JP2000515085A - 放射線吸収剤をポリマーに組み込む方法および組成物 - Google Patents
放射線吸収剤をポリマーに組み込む方法および組成物Info
- Publication number
- JP2000515085A JP2000515085A JP10507589A JP50758998A JP2000515085A JP 2000515085 A JP2000515085 A JP 2000515085A JP 10507589 A JP10507589 A JP 10507589A JP 50758998 A JP50758998 A JP 50758998A JP 2000515085 A JP2000515085 A JP 2000515085A
- Authority
- JP
- Japan
- Prior art keywords
- dye
- polymer
- precursor
- crosslinkable
- product
- 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.)
- Ceased
Links
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- NWBTXZPDTSKZJU-UHFFFAOYSA-N 3-[dimethyl(trimethylsilyloxy)silyl]propyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCC[Si](C)(C)O[Si](C)(C)C NWBTXZPDTSKZJU-UHFFFAOYSA-N 0.000 description 1
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- INOIOAWTVPHTCJ-UHFFFAOYSA-N 6-acetamido-4-hydroxy-3-[[4-(2-sulfooxyethylsulfonyl)phenyl]diazenyl]naphthalene-2-sulfonic acid Chemical compound CC(=O)NC1=CC=C2C=C(C(N=NC3=CC=C(C=C3)S(=O)(=O)CCOS(O)(=O)=O)=C(O)C2=C1)S(O)(=O)=O INOIOAWTVPHTCJ-UHFFFAOYSA-N 0.000 description 1
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- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
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- GKZCMEUEEFOXIJ-UHFFFAOYSA-N Lanosol Chemical compound OCC1=CC(O)=C(O)C(Br)=C1Br GKZCMEUEEFOXIJ-UHFFFAOYSA-N 0.000 description 1
- 229920002861 MOWIOL ® 3-83 Polymers 0.000 description 1
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- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 description 1
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- IAXXETNIOYFMLW-COPLHBTASA-N [(1s,3s,4s)-4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl] 2-methylprop-2-enoate Chemical compound C1C[C@]2(C)[C@@H](OC(=O)C(=C)C)C[C@H]1C2(C)C IAXXETNIOYFMLW-COPLHBTASA-N 0.000 description 1
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- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
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- 125000003282 alkyl amino group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 239000001000 anthraquinone dye Substances 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
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- 125000004429 atom Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 150000001558 benzoic acid derivatives Chemical class 0.000 description 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- MQDJYUACMFCOFT-UHFFFAOYSA-N bis[2-(1-hydroxycyclohexyl)phenyl]methanone Chemical compound C=1C=CC=C(C(=O)C=2C(=CC=CC=2)C2(O)CCCCC2)C=1C1(O)CCCCC1 MQDJYUACMFCOFT-UHFFFAOYSA-N 0.000 description 1
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- KBLWLMPSVYBVDK-UHFFFAOYSA-N cyclohexyl prop-2-enoate Chemical compound C=CC(=O)OC1CCCCC1 KBLWLMPSVYBVDK-UHFFFAOYSA-N 0.000 description 1
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- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- LOKCTEFSRHRXRJ-UHFFFAOYSA-I dipotassium trisodium dihydrogen phosphate hydrogen phosphate dichloride Chemical compound P(=O)(O)(O)[O-].[K+].P(=O)(O)([O-])[O-].[Na+].[Na+].[Cl-].[K+].[Cl-].[Na+] LOKCTEFSRHRXRJ-UHFFFAOYSA-I 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 125000005066 dodecenyl group Chemical group C(=CCCCCCCCCCC)* 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
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- FYUWIEKAVLOHSE-UHFFFAOYSA-N ethenyl acetate;1-ethenylpyrrolidin-2-one Chemical compound CC(=O)OC=C.C=CN1CCCC1=O FYUWIEKAVLOHSE-UHFFFAOYSA-N 0.000 description 1
- MEGHWIAOTJPCHQ-UHFFFAOYSA-N ethenyl butanoate Chemical compound CCCC(=O)OC=C MEGHWIAOTJPCHQ-UHFFFAOYSA-N 0.000 description 1
- BLZSRIYYOIZLJL-UHFFFAOYSA-N ethenyl pentanoate Chemical compound CCCCC(=O)OC=C BLZSRIYYOIZLJL-UHFFFAOYSA-N 0.000 description 1
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- 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
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- 235000011187 glycerol Nutrition 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000006038 hexenyl group Chemical group 0.000 description 1
- 230000036571 hydration Effects 0.000 description 1
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- 238000007654 immersion Methods 0.000 description 1
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- 125000003253 isopropoxy group Chemical group [H]C([H])([H])C([H])(O*)C([H])([H])[H] 0.000 description 1
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- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- HNEGQIOMVPPMNR-NSCUHMNNSA-N mesaconic acid Chemical compound OC(=O)C(/C)=C/C(O)=O HNEGQIOMVPPMNR-NSCUHMNNSA-N 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 125000005641 methacryl group Chemical group 0.000 description 1
- HEDRLUNVSRWFAG-UHFFFAOYSA-N methoxycarbonyl prop-2-enoate Chemical class COC(=O)OC(=O)C=C HEDRLUNVSRWFAG-UHFFFAOYSA-N 0.000 description 1
- NXMXPVQZFYYPGD-UHFFFAOYSA-N methyl 2-methylprop-2-enoate;methyl prop-2-enoate Chemical compound COC(=O)C=C.COC(=O)C(C)=C NXMXPVQZFYYPGD-UHFFFAOYSA-N 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- HNEGQIOMVPPMNR-UHFFFAOYSA-N methylfumaric acid Natural products OC(=O)C(C)=CC(O)=O HNEGQIOMVPPMNR-UHFFFAOYSA-N 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 239000012452 mother liquor Substances 0.000 description 1
- MGARLISKINLYPI-UHFFFAOYSA-N n-(2,2-dimethoxyethyl)-2-methylprop-2-enamide Chemical compound COC(OC)CNC(=O)C(C)=C MGARLISKINLYPI-UHFFFAOYSA-N 0.000 description 1
- OMNKZBIFPJNNIO-UHFFFAOYSA-N n-(2-methyl-4-oxopentan-2-yl)prop-2-enamide Chemical compound CC(=O)CC(C)(C)NC(=O)C=C OMNKZBIFPJNNIO-UHFFFAOYSA-N 0.000 description 1
- 125000006606 n-butoxy group Chemical group 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000003506 n-propoxy group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])O* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- KKFHAJHLJHVUDM-UHFFFAOYSA-N n-vinylcarbazole Chemical compound C1=CC=C2N(C=C)C3=CC=CC=C3C2=C1 KKFHAJHLJHVUDM-UHFFFAOYSA-N 0.000 description 1
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- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
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- 125000004365 octenyl group Chemical group C(=CCCCCCC)* 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
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- 230000035699 permeability Effects 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 239000002953 phosphate buffered saline Substances 0.000 description 1
- 229920002120 photoresistant polymer Polymers 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
- 239000003495 polar organic solvent Substances 0.000 description 1
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- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- LYBIZMNPXTXVMV-UHFFFAOYSA-N propan-2-yl prop-2-enoate Chemical compound CC(C)OC(=O)C=C LYBIZMNPXTXVMV-UHFFFAOYSA-N 0.000 description 1
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
- NHARPDSAXCBDDR-UHFFFAOYSA-N propyl 2-methylprop-2-enoate Chemical compound CCCOC(=O)C(C)=C NHARPDSAXCBDDR-UHFFFAOYSA-N 0.000 description 1
- PNXMTCDJUBJHQJ-UHFFFAOYSA-N propyl prop-2-enoate Chemical compound CCCOC(=O)C=C PNXMTCDJUBJHQJ-UHFFFAOYSA-N 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- WXQMFIJLJLLQIS-UHFFFAOYSA-N reactive blue 21 Chemical compound [Cu+2].C1=CC(S(=O)(=O)CCO)=CC=C1NS(=O)(=O)C1=CC=C2C([N-]3)=NC(C=4C5=CC=C(C=4)S(O)(=O)=O)=NC5=NC(C=4C5=CC=C(C=4)S(O)(=O)=O)=NC5=NC([N-]4)=C(C=C(C=C5)S(O)(=O)=O)C5=C4N=C3C2=C1 WXQMFIJLJLLQIS-UHFFFAOYSA-N 0.000 description 1
- 239000004627 regenerated cellulose Substances 0.000 description 1
- 238000001226 reprecipitation Methods 0.000 description 1
- 229910052594 sapphire Inorganic materials 0.000 description 1
- 239000010980 sapphire Substances 0.000 description 1
- 238000007650 screen-printing Methods 0.000 description 1
- 125000005920 sec-butoxy group Chemical group 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 229910000162 sodium phosphate Inorganic materials 0.000 description 1
- 235000011008 sodium phosphates Nutrition 0.000 description 1
- MNCGMVDMOKPCSQ-UHFFFAOYSA-M sodium;2-phenylethenesulfonate Chemical compound [Na+].[O-]S(=O)(=O)C=CC1=CC=CC=C1 MNCGMVDMOKPCSQ-UHFFFAOYSA-M 0.000 description 1
- MZSDGDXXBZSFTG-UHFFFAOYSA-M sodium;benzenesulfonate Chemical compound [Na+].[O-]S(=O)(=O)C1=CC=CC=C1 MZSDGDXXBZSFTG-UHFFFAOYSA-M 0.000 description 1
- BWYYYTVSBPRQCN-UHFFFAOYSA-M sodium;ethenesulfonate Chemical compound [Na+].[O-]S(=O)(=O)C=C BWYYYTVSBPRQCN-UHFFFAOYSA-M 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 230000002269 spontaneous effect Effects 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 125000004213 tert-butoxy group Chemical group [H]C([H])([H])C(O*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- JRMUNVKIHCOMHV-UHFFFAOYSA-M tetrabutylammonium bromide Chemical compound [Br-].CCCC[N+](CCCC)(CCCC)CCCC JRMUNVKIHCOMHV-UHFFFAOYSA-M 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 1
- AGXLJXZOBXXTBA-UHFFFAOYSA-K trisodium phosphate decahydrate Chemical compound O.O.O.O.O.O.O.O.O.O.[Na+].[Na+].[Na+].[O-]P([O-])([O-])=O AGXLJXZOBXXTBA-UHFFFAOYSA-K 0.000 description 1
- 239000010981 turquoise Substances 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
- 238000003828 vacuum filtration Methods 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 238000004073 vulcanization Methods 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2/00—Processes of polymerisation
- C08F2/44—Polymerisation in the presence of compounding ingredients, e.g. plasticisers, dyestuffs, fillers
-
- 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
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S525/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S525/937—Utility as body contact e.g. implant, contact lens or I.U.D.
Landscapes
- Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- Medicinal Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Eyeglasses (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Treatments Of Macromolecular Shaped Articles (AREA)
- Casting Or Compression Moulding Of Plastics Or The Like (AREA)
- Polymerisation Methods In General (AREA)
- Surface Treatment Of Optical Elements (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US69115796A | 1996-08-01 | 1996-08-01 | |
| US08/691,157 | 1996-08-01 | ||
| PCT/EP1997/004174 WO1998005690A1 (en) | 1996-08-01 | 1997-07-31 | Method and composition for incorporating radiation-absorbing agents into polymers |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2000515085A true JP2000515085A (ja) | 2000-11-14 |
| JP2000515085A5 JP2000515085A5 (enExample) | 2005-03-10 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP10507589A Ceased JP2000515085A (ja) | 1996-08-01 | 1997-07-31 | 放射線吸収剤をポリマーに組み込む方法および組成物 |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US6162844A (enExample) |
| EP (1) | EP0915914B1 (enExample) |
| JP (1) | JP2000515085A (enExample) |
| KR (1) | KR20000029695A (enExample) |
| CN (1) | CN1228788A (enExample) |
| AR (1) | AR008108A1 (enExample) |
| AT (1) | ATE263192T1 (enExample) |
| AU (1) | AU4012997A (enExample) |
| BR (1) | BR9711106A (enExample) |
| CA (1) | CA2261839A1 (enExample) |
| DE (1) | DE69728402T2 (enExample) |
| ID (1) | ID17749A (enExample) |
| IL (1) | IL128282A0 (enExample) |
| NO (1) | NO990441L (enExample) |
| WO (1) | WO1998005690A1 (enExample) |
| ZA (1) | ZA976812B (enExample) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2012022351A (ja) * | 2004-04-30 | 2012-02-02 | Abbott Medical Optics Inc | 高選択性紫色光透過性フィルターを有する眼用器具 |
| JP2018536194A (ja) * | 2015-12-02 | 2018-12-06 | ノバルティス アーゲー | 水溶性ｕｖ吸収化合物およびその使用 |
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| AR013444A1 (es) * | 1997-08-28 | 2000-12-27 | Novartis Ag | Metodo para incorporar agentes absorbentes de radiacion en polimeros y articulo |
| CA2307634C (en) * | 1997-11-14 | 2008-02-05 | Novartis Ag | Methods and compositions for manufacturing tinted ophthalmic lenses |
| US6149692A (en) * | 1998-08-27 | 2000-11-21 | Novartis Ag | Method and composition for incorporating radiation-absorbing agents into polymers |
| US6510005B1 (en) * | 1998-10-27 | 2003-01-21 | Irving S. Goldstein | Filter for illusion apparatus |
| US6149842A (en) * | 1998-11-12 | 2000-11-21 | Novartis Ag | Methods and compositions for manufacturing tinted ophthalmic lenses |
| ATE373682T1 (de) | 2000-03-13 | 2007-10-15 | Biocure Inc | Embolische zusammensetzungen |
| CA2402774C (en) * | 2000-03-13 | 2011-09-06 | Biocure, Inc. | Microsphere hydrogel biomedical articles |
| CA2401865C (en) * | 2000-03-24 | 2010-01-12 | Novartis Ag | Crosslinkable or polymerizable prepolymers |
| US6579096B2 (en) * | 2000-08-08 | 2003-06-17 | Paul C. Chiu | Method and system for selectively staining dental composite resin |
| US6774178B2 (en) | 2001-01-05 | 2004-08-10 | Novartis Ag | Tinted, high Dk ophthalmic molding and a method for making same |
| TWI261057B (en) * | 2001-03-07 | 2006-09-01 | Novartis Ag | Process for the manufacture of moldings |
| US7879267B2 (en) * | 2001-08-02 | 2011-02-01 | J&J Vision Care, Inc. | Method for coating articles by mold transfer |
| US20030141490A1 (en) * | 2001-12-21 | 2003-07-31 | Walters Robert W. | Photochromic polymer compositions and articles thereof |
| CN100349935C (zh) * | 2002-02-15 | 2007-11-21 | Zms有限责任公司 | 用于生物医学应用的聚合方法和材料 |
| JP4751067B2 (ja) * | 2002-08-14 | 2011-08-17 | ノバルティス アーゲー | 放射線硬化性プレポリマー |
| US20050085585A1 (en) | 2002-10-23 | 2005-04-21 | Quinn Michael H. | Polymerizable materials |
| US7288578B2 (en) * | 2002-11-01 | 2007-10-30 | Novartis Ag | Biocompatible inks, preparation, and uses thereof |
| US7216975B2 (en) * | 2003-07-15 | 2007-05-15 | Shinn-Gwo Hong | Method for preparing the reactive tinting compound and the tinted contact lens |
| ATE489058T1 (de) * | 2004-06-29 | 2010-12-15 | Inc Biocure | Bandscheiben-nucleus-pulposus-implantat |
| US8030369B2 (en) * | 2004-10-13 | 2011-10-04 | Novartis Ag | Contact lenses with improved wearing comfort |
| US8899547B2 (en) | 2004-11-18 | 2014-12-02 | Qspex Technologies, Inc. | Molds and method of using the same for optical lenses |
| US20070149641A1 (en) * | 2005-12-28 | 2007-06-28 | Goupil Dennis W | Injectable bone cement |
| RU2555704C2 (ru) | 2009-09-15 | 2015-07-10 | Новартис Аг | Преполимеры, применимые для изготовления поглощающих ультрафиолетовое излучение контактных линз |
| TWI573818B (zh) | 2010-07-30 | 2017-03-11 | 諾華公司 | 兩親性聚矽氧烷預聚物及其用途 |
| US8993651B2 (en) | 2010-10-06 | 2015-03-31 | Novartis Ag | Polymerizable chain-extended polysiloxanes with pendant hydrophilic groups |
| US8835525B2 (en) | 2010-10-06 | 2014-09-16 | Novartis Ag | Chain-extended polysiloxane crosslinkers with dangling hydrophilic polymer chains |
| KR101565220B1 (ko) | 2010-10-06 | 2015-11-02 | 노파르티스 아게 | 수-가공성 실리콘-함유 예비중합체 및 그의 용도 |
| US9042019B2 (en) | 2011-04-15 | 2015-05-26 | Qspex Technologies, Inc. | Anti-reflective lenses and methods for manufacturing the same |
| US9335443B2 (en) | 2011-04-15 | 2016-05-10 | Qspex Technologies, Inc. | Anti-reflective lenses and methods for manufacturing the same |
| EP3788084A1 (en) | 2018-05-01 | 2021-03-10 | Bausch & Lomb Incorporated | Ophthalmic devices containing uv blocker and methods for their preparation |
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- 1997-07-31 WO PCT/EP1997/004174 patent/WO1998005690A1/en not_active Ceased
- 1997-07-31 JP JP10507589A patent/JP2000515085A/ja not_active Ceased
- 1997-07-31 ZA ZA9706812A patent/ZA976812B/xx unknown
- 1997-07-31 EP EP97937535A patent/EP0915914B1/en not_active Expired - Lifetime
- 1997-07-31 ID IDP972654A patent/ID17749A/id unknown
- 1997-07-31 AT AT97937535T patent/ATE263192T1/de not_active IP Right Cessation
- 1997-07-31 CN CN97197540A patent/CN1228788A/zh active Pending
- 1997-07-31 AU AU40129/97A patent/AU4012997A/en not_active Abandoned
- 1997-07-31 IL IL12828297A patent/IL128282A0/xx unknown
- 1997-07-31 KR KR1019997000774A patent/KR20000029695A/ko not_active Withdrawn
- 1997-07-31 BR BR9711106A patent/BR9711106A/pt unknown
- 1997-07-31 DE DE69728402T patent/DE69728402T2/de not_active Expired - Lifetime
- 1997-07-31 CA CA002261839A patent/CA2261839A1/en not_active Abandoned
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1999
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| JPH06235887A (ja) * | 1992-10-26 | 1994-08-23 | Johnson & Johnson Vision Prod Inc | 色付きコンタクトレンズの製造方法 |
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Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2012022351A (ja) * | 2004-04-30 | 2012-02-02 | Abbott Medical Optics Inc | 高選択性紫色光透過性フィルターを有する眼用器具 |
| JP2018536194A (ja) * | 2015-12-02 | 2018-12-06 | ノバルティス アーゲー | 水溶性ｕｖ吸収化合物およびその使用 |
Also Published As
| Publication number | Publication date |
|---|---|
| EP0915914B1 (en) | 2004-03-31 |
| ATE263192T1 (de) | 2004-04-15 |
| CA2261839A1 (en) | 1998-02-12 |
| NO990441D0 (no) | 1999-01-29 |
| WO1998005690A1 (en) | 1998-02-12 |
| KR20000029695A (ko) | 2000-05-25 |
| BR9711106A (pt) | 1999-08-17 |
| ID17749A (id) | 1998-01-22 |
| CN1228788A (zh) | 1999-09-15 |
| US6162844A (en) | 2000-12-19 |
| AR008108A1 (es) | 1999-12-09 |
| ZA976812B (en) | 1998-03-03 |
| EP0915914A1 (en) | 1999-05-19 |
| DE69728402T2 (de) | 2005-02-24 |
| IL128282A0 (en) | 1999-11-30 |
| AU4012997A (en) | 1998-02-25 |
| DE69728402D1 (de) | 2004-05-06 |
| NO990441L (no) | 1999-03-23 |
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