the Invention] However, the material strength of silicone rubber itself is only about 1/10 that of plastic materials such as acrylic and polypropylene, so the shape of the support part as shown in FIG. Intraocular lenses that are integrated with silicone rubber, that is, both the optical part l and the support gB2 are made of silicone rubber, have been proposed in the past. Compared to an intraocular lens in which the portion 1 is made of acrylic and the strip-shaped support 12 is made of a plastic material such as polypropylene,
Since the support part 2 has little springiness, it has poor intraocular retention, and there are problems in that it may pop out of the eyeball or become misaligned after surgery.
この問題を解決するために、例えばシリコーンゴムの光
学部と、ポリプロピレン等のプラスチック材料の支持部
で構成される眼内レンズも考えられるが、前述したよう
にシリコーンゴム以外の材料で構成される支持部と眼内
組織との癒着の問題点が残り、十分な解決案には至って
いない。To solve this problem, an intraocular lens can be considered, for example, consisting of an optical part made of silicone rubber and a support part made of a plastic material such as polypropylene, but as mentioned above, the support part is made of a material other than silicone rubber. The problem of adhesion between the eyelid and intraocular tissue remains, and no satisfactory solution has been found.
[発明の目的]
本発明の目的は、上述の問題点を解消し、芯材を挿入す
ることにより支持部に適度のばね性を持たせ、眼内保持
性を高めると共に、生体適合性をも併せ持つ眼内レンズ
を提供することにある。[Objective of the Invention] The object of the present invention is to solve the above-mentioned problems, to provide the supporting portion with appropriate springiness by inserting a core material, to improve intraocular retention, and to achieve biocompatibility. Our objective is to provide an intraocular lens that has both of these features.
[発明の概要]
上述の目的を達成するための本発明の要旨は、光学部と
、該光学部を保持する支持部とから構成した眼内レンズ
において、少なくとも前記支持部はばね性を有する芯材
と外層材との二層構造としたことを特徴とする眼内レン
ズである。[Summary of the Invention] The gist of the present invention to achieve the above object is to provide an intraocular lens comprising an optical part and a support part for holding the optical part, in which at least the support part has a core having spring properties. This intraocular lens is characterized by having a two-layer structure consisting of a material and an outer layer.
[発明の実施例]
本発明を第1図〜第3図に図示の実施例に基づいて詳細
に説明する。[Embodiments of the Invention] The present invention will be described in detail based on embodiments illustrated in FIGS. 1 to 3.
第1図は第1の実施例による眼内レンズの平面図であり
、lは光学部、2は支持部である。光学部1は例えばシ
リコーンゴムで形成され、同じシリコーンゴムを外層材
3に持つ支持部2の内部には、例えばポリプロピレン等
のプラスチック材料から成る芯材4が埋め込まれている
。FIG. 1 is a plan view of the intraocular lens according to the first embodiment, where l is an optical part and 2 is a support part. The optical part 1 is made of silicone rubber, for example, and a core material 4 made of a plastic material such as polypropylene is embedded inside a support part 2 having an outer layer 3 made of the same silicone rubber.
この第1図に示す眼内レンズは、例えば次に述べるよう
な方法で作成される。即ち、予めループ状に成型された
例えばポリプロピレン等のプラスチック材料から成る線
材を芯材4として型内の所定の場所にインサートしてお
き、その後に型内に外層材3となるシリコーンゴムを流
し込んで光学部1を形成すると同時に一体物とする方法
が先ず挙げられる。型には線材の太さよりも大きい溝を
予め設けておくことによって、シリコーンゴムは支持部
2の方まで流れてゆき、最終的には第1図に示すように
芯材4がポリプロピレン等のプラスチックで、外層材3
がシリコーンゴムの支持部2が製作される。The intraocular lens shown in FIG. 1 is produced, for example, by the method described below. That is, a wire rod made of a plastic material such as polypropylene, which has been formed into a loop shape in advance, is inserted into a predetermined position in a mold as a core material 4, and then silicone rubber, which will become an outer layer material 3, is poured into the mold. Firstly, there is a method of forming the optical part 1 and simultaneously making it into an integrated object. By pre-preparing a groove in the mold that is larger than the thickness of the wire, the silicone rubber flows to the support part 2, and as shown in Figure 1, the core material 4 is made of plastic such as polypropylene. So, outer layer material 3
However, the support part 2 made of silicone rubber is manufactured.
また、他の製造方法としては、ループ状に成型されたポ
リプロピレン等のプラスチック線材の芯材4に予めシリ
コーンコーティングを施し、その後にコーティングされ
た支持部2を型内の所定の場所にインサートしておき、
シリコーンゴムを流し込んで光学部1を形成すると共に
一体化とする方法がある。Another manufacturing method is to apply silicone coating to the core material 4 of a plastic wire such as polypropylene molded into a loop shape in advance, and then insert the coated support part 2 into a predetermined position in the mold. Ok,
There is a method of forming the optical part 1 by pouring silicone rubber and integrating it.
このように構成された眼内レンズは、ポリプロピレン等
のプラスチック材料を芯材4に持つ支持部2であるため
、適度なばね性があり、眼内保持性に優れ、更にシリコ
ーンゴムから成る外層材3によって眼内組織とのE@着
も生ずることがない。The intraocular lens constructed in this way has a supporting part 2 having a core material 4 made of a plastic material such as polypropylene, so it has appropriate springiness and excellent intraocular retention. 3, no E@ adhesion with intraocular tissue occurs.
第2図Ca)は第2の実施例による眼内レンズの平面図
、(b)は断面図であり、例えばシリコーンゴムを外層
材3に持つ光学部l及び支持部2の双方の内部に、例え
ばアクリル等の透明プラスチック材料から成る芯材4が
埋め込まれている。FIG. 2(b) is a plan view of the intraocular lens according to the second embodiment, and FIG. 2(b) is a sectional view of the intraocular lens according to the second embodiment. A core material 4 made of a transparent plastic material such as acrylic is embedded.
この構成の眼内レンズは、第1図に示す眼内レンズより
も支持部2のばね性がより十分に確保でき、眼内保持性
が更に優れている。The intraocular lens with this configuration can ensure more sufficient springiness of the support portion 2 than the intraocular lens shown in FIG. 1, and is even more excellent in intraocular retention.
第3図(a)は第3の実施例による眼内レンズの平面図
、(b)はその断面図であり、第2の実施例と同様に光
学部1の内部にも例えばポリプロピレン等のプラスチッ
ク材料から成る芯材4が埋め込まれているが、この芯材
4は光学部1では周縁部のみである点が第2の実施例と
異なる。この構成では、内部に埋め込む芯材4が第2の
実施例と異なり、特に透明である必要がない、なお、こ
の第3の実施例においては、光学部1の周りに独立的に
周辺部を設け、この周辺部に芯材4を埋め込んでもよい
。FIG. 3(a) is a plan view of an intraocular lens according to the third embodiment, and FIG. 3(b) is a cross-sectional view thereof. As in the second embodiment, the inside of the optical part 1 is also made of plastic such as polypropylene. Although a core material 4 made of a material is embedded, this core material 4 is different from the second embodiment in that the core material 4 is present only at the peripheral portion of the optical section 1. In this configuration, unlike the second embodiment, the core material 4 to be embedded inside does not need to be particularly transparent; The core material 4 may be embedded in the peripheral portion.
また、上述の実施例においては、支持部2は全て所謂開
ループ形状としたが、支持部2は閉ループでも勿論支障
はない、その場合には、上述の実施例に対応するように
、芯材4が光学部1と支持部2の接続部付近から先の支
持部2の内部のみにあるもの、芯材4が光学部1の投影
面積のほぼ全体にあるもの、そして光学部1の周縁部に
位置するもの等を種々選択してもよいし、また前述のよ
うに芯材4を光学部1の周りに独立して設けた周辺部の
中に埋め込んでもよい、更には、芯材4は眼内レンズの
光学部1、支持部2の内部において部分的に配置しても
よいし、それらが全て同じ材質である必要もない。In addition, in the above-mentioned embodiment, all of the support parts 2 were formed into a so-called open loop shape, but it goes without saying that the support part 2 may have a closed loop shape.In that case, the core material may be 4 is located only inside the support part 2 from the vicinity of the connection between the optical part 1 and the support part 2, the core material 4 is located on almost the entire projected area of the optical part 1, and the peripheral part of the optical part 1. The core material 4 may be located in a variety of ways, or the core material 4 may be embedded in a peripheral area provided independently around the optical part 1 as described above. It may be partially arranged inside the optical part 1 and the support part 2 of the intraocular lens, and it is not necessary that they are all made of the same material.
芯材4の材質として、上述した実施例においてはポリプ
ロピレン、アクリル等を例に挙げたが、ポリフッ化ビニ
リデン、ポリイミド等のプラスチック材料であってもよ
いし、形状記憶合金等の金属であってもよい、また、実
施例においては光学部1は両凸型としているが、平凸型
やメニスカス型などの形状の眼内レンズとしてもよいこ
とは云うまでもない。As the material of the core material 4, polypropylene, acrylic, etc. were given as examples in the above-mentioned embodiments, but it may also be a plastic material such as polyvinylidene fluoride, polyimide, or a metal such as a shape memory alloy. In addition, in the embodiment, the optical part 1 is biconvex, but it goes without saying that an intraocular lens having a plano-convex or meniscus shape may also be used.
更に、外層材3となる材料が一般に良く知られたジメチ
ルシロキサンというシリコーンゴムでなくとも、生体適
合性に優れたシリコーンゴムであれば、芳香族誘導体置
換基などを有する高屈折率のシリコーンゴムであっても
よい、また、外層材3に親水性付与、紫外線遮断性付与
等の目的、或いは外層材3からの組成物の溶出防止の目
的でプラズマ重合膜等の成膜処理を施しておけば、より
生体適合性にも優れ生体にとっても安全である。Furthermore, even if the material to be the outer layer material 3 is not the generally well-known silicone rubber called dimethylsiloxane, as long as it is a silicone rubber with excellent biocompatibility, it can be a silicone rubber with a high refractive index having an aromatic derivative substituent. In addition, if the outer layer material 3 is subjected to a film forming treatment such as a plasma polymerized film for the purpose of imparting hydrophilicity, ultraviolet blocking property, etc., or for the purpose of preventing elution of the composition from the outer layer material 3. , it has better biocompatibility and is safe for living organisms.
[発明の効果]
以上説明したように本発明に係る眼内レンズは、その支
持部或いは光学部と支持部の両方を芯材と外層材とから
構成することにより、芯材で支持部に適度のばね性を持
たせ、眼内保持性を高めることによって、手術後に眼球
から飛び出してしまったり1位置ずれが生じたりする問
題点を解消し、眼内組織に対して癒着のない材料で外層
材を形成することによって、生体適合性をも併せ持つと
いう効果がある。[Effects of the Invention] As explained above, the intraocular lens according to the present invention has both the supporting part or the optical part and the supporting part composed of a core material and an outer layer material, so that the core material can provide a suitable amount of support to the supporting part. By providing springiness and improving intraocular retention, we have solved the problem of the eyeball popping out of the eyeball after surgery or being misaligned. By forming this, it has the effect of also having biocompatibility.
図面は第1図〜第3図は本発明に係る眼内レンズの実施
例を示し、第1図は第1の実施例の平面図、第2図(a
)は第2の実施例の平面図、(b)はそのA−A’断面
図、@3図(a)は第3の実施例の平面図、(b)はそ
のB−B’断面図であり、第4図、第5図は従来の眼内
レンズの平面図である。
符号1は光学部、2は支持部、3は外層材、4は芯材で
ある。
特許出願人 キャノン株式会社
第1図 第2図
第3図
CG)In the drawings, FIGS. 1 to 3 show an embodiment of the intraocular lens according to the present invention, and FIG. 1 is a plan view of the first embodiment, and FIG.
) is a plan view of the second embodiment, (b) is a sectional view taken along the line AA', @3 (a) is a plan view of the third embodiment, and (b) is a sectional view taken along the line BB'. 4 and 5 are plan views of conventional intraocular lenses. Reference numeral 1 is an optical part, 2 is a support part, 3 is an outer layer material, and 4 is a core material. Patent applicant Canon Co., Ltd. Figure 1 Figure 2 Figure 3 CG)
Claims (1)
した眼内レンズにおいて、少なくとも前記支持部はばね
性を有する芯材と外層材との二層構造としたことを特徴
とする眼内レンズ。1. An intraocular lens comprising an optical part and a support part for holding the optical part, characterized in that at least the support part has a two-layer structure of a core material having spring properties and an outer layer material. .
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63133151A JPH01300948A (en) | 1988-05-31 | 1988-05-31 | Intraocular lens |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63133151A JPH01300948A (en) | 1988-05-31 | 1988-05-31 | Intraocular lens |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH01300948A true JPH01300948A (en) | 1989-12-05 |
Family
ID=15097902
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP63133151A Pending JPH01300948A (en) | 1988-05-31 | 1988-05-31 | Intraocular lens |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01300948A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2005506875A (en) * | 2001-10-22 | 2005-03-10 | シノプトクス, インコーポレーテッド | Deformable intraocular multifocal lens |
WO2018134674A1 (en) | 2017-01-20 | 2018-07-26 | 興和株式会社 | Intraocular lens and method for producing same |
-
1988
- 1988-05-31 JP JP63133151A patent/JPH01300948A/en active Pending
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2005506875A (en) * | 2001-10-22 | 2005-03-10 | シノプトクス, インコーポレーテッド | Deformable intraocular multifocal lens |
WO2018134674A1 (en) | 2017-01-20 | 2018-07-26 | 興和株式会社 | Intraocular lens and method for producing same |
JP2018183197A (en) * | 2017-01-20 | 2018-11-22 | 興和株式会社 | Intraocular lens, and manufacturing method thereof |
KR20190104196A (en) | 2017-01-20 | 2019-09-06 | 코와 가부시키가이샤 | Intraocular Lens and Manufacturing Method Thereof |
CN110325150A (en) * | 2017-01-20 | 2019-10-11 | 兴和株式会社 | Intraocular lens and its manufacturing method |
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