NO853097L - Fremgangsmaate ved fremstilling av iodforbindelser. - Google Patents
Fremgangsmaate ved fremstilling av iodforbindelser.Info
- Publication number
- NO853097L NO853097L NO853097A NO853097A NO853097L NO 853097 L NO853097 L NO 853097L NO 853097 A NO853097 A NO 853097A NO 853097 A NO853097 A NO 853097A NO 853097 L NO853097 L NO 853097L
- Authority
- NO
- Norway
- Prior art keywords
- iodine
- solution
- polydextrose
- water
- available
- Prior art date
Links
- 238000002360 preparation method Methods 0.000 title claims description 44
- 238000000034 method Methods 0.000 title description 12
- 150000002497 iodine compounds Chemical class 0.000 title 1
- 229910052740 iodine Inorganic materials 0.000 claims description 373
- 239000011630 iodine Substances 0.000 claims description 370
- DLRVVLDZNNYCBX-UHFFFAOYSA-N Polydextrose Polymers OC1C(O)C(O)C(CO)OC1OCC1C(O)C(O)C(O)C(O)O1 DLRVVLDZNNYCBX-UHFFFAOYSA-N 0.000 claims description 303
- 239000001259 polydextrose Substances 0.000 claims description 151
- 229940035035 polydextrose Drugs 0.000 claims description 151
- 235000013856 polydextrose Nutrition 0.000 claims description 150
- 229920001100 Polydextrose Polymers 0.000 claims description 149
- 230000002070 germicidal effect Effects 0.000 claims description 39
- 239000000872 buffer Substances 0.000 claims description 28
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 claims description 12
- 229930006000 Sucrose Natural products 0.000 claims description 12
- 239000005720 sucrose Substances 0.000 claims description 12
- 239000004094 surface-active agent Substances 0.000 claims description 8
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 claims description 6
- 230000001580 bacterial effect Effects 0.000 claims description 4
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims 9
- 238000011200 topical administration Methods 0.000 claims 3
- 229920001577 copolymer Polymers 0.000 claims 2
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 330
- 239000000243 solution Substances 0.000 description 273
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 118
- PEDCQBHIVMGVHV-UHFFFAOYSA-N glycerol group Chemical group OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 72
- 229920000642 polymer Polymers 0.000 description 72
- 238000003756 stirring Methods 0.000 description 61
- 229920001917 Ficoll Polymers 0.000 description 52
- 239000000203 mixture Substances 0.000 description 31
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 28
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 25
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 25
- 239000000843 powder Substances 0.000 description 20
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 18
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid group Chemical group C(CC(O)(C(=O)O)CC(=O)O)(=O)O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 16
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 15
- 238000002835 absorbance Methods 0.000 description 15
- 239000007864 aqueous solution Substances 0.000 description 15
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 15
- 230000015572 biosynthetic process Effects 0.000 description 14
- 238000006243 chemical reaction Methods 0.000 description 13
- 150000002500 ions Chemical class 0.000 description 13
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 13
- 239000003599 detergent Substances 0.000 description 12
- 230000001965 increasing effect Effects 0.000 description 12
- 229940035535 iodophors Drugs 0.000 description 12
- 230000002421 anti-septic effect Effects 0.000 description 10
- 229920001282 polysaccharide Polymers 0.000 description 10
- 210000001519 tissue Anatomy 0.000 description 10
- 230000007423 decrease Effects 0.000 description 9
- 229920000620 organic polymer Polymers 0.000 description 9
- IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 9
- 230000002829 reductive effect Effects 0.000 description 8
- 239000007787 solid Substances 0.000 description 8
- 238000010438 heat treatment Methods 0.000 description 7
- 238000002844 melting Methods 0.000 description 7
- 230000008018 melting Effects 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- 238000012360 testing method Methods 0.000 description 7
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical group OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 6
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 6
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- 238000009472 formulation Methods 0.000 description 6
- 150000002496 iodine Chemical class 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- 239000002798 polar solvent Substances 0.000 description 6
- 238000004458 analytical method Methods 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- 238000004108 freeze drying Methods 0.000 description 5
- 150000004676 glycans Chemical class 0.000 description 5
- 229910000043 hydrogen iodide Inorganic materials 0.000 description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 5
- 238000002329 infrared spectrum Methods 0.000 description 5
- 230000003993 interaction Effects 0.000 description 5
- XMBWDFGMSWQBCA-UHFFFAOYSA-M iodide Chemical compound [I-] XMBWDFGMSWQBCA-UHFFFAOYSA-M 0.000 description 5
- 229940006461 iodide ion Drugs 0.000 description 5
- 239000005017 polysaccharide Substances 0.000 description 5
- WRTMQOHKMFDUKX-UHFFFAOYSA-N triiodide Chemical compound I[I-]I WRTMQOHKMFDUKX-UHFFFAOYSA-N 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 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 4
- 241001465754 Metazoa Species 0.000 description 4
- 229920000153 Povidone-iodine Polymers 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 4
- 206010052428 Wound Diseases 0.000 description 4
- 208000027418 Wounds and injury Diseases 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 239000012736 aqueous medium Substances 0.000 description 4
- 229960004106 citric acid Drugs 0.000 description 4
- 238000010668 complexation reaction Methods 0.000 description 4
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- 239000000463 material Substances 0.000 description 4
- 239000011159 matrix material Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 238000004448 titration Methods 0.000 description 4
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 3
- 102000004190 Enzymes Human genes 0.000 description 3
- 108090000790 Enzymes Proteins 0.000 description 3
- 229920003081 Povidone K 30 Polymers 0.000 description 3
- 241000191967 Staphylococcus aureus Species 0.000 description 3
- 239000003945 anionic surfactant Substances 0.000 description 3
- 230000000844 anti-bacterial effect Effects 0.000 description 3
- 210000004027 cell Anatomy 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000004132 cross linking Methods 0.000 description 3
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 3
- 229910000397 disodium phosphate Inorganic materials 0.000 description 3
- 235000019800 disodium phosphate Nutrition 0.000 description 3
- 238000010494 dissociation reaction Methods 0.000 description 3
- 230000005593 dissociations Effects 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000000605 extraction Methods 0.000 description 3
- 239000012847 fine chemical Substances 0.000 description 3
- 150000004694 iodide salts Chemical class 0.000 description 3
- 244000005700 microbiome Species 0.000 description 3
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- 230000007935 neutral effect Effects 0.000 description 3
- 239000008188 pellet Substances 0.000 description 3
- 230000009257 reactivity Effects 0.000 description 3
- FVAUCKIRQBBSSJ-UHFFFAOYSA-M sodium iodide Chemical compound [Na+].[I-] FVAUCKIRQBBSSJ-UHFFFAOYSA-M 0.000 description 3
- 239000001488 sodium phosphate Substances 0.000 description 3
- 239000000600 sorbitol Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- DHCDFWKWKRSZHF-UHFFFAOYSA-L thiosulfate(2-) Chemical compound [O-]S([S-])(=O)=O DHCDFWKWKRSZHF-UHFFFAOYSA-L 0.000 description 3
- 231100000331 toxic Toxicity 0.000 description 3
- 230000002588 toxic effect Effects 0.000 description 3
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- 230000001988 toxicity Effects 0.000 description 3
- 230000000007 visual effect Effects 0.000 description 3
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 229930182555 Penicillin Natural products 0.000 description 2
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- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 239000004133 Sodium thiosulphate Substances 0.000 description 2
- 229920002472 Starch Polymers 0.000 description 2
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- YWEUIGNSBFLMFL-UHFFFAOYSA-N diphosphonate Chemical compound O=P(=O)OP(=O)=O YWEUIGNSBFLMFL-UHFFFAOYSA-N 0.000 description 2
- 239000012153 distilled water Substances 0.000 description 2
- 239000008103 glucose Substances 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- 229940071870 hydroiodic acid Drugs 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
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- -1 hypoiodite ion Chemical class 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- TWNIBLMWSKIRAT-VFUOTHLCSA-N levoglucosan Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@H]2CO[C@@H]1O2 TWNIBLMWSKIRAT-VFUOTHLCSA-N 0.000 description 2
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- DLYUQMMRRRQYAE-UHFFFAOYSA-N phosphorus pentoxide Inorganic materials O1P(O2)(=O)OP3(=O)OP1(=O)OP2(=O)O3 DLYUQMMRRRQYAE-UHFFFAOYSA-N 0.000 description 2
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- OHVLMTFVQDZYHP-UHFFFAOYSA-N 1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)-2-[4-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]piperazin-1-yl]ethanone Chemical compound N1N=NC=2CN(CCC=21)C(CN1CCN(CC1)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)=O OHVLMTFVQDZYHP-UHFFFAOYSA-N 0.000 description 1
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- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 230000000153 supplemental effect Effects 0.000 description 1
- 235000019605 sweet taste sensations Nutrition 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 230000009885 systemic effect Effects 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 238000002211 ultraviolet spectrum Methods 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
- 239000000080 wetting agent Substances 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
-
- 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
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Plant Pathology (AREA)
- Environmental Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- Zoology (AREA)
- Pest Control & Pesticides (AREA)
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Toxicology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Medicinal Preparation (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/638,558 US4576818A (en) | 1984-08-07 | 1984-08-07 | Iodophor composition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO853097L true NO853097L (no) | 1986-02-10 |
Family
ID=24560525
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO853097A NO853097L (no) | 1984-08-07 | 1985-08-06 | Fremgangsmaate ved fremstilling av iodforbindelser. |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US4576818A (da) |
| EP (1) | EP0172984A1 (da) |
| JP (1) | JPS6147405A (da) |
| KR (1) | KR860001524A (da) |
| AU (1) | AU576612B2 (da) |
| DK (1) | DK332185A (da) |
| ES (1) | ES542273A0 (da) |
| FI (1) | FI852868L (da) |
| IL (1) | IL74702A0 (da) |
| IN (1) | IN162218B (da) |
| NO (1) | NO853097L (da) |
| NZ (1) | NZ211500A (da) |
| PH (1) | PH20620A (da) |
| PT (1) | PT80389B (da) |
| YU (1) | YU126985A (da) |
| ZA (1) | ZA852166B (da) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4668510A (en) * | 1984-08-07 | 1987-05-26 | Euroceltique, S.A. | Iodophor composition |
| NL8500774A (nl) * | 1985-03-18 | 1986-10-16 | Dagra Nv | Werkwijze ter bereiding van een vrij vloeiend, homogeen povidonjood wondpoeder. |
| GB8520664D0 (en) * | 1985-08-17 | 1985-09-25 | Euro Celtique Sa | Suppository |
| DE3540246A1 (de) * | 1985-11-13 | 1987-05-14 | Henkel Kgaa | Verwendung von alkoxyhydroxyfettsaeuren als korrosionsinhibitoren in oelen und oelhaltigen emulsionen |
| US4719106A (en) * | 1986-04-11 | 1988-01-12 | Euroceltique S.A. | Iodophor composition with immediate and long action microbicidal action |
| GB8613689D0 (en) * | 1986-06-05 | 1986-07-09 | Euro Celtique Sa | Pharmaceutical composition |
| GB8622012D0 (en) * | 1986-09-12 | 1986-10-22 | Euro Celtique Sa | Solid iodophor composition |
| US5322695A (en) * | 1987-01-09 | 1994-06-21 | Hercon Laboratories Corporation | Moisture-vapor-permeable dressing |
| US4904480A (en) * | 1988-09-19 | 1990-02-27 | Becton, Dickinson And Company | Radiation compatible iodine formulation |
| DE4414254A1 (de) * | 1994-04-23 | 1995-10-26 | Basf Ag | Iodophor aus Poly-N-vinyllactam und Dextrin |
| US6777003B1 (en) * | 1995-06-07 | 2004-08-17 | Cognis Corporation | Iodine complex of alkyl polyglycosides |
| DE19717191A1 (de) | 1997-04-24 | 1998-10-29 | Basf Ag | Flüssiges Iodophor aus Poly-N-vinyllactam, Dextrin und Alkoholen |
| KR100317476B1 (ko) * | 2001-05-17 | 2001-12-22 | 박선규 | 강인성 식물의 인피섬유 정련 방법 |
| HUP0105261A2 (hu) * | 2001-12-06 | 2003-08-28 | Szilveszter Török | Természetes anyagú, szerves kötésű jódtartalmú készítmények jód élő szervezetbe történő bevitelére, továbbá eljárások azok előállítására |
| KR100704726B1 (ko) * | 2006-10-27 | 2007-04-09 | 박선규 | 인피섬유의 정련에 유용한 엔테로박터 저고비애 에이취엘2006 및 이를 이용한 인피섬유의 정련방법 |
| US10258647B2 (en) | 2015-09-01 | 2019-04-16 | Particle Dynamics International, Llc | Iron-polysaccharide complexes and methods for the preparation thereof |
| WO2023168122A1 (en) * | 2022-03-04 | 2023-09-07 | The Regents Of The University Of California | Compositions and methods for targeted delivery of chemicals and biomolecules to plants and fungi |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB815421A (en) * | 1957-08-26 | 1959-06-24 | Ohio Commw Eng Co | Iodo-dextran and methods for producing the same |
| US1925135A (en) * | 1926-03-13 | 1933-09-05 | Merck & Co Inc | Iodine composition |
| US2022729A (en) * | 1933-07-19 | 1935-12-03 | Mackie Henkels Inc | Stable colloidal solution of iodine |
| US3928581A (en) * | 1972-09-13 | 1975-12-23 | Astra Laekemedel Ab | Certain polymer-iron complexes for treatment of iron deficiency |
| US4010259A (en) * | 1975-07-17 | 1977-03-01 | Johansson J A Olof | Disinfectants containing iodine complexed to a hydrophilic organic carrier |
| US4470975A (en) * | 1977-10-21 | 1984-09-11 | The Johns Hopkins University | Method and composition for the elimination of water from an animal body |
| US4401651A (en) * | 1979-04-18 | 1983-08-30 | Knutson Richard A | Wound-healing compositions containing povidone-iodine |
| US4459280A (en) * | 1982-07-23 | 1984-07-10 | G. D. Searle & Co. | Psyllium hydrophilic mucilloid composition |
-
1984
- 1984-08-07 US US06/638,558 patent/US4576818A/en not_active Expired - Fee Related
-
1985
- 1985-03-15 IN IN194/CAL/85A patent/IN162218B/en unknown
- 1985-03-19 EP EP85103148A patent/EP0172984A1/en not_active Withdrawn
- 1985-03-19 NZ NZ211500A patent/NZ211500A/en unknown
- 1985-03-22 ZA ZA852166A patent/ZA852166B/xx unknown
- 1985-03-25 IL IL74702A patent/IL74702A0/xx unknown
- 1985-04-16 ES ES542273A patent/ES542273A0/es active Granted
- 1985-05-03 PT PT80389A patent/PT80389B/pt unknown
- 1985-06-19 PH PH32424A patent/PH20620A/en unknown
- 1985-07-22 DK DK332185A patent/DK332185A/da not_active Application Discontinuation
- 1985-07-23 FI FI852868A patent/FI852868L/fi not_active Application Discontinuation
- 1985-08-05 AU AU45846/85A patent/AU576612B2/en not_active Ceased
- 1985-08-06 NO NO853097A patent/NO853097L/no unknown
- 1985-08-07 JP JP60172560A patent/JPS6147405A/ja active Pending
- 1985-08-07 YU YU01269/85A patent/YU126985A/xx unknown
- 1985-08-07 KR KR1019850005700A patent/KR860001524A/ko not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| PT80389B (en) | 1986-12-15 |
| FI852868L (fi) | 1986-02-08 |
| NZ211500A (en) | 1988-03-30 |
| YU126985A (en) | 1987-12-31 |
| JPS6147405A (ja) | 1986-03-07 |
| IL74702A0 (en) | 1985-06-30 |
| US4576818A (en) | 1986-03-18 |
| KR860001524A (ko) | 1986-03-20 |
| AU576612B2 (en) | 1988-09-01 |
| PH20620A (en) | 1987-03-06 |
| DK332185A (da) | 1986-02-08 |
| FI852868A0 (fi) | 1985-07-23 |
| ES8603268A1 (es) | 1985-12-16 |
| AU4584685A (en) | 1986-02-13 |
| PT80389A (en) | 1985-06-01 |
| IN162218B (da) | 1988-04-16 |
| DK332185D0 (da) | 1985-07-22 |
| EP0172984A1 (en) | 1986-03-05 |
| ES542273A0 (es) | 1985-12-16 |
| ZA852166B (en) | 1986-03-26 |
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