JP2015530451A5 - - Google Patents
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- JP2015530451A5 JP2015530451A5 JP2015533605A JP2015533605A JP2015530451A5 JP 2015530451 A5 JP2015530451 A5 JP 2015530451A5 JP 2015533605 A JP2015533605 A JP 2015533605A JP 2015533605 A JP2015533605 A JP 2015533605A JP 2015530451 A5 JP2015530451 A5 JP 2015530451A5
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- Prior art keywords
- poly
- acid
- polymer
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- group
- Prior art date
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- 229920001223 polyethylene glycol Polymers 0.000 claims description 14
- 150000001875 compounds Chemical class 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 12
- -1 4-benzoylbenzylamine 2-aminobenzophenone Chemical compound 0.000 claims description 11
- 229920000642 polymer Polymers 0.000 claims description 8
- 239000002202 Polyethylene glycol Substances 0.000 claims description 7
- NPFYZDNDJHZQKY-UHFFFAOYSA-N 4-Hydroxybenzophenone Chemical compound C1=CC(O)=CC=C1C(=O)C1=CC=CC=C1 NPFYZDNDJHZQKY-UHFFFAOYSA-N 0.000 claims description 6
- IFQUPKAISSPFTE-UHFFFAOYSA-N 4-benzoylbenzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1C(=O)C1=CC=CC=C1 IFQUPKAISSPFTE-UHFFFAOYSA-N 0.000 claims description 5
- 239000011248 coating agent Substances 0.000 claims description 5
- 238000000576 coating method Methods 0.000 claims description 5
- KIUKXJAPPMFGSW-DNGZLQJQSA-N (2S,3S,4S,5R,6R)-6-[(2S,3R,4R,5S,6R)-3-Acetamido-2-[(2S,3S,4R,5R,6R)-6-[(2R,3R,4R,5S,6R)-3-acetamido-2,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-2-carboxy-4,5-dihydroxyoxan-3-yl]oxy-5-hydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid Chemical compound CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@H](O[C@H]2[C@@H]([C@@H](O[C@H]3[C@@H]([C@@H](O)[C@H](O)[C@H](O3)C(O)=O)O)[C@H](O)[C@@H](CO)O2)NC(C)=O)[C@@H](C(O)=O)O1 KIUKXJAPPMFGSW-DNGZLQJQSA-N 0.000 claims description 4
- FGTYTUFKXYPTML-UHFFFAOYSA-N 2-benzoylbenzoic acid Chemical compound OC(=O)C1=CC=CC=C1C(=O)C1=CC=CC=C1 FGTYTUFKXYPTML-UHFFFAOYSA-N 0.000 claims description 4
- ASDLSKCKYGVMAI-UHFFFAOYSA-N 9,10-dioxoanthracene-2-carboxylic acid Chemical compound C1=CC=C2C(=O)C3=CC(C(=O)O)=CC=C3C(=O)C2=C1 ASDLSKCKYGVMAI-UHFFFAOYSA-N 0.000 claims description 4
- 239000004793 Polystyrene Substances 0.000 claims description 4
- XCBRWBLKNAXUAM-UHFFFAOYSA-N [4-(aminomethyl)phenyl]-phenylmethanone;hydrochloride Chemical compound Cl.C1=CC(CN)=CC=C1C(=O)C1=CC=CC=C1 XCBRWBLKNAXUAM-UHFFFAOYSA-N 0.000 claims description 4
- 239000003125 aqueous solvent Substances 0.000 claims description 4
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims description 4
- 229920002674 hyaluronan Polymers 0.000 claims description 4
- 229960003160 hyaluronic acid Drugs 0.000 claims description 4
- GTDQGKWDWVUKTI-UHFFFAOYSA-N o-aminoacetophenone Chemical compound CC(=O)C1=CC=CC=C1N GTDQGKWDWVUKTI-UHFFFAOYSA-N 0.000 claims description 4
- 229920002401 polyacrylamide Polymers 0.000 claims description 4
- 150000003839 salts Chemical class 0.000 claims description 4
- 238000001179 sorption measurement Methods 0.000 claims description 4
- RXCOGDYOZQGGMK-UHFFFAOYSA-N (3,4-diaminophenyl)-phenylmethanone Chemical compound C1=C(N)C(N)=CC=C1C(=O)C1=CC=CC=C1 RXCOGDYOZQGGMK-UHFFFAOYSA-N 0.000 claims description 3
- KORKIRUGUNPQML-UHFFFAOYSA-N 2-(2-aminobenzoyl)benzoic acid Chemical compound NC1=CC=CC=C1C(=O)C1=CC=CC=C1C(O)=O KORKIRUGUNPQML-UHFFFAOYSA-N 0.000 claims description 3
- UFQYYMAIVVSKPU-UHFFFAOYSA-N [4-(aminomethyl)phenyl]-phenylmethanone Chemical compound C1=CC(CN)=CC=C1C(=O)C1=CC=CC=C1 UFQYYMAIVVSKPU-UHFFFAOYSA-N 0.000 claims description 3
- 150000008366 benzophenones Chemical class 0.000 claims description 3
- WXNRYSGJLQFHBR-UHFFFAOYSA-N bis(2,4-dihydroxyphenyl)methanone Chemical compound OC1=CC(O)=CC=C1C(=O)C1=CC=C(O)C=C1O WXNRYSGJLQFHBR-UHFFFAOYSA-N 0.000 claims description 3
- 239000000463 material Substances 0.000 claims description 3
- 229920002223 polystyrene Polymers 0.000 claims description 3
- FUADXEJBHCKVBN-UHFFFAOYSA-N (3-aminophenyl)-phenylmethanone Chemical compound NC1=CC=CC(C(=O)C=2C=CC=CC=2)=C1 FUADXEJBHCKVBN-UHFFFAOYSA-N 0.000 claims description 2
- RBKHNGHPZZZJCI-UHFFFAOYSA-N (4-aminophenyl)-phenylmethanone Chemical compound C1=CC(N)=CC=C1C(=O)C1=CC=CC=C1 RBKHNGHPZZZJCI-UHFFFAOYSA-N 0.000 claims description 2
- FBMQNRKSAWNXBT-UHFFFAOYSA-N 1,4-diaminoanthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C(N)=CC=C2N FBMQNRKSAWNXBT-UHFFFAOYSA-N 0.000 claims description 2
- KHUFHLFHOQVFGB-UHFFFAOYSA-N 1-aminoanthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2N KHUFHLFHOQVFGB-UHFFFAOYSA-N 0.000 claims description 2
- QDAWXRKTSATEOP-UHFFFAOYSA-N 2-acetylbenzoic acid Chemical compound CC(=O)C1=CC=CC=C1C(O)=O QDAWXRKTSATEOP-UHFFFAOYSA-N 0.000 claims description 2
- HEQOJEGTZCTHCF-UHFFFAOYSA-N 2-amino-1-phenylethanone Chemical compound NCC(=O)C1=CC=CC=C1 HEQOJEGTZCTHCF-UHFFFAOYSA-N 0.000 claims description 2
- VVQULFWWOHEBQC-UHFFFAOYSA-N 2-amino-7-methylthioxanthen-9-one Chemical compound C1=C(N)C=C2C(=O)C3=CC(C)=CC=C3SC2=C1 VVQULFWWOHEBQC-UHFFFAOYSA-N 0.000 claims description 2
- AMIULHAFCHLPIK-UHFFFAOYSA-N 3-(9-oxothioxanthen-2-yl)oxypropane-1-sulfonic acid Chemical compound C1=CC=C2C(=O)C3=CC(OCCCS(=O)(=O)O)=CC=C3SC2=C1 AMIULHAFCHLPIK-UHFFFAOYSA-N 0.000 claims description 2
- QBHDSQZASIBAAI-UHFFFAOYSA-N 4-acetylbenzoic acid Chemical compound CC(=O)C1=CC=C(C(O)=O)C=C1 QBHDSQZASIBAAI-UHFFFAOYSA-N 0.000 claims description 2
- ZLSMCQSGRWNEGX-UHFFFAOYSA-N bis(4-aminophenyl)methanone Chemical compound C1=CC(N)=CC=C1C(=O)C1=CC=C(N)C=C1 ZLSMCQSGRWNEGX-UHFFFAOYSA-N 0.000 claims description 2
- 235000019260 propionic acid Nutrition 0.000 claims description 2
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 claims description 2
- 229920000307 polymer substrate Polymers 0.000 claims 6
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims 3
- 239000002253 acid Substances 0.000 claims 3
- 150000007513 acids Chemical class 0.000 claims 3
- 239000007864 aqueous solution Substances 0.000 claims 3
- 230000005855 radiation Effects 0.000 claims 3
- 150000003923 2,5-pyrrolediones Chemical class 0.000 claims 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims 2
- 229920000089 Cyclic olefin copolymer Polymers 0.000 claims 2
- 239000004713 Cyclic olefin copolymer Substances 0.000 claims 2
- 229920000106 Liquid crystal polymer Polymers 0.000 claims 2
- 239000004977 Liquid-crystal polymers (LCPs) Substances 0.000 claims 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims 2
- 239000004952 Polyamide Substances 0.000 claims 2
- 239000004698 Polyethylene Substances 0.000 claims 2
- 229920000954 Polyglycolide Polymers 0.000 claims 2
- 239000004642 Polyimide Substances 0.000 claims 2
- 239000004743 Polypropylene Substances 0.000 claims 2
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 claims 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical group [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims 2
- 150000001412 amines Chemical class 0.000 claims 2
- LOKCTEFSRHRXRJ-UHFFFAOYSA-I dipotassium trisodium dihydrogen phosphate hydrogen phosphate dichloride Chemical compound P(=O)(O)(O)[O-].[K+].P(=O)(O)([O-])[O-].[Na+].[Na+].[Cl-].[K+].[Cl-].[Na+] LOKCTEFSRHRXRJ-UHFFFAOYSA-I 0.000 claims 2
- 150000002148 esters Chemical class 0.000 claims 2
- 239000002953 phosphate buffered saline Substances 0.000 claims 2
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 claims 2
- 229920000747 poly(lactic acid) Polymers 0.000 claims 2
- 229920003229 poly(methyl methacrylate) Polymers 0.000 claims 2
- 229920002647 polyamide Polymers 0.000 claims 2
- 229920001610 polycaprolactone Polymers 0.000 claims 2
- 229920000573 polyethylene Polymers 0.000 claims 2
- 229920001721 polyimide Polymers 0.000 claims 2
- 239000004926 polymethyl methacrylate Substances 0.000 claims 2
- 229920006324 polyoxymethylene Polymers 0.000 claims 2
- 229920001155 polypropylene Polymers 0.000 claims 2
- 229920002635 polyurethane Polymers 0.000 claims 2
- 239000004814 polyurethane Substances 0.000 claims 2
- 239000002904 solvent Substances 0.000 claims 2
- 238000009281 ultraviolet germicidal irradiation Methods 0.000 claims 2
- 125000003504 2-oxazolinyl group Chemical class O1C(=NCC1)* 0.000 claims 1
- CDSULTPOCMWJCM-UHFFFAOYSA-N 4h-chromene-2,3-dione Chemical class C1=CC=C2OC(=O)C(=O)CC2=C1 CDSULTPOCMWJCM-UHFFFAOYSA-N 0.000 claims 1
- FHVDTGUDJYJELY-UHFFFAOYSA-N 6-{[2-carboxy-4,5-dihydroxy-6-(phosphanyloxy)oxan-3-yl]oxy}-4,5-dihydroxy-3-phosphanyloxane-2-carboxylic acid Chemical compound O1C(C(O)=O)C(P)C(O)C(O)C1OC1C(C(O)=O)OC(OP)C(O)C1O FHVDTGUDJYJELY-UHFFFAOYSA-N 0.000 claims 1
- RZVHIXYEVGDQDX-UHFFFAOYSA-N 9,10-anthraquinone Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3C(=O)C2=C1 RZVHIXYEVGDQDX-UHFFFAOYSA-N 0.000 claims 1
- XHOMPHZFIGVJJN-UHFFFAOYSA-N 9h-thioxanthene-2-carboxylic acid Chemical compound C1=CC=C2CC3=CC(C(=O)O)=CC=C3SC2=C1 XHOMPHZFIGVJJN-UHFFFAOYSA-N 0.000 claims 1
- 229920000936 Agarose Polymers 0.000 claims 1
- 102000008186 Collagen Human genes 0.000 claims 1
- 108010035532 Collagen Proteins 0.000 claims 1
- 229920002307 Dextran Polymers 0.000 claims 1
- 239000004593 Epoxy Substances 0.000 claims 1
- 108010010803 Gelatin Proteins 0.000 claims 1
- HTTJABKRGRZYRN-UHFFFAOYSA-N Heparin Chemical compound OC1C(NC(=O)C)C(O)OC(COS(O)(=O)=O)C1OC1C(OS(O)(=O)=O)C(O)C(OC2C(C(OS(O)(=O)=O)C(OC3C(C(O)C(O)C(O3)C(O)=O)OS(O)(=O)=O)C(CO)O2)NS(O)(=O)=O)C(C(O)=O)O1 HTTJABKRGRZYRN-UHFFFAOYSA-N 0.000 claims 1
- 229920002125 Sokalan® Polymers 0.000 claims 1
- 150000008062 acetophenones Chemical class 0.000 claims 1
- HAXFWIACAGNFHA-UHFFFAOYSA-N aldrithiol Chemical compound C=1C=CC=NC=1SSC1=CC=CC=N1 HAXFWIACAGNFHA-UHFFFAOYSA-N 0.000 claims 1
- 229940072056 alginate Drugs 0.000 claims 1
- 229920000615 alginic acid Polymers 0.000 claims 1
- 235000010443 alginic acid Nutrition 0.000 claims 1
- 229910021529 ammonia Inorganic materials 0.000 claims 1
- 239000012491 analyte Substances 0.000 claims 1
- 150000008365 aromatic ketones Chemical class 0.000 claims 1
- 239000007795 chemical reaction product Substances 0.000 claims 1
- 229920001436 collagen Polymers 0.000 claims 1
- 229920001577 copolymer Polymers 0.000 claims 1
- 238000004132 cross linking Methods 0.000 claims 1
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 claims 1
- 229910000397 disodium phosphate Inorganic materials 0.000 claims 1
- 235000019800 disodium phosphate Nutrition 0.000 claims 1
- 229920000159 gelatin Polymers 0.000 claims 1
- 239000008273 gelatin Substances 0.000 claims 1
- 235000019322 gelatine Nutrition 0.000 claims 1
- 235000011852 gelatine desserts Nutrition 0.000 claims 1
- 229920000669 heparin Polymers 0.000 claims 1
- 229960002897 heparin Drugs 0.000 claims 1
- 230000002209 hydrophobic effect Effects 0.000 claims 1
- 150000002634 lipophilic molecules Chemical class 0.000 claims 1
- 150000007522 mineralic acids Chemical class 0.000 claims 1
- 238000002156 mixing Methods 0.000 claims 1
- 229920000765 poly(2-oxazolines) Polymers 0.000 claims 1
- 239000004417 polycarbonate Substances 0.000 claims 1
- 229920000515 polycarbonate Polymers 0.000 claims 1
- 229920000728 polyester Polymers 0.000 claims 1
- 229920001195 polyisoprene Polymers 0.000 claims 1
- 239000001103 potassium chloride Substances 0.000 claims 1
- 235000011164 potassium chloride Nutrition 0.000 claims 1
- QLNJFJADRCOGBJ-UHFFFAOYSA-N propionamide Chemical compound CCC(N)=O QLNJFJADRCOGBJ-UHFFFAOYSA-N 0.000 claims 1
- 229910000029 sodium carbonate Inorganic materials 0.000 claims 1
- YRHRIQCWCFGUEQ-UHFFFAOYSA-N thioxanthen-9-one Chemical class C1=CC=C2C(=O)C3=CC=CC=C3SC2=C1 YRHRIQCWCFGUEQ-UHFFFAOYSA-N 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 1
- 239000012965 benzophenone Substances 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 4
- 229920002379 silicone rubber Polymers 0.000 description 3
- 239000004945 silicone rubber Substances 0.000 description 3
- 208000005422 Foreign-Body reaction Diseases 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 230000021164 cell adhesion Effects 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 2
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 2
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 2
- 102000004169 proteins and genes Human genes 0.000 description 2
- 108090000623 proteins and genes Proteins 0.000 description 2
- MAOBFOXLCJIFLV-UHFFFAOYSA-N (2-aminophenyl)-phenylmethanone Chemical compound NC1=CC=CC=C1C(=O)C1=CC=CC=C1 MAOBFOXLCJIFLV-UHFFFAOYSA-N 0.000 description 1
- MSKSQCLPULZWNO-UHFFFAOYSA-N 2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethanamine Chemical compound COCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCN MSKSQCLPULZWNO-UHFFFAOYSA-N 0.000 description 1
- KUIUTGJAYHAGTC-FLAUAXFRSA-N 2-aminoacetic acid (2S)-2-amino-3-methylbutanoic acid (2S)-pyrrolidine-2-carboxylic acid Chemical compound NCC(O)=O.NCC(O)=O.CC(C)[C@H](N)C(O)=O.CC(C)[C@H](N)C(O)=O.OC(=O)[C@@H]1CCCN1 KUIUTGJAYHAGTC-FLAUAXFRSA-N 0.000 description 1
- FGTYTUFKXYPTML-UHFFFAOYSA-M 2-benzoylbenzoate Chemical compound [O-]C(=O)C1=CC=CC=C1C(=O)C1=CC=CC=C1 FGTYTUFKXYPTML-UHFFFAOYSA-M 0.000 description 1
- PPFNJKRRFYQNLD-UHFFFAOYSA-N 9-oxothioxanthene-2-carboxylic acid Chemical compound C1=CC=C2C(=O)C3=CC(C(=O)O)=CC=C3SC2=C1 PPFNJKRRFYQNLD-UHFFFAOYSA-N 0.000 description 1
- PVVTWNMXEHROIA-UHFFFAOYSA-N Pegamine Natural products C1=CC=C2NC(CCCO)=NC(=O)C2=C1 PVVTWNMXEHROIA-UHFFFAOYSA-N 0.000 description 1
- 239000012062 aqueous buffer Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- DKYWVDODHFEZIM-UHFFFAOYSA-N ketoprofen Chemical compound OC(=O)C(C)C1=CC=CC(C(=O)C=2C=CC=CC=2)=C1 DKYWVDODHFEZIM-UHFFFAOYSA-N 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2019071302A JP6982023B2 (ja) | 2012-09-28 | 2019-04-03 | ポリマー基板にコーティングを適用するための方法 |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP12186613.1 | 2012-09-28 | ||
| EP12186613 | 2012-09-28 | ||
| PCT/EP2013/070176 WO2014049113A1 (en) | 2012-09-28 | 2013-09-27 | A method for applying a coating to a polymeric substrate |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2019071302A Division JP6982023B2 (ja) | 2012-09-28 | 2019-04-03 | ポリマー基板にコーティングを適用するための方法 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2015530451A JP2015530451A (ja) | 2015-10-15 |
| JP2015530451A5 true JP2015530451A5 (enExample) | 2016-11-17 |
Family
ID=47002684
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2015533605A Pending JP2015530451A (ja) | 2012-09-28 | 2013-09-27 | ポリマー基板にコーティングを適用するための方法 |
| JP2019071302A Active JP6982023B2 (ja) | 2012-09-28 | 2019-04-03 | ポリマー基板にコーティングを適用するための方法 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2019071302A Active JP6982023B2 (ja) | 2012-09-28 | 2019-04-03 | ポリマー基板にコーティングを適用するための方法 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US10519339B2 (enExample) |
| EP (1) | EP2900740B1 (enExample) |
| JP (2) | JP2015530451A (enExample) |
| CN (1) | CN104769022B (enExample) |
| DK (1) | DK2900740T3 (enExample) |
| WO (1) | WO2014049113A1 (enExample) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US10835905B2 (en) | 2011-05-25 | 2020-11-17 | Cidra Corporate Services Inc. | Recovery media for mineral processing |
| BR112018013799A2 (en) * | 2016-01-07 | 2018-12-11 | Cidra Corporate Services Llc | Open cell or crosslinked foam functionalized open mesh structure for the selective separation of mineral particles in an aqueous system |
| US10883901B1 (en) | 2016-10-14 | 2021-01-05 | Triad National Security, Llc | High efficiency environmental sampling with rapidly cured peelable coatings |
| CN106905158B (zh) * | 2017-01-26 | 2020-01-14 | 中国科学院长春应用化学研究所 | 一种直接改性基底的二苯甲酮型分子及其应用 |
| JP6952340B2 (ja) * | 2017-01-30 | 2021-10-20 | 東京都公立大学法人 | 表面処理剤 |
| EP3536402A1 (de) | 2018-03-09 | 2019-09-11 | Ibidi Gmbh | Probenkammer |
| CN110026167A (zh) * | 2019-04-30 | 2019-07-19 | 江苏迅驰新能源科技股份有限公司 | 一种清除甲醛的颗粒吸附材料及其制备方法 |
| JP7600274B2 (ja) * | 2020-06-19 | 2024-12-16 | レノボ・（ベイジン）・リミテッド | 小データ伝送のための方法および装置 |
| US11946834B1 (en) | 2020-10-30 | 2024-04-02 | Triad National Security, Llc | High efficiency active environmental sampling of chemical traces |
| CA3204018A1 (en) * | 2021-01-04 | 2022-07-07 | Eoin SCANLAN | Methods of coating polymers and reduction in protein aggregation |
| CN115475662B (zh) * | 2022-10-18 | 2023-05-02 | 广东工业大学 | 一种具有催化净化异味功能的聚丙烯改性材料及其制备方法 |
| CN117343262A (zh) * | 2023-10-31 | 2024-01-05 | 清华大学 | 一种紫外光照调控力学性能的聚氨酯脲薄膜及其制备方法 |
Family Cites Families (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4602097A (en) | 1984-06-11 | 1986-07-22 | Ulano Corporation | Water soluble photoinitiator benzophenone and thioxanthenone ethoxy-ether derivatives |
| SE444950B (sv) | 1984-09-28 | 1986-05-20 | Ytkemiska Inst | Ytbelagd artikel, forfarande och medel for framstellning derav samt anvendning derav |
| EP0274596A3 (en) | 1986-12-22 | 1989-11-29 | General Electric Company | Aromatic carbonate resin articles coated with a photocured acrylic coating |
| US5264533A (en) | 1988-06-16 | 1993-11-23 | Basf Aktiengesellschaft | Benzophenone derivatives and their preparation |
| DE3856430T2 (de) | 1988-07-22 | 2001-05-03 | Surmodics, Inc. | Herstellung von polymeren oberflächen |
| US5863650A (en) | 1997-05-05 | 1999-01-26 | Bioengineered Materials, Inc. | Interfacial coatings |
| DE10149587B4 (de) | 2001-10-09 | 2006-05-11 | Gkss-Forschungszentrum Geesthacht Gmbh | Photoreaktiv beschichtete Kompositmembran für die Affinitätstrennung, Verfahren zu deren Herstellung und deren Verwendung |
| ITTO20020362A1 (it) | 2002-04-30 | 2003-10-30 | Metlac S P A | Sistema multirivestimento con proprieta' di barriera ai gas, fotoreticolabile mediante radiazione uv particolarmente idoneo per la protezion |
| DE10238559A1 (de) * | 2002-08-22 | 2004-03-04 | Fresenius Medical Care Deutschland Gmbh | Verfahren zur Immobilisierung von Hydrogel-bildenden Polymeren auf Polymersubstratoberflächen |
| DE10362060B4 (de) | 2003-10-21 | 2009-07-09 | Altana Coatings & Sealants Gmbh | Verpackungsmaterial mit einer Barriereschicht für Gase |
| WO2006063181A1 (en) | 2004-12-06 | 2006-06-15 | Surmodics, Inc. | Multifunctional medical articles |
| US7717273B2 (en) | 2006-05-24 | 2010-05-18 | Millipore Corporation | Membrane surface modification by radiation-induced polymerization |
| US20100113871A1 (en) * | 2006-09-13 | 2010-05-06 | Aylvin Jorge Angelo Athanasius Dias | Antimicrobial coating |
| WO2008071796A1 (en) | 2006-12-15 | 2008-06-19 | Coloplast A/S | Coatings prepared from poly(ethylene oxide) and photo-initator-containing scaffolds |
| WO2009091224A2 (en) | 2008-01-18 | 2009-07-23 | Lg Chem, Ltd. | Optical film, preparation method of the same, and liquid crystal display comprising the same |
| TWI377413B (en) | 2008-03-06 | 2012-11-21 | Taiwan Tft Lcd Ass | Methods for fabricating liquid crystal display substrate and liquid crystal cell |
| DE102008035310A1 (de) | 2008-07-23 | 2010-01-28 | Karl Storz Gmbh & Co. Kg | Medizinisches Instrument mit einem flexiblen Dichtungssystem |
-
2013
- 2013-09-27 US US14/431,799 patent/US10519339B2/en active Active
- 2013-09-27 JP JP2015533605A patent/JP2015530451A/ja active Pending
- 2013-09-27 WO PCT/EP2013/070176 patent/WO2014049113A1/en not_active Ceased
- 2013-09-27 CN CN201380058417.7A patent/CN104769022B/zh active Active
- 2013-09-27 EP EP13766560.0A patent/EP2900740B1/en active Active
- 2013-09-27 DK DK13766560.0T patent/DK2900740T3/da active
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2019
- 2019-04-03 JP JP2019071302A patent/JP6982023B2/ja active Active
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