BRPI0707305A2 - agentes antimicrobianos poliméricos - Google Patents
agentes antimicrobianos poliméricos Download PDFInfo
- Publication number
- BRPI0707305A2 BRPI0707305A2 BRPI0707305-4A BRPI0707305A BRPI0707305A2 BR PI0707305 A2 BRPI0707305 A2 BR PI0707305A2 BR PI0707305 A BRPI0707305 A BR PI0707305A BR PI0707305 A2 BRPI0707305 A2 BR PI0707305A2
- Authority
- BR
- Brazil
- Prior art keywords
- alkyl
- substituted
- polymer
- copolymer
- formula
- Prior art date
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- 239000004599 antimicrobial Substances 0.000 title claims abstract description 25
- 229920000642 polymer Polymers 0.000 claims abstract description 139
- NOWKCMXCCJGMRR-UHFFFAOYSA-N Aziridine Chemical compound C1CN1 NOWKCMXCCJGMRR-UHFFFAOYSA-N 0.000 claims abstract description 56
- 238000000576 coating method Methods 0.000 claims abstract description 50
- 125000004433 nitrogen atom Chemical group N* 0.000 claims abstract description 44
- 239000004753 textile Substances 0.000 claims abstract description 8
- 125000000217 alkyl group Chemical group 0.000 claims description 98
- 229920001577 copolymer Polymers 0.000 claims description 88
- -1 polysiloxane Polymers 0.000 claims description 75
- 239000000203 mixture Substances 0.000 claims description 72
- 230000000845 anti-microbial effect Effects 0.000 claims description 63
- 125000001424 substituent group Chemical group 0.000 claims description 55
- 238000002360 preparation method Methods 0.000 claims description 54
- 150000003863 ammonium salts Chemical class 0.000 claims description 37
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims description 36
- 229910052736 halogen Inorganic materials 0.000 claims description 35
- KDCGOANMDULRCW-UHFFFAOYSA-N 7H-purine Chemical compound N1=CNC2=NC=NC2=C1 KDCGOANMDULRCW-UHFFFAOYSA-N 0.000 claims description 33
- 150000002367 halogens Chemical class 0.000 claims description 31
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 30
- 239000011248 coating agent Substances 0.000 claims description 29
- 238000000034 method Methods 0.000 claims description 29
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims description 27
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 25
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 claims description 22
- 238000009472 formulation Methods 0.000 claims description 21
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 20
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 claims description 17
- 125000000623 heterocyclic group Chemical group 0.000 claims description 17
- 229920003023 plastic Polymers 0.000 claims description 17
- 239000004033 plastic Substances 0.000 claims description 17
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 claims description 16
- 239000000463 material Substances 0.000 claims description 16
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 15
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 15
- 239000002023 wood Substances 0.000 claims description 14
- 125000003545 alkoxy group Chemical group 0.000 claims description 13
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 claims description 12
- 125000003342 alkenyl group Chemical group 0.000 claims description 10
- 229910052757 nitrogen Inorganic materials 0.000 claims description 10
- 125000005157 alkyl carboxy group Chemical group 0.000 claims description 9
- 239000001257 hydrogen Substances 0.000 claims description 9
- 229910052739 hydrogen Inorganic materials 0.000 claims description 9
- 230000008569 process Effects 0.000 claims description 9
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 8
- 229910006069 SO3H Inorganic materials 0.000 claims description 8
- 230000009471 action Effects 0.000 claims description 8
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims description 8
- 229910052751 metal Inorganic materials 0.000 claims description 8
- 239000002184 metal Substances 0.000 claims description 8
- 125000001624 naphthyl group Chemical group 0.000 claims description 8
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 8
- 239000000123 paper Substances 0.000 claims description 8
- 125000004429 atom Chemical group 0.000 claims description 7
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 7
- 238000004140 cleaning Methods 0.000 claims description 7
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 7
- 239000010985 leather Substances 0.000 claims description 7
- 229920001296 polysiloxane Polymers 0.000 claims description 7
- 125000004434 sulfur atom Chemical group 0.000 claims description 7
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 6
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 claims description 6
- 150000001768 cations Chemical group 0.000 claims description 6
- 229920006395 saturated elastomer Polymers 0.000 claims description 6
- 125000004400 (C1-C12) alkyl group Chemical group 0.000 claims description 5
- 125000005090 alkenylcarbonyl group Chemical group 0.000 claims description 5
- 125000005843 halogen group Chemical group 0.000 claims description 5
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- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 4
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 4
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 4
- 239000008199 coating composition Substances 0.000 claims description 4
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- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 3
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 claims description 3
- 125000002947 alkylene group Chemical group 0.000 claims description 3
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 230000000249 desinfective effect Effects 0.000 claims description 3
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 claims description 3
- 230000007935 neutral effect Effects 0.000 claims description 3
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- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims description 3
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims description 2
- 241000252505 Characidae Species 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
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- 125000000753 cycloalkyl group Chemical group 0.000 claims description 2
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- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical group OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims description 2
- 229920005615 natural polymer Polymers 0.000 claims description 2
- 125000004642 (C1-C12) alkoxy group Chemical group 0.000 claims 1
- 125000001589 carboacyl group Chemical group 0.000 claims 1
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- 230000001988 toxicity Effects 0.000 abstract description 2
- 150000001875 compounds Chemical class 0.000 description 26
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 25
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- 239000006071 cream Substances 0.000 description 16
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 14
- 239000011230 binding agent Substances 0.000 description 12
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- 239000000047 product Substances 0.000 description 10
- 238000011282 treatment Methods 0.000 description 10
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 9
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- 230000000844 anti-bacterial effect Effects 0.000 description 8
- 229920002118 antimicrobial polymer Polymers 0.000 description 8
- 150000004820 halides Chemical class 0.000 description 8
- 239000000178 monomer Substances 0.000 description 8
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- 239000007787 solid Substances 0.000 description 8
- 239000000243 solution Substances 0.000 description 8
- 239000002253 acid Substances 0.000 description 7
- 150000001412 amines Chemical class 0.000 description 7
- AGEZXYOZHKGVCM-UHFFFAOYSA-N benzyl bromide Chemical compound BrCC1=CC=CC=C1 AGEZXYOZHKGVCM-UHFFFAOYSA-N 0.000 description 7
- 239000007788 liquid Substances 0.000 description 7
- 150000003839 salts Chemical class 0.000 description 7
- 239000000758 substrate Substances 0.000 description 7
- 229920001169 thermoplastic Polymers 0.000 description 7
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- 230000003373 anti-fouling effect Effects 0.000 description 6
- 125000003118 aryl group Chemical group 0.000 description 6
- 239000002781 deodorant agent Substances 0.000 description 6
- 239000006210 lotion Substances 0.000 description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
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- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
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- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
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- 230000002087 whitening effect Effects 0.000 description 4
- 241000228245 Aspergillus niger Species 0.000 description 3
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
- 241000196324 Embryophyta Species 0.000 description 3
- 241000588724 Escherichia coli Species 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
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- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
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- A01N33/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
- A01N33/02—Amines; Quaternary ammonium compounds
- A01N33/04—Nitrogen directly attached to aliphatic or cycloaliphatic carbon atoms
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- A—HUMAN NECESSITIES
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- A01N33/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
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- A01N33/08—Amines; Quaternary ammonium compounds containing oxygen or sulfur
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- A—HUMAN NECESSITIES
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- A01N33/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
- A01N33/02—Amines; Quaternary ammonium compounds
- A01N33/12—Quaternary ammonium compounds
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- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/12—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group, wherein Cn means a carbon skeleton not containing a ring; Thio analogues thereof
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- A—HUMAN NECESSITIES
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
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Landscapes
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- Cosmetics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
- Compositions Of Macromolecular Compounds (AREA)
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| US20090117367A1 (en) * | 2007-09-28 | 2009-05-07 | General Electric Company | Article and associated method |
| CN101394739A (zh) * | 2006-02-28 | 2009-03-25 | 西巴控股公司 | 抗微生物化合物 |
| BRPI0712124A2 (pt) * | 2006-06-02 | 2012-01-17 | Ciba Holding Inc | ácidos e sais antimicrobianos |
| US7906544B2 (en) * | 2007-01-26 | 2011-03-15 | North Carolina State University | Inhibition of bacterial biofilms with imidazole derivatives |
| US20090060984A1 (en) * | 2007-09-05 | 2009-03-05 | John Texter | Anionic surfactants lethal to gram-positive bacteria |
| US8278340B2 (en) | 2007-11-27 | 2012-10-02 | North Carolina State University | Inhibition of biofilms in plants with imidazole derivatives |
| US9005643B2 (en) * | 2008-04-04 | 2015-04-14 | North Carolina State University | Inhibition of bacterial biofilms with imidazole-phenyl derivatives |
| US7897631B2 (en) * | 2008-04-21 | 2011-03-01 | North Carolina State University | Inhibition and dispersion of bacterial biofilms with imidazole-triazole derivatives |
| US20110294668A1 (en) | 2008-12-08 | 2011-12-01 | North Carolina State University | Inhibition and dispersion of biofilms in plants with imidazole-triazole derivatives |
| TW201111457A (en) * | 2009-06-10 | 2011-04-01 | Glaxosmithkline Llc | Novel article |
| US9221765B2 (en) | 2009-06-10 | 2015-12-29 | North Carolina State University | Inhibition and dispersion of bacterial biofilms with benzimidazole derivatives |
| CN101628952B (zh) * | 2009-08-20 | 2011-04-20 | 合肥工业大学 | 胍类高分子型抗菌剂的制备方法 |
| CA2797709C (en) | 2010-04-28 | 2018-07-31 | Jason J. Locklin | Photochemical cross-linkable polymers, methods of making photochemical cross-linkable polymers, methods of using photochemical cross-linkable polymers, and methods of making articles containing photochemical cross-linkable polymers |
| WO2012135016A2 (en) | 2011-03-25 | 2012-10-04 | North Carolina State University | Inhibition of bacterial biofilms and microbial growth with imidazole derivatives |
| US8721936B2 (en) | 2011-04-21 | 2014-05-13 | University Of Georgia Research Foundation, Inc. | Devices and methods for forming non-spherical particles |
| AT511386B1 (de) * | 2011-05-03 | 2013-03-15 | Ke Kelit Kunststoffwerk Gmbh | Kontaktbiozid |
| WO2013012666A2 (en) * | 2011-07-15 | 2013-01-24 | The University Of Georgia Research Foundation, Inc. | Compounds, methods of making, and methods of use |
| WO2013012664A2 (en) | 2011-07-15 | 2013-01-24 | The University Of Georgia Research Foundation, Inc | Permanent attachment of agents to surfaces containing c-h functionality |
| WO2013019918A2 (en) | 2011-08-04 | 2013-02-07 | The University Of Georgia Research Foundation, Inc. | Permanent attachment of ammonium and guanidine-based antimicrobials to surfaces containing-oh functionality |
| US9839213B2 (en) | 2011-10-14 | 2017-12-12 | The University Of Georgia Research Foundation, Inc. | Photochemical cross-linkable polymers, methods of making photochemical cross-linkable polymers, methods of using photochemical cross-linkable polymers, and methods of making articles containing photochemical cross-linkable polymers |
| DE102012219951A1 (de) * | 2012-10-31 | 2014-04-30 | Henkel Ag & Co. Kgaa | Polymere zur antimikrobiellen Ausrüstung |
| AU2013359919A1 (en) | 2012-12-11 | 2015-07-02 | Nano Safe Coatings Incorporated (A Florida Corporation 3 P14000024914) | UV cured benzophenone terminated quaternary ammonium antimicrobials for surfaces |
| AT515029B1 (de) | 2013-10-21 | 2015-12-15 | Polymer Competence Ct Leoben | Kontaktbiozide auf Basis von Poly(oxazin)en, Poly(oxazpein)en und Poly(oxazozin)en |
| CN103554491B (zh) * | 2013-10-25 | 2016-06-29 | 华南理工大学 | 聚乙烯亚胺抗菌功能化聚合物及其制备方法与应用 |
| WO2016039425A1 (ja) * | 2014-09-10 | 2016-03-17 | 株式会社日本触媒 | ポリアルキレンイミン誘導体を含む抗菌剤 |
| US11033023B2 (en) | 2014-11-26 | 2021-06-15 | Microban Products Company | Surface disinfectant with residual biocidal property |
| US10842147B2 (en) | 2014-11-26 | 2020-11-24 | Microban Products Company | Surface disinfectant with residual biocidal property |
| US10834922B2 (en) | 2014-11-26 | 2020-11-17 | Microban Products Company | Surface disinfectant with residual biocidal property |
| US10925281B2 (en) | 2014-11-26 | 2021-02-23 | Microban Products Company | Surface disinfectant with residual biocidal property |
| BR112018003786B1 (pt) | 2015-08-27 | 2022-05-17 | Nano Safe Coatings Incorporated (A Florida Corporation 3 P 14000024914) | Preparação de antimicrobianos contendo sulfonamida e composições de tratamento de substrato de antimicrobianos contendo sulfonamida |
| JP6609151B2 (ja) * | 2015-09-30 | 2019-11-20 | 株式会社日本触媒 | ポリアルキレンイミン誘導体 |
| EP3379932A4 (en) * | 2015-11-23 | 2019-05-01 | Microban Products Company | SURFACE DISINFECTANT WITH REMAINING BIOCIDAL PROPERTIES |
| EP3379931B1 (en) * | 2015-11-23 | 2024-07-17 | Microban Products Company | Surface disinfectant with residual biocidal property |
| US11384172B2 (en) * | 2015-12-14 | 2022-07-12 | Jsr Corporation | Polymer, antimicrobial agent, disinfectant, antimicrobial material, disinfectant material, antimicrobial method, and disinfecting method |
| US11503824B2 (en) | 2016-05-23 | 2022-11-22 | Microban Products Company | Touch screen cleaning and protectant composition |
| US11766386B2 (en) * | 2016-11-07 | 2023-09-26 | 3M Innovative Properties Company | Medical composition containing guanidinyl-containing polymer(s) and carrageenane(s) |
| CN107200798A (zh) * | 2017-06-12 | 2017-09-26 | 厦门建霖健康家居股份有限公司 | 一种具有广谱抗菌的抗菌剂 |
| CN107141474A (zh) * | 2017-07-04 | 2017-09-08 | 南开大学 | 含三氯生的聚（β‑氨酯）制备方法及在选择性杀灭口腔变形链球菌生物被膜中的应用 |
| JP7159084B2 (ja) * | 2018-03-15 | 2022-10-24 | ライオン株式会社 | 義歯ケア用組成物、義歯用抗菌剤、及び義歯用バイオフィルム形成抑制剤 |
| US11466122B2 (en) | 2018-10-18 | 2022-10-11 | Milliken & Company | Polyethyleneimine compounds containing N-halamine and derivatives thereof |
| US11518963B2 (en) | 2018-10-18 | 2022-12-06 | Milliken & Company | Polyethyleneimine compounds containing N-halamine and derivatives thereof |
| US11732218B2 (en) * | 2018-10-18 | 2023-08-22 | Milliken & Company | Polyethyleneimine compounds containing N-halamine and derivatives thereof |
| US11299591B2 (en) | 2018-10-18 | 2022-04-12 | Milliken & Company | Polyethyleneimine compounds containing N-halamine and derivatives thereof |
| JP7305158B2 (ja) * | 2019-05-13 | 2023-07-10 | 国立大学法人滋賀医科大学 | 修飾ポリエチレンイミン及びその製造方法 |
| CN111345298B (zh) * | 2020-04-26 | 2020-12-01 | 润贝航空科技股份有限公司 | 一种水溶性季铵盐消毒剂 |
| IT202100000848A1 (it) | 2021-01-19 | 2022-07-19 | Univ Degli Studi Roma La Sapienza | Rivestimento antimicrobico multistrato rimovibile resistente all’acqua per superfici da contatto e suo metodo di preparazione |
| CN119505619B (zh) * | 2024-10-11 | 2025-11-25 | 浙江大学绍兴研究院 | 一种双重杀菌-抗黏复合交联涂层及其制备方法和用途 |
Family Cites Families (20)
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| US3301783A (en) * | 1960-08-04 | 1967-01-31 | Petrolite Corp | Lubricating composition |
| US3116969A (en) * | 1961-03-22 | 1964-01-07 | Worth Chemical Products Compan | Chemical coating for filters |
| US4325940A (en) * | 1976-11-24 | 1982-04-20 | Kewanee Industries, Inc. | Anti-microbial, cosmetic and water-treating ionene polymeric compounds |
| US4597898A (en) * | 1982-12-23 | 1986-07-01 | The Proctor & Gamble Company | Detergent compositions containing ethoxylated amines having clay soil removal/anti-redeposition properties |
| US5405919A (en) * | 1992-08-24 | 1995-04-11 | The United States Of America As Represented By The Secretary Of Health And Human Services | Polymer-bound nitric oxide/nucleophile adduct compositions, pharmaceutical compositions and methods of treating biological disorders |
| US5300287A (en) * | 1992-11-04 | 1994-04-05 | Alcon Laboratories, Inc. | Polymeric antimicrobials and their use in pharmaceutical compositions |
| US6071866A (en) * | 1994-06-01 | 2000-06-06 | Lever Brothers Company, Division Of Conopco, Inc. | Mild antimicrobial liquid cleansing formulations comprising hydroxy acid buffering compound or compounds as potentiator of antimicrobial effectiveness |
| US5635462A (en) * | 1994-07-08 | 1997-06-03 | Gojo Industries, Inc. | Antimicrobial cleansing compositions |
| JP3526661B2 (ja) * | 1995-06-23 | 2004-05-17 | ミヨシ油脂株式会社 | 抗菌剤、抗菌性樹脂及び抗菌性塗料 |
| JP3688040B2 (ja) * | 1995-12-14 | 2005-08-24 | ミヨシ油脂株式会社 | 抗菌剤 |
| GB9526325D0 (en) * | 1995-12-22 | 1996-02-21 | Bp Exploration Operating | Inhibitors |
| US6121226A (en) * | 1996-05-03 | 2000-09-19 | The Procter & Gamble Company | Compositions comprising cotton soil release polymers and protease enzymes |
| CN1162528C (zh) * | 1996-05-03 | 2004-08-18 | 普罗格特-甘布尔公司 | 棉料去污聚合物 |
| WO1997046218A2 (en) * | 1996-06-04 | 1997-12-11 | Ciba Specialty Chemicals Holding Inc. | Concentrated liquid formulations comprising a microbicidally active ingredient |
| DE69715444T2 (de) * | 1996-07-10 | 2003-04-30 | Steris Inc. (N.D.Ges.D. Staates Delaware), Temecula | Triclosan enthaltende hautreinigungsmittel mit verbesserter wirksamkeit |
| US6258368B1 (en) * | 1997-06-04 | 2001-07-10 | The Procter & Gamble Company | Antimicrobial wipes |
| US6811771B1 (en) * | 1999-04-27 | 2004-11-02 | Ebara Corporation | Bactericidal organic polymeric material |
| US6861397B2 (en) * | 1999-06-23 | 2005-03-01 | The Dial Corporation | Compositions having enhanced deposition of a topically active compound on a surface |
| US6872241B2 (en) * | 2001-10-19 | 2005-03-29 | Innovative Construction And Building Materials, Llc | Anti-pathogenic air filtration media and air handling devices having protective capabilities against infectious airborne mircoorganisms |
| GB0221942D0 (en) * | 2002-09-20 | 2002-10-30 | Univ Strathclyde | Drug delivery |
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- 2007-01-23 US US11/656,863 patent/US20070231291A1/en not_active Abandoned
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| AU2007209376B2 (en) | 2013-02-07 |
| AU2007209376A1 (en) | 2007-08-02 |
| WO2007085552A3 (en) | 2008-03-27 |
| CA2636739A1 (en) | 2007-08-02 |
| WO2007085552A2 (en) | 2007-08-02 |
| US20070231291A1 (en) | 2007-10-04 |
| KR20080086520A (ko) | 2008-09-25 |
| JP2009524719A (ja) | 2009-07-02 |
| CN101374885A (zh) | 2009-02-25 |
| EP1984426A2 (en) | 2008-10-29 |
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