JP3348866B2 - Intraocular lens and processing method thereof - Google Patents

Intraocular lens and processing method thereof

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Publication number
JP3348866B2
JP3348866B2 JP24664491A JP24664491A JP3348866B2 JP 3348866 B2 JP3348866 B2 JP 3348866B2 JP 24664491 A JP24664491 A JP 24664491A JP 24664491 A JP24664491 A JP 24664491A JP 3348866 B2 JP3348866 B2 JP 3348866B2
Authority
JP
Japan
Prior art keywords
optical
prepolymer
support
intraocular lens
unit
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.)
Expired - Fee Related
Application number
JP24664491A
Other languages
Japanese (ja)
Other versions
JPH0556988A (en
Inventor
力 砂田
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Nidek Co Ltd
Original Assignee
Nidek Co Ltd
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 Nidek Co Ltd filed Critical Nidek Co Ltd
Priority to JP24664491A priority Critical patent/JP3348866B2/en
Publication of JPH0556988A publication Critical patent/JPH0556988A/en
Application granted granted Critical
Publication of JP3348866B2 publication Critical patent/JP3348866B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【産業上の利用分野】本発明は、眼組織の水晶体の代用
として使用される眼内レンズ及びその加工方法に関す
る。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an intraocular lens used as a substitute for a lens of ocular tissue and a method of processing the same.

【0002】[0002]

【従来の技術】白内障により水晶体を摘出した後等に水
晶体の代わりとして挿入される眼内レンズは、一般的に
は、レンズの役割を果たす光学部とこれを眼内に保持す
るための光学支持部(ル−プ)とからなるのが一般的で
ある。このような眼内レンズには、光学部と光学支持部
を一体的に加工するいわゆるシングルピ−スと呼ばれる
ものと、光学部と支持部を別個に加工し、これをカシメ
により一体にするいわゆるスリ−ピ−スと呼ばれるもの
とがある。
2. Description of the Related Art An intraocular lens which is inserted as a substitute for a crystalline lens, for example, after a crystalline lens is extracted due to a cataract, generally includes an optical part serving as a lens and an optical support for holding the optical part in the eye. It generally comprises a loop. Such an intraocular lens includes a so-called single piece in which an optical unit and an optical support unit are integrally processed, and a so-called three-piece unit in which the optical unit and the support unit are separately processed and integrated by caulking. -There is something called a piece.

【0003】[0003]

【発明が解決しようとする課題】しかしながら、前者に
は次のような欠点がある。基材として高分子量のものを
選択するときは、支持部が脆く折損しやすい。また、低
分子量のものを選択するときは、支持部は柔軟である
が、後発白内障が起きたときの光凝固治療で光学部が破
損しやすい。後者のスリ−ピ−スの場合は、カシメ加工
のための専用の装置を用意しなければならず、コスト高
の要因となる。さらに、高分子量の光学部と低分子量の
光学支持部を用いるときは、カシメによる接合強度が弱
く折損しやすいという欠点がある。
However, the former has the following disadvantages. When a high molecular weight substrate is selected, the support is brittle and easily broken. When selecting a low-molecular-weight one, the support part is flexible, but the optical part is easily damaged by photocoagulation treatment when late cataract occurs. In the latter case, a dedicated device for crimping has to be prepared, which causes an increase in cost. Further, when a high molecular weight optical part and a low molecular weight optical support part are used, there is a disadvantage that the bonding strength by caulking is weak and the fiber is easily broken.

【0004】本発明は、上記欠点に鑑み案出されたもの
で、その第1の目的は光学部と光学支持部との接合強度
が強いスリ−ピ−スタイプの眼内レンズを提供すること
にある。第2の目的は、光凝固手術などで光学部が破損
することがなく、光学支持部も柔軟性に富み、眼内挿入
時に安定性の良い眼内レンズの提供することにある。第
3の目的は、これらの眼内レンズの加工方法を提供する
ことにある。
SUMMARY OF THE INVENTION The present invention has been made in view of the above-mentioned drawbacks, and a first object of the present invention is to provide a sleeper type intraocular lens having a high bonding strength between an optical part and an optical support part. is there. A second object is to provide an intraocular lens in which the optical section is not damaged by photocoagulation surgery or the like, the optical support section is rich in flexibility, and the stability during insertion into the eye is good. A third object is to provide a method for processing these intraocular lenses.

【0005】[0005]

【課題を解決するための手段】上記目的を達成するため
に、本発明は以下のことを特徴とする。すなわち、 (1) 予め切削加工にて得られた光学部と該光学部を
手術眼の所定位置に支持するための光学支持部とからな
り、光学支持部は光学部の周辺部に形成された取付穴に
取付け加工された眼内レンズにおいて、前記光学部及び
前記光学支持部と重合可能なモノマに重合開始剤を添加
し、加熱によってラジカル重合させるとともに重合反応
を途中終了させることにより得られるラジカルが残った
プレポリマを両者の間に介在させた後、該プレポリマに
再度熱を加え重合させることで光学部と光学支持部が化
学的に結合し、前記光学部と光学支持部材との結合強度
が引張試験にて150g以上であることを特徴としてい
る。
In order to achieve the above object, the present invention is characterized by the following. That is, (1) an optical part obtained by a cutting process in advance and an optical support part for supporting the optical part at a predetermined position of a surgical eye, and the optical support part is formed around the optical part. In the intraocular lens mounted in the mounting hole, a polymerization initiator is added to a monomer polymerizable with the optical unit and the optical support unit, and radical polymerization is performed by heating, and a polymerization reaction is performed.
Radicals obtained by terminating
After the prepolymer is interposed between the two,
The optical part and the optical support part are chemically bonded by heating and polymerizing again, and the bonding strength between the optical part and the optical support member.
Is 150 g or more in a tensile test .

【0006】(2) (1)の光学部は光学支持部と比
較して相対的に高分子の物質から構成されていることを
特徴としている。
(2) The optical part of (1) is compared with the optical support part.
That it is composed of relatively high-molecular substances
Features.

【0007】(3) 光学部と該光学部とをそれぞれ別
個に所定形状に加工した後、光学支持部を光学部の周辺
部に形成された取付穴に取付け加工する眼内レンズの加
工方法において、前記光学部及び前記光学支持部と重合
可能なモノマに重合開始剤を添加し、加熱によってラジ
カル重合させるとともに重合反応を途中終了させること
により得られるラジカルが残ったプレポリマを得る工程
と、光学部に形成された取付穴又は光学支持部の少なく
とも一方に前記プレポリマを塗布する塗布工程と、光学
部の取付穴に光学支持部の先端を挿入する工程と、前記
プレポリマに再度熱を加え重合させることで光学部と光
学支持部とを化学的に結合させる工程と、からなること
を特徴としている。
(3) A method of processing an intraocular lens in which an optical part and an optical part are separately processed into a predetermined shape, and then an optical support part is mounted in a mounting hole formed in a peripheral part of the optical part. , a polymerization initiator is added to the polymerizable monomer and the optical unit and the optical support portion, Raj by heating
Terminate the polymerization reaction in the middle of the cal polymerization
A step of obtaining a prepolymer in which radicals obtained by remain, an application step of applying the prepolymer to at least one of a mounting hole or an optical support formed in the optical unit, and a tip of the optical support in the mounting hole of the optical unit. It is characterized by comprising a step of inserting, and a step of chemically bonding the optical part and the optical support part by applying heat again to the prepolymer and polymerizing it.

【0008】[0008]

【0009】[0009]

【0010】[0010]

【0011】[0011]

【0012】[0012]

【0013】[0013]

【実施例】以下に本発明の実施例を図1を参考にしなが
ら説明する。図1は本発明の1実施例を示すフロ−チャ
−トである。ポリメチルメタクリレ−トを主原料とする
板材(必要により紫外線吸収材等を混入させる)を円盤
状に打ち抜く(ステップ1)。ポリメチルメタクリレ−
トは比較的高分子量(分子量約100万)のものを用い
る。眼内レンズの光学部は円盤状に打ち抜かれたいわゆ
るコアを直径4〜8mmで、所定の屈折力を持つように切
削加工して作られる(ステップ2)。光学部には光学支
持部取付穴(直径0.15〜0.25mm)やマニピュレ
−ションホ−ルといった穴の加工が施される(ステップ
3)。一方、光学支持部は比較的低分子量(分子量約2
0万〜30万)のポリメチルメタクリレ−トの線材をル
−プ状に成形し、適当な長さに切断して使用に供する
(直径0.1〜0.2mm、長さ5〜8mm) (ステップ
4)。
An embodiment of the present invention will be described below with reference to FIG. FIG. 1 is a flowchart showing one embodiment of the present invention. A plate material made of polymethyl methacrylate as a main raw material (an ultraviolet absorber or the like is mixed as necessary) is punched into a disk shape (step 1). Polymethyl methacrylate
The material used has a relatively high molecular weight (molecular weight of about 1,000,000). The optical part of the intraocular lens is made by cutting a so-called core punched into a disk shape to have a predetermined refractive power with a diameter of 4 to 8 mm (step 2). The optical part is machined with holes such as an optical support part mounting hole (0.15-0.25 mm in diameter) and a manipulation hole (step 3). On the other hand, the optical support has a relatively low molecular weight (molecular weight of about 2).
(100,000 to 300,000) polymethyl methacrylate wire is formed into a loop, cut into appropriate lengths, and used (diameter 0.1 to 0.2 mm, length 5 to 8 mm). ) (Step 4).

【0014】また、光学部と前記光学支持部と化学的に
結合する中間物質としてプレポリマを用意する。プレポ
リマはメチルメタクリレ−トのモノマに重合開始剤であ
る過酸化ベンゾイルを添加し(ステップ5)、摂氏70
度前後で6〜8時間反応させたものである(ステップ
6)。
Further, a prepolymer is prepared as an intermediate substance chemically bonded to the optical part and the optical support part. The prepolymer was prepared by adding benzoyl peroxide as a polymerization initiator to a monomer of methyl methacrylate (step 5), and the temperature was reduced to 70 degrees Celsius.
The reaction was carried out for about 6 to 8 hours before and after the temperature (step 6).

【0015】次に、プレポリマの塗布工程を行う。プレ
ポリマの塗布は、光学支持部の先端をプレポリマ液中に
浸漬し(ステップ7)、または、プレポリマ液を針状の
器具で光学支持部取付穴に注入して(ステップ8)、こ
れを行う。プレポリマの塗布は、光学支持部及び光学支
持部取付穴の少なくとも一方になされれば良い。プレポ
リマの塗布工程後、光学支持部の先端を光学支持部取付
穴に挿入する(ステップ9)。この状態で、眼内レンズ
を摂氏60〜70度に加熱された空間に24時間置き、
プレポリマを重合し、硬化させる(ステップ10)。
Next, a prepolymer coating step is performed. The prepolymer is applied by dipping the tip of the optical support into the prepolymer liquid (step 7) or by injecting the prepolymer liquid into the optical support mounting hole with a needle-like instrument (step 8). The prepolymer may be applied to at least one of the optical support portion and the optical support portion mounting hole. After the prepolymer application step, the tip of the optical support is inserted into the optical support mounting hole (step 9). In this state, place the intraocular lens in a space heated to 60 to 70 degrees Celsius for 24 hours,
The prepolymer is polymerized and cured (step 10).

【0016】このようにして得られた眼内レンズの光学
部と光学支持部の結合強度をいわゆる引張試験により試
験した。従来のカシメ加工による接合方法の接合強度が
約90g であるのに対して、本実施例の場合接合強度は
約150g 以上と飛躍的に向上した(引張試験によ
る)。しかも、150g の負荷により破損したのは、接
合部ではなく光学支持部材それ自体であった。なお、上
記実施例は光学部、光学支持部、中間接合物としていず
れもメチルメタクリレ−ト系を使用したが、光学部、光
学支持部及び中間接合物の構成分子は必ずしも同種であ
る必要はなく、光学部と光学支持部と重合可能な中間接
合物であり、身体に安全なものを選択すれば良い。光学
部、光学支持部及び中間接合物に適する単体の例として
は、メチルメタクリレ−トの他、ヒドロキシエチルメタ
クリレ−トやメタクリル酸ブチル等の物質があげられ
る。
The bonding strength between the optical part and the optical support part of the thus obtained intraocular lens was tested by a so-called tensile test. While the joining strength of the conventional joining method by caulking is about 90 g, the joining strength of the present embodiment is remarkably improved to about 150 g or more (by a tensile test). In addition, it was the optical support member itself, not the joint, that was damaged by the 150 g load. In the above-described embodiment, methyl methacrylate was used as the optical part, the optical support part, and the intermediate conjugate, but the constituent molecules of the optical part, the optical support part, and the intermediate conjugate need not necessarily be the same kind. Instead, an intermediate joint that can be polymerized between the optical unit and the optical support unit and that is safe for the body may be selected. Examples of simple substances suitable for the optical part, the optical support part, and the intermediate joint include, in addition to methyl methacrylate, substances such as hydroxyethyl methacrylate and butyl methacrylate.

【0017】[0017]

【発明の効果】以上の説明から明らかなように、本発明
によれば、予め切削加工にて得られた光学部に対して光
学支持部を中間物質を介して化学的に結合するので、従
来のカシメによる接合強度よりも強い接合強度が得られ
る。また、光凝固手術などで光学部が破損することがな
く、光学支持部も柔軟性に富んだ眼内レンズを容易に得
ることができ
As is clear from the above description, according to the present invention, light is applied to the optical portion obtained by cutting in advance.
Chemical supports are chemically bonded via intermediates,
Stronger joint strength than conventional caulking
You. Also, without the optical unit in such photocoagulation surgery is damaged, it is possible to obtain easily an intraocular lens rich in even flexible optical support.

【図面の簡単な説明】[Brief description of the drawings]

【図1】本発明の1実施例を示すフローチャートであ
る。
FIG. 1 is a flowchart showing one embodiment of the present invention.

Claims (3)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 予め切削加工にて得られた光学部と該光
学部を手術眼の所定位置に支持するための光学支持部と
からなり、光学支持部は光学部の周辺部に形成された取
付穴に取付け加工された眼内レンズにおいて、前記光学
部及び前記光学支持部と重合可能なモノマに重合開始剤
を添加し、加熱によってラジカル重合させるとともに重
合反応を途中終了させることにより得られるラジカルが
残ったプレポリマを両者の間に介在させた後、該プレポ
リマに再度熱を加え重合させることで光学部と光学支持
部が化学的に結合し、前記光学部と光学支持部材との結
合強度が引張試験にて150g以上であることを特徴と
する眼内レンズ。
1. An optical part obtained by a cutting process in advance and an optical support part for supporting the optical part at a predetermined position of a surgical eye, and the optical support part is formed around the optical part. In the intraocular lens mounted in the mounting hole, a polymerization initiator is added to a monomer that can be polymerized with the optical unit and the optical support unit, and radical polymerization is performed by heating, and polymerization is performed.
The radical obtained by terminating the combined reaction is
After the remaining prepolymer is interposed between the two, heat is applied to the prepolymer again to cause polymerization , whereby the optical portion and the optical support portion are chemically bonded to each other, and the optical portion and the optical support member are connected to each other.
An intraocular lens having a combined strength of 150 g or more in a tensile test .
【請求項2】 請求項1の光学部は光学支持部と比較し
て相対的に高分子の物質から構成されていることを特徴
とする眼内レンズ。
2. The intraocular lens according to claim 1, wherein the optical section is made of a relatively high-molecular substance as compared with the optical support section.
【請求項3】 光学部と該光学部とをそれぞれ別個に所
定形状に加工した後、光学支持部を光学部の周辺部に形
成された取付穴に取付け加工する眼内レンズの加工方法
において、前記光学部及び前記光学支持部と重合可能な
モノマに重合開始剤を添加し、加熱によってラジカル重
合させるとともに重合反応を途中終了させることにより
得られるラジカルが残ったプレポリマを得る工程と、光
学部に形成された取付穴又は光学支持部の少なくとも一
方に前記プレポリマを塗布する塗布工程と、光学部の取
付穴に光学支持部の先端を挿入する工程と、前記プレポ
リマに再度熱を加え重合させることで光学部と光学支持
部とを化学的に結合させる工程と、からなることを特徴
とする眼内レンズの加工方法。
3. A method for processing an intraocular lens, wherein an optical part and an optical part are separately processed into a predetermined shape, and an optical support part is mounted on a mounting hole formed in a peripheral part of the optical part. A polymerization initiator is added to a monomer polymerizable with the optical unit and the optical support unit, and radical polymerization is performed by heating.
And by terminating the polymerization reaction
A step of obtaining a prepolymer in which the obtained radical remains, a coating step of applying the prepolymer to at least one of a mounting hole or an optical support formed in the optical unit, and inserting a tip of the optical support into the mounting hole of the optical unit. And a step of chemically bonding the optical part and the optical support part by applying heat again to the prepolymer to polymerize the prepolymer.
JP24664491A 1991-08-31 1991-08-31 Intraocular lens and processing method thereof Expired - Fee Related JP3348866B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP24664491A JP3348866B2 (en) 1991-08-31 1991-08-31 Intraocular lens and processing method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP24664491A JP3348866B2 (en) 1991-08-31 1991-08-31 Intraocular lens and processing method thereof

Publications (2)

Publication Number Publication Date
JPH0556988A JPH0556988A (en) 1993-03-09
JP3348866B2 true JP3348866B2 (en) 2002-11-20

Family

ID=17151482

Family Applications (1)

Application Number Title Priority Date Filing Date
JP24664491A Expired - Fee Related JP3348866B2 (en) 1991-08-31 1991-08-31 Intraocular lens and processing method thereof

Country Status (1)

Country Link
JP (1) JP3348866B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH11197165A (en) * 1998-01-16 1999-07-27 Menicon Co Ltd Intraocular lens and production of intraocular lens

Also Published As

Publication number Publication date
JPH0556988A (en) 1993-03-09

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