NO323049B1 - Desinfiseringssammensetning - Google Patents

Desinfiseringssammensetning Download PDF

Info

Publication number: NO323049B1
Authority: NO; Norway
Prior art keywords: alcohol; weight; composition; disinfectant; composition according
Prior art date: 1998-03-19

Application number

NO20004609A

Other languages

English (en)

Norwegian (no)

Other versions

NO20004609L (no

NO20004609D0 (no

Inventor

Erik Brandsborg

Preben Borelli

Original Assignee

Bifodan As

Priority date (The priority date 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 date listed.)

1998-03-19

Filing date

2000-09-15

Publication date

2006-12-27

2000-09-15 Application filed by Bifodan As filed Critical Bifodan As

2000-09-15 Publication of NO20004609L publication Critical patent/NO20004609L/no

2000-09-15 Publication of NO20004609D0 publication Critical patent/NO20004609D0/no

2006-12-27 Publication of NO323049B1 publication Critical patent/NO323049B1/no

Links

239000000203 mixture Substances 0.000 title claims description 66
230000000249 desinfective effect Effects 0.000 title description 3
ARIWANIATODDMH-UHFFFAOYSA-N rac-1-monolauroylglycerol Chemical compound CCCCCCCCCCCC(=O)OCC(O)CO ARIWANIATODDMH-UHFFFAOYSA-N 0.000 claims description 30
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 22
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 16
DBHODFSFBXJZNY-UHFFFAOYSA-N 2,4-dichlorobenzyl alcohol Chemical compound OCC1=CC=C(Cl)C=C1Cl DBHODFSFBXJZNY-UHFFFAOYSA-N 0.000 claims description 15
229960004698 dichlorobenzyl alcohol Drugs 0.000 claims description 15
229940068939 glyceryl monolaurate Drugs 0.000 claims description 13
238000004659 sterilization and disinfection Methods 0.000 claims description 8
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 6
239000000416 hydrocolloid Substances 0.000 claims description 5
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 4
229920001285 xanthan gum Polymers 0.000 claims description 4
239000000230 xanthan gum Substances 0.000 claims description 4
229940082509 xanthan gum Drugs 0.000 claims description 4
235000010493 xanthan gum Nutrition 0.000 claims description 4
239000000377 silicon dioxide Substances 0.000 claims description 2
235000015112 vegetable and seed oil Nutrition 0.000 claims description 2
239000008158 vegetable oil Substances 0.000 claims description 2
239000000645 desinfectant Substances 0.000 description 27
238000012360 testing method Methods 0.000 description 16
210000002445 nipple Anatomy 0.000 description 15
235000013336 milk Nutrition 0.000 description 14
239000008267 milk Substances 0.000 description 14
210000004080 milk Anatomy 0.000 description 14
239000000243 solution Substances 0.000 description 11
241000283690 Bos taurus Species 0.000 description 10
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 9
241001465754 Metazoa Species 0.000 description 9
210000000481 breast Anatomy 0.000 description 9
244000005700 microbiome Species 0.000 description 9
230000000845 anti-microbial effect Effects 0.000 description 6
210000004027 cell Anatomy 0.000 description 6
230000000694 effects Effects 0.000 description 6
210000000265 leukocyte Anatomy 0.000 description 6
230000000844 anti-bacterial effect Effects 0.000 description 5
239000004599 antimicrobial Substances 0.000 description 5
208000015181 infectious disease Diseases 0.000 description 5
230000003641 microbiacidal effect Effects 0.000 description 5
239000000725 suspension Substances 0.000 description 5
206010061218 Inflammation Diseases 0.000 description 4
239000002253 acid Substances 0.000 description 4
239000003795 chemical substances by application Substances 0.000 description 4
150000001875 compounds Chemical class 0.000 description 4
239000000194 fatty acid Substances 0.000 description 4
239000000499 gel Substances 0.000 description 4
230000004054 inflammatory process Effects 0.000 description 4
208000004396 mastitis Diseases 0.000 description 4
238000002360 preparation method Methods 0.000 description 4
230000002195 synergetic effect Effects 0.000 description 4
ARIWANIATODDMH-AWEZNQCLSA-N 1-lauroyl-sn-glycerol Chemical compound CCCCCCCCCCCC(=O)OC[C@@H](O)CO ARIWANIATODDMH-AWEZNQCLSA-N 0.000 description 3
WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
240000004808 Saccharomyces cerevisiae Species 0.000 description 3
235000014680 Saccharomyces cerevisiae Nutrition 0.000 description 3
239000000654 additive Substances 0.000 description 3
230000003110 anti-inflammatory effect Effects 0.000 description 3
235000013365 dairy product Nutrition 0.000 description 3
235000014113 dietary fatty acids Nutrition 0.000 description 3
238000007598 dipping method Methods 0.000 description 3
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150000004665 fatty acids Chemical class 0.000 description 3
230000000855 fungicidal effect Effects 0.000 description 3
230000000813 microbial effect Effects 0.000 description 3
239000002674 ointment Substances 0.000 description 3
210000001082 somatic cell Anatomy 0.000 description 3
FJKROLUGYXJWQN-UHFFFAOYSA-N 4-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 2
108091003079 Bovine Serum Albumin Proteins 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
241000194031 Enterococcus faecium Species 0.000 description 2
206010017533 Fungal infection Diseases 0.000 description 2
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
LCTONWCANYUPML-UHFFFAOYSA-N Pyruvic acid Chemical compound CC(=O)C(O)=O LCTONWCANYUPML-UHFFFAOYSA-N 0.000 description 2
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
150000001298 alcohols Chemical class 0.000 description 2
235000013351 cheese Nutrition 0.000 description 2
239000002537 cosmetic Substances 0.000 description 2
230000001877 deodorizing effect Effects 0.000 description 2
POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
210000002919 epithelial cell Anatomy 0.000 description 2
CRDAMVZIKSXKFV-UHFFFAOYSA-N farnesol Chemical compound CC(C)=CCCC(C)=CCCC(C)=CCO CRDAMVZIKSXKFV-UHFFFAOYSA-N 0.000 description 2
235000013305 food Nutrition 0.000 description 2
239000000417 fungicide Substances 0.000 description 2
230000002779 inactivation Effects 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
231100000252 nontoxic Toxicity 0.000 description 2
230000003000 nontoxic effect Effects 0.000 description 2
QYSGYZVSCZSLHT-UHFFFAOYSA-N octafluoropropane Chemical compound FC(F)(F)C(F)(F)C(F)(F)F QYSGYZVSCZSLHT-UHFFFAOYSA-N 0.000 description 2
QELSKZZBTMNZEB-UHFFFAOYSA-N propylparaben Chemical compound CCCOC(=O)C1=CC=C(O)C=C1 QELSKZZBTMNZEB-UHFFFAOYSA-N 0.000 description 2
239000000126 substance Substances 0.000 description 2
239000004094 surface-active agent Substances 0.000 description 2
239000012085 test solution Substances 0.000 description 2
238000005406 washing Methods 0.000 description 2
LDVVTQMJQSCDMK-UHFFFAOYSA-N 1,3-dihydroxypropan-2-yl formate Chemical compound OCC(CO)OC=O LDVVTQMJQSCDMK-UHFFFAOYSA-N 0.000 description 1
WBIQQQGBSDOWNP-UHFFFAOYSA-N 2-dodecylbenzenesulfonic acid Chemical compound CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O WBIQQQGBSDOWNP-UHFFFAOYSA-N 0.000 description 1
QCDWFXQBSFUVSP-UHFFFAOYSA-N 2-phenoxyethanol Chemical compound OCCOC1=CC=CC=C1 QCDWFXQBSFUVSP-UHFFFAOYSA-N 0.000 description 1
DWKQNRUYIOGYLP-UHFFFAOYSA-N 3-methyl-2-pentylphenol Chemical compound CCCCCC1=C(C)C=CC=C1O DWKQNRUYIOGYLP-UHFFFAOYSA-N 0.000 description 1
229940090248 4-hydroxybenzoic acid Drugs 0.000 description 1
241000894006 Bacteria Species 0.000 description 1
208000035143 Bacterial infection Diseases 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
WQZGKKKJIJFFOK-QTVWNMPRSA-N D-mannopyranose Chemical compound OC[C@H]1OC(O)[C@@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-QTVWNMPRSA-N 0.000 description 1
206010059866 Drug resistance Diseases 0.000 description 1
241000588724 Escherichia coli Species 0.000 description 1
241000192125 Firmicutes Species 0.000 description 1
241000233866 Fungi Species 0.000 description 1
IAJILQKETJEXLJ-UHFFFAOYSA-N Galacturonsaeure Natural products O=CC(O)C(O)C(O)C(O)C(O)=O IAJILQKETJEXLJ-UHFFFAOYSA-N 0.000 description 1
241000173371 Garcinia indica Species 0.000 description 1
108010010803 Gelatin Proteins 0.000 description 1
WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
241000282412 Homo Species 0.000 description 1
239000005639 Lauric acid Substances 0.000 description 1
241000124008 Mammalia Species 0.000 description 1
208000031888 Mycoses Diseases 0.000 description 1
239000004264 Petrolatum Substances 0.000 description 1
241000588770 Proteus mirabilis Species 0.000 description 1
241000589517 Pseudomonas aeruginosa Species 0.000 description 1
208000035415 Reinfection Diseases 0.000 description 1
239000005708 Sodium hypochlorite Substances 0.000 description 1
241000191967 Staphylococcus aureus Species 0.000 description 1
229920002472 Starch Polymers 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
239000013543 active substance Substances 0.000 description 1
230000000996 additive effect Effects 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
125000000217 alkyl group Chemical group 0.000 description 1
239000013566 allergen Substances 0.000 description 1
AEMOLEFTQBMNLQ-WAXACMCWSA-N alpha-D-glucuronic acid Chemical compound O[C@H]1O[C@H](C(O)=O)[C@@H](O)[C@H](O)[C@H]1O AEMOLEFTQBMNLQ-WAXACMCWSA-N 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
230000001580 bacterial effect Effects 0.000 description 1
208000022362 bacterial infectious disease Diseases 0.000 description 1
239000003899 bactericide agent Substances 0.000 description 1
230000004888 barrier function Effects 0.000 description 1
239000002585 base Substances 0.000 description 1
235000019445 benzyl alcohol Nutrition 0.000 description 1
WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
230000003115 biocidal effect Effects 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
235000013877 carbamide Nutrition 0.000 description 1
150000001720 carbohydrates Chemical class 0.000 description 1
235000014633 carbohydrates Nutrition 0.000 description 1
239000000969 carrier Substances 0.000 description 1
239000005018 casein Substances 0.000 description 1
BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
235000021240 caseins Nutrition 0.000 description 1
230000002925 chemical effect Effects 0.000 description 1
229960003260 chlorhexidine Drugs 0.000 description 1
XTEGARKTQYYJKE-UHFFFAOYSA-N chloric acid Chemical compound OCl(=O)=O XTEGARKTQYYJKE-UHFFFAOYSA-N 0.000 description 1
229940005991 chloric acid Drugs 0.000 description 1
229910001919 chlorite Inorganic materials 0.000 description 1
229910052619 chlorite group Inorganic materials 0.000 description 1
QBWCMBCROVPCKQ-UHFFFAOYSA-N chlorous acid Chemical compound OCl=O QBWCMBCROVPCKQ-UHFFFAOYSA-N 0.000 description 1
238000004140 cleaning Methods 0.000 description 1
230000015271 coagulation Effects 0.000 description 1
238000005345 coagulation Methods 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
230000009918 complex formation Effects 0.000 description 1
235000020247 cow milk Nutrition 0.000 description 1
230000008260 defense mechanism Effects 0.000 description 1
150000004683 dihydrates Chemical class 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
201000010099 disease Diseases 0.000 description 1
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
238000001035 drying Methods 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
235000019197 fats Nutrition 0.000 description 1
238000000855 fermentation Methods 0.000 description 1
230000004151 fermentation Effects 0.000 description 1
239000000945 filler Substances 0.000 description 1
238000009472 formulation Methods 0.000 description 1
230000002538 fungal effect Effects 0.000 description 1
239000008273 gelatin Substances 0.000 description 1
229920000159 gelatin Polymers 0.000 description 1
235000019322 gelatine Nutrition 0.000 description 1
235000011852 gelatine desserts Nutrition 0.000 description 1
150000004676 glycans Chemical class 0.000 description 1
-1 glycerol monolaurate Chemical compound 0.000 description 1
125000003976 glyceryl group Chemical group [H]C([*])([H])C(O[H])([H])C(O[H])([H])[H] 0.000 description 1
230000036541 health Effects 0.000 description 1
150000002402 hexoses Chemical group 0.000 description 1
230000003165 hydrotropic effect Effects 0.000 description 1
150000002460 imidazoles Chemical class 0.000 description 1
210000000987 immune system Anatomy 0.000 description 1
230000000415 inactivating effect Effects 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
229940035535 iodophors Drugs 0.000 description 1
230000007794 irritation Effects 0.000 description 1
230000001665 lethal effect Effects 0.000 description 1
239000007788 liquid Substances 0.000 description 1
239000003589 local anesthetic agent Substances 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
238000000034 method Methods 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
239000004292 methyl p-hydroxybenzoate Substances 0.000 description 1
235000010270 methyl p-hydroxybenzoate Nutrition 0.000 description 1
229960002216 methylparaben Drugs 0.000 description 1
238000002156 mixing Methods 0.000 description 1
238000012986 modification Methods 0.000 description 1
230000004048 modification Effects 0.000 description 1
150000004682 monohydrates Chemical class 0.000 description 1
150000004957 nitroimidazoles Chemical class 0.000 description 1
239000002736 nonionic surfactant Substances 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
235000005985 organic acids Nutrition 0.000 description 1
LXCFILQKKLGQFO-UHFFFAOYSA-N p-hydroxybenzoic acid methyl ester Natural products COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 description 1
239000005022 packaging material Substances 0.000 description 1
244000052769 pathogen Species 0.000 description 1
235000019271 petrolatum Nutrition 0.000 description 1
229940066842 petrolatum Drugs 0.000 description 1
239000008194 pharmaceutical composition Substances 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
229960005323 phenoxyethanol Drugs 0.000 description 1
230000000704 physical effect Effects 0.000 description 1
239000000049 pigment Substances 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920005862 polyol Polymers 0.000 description 1
150000003077 polyols Chemical class 0.000 description 1
229920001282 polysaccharide Polymers 0.000 description 1
239000005017 polysaccharide Substances 0.000 description 1
239000000843 powder Substances 0.000 description 1
239000004405 propyl p-hydroxybenzoate Substances 0.000 description 1
235000010232 propyl p-hydroxybenzoate Nutrition 0.000 description 1
229960003415 propylparaben Drugs 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
239000011241 protective layer Substances 0.000 description 1
229940107700 pyruvic acid Drugs 0.000 description 1
150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
230000009467 reduction Effects 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
150000004671 saturated fatty acids Chemical class 0.000 description 1
235000003441 saturated fatty acids Nutrition 0.000 description 1
206010040872 skin infection Diseases 0.000 description 1
239000000344 soap Substances 0.000 description 1
SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 description 1
239000002904 solvent Substances 0.000 description 1
241000894007 species Species 0.000 description 1
238000005507 spraying Methods 0.000 description 1
235000019698 starch Nutrition 0.000 description 1
239000008107 starch Substances 0.000 description 1
230000003637 steroidlike Effects 0.000 description 1
238000003860 storage Methods 0.000 description 1
230000008961 swelling Effects 0.000 description 1
208000024891 symptom Diseases 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
230000009974 thixotropic effect Effects 0.000 description 1
230000000699 topical effect Effects 0.000 description 1
239000012049 topical pharmaceutical composition Substances 0.000 description 1
ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1

Classifications

- 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
- A01N31/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic oxygen or sulfur compounds
- A01N31/04—Oxygen or sulfur attached to an aliphatic side-chain of a carbocyclic ring system
- 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
- A61K31/21—Esters, e.g. nitroglycerine, selenocyanates
- A61K31/215—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
- A61K31/22—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin
- A61K31/23—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin of acids having a carboxyl group bound to a chain of seven or more carbon atoms
- 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

Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
General Health & Medical Sciences (AREA)
Pharmacology & Pharmacy (AREA)
Veterinary Medicine (AREA)
Chemical & Material Sciences (AREA)
Public Health (AREA)
Medicinal Chemistry (AREA)
Animal Behavior & Ethology (AREA)
Dentistry (AREA)
Wood Science & Technology (AREA)
Environmental Sciences (AREA)
Zoology (AREA)
Engineering & Computer Science (AREA)
Plant Pathology (AREA)
Emergency Medicine (AREA)
Epidemiology (AREA)
Agronomy & Crop Science (AREA)
Pest Control & Pesticides (AREA)
Oncology (AREA)
Chemical Kinetics & Catalysis (AREA)
Communicable Diseases (AREA)
Organic Chemistry (AREA)
General Chemical & Material Sciences (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Medicinal Preparation (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

NO20004609A 1998-03-19 2000-09-15 Desinfiseringssammensetning NO323049B1 (no)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DK38798		1998-03-19
PCT/DK1999/000130 WO1999046987A1 (en)	1998-03-19	1999-03-16	Disinfecting composition

Publications (3)

Publication Number	Publication Date
NO20004609L NO20004609L (no)	2000-09-15
NO20004609D0 NO20004609D0 (no)	2000-09-15
NO323049B1 true NO323049B1 (no)	2006-12-27

Family

ID=8092930

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO20004609A NO323049B1 (no)	1998-03-19	2000-09-15	Desinfiseringssammensetning

Country Status (18)

Country	Link
US (1)	US6414023B1 (pl)
EP (1)	EP1063886B1 (pl)
AT (1)	ATE233484T1 (pl)
AU (1)	AU740138B2 (pl)
CA (1)	CA2321658C (pl)
DE (1)	DE69905700T2 (pl)
DK (1)	DK1063886T3 (pl)
EE (1)	EE04136B1 (pl)
ES (1)	ES2191417T3 (pl)
IL (1)	IL137891A (pl)
LT (1)	LT4778B (pl)
LV (1)	LV12582B (pl)
NO (1)	NO323049B1 (pl)
NZ (1)	NZ506681A (pl)
PL (1)	PL196077B1 (pl)
PT (1)	PT1063886E (pl)
RU (1)	RU2221557C2 (pl)
WO (1)	WO1999046987A1 (pl)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US20070003508A1 (en)	2005-07-01	2007-01-04	Wooley Richard E	Methods and compositions for promoting wound healing
US20040208842A1 (en) *	2001-09-18	2004-10-21	Ritchie Branson W.	Antimicrobial cleansing compositions and methods of use
US20040151765A1 (en) *	2001-09-18	2004-08-05	Ritchie Branson W.	Methods and compositions for wound management
US8193244B1 (en)	2008-05-29	2012-06-05	Nevada Naturals, Inc.	Antimicrobial agents
US8795638B1 (en)	2003-08-26	2014-08-05	Nevada Naturals Inc.	Compositions for dental care
US20100056628A1 (en) *	2006-09-07	2010-03-04	Stockel Richard F	Preservative compositions
US20050058673A1 (en)	2003-09-09	2005-03-17	3M Innovative Properties Company	Antimicrobial compositions and methods
US20070185202A1 (en) *	2004-03-03	2007-08-09	University Of Georgia Research Foundation, Inc.	Methods and compositions for ophthalmic treatment of fungal and bacterial infections
EP2497460A1 (en)	2005-03-10	2012-09-12	3M Innovative Properties Co.	Methods of reducing microbial contamination
KR20070113281A (ko)	2005-03-10	2007-11-28	쓰리엠 이노베이티브 프로퍼티즈 컴파니	항미생물성 조성물 및 방법
US20060204558A1 (en) *	2005-03-10	2006-09-14	Kantner Steven S	Antimicrobial pet wipes and methods
JP2008533048A (ja)	2005-03-10	2008-08-21	スリーエムイノベイティブプロパティズカンパニー	耳の感染症の治療方法
US9023891B2 (en)	2008-05-29	2015-05-05	Nevada Naturals, Inc.	Synergistic antimicrobial agents
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1999
- 1999-03-16 WO PCT/DK1999/000130 patent/WO1999046987A1/en not_active Ceased
- 1999-03-16 RU RU2000126306/15A patent/RU2221557C2/ru not_active IP Right Cessation
- 1999-03-16 NZ NZ506681A patent/NZ506681A/xx not_active IP Right Cessation
- 1999-03-16 AU AU27142/99A patent/AU740138B2/en not_active Ceased
- 1999-03-16 US US09/646,523 patent/US6414023B1/en not_active Expired - Lifetime
- 1999-03-16 EP EP99907340A patent/EP1063886B1/en not_active Expired - Lifetime
- 1999-03-16 ES ES99907340T patent/ES2191417T3/es not_active Expired - Lifetime
- 1999-03-16 EE EEP200000550A patent/EE04136B1/xx not_active IP Right Cessation
- 1999-03-16 CA CA002321658A patent/CA2321658C/en not_active Expired - Fee Related
- 1999-03-16 AT AT99907340T patent/ATE233484T1/de active
- 1999-03-16 PL PL343030A patent/PL196077B1/pl unknown
- 1999-03-16 DK DK99907340T patent/DK1063886T3/da active
- 1999-03-16 DE DE69905700T patent/DE69905700T2/de not_active Expired - Lifetime
- 1999-03-16 IL IL13789199A patent/IL137891A/xx not_active IP Right Cessation
- 1999-03-16 PT PT99907340T patent/PT1063886E/pt unknown
2000
- 2000-08-22 LV LVP-00-112A patent/LV12582B/en unknown
- 2000-09-14 LT LT2000087A patent/LT4778B/lt not_active IP Right Cessation
- 2000-09-15 NO NO20004609A patent/NO323049B1/no not_active IP Right Cessation

Also Published As

Publication number	Publication date
EE04136B1 (et)	2003-10-15
LV12582B (en)	2001-03-20
ATE233484T1 (de)	2003-03-15
LT4778B (lt)	2001-04-25
CA2321658C (en)	2008-11-18
IL137891A0 (en)	2001-10-31
EP1063886A1 (en)	2001-01-03
LT2000087A (lt)	2001-01-25
PL343030A1 (en)	2001-07-30
WO1999046987A1 (en)	1999-09-23
PT1063886E (pt)	2003-07-31
CA2321658A1 (en)	1999-09-23
IL137891A (en)	2005-03-20
LV12582A (en)	2000-12-20
RU2221557C2 (ru)	2004-01-20
ES2191417T3 (es)	2003-09-01
AU740138B2 (en)	2001-11-01
EP1063886B1 (en)	2003-03-05
US6414023B1 (en)	2002-07-02
PL196077B1 (pl)	2007-12-31
DE69905700T2 (de)	2003-11-13
AU2714299A (en)	1999-10-11
DE69905700D1 (de)	2003-04-10
EE200000550A (et)	2002-04-15
DK1063886T3 (da)	2003-06-23
NO20004609L (no)	2000-09-15
NZ506681A (en)	2002-12-20
NO20004609D0 (no)	2000-09-15

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2015-10-26	MM1K	Lapsed by not paying the annual fees

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