JPS6345210A - Sterilizing composition and sterilization - Google Patents
Sterilizing composition and sterilizationInfo
- Publication number
- JPS6345210A JPS6345210A JP62201681A JP20168187A JPS6345210A JP S6345210 A JPS6345210 A JP S6345210A JP 62201681 A JP62201681 A JP 62201681A JP 20168187 A JP20168187 A JP 20168187A JP S6345210 A JPS6345210 A JP S6345210A
- Authority
- JP
- Japan
- Prior art keywords
- lactic acid
- acid
- acidic substance
- composition
- sterilizing 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.)
- Pending
Links
- 239000000203 mixture Substances 0.000 title claims description 62
- 230000001954 sterilising effect Effects 0.000 title claims description 42
- 238000004659 sterilization and disinfection Methods 0.000 title claims description 24
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 claims description 66
- 239000004310 lactic acid Substances 0.000 claims description 33
- 235000014655 lactic acid Nutrition 0.000 claims description 33
- QBWCMBCROVPCKQ-UHFFFAOYSA-N chlorous acid Chemical compound OCl=O QBWCMBCROVPCKQ-UHFFFAOYSA-N 0.000 claims description 26
- 239000000126 substance Substances 0.000 claims description 19
- 238000000034 method Methods 0.000 claims description 18
- 230000001580 bacterial effect Effects 0.000 claims description 16
- 229910001919 chlorite Inorganic materials 0.000 claims description 16
- 229910052619 chlorite group Inorganic materials 0.000 claims description 16
- 230000002378 acidificating effect Effects 0.000 claims description 12
- 239000012736 aqueous medium Substances 0.000 claims description 7
- 150000007522 mineralic acids Chemical class 0.000 claims description 6
- 150000007524 organic acids Chemical class 0.000 claims description 4
- 239000007921 spray Substances 0.000 claims description 3
- 229940077239 chlorous acid Drugs 0.000 claims description 2
- 150000003839 salts Chemical class 0.000 claims description 2
- 238000004506 ultrasonic cleaning Methods 0.000 claims description 2
- OSVXSBDYLRYLIG-UHFFFAOYSA-N dioxidochlorine(.) Chemical compound O=Cl=O OSVXSBDYLRYLIG-UHFFFAOYSA-N 0.000 description 35
- 235000019398 chlorine dioxide Nutrition 0.000 description 21
- 239000002253 acid Substances 0.000 description 15
- 239000004155 Chlorine dioxide Substances 0.000 description 14
- 241000894006 Bacteria Species 0.000 description 13
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 12
- UKLNMMHNWFDKNT-UHFFFAOYSA-M sodium chlorite Chemical compound [Na+].[O-]Cl=O UKLNMMHNWFDKNT-UHFFFAOYSA-M 0.000 description 11
- 229960002218 sodium chlorite Drugs 0.000 description 11
- 239000000243 solution Substances 0.000 description 9
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 8
- 238000004140 cleaning Methods 0.000 description 8
- 239000000645 desinfectant Substances 0.000 description 8
- 230000000249 desinfective effect Effects 0.000 description 8
- 230000002070 germicidal effect Effects 0.000 description 8
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 7
- 230000000844 anti-bacterial effect Effects 0.000 description 7
- 239000000460 chlorine Substances 0.000 description 7
- 229910052801 chlorine Inorganic materials 0.000 description 7
- 150000001875 compounds Chemical class 0.000 description 7
- 206010052428 Wound Diseases 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
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 208000027418 Wounds and injury Diseases 0.000 description 5
- 150000007513 acids Chemical class 0.000 description 5
- 210000004027 cell Anatomy 0.000 description 5
- 235000013305 food Nutrition 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- 231100000419 toxicity Toxicity 0.000 description 5
- 230000001988 toxicity Effects 0.000 description 5
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 235000011054 acetic acid Nutrition 0.000 description 4
- 239000000443 aerosol Substances 0.000 description 4
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 4
- 210000002421 cell wall Anatomy 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000007789 gas Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 244000005700 microbiome Species 0.000 description 4
- 238000011012 sanitization Methods 0.000 description 4
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 239000007844 bleaching agent Substances 0.000 description 3
- 239000006172 buffering agent Substances 0.000 description 3
- 239000006227 byproduct Substances 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 150000001805 chlorine compounds Chemical class 0.000 description 3
- -1 chlorite ions Chemical class 0.000 description 3
- BEFDCLMNVWHSGT-UHFFFAOYSA-N ethenylcyclopentane Chemical compound C=CC1CCCC1 BEFDCLMNVWHSGT-UHFFFAOYSA-N 0.000 description 3
- WQYVRQLZKVEZGA-UHFFFAOYSA-N hypochlorite Inorganic materials Cl[O-] WQYVRQLZKVEZGA-UHFFFAOYSA-N 0.000 description 3
- 239000000543 intermediate Substances 0.000 description 3
- 231100001231 less toxic Toxicity 0.000 description 3
- 230000002335 preservative effect Effects 0.000 description 3
- 239000004334 sorbic acid Substances 0.000 description 3
- 235000010199 sorbic acid Nutrition 0.000 description 3
- 229940075582 sorbic acid Drugs 0.000 description 3
- 230000009182 swimming Effects 0.000 description 3
- 210000001519 tissue Anatomy 0.000 description 3
- TUSDEZXZIZRFGC-UHFFFAOYSA-N 1-O-galloyl-3,6-(R)-HHDP-beta-D-glucose Natural products OC1C(O2)COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC1C(O)C2OC(=O)C1=CC(O)=C(O)C(O)=C1 TUSDEZXZIZRFGC-UHFFFAOYSA-N 0.000 description 2
- HORNXRXVQWOLPJ-UHFFFAOYSA-N 3-chlorophenol Chemical compound OC1=CC=CC(Cl)=C1 HORNXRXVQWOLPJ-UHFFFAOYSA-N 0.000 description 2
- CYDQOEWLBCCFJZ-UHFFFAOYSA-N 4-(4-fluorophenyl)oxane-4-carboxylic acid Chemical compound C=1C=C(F)C=CC=1C1(C(=O)O)CCOCC1 CYDQOEWLBCCFJZ-UHFFFAOYSA-N 0.000 description 2
- 241000251468 Actinopterygii Species 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- 102000004190 Enzymes Human genes 0.000 description 2
- 108090000790 Enzymes Proteins 0.000 description 2
- 239000001263 FEMA 3042 Substances 0.000 description 2
- LRBQNJMCXXYXIU-PPKXGCFTSA-N Penta-digallate-beta-D-glucose Natural products OC1=C(O)C(O)=CC(C(=O)OC=2C(=C(O)C=C(C=2)C(=O)OC[C@@H]2[C@H]([C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)O2)OC(=O)C=2C=C(OC(=O)C=3C=C(O)C(O)=C(O)C=3)C(O)=C(O)C=2)O)=C1 LRBQNJMCXXYXIU-PPKXGCFTSA-N 0.000 description 2
- 241000700605 Viruses Species 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 230000002421 anti-septic effect Effects 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 230000003115 biocidal effect Effects 0.000 description 2
- 238000004061 bleaching Methods 0.000 description 2
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 239000001530 fumaric acid Substances 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- QWPPOHNGKGFGJK-UHFFFAOYSA-N hypochlorous acid Chemical group ClO QWPPOHNGKGFGJK-UHFFFAOYSA-N 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 230000001590 oxidative effect Effects 0.000 description 2
- 150000002989 phenols Chemical class 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000003755 preservative agent Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000003380 propellant Substances 0.000 description 2
- 238000007086 side reaction Methods 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 239000001540 sodium lactate Substances 0.000 description 2
- 229940005581 sodium lactate Drugs 0.000 description 2
- 235000011088 sodium lactate Nutrition 0.000 description 2
- 235000015523 tannic acid Nutrition 0.000 description 2
- LRBQNJMCXXYXIU-NRMVVENXSA-N tannic acid Chemical compound OC1=C(O)C(O)=CC(C(=O)OC=2C(=C(O)C=C(C=2)C(=O)OC[C@@H]2[C@H]([C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)O2)OC(=O)C=2C=C(OC(=O)C=3C=C(O)C(O)=C(O)C=3)C(O)=C(O)C=2)O)=C1 LRBQNJMCXXYXIU-NRMVVENXSA-N 0.000 description 2
- 229940033123 tannic acid Drugs 0.000 description 2
- 229920002258 tannic acid Polymers 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- 239000000080 wetting agent Substances 0.000 description 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
- 240000005528 Arctium lappa Species 0.000 description 1
- 235000003130 Arctium lappa Nutrition 0.000 description 1
- 235000008078 Arctium minus Nutrition 0.000 description 1
- ZKQDCIXGCQPQNV-UHFFFAOYSA-N Calcium hypochlorite Chemical compound [Ca+2].Cl[O-].Cl[O-] ZKQDCIXGCQPQNV-UHFFFAOYSA-N 0.000 description 1
- 241000222120 Candida <Saccharomycetales> Species 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- QDHHCQZDFGDHMP-UHFFFAOYSA-N Chloramine Chemical compound ClN QDHHCQZDFGDHMP-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- 102000004867 Hydro-Lyases Human genes 0.000 description 1
- 108090001042 Hydro-Lyases Proteins 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
- JVTAAEKCZFNVCJ-UHFFFAOYSA-M Lactate Chemical compound CC(O)C([O-])=O JVTAAEKCZFNVCJ-UHFFFAOYSA-M 0.000 description 1
- 240000007643 Phytolacca americana Species 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 241000588767 Proteus vulgaris Species 0.000 description 1
- 229920001131 Pulp (paper) Polymers 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- 241000607479 Yersinia pestis Species 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 229960000583 acetic acid Drugs 0.000 description 1
- 239000012445 acidic reagent Substances 0.000 description 1
- 239000003619 algicide Substances 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 210000003484 anatomy Anatomy 0.000 description 1
- 230000015572 biosynthetic process Effects 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
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 230000005779 cell damage Effects 0.000 description 1
- 230000010261 cell growth Effects 0.000 description 1
- 230000019522 cellular metabolic process Effects 0.000 description 1
- 235000013339 cereals Nutrition 0.000 description 1
- 235000013351 cheese Nutrition 0.000 description 1
- WIIZWVCIJKGZOK-RKDXNWHRSA-N chloramphenicol Chemical compound ClC(Cl)C(=O)N[C@H](CO)[C@H](O)C1=CC=C([N+]([O-])=O)C=C1 WIIZWVCIJKGZOK-RKDXNWHRSA-N 0.000 description 1
- 229940099041 chlorine dioxide Drugs 0.000 description 1
- 229940097572 chloromycetin Drugs 0.000 description 1
- 229930002875 chlorophyll Natural products 0.000 description 1
- 235000019804 chlorophyll Nutrition 0.000 description 1
- ATNHDLDRLWWWCB-AENOIHSZSA-M chlorophyll a Chemical compound C1([C@@H](C(=O)OC)C(=O)C2=C3C)=C2N2C3=CC(C(CC)=C3C)=[N+]4C3=CC3=C(C=C)C(C)=C5N3[Mg-2]42[N+]2=C1[C@@H](CCC(=O)OC\C=C(/C)CCC[C@H](C)CCC[C@H](C)CCCC(C)C)[C@H](C)C2=C5 ATNHDLDRLWWWCB-AENOIHSZSA-M 0.000 description 1
- 229960004106 citric acid Drugs 0.000 description 1
- 235000015165 citric acid Nutrition 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 210000000805 cytoplasm Anatomy 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000000593 degrading effect Effects 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000002360 explosive Substances 0.000 description 1
- 238000000855 fermentation Methods 0.000 description 1
- 230000004151 fermentation Effects 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 1
- 229960002598 fumaric acid Drugs 0.000 description 1
- 235000011087 fumaric acid Nutrition 0.000 description 1
- 238000003958 fumigation Methods 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 231100001261 hazardous Toxicity 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 229940001447 lactate Drugs 0.000 description 1
- 229960000448 lactic acid Drugs 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 229960002523 mercuric chloride Drugs 0.000 description 1
- LWJROJCJINYWOX-UHFFFAOYSA-L mercury dichloride Chemical compound Cl[Hg]Cl LWJROJCJINYWOX-UHFFFAOYSA-L 0.000 description 1
- 230000002503 metabolic effect Effects 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- 230000003641 microbiacidal effect Effects 0.000 description 1
- 210000003205 muscle Anatomy 0.000 description 1
- 150000007523 nucleic acids Chemical class 0.000 description 1
- 102000039446 nucleic acids Human genes 0.000 description 1
- 108020004707 nucleic acids Proteins 0.000 description 1
- 235000019645 odor Nutrition 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000005416 organic matter Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000009896 oxidative bleaching Methods 0.000 description 1
- 230000020477 pH reduction Effects 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 229940007042 proteus vulgaris Drugs 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000000527 sonication Methods 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- 230000003330 sporicidal effect Effects 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- 235000019640 taste Nutrition 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 231100000816 toxic dose Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 239000001226 triphosphate Substances 0.000 description 1
- 235000011178 triphosphate Nutrition 0.000 description 1
- UNXRWKVEANCORM-UHFFFAOYSA-N triphosphoric acid Chemical compound OP(O)(=O)OP(O)(=O)OP(O)(O)=O UNXRWKVEANCORM-UHFFFAOYSA-N 0.000 description 1
- 238000002604 ultrasonography Methods 0.000 description 1
- 239000000052 vinegar Substances 0.000 description 1
- 235000021419 vinegar Nutrition 0.000 description 1
- 230000003253 viricidal effect Effects 0.000 description 1
- 235000011845 white flour Nutrition 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
Landscapes
- Apparatus For Disinfection Or Sterilisation (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Abstract] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
本発明は殺菌用組成物および殺菌方法て関し、特に洗浄
、衛生化および殺菌のための種々の用途に有利に使用す
ることのできる組成物に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a sterilizing composition and a sterilizing method, and more particularly to a composition that can be advantageously used in a variety of cleaning, sanitizing, and sterilizing applications.
種々のタイツの洗浄、衛生化および殺菌のtめの組成物
中に、塩素化合物を用いることはよく知られている。こ
の塩素化合物は、例えば、第1次世昇天戦中に傷口洗浄
剤として用いられ九次亜塩素酸ナトリウムや、m−クロ
ロフェノールの如き塩素化フェノール類があるが、これ
ら化合物はある場合には、非塩素化フェノール類に比較
して殺菌作用が強い反面毒性が弱く、それ故m−クロロ
フェノール係数は、7.4 (B、 typhosus
)および5.8 (S、 aureus)である。The use of chlorine compounds in various tights cleaning, sanitizing and disinfecting compositions is well known. These chlorine compounds include, for example, chlorinated phenols such as nine-hypohydrous sodium chlorite, which was used as a wound cleansing agent during the First War of Ascension, and m-chlorophenol. Compared to non-chlorinated phenols, it has a stronger bactericidal effect but less toxicity, so the m-chlorophenol coefficient is 7.4 (B, typhosus
) and 5.8 (S, aureus).
”を何らかの形で殺菌に有用であることが認められてい
る他の塩素化合物は、その使用制限がなしとすると、塩
素ガス自体、二酸化塩素、クロルアミンT1塩化第2水
銀、次亜塩素酸カルシウム(標準的表水泳プール殺菌剤
)、クロルアピクリン(害虫駆除剤)、クロロフォルム
(薫蒸消毒剤)クロルアダン(殺虫剤)、塩化亜鉛(保
存剤)およびクロロマイセチン(抗生剤)等がある。Other chlorine compounds that have been recognized to be useful in some form of disinfection are chlorine gas itself, chlorine dioxide, chloramine T1, mercuric chloride, calcium hypochlorite (assuming there are no restrictions on their use). These include standard surface swimming pool disinfectants), chlorapicrin (pest control agent), chloroform (fumigation disinfectant), chloradan (insecticide), zinc chloride (preservative) and chloromycetin (antibiotic).
とりわけ二酸化塩素は有効な殺菌剤であることが知られ
ている。この化合物は極めて用途が広く、まt漂白剤と
して、例えば、綿や木材パルプその他セルロース性繊維
物質中に存在する天然の着色剤の酸化漂白に用いられて
おり、酸化機能を行うにもかかわらずFR雄物質に関し
て無害である。Chlorine dioxide, in particular, is known to be an effective disinfectant. This compound is extremely versatile and is used as a bleaching agent, for example in the oxidative bleaching of natural colorants present in cotton, wood pulp and other cellulosic fibrous materials, even though it performs an oxidizing function. Harmless with respect to FR male material.
更に、二酸化塩素は以前から上水道の処理に用いられて
おり、′1几現在粉剤として水泳プール用に、および液
剤として家庭及び工場の洗浄及び殺菌用に市販されてい
る。一般に二酸化塩素は、臭や味の除去、異類その他の
有機物質の破壊や除去の点でガス状の塩素よりも優れて
おり、殺菌剤、殺ビールス剤まtは殺胞子剤として塩素
ガスに優ることはないとしても、少くとも同様に有効で
あると考えられており、更に防腐性の点においても塩素
のようにPHに対して敏感ではない。すなわち二酸化塩
素にその殺菌能力を塩素ガスよりはるかに大きい程度ま
で、また、より広いPH範囲にわ乏って保持するという
利点を有する。Additionally, chlorine dioxide has long been used in the treatment of water supplies and is currently commercially available as a powder for swimming pools and as a liquid for cleaning and disinfecting homes and industries. In general, chlorine dioxide is superior to gaseous chlorine in eliminating odors and tastes, and in destroying and removing foreign and other organic substances, and is superior to chlorine gas as a disinfectant, virucidal, or sporicidal agent. It is believed to be at least as effective, if not more effective, and is also less sensitive to pH than chlorine in terms of preservative properties. Thus, chlorine dioxide has the advantage of retaining its disinfecting ability to a much greater degree than chlorine gas and over a wider pH range.
しかしながら、上記のように二酸化塩素の使用により得
られる多くの有利さにもかかわらず、実際にはなおいく
つかの困難に出会う。However, despite the many advantages afforded by the use of chlorine dioxide as described above, some difficulties are still encountered in practice.
例えば、濃厚ガスとしての二酸化塩素は、爆発性があり
、ま之有毒である几め、通常、中間ま之は少量のユーザ
ーに対しては、ガス状では輸送されない。それ故、貯M
、輸送および取扱いの点から安全な亜塩素酸す) IJ
ウム粉末のような二酸化塩素を遊離する化合物を用いる
のが普通である。該物質から二酸化塩素を発生させるに
は、通常次に示す三つの方法のいずれかにより行う。For example, chlorine dioxide, as a concentrated gas, is explosive and toxic, and intermediate gases are usually not transported in gaseous form to small volume users. Therefore, saving M
, safe transport and handling) IJ
It is common to use compounds that liberate chlorine dioxide, such as chlorine powder. Chlorine dioxide is usually generated from the substance by one of the following three methods.
(1)酸の添加
H” + NaC402HC202+Na”5HC−C
O24CJ 02+HC,!+2H20(2)漂白剤(
次亜塩素酸基)の添加
2NaC−!02+NaC10+H2O2CJOz+N
aOH+NaCJ’
(3)塩素の添加
2NaCJO2+C422CJO2+2NaCJ二酸化
塩素、これは以後CjQzとも呼ぶが、これの反応(1
)による発生は、一般に比較的安価な無機の酸、例えば
塩酸、硫酸などによりもtらされる。家庭での使用には
、時々、リン酸又は酢酸(酢)が指示されるが、これは
、これら酸が取扱いに比較的安全であシ、又、一般に容
易に手に入る九めである。(1) Addition of acid H"+NaC402HC202+Na"5HC-C
O24CJ 02+HC,! +2H20 (2) Bleach (
Addition of hypochlorous acid group) 2NaC-! 02+NaC10+H2O2CJOz+N
aOH+NaCJ' (3) Addition of chlorine 2NaCJO2+C422CJO2+2NaCJ chlorine dioxide, which is also referred to as CjQz from now on, the reaction (1
) is also generally caused by relatively inexpensive inorganic acids such as hydrochloric acid and sulfuric acid. For home use, phosphoric acid or acetic acid (vinegar) are sometimes indicated, since these acids are relatively safe to handle and are generally readily available.
これまで推實され又実施されて来之よつな酸により亜塩
素酸ナトリウムからのC2O4の発生は、大部分効果の
ないことが証明されている。例えば、使用され之酸性物
質がそれにより放出され7をCJQzと反応し、有用な
目的に利用し得る活、性成分の有効量を減じる傾向がし
ばしば見い出されている。Conventional acid generation of C2O4 from sodium chlorite hitherto estimated and practiced has proven to be largely ineffective. For example, it has often been found that the acidic substances used thereby tend to be released and react with CJQz, reducing the effective amount of the active ingredients available for useful purposes.
更に、亜塩素酸ナトリウムの酸性化に由来する組成物は
通常所望の殺菌効果、殊に殺菌率の点からの所望の効果
を示さない。この欠点を補う之めに、亜塩素酸ナトIJ
ウムと酸の濃度を上げる必要が生じ、これが殊にこの組
成物を閉め切っ之空間で用いる時には、毒性の問題を生
じ得ることになる。Furthermore, compositions derived from acidification of sodium chlorite usually do not exhibit the desired disinfecting effect, especially in terms of disinfection rate. In order to compensate for this drawback, sodium chlorite IJ
It becomes necessary to increase the concentration of umum and acid, which can lead to toxicity problems, especially when the composition is used in an enclosed space.
亜塩素酸ナトリウムと酸性物質の相互作用から得られる
組成物は、C2O4や亜塩素酸のような活性塩素を含む
副生成物に対する真に有効な溶媒を提供しないというこ
とからもう1つの問題が生ずる。Another problem arises from the fact that the compositions resulting from the interaction of sodium chlorite and acidic substances do not provide a truly effective solvent for by-products containing active chlorine such as C2O4 and chlorite. .
これら、ガス性成分をある程度吸い込むと、勿論健康に
害があり、その之め個人の安全性に対する危険が重要な
問題となる。友しかに、この毒性の問題は殺菌組成物の
一般的な使用について、殊に人間の処理の点で厳しい制
限tnするものである。Inhalation of these gaseous components to some extent is, of course, harmful to health, and therefore the risk to personal safety becomes an important issue. Admittedly, this toxicity problem places severe limitations on the general use of fungicidal compositions, particularly for human treatment.
本発明者は上記のような欠点を克服する九めに種々研究
し、実験を行ったが、亜塩素酸塩と反応する各種酸性物
質のうち乳酸を選ぶことにより、すぐれ几殺菌効果を得
られ、実用上極めて有利な殺菌剤となることを見い出し
九〇
本発明はこの知見に基づきなされ几もので広範囲の条件
下で安定して細菌および細菌を生ずる有機体その他有害
物質に対し高度な殺菌効果を生ずるとともに、逃散的副
反応による有効成分の損失を最少とし、しかも通常その
使用が指示されるような条件下での毒性が無視し得る程
度のものであり、またそれ故に食品置場、rutens
il、医療用バードウニア、人間の解剖その他の種々の
タイプの傷の殺菌処理に関連し九極めて有用な殺菌用組
成物および殺菌方法を提供するものである。The present inventor conducted various studies and experiments to overcome the above-mentioned drawbacks, and found that by selecting lactic acid from various acidic substances that react with chlorite, an excellent sterilization effect could be obtained. Based on this knowledge, the present invention has been made based on this knowledge and has a high degree of bactericidal effect against bacteria, bacteria-producing organisms, and other harmful substances, stably under a wide range of conditions. It also minimizes the loss of active ingredient due to fugitive side reactions, and has negligible toxicity under the conditions under which its use is normally indicated, and is therefore suitable for food storage, rutens, etc.
The present invention provides a sterilizing composition and a sterilizing method that are extremely useful in connection with the sterilizing treatment of various types of wounds, including medical burdock, human anatomy, and other types of wounds.
前述及び関連の諸口的は本発明により得られ、本発明は
そのより広い意味において殺菌性金有する組成物および
較菌方法を提供するものであり、この組成物の製造法は
亜塩素酸ナトリウムを、有機酸及びこれと無機酸との混
合物より成る群より選ばれた本質的に水溶性の酸性物質
と接触させることを含み、この酸性物質は少くとも15
重1パーセントの乳酸を含み、又この接触は水性媒体中
で又その水性媒体のPHt約7以下に下げるのに充分な
量の核酸の存在下に行なわれるものである。The foregoing and related aspects are obtained by the present invention, which in its broader sense provides a germicidal composition and a method for calibrating the composition, which method comprises adding sodium chlorite to the composition. , with an essentially water-soluble acidic substance selected from the group consisting of organic acids and mixtures thereof with inorganic acids, the acidic substance having at least 15
1 percent by weight of lactic acid, and the contacting is in an aqueous medium and in the presence of an amount of nucleic acid sufficient to lower the PHt of the aqueous medium to about 7 or less.
更にこの実施態様において本発明は殺菌組成物それ自体
又はそれをその場で生成し得る反応物質のいずれかを、
閉鎖され几空間と同じく種々の種類の物質を含む細菌担
体に使用することを含む前記組成物を利用する洗浄、衛
生化、及び殺菌の方法を提供する。Further in this embodiment, the invention provides that either the germicidal composition itself or the reactants capable of producing it in situ,
A method of cleaning, sanitizing, and disinfecting is provided that utilizes the composition, including its use in closed, cubical spaces as well as bacterial carriers containing various types of materials.
ここに提供されている組成物及び方法における乳酸の使
用は重要である。例えば、この特別の化合物は前述の条
件下で亜塩素酸ナトリウムと協力して相乗的に働き非常
に効力のある殺菌組成物全提供することが知られている
。この結果はいささか驚くべきものである。なぜならば
通常乳酸はいくらか類似の酸化合物の場合のようにそれ
によシ生ずる副生成物の二酸化塩素と反応して、そうで
なければ有用な目的に役立つはずの乳酸と二酸化塩素と
の有効lを減少させるものと考えられるからである。又
、この反応中に生ずる乳酸塩は通常漂白作業や水道の殺
菌や有機物の除去の時には不純物と考えられもしよう。The use of lactic acid in the compositions and methods provided herein is significant. For example, this particular compound is known to work synergistically with sodium chlorite under the aforementioned conditions to provide a highly effective disinfectant composition. This result is somewhat surprising. This is because lactic acid normally reacts with the resulting by-product chlorine dioxide, as is the case with some similar acid compounds, to eliminate the available lactic acid and chlorine dioxide that would otherwise serve a useful purpose. This is because it is thought to reduce the Also, the lactate produced during this reaction would normally be considered an impurity during bleaching operations, water sterilization, and organic matter removal.
しかしながら、本発明ではこのような望しくない副反応
が、随伴する有害な効果と同様に、もしあつtとしても
、それが無視しうる程度に過ぎないことは明らかである
。However, it is clear that in the present invention, such undesirable side reactions, as well as the attendant deleterious effects, are negligible, if any at all.
この組成物を製造するには、乳酸を水性媒体中で亜塩素
酸ナトリウムと接触させ、この酸は該組成物のPHを約
7以下に下げるのに充分な程使用する。水道の必要条件
は通常この酸と亜塩素酸塩(より満されるが、これら両
物質は水性溶液中の濃度を変えて利用される。亜塩素酸
塩化合物と乳酸の相対的割合は水性媒体中のPHが約7
以下に々るように選ぶ。酸の必要量は勿論一部分は、混
合しfc時の酸と亜塩素酸塩組成物それぞれの全稀釈液
と同じく酸試薬溶液の強度により決定される。To prepare this composition, lactic acid is contacted with sodium chlorite in an aqueous medium, and the acid is used in an amount sufficient to lower the pH of the composition to about 7 or less. Water supply requirements are usually met by this acid and chlorite (both of these substances are utilized in varying concentrations in aqueous solution. The relative proportions of chlorite compounds and lactic acid are The pH inside is about 7
Choose from the following. The amount of acid required is of course determined in part by the strength of the acid reagent solution as well as the total dilution of the acid and chlorite compositions respectively at the time of mixing and fc.
しかし々から、必要量は凛準方法てより容易に前もって
決定することができる。However, the required amount can be determined in advance more easily in a reasonable manner.
亜塩素酸塩と乳酸との接触、即ち反応により得られる殺
菌組成物は、二酸化塩素、亜塩素駿、乳酸及び乳酸ナト
リウムを含む混合物を含んでいる。The disinfectant composition obtained by contacting or reacting chlorite with lactic acid comprises a mixture comprising chlorine dioxide, chlorite, lactic acid and sodium lactate.
前述の物質の平衡混合物は錯化合物の形で存在すると思
われ、分析によると少くとも上に列挙した成分の存在が
示されている。この混合物又は錯化合物は比較的安定で
ある。しかしながら、最適の殺菌効果の之めにはこの組
成物をその生成から約48時間までの期間内に用いるべ
きである。しかしながら、乳酸と亜塩素酸化合物とが別
々のパッケージによりお互いに分離されているならば、
これは単−又は共通の容器を用いてできるであろうが、
この場合亜塩素酸塩と乳酸の材料の接触全使用時まで禁
じておくのであれば、棚ざらし期間についての制限は殆
んど無い。Equilibrium mixtures of the aforementioned substances are believed to exist in the form of complex compounds, and analysis shows the presence of at least the components listed above. This mixture or complex compound is relatively stable. However, for optimal bactericidal efficacy, the composition should be used within a period of up to about 48 hours after its preparation. However, if lactic acid and chlorite are separated from each other by separate packaging,
This could be done using a single or common container, but
In this case, if contact between chlorite and lactic acid materials is prohibited until the time of full use, there is almost no restriction on the period of exposure.
それ故、亜塩素酸塩と乳酸の材料全軽く指で圧し友だけ
で動くパルプ式調剤手段を備え之エア。Therefore, the chlorite and lactic acid ingredients are all lightly pressed with the fingers and are equipped with a pulp-type dispensing means that can be moved by just using the air.
ゾル型の別々の容器の区画に閉じ込めて、殆んど同時に
この亜塩素酸塩と乳酸の成分が細いスプレーの形で混合
、放出されるようにするのもよい。必要なエアロゾル圧
力は、炭化水素及び/又はハロゲン化、例えば塩素化、
弗素化しt炭化水素を含む公知の推進ガスにより供給さ
れ得る。使用する推進ガスの量はエアロゾル容器の中味
を本質的に完全に排除又は排出させるものでなければな
らない。この点について有用な容器の構造はいずれにせ
よこの分野の技術に公知のものである。The chlorite and lactic acid components may be mixed and released in a thin spray at nearly the same time by being confined in separate container compartments in a sol type. The required aerosol pressure is determined by the hydrocarbon and/or halogenated, e.g. chlorinated,
It can be supplied by known propellant gases including fluorinated tertiary hydrocarbons. The amount of propellant gas used must be such as to cause essentially complete displacement or evacuation of the contents of the aerosol container. Container constructions useful in this regard are in any case known in the art.
或いは又、亜塩素酸塩と乳酸とを別々に包装してこれを
一つの単位として家庭での消費者がこれを混合して使用
するように適当な指示をつけて売ってもよいだろう。Alternatively, the chlorite and lactic acid could be packaged separately and sold as a unit with appropriate instructions for mixing and use by the consumer at home.
この組成物製品は多くの面で利点がある。例えば1必要
な制限なしに、 S、 aureus、 S、 alb
us。This composition product is advantageous in many ways. For example 1, without any necessary restrictions, S, aureus, S, alb
us.
psuedomonas、 E、 colt、 Pro
teusvulgaris。psuedomonas, E, colt, Pro
teusvulgaris.
streppyoogen*s、 Candida a
lbicans (乾燥)胞子、B、5ubtilus
(乾燥)胞子などを含むバクテリア類に関してこの
組成物の著しい殺菌性は、特にこの組成物の毒性濃度の
低さと同様にこの組成物が殺菌に用いられる温度の低さ
く約50℃)の点でも驚くべものであることを証明し念
。streppyogen*s, Candida a
lbicans (dried) spores, B, 5ubtilus
The remarkable bactericidal properties of this composition with respect to bacteria, including (dry) spores, etc., are particularly due to the low toxic concentration of this composition as well as the low temperature at which it is used for sterilization (approximately 50°C). I hope it proves to be amazing.
更に、テスH−した微生物は50℃の水道水を用い之と
きには約10分以内に、又超音波クリーナーでこの組成
物を用いt時には5分以下で完全に死滅し几。Furthermore, the tested microorganisms were completely killed within about 10 minutes when using tap water at 50°C, and within 5 minutes when using this composition in an ultrasonic cleaner.
大規模なテストにより本組成物は例えばサラシ粉よシも
刺激性も毒性も少いことが確証されている。この後者は
長い間局所的に比較的無害であるとされてきたものであ
る。一般にctozの溶液は有害ではないと考えられる
べきであシ、又有害な結果を生ずることなく河川などに
織物加工業者により当然のこととして流されている。事
実、このような溶液は一般に公共及び家庭の養魚池の魚
り/りをきれいKするのに用いられている。更にcto
zはコテージチーズを含む種々の食品の保存剤として用
いられており、又食品容器の衛生化に使用され、これに
より処理しt後は洗う必要がないとされている。本組成
物は通常のcto2殺菌溶液よりも毒性が少くさえあり
、従って前述の諸口的に対して開放性の傷口の処理や外
科医の手の洗浄その他と同様に有効に使用することがで
きる。Extensive testing has confirmed that the composition is less irritating and less toxic than, for example, white flour. The latter has long been considered relatively harmless locally. In general, solutions of ctoz should be considered non-hazardous and are routinely poured into rivers and the like by textile processors without harmful consequences. In fact, such solutions are commonly used to clean fish stocks in public and domestic fish ponds. Further cto
Z is used as a preservative for various foods, including cottage cheese, and is also used to sanitize food containers, so that they do not need to be washed after processing. The compositions are even less toxic than conventional CTO2 antiseptic solutions, and therefore can be used effectively in the treatment of open wounds, cleaning surgeons' hands, and the like, as well as those mentioned above.
傷口の洗浄剤として用いる時には、適当なPHを保つ几
めに緩衡剤を用いるのが有利であることがしばしば証明
されている。When used as a wound cleanser, it has often proven advantageous to use a buffering agent to help maintain a suitable pH.
何らかの理論により理解されるつもりはないが、次のこ
とは本発明の組成物により得られる点に効果的な殺菌性
の説明の中で自明のことである。例えばctozは塩素
よりも約5倍水に溶けやすく、それ故揮発により失われ
ることが、ずっと少いように思われる。更に亜塩素酸塩
イオンは次亜塩素酸塩イオンよシ有意に腐蝕性が少く、
例えば、布の漂白の場合、C6O2の存在によって布が
次亜塩素酸塩の劣化作用から守られる程である。漂白剤
の殺菌力は一般に、それが細胞壁を通って拡散しバクテ
リアの急所に達し、次亜塩素酸と酵素、即ち三燐酸脱水
酵素との反応に由来する殺生作用によるものである。他
の権威者は、C2O2はバクテリアの細胞の代謝を促進
し細胞の成長に損害を与えると考えている。又他の信頼
すべき権威者はClO2中の塩素イオンが胞子の壁を通
過する時に8種類の可能な酸化状態を通ると主張してい
る。Without wishing to be bound by any theory, the following is self-evident in explaining the highly effective microbicidal properties provided by the compositions of the present invention. For example, ctoz is about five times more soluble in water than chlorine, and therefore appears to be much less likely to be lost to volatilization. Additionally, chlorite ions are significantly less corrosive than hypochlorite ions;
For example, in the case of fabric bleaching, the presence of C6O2 is sufficient to protect the fabric from the degrading effects of hypochlorite. Bleach's disinfecting power is generally due to its biocidal action, which is derived from the reaction between hypochlorous acid and the enzyme triphosphate dehydratase, as it diffuses through cell walls and reaches the vital points of bacteria. Other authorities believe that C2O2 accelerates bacterial cell metabolism and damages cell growth. Other reputable authorities claim that the chloride ions in ClO2 pass through eight possible oxidation states as they pass through the spore wall.
殺藻剤としてClO2は葉緑素を破壊し、細胞を分解し
て水分が原形質から失われ、その後細胞を完全に破壊又
は酸化して水のフィルター上に泥状残:(ヲ全く残さな
いようにする。乳酸の存在は前述のメカニズムを高め又
は増大させると思われる。As an algaecide, ClO2 destroys chlorophyll, decomposes cells, causing water to be lost from the protoplasm, and then completely destroys or oxidizes the cells, leaving no muddy residue on the water filter. The presence of lactic acid appears to enhance or augment the aforementioned mechanisms.
例えば、筋肉の働き及び広範囲に亘るバクテリアの発酵
の自然の副産物である乳酸は、他のそして密接な関連の
ある酸のようにバクテリアの環境にあっては1異物″で
はない。この点で、乳酸は”拒否″されることなくバク
テリアの細胞の壁にはるかによりよく浸透することがで
き、そしてそうすることによりClO2あるいは亜塩素
酸分子を一緒に運び込む。バクテリアの細胞に浸透して
しまうと、乳酸とその塩とは細胞の代謝活性に影響を及
ぼして特にClO2又はそれより誘導され之生成物の殺
菌作用に感受性のある中間化合物を生成することが極め
てあり得ることになる。更に他の半安定性の塩素中間物
の生成が促進されてこれら又はClO2は決定的な代謝
過程で酵素を不活性にすることもあろう。更に細胞壁の
外側に余分に存在する塩素イオンの酸化作用がこの細胞
壁を被覆している乳酸によって増進されることもあシう
ることである。For example, lactic acid, a natural by-product of muscle work and widespread bacterial fermentation, is not foreign to the bacterial environment like other and closely related acids. In this regard, Lactic acid is much better able to penetrate the bacterial cell wall without being "rejected," and in doing so carries with it ClO2 or chlorite molecules.Once it penetrates the bacterial cell, It is very likely that lactic acid and its salts can influence the metabolic activity of cells and produce intermediate compounds which are particularly susceptible to the bactericidal action of ClO2 or its derived products. These or ClO2 may also inactivate enzymes in critical metabolic processes by promoting the formation of stable chlorine intermediates.Moreover, the oxidative effect of the excess chloride ions on the outside of the cell wall It may also be enhanced by the lactic acid coating.
前述の説明にもかかわらず、どのようなことがあっても
乳酸を特に亜塩素酸物質に添加して効力を有する殺菌組
成物を作ることは本発明により確定し几ことである。Notwithstanding the foregoing, it is determined by the present invention that lactic acid can be added to particularly chlorite materials to produce efficacious germicidal compositions.
この殺菌組成物は超音波クリーナー装置で使用すると特
に有効である。超音波のみ又はキャビテーションの殺菌
性については長年研究されて来た。This germicidal composition is particularly effective when used in ultrasonic cleaner devices. The bactericidal properties of ultrasound alone or cavitation have been studied for many years.
もしも強度が例えば1d当り100ワット以上のように
充分に高ければ、キャビテーションは全細胞を殺すばか
りではなくそれらを破壊してしまうグであろう。しかし
ながら、従来の超音波クリーナーでは強度は1−当り1
ワツトのオーダーではるかに小さいものである。しかし
この強度レベルでは、バクテリアは、バクテリアの塊や
粒が分離するために超音波処理をしない場合よりも速い
速度で培養されるであろう。しかしながら、この殺菌組
成物を超音波クリーナー装置で低い又は通常のレベルの
強度で用いると以前に用いられた殺菌組成物よりもはる
かに有効であることが証明される。それ故、本組成物は
臭いがないのと同様に、毒性がずっと少く、汚染が少く
、又低温でもより有効である。超音波クリーナー装置に
本組成物を使用すると、外科医、歯科医及び食品加工者
その他は一回の操作で素速く器具や装置の洗浄と殺菌の
両方を行うことができる。このような用法によりバクテ
リアの塊は壊してばらばらにされ几り又はバクテリアが
器具や装置から離されてバクテリアが溶液に完全に曝さ
れ、その几め又その殺菌効果に曝されることになると思
われる。しばしばバクテリアを取シ囲み、さもなければ
これを保護している顕微鏡的泡が破壊される。これら泡
はキャビテーションにより生ずる泡と同様にctozで
満される。この非常に小さい泡はしばしば洗浄される器
具や装置のかき傷や小さい割れ目やその他の欠(5!K
<つついて殺菌が充分性われるようにする。If the intensity is high enough, for example over 100 watts per d, cavitation will not only kill all cells but also destroy them. However, in conventional ultrasonic cleaners, the intensity is 1
It is much smaller on the order of Watsuto. However, at this intensity level, bacteria will grow at a faster rate than without sonication due to the separation of bacterial clumps and grains. However, the use of this germicidal composition in ultrasonic cleaner devices at low or normal levels of intensity has proven to be much more effective than previously used germicidal compositions. Therefore, as well as being odorless, the composition is much less toxic, less polluting, and more effective at lower temperatures. Use of the present compositions in ultrasonic cleaner devices allows surgeons, dentists, food processors, and others to quickly both clean and sterilize instruments and equipment in a single operation. It is believed that such usage will break up the bacterial clumps, break them up, and remove them from the utensils and equipment, exposing them completely to the solution and its disinfecting effects. It will be done. Often the microscopic bubbles that surround and otherwise protect the bacteria are destroyed. These bubbles are filled with ctoz similar to bubbles produced by cavitation. These very small bubbles are often found in scratches, small cracks and other defects in instruments and equipment being cleaned (5!K).
<Poke to ensure sufficient sterilization.
更に、キャビテーションは殺菌組成物がバクテリアの細
胞壁を攻撃するようにし、これにより殺菌組成物がバク
テリアの内部に拡散するのを促進する。Additionally, cavitation causes the disinfectant composition to attack the cell walls of the bacteria, thereby facilitating diffusion of the disinfectant composition into the interior of the bacteria.
それ故、本発明によれば、超音波クリーナー装置本来の
利点と本組成物の優れ友殺菌性との組合せによυ、バク
テリア、ビールス、胞子などの集積に場所を提供してい
る種々の物質の洗浄、衛生化及び殺菌の九めの効果的な
方法が提供される。Therefore, according to the present invention, the combination of the inherent advantages of ultrasonic cleaner devices and the excellent bactericidal properties of the present composition makes it possible to eliminate various substances that provide a place for the accumulation of bacteria, viruses, spores, etc. A ninth effective method of cleaning, sanitizing and disinfecting is provided.
亜塩素酸塩物質との組合せで乳酸のみを用いることは、
本発明の特に好ましい実施態様を構成する。しかしなが
ら、有機あるいは無機の酸を含む他の酸と組合せて乳酸
を用いることも又有効である。適当な有機数としては、
例えば酢酸、クエン酸、ソルビン酸、フマル酸、タンニ
ン酸など金含む炭素数が2から約16の水溶性又は水分
散性のモノカルボキシル及びポリカルボキシル酸がある
。Using lactic acid alone in combination with chlorite substances
This constitutes a particularly preferred embodiment of the invention. However, it is also effective to use lactic acid in combination with other acids, including organic or inorganic acids. An appropriate organic number is
Examples include water-soluble or water-dispersible monocarboxylic and polycarboxylic acids containing gold and having 2 to about 16 carbon atoms, such as acetic acid, citric acid, sorbic acid, fumaric acid, and tannic acid.
適当な無機酸としては、例えば硫酸、塩酸、燐酸などが
ある。酸混合物を用いる時には、確実に効果的な結果を
得る九めには、乳酸は全混合物の少くとも約15重量パ
ーセント、好ましくは少くとも約45重量パーセントを
占めるものとする。Suitable inorganic acids include, for example, sulfuric acid, hydrochloric acid, phosphoric acid, and the like. When using acid mixtures, to ensure effective results, lactic acid should account for at least about 15 weight percent of the total mixture, preferably at least about 45 weight percent.
亜塩素酸ナトリウムの使用がctoz放出物質として好
ましいとはいえ、他の水溶性カチオンも、ナトリウムの
代りに用いることができ、それらにはカリウムのような
他のアルカリ金属やアルカリ土類金属があるが、前者が
特に好ましい。Although the use of sodium chlorite is preferred as the ctoz releasing agent, other water-soluble cations can also be used in place of sodium, including other alkali metals and alkaline earth metals such as potassium. However, the former is particularly preferred.
ここに用いられる1基質5ubstrate ”や“細
菌担体gsrrn carrier ”の語は、細菌、
ビールス、胞子、バクテリア、菌類、即ちすべてのタイ
ツ賢生的微生物。集、。場□提供、得、す、ア。As used herein, the terms ``substrate'' and ``bacterial carrier'' refer to bacteria,
Viruses, spores, bacteria, fungi, all tight microorganisms. collection,. Place □ offer, get, su, a.
タイプの硬い表面又は担体を指すものである。その明白
な例としては、外科及び歯科の器具、食品容器、人間の
組織、水泳プール、家庭の流し、ごみ容器、浴室の用具
などがある。洗浄作用は湿潤剤を加えることにより促進
され、この後者は洗浄作用に適合し、又ClO2と反応
するいかなる傾向ともかかわりがない。このように使用
するのに特シて有効な湿潤剤としては、Du pon
t社から出されている市販のフルオロカーボン表面活性
剤がある。エアロゾルタイプの本組成物は閉鎖空間の中
で運ばれるような空気伝染又は大気的細菌の破壊に効果
的に用いられる。ここで用いる“細菌担体germ c
arrier ”の語はこのような大気的、ガス的担体
を指すものである。type of hard surface or carrier. Obvious examples include surgical and dental instruments, food containers, human tissue, swimming pools, household sinks, garbage containers, bathroom utensils, etc. The cleaning action is facilitated by adding a wetting agent, the latter being compatible with the cleaning action and free from any tendency to react with ClO2. A particularly effective wetting agent for use in this manner is Du pon
There are commercially available fluorocarbon surfactants available from T.T. The aerosol type of the composition is effectively used for the destruction of airborne or atmospheric bacteria such as those carried in confined spaces. “Bacterial carrier germ c” used here
The term "arrier" refers to such an atmospheric, gaseous carrier.
傷口の洗浄剤としてこの殺菌組成物を人間の組織に用い
るような例では、PHをこのような組織に適合するよう
に保持し得るような緩衡剤を含めるのがよい。この之め
にアルカリ金属重炭酸塩のような従来の緩衝剤が用いら
れる。In instances where the antiseptic composition is used on human tissue as a wound cleanser, a buffering agent may be included to maintain the pH compatible with such tissue. Conventional buffering agents such as alkali metal bicarbonates are used for this purpose.
本組成物は比較的広い範囲の濃度で用いることができ、
その根本的な必要事項は、少くとも少量でも有効な殺菌
量全用いるべきであるということである。用いられる量
の上限は多くの場合、それを越えると更に有利な効果は
得られないという点てよシ決められる。特別な場合にお
ける必要表有動量は又温度とか、溶液からのClO2の
損失を招くようなある種のタイプのスペクトル放射線の
ような因子により影響を受ける。しかしながら一般に、
溶液中約100乃至5000ppmの範囲の量、好まし
くは約2700乃至3300ppmの濃度で亜塩素酸化
合物を用いると効果のある殺菌結果を得る。The composition can be used in a relatively wide range of concentrations;
The fundamental requirement is that at least the entire effective germicidal dose should be used, even in small amounts. The upper limit of the amount used is often determined by the fact that no further advantageous effects can be achieved beyond this amount. The required surface activity in a particular case is also influenced by factors such as temperature and certain types of spectral radiation that cause loss of ClO2 from the solution. However, in general,
Effective disinfection results are obtained using chlorite compounds in amounts ranging from about 100 to 5000 ppm, preferably at concentrations of about 2700 to 3300 ppm in solution.
以下の実施例は説明の定めにのみ示すもので、本発明を
限定するものと考えられてはならない。The following examples are given by way of illustration only and are not to be considered as limiting the invention.
他に断りのない限り部及びパーセンテージはすべて重量
によるものである。All parts and percentages are by weight unless otherwise noted.
実施例1
亜塩素酸ナトリウム3000ppm f含む亜塩素酸
ナトリウムの水溶液に、得られる溶液のPHt″約3に
まで下げるに充分な量の乳酸水溶液を加える。このよう
Kして得られ九溶液の一部を取り、分析するとこれが二
酸化塩素、亜塩素酸、乳酸及び乳酸ナトリウムより成っ
ていることが解る。本組成物の殺菌効果を温い水道水(
約50℃)を用い、次のものについてテス)Le。Example 1 To an aqueous solution of sodium chlorite containing 3000 ppm of sodium chlorite is added an aqueous lactic acid solution in an amount sufficient to lower the PHt of the resulting solution to approximately 3. When a sample is taken and analyzed, it is found that it is composed of chlorine dioxide, chlorous acid, lactic acid, and sodium lactate.
(approximately 50° C.) and test the following: Le.
a) S、aureus
b) S、albus
c) Psuedomonas
d)E、coli
e) prot@us vulgarisf) 5
trep Pyogenesg) (andida
Albieiua (乾燥)胞子h) B、5ub
tilus (乾燥)胞子各側についてのテストは確認
し几バクテリア試料paniシリンダーと5urica
l knotに飽和するまで浸は込ませて行つ之。次
いでテスト試料を前述のようにして製し几殺菌組成物に
浸し友。各場合とも、約10分間で微生物は完全に死ん
だ。a) S, aureus b) S, albus c) Psuedomonas d) E, coli e) prot@us vulgarisf) 5
trep Pyogenesg) (andida
Albieiua (dried) spore h) B, 5ub
Tilus (dried) spores tested on each side and confirmed bacteria sample pan cylinder and 5urica
Immerse it in the l knot until it is saturated. The test specimens were then immersed in a sterilizing composition prepared as described above. In each case, the microorganisms were completely killed in about 10 minutes.
実施例2
実施例1を繰返し九が、テストは室温で強度が1−当り
1ワツトの超音波クリーナー装置を用いて行った。この
場合、テストし几微生物は5分以内に完全に死んだ。Example 2 Example 1 was repeated nine times, but the test was conducted at room temperature using an ultrasonic cleaner device with an intensity of 1 watt per minute. In this case, the tested microorganisms were completely killed within 5 minutes.
前述の結果は、テストの間一般に低温であつ九というこ
ととこの殺菌組成物の毒性が比較的低いレベルであると
いう点で、特に驚くべきものである。The foregoing results are particularly surprising in view of the generally low temperatures during testing and the relatively low level of toxicity of this germicidal composition.
前述の実施例を繰返し九が、乳酸をすべて、(a)燐酸
、(b)酢酸、(c)ソルビン酸、(d)フマル酸、(
、)スルファミノ酸、(f)コハク酸、(g)ホウ酸、
(h)タンニン酸、及び(i)クエン酸にそれぞれ代え
た場合、得られた結果は殺菌の速度と殺菌の完全さの面
で、乳酸により得られ九結果と比較し几場合、著しく劣
ってい几。やはり、この結果はテストした酸のいくつか
と乳酸との密接な関係からみていささか驚くべきもので
ある。Repeating the previous example, nine times the lactic acid was replaced with (a) phosphoric acid, (b) acetic acid, (c) sorbic acid, (d) fumaric acid, (
,) sulfamino acid, (f) succinic acid, (g) boric acid,
When substituting (h) tannic acid and (i) citric acid, the results obtained were significantly inferior, in terms of speed of sterilization and completeness of sterilization, to the results obtained with lactic acid.几. Again, this result is somewhat surprising in view of the close relationship between some of the acids tested and lactic acid.
実施例1及び2を繰返したが、乳酸の一部をそれぞれ約
80%までの燐酸、酢酸、ソルビン酸その他に置き代え
九時、有効な殺菌組成物は得られ九が、その改善され几
殺菌効果は実施例1及び2の組成物を特徴づけ九もの程
著しいものではなかつ几。Examples 1 and 2 were repeated, but a portion of the lactic acid was replaced with up to about 80% of each of phosphoric acid, acetic acid, sorbic acid, etc., and an effective sterilizing composition was obtained, but with improved sterilization. The effects were not as significant as those characterizing the compositions of Examples 1 and 2.
手続補正書
昭和62年9月7日
特許庁長官 小 川 邦 夫 殿
1、ゎイ’toあ 隻
昭和62年8月12日提出の特許願
2、発明の名称
殺菌用組成物および殺菌方法
3、補正をする者
事件との関係 特許出願人
氏 名 ホワード・アリガー
4、代理人〒101
住 所 東京都千代田区内神田1丁目15番16号東
光ビル6階 電話295−1480
特許請求の範囲
徴とする殺菌用組成物。Procedural amendment September 7, 1988 Director General of the Patent Office Kunio Ogawa 1. Patent application filed on August 12, 1986 2. Title of invention: Sterilizing composition and sterilizing method 3 , Relationship with the case of the person making the amendment Patent applicant Name: Howard Alliger 4, Agent: 101 Address: 6th floor, Toko Building, 1-15-16 Uchikanda, Chiyoda-ku, Tokyo Telephone: 295-1480 Scope of claims A sterilizing composition.
全殺菌組成物の有効な殺菌量と、殺菌担体を接触させる
ことを特徴とする殺菌方法。A sterilization method comprising contacting an effective sterilization amount of a total sterilization composition with a sterilization carrier.
(3)上記細菌担体との接触は、バルブ調剤手段を備え
た加圧エアゾル容器から上記殺菌組成物を分散ゼしめる
ことにより行うようにした特許請求の範囲第2項記載の
殺菌方法。(3) The sterilization method according to claim 2, wherein the contact with the bacterial carrier is carried out by dispersing and zesting the sterilizing composition from a pressurized aerosol container equipped with a valve dispensing means.
(4)上記細菌担体との接触は、超音波洗浄装置内に上
記殺菌組成物を投入せしめることにより行うようにした
特許請求の範囲第2項記載の殺菌方法。(4) The sterilization method according to claim 2, wherein the contact with the bacterial carrier is carried out by introducing the sterilization composition into an ultrasonic cleaning device.
(5)上記細菌担体との接触は、上記殺菌組成物を超音
波噴霧発生装置より分散せしめることにより行うように
した特許請求の範囲第2項記載の殺菌方法。(5) The sterilization method according to claim 2, wherein the contact with the bacterial carrier is carried out by dispersing the sterilizing composition using an ultrasonic spray generator.
Claims (7)
に水溶性の有機あるいは無機酸の群の中から選ばれた酸
性物質を水性媒体中で亜塩素酸塩に接触せしめてなり、
かつ上記酸性物質は水性媒体のPHを約7以下とするの
に充分な量が含有されていることを特徴とする殺菌用組
成物。(1) contacting chlorite in an aqueous medium with an acidic substance selected from the group of inorganically water-soluble organic or inorganic acids containing at least 15 percent by weight of lactic acid;
A sterilizing composition characterized in that the acidic substance is contained in an amount sufficient to adjust the pH of the aqueous medium to about 7 or less.
第1項記載の殺菌用組成物。(2) The sterilizing composition according to claim 1, wherein the acidic substance consists of lactic acid only.
群の中から選ばれた本質的に水溶性の酸性物質と反応さ
せ、この酸性物質は少くとも15重量パーセントの乳酸
を含み、この接触は水性媒体中でこの水性媒体のPHを
約7以下にするに充分な量の上記酸性物質の存在下で行
うことにより得られる殺菌組成物の有効な殺菌量と、細
菌担体を接触させることを特徴とする殺菌方法。(3) reacting chlorous acid or a salt thereof with an essentially water-soluble acidic substance selected from the group of organic or inorganic acids, the acidic substance containing at least 15 weight percent lactic acid; This contacting is carried out in an aqueous medium in the presence of an amount of the above acidic substance sufficient to bring the pH of the aqueous medium to about 7 or less, thereby bringing the bacterial carrier into contact with an effective sterilizing amount of the sterilizing composition obtained. A sterilization method characterized by:
囲第3項記載の殺菌方法。(4) The sterilization method according to claim 3, wherein the acidic substance is only lactic acid.
た加圧ニアゾル容器から上記殺菌組成物を分散せしめる
ことにより行うようにした特許請求の範囲第3項記載の
殺菌方法。(5) The sterilization method according to claim 3, wherein the contact with the bacterial carrier is carried out by dispersing the sterilizing composition from a pressurized Niasol container equipped with a valve dispensing means.
殺菌組成物を投入せしめることにより行うようにした特
許請求の範囲第3項記載の殺菌方法。(6) The sterilization method according to claim 3, wherein the contact with the bacterial carrier is carried out by introducing the sterilizing composition into an ultrasonic cleaning device.
波噴霧発生装置より分散せしめることにより行うように
した特許請求の範囲第3項記載の殺菌方法。(7) The sterilization method according to claim 3, wherein the contact with the bacterial carrier is carried out by dispersing the sterilizing composition using an ultrasonic spray generator.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62201681A JPS6345210A (en) | 1987-08-12 | 1987-08-12 | Sterilizing composition and sterilization |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62201681A JPS6345210A (en) | 1987-08-12 | 1987-08-12 | Sterilizing composition and sterilization |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS6345210A true JPS6345210A (en) | 1988-02-26 |
Family
ID=16445138
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP62201681A Pending JPS6345210A (en) | 1987-08-12 | 1987-08-12 | Sterilizing composition and sterilization |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6345210A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0420350U (en) * | 1990-06-13 | 1992-02-20 |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4084747A (en) * | 1976-03-26 | 1978-04-18 | Howard Alliger | Germ killing composition and method |
JPS6143322A (en) * | 1984-08-06 | 1986-03-01 | Yoshito Iwasa | Stepping type keyboard |
-
1987
- 1987-08-12 JP JP62201681A patent/JPS6345210A/en active Pending
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4084747A (en) * | 1976-03-26 | 1978-04-18 | Howard Alliger | Germ killing composition and method |
JPS6143322A (en) * | 1984-08-06 | 1986-03-01 | Yoshito Iwasa | Stepping type keyboard |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0420350U (en) * | 1990-06-13 | 1992-02-20 |
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