HRP20110420T1 - Materijali za oftalmičke i otorinolaringološke uređaje - Google Patents
Materijali za oftalmičke i otorinolaringološke uređaje Download PDFInfo
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- HRP20110420T1 HRP20110420T1 HR20110420T HRP20110420T HRP20110420T1 HR P20110420 T1 HRP20110420 T1 HR P20110420T1 HR 20110420 T HR20110420 T HR 20110420T HR P20110420 T HRP20110420 T HR P20110420T HR P20110420 T1 HRP20110420 T1 HR P20110420T1
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- 239000000463 material Substances 0.000 title claims abstract 16
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims abstract 11
- 239000000178 monomer Substances 0.000 claims abstract 9
- CBOIHMRHGLHBPB-UHFFFAOYSA-N hydroxymethyl Chemical compound O[CH2] CBOIHMRHGLHBPB-UHFFFAOYSA-N 0.000 claims abstract 7
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims abstract 4
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 claims abstract 4
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims abstract 2
- 238000004132 cross linking Methods 0.000 claims abstract 2
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims abstract 2
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims abstract 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 9
- 239000002861 polymer material Substances 0.000 claims 6
- 239000004615 ingredient Substances 0.000 claims 3
- LEJBBGNFPAFPKQ-UHFFFAOYSA-N 2-(2-prop-2-enoyloxyethoxy)ethyl prop-2-enoate Chemical compound C=CC(=O)OCCOCCOC(=O)C=C LEJBBGNFPAFPKQ-UHFFFAOYSA-N 0.000 claims 2
- XFCMNSHQOZQILR-UHFFFAOYSA-N 2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOC(=O)C(C)=C XFCMNSHQOZQILR-UHFFFAOYSA-N 0.000 claims 2
- INQDDHNZXOAFFD-UHFFFAOYSA-N 2-[2-(2-prop-2-enoyloxyethoxy)ethoxy]ethyl prop-2-enoate Chemical compound C=CC(=O)OCCOCCOCCOC(=O)C=C INQDDHNZXOAFFD-UHFFFAOYSA-N 0.000 claims 2
- KUDUQBURMYMBIJ-UHFFFAOYSA-N 2-prop-2-enoyloxyethyl prop-2-enoate Chemical compound C=CC(=O)OCCOC(=O)C=C KUDUQBURMYMBIJ-UHFFFAOYSA-N 0.000 claims 2
- 239000006096 absorbing agent Substances 0.000 claims 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 2
- WTJTUKSVRGVSNZ-UHFFFAOYSA-N 2-(2-phenoxyethoxy)ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOC1=CC=CC=C1 WTJTUKSVRGVSNZ-UHFFFAOYSA-N 0.000 claims 1
- QFNYOIKHNYCFRG-UHFFFAOYSA-N 2-(2-phenoxyethoxy)ethyl prop-2-enoate Chemical compound C=CC(=O)OCCOCCOC1=CC=CC=C1 QFNYOIKHNYCFRG-UHFFFAOYSA-N 0.000 claims 1
- PAVGMLBHCOPIEI-UHFFFAOYSA-N 2-(2-phenylmethoxyethoxy)ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOCC1=CC=CC=C1 PAVGMLBHCOPIEI-UHFFFAOYSA-N 0.000 claims 1
- LFYRACKKHOZCAV-UHFFFAOYSA-N 2-(2-phenylmethoxyethoxy)ethyl prop-2-enoate Chemical compound C=CC(=O)OCCOCCOCC1=CC=CC=C1 LFYRACKKHOZCAV-UHFFFAOYSA-N 0.000 claims 1
- HWSSEYVMGDIFMH-UHFFFAOYSA-N 2-[2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOCCOC(=O)C(C)=C HWSSEYVMGDIFMH-UHFFFAOYSA-N 0.000 claims 1
- CEXQWAAGPPNOQF-UHFFFAOYSA-N 2-phenoxyethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOC1=CC=CC=C1 CEXQWAAGPPNOQF-UHFFFAOYSA-N 0.000 claims 1
- RZVINYQDSSQUKO-UHFFFAOYSA-N 2-phenoxyethyl prop-2-enoate Chemical compound C=CC(=O)OCCOC1=CC=CC=C1 RZVINYQDSSQUKO-UHFFFAOYSA-N 0.000 claims 1
- ILZXXGLGJZQLTR-UHFFFAOYSA-N 2-phenylethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCC1=CC=CC=C1 ILZXXGLGJZQLTR-UHFFFAOYSA-N 0.000 claims 1
- HPSGLFKWHYAKSF-UHFFFAOYSA-N 2-phenylethyl prop-2-enoate Chemical compound C=CC(=O)OCCC1=CC=CC=C1 HPSGLFKWHYAKSF-UHFFFAOYSA-N 0.000 claims 1
- CWVFILUMTNJKBN-UHFFFAOYSA-N 2-phenylmethoxyethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCC1=CC=CC=C1 CWVFILUMTNJKBN-UHFFFAOYSA-N 0.000 claims 1
- ROJWTNWAEYEKMO-UHFFFAOYSA-N 2-phenylmethoxyethyl prop-2-enoate Chemical compound C=CC(=O)OCCOCC1=CC=CC=C1 ROJWTNWAEYEKMO-UHFFFAOYSA-N 0.000 claims 1
- DJENTNKTVLSRNS-UHFFFAOYSA-N 3-phenylmethoxypropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCOCC1=CC=CC=C1 DJENTNKTVLSRNS-UHFFFAOYSA-N 0.000 claims 1
- SJOIDEGZPXSHOC-UHFFFAOYSA-N 3-phenylmethoxypropyl prop-2-enoate Chemical compound C=CC(=O)OCCCOCC1=CC=CC=C1 SJOIDEGZPXSHOC-UHFFFAOYSA-N 0.000 claims 1
- RXXZODOCQIRRQA-UHFFFAOYSA-N 3-phenylpropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCC1=CC=CC=C1 RXXZODOCQIRRQA-UHFFFAOYSA-N 0.000 claims 1
- PKBZUGSITIBLFK-UHFFFAOYSA-N 3-phenylpropyl prop-2-enoate Chemical compound C=CC(=O)OCCCC1=CC=CC=C1 PKBZUGSITIBLFK-UHFFFAOYSA-N 0.000 claims 1
- XOJWAAUYNWGQAU-UHFFFAOYSA-N 4-(2-methylprop-2-enoyloxy)butyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCCOC(=O)C(C)=C XOJWAAUYNWGQAU-UHFFFAOYSA-N 0.000 claims 1
- DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 claims 1
- IGVCHZAHFGFESB-UHFFFAOYSA-N 4-phenylbutyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCCC1=CC=CC=C1 IGVCHZAHFGFESB-UHFFFAOYSA-N 0.000 claims 1
- MXNDNUJKPFXJJX-UHFFFAOYSA-N 4-phenylbutyl prop-2-enoate Chemical compound C=CC(=O)OCCCCC1=CC=CC=C1 MXNDNUJKPFXJJX-UHFFFAOYSA-N 0.000 claims 1
- JHWGFJBTMHEZME-UHFFFAOYSA-N 4-prop-2-enoyloxybutyl prop-2-enoate Chemical compound C=CC(=O)OCCCCOC(=O)C=C JHWGFJBTMHEZME-UHFFFAOYSA-N 0.000 claims 1
- RXPPWNDYCIQFQB-UHFFFAOYSA-N 5-phenylpentyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCCCC1=CC=CC=C1 RXPPWNDYCIQFQB-UHFFFAOYSA-N 0.000 claims 1
- FBOYEYXUKAKVDL-UHFFFAOYSA-N 5-phenylpentyl prop-2-enoate Chemical compound C=CC(=O)OCCCCCC1=CC=CC=C1 FBOYEYXUKAKVDL-UHFFFAOYSA-N 0.000 claims 1
- SAPGBCWOQLHKKZ-UHFFFAOYSA-N 6-(2-methylprop-2-enoyloxy)hexyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCCCCOC(=O)C(C)=C SAPGBCWOQLHKKZ-UHFFFAOYSA-N 0.000 claims 1
- FIHBHSQYSYVZQE-UHFFFAOYSA-N 6-prop-2-enoyloxyhexyl prop-2-enoate Chemical compound C=CC(=O)OCCCCCCOC(=O)C=C FIHBHSQYSYVZQE-UHFFFAOYSA-N 0.000 claims 1
- FNFHMERPSBNGRL-UHFFFAOYSA-N [4-(2-methylprop-2-enoyloxymethyl)phenyl]methyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC1=CC=C(COC(=O)C(C)=C)C=C1 FNFHMERPSBNGRL-UHFFFAOYSA-N 0.000 claims 1
- UJTHMGMWSSOKMD-UHFFFAOYSA-N [4-(prop-2-enoyloxymethyl)phenyl]methyl prop-2-enoate Chemical compound C=CC(=O)OCC1=CC=C(COC(=O)C=C)C=C1 UJTHMGMWSSOKMD-UHFFFAOYSA-N 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- AOJOEFVRHOZDFN-UHFFFAOYSA-N benzyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC1=CC=CC=C1 AOJOEFVRHOZDFN-UHFFFAOYSA-N 0.000 claims 1
- GCTPMLUUWLLESL-UHFFFAOYSA-N benzyl prop-2-enoate Chemical compound C=CC(=O)OCC1=CC=CC=C1 GCTPMLUUWLLESL-UHFFFAOYSA-N 0.000 claims 1
- 239000003086 colorant Substances 0.000 claims 1
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 claims 1
- 239000003999 initiator Substances 0.000 claims 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 238000006116 polymerization reaction Methods 0.000 claims 1
- 230000005855 radiation Effects 0.000 claims 1
- 150000003254 radicals Chemical class 0.000 claims 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
- -1 CH (CH3) 2 Chemical group 0.000 abstract 1
Classifications
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- 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
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/12—Esters of monohydric alcohols or phenols
- C08F220/16—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
- C08F220/18—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L27/00—Materials for grafts or prostheses or for coating grafts or prostheses
- A61L27/14—Macromolecular materials
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L27/00—Materials for grafts or prostheses or for coating grafts or prostheses
- A61L27/14—Macromolecular materials
- A61L27/16—Macromolecular materials obtained by reactions only involving carbon-to-carbon unsaturated bonds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L27/00—Materials for grafts or prostheses or for coating grafts or prostheses
- A61L27/50—Materials characterised by their function or physical properties, e.g. injectable or lubricating compositions, shape-memory materials, surface modified materials
-
- 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
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/02—Prostheses implantable into the body
- A61F2/14—Eye parts, e.g. lenses, corneal implants; Implanting instruments specially adapted therefor; Artificial eyes
- A61F2/16—Intraocular lenses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2430/00—Materials or treatment for tissue regeneration
- A61L2430/16—Materials or treatment for tissue regeneration for reconstruction of eye parts, e.g. intraocular lens, cornea
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- 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
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/13—Hollow or container type article [e.g., tube, vase, etc.]
- Y10T428/1352—Polymer or resin containing [i.e., natural or synthetic]
Abstract
Polimerni materijal za oftalmički ili otorinolaringološki uređaj, naznačen time što sadržia) 70 do 98 % (težinski) monofunkcionalnog akrilatnog ili metakrilatnog monomera formule [1]: gdjeB = -O(CH2)n-, -(OCH2CH2)n-, -NH(CH2)n- ili -NCH3(CH2)n-;R1 = H, CH3, CH2CH3 ili CH2OH; n = 0-12; A = C6H5 ili O(CH2)mC6H5, gdje je skupina C6H5 izborno supstituirana s -(CH2)nH, -O(CH2)nH, -CH(CH3)2, -C6H5, -OC6H5, -CH2C6H5, F, Cl, Br ili I; im = 0-18; b) 0,5 do 3 % (težinski) difunkcionalnog akrilatnog ili metakrilatnog monomera za umrežavanje formule [2]: gdjeR2 i R3 neovisno = H, CH3, CH2CH3 ili CH2OH; W i W' neovisno = O(CH2)d, NH(CH2)d, NCH3(CH2)d, O(CH2)dC6H4, O(CH2CH2O)dCH2, O(CH2CH2CH2O)dCH2, O(CH2CH2CH2CH2O)dCH2 ili ništa; J = (CH2)a, O(CH2CH2O)b, O ili ništa, uz uvjet da ako W i W' = ništa, J # ništa; d = 0-12; a = 1-12; ib = 1-24; ic) 0,5 do 15 % (težinski) hidrofilnog pobočnog makromera formule [3a], [3b], [3c], [3d] ili [3e]: gdje za formule [3a], [3b], [3c], [3d] i [3e]: e = 1-50; X = -O-, NH-, -N(CH3)-, -N(CH2CH3)- ili -N(C6H5)-;Y = -H, -(CH2)pOH, -CH2CH2N(CH3)2, -CH2CH2N(CH2CH3)2, -CH2CH(OH)CH2OH, -(CH2CH2O)qCH3, -(CH2CH2O)qH, -(CH2CH2O)qC6H5 ilip = 1-12; q = 1-230; T i T' neovisno = O(CH2)d', NH(CH2)d', NCH3(CH2)d', O(CH2)d'C6H4, O(CH2CH2O)d'CH2, O(CH2CH2CH2O)d'CH2, O(CH2CH2CH2CH2O)d'CH2 ili ništa; K = (CH2)a', O(CH2CH2O)b', O ili ništa, uz uvjet da ako T i T' = ništa, K # ništa; d' = 0-12; a' = 1-12; b' = 1-24; L = H, Cl, Br, -CH2C(O)CH3, CH2C(O)C(CH3)3, -CH2C(O)C6H5, -CH2C(O)C6H4OH, -CH2C(O)C6H4OCH3,ili -CH2CH=CH2;R4 i R5 neovisno = H, CH3, CH2CH3, CH2CH2CH3, CH(CH3)2, CH2CH2CH2CH3 ili CH2CH(CH3)2;R6 = -CO2CH3, -CO2CH2CH3, -CN ili -CONHCH2CH2CH2CH3;R7 i R8 neovisno = H, CH3, CH2CH3 ili CH2OH; M = -(CH2)a''-; ia'' = 2-20. Patent sadrži još 20 patentnih zahtjeva.
Claims (21)
1. Polimerni materijal za oftalmički ili otorinolaringološki uređaj, naznačen time što sadrži
a) 70 do 98 % (težinski) monofunkcionalnog akrilatnog ili metakrilatnog monomera formule [1]:
[image]
gdje
B = -O(CH2)n-, -(OCH2CH2)n-, -NH(CH2)n- ili -NCH3(CH2)n-;
R1 = H, CH3, CH2CH3 ili CH2OH;
n = 0-12;
A = C6H5 ili O(CH2)mC6H5, gdje je skupina C6H5 izborno supstituirana s -(CH2)nH, -O(CH2)nH, -CH(CH3)2, -C6H5, -OC6H5, -CH2C6H5, F, Cl, Br ili I; i
m = 0-18;
b) 0,5 do 3 % (težinski) difunkcionalnog akrilatnog ili metakrilatnog monomera za umrežavanje formule [2]:
[image]
gdje
R2 i R3 neovisno = H, CH3, CH2CH3 ili CH2OH;
W i W' neovisno = O(CH2)d, NH(CH2)d, NCH3(CH2)d, O(CH2)dC6H4, O(CH2CH2O)dCH2, O(CH2CH2CH2O)dCH2, O(CH2CH2CH2CH2O)dCH2 ili ništa;
J = (CH2)a, O(CH2CH2O)b, O ili ništa, uz uvjet da ako W i W' = ništa, J # ništa;
d = 0-12;
a = 1-12; i
b = 1-24;
i
c) 0,5 do 15 % (težinski) hidrofilnog pobočnog makromera formule [3a], [3b], [3c], [3d] ili [3e]:
[image]
gdje za formule [3a], [3b], [3c], [3d] i [3e]:
e = 1-50;
X = -O-, NH-, -N(CH3)-, -N(CH2CH3)- ili -N(C6H5)-;
Y = -H, -(CH2)pOH, -CH2CH2N(CH3)2, -CH2CH2N(CH2CH3)2, -CH2CH(OH)CH2OH, -(CH2CH2O)qCH3, -(CH2CH2O)qH, -(CH2CH2O)qC6H5 ili
[image]
p = 1-12;
q = 1-230;
T i T' neovisno = O(CH2)d', NH(CH2)d', NCH3(CH2)d', O(CH2)d'C6H4, O(CH2CH2O)d'CH2, O(CH2CH2CH2O)d'CH2, O(CH2CH2CH2CH2O)d'CH2 ili ništa;
K = (CH2)a', O(CH2CH2O)b', O ili ništa, uz uvjet da ako T i T' = ništa, K # ništa;
d' = 0-12;
a' = 1-12;
b' = 1-24;
L = H, Cl, Br, -CH2C(O)CH3, CH2C(O)C(CH3)3, -CH2C(O)C6H5, -CH2C(O)C6H4OH, -CH2C(O)C6H4OCH3,
[image]
ili -CH2CH=CH2;
R4 i R5 neovisno = H, CH3, CH2CH3, CH2CH2CH3, CH(CH3)2, CH2CH2CH2CH3 ili CH2CH(CH3)2;
R6 = -CO2CH3, -CO2CH2CH3, -CN ili -CONHCH2CH2CH2CH3;
R7 i R8 neovisno = H, CH3, CH2CH3 ili CH2OH;
M = -(CH2)a''-; i
a'' = 2-20.
2. Polimerni materijal za navedeni uređaj u skladu s patentnim zahtjevom 1, naznačen time što za monomer formule [1]:
B = -O(CH2)n- ili -(OCH2CH2)n-;
R1 = -H ili -CH3;
n = 1-5;
A = -C6H5, O(CH2)mC6H5; i
m = 0-4.
3. Polimerni materijal za navedeni uređaj u skladu s patentnim zahtjevom 1, naznačen time što za monomer formule [2]:
R2 i R3 neovisno = H ili CH3;
W i W' neovisno = O(CH2)d', O(CH2)dC6H4 ili ništa;
J = O(CH2CH2O)b ili ništa, uz uvjet da ako W i W' = ništa, J # ništa;
d = 0-6; i
b = 1-10.
4. Polimerni materijal za navedeni uređaj u skladu s patentnim zahtjevom 1, naznačen time što za makromer formule [3]:
e = 2-40;
X = -O- ili -N(CH3)-;
Y = (CH2CH2O)qCH3, -(CH2CH2O)qH ili -(CH2CH2O)qC6H5;
q = 2-23;
T i T' neovisno = O(CH2)d' ili ništa;
K = O(CH2CH2O)b' ili ništa, uz uvjet da ako T i T' = ništa, K # ništa;
d' = 0-6;
b' = 1 -10;
L = H, Cl, Br, -CH2C(O)C6H5, -CH2C(O)C6H4OH, -CH2C(O)C6H4OCH3 ili -CH2CH=CH2;
R4 i R5 neovisno = H, CH3 ili CH2CH3;
R6 = -CO2CH3, -CO2CH2CH3, -CN ili -CONHCH2CH2CH2CH3;
R7 i R8 neovisno = H ili CH3; i
a'' = 2-12.
5. Polimerni materijal za navedeni uređaj u skladu s patentnim zahtjevom 4, naznačen time što za makromer formule [3]:
e = 5-30;
X = -O-;
Y = (CH2CH2O)qCH3;
q = 4-15;
T i T' neovisno = O(CH2)d', O(CH2)d', C6H4 ili ništa;
K = O(CH2CH2O)b' ili ništa, uz uvjet da ako T i T' = ništa, K # ništa;
d' = 0-6;
b' = 1-10;
L = H, -CH2C(O)C6H5, -CH2C(O)C6H4OCH3 ili -CH2CH=CH2;
R4 i R5 neovisno = H, CH3 ili CH2CH3;
R6 = -CO2CH3, -CO2CH2CH3, -CN ili -CONHCH2CH2CH2CH3;
R7 i R8 neovisno = H ili CH3; i
a'' = 2-12.
6. Polimerni materijal za navedeni uređaj u skladu s patentnim zahtjevom 1, naznačen time što monomer formule [1] se bira iz skupine koju čine benzil-metakrilat; 2-feniletil-metakrilat; 3-fenilpropil-metakrilat; 4-fenilbutil-metakrilat; 5-fenilpentil-metakrilat; 2-fenoksietil-metakrilat; 2-(2-fenoksietoksi)etil-metakrilat; 2-benziloksietil-metakrilat; 2-(2-(benziloksi)etoksi)etil-metakrilat; 3-benziloksipropil-metakrilat; benzil-akrilat; 2-feniletil-akrilat; 3-fenilpropil-akrilat; 4-fenilbutil-akrilat; 5-fenilpentil-akrilat; 2-fenoksietil-akrilat; 2-(2-fenoksietoksi)etil-akrilat; 2-benziloksietil-akrilat; 2-(2-(benziloksi)etoksi)etil-akrilat; te 3-benziloksipropil-akrilat.
7. Polimerni materijal za navedeni uređaj u skladu s patentnim zahtjevom 1, naznačen time što monomer formule [2] se bira iz skupine koju čine etilen-glikol-dimetakrilat; dietilen-glikol-dimetakrilat; trietilen-glikol-dimetakrilat; 1,6-heksandiol-dimetakrilat; 1,4-butandiol-dimetakrilat; 1,4-benzendimetanol-dimetakrilat; etilen-glikol-diakrilat; dietilen-glikol-diakrilat; trietilen-glikol-diakrilat; 1,6-heksandiol-diakrilat; 1,4-butandiol-diakrilat; te 1,4-benzendimetanol-diakrilat.
8. Polimerni materijal za navedeni uređaj u skladu s patentnim zahtjevom 1, naznačen time što količina of monomer [1] je 80 to 95 % (težinski).
9. Polimerni materijal za navedeni uređaj u skladu s patentnim zahtjevom 1, naznačen time što količina hidrofilnog pobočnog makromera je 1 do 10 % (težinski).
10. Polimerni materijal za navedeni uređaj u skladu s patentnim zahtjevom 9, naznačen time što količina hidrofilnog pobočnog makromera je 1 do 5 % (težinski).
11. Polimerni materijal za navedeni uređaj u skladu s patentnim zahtjevom 10, naznačen time što količina hidrofilnog pobočnog makromera je 2 do 4 % (težinski).
12. Polimerni materijal za navedeni uređaj u skladu s patentnim zahtjevom 1, naznačen time što hidrofilni pobočni makromer je makromer formule [3a].
13. Polimerni materijal za navedeni uređaj u skladu s patentnim zahtjevom 1, naznačen time što hidrofilni pobočni makromer je makromer formule [3b].
14. Polimerni materijal za navedeni uređaj u skladu s patentnim zahtjevom 1, naznačen time što hidrofilni pobočni makromer je makromer formule [3c].
15. Polimerni materijal za navedeni uređaj u skladu s patentnim zahtjevom 1, naznačen time što hidrofilni pobočni makromer je makromer formule [3d].
16. Polimerni materijal za navedeni uređaj u skladu s patentnim zahtjevom 1, naznačen time što hidrofilni pobočni makromer je makromer formule [3e].
17. Polimerni materijal za navedeni uređaj u skladu s patentnim zahtjevom 1, naznačen time što dodatno sadrži sastojak kojeg se bira iz skupine koju čine polimerizabilni UV apsorberi i polimerizabilne boje.
18. Polimerni materijal za navedeni uređaj u skladu s patentnim zahtjevom 17, naznačen time što sadrži 0,1-5 % (težinski) polimerizabilnog UV apsorbera i 0,01-0,5 % (težinski) polimerizabilne boje.
19. Postupak priprave polimernog materijala za oftalmički ili otorinolaringološki uređaj u skladu s patentnim zahtjevom 1, naznačen time što sastojke [1], [2] i [3], kao i sve daljnje izborne sastojke se međusobno miješa, te polimerizira uz pomoć radikalnog inicijatora kako bi se pokrenulo polimerizaciju uz djelovanje topline ili zračenja.
20. Oftalmički ili otorinolaringološki uređaj, naznačen time što sadrži polimerni materijal za navedeni uređaj u skladu s patentnim zahtjevom 1, gdje se oftalmički ili otorinolaringološki uređaj bira iz skupine koju čine intraokularne leće; kontaktne leće; keratoproteze; kornealni umetci ili prsteni; otološke cijevi za propuhivanje; te nazalni usatci.
21. Oftalmički ili otorinolaringološki uređaj u skladu s patentnim zahtjevom 20, naznačen time što navedeni oftalmički ili otorinolaringološki uređaj je intraokularna leća.
Applications Claiming Priority (2)
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US97800007P | 2007-10-05 | 2007-10-05 | |
PCT/US2008/078646 WO2009046235A1 (en) | 2007-10-05 | 2008-10-03 | Ophthalmic and otorhinolaryngological device materials |
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HRP20110420T1 true HRP20110420T1 (hr) | 2011-07-31 |
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US (4) | US8048154B2 (hr) |
EP (1) | EP2192933B1 (hr) |
JP (2) | JP5623280B2 (hr) |
KR (1) | KR101513131B1 (hr) |
CN (1) | CN101815541B (hr) |
AR (1) | AR068661A1 (hr) |
AT (1) | ATE510568T1 (hr) |
AU (1) | AU2008308607B2 (hr) |
BR (1) | BRPI0817627B8 (hr) |
CA (1) | CA2700150C (hr) |
CY (1) | CY1112248T1 (hr) |
DK (1) | DK2192933T3 (hr) |
ES (1) | ES2364892T3 (hr) |
HK (1) | HK1139339A1 (hr) |
HR (1) | HRP20110420T1 (hr) |
IL (1) | IL204609A (hr) |
MX (1) | MX2010003183A (hr) |
NZ (1) | NZ585017A (hr) |
PL (1) | PL2192933T3 (hr) |
PT (1) | PT2192933E (hr) |
RU (1) | RU2467769C2 (hr) |
SI (1) | SI2192933T1 (hr) |
TW (1) | TWI426932B (hr) |
WO (1) | WO2009046235A1 (hr) |
ZA (1) | ZA201002393B (hr) |
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TWI473629B (zh) * | 2010-01-18 | 2015-02-21 | Alcon Inc | 用於眼用晶體材料之可見光吸收劑 |
US8362177B1 (en) | 2010-05-05 | 2013-01-29 | Novartis Ag | High refractive index ophthalmic device materials with reduced tack |
TWI473823B (zh) | 2010-06-21 | 2015-02-21 | Novartis Ag | 具有經降低的閃光之高折射率、丙烯酸系眼科裝置材料 |
TWI517861B (zh) | 2011-02-08 | 2016-01-21 | 諾華公司 | 低黏度疏水性眼科裝置材料 |
TWI513768B (zh) | 2011-06-01 | 2015-12-21 | Novartis Ag | 疏水性丙烯酸系眼內水晶體材料 |
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-
2008
- 2008-10-02 TW TW097137895A patent/TWI426932B/zh not_active IP Right Cessation
- 2008-10-03 CA CA2700150A patent/CA2700150C/en not_active Expired - Fee Related
- 2008-10-03 EP EP08835579A patent/EP2192933B1/en active Active
- 2008-10-03 ES ES08835579T patent/ES2364892T3/es active Active
- 2008-10-03 DK DK08835579.7T patent/DK2192933T3/da active
- 2008-10-03 US US12/244,814 patent/US8048154B2/en active Active
- 2008-10-03 PT PT08835579T patent/PT2192933E/pt unknown
- 2008-10-03 WO PCT/US2008/078646 patent/WO2009046235A1/en active Application Filing
- 2008-10-03 CN CN2008801101801A patent/CN101815541B/zh not_active Expired - Fee Related
- 2008-10-03 AT AT08835579T patent/ATE510568T1/de active
- 2008-10-03 KR KR1020107009759A patent/KR101513131B1/ko active IP Right Grant
- 2008-10-03 MX MX2010003183A patent/MX2010003183A/es active IP Right Grant
- 2008-10-03 AR ARP080104337A patent/AR068661A1/es not_active Application Discontinuation
- 2008-10-03 PL PL08835579T patent/PL2192933T3/pl unknown
- 2008-10-03 JP JP2010528145A patent/JP5623280B2/ja active Active
- 2008-10-03 SI SI200830288T patent/SI2192933T1/sl unknown
- 2008-10-03 RU RU2010117690/15A patent/RU2467769C2/ru not_active IP Right Cessation
- 2008-10-03 BR BRPI0817627A patent/BRPI0817627B8/pt not_active IP Right Cessation
- 2008-10-03 AU AU2008308607A patent/AU2008308607B2/en not_active Ceased
- 2008-10-03 NZ NZ585017A patent/NZ585017A/en not_active IP Right Cessation
-
2010
- 2010-03-18 IL IL204609A patent/IL204609A/en not_active IP Right Cessation
- 2010-04-06 ZA ZA2010/02393A patent/ZA201002393B/en unknown
- 2010-06-19 HK HK10106093.1A patent/HK1139339A1/xx not_active IP Right Cessation
-
2011
- 2011-06-03 HR HR20110420T patent/HRP20110420T1/hr unknown
- 2011-06-29 US US13/171,817 patent/US8163862B2/en active Active
- 2011-07-13 CY CY20111100684T patent/CY1112248T1/el unknown
- 2011-08-17 US US13/211,416 patent/US8728157B2/en active Active
-
2014
- 2014-03-28 US US14/228,679 patent/US8900297B2/en active Active
- 2014-07-24 JP JP2014150421A patent/JP2014198265A/ja not_active Withdrawn
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