KR950006932B1 - 콘택트렌즈 소독 시스템 - Google Patents
콘택트렌즈 소독 시스템 Download PDFInfo
- Publication number
- KR950006932B1 KR950006932B1 KR1019920701182A KR920701182A KR950006932B1 KR 950006932 B1 KR950006932 B1 KR 950006932B1 KR 1019920701182 A KR1019920701182 A KR 1019920701182A KR 920701182 A KR920701182 A KR 920701182A KR 950006932 B1 KR950006932 B1 KR 950006932B1
- Authority
- KR
- South Korea
- Prior art keywords
- solution
- alkyl
- pyrrolidone
- lens
- fungicides
- 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
- 230000000249 desinfective effect Effects 0.000 title claims description 8
- 239000000243 solution Substances 0.000 claims description 38
- 238000000034 method Methods 0.000 claims description 21
- 239000000203 mixture Substances 0.000 claims description 20
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical group [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 16
- 125000000217 alkyl group Chemical group 0.000 claims description 13
- 239000000417 fungicide Substances 0.000 claims description 13
- 239000007788 liquid Substances 0.000 claims description 9
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 claims description 8
- 239000007864 aqueous solution Substances 0.000 claims description 7
- 239000000843 powder Substances 0.000 claims description 6
- 230000000844 anti-bacterial effect Effects 0.000 claims description 5
- 239000002904 solvent Substances 0.000 claims description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 4
- 229920002413 Polyhexanide Polymers 0.000 claims description 3
- -1 alkyl pyrrolidone Chemical compound 0.000 claims description 3
- VAZJLPXFVQHDFB-UHFFFAOYSA-N 1-(diaminomethylidene)-2-hexylguanidine Polymers CCCCCCN=C(N)N=C(N)N VAZJLPXFVQHDFB-UHFFFAOYSA-N 0.000 claims description 2
- 239000003899 bactericide agent Substances 0.000 claims description 2
- 230000000855 fungicidal effect Effects 0.000 claims 2
- 239000003761 preservation solution Substances 0.000 claims 2
- 239000008247 solid mixture Substances 0.000 claims 2
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 claims 1
- 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
- 125000003438 dodecyl 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])C([H])([H])C([H])([H])* 0.000 claims 1
- 125000002347 octyl 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])[H] 0.000 claims 1
- 238000004321 preservation Methods 0.000 claims 1
- 238000004140 cleaning Methods 0.000 description 16
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 15
- 239000003826 tablet Substances 0.000 description 13
- 238000012360 testing method Methods 0.000 description 10
- 238000004659 sterilization and disinfection Methods 0.000 description 9
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 8
- 238000009472 formulation Methods 0.000 description 8
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 6
- 241000894006 Bacteria Species 0.000 description 6
- 239000000872 buffer 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
- 239000000882 contact lens solution Substances 0.000 description 6
- 150000004040 pyrrolidinones Chemical class 0.000 description 6
- 239000004094 surface-active agent Substances 0.000 description 5
- 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 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- 239000001361 adipic acid Substances 0.000 description 4
- 235000011037 adipic acid Nutrition 0.000 description 4
- 230000003115 biocidal effect Effects 0.000 description 4
- 239000003599 detergent Substances 0.000 description 4
- 239000002736 nonionic surfactant Substances 0.000 description 4
- 150000002978 peroxides Chemical class 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- 239000011343 solid material Substances 0.000 description 4
- 241000222122 Candida albicans Species 0.000 description 3
- 229910052783 alkali metal Inorganic materials 0.000 description 3
- 239000003945 anionic surfactant Substances 0.000 description 3
- 235000010323 ascorbic acid Nutrition 0.000 description 3
- 229960005070 ascorbic acid Drugs 0.000 description 3
- 239000011668 ascorbic acid Substances 0.000 description 3
- 229960003333 chlorhexidine gluconate Drugs 0.000 description 3
- 239000000645 desinfectant Substances 0.000 description 3
- 239000003352 sequestering agent Substances 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- RGHNJXZEOKUKBD-SQOUGZDYSA-N D-gluconic acid Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O RGHNJXZEOKUKBD-SQOUGZDYSA-N 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 2
- 238000002835 absorbance Methods 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- 230000001580 bacterial effect Effects 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- YZIYKJHYYHPJIB-UUPCJSQJSA-N chlorhexidine gluconate Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O.OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O.C1=CC(Cl)=CC=C1NC(=N)NC(=N)NCCCCCCNC(=N)NC(=N)NC1=CC=C(Cl)C=C1 YZIYKJHYYHPJIB-UUPCJSQJSA-N 0.000 description 2
- 235000015165 citric acid Nutrition 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 150000004985 diamines Chemical group 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000007938 effervescent tablet Substances 0.000 description 2
- 239000003623 enhancer Substances 0.000 description 2
- 150000002484 inorganic compounds Chemical class 0.000 description 2
- 229910010272 inorganic material Inorganic materials 0.000 description 2
- 229910052740 iodine Inorganic materials 0.000 description 2
- 239000011630 iodine Substances 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 244000005700 microbiome Species 0.000 description 2
- 231100000344 non-irritating Toxicity 0.000 description 2
- 230000001590 oxidative effect Effects 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 229920000570 polyether Polymers 0.000 description 2
- 229940071089 sarcosinate Drugs 0.000 description 2
- FSYKKLYZXJSNPZ-UHFFFAOYSA-N sarcosine Chemical compound C[NH2+]CC([O-])=O FSYKKLYZXJSNPZ-UHFFFAOYSA-N 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 229940079862 sodium lauryl sarcosinate Drugs 0.000 description 2
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 2
- 229960001922 sodium perborate Drugs 0.000 description 2
- BZCOSCNPHJNQBP-UPHRSURJSA-N (z)-2,3-dihydroxybut-2-enedioic acid Chemical compound OC(=O)C(\O)=C(\O)C(O)=O BZCOSCNPHJNQBP-UPHRSURJSA-N 0.000 description 1
- 229940043375 1,5-pentanediol Drugs 0.000 description 1
- WQNHWIYLCRZRLR-UHFFFAOYSA-N 2-(3-hydroxy-2,5-dioxooxolan-3-yl)acetic acid Chemical compound OC(=O)CC1(O)CC(=O)OC1=O WQNHWIYLCRZRLR-UHFFFAOYSA-N 0.000 description 1
- CQVKMVQRSNNAGO-UHFFFAOYSA-N 2-[4-formyl-3-methyl-n-(2-methylsulfonyloxyethyl)anilino]ethyl methanesulfonate Chemical compound CC1=CC(N(CCOS(C)(=O)=O)CCOS(C)(=O)=O)=CC=C1C=O CQVKMVQRSNNAGO-UHFFFAOYSA-N 0.000 description 1
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- LXAHHHIGZXPRKQ-UHFFFAOYSA-N 5-fluoro-2-methylpyridine Chemical compound CC1=CC=C(F)C=N1 LXAHHHIGZXPRKQ-UHFFFAOYSA-N 0.000 description 1
- ODHCTXKNWHHXJC-VKHMYHEASA-N 5-oxo-L-proline Chemical class OC(=O)[C@@H]1CCC(=O)N1 ODHCTXKNWHHXJC-VKHMYHEASA-N 0.000 description 1
- BDDLHHRCDSJVKV-UHFFFAOYSA-N 7028-40-2 Chemical compound CC(O)=O.CC(O)=O.CC(O)=O.CC(O)=O BDDLHHRCDSJVKV-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 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
- 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
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- JPVYNHNXODAKFH-UHFFFAOYSA-N Cu2+ Chemical compound [Cu+2] JPVYNHNXODAKFH-UHFFFAOYSA-N 0.000 description 1
- RGHNJXZEOKUKBD-SQOUGZDYSA-M D-gluconate Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O RGHNJXZEOKUKBD-SQOUGZDYSA-M 0.000 description 1
- RGHNJXZEOKUKBD-UHFFFAOYSA-N D-gluconic acid Natural products OCC(O)C(O)C(O)C(O)C(O)=O RGHNJXZEOKUKBD-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- ALQSHHUCVQOPAS-UHFFFAOYSA-N Pentane-1,5-diol Chemical compound OCCCCCO ALQSHHUCVQOPAS-UHFFFAOYSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-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
- 235000021355 Stearic acid Nutrition 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- 229920002359 Tetronic® Polymers 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 150000007854 aminals Chemical class 0.000 description 1
- 239000002280 amphoteric surfactant Substances 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 229940091771 aspergillus fumigatus Drugs 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 239000007975 buffered saline Substances 0.000 description 1
- 229940095731 candida albicans Drugs 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229960003260 chlorhexidine Drugs 0.000 description 1
- 230000001332 colony forming effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 229910001431 copper ion Inorganic materials 0.000 description 1
- 235000021438 curry Nutrition 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- BZCOSCNPHJNQBP-OWOJBTEDSA-N dihydroxyfumaric acid Chemical compound OC(=O)C(\O)=C(/O)C(O)=O BZCOSCNPHJNQBP-OWOJBTEDSA-N 0.000 description 1
- SPCNPOWOBZQWJK-UHFFFAOYSA-N dimethoxy-(2-propan-2-ylsulfanylethylsulfanyl)-sulfanylidene-$l^{5}-phosphane Chemical compound COP(=S)(OC)SCCSC(C)C SPCNPOWOBZQWJK-UHFFFAOYSA-N 0.000 description 1
- VTIIJXUACCWYHX-UHFFFAOYSA-L disodium;carboxylatooxy carbonate Chemical compound [Na+].[Na+].[O-]C(=O)OOC([O-])=O VTIIJXUACCWYHX-UHFFFAOYSA-L 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229960001484 edetic acid Drugs 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- BEFDCLMNVWHSGT-UHFFFAOYSA-N ethenylcyclopentane Chemical compound C=CC1CCCC1 BEFDCLMNVWHSGT-UHFFFAOYSA-N 0.000 description 1
- 125000004494 ethyl ester group Chemical group 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 125000005313 fatty acid group Chemical group 0.000 description 1
- 210000003811 finger Anatomy 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 description 1
- 229940050410 gluconate Drugs 0.000 description 1
- 239000000174 gluconic acid Substances 0.000 description 1
- 235000012208 gluconic acid Nutrition 0.000 description 1
- 229920001477 hydrophilic polymer Polymers 0.000 description 1
- 230000000774 hypoallergenic effect Effects 0.000 description 1
- JBFYUZGYRGXSFL-UHFFFAOYSA-N imidazolide Chemical compound C1=C[N-]C=N1 JBFYUZGYRGXSFL-UHFFFAOYSA-N 0.000 description 1
- MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical compound C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 description 1
- 150000002462 imidazolines Chemical class 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 230000003204 osmotic effect Effects 0.000 description 1
- RARSHUDCJQSEFJ-UHFFFAOYSA-N p-Hydroxypropiophenone Chemical compound CCC(=O)C1=CC=C(O)C=C1 RARSHUDCJQSEFJ-UHFFFAOYSA-N 0.000 description 1
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical class OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 239000008363 phosphate buffer Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229920001983 poloxamer Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 239000001508 potassium citrate Substances 0.000 description 1
- 229960002635 potassium citrate Drugs 0.000 description 1
- QEEAPRPFLLJWCF-UHFFFAOYSA-K potassium citrate (anhydrous) Chemical compound [K+].[K+].[K+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O QEEAPRPFLLJWCF-UHFFFAOYSA-K 0.000 description 1
- 235000011082 potassium citrates Nutrition 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 150000004728 pyruvic acid derivatives Chemical class 0.000 description 1
- 238000006722 reduction reaction Methods 0.000 description 1
- 235000015424 sodium Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 239000001509 sodium citrate Substances 0.000 description 1
- 229940045872 sodium percarbonate Drugs 0.000 description 1
- ADWNFGORSPBALY-UHFFFAOYSA-M sodium;2-[dodecyl(methyl)amino]acetate Chemical compound [Na+].CCCCCCCCCCCCN(C)CC([O-])=O ADWNFGORSPBALY-UHFFFAOYSA-M 0.000 description 1
- YKLJGMBLPUQQOI-UHFFFAOYSA-M sodium;oxidooxy(oxo)borane Chemical compound [Na+].[O-]OB=O YKLJGMBLPUQQOI-UHFFFAOYSA-M 0.000 description 1
- 235000010199 sorbic acid Nutrition 0.000 description 1
- 239000004334 sorbic acid Substances 0.000 description 1
- 229940075582 sorbic acid Drugs 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000012086 standard solution Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000008174 sterile solution Substances 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- DHCDFWKWKRSZHF-UHFFFAOYSA-L thiosulfate(2-) Chemical compound [O-]S([S-])(=O)=O DHCDFWKWKRSZHF-UHFFFAOYSA-L 0.000 description 1
- 210000003813 thumb Anatomy 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- AQLJVWUFPCUVLO-UHFFFAOYSA-N urea hydrogen peroxide Chemical compound OO.NC(N)=O AQLJVWUFPCUVLO-UHFFFAOYSA-N 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
Classifications
-
- 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
- A61L12/00—Methods or apparatus for disinfecting or sterilising contact lenses; Accessories therefor
- A61L12/08—Methods or apparatus for disinfecting or sterilising contact lenses; Accessories therefor using chemical substances
- A61L12/14—Organic compounds not covered by groups A61L12/10 or A61L12/12
- A61L12/141—Biguanides, e.g. chlorhexidine
- A61L12/142—Polymeric biguanides
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/36—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom five-membered rings
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- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Environmental Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Pest Control & Pesticides (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Agronomy & Crop Science (AREA)
- Chemical & Material Sciences (AREA)
- Plant Pathology (AREA)
- General Chemical & Material Sciences (AREA)
- Epidemiology (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Detergent Compositions (AREA)
- Apparatus For Disinfection Or Sterilisation (AREA)
- Eyeglasses (AREA)
Abstract
Description
Claims (16)
- 콘택트렌즈를 N-알킬-2-피롤리돈(여기서, 피롤리돈의 알킬 그룹은 C8-C20알킬잔기이다) 및 임의로는 추가의 살균제를 포함하는 수용액과 접촉시킴을 특징으로 하는 콘택트렌즈를 소독하는 방법.
- 제1항에 있어서, 알킬 잔기가 C8-C12잔기인 방법.
- 제2항에 있어서, 알킬 잔기가 옥틸, 데실 또는 도데실인 방법.
- 제1항 내지 제3항중 어느 한 항에 있어서, 용액중 피롤리돈의 농도가 용액의 약 0.001 내지 약 0.2중량%인 방법.
- 제1항 내지 제4항중 어느 한 항에 있어서, 추가의 살균제를 용액에 포함시키는 방법.
- 제5항에 있어서, 추가의 살균제가 폴리헥사메틸렌 비구아니드인 방법.
- N-알킬-2-피롤리돈 및 임의로는 추가의 살균제를 포함하는, 정제 또는 산제 형태의 수용성 고체 조성물로 포함하는 콘택트렌즈 소독용 조성물.
- C8-C20N-알킬-2-피롤리돈 및 임의로는 추가의 살균제 및 용매를 포함하는 렌즈 보존 용액.
- 제8항에 있어서, 용매가 등장성 염수용액인 렌즈 보존 용액.
- (a) 수성 액체의 특정량이 함유됨을 표시하기 위한 눈금이 매겨진 용기 ; (b) 수용액중에 액침시킨 하나 이상의 콘택트렌즈를 지지시키는 장치 ; 및 (c) N-알킬-2-피롤리돈 및 임의로는 추가의 살균제를 포함하는 정제 또는 산제의 단위 투여량(이는 특정량의 수성 액체중에 용해시키는 경우 피롤리돈의 농도가 용액의 약 0.001 내지 약 0.2중량%인 액체를 생성시킨다)을 포함하는 콘택트랜즈 소독용 키트.
- 제10항에 있어서, 피롤리돈이 C8-C20알킬 피롤리돈인 키트.
- 콘택트렌즈 소독에 유용한 정제 또는 산제 형태의 수용성 고체 조성물을 제조하기 위한, N-알킬-2-피롤리돈(여기서, 알킬 그룹은 C8-C20알킬잔기이다)의 용도.
- 제12항에 있어서, 조성물이 추가의 살균제를 함유하는 용도.
- 렌즈 보존에 유용한 용액을 제조하기 위한, N-알킬-2-피톨리돈(여기서, 알킬 그룹은 C8-C20알킬잔기이다)의 용도.
- 제14항에 있어서, 용액이 추가의 살균제를 함유하는 용도.
- 제14항 또는 제15항에 있어서, 용매가 등장성 염수용액인 용도.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP07/439,769 | 1989-11-21 | ||
| US07/439,769 US5035859A (en) | 1989-11-21 | 1989-11-21 | Contact lens disinfecting system |
| PCT/US1990/006656 WO1991007192A1 (en) | 1989-11-21 | 1990-11-20 | Contact lens disinfecting system |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR950006932B1 true KR950006932B1 (ko) | 1995-06-26 |
Family
ID=23746067
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1019920701182A Expired - Lifetime KR950006932B1 (ko) | 1989-11-21 | 1990-11-20 | 콘택트렌즈 소독 시스템 |
Country Status (19)
| Country | Link |
|---|---|
| US (1) | US5035859A (ko) |
| EP (1) | EP0502074A1 (ko) |
| JP (1) | JPH0622543B2 (ko) |
| KR (1) | KR950006932B1 (ko) |
| CN (1) | CN1051841A (ko) |
| AU (1) | AU636942B2 (ko) |
| BR (1) | BR9007858A (ko) |
| CA (1) | CA2069094A1 (ko) |
| CS (1) | CS574590A2 (ko) |
| HU (2) | HUT60636A (ko) |
| IE (1) | IE904184A1 (ko) |
| IL (1) | IL96416A (ko) |
| MY (1) | MY106166A (ko) |
| NZ (1) | NZ236145A (ko) |
| PH (1) | PH27308A (ko) |
| PL (1) | PL287846A1 (ko) |
| PT (1) | PT95937A (ko) |
| WO (1) | WO1991007192A1 (ko) |
| ZA (1) | ZA909309B (ko) |
Families Citing this family (31)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU636908B2 (en) * | 1989-08-01 | 1993-05-13 | Schering Corporation | Contact lens disinfecting system |
| US5399284A (en) * | 1991-04-03 | 1995-03-21 | Chemische Fabrik Dr. Weigert (Gmbh & Co.) | Process for removing starch-containing contamination from dishes and surfactant concentrates suitable for this process |
| AU2668192A (en) * | 1991-10-21 | 1993-05-21 | Isp Investments Inc. | Oil removal compositions |
| US5470508A (en) * | 1992-01-24 | 1995-11-28 | Isp Investments Inc. | Aqueous oil removal composition containing higher-alkyl pyrrolidone |
| EP0639070B2 (en) * | 1992-05-06 | 2010-09-08 | Alcon Laboratories, Inc. | Use of borate-polyol complexes in ophthalmic compositions |
| US5424072A (en) * | 1992-07-27 | 1995-06-13 | Isp Investments Inc. | Water soluble wetting agent for pesticide formulations |
| US5323337A (en) * | 1992-08-04 | 1994-06-21 | Loral Aerospace Corp. | Signal detector employing mean energy and variance of energy content comparison for noise detection |
| WO1994019027A1 (en) * | 1993-02-26 | 1994-09-01 | Wesley-Jessen Corporation | Method and composition for disinfecting contact lenses |
| JP3686434B2 (ja) * | 1993-10-01 | 2005-08-24 | 千寿製薬株式会社 | コンタクトレンズ用剤の安定化方法 |
| US5935584A (en) * | 1994-01-13 | 1999-08-10 | Elizabeth Arden Company | Vitamin C delivery system |
| EP0782610A4 (en) * | 1994-09-23 | 1999-07-28 | Church & Dwight Co Inc | AQUEOUS CLEANER FOR METALS |
| WO1996025183A2 (en) * | 1995-02-17 | 1996-08-22 | Allergan, Inc. | Ophthalmic compositions including peptides and peptide derivatives and methods for using same |
| US5888752A (en) * | 1995-05-16 | 1999-03-30 | Bayer Corporation | Universal rinse reagent and method for use in hematological analyses of whole blood samples |
| US5741520A (en) * | 1995-10-06 | 1998-04-21 | Southland, Ltd. | Disinfectant effervescent tablet formulation |
| US5922279A (en) * | 1996-02-28 | 1999-07-13 | Bausch & Lomb Incorporated | Treatment of contact lenses with an aqueous solution including pyrrolidone compounds |
| JPH1071190A (ja) * | 1996-08-30 | 1998-03-17 | Tomey Technol Corp | コンタクトレンズ用液剤 |
| ES2286862T3 (es) * | 1997-11-12 | 2007-12-01 | BAUSCH & LOMB INCORPORATED | Limpieza y desinfeccion de lentillas de contacto con biguanida y un tampon de fosfato y borato. |
| US6063745A (en) * | 1997-11-26 | 2000-05-16 | Allergan | Mutli-purpose contact lens care compositions |
| JP4629976B2 (ja) * | 2001-08-16 | 2011-02-09 | ヴァイトマン プラスチックス テクノロジー アクチエンゲゼルシャフト | シーリングカバーの製造方法ならびにその方法によって製造されたシーリングカバー |
| US20080095863A1 (en) * | 2006-10-24 | 2008-04-24 | Alcon Manufacturing Ltd. | 2-pyrrolidone derivatives for preservation of ophthalmic, otic and nasal compositions |
| WO2008052037A2 (en) * | 2006-10-24 | 2008-05-02 | Alcon Research, Ltd. | Packaging materials for formulations containing 2-pyrrolidone derivatives |
| GB201010374D0 (en) * | 2010-06-21 | 2010-08-04 | Mtp Innovations Ltd | Disinfectant composition |
| FR2984351B1 (fr) * | 2011-12-20 | 2015-03-13 | Condat Sa | Nouveau lubrifiant pour la forge sous forme de poudre ou de poudre compactee |
| US9241483B2 (en) * | 2012-06-29 | 2016-01-26 | Contec, Inc. | Fast-acting disinfectant compositions for reducing or eliminating microbial populations |
| WO2017044062A1 (en) * | 2015-09-09 | 2017-03-16 | Yeditepe Universitesi | Antimicrobial and antiviral composite polymer surfaces |
| EP3879984B1 (en) | 2018-11-12 | 2024-05-29 | Diversey, Inc. | C3-c6 n-alkyl-gamma-butyrolactam- and peroxygen-containing antimicrobial compositions |
| US20210315207A1 (en) * | 2018-12-04 | 2021-10-14 | Virox Technologies Inc. | C3-c5 n-alkyl-gamma-butyrolactam-containing antimicrobial compositions and uses thereof |
| US12053540B2 (en) | 2018-12-04 | 2024-08-06 | Virox Technologies Inc. | Antimicrobial compositions containing solvents including a C3-C5 N-alkyl-gamma-butyrolactam |
| US12532886B2 (en) | 2018-12-04 | 2026-01-27 | Virox Technologies Inc. | Method of killing microbes using C3-C5 n-alkyl-gamma-butyrolactams and antimicrobial compositions containing same |
| BR112021006553A2 (pt) * | 2018-12-04 | 2021-07-13 | Virox Technologies Inc. | composições antimicrobianas contendo c3-c5 n-alquil-gama-butirolactama e usos dos mesmos |
| US12052990B2 (en) | 2018-12-04 | 2024-08-06 | Virox Technologies Inc. | C3-C5 n-alkyl-gamma-butyrolactam containing antimicrobial compositions and methods of using same |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4013576A (en) * | 1973-11-21 | 1977-03-22 | Wesley-Jessen Inc. | Contact lens treating composition |
| FR2517208A1 (fr) * | 1981-12-02 | 1983-06-03 | Pos Lab | Composition pour le nettoyage et la sterilisation de protheses oculaires et auriculaires |
| US4836986A (en) * | 1984-09-28 | 1989-06-06 | Bausch & Lomb Incorporated | Disinfecting and preserving systems and methods of use |
| US4782078A (en) * | 1986-01-16 | 1988-11-01 | Ppg Industries, Inc. | Halophor biocidal compositions |
| DE3751821T2 (de) * | 1986-06-27 | 1996-10-31 | Isp Investments Inc | Oberflächenaktive laktame |
| US4719287A (en) * | 1986-06-27 | 1988-01-12 | Gaf Corporation | Higher alkyl pyrrolidone extractants for water soluble phenolic or carboxylic antibiotics |
| US4828569A (en) * | 1987-07-30 | 1989-05-09 | Wen-Don Corporation | Detergent compositions for removing iodine stains |
-
1989
- 1989-11-21 US US07/439,769 patent/US5035859A/en not_active Expired - Fee Related
-
1990
- 1990-11-20 ZA ZA909309A patent/ZA909309B/xx unknown
- 1990-11-20 CS CS905745A patent/CS574590A2/cs unknown
- 1990-11-20 IL IL9641690A patent/IL96416A/en not_active IP Right Cessation
- 1990-11-20 WO PCT/US1990/006656 patent/WO1991007192A1/en not_active Ceased
- 1990-11-20 MY MYPI90002037A patent/MY106166A/en unknown
- 1990-11-20 NZ NZ236145A patent/NZ236145A/xx unknown
- 1990-11-20 AU AU68796/91A patent/AU636942B2/en not_active Ceased
- 1990-11-20 JP JP3500852A patent/JPH0622543B2/ja not_active Expired - Lifetime
- 1990-11-20 PT PT95937A patent/PT95937A/pt not_active Application Discontinuation
- 1990-11-20 IE IE418490A patent/IE904184A1/en unknown
- 1990-11-20 PH PH41584A patent/PH27308A/en unknown
- 1990-11-20 PL PL28784690A patent/PL287846A1/xx unknown
- 1990-11-20 HU HU9201684A patent/HUT60636A/hu unknown
- 1990-11-20 CA CA002069094A patent/CA2069094A1/en not_active Abandoned
- 1990-11-20 EP EP91900075A patent/EP0502074A1/en not_active Ceased
- 1990-11-20 HU HU9201684A patent/HU211199B/hu not_active IP Right Cessation
- 1990-11-20 KR KR1019920701182A patent/KR950006932B1/ko not_active Expired - Lifetime
- 1990-11-20 BR BR909007858A patent/BR9007858A/pt unknown
- 1990-11-21 CN CN90109297A patent/CN1051841A/zh active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| US5035859A (en) | 1991-07-30 |
| AU6879691A (en) | 1991-06-13 |
| CA2069094A1 (en) | 1991-05-22 |
| HU9201684D0 (en) | 1992-09-28 |
| IE904184A1 (en) | 1991-05-22 |
| JPH0622543B2 (ja) | 1994-03-30 |
| BR9007858A (pt) | 1992-09-29 |
| PT95937A (pt) | 1991-09-13 |
| AU636942B2 (en) | 1993-05-13 |
| EP0502074A1 (en) | 1992-09-09 |
| PH27308A (en) | 1993-05-28 |
| CN1051841A (zh) | 1991-06-05 |
| HUT60636A (en) | 1992-10-28 |
| IL96416A (en) | 1995-01-24 |
| PL287846A1 (en) | 1991-07-29 |
| ZA909309B (en) | 1991-07-31 |
| NZ236145A (en) | 1993-04-28 |
| WO1991007192A1 (en) | 1991-05-30 |
| MY106166A (en) | 1995-03-31 |
| CS574590A2 (en) | 1991-12-17 |
| HU211199B (en) | 1995-11-28 |
| JPH05500019A (ja) | 1993-01-14 |
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