CS205116B2 - Method of preparing silicone copolymers grafted by hydrophylic monomers - Google Patents
Method of preparing silicone copolymers grafted by hydrophylic monomers Download PDFInfo
- Publication number
- CS205116B2 CS205116B2 CS782085A CS208578A CS205116B2 CS 205116 B2 CS205116 B2 CS 205116B2 CS 782085 A CS782085 A CS 782085A CS 208578 A CS208578 A CS 208578A CS 205116 B2 CS205116 B2 CS 205116B2
- Authority
- CS
- Czechoslovakia
- Prior art keywords
- grafting
- silicone
- copolymers
- hydrophilic
- contact lens
- Prior art date
Links
- 229920001296 polysiloxane Polymers 0.000 title claims abstract description 34
- 238000000034 method Methods 0.000 title claims abstract description 30
- 239000000178 monomer Substances 0.000 title claims abstract description 23
- 230000005855 radiation Effects 0.000 claims abstract description 23
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 8
- 239000001301 oxygen Substances 0.000 claims abstract description 8
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 8
- 238000002360 preparation method Methods 0.000 claims abstract description 4
- 238000004519 manufacturing process Methods 0.000 claims description 13
- 229920001577 copolymer Polymers 0.000 claims description 9
- 238000006243 chemical reaction Methods 0.000 claims description 7
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- 150000001875 compounds Chemical class 0.000 abstract description 10
- 229920000578 graft copolymer Polymers 0.000 abstract description 5
- 229920002050 silicone resin Polymers 0.000 abstract 2
- 238000009281 ultraviolet germicidal irradiation Methods 0.000 abstract 1
- 229920005573 silicon-containing polymer Polymers 0.000 description 24
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 11
- 239000000203 mixture Substances 0.000 description 10
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 9
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 9
- 229910052753 mercury Inorganic materials 0.000 description 9
- 239000000463 material Substances 0.000 description 7
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 7
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 7
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- 229920000642 polymer Polymers 0.000 description 6
- 229910052697 platinum Inorganic materials 0.000 description 5
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 5
- 239000002253 acid Substances 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 229910004298 SiO 2 Inorganic materials 0.000 description 3
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 3
- 230000005587 bubbling Effects 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 238000007334 copolymerization reaction Methods 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 125000000623 heterocyclic group Chemical group 0.000 description 2
- 150000002433 hydrophilic molecules Chemical class 0.000 description 2
- 230000005865 ionizing radiation Effects 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 229920001558 organosilicon polymer Polymers 0.000 description 2
- -1 polysiloxanes Polymers 0.000 description 2
- 239000010453 quartz Substances 0.000 description 2
- 238000004383 yellowing Methods 0.000 description 2
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 1
- JSOWQCTXCCXWCJ-UHFFFAOYSA-N 1-ethylpyrrolidin-2-one;prop-2-enoic acid Chemical compound OC(=O)C=C.CCN1CCCC1=O JSOWQCTXCCXWCJ-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 230000003321 amplification Effects 0.000 description 1
- 229940045985 antineoplastic platinum compound Drugs 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 210000004087 cornea Anatomy 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 239000004205 dimethyl polysiloxane Substances 0.000 description 1
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002148 esters Chemical group 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 125000001183 hydrocarbyl group Chemical group 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 230000001678 irradiating effect Effects 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 238000003199 nucleic acid amplification method Methods 0.000 description 1
- 150000003057 platinum Chemical class 0.000 description 1
- 150000003058 platinum compounds Chemical class 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical group O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
- 230000002285 radioactive effect Effects 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
- C08J7/12—Chemical modification
- C08J7/16—Chemical modification with polymerisable compounds
- C08J7/18—Chemical modification with polymerisable compounds using wave energy or particle radiation
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29D—PRODUCING PARTICULAR ARTICLES FROM PLASTICS OR FROM SUBSTANCES IN A PLASTIC STATE
- B29D11/00—Producing optical elements, e.g. lenses or prisms
- B29D11/00009—Production of simple or compound lenses
- B29D11/00038—Production of contact lenses
- B29D11/00125—Auxiliary operations, e.g. removing oxygen from the mould, conveying moulds from a storage to the production line in an inert atmosphere
- B29D11/00134—Curing of the contact lens material
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29D—PRODUCING PARTICULAR ARTICLES FROM PLASTICS OR FROM SUBSTANCES IN A PLASTIC STATE
- B29D11/00—Producing optical elements, e.g. lenses or prisms
- B29D11/00865—Applying coatings; tinting; colouring
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B1/00—Optical elements characterised by the material of which they are made; Optical coatings for optical elements
- G02B1/04—Optical elements characterised by the material of which they are made; Optical coatings for optical elements made of organic materials, e.g. plastics
- G02B1/041—Lenses
- G02B1/043—Contact lenses
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2383/00—Characterised by the use of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen, or carbon only; Derivatives of such polymers
- C08J2383/04—Polysiloxanes
Landscapes
- Engineering & Computer Science (AREA)
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- Mechanical Engineering (AREA)
- Ophthalmology & Optometry (AREA)
- Manufacturing & Machinery (AREA)
- Medicinal Chemistry (AREA)
- Organic Chemistry (AREA)
- Polymers & Plastics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Toxicology (AREA)
- General Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Eyeglasses (AREA)
- Treatments Of Macromolecular Shaped Articles (AREA)
- Silicon Polymers (AREA)
- Graft Or Block Polymers (AREA)
- Macromonomer-Based Addition Polymer (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR7709766A FR2385763A1 (fr) | 1977-03-31 | 1977-03-31 | Procede de preparation de copolymeres greffes de silicones |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CS205116B2 true CS205116B2 (en) | 1981-04-30 |
Family
ID=9188842
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CS782085A CS205116B2 (en) | 1977-03-31 | 1978-03-31 | Method of preparing silicone copolymers grafted by hydrophylic monomers |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US4229273A (de) |
| JP (1) | JPS53121874A (de) |
| AT (1) | AT380962B (de) |
| BE (1) | BE865071A (de) |
| BR (1) | BR7801971A (de) |
| CH (1) | CH630103A5 (de) |
| CS (1) | CS205116B2 (de) |
| DD (1) | DD137238A5 (de) |
| DE (1) | DE2813558C2 (de) |
| ES (1) | ES468279A1 (de) |
| FR (1) | FR2385763A1 (de) |
| GB (1) | GB1598754A (de) |
| HU (1) | HU180453B (de) |
| NL (1) | NL7803234A (de) |
| SU (1) | SU973027A3 (de) |
Families Citing this family (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3004685C2 (de) * | 1980-02-08 | 1986-07-31 | Titmus Eurocon Kontaktlinsen GmbH, 8750 Aschaffenburg | Verfahren zur Hydrophilierung von Kontaktlinsen aus Siliconkautschuk |
| US4761436A (en) * | 1985-10-21 | 1988-08-02 | Shin-Etsu Chemical Co., Ltd. | Contact lens comprising triorganovinylsilane polymers |
| US4983702A (en) * | 1988-09-28 | 1991-01-08 | Ciba-Geigy Corporation | Crosslinked siloxane-urethane polymer contact lens |
| US4978481A (en) * | 1989-01-13 | 1990-12-18 | Ciba-Geigy Corporation | Process for the encapsulation of preformed substrates by graft copolymerization |
| US4968532A (en) * | 1989-01-13 | 1990-11-06 | Ciba-Geigy Corporation | Process for graft copolymerization on surfaces of preformed substrates to modify surface properties |
| US5274028A (en) * | 1990-12-06 | 1993-12-28 | Baxter International Inc. | Polyvinyl pyrrolidone-grafted coatings on preformed polymers |
| US5760100B1 (en) | 1994-09-06 | 2000-11-14 | Ciba Vision Corp | Extended wear ophthalmic lens |
| US7468398B2 (en) | 1994-09-06 | 2008-12-23 | Ciba Vision Corporation | Extended wear ophthalmic lens |
| EP0814116A1 (de) * | 1996-06-19 | 1997-12-29 | Hüls Aktiengesellschaft | Hydrophile Beschichtung von Oberflächen polymerer Substrate |
| US6132561A (en) * | 1997-10-13 | 2000-10-17 | Mincher; Bruce J. | Process for the solvent extraction for the radiolysis and dehalogenation of halogenated organic compounds in soils, sludges, sediments and slurries |
| ES2222373T3 (es) * | 2000-03-24 | 2005-02-01 | Novartis Ag | Prepolimeros reticulares o polimerizables. |
| US20040152963A1 (en) * | 2001-04-27 | 2004-08-05 | March Wayne Front | Apparatus for measuring blood glucose concentrations |
| US7438411B2 (en) * | 2005-05-07 | 2008-10-21 | Nanospectra Biosciences, Inc. | Plasmon resonant based eye protection |
| JP5669396B2 (ja) * | 2006-12-13 | 2015-02-12 | ノバルティス アーゲー | 化学線硬化性シリコーンヒドロゲルコポリマーおよびその使用 |
| EP2129513B1 (de) * | 2007-03-22 | 2016-08-03 | Novartis AG | Präpolymere mit baumelnden polysiloxanhaltigen polymerketten |
| MX2009010109A (es) * | 2007-03-22 | 2009-10-12 | Novartis Ag | Prepolimeros que contienen silicona con cadenas polimericas hidrofilicas. |
| US8044111B2 (en) * | 2007-11-30 | 2011-10-25 | Novartis Ag | Actinically-crosslinkable silicone-containing block copolymers |
| ATE552517T1 (de) * | 2007-12-10 | 2012-04-15 | Novartis Ag | Verfahren zur herstellung von silikonhydrogel- kontaktlinsen |
| TWI522395B (zh) | 2010-07-30 | 2016-02-21 | 諾華公司 | 兩親性聚矽氧烷預聚物及其用途 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1526934A (fr) * | 1966-12-01 | 1968-05-31 | Commissariat Energie Atomique | Procédé de préparation des silicones hydrophiles par greffage radiochimique |
| US3959102A (en) * | 1973-08-06 | 1976-05-25 | Essilor International (Compagnie Generale D'optique S.A.) | Method for preparing a crosslinked graft copolymer of silicone and polyvinylpyrrolidone for use as a contact lens, and a contact lens produced thereby |
| GB1480880A (en) * | 1974-05-06 | 1977-07-27 | Bausch & Lomb | Shaped body of a simultaneously interpenetrating network polymer and method of preparing same |
-
1977
- 1977-03-31 FR FR7709766A patent/FR2385763A1/fr active Granted
-
1978
- 1978-03-16 AT AT0187578A patent/AT380962B/de not_active IP Right Cessation
- 1978-03-20 BE BE186075A patent/BE865071A/xx not_active IP Right Cessation
- 1978-03-28 HU HU78EI786A patent/HU180453B/hu unknown
- 1978-03-28 CH CH326778A patent/CH630103A5/fr not_active IP Right Cessation
- 1978-03-28 NL NL7803234A patent/NL7803234A/xx not_active Application Discontinuation
- 1978-03-28 ES ES468279A patent/ES468279A1/es not_active Expired
- 1978-03-29 DE DE2813558A patent/DE2813558C2/de not_active Expired
- 1978-03-29 JP JP3650178A patent/JPS53121874A/ja active Pending
- 1978-03-30 GB GB12495/78A patent/GB1598754A/en not_active Expired
- 1978-03-30 BR BR7801971A patent/BR7801971A/pt unknown
- 1978-03-30 DD DD78204484A patent/DD137238A5/de unknown
- 1978-03-31 CS CS782085A patent/CS205116B2/cs unknown
- 1978-03-31 SU SU782599202A patent/SU973027A3/ru active
-
1979
- 1979-05-23 US US06/041,734 patent/US4229273A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| DD137238A5 (de) | 1979-08-22 |
| CH630103A5 (fr) | 1982-05-28 |
| FR2385763B1 (de) | 1980-12-05 |
| DE2813558C2 (de) | 1983-01-05 |
| BE865071A (fr) | 1978-07-17 |
| GB1598754A (en) | 1981-09-23 |
| HU180453B (en) | 1983-03-28 |
| ES468279A1 (es) | 1978-11-16 |
| DE2813558A1 (de) | 1978-10-12 |
| NL7803234A (nl) | 1978-10-03 |
| SU973027A3 (ru) | 1982-11-07 |
| BR7801971A (pt) | 1978-12-26 |
| US4229273A (en) | 1980-10-21 |
| FR2385763A1 (fr) | 1978-10-27 |
| AT380962B (de) | 1986-08-11 |
| ATA187578A (de) | 1985-12-15 |
| JPS53121874A (en) | 1978-10-24 |
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