JP2010520316A5 - - Google Patents
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- JP2010520316A5 JP2010520316A5 JP2009551200A JP2009551200A JP2010520316A5 JP 2010520316 A5 JP2010520316 A5 JP 2010520316A5 JP 2009551200 A JP2009551200 A JP 2009551200A JP 2009551200 A JP2009551200 A JP 2009551200A JP 2010520316 A5 JP2010520316 A5 JP 2010520316A5
- Authority
- JP
- Japan
- Prior art keywords
- coating
- coating formulation
- copolymers
- hydrophilic
- polymer
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- 239000000203 mixture Substances 0.000 claims description 6
- 238000010546 Norrish type I reaction Methods 0.000 claims description 4
- 239000008199 coating composition Substances 0.000 claims 12
- 239000011248 coating agent Substances 0.000 claims 11
- 238000000576 coating method Methods 0.000 claims 11
- 229920001577 copolymer Polymers 0.000 claims 6
- 229920001519 homopolymer Polymers 0.000 claims 6
- 229920000642 polymer Polymers 0.000 claims 6
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 claims 2
- 238000010547 Norrish type II reaction Methods 0.000 claims 2
- 239000012530 fluid Substances 0.000 claims 2
- 239000000178 monomer Substances 0.000 claims 2
- 229920000867 polyelectrolyte Polymers 0.000 claims 2
- 150000003839 salts Chemical class 0.000 claims 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims 2
- 238000009736 wetting Methods 0.000 claims 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical class COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims 1
- 239000004721 Polyphenylene oxide Substances 0.000 claims 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims 1
- 230000003213 activating effect Effects 0.000 claims 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 claims 1
- 239000012965 benzophenone Substances 0.000 claims 1
- 150000008366 benzophenones Chemical class 0.000 claims 1
- 230000005670 electromagnetic radiation Effects 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- 238000009472 formulation Methods 0.000 claims 1
- 239000001530 fumaric acid Substances 0.000 claims 1
- 229920001477 hydrophilic polymer Polymers 0.000 claims 1
- 239000003999 initiator Substances 0.000 claims 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims 1
- 239000011976 maleic acid Substances 0.000 claims 1
- 239000012528 membrane Substances 0.000 claims 1
- 229920000570 polyether Polymers 0.000 claims 1
- 238000006116 polymerization reaction Methods 0.000 claims 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 claims 1
- 239000000758 substrate Substances 0.000 claims 1
- 125000000542 sulfonic acid group Chemical group 0.000 claims 1
- -1 Ciba-Geigy) Chemical compound 0.000 description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
- AUHZEENZYGFFBQ-UHFFFAOYSA-N 1,3,5-trimethylbenzene Chemical compound CC1=CC(C)=CC(C)=C1 AUHZEENZYGFFBQ-UHFFFAOYSA-N 0.000 description 2
- KWVGIHKZDCUPEU-UHFFFAOYSA-N 2,2-dimethoxy-2-phenylacetophenone Chemical compound C=1C=CC=CC=1C(OC)(OC)C(=O)C1=CC=CC=C1 KWVGIHKZDCUPEU-UHFFFAOYSA-N 0.000 description 2
- GJKGAPPUXSSCFI-UHFFFAOYSA-N 2-Hydroxy-4'-(2-hydroxyethoxy)-2-methylpropiophenone Chemical compound CC(C)(O)C(=O)C1=CC=C(OCCO)C=C1 GJKGAPPUXSSCFI-UHFFFAOYSA-N 0.000 description 2
- UHFFVFAKEGKNAQ-UHFFFAOYSA-N 2-benzyl-2-(dimethylamino)-1-(4-morpholin-4-ylphenyl)butan-1-one Chemical compound C=1C=C(N2CCOCC2)C=CC=1C(=O)C(CC)(N(C)C)CC1=CC=CC=C1 UHFFVFAKEGKNAQ-UHFFFAOYSA-N 0.000 description 2
- LWRBVKNFOYUCNP-UHFFFAOYSA-N 2-methyl-1-(4-methylsulfanylphenyl)-2-morpholin-4-ylpropan-1-one Chemical compound C1=CC(SC)=CC=C1C(=O)C(C)(C)N1CCOCC1 LWRBVKNFOYUCNP-UHFFFAOYSA-N 0.000 description 2
- LFOXEOLGJPJZAA-UHFFFAOYSA-N [(2,6-dimethoxybenzoyl)-(2,4,4-trimethylpentyl)phosphoryl]-(2,6-dimethoxyphenyl)methanone Chemical compound COC1=CC=CC(OC)=C1C(=O)P(=O)(CC(C)CC(C)(C)C)C(=O)C1=C(OC)C=CC=C1OC LFOXEOLGJPJZAA-UHFFFAOYSA-N 0.000 description 2
- 150000008062 acetophenones Chemical class 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- UFUASNAHBMBJIX-UHFFFAOYSA-N propan-1-one Chemical compound CC[C]=O UFUASNAHBMBJIX-UHFFFAOYSA-N 0.000 description 2
- QNODIIQQMGDSEF-UHFFFAOYSA-N (1-hydroxycyclohexyl)-phenylmethanone Chemical compound C=1C=CC=CC=1C(=O)C1(O)CCCCC1 QNODIIQQMGDSEF-UHFFFAOYSA-N 0.000 description 1
- CKGKXGQVRVAKEA-UHFFFAOYSA-N (2-methylphenyl)-phenylmethanone Chemical class CC1=CC=CC=C1C(=O)C1=CC=CC=C1 CKGKXGQVRVAKEA-UHFFFAOYSA-N 0.000 description 1
- JDPDLMITLVAWKZ-UHFFFAOYSA-N 1,3-dioxolan-4-yl(phenyl)methanone Chemical class C=1C=CC=CC=1C(=O)C1COCO1 JDPDLMITLVAWKZ-UHFFFAOYSA-N 0.000 description 1
- 239000012956 1-hydroxycyclohexylphenyl-ketone Substances 0.000 description 1
- MEYARNKYUHUVBB-UHFFFAOYSA-N 2-hydroxy-1-[2-(hydroxymethyl)phenyl]-2-phenylethanone Chemical compound OCC1=CC=CC=C1C(=O)C(O)C1=CC=CC=C1 MEYARNKYUHUVBB-UHFFFAOYSA-N 0.000 description 1
- XMLYCEVDHLAQEL-UHFFFAOYSA-N 2-hydroxy-2-methyl-1-phenylpropan-1-one Chemical compound CC(C)(O)C(=O)C1=CC=CC=C1 XMLYCEVDHLAQEL-UHFFFAOYSA-N 0.000 description 1
- RIWRBSMFKVOJMN-UHFFFAOYSA-N 2-methyl-1-phenylpropan-2-ol Chemical compound CC(C)(O)CC1=CC=CC=C1 RIWRBSMFKVOJMN-UHFFFAOYSA-N 0.000 description 1
- ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical class C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- MQDJYUACMFCOFT-UHFFFAOYSA-N bis[2-(1-hydroxycyclohexyl)phenyl]methanone Chemical compound C=1C=CC=C(C(=O)C=2C(=CC=CC=2)C2(O)CCCCC2)C=1C1(O)CCCCC1 MQDJYUACMFCOFT-UHFFFAOYSA-N 0.000 description 1
- PODOEQVNFJSWIK-UHFFFAOYSA-N diphenylphosphoryl-(2,4,6-trimethoxyphenyl)methanone Chemical compound COC1=CC(OC)=CC(OC)=C1C(=O)P(=O)(C=1C=CC=CC=1)C1=CC=CC=C1 PODOEQVNFJSWIK-UHFFFAOYSA-N 0.000 description 1
- VFHVQBAGLAREND-UHFFFAOYSA-N diphenylphosphoryl-(2,4,6-trimethylphenyl)methanone Chemical compound CC1=CC(C)=CC(C)=C1C(=O)P(=O)(C=1C=CC=CC=1)C1=CC=CC=C1 VFHVQBAGLAREND-UHFFFAOYSA-N 0.000 description 1
- 239000012949 free radical photoinitiator Substances 0.000 description 1
- KRIOVPPHQSLHCZ-UHFFFAOYSA-N propiophenone Chemical compound CCC(=O)C1=CC=CC=C1 KRIOVPPHQSLHCZ-UHFFFAOYSA-N 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP07004101 | 2007-02-28 | ||
| EP07004101.7 | 2007-02-28 | ||
| US90760707P | 2007-04-11 | 2007-04-11 | |
| US60/907,607 | 2007-04-11 | ||
| PCT/EP2008/052396 WO2008104572A2 (en) | 2007-02-28 | 2008-02-27 | Hydrophilic coating |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2010520316A JP2010520316A (ja) | 2010-06-10 |
| JP2010520316A5 true JP2010520316A5 (OSRAM) | 2014-05-22 |
| JP5587611B2 JP5587611B2 (ja) | 2014-09-10 |
Family
ID=38331685
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2009551200A Active JP5587611B2 (ja) | 2007-02-28 | 2008-02-27 | 親水性コーティング |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US8809411B2 (OSRAM) |
| EP (1) | EP2114477B1 (OSRAM) |
| JP (1) | JP5587611B2 (OSRAM) |
| CN (1) | CN101622020B (OSRAM) |
| BR (1) | BRPI0808105A2 (OSRAM) |
| DK (1) | DK2114477T3 (OSRAM) |
| ES (1) | ES2387699T3 (OSRAM) |
| MX (1) | MX339467B (OSRAM) |
| MY (1) | MY146399A (OSRAM) |
| WO (1) | WO2008104572A2 (OSRAM) |
Families Citing this family (76)
| Publication number | Priority date | Publication date | Assignee | Title |
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| ATE514491T1 (de) | 2004-11-29 | 2011-07-15 | Dsm Ip Assets Bv | Verfahren zur verringerung der menge von migrierbaren komponenten von polymerbeschichtungen |
| US8512795B2 (en) * | 2005-12-09 | 2013-08-20 | Dsm Ip Assets B.V. | Hydrophilic coating comprising a polyelectrolyte |
| US20100113871A1 (en) * | 2006-09-13 | 2010-05-06 | Aylvin Jorge Angelo Athanasius Dias | Antimicrobial coating |
| EP2061526B1 (en) * | 2006-09-13 | 2015-07-29 | DSM IP Assets B.V. | Coated medical device |
| EP2125061A2 (en) * | 2007-02-28 | 2009-12-02 | DSM IP Assets B.V. | Hydrophilic coating |
| WO2009112548A1 (en) * | 2008-03-12 | 2009-09-17 | Dsm Ip Assets B.V. | Hydrophilic coating |
| US8795830B2 (en) * | 2009-01-09 | 2014-08-05 | Dsm Ip Assets B.V. | Primer for coating coiled wires |
| CN102427834A (zh) | 2009-04-28 | 2012-04-25 | 苏尔莫迪克斯公司 | 用于递送生物活性剂的装置和方法 |
| JP5907957B2 (ja) * | 2010-06-16 | 2016-04-26 | ディーエスエム アイピー アセッツ ビー．ブイ． | 親水性コーティングを製造するためのコーティング配合物 |
| US10213529B2 (en) | 2011-05-20 | 2019-02-26 | Surmodics, Inc. | Delivery of coated hydrophobic active agent particles |
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| CN102320780B (zh) * | 2011-06-30 | 2013-02-27 | 周迪 | 一种用于内墙的水溶性环保涂料及其制备方法 |
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2008
- 2008-02-27 BR BRPI0808105-0A2A patent/BRPI0808105A2/pt active Search and Examination
- 2008-02-27 WO PCT/EP2008/052396 patent/WO2008104572A2/en not_active Ceased
- 2008-02-27 US US12/528,102 patent/US8809411B2/en active Active
- 2008-02-27 CN CN200880006605.4A patent/CN101622020B/zh active Active
- 2008-02-27 MY MYPI20093555A patent/MY146399A/en unknown
- 2008-02-27 ES ES08717200T patent/ES2387699T3/es active Active
- 2008-02-27 JP JP2009551200A patent/JP5587611B2/ja active Active
- 2008-02-27 DK DK08717200.3T patent/DK2114477T3/da active
- 2008-02-27 MX MX2009009139A patent/MX339467B/es active IP Right Grant
- 2008-02-27 EP EP08717200A patent/EP2114477B1/en active Active
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