ZA200503974B - Use of multifunctional surface active agents to clean contact lenses - Google Patents
Use of multifunctional surface active agents to clean contact lenses Download PDFInfo
- Publication number
- ZA200503974B ZA200503974B ZA200503974A ZA200503974A ZA200503974B ZA 200503974 B ZA200503974 B ZA 200503974B ZA 200503974 A ZA200503974 A ZA 200503974A ZA 200503974 A ZA200503974 A ZA 200503974A ZA 200503974 B ZA200503974 B ZA 200503974B
- Authority
- ZA
- South Africa
- Prior art keywords
- solution
- lens
- following formula
- alkyl
- defined above
- Prior art date
Links
- 239000004094 surface-active agent Substances 0.000 title claims description 12
- 239000000243 solution Substances 0.000 claims description 45
- 239000000203 mixture Substances 0.000 claims description 30
- 239000003795 chemical substances by application Substances 0.000 claims description 22
- 238000000034 method Methods 0.000 claims description 19
- 150000001875 compounds Chemical class 0.000 claims description 18
- 238000004140 cleaning Methods 0.000 claims description 15
- 239000004599 antimicrobial Substances 0.000 claims description 14
- 125000000129 anionic group Chemical group 0.000 claims description 12
- -1 alkyl iminodiacetates Chemical class 0.000 claims description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 9
- 239000003945 anionic surfactant Substances 0.000 claims description 8
- 239000007864 aqueous solution Substances 0.000 claims description 7
- OUDSFQBUEBFSPS-UHFFFAOYSA-N ethylenediaminetriacetic acid Chemical compound OC(=O)CNCCN(CC(O)=O)CC(O)=O OUDSFQBUEBFSPS-UHFFFAOYSA-N 0.000 claims description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 5
- 239000005977 Ethylene Substances 0.000 claims description 5
- 230000000813 microbial effect Effects 0.000 claims description 5
- 229920002413 Polyhexanide Polymers 0.000 claims description 4
- 238000011109 contamination Methods 0.000 claims description 4
- VAZJLPXFVQHDFB-UHFFFAOYSA-N 1-(diaminomethylidene)-2-hexylguanidine Polymers CCCCCCN=C(N)N=C(N)N VAZJLPXFVQHDFB-UHFFFAOYSA-N 0.000 claims description 3
- IFYDWYVPVAMGRO-UHFFFAOYSA-N n-[3-(dimethylamino)propyl]tetradecanamide Chemical compound CCCCCCCCCCCCCC(=O)NCCCN(C)C IFYDWYVPVAMGRO-UHFFFAOYSA-N 0.000 claims description 3
- 229920000642 polymer Polymers 0.000 claims description 3
- 238000002791 soaking Methods 0.000 claims description 3
- 125000003342 alkenyl group Chemical group 0.000 claims 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 1
- 230000000249 desinfective effect Effects 0.000 claims 1
- 244000145841 kine Species 0.000 claims 1
- 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 1
- 102000004169 proteins and genes Human genes 0.000 description 14
- 108090000623 proteins and genes Proteins 0.000 description 14
- 102000016943 Muramidase Human genes 0.000 description 11
- 108010014251 Muramidase Proteins 0.000 description 11
- 108010062010 N-Acetylmuramoyl-L-alanine Amidase Proteins 0.000 description 11
- 229960000274 lysozyme Drugs 0.000 description 11
- 235000010335 lysozyme Nutrition 0.000 description 11
- 239000004325 lysozyme Substances 0.000 description 11
- 230000000845 anti-microbial effect Effects 0.000 description 9
- 239000000463 material Substances 0.000 description 6
- 239000003139 biocide Substances 0.000 description 5
- 239000002738 chelating agent Substances 0.000 description 5
- 102000004190 Enzymes Human genes 0.000 description 4
- 108090000790 Enzymes Proteins 0.000 description 4
- 108091005804 Peptidases Proteins 0.000 description 4
- 102000035195 Peptidases Human genes 0.000 description 4
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 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
- 238000009472 formulation Methods 0.000 description 4
- 150000002430 hydrocarbons Chemical group 0.000 description 4
- 150000002632 lipids Chemical class 0.000 description 4
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 150000001414 amino alcohols Chemical class 0.000 description 3
- 239000011575 calcium Substances 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 239000012459 cleaning agent Substances 0.000 description 3
- 230000008021 deposition Effects 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 239000002953 phosphate buffered saline Substances 0.000 description 3
- 229920001983 poloxamer Polymers 0.000 description 3
- 229940024999 proteolytic enzymes for treatment of wounds and ulcers Drugs 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- DTQVDTLACAAQTR-UHFFFAOYSA-N trifluoroacetic acid Substances OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 3
- 229940058020 2-amino-2-methyl-1-propanol Drugs 0.000 description 2
- 101100162013 Arabidopsis thaliana MAPDA gene Proteins 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- 108700015005 N6-mAMP deaminase activity proteins Proteins 0.000 description 2
- CBTVGIZVANVGBH-UHFFFAOYSA-N aminomethyl propanol Chemical compound CC(C)(N)CO CBTVGIZVANVGBH-UHFFFAOYSA-N 0.000 description 2
- 230000003115 biocidal effect Effects 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 239000008139 complexing agent Substances 0.000 description 2
- 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 2
- 238000000605 extraction Methods 0.000 description 2
- 230000002209 hydrophobic effect Effects 0.000 description 2
- 244000005700 microbiome Species 0.000 description 2
- 229920001987 poloxamine Polymers 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 239000001509 sodium citrate Substances 0.000 description 2
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 2
- 238000004659 sterilization and disinfection Methods 0.000 description 2
- HFDVRLIODXPAHB-UHFFFAOYSA-N 1-tetradecene Chemical group CCCCCCCCCCCCC=C HFDVRLIODXPAHB-UHFFFAOYSA-N 0.000 description 1
- VTUFDOOSZOYXFC-UHFFFAOYSA-N 2-amino-1-(diaminomethylidene)guanidine Chemical compound NNC(=N)NC(N)=N VTUFDOOSZOYXFC-UHFFFAOYSA-N 0.000 description 1
- JCBPETKZIGVZRE-UHFFFAOYSA-N 2-aminobutan-1-ol Chemical compound CCC(N)CO JCBPETKZIGVZRE-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical group CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 1
- 229940123208 Biguanide Drugs 0.000 description 1
- GHXZTYHSJHQHIJ-UHFFFAOYSA-N Chlorhexidine Chemical compound C=1C=C(Cl)C=CC=1NC(N)=NC(N)=NCCCCCCN=C(N)N=C(N)NC1=CC=C(Cl)C=C1 GHXZTYHSJHQHIJ-UHFFFAOYSA-N 0.000 description 1
- 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 1
- DBVJJBKOTRCVKF-UHFFFAOYSA-N Etidronic acid Chemical compound OP(=O)(O)C(O)(C)P(O)(O)=O DBVJJBKOTRCVKF-UHFFFAOYSA-N 0.000 description 1
- 208000001860 Eye Infections Diseases 0.000 description 1
- MNLRQHMNZILYPY-MDMHTWEWSA-N N-acetyl-alpha-D-muramic acid Chemical compound OC(=O)[C@@H](C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](O)[C@@H]1NC(C)=O MNLRQHMNZILYPY-MDMHTWEWSA-N 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
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 238000003287 bathing Methods 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 239000006172 buffering agent Substances 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- 210000002421 cell wall Anatomy 0.000 description 1
- 230000009920 chelation Effects 0.000 description 1
- 229960003260 chlorhexidine Drugs 0.000 description 1
- 230000000593 degrading effect Effects 0.000 description 1
- 229940061607 dibasic sodium phosphate Drugs 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 229940047642 disodium cocoamphodiacetate Drugs 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
- 229940079881 disodium lauroamphodiacetate Drugs 0.000 description 1
- QKQCPXJIOJLHAL-UHFFFAOYSA-L disodium;2-[2-(carboxylatomethoxy)ethyl-[2-(dodecanoylamino)ethyl]amino]acetate Chemical compound [Na+].[Na+].CCCCCCCCCCCC(=O)NCCN(CC([O-])=O)CCOCC([O-])=O QKQCPXJIOJLHAL-UHFFFAOYSA-L 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 239000002563 ionic surfactant Substances 0.000 description 1
- 230000007794 irritation Effects 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229940045641 monobasic sodium phosphate Drugs 0.000 description 1
- 150000004682 monohydrates Chemical class 0.000 description 1
- 229910000403 monosodium phosphate Inorganic materials 0.000 description 1
- 235000019799 monosodium phosphate Nutrition 0.000 description 1
- 230000037125 natural defense Effects 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 229940055695 pancreatin Drugs 0.000 description 1
- 239000008363 phosphate buffer Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 230000004962 physiological condition Effects 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 239000006254 rheological additive Substances 0.000 description 1
- 239000011734 sodium Substances 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
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 239000012085 test solution Substances 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- BSVBQGMMJUBVOD-UHFFFAOYSA-N trisodium borate Chemical compound [Na+].[Na+].[Na+].[O-]B([O-])[O-] BSVBQGMMJUBVOD-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
- 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)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US43616302P | 2002-12-23 | 2002-12-23 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ZA200503974B true ZA200503974B (en) | 2006-08-30 |
Family
ID=32682353
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ZA200503974A ZA200503974B (en) | 2002-12-23 | 2003-12-17 | Use of multifunctional surface active agents to clean contact lenses |
Country Status (21)
| Country | Link |
|---|---|
| US (2) | US6995123B2 (https=) |
| EP (1) | EP1576081B1 (https=) |
| JP (1) | JP4486895B2 (https=) |
| KR (1) | KR100950132B1 (https=) |
| CN (1) | CN1732255B (https=) |
| AR (1) | AR043317A1 (https=) |
| AT (1) | ATE368098T1 (https=) |
| AU (1) | AU2003301080B2 (https=) |
| BR (1) | BR0317653B1 (https=) |
| CA (1) | CA2507377C (https=) |
| CY (1) | CY1107407T1 (https=) |
| DE (1) | DE60315191T2 (https=) |
| DK (1) | DK1576081T3 (https=) |
| ES (1) | ES2287577T3 (https=) |
| MX (1) | MXPA05006850A (https=) |
| NO (1) | NO337439B1 (https=) |
| NZ (1) | NZ541289A (https=) |
| PT (1) | PT1576081E (https=) |
| TW (1) | TWI322828B (https=) |
| WO (1) | WO2004058929A1 (https=) |
| ZA (1) | ZA200503974B (https=) |
Families Citing this family (23)
| 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 |
| US20110046033A1 (en) * | 2008-01-31 | 2011-02-24 | Jinzhong Zhang | Multipurpose Lens Care Solution with Benefits to Corneal Epithelial Barrier Function |
| US8119112B2 (en) | 2008-01-31 | 2012-02-21 | Bausch & Lomb Incorporated | Ophthalmic compositions with an amphoteric surfactant and hyaluronic acid |
| US9096819B2 (en) | 2008-01-31 | 2015-08-04 | Bausch & Lomb Incorporated | Ophthalmic compositions with an amphoteric surfactant and an anionic biopolymer |
| ES2638771T3 (es) * | 2008-03-17 | 2017-10-24 | Novartis Ag | Composiciones farmacéuticas 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 |
| US11723852B2 (en) | 2011-10-31 | 2023-08-15 | Kane Biotech Inc. | Antimicrobial-antibiofilm compositions and methods of use thereof for personal care products |
| US8664180B2 (en) | 2012-02-06 | 2014-03-04 | Bausch & Lomb Incorporated | Ophthalmic compositions containing diglycine |
| US8324171B1 (en) | 2012-02-06 | 2012-12-04 | Bausch & Lomb Incorporated | Ophthalmic compositions containing diglycine |
| JP2015509495A (ja) | 2012-02-24 | 2015-03-30 | ボシュ・アンド・ロム・インコーポレイテッドＢａｕｓｃｈ ＆ Ｌｏｍｂ Ｉｎｃｏｒｐｏｒａｔｅｄ | アルコキシル化天然ワックスを有する眼用組成物 |
| CN103893027A (zh) * | 2012-12-25 | 2014-07-02 | 青岛海芬海洋生物科技有限公司 | 一种含有海洋生物成分的沐浴液及其制备方法 |
| PL2948196T3 (pl) | 2013-01-24 | 2018-01-31 | Bausch & Lomb | Poli(azotowane/aminowane) pochodne naturalnego wosku lub jego alkoksylowana pochodna i kompozycje okulistyczne |
| JP2017519035A (ja) * | 2014-06-27 | 2017-07-13 | ケーン バイオテク インコーポレーテッド | 抗微生物性−抗バイオフィルム性組成物及び該組成物のパーソナルケア製品のための使用 |
| CN107828545A (zh) * | 2017-10-25 | 2018-03-23 | 成都纽兰晶茂商贸有限公司 | 一种电脑显示屏用清洁剂的制备方法 |
| CN114689538A (zh) * | 2020-12-30 | 2022-07-01 | 苏州三个臭皮匠生物科技有限公司 | 一种有效测量软性亲水角膜接触镜泪蛋白含量的方法 |
Family Cites Families (38)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US441042A (en) * | 1890-11-18 | Policeman s club | ||
| US3908680A (en) | 1973-10-12 | 1975-09-30 | Flow Pharma Inc | Methods for cleaning and bleaching plastic articles |
| US4013576A (en) * | 1973-11-21 | 1977-03-22 | Wesley-Jessen Inc. | Contact lens treating composition |
| US4046706A (en) | 1976-04-06 | 1977-09-06 | Flow Pharmaceuticals, Inc. | Contact lens cleaning composition |
| US4410442A (en) | 1982-01-13 | 1983-10-18 | The Procter & Gamble Company | Disinfecting solutions for hydrophilic contact lenses |
| JPS6151121A (ja) * | 1984-08-21 | 1986-03-13 | Lion Corp | コンタクトレンズ用洗浄剤 |
| US4908147A (en) | 1986-02-19 | 1990-03-13 | Ciba-Geigy Corporation | Aqueous self preserving soft contact lens solution and method |
| US5846919A (en) | 1989-01-31 | 1998-12-08 | Ciba Vision Corporation | Rapid ophthalmic disinfection solution using salt and glycol and/or lower alkanol and surfactant |
| US5298182A (en) | 1989-01-31 | 1994-03-29 | Ciba-Geigy Corporation | Rapid ophthalmic glycol/lower alkanol cleaning and disinfecting solution and method |
| GB9020594D0 (en) * | 1990-09-21 | 1990-10-31 | Procter & Gamble | Cleansing compositions |
| EP0766970A3 (en) | 1990-12-27 | 2000-02-23 | Allergan, Inc | Method and composition for disinfecting contact lenses |
| US5191081A (en) | 1991-12-12 | 1993-03-02 | W. R. Grace & Co.-Conn. | 1-cyanomethyl-4-carboxymethyl-3-ketopiperazine, salts thereof and process for their preparation |
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-
2003
- 2003-11-05 TW TW092130942A patent/TWI322828B/zh not_active IP Right Cessation
- 2003-12-17 DE DE60315191T patent/DE60315191T2/de not_active Expired - Lifetime
- 2003-12-17 ZA ZA200503974A patent/ZA200503974B/en unknown
- 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 PT PT03814179T patent/PT1576081E/pt unknown
- 2003-12-17 BR BRPI0317653-3A patent/BR0317653B1/pt not_active IP Right Cessation
- 2003-12-17 CA CA002507377A patent/CA2507377C/en not_active Expired - Lifetime
- 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 KR KR1020057011883A patent/KR100950132B1/ko not_active Expired - Fee Related
- 2003-12-17 CN CN2003801073955A patent/CN1732255B/zh not_active Expired - Lifetime
- 2003-12-17 JP JP2004563783A patent/JP4486895B2/ja not_active Expired - Lifetime
- 2003-12-17 US US10/738,202 patent/US6995123B2/en not_active Expired - Lifetime
- 2003-12-17 WO PCT/US2003/040427 patent/WO2004058929A1/en not_active Ceased
- 2003-12-17 MX MXPA05006850A patent/MXPA05006850A/es active IP Right Grant
- 2003-12-17 AT AT03814179T patent/ATE368098T1/de active
- 2003-12-17 ES ES03814179T patent/ES2287577T3/es not_active Expired - Lifetime
- 2003-12-19 AR ARP030104754A patent/AR043317A1/es not_active Application Discontinuation
-
2005
- 2005-07-22 NO NO20053580A patent/NO337439B1/no not_active IP Right Cessation
- 2005-08-24 US US11/210,331 patent/US20050282715A1/en not_active Abandoned
-
2007
- 2007-08-02 CY CY20071101033T patent/CY1107407T1/el unknown
Also Published As
| Publication number | Publication date |
|---|---|
| EP1576081A1 (en) | 2005-09-21 |
| BR0317653B1 (pt) | 2014-05-27 |
| TWI322828B (en) | 2010-04-01 |
| KR100950132B1 (ko) | 2010-03-30 |
| TW200427473A (en) | 2004-12-16 |
| CY1107407T1 (el) | 2012-12-19 |
| DK1576081T3 (da) | 2007-10-01 |
| CN1732255B (zh) | 2010-08-18 |
| WO2004058929A1 (en) | 2004-07-15 |
| NO20053580L (no) | 2005-07-22 |
| PT1576081E (pt) | 2007-08-10 |
| EP1576081B1 (en) | 2007-07-25 |
| CN1732255A (zh) | 2006-02-08 |
| ATE368098T1 (de) | 2007-08-15 |
| ES2287577T3 (es) | 2007-12-16 |
| AU2003301080B2 (en) | 2010-01-14 |
| MXPA05006850A (es) | 2005-08-16 |
| JP4486895B2 (ja) | 2010-06-23 |
| DE60315191T2 (de) | 2007-11-22 |
| US6995123B2 (en) | 2006-02-07 |
| CA2507377C (en) | 2008-02-19 |
| US20050282715A1 (en) | 2005-12-22 |
| JP2006511837A (ja) | 2006-04-06 |
| KR20050089981A (ko) | 2005-09-09 |
| AU2003301080A1 (en) | 2004-07-22 |
| CA2507377A1 (en) | 2004-07-15 |
| BR0317653A (pt) | 2005-11-29 |
| HK1075464A1 (en) | 2005-12-16 |
| AR043317A1 (es) | 2005-07-27 |
| NZ541289A (en) | 2008-05-30 |
| DE60315191D1 (de) | 2007-09-06 |
| US20040127372A1 (en) | 2004-07-01 |
| NO337439B1 (no) | 2016-04-11 |
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