CN1732255B - 多功能表面活性剂清洗隐形眼镜的用途 - Google Patents
多功能表面活性剂清洗隐形眼镜的用途 Download PDFInfo
- Publication number
- CN1732255B CN1732255B CN2003801073955A CN200380107395A CN1732255B CN 1732255 B CN1732255 B CN 1732255B CN 2003801073955 A CN2003801073955 A CN 2003801073955A CN 200380107395 A CN200380107395 A CN 200380107395A CN 1732255 B CN1732255 B CN 1732255B
- Authority
- CN
- China
- Prior art keywords
- solution
- eyeglass
- alkyl
- contact lens
- composition
- 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.)
- Expired - Lifetime
Links
- 239000004094 surface-active agent Substances 0.000 title abstract description 17
- 238000004140 cleaning Methods 0.000 claims abstract description 42
- 239000000203 mixture Substances 0.000 claims abstract description 34
- 239000003945 anionic surfactant Substances 0.000 claims abstract description 8
- OUDSFQBUEBFSPS-UHFFFAOYSA-N ethylenediaminetriacetic acid Chemical compound OC(=O)CNCCN(CC(O)=O)CC(O)=O OUDSFQBUEBFSPS-UHFFFAOYSA-N 0.000 claims description 11
- 239000013543 active substance Substances 0.000 claims description 8
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- 125000005277 alkyl imino group Chemical group 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 3
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 3
- 239000004348 Glyceryl diacetate Substances 0.000 claims description 2
- 125000003342 alkenyl group Chemical group 0.000 claims description 2
- 229910052799 carbon Inorganic materials 0.000 claims description 2
- 235000019443 glyceryl diacetate Nutrition 0.000 claims description 2
- 102000004169 proteins and genes Human genes 0.000 abstract description 5
- 108090000623 proteins and genes Proteins 0.000 abstract description 5
- 239000000243 solution Substances 0.000 description 49
- 230000000694 effects Effects 0.000 description 27
- 238000002360 preparation method Methods 0.000 description 24
- 108010064696 N,O-diacetylmuramidase Proteins 0.000 description 16
- 238000000034 method Methods 0.000 description 11
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 10
- 238000000605 extraction Methods 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- 230000000845 anti-microbial effect Effects 0.000 description 9
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 7
- 239000000872 buffer Substances 0.000 description 7
- 239000003795 chemical substances by application Substances 0.000 description 7
- 150000001875 compounds Chemical class 0.000 description 7
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 239000003513 alkali Substances 0.000 description 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 238000002791 soaking Methods 0.000 description 6
- 239000001509 sodium citrate Substances 0.000 description 6
- HRXKRNGNAMMEHJ-UHFFFAOYSA-K trisodium citrate Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O HRXKRNGNAMMEHJ-UHFFFAOYSA-K 0.000 description 6
- 229940038773 trisodium citrate Drugs 0.000 description 6
- 108010014251 Muramidase Proteins 0.000 description 5
- 102000016943 Muramidase Human genes 0.000 description 5
- 108010062010 N-Acetylmuramoyl-L-alanine Amidase Proteins 0.000 description 5
- 229920002359 Tetronic® Polymers 0.000 description 5
- DPDMMXDBJGCCQC-UHFFFAOYSA-N [Na].[Cl] Chemical compound [Na].[Cl] DPDMMXDBJGCCQC-UHFFFAOYSA-N 0.000 description 5
- 238000010521 absorption reaction Methods 0.000 description 5
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 5
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 5
- 239000004327 boric acid Substances 0.000 description 5
- 229960000274 lysozyme Drugs 0.000 description 5
- 239000004325 lysozyme Substances 0.000 description 5
- 235000010335 lysozyme Nutrition 0.000 description 5
- 230000035479 physiological effects, processes and functions Effects 0.000 description 5
- 239000003352 sequestering agent Substances 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- DTQVDTLACAAQTR-UHFFFAOYSA-N trifluoroacetic acid Substances OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 5
- MEIRRNXMZYDVDW-MQQKCMAXSA-N (2E,4E)-2,4-hexadien-1-ol Chemical compound C\C=C\C=C\CO MEIRRNXMZYDVDW-MQQKCMAXSA-N 0.000 description 4
- 101100162013 Arabidopsis thaliana MAPDA gene Proteins 0.000 description 4
- 108090000790 Enzymes Proteins 0.000 description 4
- 102000004190 Enzymes Human genes 0.000 description 4
- 108700015005 N6-mAMP deaminase activity proteins Proteins 0.000 description 4
- -1 amino guanyl guanidine Chemical compound 0.000 description 4
- 230000003115 biocidal effect Effects 0.000 description 4
- 239000008367 deionised water Substances 0.000 description 4
- 229910021641 deionized water Inorganic materials 0.000 description 4
- 229940088598 enzyme Drugs 0.000 description 4
- 150000002632 lipids Chemical class 0.000 description 4
- 230000000813 microbial effect Effects 0.000 description 4
- 244000005700 microbiome Species 0.000 description 4
- 239000008213 purified water Substances 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- OIQXFRANQVWXJF-LIQNAMIISA-N (1s,2z,4r)-2-benzylidene-4,7,7-trimethylbicyclo[2.2.1]heptan-3-one Chemical compound O=C([C@]1(C)CC[C@H]2C1(C)C)\C2=C/C1=CC=CC=C1 OIQXFRANQVWXJF-LIQNAMIISA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 150000001414 amino alcohols Chemical class 0.000 description 3
- 239000003139 biocide Substances 0.000 description 3
- 238000011109 contamination Methods 0.000 description 3
- 239000003814 drug Substances 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 150000002500 ions Chemical class 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- 229920001983 poloxamer Polymers 0.000 description 3
- 230000002797 proteolythic effect Effects 0.000 description 3
- 230000001954 sterilising effect Effects 0.000 description 3
- 238000004659 sterilization and disinfection Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- RVGRUAULSDPKGF-UHFFFAOYSA-N Poloxamer Chemical compound C1CO1.CC1CO1 RVGRUAULSDPKGF-UHFFFAOYSA-N 0.000 description 2
- 229920002413 Polyhexanide Polymers 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- 229910021538 borax Inorganic materials 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 239000012459 cleaning agent Substances 0.000 description 2
- 239000008139 complexing agent Substances 0.000 description 2
- 238000000151 deposition Methods 0.000 description 2
- 239000000645 desinfectant Substances 0.000 description 2
- UQGFMSUEHSUPRD-UHFFFAOYSA-N disodium;3,7-dioxido-2,4,6,8,9-pentaoxa-1,3,5,7-tetraborabicyclo[3.3.1]nonane Chemical compound [Na+].[Na+].O1B([O-])OB2OB([O-])OB1O2 UQGFMSUEHSUPRD-UHFFFAOYSA-N 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 230000005284 excitation Effects 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 230000002209 hydrophobic effect Effects 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000012452 mother liquor Substances 0.000 description 2
- GRZMEERIPCJGSO-UHFFFAOYSA-N oxalic acid;sodium Chemical compound [Na].[Na].OC(=O)C(O)=O GRZMEERIPCJGSO-UHFFFAOYSA-N 0.000 description 2
- 229960000502 poloxamer Drugs 0.000 description 2
- 238000010926 purge Methods 0.000 description 2
- 239000011435 rock Substances 0.000 description 2
- 239000004328 sodium tetraborate Substances 0.000 description 2
- 235000010339 sodium tetraborate Nutrition 0.000 description 2
- LJCJRRKKAKAKRV-UHFFFAOYSA-N (2-amino-2-methylpropyl) 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical group CC(C)(N)COC(=O)CCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 LJCJRRKKAKAKRV-UHFFFAOYSA-N 0.000 description 1
- ZLNXPOHTTBSBIH-HNNXBMFYSA-N (2s)-2-(dodecylamino)pentanedioic acid Chemical compound CCCCCCCCCCCCN[C@H](C(O)=O)CCC(O)=O ZLNXPOHTTBSBIH-HNNXBMFYSA-N 0.000 description 1
- VAZJLPXFVQHDFB-UHFFFAOYSA-N 1-(diaminomethylidene)-2-hexylguanidine Polymers CCCCCCN=C(N)N=C(N)N VAZJLPXFVQHDFB-UHFFFAOYSA-N 0.000 description 1
- MFMNADOFNGXVAW-UHFFFAOYSA-N 2-[carboxymethyl(dodecyl)amino]acetic acid Chemical compound CCCCCCCCCCCCN(CC(O)=O)CC(O)=O MFMNADOFNGXVAW-UHFFFAOYSA-N 0.000 description 1
- 229940058020 2-amino-2-methyl-1-propanol Drugs 0.000 description 1
- JCBPETKZIGVZRE-UHFFFAOYSA-N 2-aminobutan-1-ol Chemical class CCC(N)CO JCBPETKZIGVZRE-UHFFFAOYSA-N 0.000 description 1
- XNCOSPRUTUOJCJ-UHFFFAOYSA-N Biguanide Chemical compound NC(N)=NC(N)=N XNCOSPRUTUOJCJ-UHFFFAOYSA-N 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 1
- GRHQMTGLVVHYDS-UHFFFAOYSA-N C(C)(=O)O.C(C)(=O)O.C(C)(=O)O.C(CCCCCCCCCCC)NCCN Chemical compound C(C)(=O)O.C(C)(=O)O.C(C)(=O)O.C(CCCCCCCCCCC)NCCN GRHQMTGLVVHYDS-UHFFFAOYSA-N 0.000 description 1
- 208000001860 Eye Infections Diseases 0.000 description 1
- OVRNDRQMDRJTHS-FMDGEEDCSA-N N-acetyl-beta-D-glucosamine Chemical group CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O OVRNDRQMDRJTHS-FMDGEEDCSA-N 0.000 description 1
- 108010019160 Pancreatin Proteins 0.000 description 1
- 108091005804 Peptidases Proteins 0.000 description 1
- 102000035195 Peptidases Human genes 0.000 description 1
- 229920000289 Polyquaternium Polymers 0.000 description 1
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
- 235000009470 Theobroma cacao Nutrition 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- CBTVGIZVANVGBH-UHFFFAOYSA-N aminomethyl propanol Chemical compound CC(C)(N)CO CBTVGIZVANVGBH-UHFFFAOYSA-N 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 238000003556 assay Methods 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 238000012661 block copolymerization Methods 0.000 description 1
- 244000240602 cacao Species 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 230000007123 defense Effects 0.000 description 1
- 230000003544 deproteinization Effects 0.000 description 1
- 230000000249 desinfective effect Effects 0.000 description 1
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 1
- 229910000397 disodium phosphate Inorganic materials 0.000 description 1
- 235000019800 disodium phosphate Nutrition 0.000 description 1
- 231100000673 dose–response relationship Toxicity 0.000 description 1
- 230000003203 everyday effect Effects 0.000 description 1
- 208000011323 eye infectious disease Diseases 0.000 description 1
- 238000011010 flushing procedure Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- VLKZOEOYAKHREP-UHFFFAOYSA-N hexane Substances CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 1
- 125000001183 hydrocarbyl group Chemical group 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 230000000116 mitigating effect Effects 0.000 description 1
- 229940045641 monobasic sodium phosphate Drugs 0.000 description 1
- 150000004682 monohydrates Chemical class 0.000 description 1
- DZJAANPKJHXJDI-UHFFFAOYSA-N n'-methyl-n'-pentadecylpropane-1,3-diamine Chemical compound CCCCCCCCCCCCCCCN(C)CCCN DZJAANPKJHXJDI-UHFFFAOYSA-N 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- MUBZPKHOEPUJKR-UHFFFAOYSA-N oxalic acid group Chemical group C(C(=O)O)(=O)O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 1
- 229940055695 pancreatin Drugs 0.000 description 1
- 150000003009 phosphonic acids Chemical class 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- MYYHRFFZGSQEIT-UHFFFAOYSA-L polixetonium chloride Chemical compound [Cl-].[Cl-].PCC[N+](C)(C)CC[N+](C)(C)CCOP MYYHRFFZGSQEIT-UHFFFAOYSA-L 0.000 description 1
- 229960003426 polixetonium chloride Drugs 0.000 description 1
- 229920001987 poloxamine Polymers 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000012207 quantitative assay Methods 0.000 description 1
- 239000006254 rheological additive Substances 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- AJPJDKMHJJGVTQ-UHFFFAOYSA-M sodium dihydrogen phosphate Chemical compound [Na+].OP(O)([O-])=O AJPJDKMHJJGVTQ-UHFFFAOYSA-M 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
- 238000001179 sorption measurement Methods 0.000 description 1
- 230000000638 stimulation Effects 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 230000004083 survival effect Effects 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 229960004418 trolamine Drugs 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/04—Carboxylic acids or salts thereof
- C11D1/10—Amino carboxylic acids; Imino carboxylic acids; Fatty acid condensates thereof
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/88—Ampholytes; Electroneutral compounds
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/0005—Other compounding ingredients characterised by their effect
- C11D3/0078—Compositions for cleaning contact lenses, spectacles or lenses
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Detergent Compositions (AREA)
- Eyeglasses (AREA)
- Apparatus For Disinfection Or Sterilisation (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Description
成份 | 浓度(%w/v) |
聚塞氯胺-1 | 0.001 |
MAPDA | 0.0005 |
C9-ED3A | 0.1 |
山梨醇 | 1.2 |
硼酸 | 0.6 |
柠檬酸钠 | 0.65 |
氯化钠 | 0.1 |
四聚醇胺1304 | 0.1 |
成份 | 浓度(%w/v) |
EDTA | 0.05 |
AMP(95%) | 0.45 |
纯化水 | QS |
PH | 7.8 |
Claims (5)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US43616302P | 2002-12-23 | 2002-12-23 | |
US60/436,163 | 2002-12-23 | ||
PCT/US2003/040427 WO2004058929A1 (en) | 2002-12-23 | 2003-12-17 | Use of multifunctional surface active agents to clean contact lenses |
Publications (2)
Publication Number | Publication Date |
---|---|
CN1732255A CN1732255A (zh) | 2006-02-08 |
CN1732255B true CN1732255B (zh) | 2010-08-18 |
Family
ID=32682353
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN2003801073955A Expired - Lifetime CN1732255B (zh) | 2002-12-23 | 2003-12-17 | 多功能表面活性剂清洗隐形眼镜的用途 |
Country Status (22)
Country | Link |
---|---|
US (2) | US6995123B2 (zh) |
EP (1) | EP1576081B1 (zh) |
JP (1) | JP4486895B2 (zh) |
KR (1) | KR100950132B1 (zh) |
CN (1) | CN1732255B (zh) |
AR (1) | AR043317A1 (zh) |
AT (1) | ATE368098T1 (zh) |
AU (1) | AU2003301080B2 (zh) |
BR (1) | BR0317653B1 (zh) |
CA (1) | CA2507377C (zh) |
CY (1) | CY1107407T1 (zh) |
DE (1) | DE60315191T2 (zh) |
DK (1) | DK1576081T3 (zh) |
ES (1) | ES2287577T3 (zh) |
HK (1) | HK1075464A1 (zh) |
MX (1) | MXPA05006850A (zh) |
NO (1) | NO337439B1 (zh) |
NZ (1) | NZ541289A (zh) |
PT (1) | PT1576081E (zh) |
TW (1) | TWI322828B (zh) |
WO (1) | WO2004058929A1 (zh) |
ZA (1) | ZA200503974B (zh) |
Families Citing this family (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8071345B2 (en) * | 2006-03-31 | 2011-12-06 | Novozymes A/S | Stabilized subtilisin composition |
US20070264226A1 (en) * | 2006-05-10 | 2007-11-15 | Karagoezian Hampar L | Synergistically enhanced disinfecting solutions |
US8138156B2 (en) * | 2006-10-18 | 2012-03-20 | Bausch & Lomb Incorporated | Ophthalmic compositions containing diglycine |
US7897553B2 (en) * | 2006-10-23 | 2011-03-01 | Bausch & Lomb Incorporated | Biguanide composition with low terminal amine |
US8759321B2 (en) * | 2007-06-13 | 2014-06-24 | Bausch & Lomb Incorporated | Ophthalmic composition with hyaluronic acid and polymeric biguanide |
US8119112B2 (en) | 2008-01-31 | 2012-02-21 | Bausch & Lomb Incorporated | Ophthalmic compositions with an amphoteric surfactant and hyaluronic acid |
US20110046033A1 (en) * | 2008-01-31 | 2011-02-24 | Jinzhong Zhang | Multipurpose Lens Care Solution with Benefits to Corneal Epithelial Barrier Function |
US9096819B2 (en) | 2008-01-31 | 2015-08-04 | Bausch & Lomb Incorporated | Ophthalmic compositions with an amphoteric surfactant and an anionic biopolymer |
MX2010009336A (es) * | 2008-03-17 | 2010-09-24 | Alcon Res Ltd | Composiciones farmaceuticas acuosas que contienen complejos de borato-poliol. |
US8629099B2 (en) * | 2008-03-25 | 2014-01-14 | Bausch & Lomb Incorporated | Ophthalmic compositions comprising a dipeptide |
TWI489997B (zh) * | 2009-06-19 | 2015-07-01 | Alcon Res Ltd | 含有硼酸-多元醇錯合物之水性藥學組成物 |
US20110142786A1 (en) * | 2009-09-16 | 2011-06-16 | Erning Xia | Lens care solutions functionalized alkyldimonium hydroxypropyl alkylglucosides |
US8501200B2 (en) | 2010-04-26 | 2013-08-06 | Bausch & Lomb Incorporated | Ophthalmic compositions with biguanide and PEG-glycerol esters |
JP5927803B2 (ja) * | 2011-08-05 | 2016-06-01 | 三浦工業株式会社 | 界面活性剤組成物 |
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- 2003-11-05 TW TW092130942A patent/TWI322828B/zh not_active IP Right Cessation
- 2003-12-17 US US10/738,202 patent/US6995123B2/en not_active Expired - Lifetime
- 2003-12-17 JP JP2004563783A patent/JP4486895B2/ja not_active Expired - Lifetime
- 2003-12-17 CA CA002507377A patent/CA2507377C/en not_active Expired - Lifetime
- 2003-12-17 DE DE60315191T patent/DE60315191T2/de not_active Expired - Lifetime
- 2003-12-17 CN CN2003801073955A patent/CN1732255B/zh not_active Expired - Lifetime
- 2003-12-17 KR KR1020057011883A patent/KR100950132B1/ko not_active IP Right Cessation
- 2003-12-17 ES ES03814179T patent/ES2287577T3/es not_active Expired - Lifetime
- 2003-12-17 NZ NZ541289A patent/NZ541289A/en not_active IP Right Cessation
- 2003-12-17 DK DK03814179T patent/DK1576081T3/da active
- 2003-12-17 MX MXPA05006850A patent/MXPA05006850A/es active IP Right Grant
- 2003-12-17 BR BRPI0317653-3A patent/BR0317653B1/pt not_active IP Right Cessation
- 2003-12-17 WO PCT/US2003/040427 patent/WO2004058929A1/en active IP Right Grant
- 2003-12-17 PT PT03814179T patent/PT1576081E/pt unknown
- 2003-12-17 AU AU2003301080A patent/AU2003301080B2/en not_active Ceased
- 2003-12-17 EP EP03814179A patent/EP1576081B1/en not_active Expired - Lifetime
- 2003-12-17 AT AT03814179T patent/ATE368098T1/de active
- 2003-12-17 ZA ZA200503974A patent/ZA200503974B/en unknown
- 2003-12-19 AR ARP030104754A patent/AR043317A1/es not_active Application Discontinuation
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2005
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- 2005-08-24 US US11/210,331 patent/US20050282715A1/en not_active Abandoned
- 2005-09-26 HK HK05108467A patent/HK1075464A1/xx not_active IP Right Cessation
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Also Published As
Publication number | Publication date |
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JP4486895B2 (ja) | 2010-06-23 |
ES2287577T3 (es) | 2007-12-16 |
TW200427473A (en) | 2004-12-16 |
CN1732255A (zh) | 2006-02-08 |
DE60315191D1 (de) | 2007-09-06 |
ATE368098T1 (de) | 2007-08-15 |
PT1576081E (pt) | 2007-08-10 |
MXPA05006850A (es) | 2005-08-16 |
US20040127372A1 (en) | 2004-07-01 |
BR0317653A (pt) | 2005-11-29 |
ZA200503974B (en) | 2006-08-30 |
NO20053580L (no) | 2005-07-22 |
KR20050089981A (ko) | 2005-09-09 |
WO2004058929A1 (en) | 2004-07-15 |
DE60315191T2 (de) | 2007-11-22 |
DK1576081T3 (da) | 2007-10-01 |
EP1576081A1 (en) | 2005-09-21 |
EP1576081B1 (en) | 2007-07-25 |
US6995123B2 (en) | 2006-02-07 |
US20050282715A1 (en) | 2005-12-22 |
NZ541289A (en) | 2008-05-30 |
AU2003301080A1 (en) | 2004-07-22 |
AR043317A1 (es) | 2005-07-27 |
KR100950132B1 (ko) | 2010-03-30 |
HK1075464A1 (en) | 2005-12-16 |
JP2006511837A (ja) | 2006-04-06 |
TWI322828B (en) | 2010-04-01 |
BR0317653B1 (pt) | 2014-05-27 |
CA2507377C (en) | 2008-02-19 |
NO337439B1 (no) | 2016-04-11 |
CA2507377A1 (en) | 2004-07-15 |
CY1107407T1 (el) | 2012-12-19 |
AU2003301080B2 (en) | 2010-01-14 |
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