TW201827854A - 眼用鏡片材料及眼用鏡片 - Google Patents
眼用鏡片材料及眼用鏡片 Download PDFInfo
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- TW201827854A TW201827854A TW106102051A TW106102051A TW201827854A TW 201827854 A TW201827854 A TW 201827854A TW 106102051 A TW106102051 A TW 106102051A TW 106102051 A TW106102051 A TW 106102051A TW 201827854 A TW201827854 A TW 201827854A
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- Prior art keywords
- ophthalmic lens
- lens material
- mass percentage
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- material according
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- 239000000463 material Substances 0.000 title claims abstract description 44
- 239000000178 monomer Substances 0.000 claims abstract description 27
- 150000003839 salts Chemical class 0.000 claims abstract description 22
- 239000003999 initiator Substances 0.000 claims abstract description 16
- 239000002904 solvent Substances 0.000 claims abstract description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 43
- KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical compound [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 claims description 15
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 14
- OKKRPWIIYQTPQF-UHFFFAOYSA-N Trimethylolpropane trimethacrylate Chemical compound CC(=C)C(=O)OCC(CC)(COC(=O)C(C)=C)COC(=O)C(C)=C OKKRPWIIYQTPQF-UHFFFAOYSA-N 0.000 claims description 13
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 12
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 claims description 12
- 239000003431 cross linking reagent Substances 0.000 claims description 11
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 claims description 9
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 claims description 7
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims description 7
- 239000007983 Tris buffer Substances 0.000 claims description 7
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 6
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 claims description 5
- DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 claims description 4
- SCVFZCLFOSHCOH-UHFFFAOYSA-M potassium acetate Chemical compound [K+].CC([O-])=O SCVFZCLFOSHCOH-UHFFFAOYSA-M 0.000 claims description 4
- DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 claims description 3
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 claims description 3
- 229910052732 germanium Inorganic materials 0.000 claims description 3
- GNPVGFCGXDBREM-UHFFFAOYSA-N germanium atom Chemical compound [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 claims description 3
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 claims description 3
- 229910001629 magnesium chloride Inorganic materials 0.000 claims description 3
- 150000002978 peroxides Chemical class 0.000 claims description 3
- 239000011780 sodium chloride Substances 0.000 claims description 3
- 239000012956 1-hydroxycyclohexylphenyl-ketone Substances 0.000 claims description 2
- PIZHFBODNLEQBL-UHFFFAOYSA-N 2,2-diethoxy-1-phenylethanone Chemical compound CCOC(OCC)C(=O)C1=CC=CC=C1 PIZHFBODNLEQBL-UHFFFAOYSA-N 0.000 claims description 2
- JJBFVQSGPLGDNX-UHFFFAOYSA-N 2-(2-methylprop-2-enoyloxy)propyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC(C)COC(=O)C(C)=C JJBFVQSGPLGDNX-UHFFFAOYSA-N 0.000 claims description 2
- WYGWHHGCAGTUCH-UHFFFAOYSA-N 2-[(2-cyano-4-methylpentan-2-yl)diazenyl]-2,4-dimethylpentanenitrile Chemical compound CC(C)CC(C)(C#N)N=NC(C)(C#N)CC(C)C WYGWHHGCAGTUCH-UHFFFAOYSA-N 0.000 claims description 2
- BQZJOQXSCSZQPS-UHFFFAOYSA-N 2-methoxy-1,2-diphenylethanone Chemical compound C=1C=CC=CC=1C(OC)C(=O)C1=CC=CC=C1 BQZJOQXSCSZQPS-UHFFFAOYSA-N 0.000 claims description 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims description 2
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 claims description 2
- 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 claims description 2
- 235000013870 dimethyl polysiloxane Nutrition 0.000 claims description 2
- 239000004205 dimethyl polysiloxane Substances 0.000 claims description 2
- AUONHKJOIZSQGR-UHFFFAOYSA-N oxophosphane Chemical compound P=O AUONHKJOIZSQGR-UHFFFAOYSA-N 0.000 claims description 2
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 claims description 2
- 235000011056 potassium acetate Nutrition 0.000 claims description 2
- 229960000834 vinyl ether Drugs 0.000 claims description 2
- AVTLBBWTUPQRAY-UHFFFAOYSA-N 2-(2-cyanobutan-2-yldiazenyl)-2-methylbutanenitrile Chemical compound CCC(C)(C#N)N=NC(C)(CC)C#N AVTLBBWTUPQRAY-UHFFFAOYSA-N 0.000 claims 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims 1
- ILGAYROEISMOJM-UHFFFAOYSA-N C(C1=CC=CC=C1)(C1=CC=CC=C1)[PH2]=O Chemical compound C(C1=CC=CC=C1)(C1=CC=CC=C1)[PH2]=O ILGAYROEISMOJM-UHFFFAOYSA-N 0.000 claims 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 239000004971 Cross linker Substances 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 150000001450 anions Chemical class 0.000 description 18
- 150000001768 cations Chemical class 0.000 description 18
- MSXVEPNJUHWQHW-UHFFFAOYSA-N 2-methylbutan-2-ol Chemical compound CCC(C)(C)O MSXVEPNJUHWQHW-UHFFFAOYSA-N 0.000 description 6
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- NGDNVOAEIVQRFH-UHFFFAOYSA-N 2-nonanol Chemical compound CCCCCCCC(C)O NGDNVOAEIVQRFH-UHFFFAOYSA-N 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 4
- 208000030533 eye disease Diseases 0.000 description 4
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 4
- OZAIFHULBGXAKX-VAWYXSNFSA-N AIBN Substances N#CC(C)(C)\N=N\C(C)(C)C#N OZAIFHULBGXAKX-VAWYXSNFSA-N 0.000 description 3
- 208000003556 Dry Eye Syndromes Diseases 0.000 description 3
- 206010013774 Dry eye Diseases 0.000 description 3
- 230000036571 hydration Effects 0.000 description 3
- 238000006703 hydration reaction Methods 0.000 description 3
- 150000002500 ions Chemical class 0.000 description 3
- 230000005923 long-lasting effect Effects 0.000 description 3
- 239000011259 mixed solution Substances 0.000 description 3
- 230000003020 moisturizing effect Effects 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 3
- CETWDUZRCINIHU-UHFFFAOYSA-N 2-heptanol Chemical compound CCCCCC(C)O CETWDUZRCINIHU-UHFFFAOYSA-N 0.000 description 2
- WFRBDWRZVBPBDO-UHFFFAOYSA-N 2-methyl-2-pentanol Chemical compound CCCC(C)(C)O WFRBDWRZVBPBDO-UHFFFAOYSA-N 0.000 description 2
- DLHQZZUEERVIGQ-UHFFFAOYSA-N 3,7-dimethyl-3-octanol Chemical compound CCC(C)(O)CCCC(C)C DLHQZZUEERVIGQ-UHFFFAOYSA-N 0.000 description 2
- MXLMTQWGSQIYOW-UHFFFAOYSA-N 3-methyl-2-butanol Chemical compound CC(C)C(C)O MXLMTQWGSQIYOW-UHFFFAOYSA-N 0.000 description 2
- PQOSNJHBSNZITJ-UHFFFAOYSA-N 3-methyl-3-heptanol Chemical compound CCCCC(C)(O)CC PQOSNJHBSNZITJ-UHFFFAOYSA-N 0.000 description 2
- FRDAATYAJDYRNW-UHFFFAOYSA-N 3-methyl-3-pentanol Chemical compound CCC(C)(O)CC FRDAATYAJDYRNW-UHFFFAOYSA-N 0.000 description 2
- -1 Irgacure-1173 Chemical compound 0.000 description 2
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 2
- NIHNNTQXNPWCJQ-UHFFFAOYSA-N fluorene Chemical compound C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 description 2
- QNVRIHYSUZMSGM-UHFFFAOYSA-N hexan-2-ol Chemical compound CCCCC(C)O QNVRIHYSUZMSGM-UHFFFAOYSA-N 0.000 description 2
- ZOCHHNOQQHDWHG-UHFFFAOYSA-N hexan-3-ol Chemical compound CCCC(O)CC ZOCHHNOQQHDWHG-UHFFFAOYSA-N 0.000 description 2
- 230000004402 high myopia Effects 0.000 description 2
- QYPPRTNMGCREIM-UHFFFAOYSA-N methylarsonic acid Chemical compound C[As](O)(O)=O QYPPRTNMGCREIM-UHFFFAOYSA-N 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- SJWFXCIHNDVPSH-UHFFFAOYSA-N octan-2-ol Chemical compound CCCCCCC(C)O SJWFXCIHNDVPSH-UHFFFAOYSA-N 0.000 description 2
- NMRPBPVERJPACX-UHFFFAOYSA-N octan-3-ol Chemical compound CCCCCC(O)CC NMRPBPVERJPACX-UHFFFAOYSA-N 0.000 description 2
- JYVLIDXNZAXMDK-UHFFFAOYSA-N pentan-2-ol Chemical compound CCCC(C)O JYVLIDXNZAXMDK-UHFFFAOYSA-N 0.000 description 2
- AQIXEPGDORPWBJ-UHFFFAOYSA-N pentan-3-ol Chemical compound CCC(O)CC AQIXEPGDORPWBJ-UHFFFAOYSA-N 0.000 description 2
- 230000005477 standard model Effects 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- NOOLISFMXDJSKH-UTLUCORTSA-N (+)-Neomenthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@@H]1O NOOLISFMXDJSKH-UTLUCORTSA-N 0.000 description 1
- VTBOTOBFGSVRMA-UHFFFAOYSA-N 1-Methylcyclohexanol Chemical compound CC1(O)CCCCC1 VTBOTOBFGSVRMA-UHFFFAOYSA-N 0.000 description 1
- JNOZGFXJZQXOSU-UHFFFAOYSA-N 1-chloro-2-methylpropan-2-ol Chemical compound CC(C)(O)CCl JNOZGFXJZQXOSU-UHFFFAOYSA-N 0.000 description 1
- JOLQKTGDSGKSKJ-UHFFFAOYSA-N 1-ethoxypropan-2-ol Chemical compound CCOCC(C)O JOLQKTGDSGKSKJ-UHFFFAOYSA-N 0.000 description 1
- LPCWIFPJLFCXRS-UHFFFAOYSA-N 1-ethylcyclopentan-1-ol Chemical compound CCC1(O)CCCC1 LPCWIFPJLFCXRS-UHFFFAOYSA-N 0.000 description 1
- CAKWRXVKWGUISE-UHFFFAOYSA-N 1-methylcyclopentan-1-ol Chemical compound CC1(O)CCCC1 CAKWRXVKWGUISE-UHFFFAOYSA-N 0.000 description 1
- QIGOESOMEANKQI-UHFFFAOYSA-N 1-methylcyclopentane-1,3-diol Chemical compound CC1(O)CCC(O)C1 QIGOESOMEANKQI-UHFFFAOYSA-N 0.000 description 1
- PLSMHHUFDLYURK-UHFFFAOYSA-N 2,3,4-trimethyl-3-pentanol Chemical compound CC(C)C(C)(O)C(C)C PLSMHHUFDLYURK-UHFFFAOYSA-N 0.000 description 1
- IKECULIHBUCAKR-UHFFFAOYSA-N 2,3-dimethylbutan-2-ol Chemical compound CC(C)C(C)(C)O IKECULIHBUCAKR-UHFFFAOYSA-N 0.000 description 1
- FMLSQAUAAGVTJO-UHFFFAOYSA-N 2,4-dimethylpentan-2-ol Chemical compound CC(C)CC(C)(C)O FMLSQAUAAGVTJO-UHFFFAOYSA-N 0.000 description 1
- QNVRIHYSUZMSGM-LURJTMIESA-N 2-Hexanol Natural products CCCC[C@H](C)O QNVRIHYSUZMSGM-LURJTMIESA-N 0.000 description 1
- GJKGAPPUXSSCFI-UHFFFAOYSA-N 2-Hydroxy-4'-(2-hydroxyethoxy)-2-methylpropiophenone Chemical compound CC(C)(O)C(=O)C1=CC=C(OCCO)C=C1 GJKGAPPUXSSCFI-UHFFFAOYSA-N 0.000 description 1
- RIWRBSMFKVOJMN-UHFFFAOYSA-N 2-methyl-1-phenylpropan-2-ol Chemical group CC(C)(O)CC1=CC=CC=C1 RIWRBSMFKVOJMN-UHFFFAOYSA-N 0.000 description 1
- RCEJCSULJQNRQQ-UHFFFAOYSA-N 2-methylbutanenitrile Chemical compound CCC(C)C#N RCEJCSULJQNRQQ-UHFFFAOYSA-N 0.000 description 1
- ACBMYYVZWKYLIP-UHFFFAOYSA-N 2-methylheptan-2-ol Chemical compound CCCCCC(C)(C)O ACBMYYVZWKYLIP-UHFFFAOYSA-N 0.000 description 1
- KRIMXCDMVRMCTC-UHFFFAOYSA-N 2-methylhexan-2-ol Chemical compound CCCCC(C)(C)O KRIMXCDMVRMCTC-UHFFFAOYSA-N 0.000 description 1
- VREDNSVJXRJXRI-UHFFFAOYSA-N 2-methylnonan-2-ol Chemical compound CCCCCCCC(C)(C)O VREDNSVJXRJXRI-UHFFFAOYSA-N 0.000 description 1
- KBCNUEXDHWDIFX-UHFFFAOYSA-N 2-methyloctan-2-ol Chemical compound CCCCCCC(C)(C)O KBCNUEXDHWDIFX-UHFFFAOYSA-N 0.000 description 1
- XGLHYBVJPSZXIF-UHFFFAOYSA-N 2-phenylbutan-2-ol Chemical compound CCC(C)(O)C1=CC=CC=C1 XGLHYBVJPSZXIF-UHFFFAOYSA-N 0.000 description 1
- BDCFWIDZNLCTMF-UHFFFAOYSA-N 2-phenylpropan-2-ol Chemical compound CC(C)(O)C1=CC=CC=C1 BDCFWIDZNLCTMF-UHFFFAOYSA-N 0.000 description 1
- NMRPBPVERJPACX-QMMMGPOBSA-N 3-Octanol Natural products CCCCC[C@@H](O)CC NMRPBPVERJPACX-QMMMGPOBSA-N 0.000 description 1
- WNDLTOTUHMHNOC-UHFFFAOYSA-N 3-ethylhexan-3-ol Chemical compound CCCC(O)(CC)CC WNDLTOTUHMHNOC-UHFFFAOYSA-N 0.000 description 1
- XKIRHOWVQWCYBT-UHFFFAOYSA-N 3-ethylpentan-3-ol Chemical compound CCC(O)(CC)CC XKIRHOWVQWCYBT-UHFFFAOYSA-N 0.000 description 1
- JEWXYDDSLPIBBO-UHFFFAOYSA-N 3-methyl-3-octanol Chemical compound CCCCCC(C)(O)CC JEWXYDDSLPIBBO-UHFFFAOYSA-N 0.000 description 1
- KYWJZCSJMOILIZ-UHFFFAOYSA-N 3-methylhexan-3-ol Chemical compound CCCC(C)(O)CC KYWJZCSJMOILIZ-UHFFFAOYSA-N 0.000 description 1
- VZBFPIMCUSPDLS-UHFFFAOYSA-N 3-methylnonan-3-ol Chemical compound CCCCCCC(C)(O)CC VZBFPIMCUSPDLS-UHFFFAOYSA-N 0.000 description 1
- BESKSSIEODQWBP-UHFFFAOYSA-N 3-tris(trimethylsilyloxy)silylpropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCC[Si](O[Si](C)(C)C)(O[Si](C)(C)C)O[Si](C)(C)C BESKSSIEODQWBP-UHFFFAOYSA-N 0.000 description 1
- GNROHGFUVTWFNG-UHFFFAOYSA-N 4-ethylheptan-4-ol Chemical compound CCCC(O)(CC)CCC GNROHGFUVTWFNG-UHFFFAOYSA-N 0.000 description 1
- IQXKGRKRIRMQCQ-UHFFFAOYSA-N 4-methylheptan-4-ol Chemical compound CCCC(C)(O)CCC IQXKGRKRIRMQCQ-UHFFFAOYSA-N 0.000 description 1
- GDCOAKPWVJCNGI-UHFFFAOYSA-N 4-methylnonan-4-ol Chemical compound CCCCCC(C)(O)CCC GDCOAKPWVJCNGI-UHFFFAOYSA-N 0.000 description 1
- RXSIKQJQLQRQQY-UHFFFAOYSA-N 4-methyloctan-4-ol Chemical compound CCCCC(C)(O)CCC RXSIKQJQLQRQQY-UHFFFAOYSA-N 0.000 description 1
- OHSMKBPEDBXYDU-UHFFFAOYSA-N 4-propan-2-ylheptan-4-ol Chemical compound CCCC(O)(C(C)C)CCC OHSMKBPEDBXYDU-UHFFFAOYSA-N 0.000 description 1
- SJTPBRMACCDJPZ-UHFFFAOYSA-N 4-propylheptan-4-ol Chemical compound CCCC(O)(CCC)CCC SJTPBRMACCDJPZ-UHFFFAOYSA-N 0.000 description 1
- NOOLISFMXDJSKH-UHFFFAOYSA-N DL-menthol Natural products CC(C)C1CCC(C)CC1O NOOLISFMXDJSKH-UHFFFAOYSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- WIELQWUKLCASNP-UHFFFAOYSA-N [PH3]=O.C(C1=CC=CC=C1)(=N)N Chemical compound [PH3]=O.C(C1=CC=CC=C1)(=N)N WIELQWUKLCASNP-UHFFFAOYSA-N 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
- XCIXKGXIYUWCLL-UHFFFAOYSA-N cyclopentanol Chemical compound OC1CCCC1 XCIXKGXIYUWCLL-UHFFFAOYSA-N 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229940041616 menthol Drugs 0.000 description 1
- QQZOPKMRPOGIEB-UHFFFAOYSA-N n-butyl methyl ketone Natural products CCCCC(C)=O QQZOPKMRPOGIEB-UHFFFAOYSA-N 0.000 description 1
- 125000002868 norbornyl group Chemical group C12(CCC(CC1)C2)* 0.000 description 1
- CXQXSVUQTKDNFP-UHFFFAOYSA-N octamethyltrisiloxane Chemical compound C[Si](C)(C)O[Si](C)(C)O[Si](C)(C)C CXQXSVUQTKDNFP-UHFFFAOYSA-N 0.000 description 1
- 238000004987 plasma desorption mass spectroscopy Methods 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
Classifications
-
- 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
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C233/02—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having nitrogen atoms of carboxamide groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals
- C07C233/09—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having nitrogen atoms of carboxamide groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals with carbon atoms of carboxamide groups bound to carbon atoms of an acyclic unsaturated carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C245/00—Compounds containing chains of at least two nitrogen atoms with at least one nitrogen-to-nitrogen multiple bond
- C07C245/22—Compounds containing chains of at least two nitrogen atoms with at least one nitrogen-to-nitrogen multiple bond containing chains of three or more nitrogen atoms with one or more nitrogen-to-nitrogen double bonds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/03—Ethers having all ether-oxygen atoms bound to acyclic carbon atoms
- C07C43/14—Unsaturated ethers
- C07C43/15—Unsaturated ethers containing only non-aromatic carbon-to-carbon double bonds
- C07C43/16—Vinyl ethers
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/76—Ketones containing a keto group bound to a six-membered aromatic ring
- C07C49/82—Ketones containing a keto group bound to a six-membered aromatic ring containing hydroxy groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/76—Ketones containing a keto group bound to a six-membered aromatic ring
- C07C49/82—Ketones containing a keto group bound to a six-membered aromatic ring containing hydroxy groups
- C07C49/83—Ketones containing a keto group bound to a six-membered aromatic ring containing hydroxy groups polycyclic
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/76—Ketones containing a keto group bound to a six-membered aromatic ring
- C07C49/84—Ketones containing a keto group bound to a six-membered aromatic ring containing ether groups, groups, groups, or groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/52—Esters of acyclic unsaturated carboxylic acids having the esterified carboxyl group bound to an acyclic carbon atom
- C07C69/533—Monocarboxylic acid esters having only one carbon-to-carbon double bond
- C07C69/54—Acrylic acid esters; Methacrylic acid esters
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
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Abstract
一種眼用鏡片材料,其包含有機單體、交聯劑、引發劑、鹽類及溶劑,該溶劑包含水。另,本發明還涉及一種應用該眼用鏡片材料製成的眼用鏡片。
Description
本發明涉及一種眼用鏡片材料及應用該眼用鏡片材料製得的眼用鏡片。
近年來,隨著近視人群的數量越來越多,隱形眼鏡因其便攜、美觀的特性而被廣泛使用。此外,對於高度近視者一般會藉由將透明晶(晶狀體)全摘除,然後植入眼內鏡片(人工晶狀體等),以使高度近視者可以看清物體。然,習知的眼用鏡片容易失水,從而引起眼睛乾澀或發紅等,使佩戴者感到不舒服,甚至引發眼部疾病。
有鑑於此,有必要提供一種新的眼用鏡片材料,以解決上述問題。
一種眼用鏡片材料,其包含有機單體、交聯劑、引發劑、鹽類及溶劑,該溶劑包含水。
一種眼用鏡片,該眼用鏡片由上述眼用鏡片材料製得。
本發明的眼用鏡片材料中包含鹽類,該鹽類可以溶解在水中,從而分離出多個陰離子和陽離子。這些陰離子和陽離子可以鍵合在水分子上,該鍵合作用使得陰離子和/或陽離子與水分子之間具有較強的結合強度。此外,鹽類溶解在水中,陰離子和陽離子很容易鍵合在水分子上,因此,水分子的離子水化度較高。在含有鹽類的水溶液中,水分子蒸發的時候,需要先破壞水分子與陰離子和/或陽離子之間的鍵合,水分子擺脫陰離子和/或陽離子之後,才可以蒸發。因此,在含有鹽類的眼用鏡片材料中,水分子蒸發的較慢,可以起到長久保濕的效果,從而使由該眼用鏡片材料製得的眼用鏡片長久濕潤,避免眼用鏡片失水引起的眼鏡乾澀及紅眼等眼部疾病。
本發明較佳實施方式提供一種眼用鏡片材料,其用於製備眼用鏡片。該眼用鏡片材料包含有機單體、交聯劑、引發劑、鹽類及溶劑。
所述眼用鏡片材料中,有機單體的質量百分含量的範圍為32~81%,交聯劑的質量百分含量的範圍為0.08~14.6% ,引發劑的質量百分含量的範圍為0.05~12.1%,鹽類的質量百分含量的範圍為 3~21.5%,溶劑的質量百分含量的範圍為5.5~51%。
所述有機單體包括親水性單體。該親水性單體包括但不限於甲基丙烯酸-2-羥基乙酯(HEMA)、甲基丙烯酸甲酯(MMA)、N,N-二甲基乙醯胺(DMA)、甲基丙烯酸縮水甘油酯(GMA) 、N-乙烯基吡咯烷酮(NVP)中的一種或幾種。
所述有機單體還包括有機矽單體。該有機矽單體包括但不限於甲基丙烯醯氧丙基三(三甲基矽氧烷基)矽烷(3-(METHACRYLOYLOXY)PROPYLTRIS(TRIMETHYLSILOXY)SILANE,TRIS)及聚二甲基矽氧烷(PDMS)中的一種或兩種。
所述交聯劑包括但不限於二甲基丙烯酸乙二醇酯(EGDMA)、三羥甲基丙烷三甲基丙烯酸酯(TMPTMA)、三(乙二醇)二甲基丙烯酸酯(TEGDMA)、三(乙二醇)二乙烯基醚(TEGDVE)、丙二醇二甲基丙烯酸酯(TMGDMA)等常規用於製備眼用鏡片的交聯劑中的一種或幾種。
所述引發劑可以為光引發劑或熱引發劑。該光引發劑包括但不限於苯偶姻甲基醚、二乙氧基苯乙酮、苯甲醯基氧化膦類光引發劑、1-羥基環己基苯基酮、Darocure型(化工行業標準型號)光引發劑及Irgacure型(化工行業標準型號)光引發劑等常規用於製備眼用鏡片的光引發劑中的一種或幾種。其中,該Darocure型光引發劑優選Darocur-1173或Darocur-2959;該Irgacure型光引發劑優選Irgacure-1173;該苯甲醯基氧化膦類光引發劑包括但不僅限於2,4,6-三甲基苯甲醯基二苯基氧化膦(2,4,6-trimethylbenzoyldiphenylophosphine oxide)、雙-(-二氯苯甲醯基)-4-N-丙苯基氧化膦、雙-(2,6-二氯苯甲醯基)-4-N-丁苯基氧化膦中的一種或幾種。所述熱引發劑包括但不限於2,2’-偶氮二(2,4-二甲基戊腈)、2,2’-偶氮二(2-甲基丙腈)、2,2’-偶氮二(2-甲基丁腈)、2,2’-偶氮二異丁腈(AIBN)、過氧化物(如過氧化苯甲醯)中的一種或幾種。
所述鹽類包括但不限於氯化鈉(NaCl)、氯化鋰(LiCl)、乙酸鉀(KAc)、氯化鎂(MgCl2
)中的一種或幾種。
所述溶劑可為水或水與醇的混合液。當溶劑為水與醇的混合液的時候,該混合溶液中水與醇的體積比的範圍為1%~95%。該醇包括但不限於聚乙二醇、聚丙二醇、2-丁醇、2-丙醇、薄荷醇、環己醇、環戊醇、2-戊醇、3-戊醇、2-己醇、3-己醇、3-甲基-2-丁醇、2-庚醇、2-辛醇、2-壬醇、2-癸醇、3-辛醇、降冰片、叔丁醇、叔戊醇、2-甲基-2-戊醇、2,3-二甲基-2-丁醇、3-甲基-3-戊醇、1-甲基環己醇、2-甲基-2-己醇、3,7-二甲基-3-辛醇、1-氯-2-甲基-2-丙醇、2-甲基-2-庚醇、2-甲基-2-辛醇、2-2-甲基-2-壬醇、2-甲基-2-癸醇、3-甲基-3-己醇,3-甲基-3-庚醇、4-甲基-4-庚醇、3-甲基-3-辛醇、4-甲基-4-辛醇、3-甲基-3-壬醇、4-甲基-4-壬醇、3-乙基-3-己醇、3-甲基-3-庚醇、4-乙基-4-庚醇、4-丙基-4-庚醇、4-異丙基-4-庚醇、2,4-二甲基-2-戊醇、1-甲基環戊醇、1-乙基環戊醇、4-羥基-4-甲基-1-環戊醇、2-苯基-2-丙醇、2-甲氧基-2-甲基-2-丙醇、2,3,4-三甲基-3-戊醇、3,7-二甲基-3-辛醇、2-苯基-2-丁醇、2-甲基-1-苯基-2-丙醇和3-乙基-3-戊醇、1-乙氧基-2-丙醇、1-甲基-2-丙醇、叔戊醇、異丙醇中的一種或幾種。
所述眼用鏡片材料中,鹽類可以溶解在水中,從而分離出多個陰離子和陽離子。這些陰離子和和/或陽離子可以鍵合在水分子上,該鍵合作用使得陰離子和/或陽離子與水分子之間具有較強的結合強度。此外,鹽類溶解在水中,陰離子和陽離子很容易鍵合在水分子上,因此,水分子的離子水化度較高。在含有鹽類的水溶液中,水分子蒸發的時候,需要先破壞水分子與陰離子和/或陽離子之間的鍵合,擺脫陰離子和/或陽離子之後,才可以蒸發。因此,在含有鹽類的眼用鏡片材料中,水分子蒸發的較慢,可以起到長久保濕的效果,從而使由該眼用鏡片材料製得的眼用鏡片長久濕潤,避免眼用鏡片失水引起的眼鏡乾澀及紅眼等眼部疾病。
一種眼用鏡片,其可為隱形眼鏡、眼內鏡片(AIOL)等,該眼內鏡片可為人工晶狀體(IOLs)等。該眼用鏡片由上述眼用鏡片材料製得。
一種眼用鏡片的製造方法,其包括以下步驟:
步驟S1,提供所述有機單體、交聯劑、引發劑、鹽類及溶劑,將該有機單體、交聯劑、引發劑、鹽類及溶劑按照預設比例混合均勻,得到混合溶液。
步驟S2,提供一眼用鏡片模具,將上述混合溶液置於眼用鏡片模具中。
步驟S3,對所述眼用鏡片模具進行加熱或紫外光照射,使所述有機單體及交聯劑在引發劑的作用下發生聚合反應,形成化學交聯的網狀結構。
步驟S4,脫模並清洗,即得到眼用鏡片。
下面藉由實施例來對本發明進行具體說明。
實施例1
本實施例的眼用鏡片材料包含HEMA、TMPTMA、Irgacure-1173、LiCl和水。
本實施例的眼用鏡片材料中,HEMA的質量百分含量為53.4%,TMPTMA的質量百分含量為0.53%,Irgacure-1173的質量百分含量為 0.23%,LiCl的質量百分含量為12.7%,水的質量百分含量為33.14%。
實施例2
本實施例的眼用鏡片材料包含HEMA、TMPTMA、Irgacure-1173、MgCl2和水。
本實施例的眼用鏡片材料中,HEMA的質量百分含量為58.34%,TMPTMA的質量百分含量為0.545%,Irgacure-1173的質量百分含量為 0.254% ,MgCl2的質量百分含量為12.45%,水的質量百分含量為28.411%。
實施例3
本實施例的眼用鏡片材料包含有機單體、TMPTMA、AIBN、LiCl和體積比為65%的乙醇水溶液。其中,有機單體包括HEMA、MAA及NVP。
本實施例的眼用鏡片材料中,HEMA的質量百分含量為52.43%、MAA的質量百分含量為0.82%、NVP 的質量百分含量為1.05%,TMPTMA的質量百分含量為0.55% ,AIBN的質量百分含量為0.26% ,LiCl的質量百分含量為10.87%,乙醇水溶液的質量百分含量為34.01% 。
實施例4
本實施例的眼用鏡片材料包含有機單體、TMPTMA、Irgacure-1173、KAc和體積比為5%的乙醇水溶液。其中,有機單體包括HEMA、MAA及NVP。
本實施例的眼用鏡片材料中,HEMA的質量百分含量為45.77%、MAA 的質量百分含量為0.71%、NVP的質量百分含量為 0.93%,TMPTMA的質量百分含量為0.49% ,Irgacure-1173的質量百分含量為0.22%,KAc的質量百分含量為22.15%,乙醇水溶液的質量百分含量為29.73%。
實施例5
本實施例的眼用鏡片材料包含有機單體、TMPTMA、Irgacure-1173、LiCl和95%的己醇水溶液。其中,有機單體包括HEMA、TRIS及DMA。
本實施例的眼用鏡片材料中,HEMA的質量百分含量為12.1%、TRIS 的質量百分含量為41.9%、DMA 的質量百分含量為0.8%,TMPTMA的質量百分含量為0.38%,Irgacure-1173的質量百分含量為0.31%,LiCl的質量百分含量為11.9%,95%的己醇水溶液的質量百分含量為32.61%。
本發明的眼用鏡片材料中包含鹽類,該鹽類可以溶解在水中,從而分離出多個陰離子和陽離子。這些陰離子和陽離子可以鍵合在水分子上,該鍵合作用使得陰離子和/或陽離子與水分子之間具有較強的結合強度。此外,鹽類溶解在水中,陰離子和陽離子很容易鍵合在水分子上,因此,水分子的離子水化度較高。在含有鹽類的水溶液中,水分子蒸發的時候,需要先破壞水分子與陰離子和/或陽離子之間的鍵合,水分子擺脫陰離子和/或陽離子之後,才可以蒸發。因此,在含有鹽類的眼用鏡片材料中,水分子蒸發的較慢,可以起到長久保濕的效果,從而使由該眼用鏡片材料製得的眼用鏡片長久濕潤,避免眼用鏡片失水引起的眼鏡乾澀及紅眼等眼部疾病。
另外,對於本領域的普通技術人員來說,可以根據本發明的技術構思做出其它各種相應的改變與變形,而所有這些改變與變形都應屬於本發明申請專利範圍的保護範圍。
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Claims (10)
- 一種眼用鏡片材料,其改良在於,該眼用鏡片材料包含有機單體、交聯劑、引發劑、鹽類及溶劑,該溶劑包含水。
- 如申請專利範圍1所述的眼用鏡片材料,其中,所述眼用鏡片材料中,有機單體的質量百分含量的範圍為32~81%,交聯劑的質量百分含量的範圍為0.08~14.6% ,引發劑的質量百分含量的範圍為0.05~12.1%,鹽類的質量百分含量的範圍為 3~21.5%,溶劑的質量百分含量的範圍為5.5~51%。
- 如申請專利範圍1所述的眼用鏡片材料,其中,所述有機單體包括親水性單體,該親水性單體包括甲基丙烯酸-2-羥基乙酯、甲基丙烯酸甲酯、N,N-二甲基乙醯胺、甲基丙烯酸縮水甘油酯、N-乙烯基吡咯烷酮中的一種或幾種。
- 如申請專利範圍3所述的眼用鏡片材料,其中,所述有機單體還包括有機矽單體,該有機矽單體包括甲基丙烯醯氧丙基三(三甲基矽氧烷基)矽烷及聚二甲基矽氧烷中的一種或兩種。
- 如申請專利範圍1所述的眼用鏡片材料,其中,所述交聯劑包括二甲基丙烯酸乙二醇酯、三羥甲基丙烷三甲基丙烯酸酯、三(乙二醇)二甲基丙烯酸酯、三(乙二醇)二乙烯基醚、及丙二醇二甲基丙烯酸酯中的一種或幾種。
- 如申請專利範圍1所述的眼用鏡片材料,其中,所述引發劑為光引發劑,該光引發劑包括苯偶姻甲基醚、二乙氧基苯乙酮、苯甲醯基氧化膦類光引發劑、1-羥基環己基苯基酮、Darocure型光引發劑及Irgacure型光引發劑中的一種或幾種,其中,該苯甲醯基氧化膦類光引發劑包括2,4,6-三甲基苯甲醯基二苯基氧化膦、雙-(-二氯苯甲醯基)-4-N-丙苯基氧化膦、雙-(2,6-二氯苯甲醯基)-4-N-丁苯基氧化膦中的一種或幾種。
- 如申請專利範圍1所述的眼用鏡片材料,其中,所述引發劑為熱引發劑,該熱引發劑包括2,2’-偶氮二(2,4-二甲基戊腈)、2,2’-偶氮二(2-甲基丙腈)、2,2’-偶氮二(2-甲基丁腈)、2,2’-偶氮二異丁腈、過氧化物中的一種或幾種。
- 如申請專利範圍1所述的眼用鏡片材料,其中,所述鹽類包括氯化鈉、氯化鋰、乙酸鉀、氯化鎂中的一種或幾種。
- 如申請專利範圍1所述的眼用鏡片材料,其中,所述溶劑還包含醇。
- 一種眼用鏡片,其改良在於,該眼用鏡片材料由申請專利範圍1至9中任意一項所述的眼用鏡片材料製得。
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US15/497,211 US10162082B2 (en) | 2017-01-20 | 2017-04-26 | Ophthalmic lens material and ophthalmic lens of such material |
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