JP2010520317A5 - - Google Patents
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- Publication number
- JP2010520317A5 JP2010520317A5 JP2009551201A JP2009551201A JP2010520317A5 JP 2010520317 A5 JP2010520317 A5 JP 2010520317A5 JP 2009551201 A JP2009551201 A JP 2009551201A JP 2009551201 A JP2009551201 A JP 2009551201A JP 2010520317 A5 JP2010520317 A5 JP 2010520317A5
- Authority
- JP
- Japan
- Prior art keywords
- coating
- coating formulation
- formulation
- 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.)
- Granted
Links
- 239000000203 mixture Substances 0.000 claims description 4
- 238000010546 Norrish type I reaction Methods 0.000 claims description 2
- 239000008199 coating composition Substances 0.000 claims 9
- 239000011248 coating agent Substances 0.000 claims 8
- 238000000576 coating method Methods 0.000 claims 8
- 229920000642 polymer Polymers 0.000 claims 6
- 239000012530 fluid Substances 0.000 claims 2
- 229920000867 polyelectrolyte Polymers 0.000 claims 2
- 238000009736 wetting Methods 0.000 claims 2
- 238000010547 Norrish type II reaction Methods 0.000 claims 1
- 239000004721 Polyphenylene oxide Substances 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
- 239000003999 initiator 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
- 239000000758 substrate Substances 0.000 claims 1
- -1 Ciba-Geigy) Chemical compound 0.000 description 7
- UFUASNAHBMBJIX-UHFFFAOYSA-N propan-1-one Chemical compound CC[C]=O UFUASNAHBMBJIX-UHFFFAOYSA-N 0.000 description 4
- 239000004480 active ingredient Substances 0.000 description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
- 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
- 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
- GUCYFKSBFREPBC-UHFFFAOYSA-N [phenyl-(2,4,6-trimethylbenzoyl)phosphoryl]-(2,4,6-trimethylphenyl)methanone Chemical compound CC1=CC(C)=CC(C)=C1C(=O)P(=O)(C=1C=CC=CC=1)C(=O)C1=C(C)C=C(C)C=C1C GUCYFKSBFREPBC-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
- WKGDNXBDNLZSKC-UHFFFAOYSA-N oxido(phenyl)phosphanium Chemical compound O=[PH2]c1ccccc1 WKGDNXBDNLZSKC-UHFFFAOYSA-N 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 |
|---|---|---|---|
| EP07004100.9 | 2007-02-28 | ||
| EP07004100 | 2007-02-28 | ||
| US90760807P | 2007-04-11 | 2007-04-11 | |
| US60/907,608 | 2007-04-11 | ||
| PCT/EP2008/052397 WO2008104573A2 (en) | 2007-02-28 | 2008-02-27 | Hydrophilic coating |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2010520317A JP2010520317A (ja) | 2010-06-10 |
| JP2010520317A5 true JP2010520317A5 (OSRAM) | 2014-05-22 |
| JP5587612B2 JP5587612B2 (ja) | 2014-09-10 |
Family
ID=38474357
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2009551201A Active JP5587612B2 (ja) | 2007-02-28 | 2008-02-27 | 親水性コーティング |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US8513320B2 (OSRAM) |
| EP (1) | EP2125061A2 (OSRAM) |
| JP (1) | JP5587612B2 (OSRAM) |
| CN (1) | CN101622019B (OSRAM) |
| BR (1) | BRPI0808118A2 (OSRAM) |
| MX (1) | MX2009009145A (OSRAM) |
| MY (1) | MY148410A (OSRAM) |
| WO (1) | WO2008104573A2 (OSRAM) |
Families Citing this family (80)
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| AU2005308920B2 (en) | 2004-11-29 | 2010-04-15 | Dsm Ip Assets B.V. | Method for reducing the amount of migrateables of polymer coatings |
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| MX2009009145A (es) | 2007-02-28 | 2009-09-03 | Dsm Ip Assets Bv | Recubrimiento hidrofilo. |
| JP5587611B2 (ja) | 2007-02-28 | 2014-09-10 | 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 |
| MY160698A (en) * | 2008-03-12 | 2017-03-15 | Dsm Ip Assets Bv | Hydrophilic coating |
| US8114429B2 (en) | 2008-09-15 | 2012-02-14 | Cv Ingenuity Corp. | Local delivery of water-soluble or water-insoluble therapeutic agents to the surface of body lumens |
| US8257722B2 (en) | 2008-09-15 | 2012-09-04 | Cv Ingenuity Corp. | Local delivery of water-soluble or water-insoluble therapeutic agents to the surface of body lumens |
| US9198968B2 (en) | 2008-09-15 | 2015-12-01 | The Spectranetics Corporation | Local delivery of water-soluble or water-insoluble therapeutic agents to the surface of body lumens |
| US8128951B2 (en) * | 2008-09-15 | 2012-03-06 | Cv Ingenuity Corp. | Local delivery of water-soluble or water-insoluble therapeutic agents to the surface of body lumens |
| BRPI1007204A2 (pt) | 2009-01-09 | 2016-02-23 | Dsm Ip Assets Bv | primer para revestimento de fios enrolados |
| WO2010129328A2 (en) | 2009-04-28 | 2010-11-11 | Surmodics, Inc. | Devices and methods for delivery of bioactive agents |
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| EP2593243B1 (en) | 2010-09-29 | 2016-07-27 | Siemens Healthcare Diagnostics Inc. | Hydrophilic coating for nonporous surfaces and microfluidic devices including same |
| US10213529B2 (en) | 2011-05-20 | 2019-02-26 | Surmodics, Inc. | Delivery of coated hydrophobic active agent particles |
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| JP2012241127A (ja) * | 2011-05-20 | 2012-12-10 | Hitachi Chemical Co Ltd | 光硬化性樹脂組成物及びこれを用いた光硬化性樹脂組成物ワニス、光硬化性樹脂組成物硬化物 |
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-
2008
- 2008-02-27 MX MX2009009145A patent/MX2009009145A/es active IP Right Grant
- 2008-02-27 CN CN200880006517.4A patent/CN101622019B/zh active Active
- 2008-02-27 US US12/528,123 patent/US8513320B2/en active Active
- 2008-02-27 MY MYPI20093556A patent/MY148410A/en unknown
- 2008-02-27 EP EP08717201A patent/EP2125061A2/en not_active Withdrawn
- 2008-02-27 WO PCT/EP2008/052397 patent/WO2008104573A2/en not_active Ceased
- 2008-02-27 JP JP2009551201A patent/JP5587612B2/ja active Active
- 2008-02-27 BR BRPI0808118-2A2A patent/BRPI0808118A2/pt not_active Application Discontinuation
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