JPH10177152A - Moisture-containing soft contact lens - Google Patents
Moisture-containing soft contact lensInfo
- Publication number
- JPH10177152A JPH10177152A JP33694996A JP33694996A JPH10177152A JP H10177152 A JPH10177152 A JP H10177152A JP 33694996 A JP33694996 A JP 33694996A JP 33694996 A JP33694996 A JP 33694996A JP H10177152 A JPH10177152 A JP H10177152A
- Authority
- JP
- Japan
- Prior art keywords
- contact lens
- meth
- soft contact
- polymer
- weight
- 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.)
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- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、含水性ソフトコン
タクトレンズに関する。更に詳細には、含水率、酸素透
過性、防汚性及び機械的強度に優れた含水性ソフトコン
タクトレンズに関する。The present invention relates to a hydrous soft contact lens. More specifically, the present invention relates to a water-containing soft contact lens excellent in water content, oxygen permeability, antifouling property and mechanical strength.
【0002】[0002]
【従来の技術】含水性ソフトコンタクトレンズは、メチ
ルメタクリレート、シロキサニルアルキルメタクリレー
ト等の単量体を主成分とする非含水性ハードコンタクト
レンズ(特公昭52−23502号公報)と比較して、
目に馴染み易く、優れた装用感、即ち、目に装着した際
に違和感のない状態を有することが知られている。一般
に、含水性ソフトコンタクトレンズとしては、2−ヒド
ロキシエチルメタクリレート(以下、「HEMA」と略
す)が主原材料として使用されており、含水性ソフトコ
ンタクトレンズとしては、機械的強度及び加工性に優れ
るという特徴がある。しかしながら、従来のこれらのソ
フトコンタクトレンズは、含水率が35%以下と低含水
率であるため、長時間の連続装用を行う場合には十分な
ものではなかった。そこで、これを改良するために、レ
ンズ材料の含水率を高めることにより装用感のより優れ
た含水性ソフトコンタクトレンズを得ることが提案され
ている。例えば、N−ビニルピロリドン、メタクリル酸
を共重合成分として、メチルメタクリレート、2−ヒド
ロキシエチルメタクリレート等を共重合させて得られる
重合体からなる高含水性ソフトコンタクトレンズが提案
されている(特公昭54−4269号公報)。2. Description of the Related Art A water-containing soft contact lens is compared with a non-water-containing hard contact lens containing a monomer such as methyl methacrylate or siloxanyl alkyl methacrylate (Japanese Patent Publication No. 52-23502).
It is known that it has a feeling of being worn easily on the eyes and having an excellent feeling of wearing, that is, a state without discomfort when worn on the eyes. Generally, 2-hydroxyethyl methacrylate (hereinafter abbreviated as "HEMA") is used as a main raw material as a hydrous soft contact lens, and as a hydrous soft contact lens, it has excellent mechanical strength and workability. There are features. However, since these conventional soft contact lenses have a low water content of 35% or less, they are not sufficient for long-time continuous wearing. Therefore, in order to improve this, it has been proposed to increase the water content of the lens material to obtain a water-containing soft contact lens having a more comfortable wearing feeling. For example, a highly water-containing soft contact lens made of a polymer obtained by copolymerizing methyl methacrylate, 2-hydroxyethyl methacrylate, or the like with N-vinylpyrrolidone and methacrylic acid as copolymer components has been proposed (Japanese Patent Publication No. Sho 54). -4269).
【0003】一方、高含水率化は優れた装用感を与える
が、N−ビニルピロリドン、メタクリル酸を用いた高含
水性ソフトコンタクトレンズにおいては、汚れが付着し
易く、強度低下、繰り返し滅菌による黄変等の種々の欠
点が生じる。On the other hand, a high water content gives an excellent feeling of wearing. However, in a high water content soft contact lens using N-vinylpyrrolidone and methacrylic acid, dirt easily adheres, strength is reduced, and yellowness due to repeated sterilization is reduced. Various drawbacks such as strangeness occur.
【0004】いずれの場合も一般に含水性ソフトコンタ
クトレンズは共通してタンパク質、脂質等の付着、細菌
の繁殖等の衛生上の問題、高含水による機械的強度の低
下等が欠点として挙げられる。これらの問題を解決する
ため、特開平5−107511号公報では、汚れの付着
を防止する目的でホスホリルコリン基を含有する(メ
タ)アクリレート単量体を主原材料としたコンタクトレ
ンズが開示されている。しかしながら、前記ホスホリル
コリン基含有(メタ)アクリレート単量体では、重合時
の発熱が大きく重合制御が困難であり、レンズの機械的
強度の低下が生じるという問題がある。In all cases, the hydrous soft contact lenses generally have disadvantages such as adhesion of proteins and lipids, hygiene problems such as propagation of bacteria, and decrease in mechanical strength due to high water content. In order to solve these problems, Japanese Patent Application Laid-Open No. Hei 5-107511 discloses a contact lens mainly composed of a (meth) acrylate monomer containing a phosphorylcholine group for the purpose of preventing adhesion of dirt. However, the phosphorylcholine group-containing (meth) acrylate monomer has a problem that heat generation at the time of polymerization is large and it is difficult to control the polymerization, resulting in a decrease in mechanical strength of the lens.
【0005】[0005]
【発明が解決しようとする課題】本発明の目的は、高含
水率、高酸素透過性を有し、安全に製造、使用でき、更
に汚れ等の付着を抑制できる、ある程度強度を保持した
含水性ソフトコンタクトレンズを提供することにある。SUMMARY OF THE INVENTION An object of the present invention is to provide a water-containing material having a high water content and high oxygen permeability, which can be manufactured and used safely, and which can suppress the adhesion of dirt and the like, and has a certain strength. It is to provide a soft contact lens.
【0006】[0006]
【課題を解決するための手段】本発明によれば、下記一
般式(1)(式中R1は、水素原子又はメチル基を示
し、nは、1〜10の数を示す)で表されるホスホリル
コリン基含有(メタ)アクリル酸エステルを構成単位と
して含む重合体(A)1〜70重量%と、室温で液状の
ビニル単量体(B)99〜30重量%とを含有する原材
料を重合して得られた重合材料を含む含水性ソフトコン
タクトレンズが提供される。According to the present invention, the present invention is represented by the following general formula (1), wherein R 1 represents a hydrogen atom or a methyl group, and n represents a number of 1 to 10. A raw material containing 1 to 70% by weight of a polymer (A) containing a phosphorylcholine group-containing (meth) acrylic acid ester as a constituent unit and 99 to 30% by weight of a vinyl monomer (B) liquid at room temperature is polymerized. The present invention provides a hydrous soft contact lens containing the polymer material obtained by the above method.
【0007】[0007]
【化2】 Embedded image
【0008】[0008]
【発明の実施の形態】本発明の含水性ソフトコンタクト
レンズは、前記式(1)で表される特定のホスホリルコ
リン基含有(メタ)アクリル酸エステルを構成単位とし
て含有する重合体(A)と、室温で液状のビニル単量体
とを含む原材料を重合させて得られた重合材料を含む。
本発明の含水性ソフトコンタクトレンズの物性は、好ま
しくは、含水率40〜80重量%、特に40〜75重量
%、酸素透過性8〜50×10-11ml/cm2・sec
・mmHg、特に10〜40×10-11ml/cm2・s
ec・mmHgであるのが望ましい。前記式(1)にお
いて、nが10を超える場合には得られる重合材料の強
度及び加工性が低下する。BEST MODE FOR CARRYING OUT THE INVENTION The water-containing soft contact lens of the present invention comprises a polymer (A) containing a specific phosphorylcholine group-containing (meth) acrylate represented by the above formula (1) as a constitutional unit, It includes a polymerized material obtained by polymerizing a raw material containing a vinyl monomer which is liquid at room temperature.
The physical properties of the water-containing soft contact lens of the present invention are preferably 40 to 80% by weight, particularly 40 to 75% by weight, and oxygen permeability of 8 to 50 × 10 −11 ml / cm 2 · sec.
・ MmHg, especially 10 to 40 × 10 -11 ml / cm 2・ s
ec · mmHg is desirable. In the above formula (1), when n exceeds 10, the strength and processability of the obtained polymer material decrease.
【0009】本発明において用いる前記特定のホスホリ
ルコリン基含有(メタ)アクリル酸エステル単量体(以
下、「PC単量体」と略す)としては、例えば、2−
(メタ)アクリロイルオキシエチル−2’−(トリメチ
ルアンモニオ)エチルホスフェート、2−(メタ)アク
リロイルオキシプロピル−2’−(トリメチルアンモニ
オ)エチルホスフェート、2−(メタ)アクリロイルオ
キシエトキシエチル−2’−(トリメチルアンモニオ)
エチルホスフェート、2−(メタ)アクリロイルオキシ
ジエトキシエチル−2’−(トリメチルアンモニオ)エ
チルホスフェート、2−(メタ)アクリロイルオキシト
リエトキシエチル−2’−(トリメチルアンモニオ)エ
チルホスフェート等を挙げることができる。The specific phosphorylcholine group-containing (meth) acrylic acid ester monomer (hereinafter abbreviated as “PC monomer”) used in the present invention includes, for example, 2-PC
(Meth) acryloyloxyethyl-2 ′-(trimethylammonio) ethyl phosphate, 2- (meth) acryloyloxypropyl-2 ′-(trimethylammonio) ethyl phosphate, 2- (meth) acryloyloxyethoxyethyl-2 ′ -(Trimethylammonio)
Ethyl phosphate, 2- (meth) acryloyloxydiethoxyethyl-2 ′-(trimethylammonio) ethyl phosphate, 2- (meth) acryloyloxytriethoxyethyl-2 ′-(trimethylammonio) ethyl phosphate and the like are mentioned. Can be.
【0010】本発明において原材料として用いる重合体
(A)は、PC単量体の1種又は2種以上の重合体であ
っても、また必要に応じてPC単量体と共重合可能な他
の単量体との共重合体であってもよい。共重合可能な他
の単量体としては、PC単量体以外の(メタ)アクリル
酸エステル類、(メタ)アクリル酸アミド類、スチレン
類等が挙げられる。これらの共重合可能な他の単量体
は、重合体(A)中に95重量%以下となるように使用
することができる。重合体(A)の原材料中の配合割合
は、1〜70重量%、好ましくは5〜50重量%であ
る。70重量%を超えると得られる重合材料に親水性及
び生体適合性を十分に付与できない。1重量%未満で
は、重合体(A)による効果が期待できない。この重合
体(A)は、後述する室温で液状のビニル単量体(B)
に溶解している状態で重合させるのが好ましく、従っ
て、その配合割合は、ビニル単量体(B)の配合量以下
が特に好ましい。重合体(A)の数平均分子量は、20
00〜200000の範囲が望ましい。この重合体
(A)は、得られるコンタクトレンズに高含水率、高酸
素透過性、防汚染性を付与できる。The polymer (A) used as a raw material in the present invention may be a polymer of one or more kinds of PC monomers. May be a copolymer with the above monomer. Examples of other copolymerizable monomers include (meth) acrylic esters other than PC monomers, (meth) acrylic amides, and styrenes. These other copolymerizable monomers can be used so as to be 95% by weight or less in the polymer (A). The blending ratio of the polymer (A) in the raw materials is 1 to 70% by weight, preferably 5 to 50% by weight. If it exceeds 70% by weight, the resulting polymer material cannot be sufficiently imparted with hydrophilicity and biocompatibility. If it is less than 1% by weight, the effect of the polymer (A) cannot be expected. The polymer (A) is a vinyl monomer (B) which is liquid at room temperature as described below.
It is preferable to carry out the polymerization in a state in which the vinyl monomer (B) is dissolved. Therefore, the blending ratio is particularly preferably equal to or less than the blending amount of the vinyl monomer (B). The number average molecular weight of the polymer (A) is 20
The range of 00 to 200,000 is desirable. The polymer (A) can impart high water content, high oxygen permeability and antifouling property to the obtained contact lens.
【0011】重合体(A)を調製するには、例えば、P
C単量体のみを、又はPC単量体と他の単量体とを、公
知のラジカル重合法、好ましくは溶液重合法等により、
連鎖移動剤の存在下又は不存在下の条件でラジカル重合
させて調製することができる。To prepare the polymer (A), for example, P
Only a C monomer, or a PC monomer and another monomer, by a known radical polymerization method, preferably a solution polymerization method, etc.
It can be prepared by radical polymerization in the presence or absence of a chain transfer agent.
【0012】本発明において原材料として用いる室温で
液状のビニル単量体(B)としては、例えば、スチレ
ン、核置換スチレン、(メタ)アクリル酸メチル、(メ
タ)アクリル酸エチル、(メタ)アクリル酸−n−ブチ
ル、(メタ)アクリル酸−N,N−ジメチル(メタ)ア
クリルアミド、(メタ)アクリル酸−2−ヒドロキシエ
チル、(メタ)アクリル酸フルオロアルキル、(メタ)
アクリル酸シリルアルキル、N−ビニルピロリドン、N
−ビニルピリジン等が挙げられ、使用に際しては単独若
しくは混合物として用いることができる。好ましくは少
なくとも1種の水溶性ビニル単量体の使用により、得ら
れるコンタクトレンズの含水率、機械的強度等を調節す
ることができる。ビニル単量体(B)の原材料中の配合
割合は、99〜30重量%、好ましくは95〜50重量
%であり、特に好ましくは前記重合体(A)の配合量以
上が望ましい。The vinyl monomer (B) at room temperature which is used as a raw material in the present invention is, for example, styrene, nucleus-substituted styrene, methyl (meth) acrylate, ethyl (meth) acrylate, (meth) acrylic acid. -N-butyl, -N, N-dimethyl (meth) acrylamide (meth) acrylate, 2-hydroxyethyl (meth) acrylate, fluoroalkyl (meth) acrylate, (meth) acrylate
Silylalkyl acrylate, N-vinylpyrrolidone, N
-Vinylpyridine and the like, and can be used alone or as a mixture when used. Preferably, by using at least one water-soluble vinyl monomer, the water content, mechanical strength, and the like of the obtained contact lens can be adjusted. The compounding ratio of the vinyl monomer (B) in the raw material is 99 to 30% by weight, preferably 95 to 50% by weight, and particularly preferably the compounding amount of the polymer (A) or more.
【0013】本発明においては、得られるコンタクトレ
ンズの耐熱性、加工性、形状安定性等を更に向上させる
ために、原材料として必要に応じて、例えば、(メタ)
アクリル酸アリル、エチレングリコールジ(メタ)アク
リル酸エステル、ジエチレングリコールジ(メタ)アク
リル酸エステル、ジエチレングリコールジ(メタ)アク
リル酸エステル、トリエチレングリコールジ(メタ)ア
クリル酸エステル、ネオペンチルグリコールジ(メタ)
アクリル酸エステル、1,4−ブタンジオールジ(メ
タ)アクリル酸エステル、ジビニルベンゼン、ジアリル
フタレート、アジピン酸ジビニル等の架橋性多官能単量
体等を用いることもできる。この必要に応じて使用でき
る原材料の配合割合は、原材料全量に対して、20重量
%以下、特に10重量%以下が好ましい。In the present invention, in order to further improve the heat resistance, processability, shape stability and the like of the obtained contact lens, if necessary, for example, (meth)
Allyl acrylate, ethylene glycol di (meth) acrylate, diethylene glycol di (meth) acrylate, diethylene glycol di (meth) acrylate, triethylene glycol di (meth) acrylate, neopentyl glycol di (meth) acrylate
Crosslinkable polyfunctional monomers such as acrylates, 1,4-butanediol di (meth) acrylate, divinylbenzene, diallyl phthalate, and divinyl adipate can also be used. The mixing ratio of the raw materials that can be used as required is preferably 20% by weight or less, particularly preferably 10% by weight or less, based on the total amount of the raw materials.
【0014】本発明において、前記原材料を重合させる
には、ラジカル重合開始剤の存在下、窒素、ヘリウム、
アルゴン等の不活性ガスで置換下又は雰囲気下において
行うことができる。具体的には、前記原材料及び重合開
始剤を、金属製、ガラス製、プラスチック製等の所望の
形状、例えば、試験管状、レンズ状等の型に注入密封
し、加熱又は光照射等により行うことができる。この重
合により得られた重合材料は、切削加工、研磨等してレ
ンズとし、更に公知の水和膨潤させる方法等により含水
性ソフトコンタクトレンズを製造することができる。ま
た、公知の注型重合法により直接レンズにする方法、光
照射しながらキャストを行う方法等によってもレンズと
することができる。重合に際しては、色素等の着色剤、
紫外線吸収剤又はこれらの機能を有する単量体等を添加
しても良い。In the present invention, to polymerize the raw materials, nitrogen, helium,
It can be carried out under a substitution or atmosphere with an inert gas such as argon. Specifically, the raw material and the polymerization initiator are injected and sealed in a desired shape such as metal, glass, plastic, or the like, for example, a test tube, a lens-shaped mold, or the like, and heated or irradiated with light. Can be. The polymerized material obtained by this polymerization is formed into a lens by cutting, polishing or the like, and a water-containing soft contact lens can be produced by a known method of swelling by hydration. The lens can also be formed by a method of directly forming a lens by a known casting polymerization method, a method of performing casting while irradiating light, or the like. Upon polymerization, a coloring agent such as a dye,
An ultraviolet absorber or a monomer having these functions may be added.
【0015】ラジカル重合開始剤としては、特に限定さ
せるものではないが、例えば、過酸化ベンゾイル、ジイ
ソプロピルペルオキシカーボネート、t−ブチルペルオ
キシ−2−エチルヘキサノエート、t−ブチルペルオキ
シピバレート、t−ブチルペルオキシジイソブチレー
ト、過酸化ラウロイル、アゾビスイソブチロニトリル
(以下、「AIBN」と略す)、アゾビス−2,4−ジ
メチルバレロニトリル、ベンゾインメチルエーテル、ベ
ンゾインエチルエーテル等が好ましく挙げられる。この
重合開始剤の仕込み量は、原材料100重量部に対して
10重量%以下、特に5重量%以下が望ましい。Examples of the radical polymerization initiator include, but are not limited to, benzoyl peroxide, diisopropylperoxycarbonate, t-butylperoxy-2-ethylhexanoate, t-butylperoxypivalate, t-butyl. Preferred are peroxydiisobutyrate, lauroyl peroxide, azobisisobutyronitrile (hereinafter abbreviated as “AIBN”), azobis-2,4-dimethylvaleronitrile, benzoin methyl ether, benzoin ethyl ether and the like. The amount of the polymerization initiator to be charged is preferably 10% by weight or less, particularly preferably 5% by weight or less based on 100 parts by weight of the raw materials.
【0016】前記原材料を重合させる際の重合温度は、
重合開始剤の種類により異なるが、20〜140℃が好
ましく、重合時間は6〜120時間が望ましい。The polymerization temperature at the time of polymerizing the raw materials is as follows:
Although it depends on the type of the polymerization initiator, the polymerization temperature is preferably from 20 to 140C, and the polymerization time is preferably from 6 to 120 hours.
【0017】[0017]
【発明の効果】本発明の含水性ソフトコンタクトレンズ
は、ホスホリルコリン基含有(メタ)アクリル酸エステ
ルを構成単位として含む重合体(A)とビニル単量体
(B)とを必須成分とする原材料を重合させた重合材料
を含むので、高含水率、高酸素透過性を有し、装用感に
も優れている。更に、タンパク質、脂質等の汚れの付着
が抑制でき、レンズの均一製造が可能であり、使用上の
安全性を確保できる。The water-containing soft contact lens of the present invention comprises a raw material comprising a polymer (A) containing a phosphorylcholine group-containing (meth) acrylate as a constitutional unit and a vinyl monomer (B) as essential components. Since it contains a polymerized polymer material, it has a high water content and high oxygen permeability, and is also excellent in wearing feeling. Furthermore, adhesion of dirt such as proteins and lipids can be suppressed, uniform production of the lens is possible, and safety in use can be ensured.
【0018】[0018]
【実施例】以下、合成例、実施例及び比較例により更に
詳細に説明するが、本発明はこれらに限定されるもので
はない。The present invention will be described in more detail with reference to Synthesis Examples, Examples and Comparative Examples, but the present invention is not limited thereto.
【0019】合成例1 2−メタクリロイルオキシエチル−2’−(トリメチル
アンモニオ)エチルホスフェート(以下、「MPC」と
略す)20g(0.072mol)と、AIBN0.2
gと、エタノール80gとからなる配合液を、撹拌機、
温度計、還流器及び窒素導入管を備えた200mlの4
つ口フラスコに仕込み、恒温槽中で50℃、10時間加
熱重合させた。重合後、大量のジイソプロピルエーテル
中に前記重合液を投入し、重合物を沈澱させ、濾別、真
空乾燥させて、白色粉末の重合体(A−1)を得た。重
合体(A−1)の収率は92%であり、GPC測定法
(ポリエチレングリコールを標準)により測定した数平
均分子量は、55800であった。 Synthesis Example 1 20 g (0.072 mol) of 2-methacryloyloxyethyl-2 ′-(trimethylammonio) ethyl phosphate (hereinafter abbreviated as “MPC”), and AIBN 0.2
g and 80 g of ethanol, a stirrer,
200 ml 4 equipped with thermometer, reflux condenser and nitrogen inlet tube
The mixture was charged in a one-necked flask and polymerized by heating at 50 ° C. for 10 hours in a thermostat. After the polymerization, the polymerization solution was poured into a large amount of diisopropyl ether to precipitate a polymer, which was separated by filtration and dried in vacuo to obtain a white powder polymer (A-1). The yield of the polymer (A-1) was 92%, and the number average molecular weight measured by GPC (using polyethylene glycol as a standard) was 55,800.
【0020】合成例2 配合液の組成を、MPC10g(0.036mol)
と、HEMA10g(0.078mol)と、AIBN
0.2gと、エタノール80gとに代えた以外は、合成
例1と同様に重合を行って白色粉末の重合体(A−2)
を得た。重合体(A−2)の収率は85%であり、実施
例1と同様に測定した数平均分子量は63700であっ
た。尚、MPCとHEMAとの仕込み重量比50/50
に対して、共重合体の重量比は50/50であった。 Synthesis Example 2 The composition of the mixed solution was changed to 10 g (0.036 mol) of MPC.
, HEMA10g (0.078mol), AIBN
Polymerization was performed in the same manner as in Synthesis Example 1 except that 0.2 g and 80 g of ethanol were used, and a polymer (A-2) as a white powder was obtained.
I got The yield of the polymer (A-2) was 85%, and the number average molecular weight measured in the same manner as in Example 1 was 63,700. The weight ratio of the charged MPC and HEMA was 50/50.
In contrast, the weight ratio of the copolymer was 50/50.
【0021】合成例3 配合液に連鎖移動剤としてのエタンジオール0.02g
を添加した以外は、合成例1と同様に重合を行い、白色
粉末の重合体(A−3)を得た。重合体(A−3)の収
率は74%であり、実施例1と同様に測定した数平均分
子量は28500であった。 Synthesis Example 3 0.02 g of ethanediol as a chain transfer agent was added to the mixture.
Polymerization was carried out in the same manner as in Synthesis Example 1 except that was added, to obtain a white powder polymer (A-3). The yield of the polymer (A-3) was 74%, and the number average molecular weight measured in the same manner as in Example 1 was 28,500.
【0022】実施例1 合成例1で得られた重合体(A−1)4gと、メタクリ
ル酸−2−ヒドロキシエチル16gと、エチレングリコ
ールジ(メタ)アクリル酸エステル0.4gとからなる
配合液を、試験管状のガラス型に注入し、系内を窒素置
換、脱気し、密封した後、加熱重合した。加熱は30℃
で10時間、30〜80℃まで24時間かけて昇温し、
重合後、硬化物を型から取り出した。硬化物を通常の加
工法により切削研磨し、水和膨潤した後、直径13m
m、厚さ0.2mmの含水性ソフトコンタクトレンズを
作製した。このコンタクトレンズの含水率、酸素透過
性、引張試験及び防汚性を、以下の測定方法にしたがっ
て測定した。結果を表1に示す。 Example 1 A mixed solution comprising 4 g of the polymer (A-1) obtained in Synthesis Example 1, 16 g of 2-hydroxyethyl methacrylate, and 0.4 g of ethylene glycol di (meth) acrylate. Was poured into a test tubular glass mold, the system was purged with nitrogen, degassed, sealed, and then heated and polymerized. Heating is 30 ° C
For 10 hours, the temperature was raised to 30 to 80 ° C. over 24 hours,
After the polymerization, the cured product was removed from the mold. The cured product is cut and polished by a normal processing method, hydrated and swelled, and has a diameter of 13 m.
m, a hydrous soft contact lens having a thickness of 0.2 mm was prepared. The water content, oxygen permeability, tensile test and antifouling property of this contact lens were measured according to the following measuring methods. Table 1 shows the results.
【0023】1.含水率:コンタクトレンズを生理食塩
水中に浸漬させ、浸漬前後の重量変化により求めた(含
水率(%)={(含水重量−乾燥時重量)/含水重量}×10
0)。 2.酸素透過係数:製科研(株)製(型式316)のフ
ィルム酸素透過測定機を用いて、35℃の生理食塩水中
で測定した。 3.引張試験:山電(株)製(型式レオナRE−330
5)の引張試験機を用い、コンタクトレンズに20gの
加重をかけ1mm/秒の引張速度で測定した。 4.防汚性:アルブミン0.39重量%、リゾチウム
0.17重量%、グロブリン0.105重量%を含む3
5℃の生理食塩水中に、2週間コンタクトレンズを浸漬
させた後、生理食塩水で洗浄し、界面活性剤でコンタク
トレンズからタンパク質を分離した。分離した蛋白質は
蛋白質定量用の試薬を注入し、UV測定法により定量し
た。1. Moisture content: The contact lens was immersed in physiological saline and determined by weight change before and after immersion (moisture content (%) = {(water content-dry weight) / water content} × 10
0). 2. Oxygen Permeability Coefficient: Measured in physiological saline at 35 ° C. using a film oxygen permeation measuring device manufactured by Seikaken Co., Ltd. (model 316). 3. Tensile test: manufactured by Yamaden Co., Ltd. (Model Leona RE-330
The contact lens was measured at a tensile speed of 1 mm / sec by applying a load of 20 g to the contact lens using the tensile tester of 5). 4. Antifouling property: containing 0.39% by weight of albumin, 0.17% by weight of lysodium and 0.105% by weight of globulin 3
After immersing the contact lens in physiological saline at 5 ° C. for 2 weeks, the contact lens was washed with physiological saline and the protein was separated from the contact lens with a surfactant. The separated proteins were injected with a reagent for protein quantification and quantified by UV measurement.
【0024】実施例2〜5 表1に示す原材料を用いた以外は、実施例1と同様に含
水性ソフトコンタクトレンズを作製し、各種測定を行っ
た。結果を表1に示す。 Examples 2 to 5 Except that the raw materials shown in Table 1 were used, water-containing soft contact lenses were prepared in the same manner as in Example 1, and various measurements were made. Table 1 shows the results.
【0025】比較例1〜4 表2に示す原材料を用いた以外は、実施例1と同様に含
水性ソフトコンタクトレンズを作製し、各種測定を行っ
た。結果を表2に示す。 Comparative Examples 1-4 A water-containing soft contact lens was prepared in the same manner as in Example 1 except that the raw materials shown in Table 2 were used, and various measurements were made. Table 2 shows the results.
【0026】表1及び2の結果から、本発明の含水性ソ
フトコンタクトレンズは、比較例に比べて含水率、酸素
透過性及び強度が高く、蛋白吸着量が少なくバランスが
良いことがわかる。From the results shown in Tables 1 and 2, it can be seen that the water-containing soft contact lens of the present invention has a higher water content, oxygen permeability and strength, a smaller amount of adsorbed protein and a better balance than the comparative example.
【0027】表中に用いた記号は以下のとおりであり、
酸素透過性の単位は、×10-11ml/cm2・sec・
mmHgである。 HEMA:メタクリル酸−2−ヒドロキシエチル(2−
ヒドロキシエチルメタクリレート)、EGMA:エチレ
ングリコールジメタクリル酸エステル、MA:メタクリ
ル酸、NVP:N−ビニルピロリドン、MPC:2−メ
タクリロイルオキシエチル−2’−(トリメチルアンモ
ニオ)エチルホスフェート。The symbols used in the table are as follows:
The unit of oxygen permeability is × 10 −11 ml / cm 2 · sec.
mmHg. HEMA: 2-hydroxyethyl methacrylate (2-
Hydroxyethyl methacrylate), EGMA: ethylene glycol dimethacrylate, MA: methacrylic acid, NVP: N-vinylpyrrolidone, MPC: 2-methacryloyloxyethyl-2 ′-(trimethylammonio) ethyl phosphate.
【0028】[0028]
【表1】 [Table 1]
【0029】[0029]
【表2】 [Table 2]
───────────────────────────────────────────────────── フロントページの続き (72)発明者 鯉沼 康美 茨城県つくば市東新井32−16 (72)発明者 猪又 潔 茨城県つくば市春日2−17−1 (72)発明者 中林 宣男 千葉県松戸市小金原5−6−20 (72)発明者 石原 一彦 東京都小平市上水本町3−16−37 ──────────────────────────────────────────────────続 き Continued on the front page (72) Inventor Yasumi Koinuma 32-16 Higashiarai, Tsukuba, Ibaraki Prefecture (72) Inventor Kiyoshi 27-1-1, Kasuga, Tsukuba, Ibaraki Prefecture (72) Inventor Norio Nakabayashi Matsudo, Chiba Prefecture (72) Inventor Kazuhiko Ishihara 3-16-37, Josuihoncho, Kodaira-shi, Tokyo
Claims (1)
子又はメチル基を示し、nは、1〜10の数を示す)で
表されるホスホリルコリン基含有(メタ)アクリル酸エ
ステルを構成単位として含む重合体(A)1〜70重量
%と、 室温で液状のビニル単量体(B)99〜30重量%とを
含有する原材料を重合して得られた重合材料を含む含水
性ソフトコンタクトレンズ。 【化1】 1. A phosphorylcholine group-containing (meth) acrylate represented by the following general formula (1), wherein R 1 represents a hydrogen atom or a methyl group, and n represents a number of 1 to 10. Containing a polymer material obtained by polymerizing a raw material containing 1 to 70% by weight of a polymer (A) containing as a structural unit and 99 to 30% by weight of a vinyl monomer (B) which is liquid at room temperature. Soft contact lenses. Embedded image
Priority Applications (1)
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JP33694996A JP3974673B2 (en) | 1996-12-17 | 1996-12-17 | Hydrous soft contact lens |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP33694996A JP3974673B2 (en) | 1996-12-17 | 1996-12-17 | Hydrous soft contact lens |
Publications (2)
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JPH10177152A true JPH10177152A (en) | 1998-06-30 |
JP3974673B2 JP3974673B2 (en) | 2007-09-12 |
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ID=18304118
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Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP4938929B2 (en) * | 1998-12-11 | 2012-05-23 | バイオコンパテイブルズ・ユーケイ・リミテツド | Crosslinked polymers and refractive devices formed therefrom |
US8318865B2 (en) | 2004-05-24 | 2012-11-27 | Shiseido Company, Ltd. | Eye lens material and method of manufacturing thereof |
US20180127529A1 (en) * | 2014-08-04 | 2018-05-10 | Elc Management Llc | Water-Absorbing (Meth) Acrylic Resin With Optical Effects, And Related Compositions |
WO2021193491A1 (en) * | 2020-03-26 | 2021-09-30 | 日油株式会社 | Adsorption inhibitor for inorganic fine particles to be used in soft contact lenses |
-
1996
- 1996-12-17 JP JP33694996A patent/JP3974673B2/en not_active Expired - Lifetime
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP4938929B2 (en) * | 1998-12-11 | 2012-05-23 | バイオコンパテイブルズ・ユーケイ・リミテツド | Crosslinked polymers and refractive devices formed therefrom |
US8318865B2 (en) | 2004-05-24 | 2012-11-27 | Shiseido Company, Ltd. | Eye lens material and method of manufacturing thereof |
US20180127529A1 (en) * | 2014-08-04 | 2018-05-10 | Elc Management Llc | Water-Absorbing (Meth) Acrylic Resin With Optical Effects, And Related Compositions |
US10676556B2 (en) * | 2014-08-04 | 2020-06-09 | Elc Management Llc | Water-absorbing (meth) acrylic resin with optical effects, and related compositions |
WO2021193491A1 (en) * | 2020-03-26 | 2021-09-30 | 日油株式会社 | Adsorption inhibitor for inorganic fine particles to be used in soft contact lenses |
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