MXPA04006836A - Composiciones y metodos antisepticos. - Google Patents
Composiciones y metodos antisepticos.Info
- Publication number
- MXPA04006836A MXPA04006836A MXPA04006836A MXPA04006836A MXPA04006836A MX PA04006836 A MXPA04006836 A MX PA04006836A MX PA04006836 A MXPA04006836 A MX PA04006836A MX PA04006836 A MXPA04006836 A MX PA04006836A MX PA04006836 A MXPA04006836 A MX PA04006836A
- Authority
- MX
- Mexico
- Prior art keywords
- weight
- acid
- present
- antiseptic composition
- compositions
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 334
- 230000002421 anti-septic effect Effects 0.000 title claims abstract description 74
- 238000000034 method Methods 0.000 title claims abstract description 54
- 229920000642 polymer Polymers 0.000 claims abstract description 170
- 229910052740 iodine Inorganic materials 0.000 claims abstract description 66
- 239000011630 iodine Substances 0.000 claims abstract description 65
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 62
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 claims abstract description 51
- 239000007853 buffer solution Substances 0.000 claims abstract description 48
- 239000004599 antimicrobial Substances 0.000 claims abstract description 42
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims abstract description 11
- 239000004094 surface-active agent Substances 0.000 claims description 81
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 45
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 42
- 150000001412 amines Chemical group 0.000 claims description 37
- 239000000178 monomer Substances 0.000 claims description 32
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 claims description 30
- 239000000872 buffer Substances 0.000 claims description 23
- 125000003277 amino group Chemical group 0.000 claims description 19
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 claims description 18
- 125000000217 alkyl group Chemical group 0.000 claims description 18
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 claims description 18
- 239000001630 malic acid Substances 0.000 claims description 18
- 235000011090 malic acid Nutrition 0.000 claims description 18
- 239000002253 acid Substances 0.000 claims description 17
- 239000004310 lactic acid Substances 0.000 claims description 15
- 235000014655 lactic acid Nutrition 0.000 claims description 15
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 15
- 235000015165 citric acid Nutrition 0.000 claims description 14
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- 238000010998 test method Methods 0.000 claims description 14
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- 125000000129 anionic group Chemical group 0.000 claims description 9
- 150000001875 compounds Chemical class 0.000 claims description 9
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- 125000004122 cyclic group Chemical group 0.000 claims description 9
- 150000003839 salts Chemical class 0.000 claims description 9
- 229920000036 polyvinylpyrrolidone Polymers 0.000 claims description 8
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 7
- 239000003960 organic solvent Substances 0.000 claims description 7
- 239000001267 polyvinylpyrrolidone Substances 0.000 claims description 7
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 claims description 7
- 230000000249 desinfective effect Effects 0.000 claims description 6
- 125000003118 aryl group Chemical group 0.000 claims description 5
- WHBMMWSBFZVSSR-UHFFFAOYSA-N 3-hydroxybutyric acid Chemical compound CC(O)CC(O)=O WHBMMWSBFZVSSR-UHFFFAOYSA-N 0.000 claims description 4
- 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 claims description 4
- 239000004744 fabric Substances 0.000 claims description 4
- 150000002596 lactones Chemical class 0.000 claims description 4
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 claims description 4
- QBYIENPQHBMVBV-HFEGYEGKSA-N (2R)-2-hydroxy-2-phenylacetic acid Chemical compound O[C@@H](C(O)=O)c1ccccc1.O[C@@H](C(O)=O)c1ccccc1 QBYIENPQHBMVBV-HFEGYEGKSA-N 0.000 claims description 3
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 claims description 3
- 206010013786 Dry skin Diseases 0.000 claims description 3
- IWYDHOAUDWTVEP-UHFFFAOYSA-N R-2-phenyl-2-hydroxyacetic acid Natural products OC(=O)C(O)C1=CC=CC=C1 IWYDHOAUDWTVEP-UHFFFAOYSA-N 0.000 claims description 3
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 claims description 3
- 230000002378 acidificating effect Effects 0.000 claims description 3
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 3
- 230000037336 dry skin Effects 0.000 claims description 3
- 229960002510 mandelic acid Drugs 0.000 claims description 3
- 239000011975 tartaric acid Substances 0.000 claims description 3
- 235000002906 tartaric acid Nutrition 0.000 claims description 3
- AFENDNXGAFYKQO-UHFFFAOYSA-N 2-hydroxybutyric acid Chemical compound CCC(O)C(O)=O AFENDNXGAFYKQO-UHFFFAOYSA-N 0.000 claims description 2
- RGHNJXZEOKUKBD-UHFFFAOYSA-N D-gluconic acid Natural products OCC(O)C(O)C(O)C(O)C(O)=O RGHNJXZEOKUKBD-UHFFFAOYSA-N 0.000 claims description 2
- 239000002202 Polyethylene glycol Substances 0.000 claims description 2
- 125000002843 carboxylic acid group Chemical group 0.000 claims description 2
- 239000000174 gluconic acid Substances 0.000 claims description 2
- 235000012208 gluconic acid Nutrition 0.000 claims description 2
- 229950006191 gluconic acid Drugs 0.000 claims description 2
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 claims description 2
- 229920001223 polyethylene glycol Polymers 0.000 claims description 2
- 229960004889 salicylic acid Drugs 0.000 claims description 2
- 229960001367 tartaric acid Drugs 0.000 claims description 2
- 239000008186 active pharmaceutical agent Substances 0.000 claims 1
- 239000003638 chemical reducing agent Substances 0.000 claims 1
- 125000006165 cyclic alkyl group Chemical group 0.000 claims 1
- 238000003958 fumigation Methods 0.000 claims 1
- 238000010791 quenching Methods 0.000 claims 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 59
- CPKVUHPKYQGHMW-UHFFFAOYSA-N 1-ethenylpyrrolidin-2-one;molecular iodine Chemical compound II.C=CN1CCCC1=O CPKVUHPKYQGHMW-UHFFFAOYSA-N 0.000 description 58
- 239000000243 solution Substances 0.000 description 55
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- 229940064804 betadine Drugs 0.000 description 36
- 239000000047 product Substances 0.000 description 35
- 210000001519 tissue Anatomy 0.000 description 24
- 229920000153 Povidone-iodine Polymers 0.000 description 23
- 230000000845 anti-microbial effect Effects 0.000 description 23
- 229960001621 povidone-iodine Drugs 0.000 description 23
- 238000009472 formulation Methods 0.000 description 22
- 239000007787 solid Substances 0.000 description 19
- 238000007792 addition Methods 0.000 description 18
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 16
- 238000005201 scrubbing Methods 0.000 description 15
- -1 ammonium carboxylate Chemical class 0.000 description 14
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 14
- 230000009467 reduction Effects 0.000 description 14
- 239000003945 anionic surfactant Substances 0.000 description 13
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- 230000007794 irritation Effects 0.000 description 12
- 239000003973 paint Substances 0.000 description 12
- 229910019142 PO4 Inorganic materials 0.000 description 11
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 11
- 230000000813 microbial effect Effects 0.000 description 11
- 235000021317 phosphate Nutrition 0.000 description 11
- 229940064004 antiseptic throat preparations Drugs 0.000 description 10
- 238000001035 drying Methods 0.000 description 10
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 9
- 241001465754 Metazoa Species 0.000 description 9
- 241000283973 Oryctolagus cuniculus Species 0.000 description 9
- 229940061720 alpha hydroxy acid Drugs 0.000 description 9
- 150000001280 alpha hydroxy acids Chemical class 0.000 description 9
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 9
- 210000004400 mucous membrane Anatomy 0.000 description 9
- 239000002736 nonionic surfactant Substances 0.000 description 9
- 125000001453 quaternary ammonium group Chemical group 0.000 description 9
- 239000000126 substance Substances 0.000 description 9
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 8
- 206010052428 Wound Diseases 0.000 description 8
- 239000006185 dispersion Substances 0.000 description 8
- 239000011734 sodium Substances 0.000 description 8
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 8
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 7
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 7
- 208000027418 Wounds and injury Diseases 0.000 description 7
- 150000007513 acids Chemical class 0.000 description 7
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- 125000000524 functional group Chemical group 0.000 description 7
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- 229940035535 iodophors Drugs 0.000 description 7
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- 229910052708 sodium Inorganic materials 0.000 description 7
- 229920002554 vinyl polymer Polymers 0.000 description 7
- JKNCOURZONDCGV-UHFFFAOYSA-N 2-(dimethylamino)ethyl 2-methylprop-2-enoate Chemical compound CN(C)CCOC(=O)C(C)=C JKNCOURZONDCGV-UHFFFAOYSA-N 0.000 description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- 150000001298 alcohols Chemical class 0.000 description 6
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- 230000001580 bacterial effect Effects 0.000 description 6
- 235000020289 caffè mocha Nutrition 0.000 description 6
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- 239000008367 deionised water Substances 0.000 description 6
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- 210000003811 finger Anatomy 0.000 description 6
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- 229940068196 placebo Drugs 0.000 description 6
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 6
- 150000003512 tertiary amines Chemical class 0.000 description 6
- JKXYOQDLERSFPT-UHFFFAOYSA-N 2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-(2-octadecoxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethanol Chemical compound CCCCCCCCCCCCCCCCCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCO JKXYOQDLERSFPT-UHFFFAOYSA-N 0.000 description 5
- 208000006069 Corneal Opacity Diseases 0.000 description 5
- 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 5
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 5
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- IAXXETNIOYFMLW-UHFFFAOYSA-N (4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl) 2-methylprop-2-enoate Chemical compound C1CC2(C)C(OC(=O)C(=C)C)CC1C2(C)C IAXXETNIOYFMLW-UHFFFAOYSA-N 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 4
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- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 4
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- 238000003756 stirring Methods 0.000 description 4
- 238000003860 storage Methods 0.000 description 4
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- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 3
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- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
- RUMACXVDVNRZJZ-UHFFFAOYSA-N 2-methylpropyl 2-methylprop-2-enoate Chemical compound CC(C)COC(=O)C(C)=C RUMACXVDVNRZJZ-UHFFFAOYSA-N 0.000 description 2
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- PQUCIEFHOVEZAU-UHFFFAOYSA-N Diammonium sulfite Chemical compound [NH4+].[NH4+].[O-]S([O-])=O PQUCIEFHOVEZAU-UHFFFAOYSA-N 0.000 description 2
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- XMRUJYGYYCLRGJ-UHFFFAOYSA-N azanium;2-[2-[2-[2-(4-nonylphenoxy)ethoxy]ethoxy]ethoxy]ethyl sulfate Chemical compound [NH4+].CCCCCCCCCC1=CC=C(OCCOCCOCCOCCOS([O-])(=O)=O)C=C1 XMRUJYGYYCLRGJ-UHFFFAOYSA-N 0.000 description 2
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- 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
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- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
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- 239000007858 starting material Substances 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
- 238000013268 sustained release Methods 0.000 description 1
- 239000012730 sustained-release form Substances 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 239000012085 test solution Substances 0.000 description 1
- 229920006029 tetra-polymer Polymers 0.000 description 1
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical compound FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
- WHRNULOCNSKMGB-UHFFFAOYSA-N tetrahydrofuran thf Chemical compound C1CCOC1.C1CCOC1 WHRNULOCNSKMGB-UHFFFAOYSA-N 0.000 description 1
- 208000037816 tissue injury Diseases 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 238000012549 training Methods 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 229960003500 triclosan Drugs 0.000 description 1
- 229940072029 trilaureth-4 phosphate Drugs 0.000 description 1
- 235000019154 vitamin C Nutrition 0.000 description 1
- 239000011718 vitamin C Substances 0.000 description 1
- 239000003643 water by type Substances 0.000 description 1
- 239000008215 water for injection Substances 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
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Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/74—Synthetic polymeric materials
- A61K31/785—Polymers containing nitrogen
- A61K31/787—Polymers containing nitrogen containing heterocyclic rings having nitrogen as a ring hetero atom
- A61K31/79—Polymers of vinyl pyrrolidone
-
- 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
- A01N59/00—Biocides, pest repellants or attractants, or plant growth regulators containing elements or inorganic compounds
- A01N59/12—Iodine, e.g. iodophors; Compounds thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/08—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
- A61K47/12—Carboxylic acids; Salts or anhydrides thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/02—Local antiseptics
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Environmental Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Dentistry (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Inorganic Chemistry (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Toxicology (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/051,719 US7147873B2 (en) | 2002-01-16 | 2002-01-16 | Antiseptic compositions and methods |
| PCT/US2002/036927 WO2003061389A1 (en) | 2002-01-16 | 2002-11-18 | Antiseptic compositions and methods |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MXPA04006836A true MXPA04006836A (es) | 2004-12-06 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MXPA04006836A MXPA04006836A (es) | 2002-01-16 | 2002-11-18 | Composiciones y metodos antisepticos. |
Country Status (13)
| Country | Link |
|---|---|
| US (4) | US7147873B2 (enExample) |
| EP (3) | EP1955594B1 (enExample) |
| JP (2) | JP4663983B2 (enExample) |
| KR (1) | KR20040076893A (enExample) |
| AT (1) | ATE421248T1 (enExample) |
| AU (1) | AU2002367455B2 (enExample) |
| BR (1) | BRPI0215517B1 (enExample) |
| CA (1) | CA2472564A1 (enExample) |
| DE (1) | DE60231007D1 (enExample) |
| ES (1) | ES2320983T3 (enExample) |
| MX (1) | MXPA04006836A (enExample) |
| NO (1) | NO20043296L (enExample) |
| WO (1) | WO2003061389A1 (enExample) |
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| US7147873B2 (en) | 2002-01-16 | 2006-12-12 | 3M Innovative Properties Company | Antiseptic compositions and methods |
| US20040180093A1 (en) * | 2003-03-12 | 2004-09-16 | 3M Innovative Properties Company | Polymer compositions with bioactive agent, medical articles, and methods |
| US20050058673A1 (en) | 2003-09-09 | 2005-03-17 | 3M Innovative Properties Company | Antimicrobial compositions and methods |
| US7320956B2 (en) * | 2004-04-01 | 2008-01-22 | 3M Innovative Properties Company | Aqueous cleaning/treatment composition for fibrous substrates |
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| US20060045914A1 (en) * | 2004-08-26 | 2006-03-02 | Isp Investments Inc. | Matrix composition for stable microemulsions |
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-
2002
- 2002-01-16 US US10/051,719 patent/US7147873B2/en not_active Expired - Lifetime
- 2002-11-18 EP EP08153434.9A patent/EP1955594B1/en not_active Expired - Lifetime
- 2002-11-18 ES ES02791259T patent/ES2320983T3/es not_active Expired - Lifetime
- 2002-11-18 AT AT02791259T patent/ATE421248T1/de not_active IP Right Cessation
- 2002-11-18 KR KR10-2004-7010931A patent/KR20040076893A/ko not_active Ceased
- 2002-11-18 JP JP2003561345A patent/JP4663983B2/ja not_active Expired - Fee Related
- 2002-11-18 EP EP16158778.7A patent/EP3064065B1/en not_active Expired - Lifetime
- 2002-11-18 DE DE60231007T patent/DE60231007D1/de not_active Expired - Lifetime
- 2002-11-18 AU AU2002367455A patent/AU2002367455B2/en not_active Ceased
- 2002-11-18 BR BRPI0215517-6A patent/BRPI0215517B1/pt not_active IP Right Cessation
- 2002-11-18 WO PCT/US2002/036927 patent/WO2003061389A1/en not_active Ceased
- 2002-11-18 CA CA002472564A patent/CA2472564A1/en not_active Abandoned
- 2002-11-18 MX MXPA04006836A patent/MXPA04006836A/es active IP Right Grant
- 2002-11-18 EP EP02791259A patent/EP1465491B1/en not_active Expired - Lifetime
-
2004
- 2004-08-06 NO NO20043296A patent/NO20043296L/no not_active Application Discontinuation
-
2006
- 2006-03-10 US US11/372,758 patent/US8840932B2/en not_active Expired - Fee Related
-
2010
- 2010-02-18 JP JP2010033458A patent/JP2010138180A/ja not_active Withdrawn
-
2011
- 2011-07-19 US US13/185,713 patent/US9277750B2/en not_active Expired - Fee Related
-
2016
- 2016-03-07 US US15/062,493 patent/US20160184346A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| AU2002367455B2 (en) | 2006-07-27 |
| US7147873B2 (en) | 2006-12-12 |
| US20110274770A1 (en) | 2011-11-10 |
| ATE421248T1 (de) | 2009-02-15 |
| US20030194447A1 (en) | 2003-10-16 |
| WO2003061389A1 (en) | 2003-07-31 |
| EP1955594A1 (en) | 2008-08-13 |
| EP1955594B1 (en) | 2016-03-09 |
| JP2005515235A (ja) | 2005-05-26 |
| DE60231007D1 (de) | 2009-03-12 |
| JP2010138180A (ja) | 2010-06-24 |
| EP3064065B1 (en) | 2020-08-12 |
| BR0215517A (pt) | 2004-12-21 |
| CA2472564A1 (en) | 2003-07-31 |
| EP1465491B1 (en) | 2009-01-21 |
| EP3064065A1 (en) | 2016-09-07 |
| US20060177511A1 (en) | 2006-08-10 |
| US9277750B2 (en) | 2016-03-08 |
| BRPI0215517B1 (pt) | 2015-08-18 |
| JP4663983B2 (ja) | 2011-04-06 |
| KR20040076893A (ko) | 2004-09-03 |
| ES2320983T3 (es) | 2009-06-01 |
| US8840932B2 (en) | 2014-09-23 |
| EP1465491A1 (en) | 2004-10-13 |
| US20160184346A1 (en) | 2016-06-30 |
| NO20043296L (no) | 2004-10-07 |
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