CS272213B2 - Method of hydrogel-forming cross-linked polymer production - Google Patents
Method of hydrogel-forming cross-linked polymer production Download PDFInfo
- Publication number
- CS272213B2 CS272213B2 CS859450A CS945085A CS272213B2 CS 272213 B2 CS272213 B2 CS 272213B2 CS 859450 A CS859450 A CS 859450A CS 945085 A CS945085 A CS 945085A CS 272213 B2 CS272213 B2 CS 272213B2
- Authority
- CS
- Czechoslovakia
- Prior art keywords
- polymer
- hydrogel
- cellulose
- vinyl
- monomer
- Prior art date
Links
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- 238000004519 manufacturing process Methods 0.000 title claims description 12
- 229920006037 cross link polymer Polymers 0.000 title description 4
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- 239000000178 monomer Substances 0.000 claims abstract description 57
- 239000000203 mixture Substances 0.000 claims description 44
- 239000000017 hydrogel Substances 0.000 claims description 32
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- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical class O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 1
- UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 210000000744 eyelid Anatomy 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 150000002367 halogens Chemical group 0.000 description 1
- 229920000140 heteropolymer Polymers 0.000 description 1
- 150000002430 hydrocarbons Chemical group 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 150000002432 hydroperoxides Chemical class 0.000 description 1
- 239000007943 implant Substances 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 230000001939 inductive effect Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000004410 intraocular pressure Effects 0.000 description 1
- 230000005865 ionizing radiation Effects 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 150000002689 maleic acids Chemical class 0.000 description 1
- 230000001404 mediated effect Effects 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- VHRYZQNGTZXDNX-UHFFFAOYSA-N methacryloyl chloride Chemical compound CC(=C)C(Cl)=O VHRYZQNGTZXDNX-UHFFFAOYSA-N 0.000 description 1
- WBYWAXJHAXSJNI-UHFFFAOYSA-N methyl p-hydroxycinnamate Natural products OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 description 1
- HTZZCJSUMTXOJL-UHFFFAOYSA-N n',3-dimethyl-2-methylidenebutanehydrazide Chemical compound CNNC(=O)C(=C)C(C)C HTZZCJSUMTXOJL-UHFFFAOYSA-N 0.000 description 1
- 229940088644 n,n-dimethylacrylamide Drugs 0.000 description 1
- YLGYACDQVQQZSW-UHFFFAOYSA-N n,n-dimethylprop-2-enamide Chemical compound CN(C)C(=O)C=C YLGYACDQVQQZSW-UHFFFAOYSA-N 0.000 description 1
- WDQKICIMIPUDBL-UHFFFAOYSA-N n-[2-(dimethylamino)ethyl]prop-2-enamide Chemical compound CN(C)CCNC(=O)C=C WDQKICIMIPUDBL-UHFFFAOYSA-N 0.000 description 1
- YPHQUSNPXDGUHL-UHFFFAOYSA-N n-methylprop-2-enamide Chemical compound CNC(=O)C=C YPHQUSNPXDGUHL-UHFFFAOYSA-N 0.000 description 1
- QNILTEGFHQSKFF-UHFFFAOYSA-N n-propan-2-ylprop-2-enamide Chemical compound CC(C)NC(=O)C=C QNILTEGFHQSKFF-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 210000003101 oviduct Anatomy 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 229960000969 phenyl salicylate Drugs 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000002504 physiological saline solution Substances 0.000 description 1
- 229960001416 pilocarpine Drugs 0.000 description 1
- 229960002139 pilocarpine hydrochloride Drugs 0.000 description 1
- RNAICSBVACLLGM-GNAZCLTHSA-N pilocarpine hydrochloride Chemical compound Cl.C1OC(=O)[C@@H](CC)[C@H]1CC1=CN=CN1C RNAICSBVACLLGM-GNAZCLTHSA-N 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920002338 polyhydroxyethylmethacrylate Polymers 0.000 description 1
- 238000011417 postcuring Methods 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- RGBXDEHYFWDBKD-UHFFFAOYSA-N propan-2-yl propan-2-yloxy carbonate Chemical compound CC(C)OOC(=O)OC(C)C RGBXDEHYFWDBKD-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000008707 rearrangement Effects 0.000 description 1
- GDESWOTWNNGOMW-UHFFFAOYSA-N resorcinol monobenzoate Chemical compound OC1=CC=CC(OC(=O)C=2C=CC=CC=2)=C1 GDESWOTWNNGOMW-UHFFFAOYSA-N 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000001223 reverse osmosis Methods 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 229940042055 systemic antimycotics triazole derivative Drugs 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
- 230000002792 vascular Effects 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
Landscapes
- Graft Or Block Polymers (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Materials For Medical Uses (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Eyeglasses (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB848431901A GB8431901D0 (en) | 1984-12-18 | 1984-12-18 | Polymeric materials |
| GB858513004A GB8513004D0 (en) | 1984-12-18 | 1985-05-22 | Hydrogel-forming polymers |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CS945085A2 CS945085A2 (en) | 1990-03-14 |
| CS272213B2 true CS272213B2 (en) | 1991-01-15 |
Family
ID=26288589
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CS859450A CS272213B2 (en) | 1984-12-18 | 1985-12-18 | Method of hydrogel-forming cross-linked polymer production |
Country Status (5)
| Country | Link |
|---|---|
| JP (1) | JPH0624584B2 (da) |
| CS (1) | CS272213B2 (da) |
| DK (1) | DK584885A (da) |
| ES (1) | ES8705900A1 (da) |
| GB (1) | GB8519071D0 (da) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4731079A (en) * | 1986-11-26 | 1988-03-15 | Kingston Technologies, Inc. | Intraocular lenses |
| JPH06347730A (ja) * | 1993-06-11 | 1994-12-22 | Tokyo Keikaku:Kk | ソフトコンタクトレンズ |
| US5914355A (en) * | 1998-05-15 | 1999-06-22 | Bausch & Lomb Incorporated | Method for making contact lenses having UV absorbing properties |
| JP4398124B2 (ja) * | 2001-11-30 | 2010-01-13 | 博夫 岩田 | 薬理活性物質の放出を温度でコントロールできるバルーンカテーテル |
| US20130313733A1 (en) * | 2012-05-25 | 2013-11-28 | Ivan Nunez | Method of making a fully polymerized uv blocking silicone hydrogel lens |
| CN110050007A (zh) * | 2017-01-10 | 2019-07-23 | 株式会社大阪曹达 | 不饱和聚酯树脂组合物 |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1495381B2 (de) * | 1963-09-07 | 1971-06-24 | Czeskoslovenska akademie ved , Prag | Verfahren zur herstellung von kontaktlinsen oder kontakt linsenrohlingen aus quellfaehigen hydrogelen |
| US3822089A (en) * | 1968-09-25 | 1974-07-02 | Akademie Ved | Contact lens blank or replica made from anhydrous, sparingly cross-linked hydrophilic copolymers |
| JPS5510050A (en) * | 1978-07-10 | 1980-01-24 | Toyota Motor Corp | Plasma ignition device |
| JPS5530601A (en) * | 1978-08-22 | 1980-03-04 | Sybron Corp | Method and device for measuring parameter of flow of fluid |
| US4433111A (en) * | 1980-10-14 | 1984-02-21 | Kelvin Lenses Limited | Fluorine-containing hydrogel-forming polymeric materials |
| JPS5923271A (ja) * | 1982-07-30 | 1984-02-06 | Fujitsu Ltd | 超音波送受信装置 |
| JPS5994731A (ja) * | 1982-11-22 | 1984-05-31 | Toray Ind Inc | ソフトコンタクトレンズの製造方法 |
| JPS606710A (ja) * | 1983-06-27 | 1985-01-14 | Toray Ind Inc | ヒドロゲル成形品の製造方法 |
-
1985
- 1985-07-29 GB GB858519071A patent/GB8519071D0/en active Pending
- 1985-12-17 ES ES550058A patent/ES8705900A1/es not_active Expired
- 1985-12-17 DK DK584885A patent/DK584885A/da not_active Application Discontinuation
- 1985-12-17 JP JP60285363A patent/JPH0624584B2/ja not_active Expired - Lifetime
- 1985-12-18 CS CS859450A patent/CS272213B2/cs unknown
Also Published As
| Publication number | Publication date |
|---|---|
| GB8519071D0 (en) | 1985-09-04 |
| CS945085A2 (en) | 1990-03-14 |
| DK584885D0 (da) | 1985-12-17 |
| ES8705900A1 (es) | 1987-06-01 |
| JPH0624584B2 (ja) | 1994-04-06 |
| DK584885A (da) | 1986-06-19 |
| JPS61145213A (ja) | 1986-07-02 |
| ES550058A0 (es) | 1987-06-01 |
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