JP2009533532A5 - - Google Patents
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- JP2009533532A5 JP2009533532A5 JP2009505539A JP2009505539A JP2009533532A5 JP 2009533532 A5 JP2009533532 A5 JP 2009533532A5 JP 2009505539 A JP2009505539 A JP 2009505539A JP 2009505539 A JP2009505539 A JP 2009505539A JP 2009533532 A5 JP2009533532 A5 JP 2009533532A5
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- JP
- Japan
- Prior art keywords
- group
- substituted
- monomer
- unsubstituted
- ether
- 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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- 239000000178 monomer Substances 0.000 claims 26
- 239000000203 mixture Substances 0.000 claims 10
- -1 carboxyureido, sulfonyl Chemical group 0.000 claims 8
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 6
- 238000006116 polymerization reaction Methods 0.000 claims 5
- 238000000034 method Methods 0.000 claims 4
- DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 claims 3
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims 3
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 claims 3
- 239000012528 membrane Substances 0.000 claims 3
- FBCQUCJYYPMKRO-UHFFFAOYSA-N prop-2-enyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC=C FBCQUCJYYPMKRO-UHFFFAOYSA-N 0.000 claims 3
- 229910052710 silicon Inorganic materials 0.000 claims 3
- 239000010703 silicon Substances 0.000 claims 3
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 claims 3
- 125000000923 (C1-C30) alkyl group Chemical group 0.000 claims 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Chemical group OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims 2
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims 2
- 239000004721 Polyphenylene oxide Substances 0.000 claims 2
- 125000003545 alkoxy group Chemical group 0.000 claims 2
- 150000005215 alkyl ethers Chemical class 0.000 claims 2
- 125000003368 amide group Chemical group 0.000 claims 2
- 125000003710 aryl alkyl group Chemical group 0.000 claims 2
- 150000008378 aryl ethers Chemical class 0.000 claims 2
- 125000003118 aryl group Chemical group 0.000 claims 2
- 125000001951 carbamoylamino group Chemical group C(N)(=O)N* 0.000 claims 2
- 125000002091 cationic group Chemical group 0.000 claims 2
- 125000000392 cycloalkenyl group Chemical group 0.000 claims 2
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 claims 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims 2
- 125000003709 fluoroalkyl group Chemical group 0.000 claims 2
- 125000004407 fluoroaryl group Chemical group 0.000 claims 2
- 125000001072 heteroaryl group Chemical group 0.000 claims 2
- 125000004446 heteroarylalkyl group Chemical group 0.000 claims 2
- 125000000623 heterocyclic group Chemical group 0.000 claims 2
- 150000002500 ions Chemical class 0.000 claims 2
- 229920000570 polyether Polymers 0.000 claims 2
- 239000002904 solvent Substances 0.000 claims 2
- SJHPCNCNNSSLPL-CSKARUKUSA-N (4e)-4-(ethoxymethylidene)-2-phenyl-1,3-oxazol-5-one Chemical compound O1C(=O)C(=C/OCC)\N=C1C1=CC=CC=C1 SJHPCNCNNSSLPL-CSKARUKUSA-N 0.000 claims 1
- VAYTZRYEBVHVLE-UHFFFAOYSA-N 1,3-dioxol-2-one Chemical compound O=C1OC=CO1 VAYTZRYEBVHVLE-UHFFFAOYSA-N 0.000 claims 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical group COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims 1
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical class OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 claims 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims 1
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 claims 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 1
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical class CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 claims 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 claims 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical group CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims 1
- 150000001298 alcohols Chemical class 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 125000003277 amino group Chemical group 0.000 claims 1
- 239000012620 biological material Substances 0.000 claims 1
- 210000004204 blood vessel Anatomy 0.000 claims 1
- 210000000481 breast Anatomy 0.000 claims 1
- 150000001732 carboxylic acid derivatives Chemical group 0.000 claims 1
- 238000000605 extraction Methods 0.000 claims 1
- 229910052731 fluorine Inorganic materials 0.000 claims 1
- 239000011737 fluorine Substances 0.000 claims 1
- 239000007789 gas Substances 0.000 claims 1
- 210000003709 heart valve Anatomy 0.000 claims 1
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims 1
- 239000000017 hydrogel Substances 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 1
- 230000002209 hydrophobic effect Effects 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 210000003734 kidney Anatomy 0.000 claims 1
- 210000004072 lung Anatomy 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 claims 1
- 229940088644 n,n-dimethylacrylamide Drugs 0.000 claims 1
- YLGYACDQVQQZSW-UHFFFAOYSA-N n,n-dimethylprop-2-enamide Chemical compound CN(C)C(=O)C=C YLGYACDQVQQZSW-UHFFFAOYSA-N 0.000 claims 1
- 238000004806 packaging method and process Methods 0.000 claims 1
- 229910000077 silane Inorganic materials 0.000 claims 1
- 125000004469 siloxy group Chemical group [SiH3]O* 0.000 claims 1
- 230000001954 sterilising effect Effects 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 1
- 210000000626 ureter Anatomy 0.000 claims 1
- LVLANIHJQRZTPY-UHFFFAOYSA-N vinyl carbamate Chemical compound NC(=O)OC=C LVLANIHJQRZTPY-UHFFFAOYSA-N 0.000 claims 1
- 229920002554 vinyl polymer Polymers 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US11/403,393 US7960447B2 (en) | 2006-04-13 | 2006-04-13 | Cationic end-capped siloxane prepolymer for reduced cross-link density |
| PCT/US2007/065851 WO2007121084A1 (en) | 2006-04-13 | 2007-04-03 | Cationic end-capped siloxane prepolymer for reduced cross-link density |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2013020229A Division JP2013100539A (ja) | 2006-04-13 | 2013-02-05 | 架橋密度を減少させるための陽イオン末端キャッピングされたシロキサンプレポリマー |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2009533532A JP2009533532A (ja) | 2009-09-17 |
| JP2009533532A5 true JP2009533532A5 (enExample) | 2010-08-12 |
Family
ID=38372428
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2009505539A Pending JP2009533532A (ja) | 2006-04-13 | 2007-04-03 | 架橋密度を減少させるための陽イオン末端キャッピングされたシロキサンプレポリマー |
| JP2013020229A Pending JP2013100539A (ja) | 2006-04-13 | 2013-02-05 | 架橋密度を減少させるための陽イオン末端キャッピングされたシロキサンプレポリマー |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2013020229A Pending JP2013100539A (ja) | 2006-04-13 | 2013-02-05 | 架橋密度を減少させるための陽イオン末端キャッピングされたシロキサンプレポリマー |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US7960447B2 (enExample) |
| EP (1) | EP2004729B1 (enExample) |
| JP (2) | JP2009533532A (enExample) |
| CN (1) | CN101421335A (enExample) |
| AT (1) | ATE438677T1 (enExample) |
| DE (1) | DE602007001881D1 (enExample) |
| ES (1) | ES2329197T3 (enExample) |
| WO (1) | WO2007121084A1 (enExample) |
Families Citing this family (28)
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| JP4708342B2 (ja) | 2003-07-25 | 2011-06-22 | デックスコム・インコーポレーテッド | 埋設可能な装置に用いる酸素増大膜システム |
| US8277713B2 (en) | 2004-05-03 | 2012-10-02 | Dexcom, Inc. | Implantable analyte sensor |
| US8744546B2 (en) | 2005-05-05 | 2014-06-03 | Dexcom, Inc. | Cellulosic-based resistance domain for an analyte sensor |
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| US8682408B2 (en) | 2008-03-28 | 2014-03-25 | Dexcom, Inc. | Polymer membranes for continuous analyte sensors |
| US11730407B2 (en) | 2008-03-28 | 2023-08-22 | Dexcom, Inc. | Polymer membranes for continuous analyte sensors |
| US8583204B2 (en) | 2008-03-28 | 2013-11-12 | Dexcom, Inc. | Polymer membranes for continuous analyte sensors |
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| CN103476779B (zh) * | 2011-02-01 | 2016-04-06 | 帝斯曼知识产权资产管理有限公司 | 具有亲水性端基的含硅酮的单体 |
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| JP5944987B2 (ja) | 2011-06-30 | 2016-07-05 | ディーエスエム アイピー アセッツ ビー.ブイ. | シリコーン含有モノマー |
| CN104321352B (zh) | 2012-03-22 | 2017-09-26 | 莫门蒂夫性能材料股份有限公司 | 可聚合的含酰胺基的有机硅化合物、含硅聚合物以及由其制备的生物医学装置 |
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| US10441676B2 (en) | 2013-01-15 | 2019-10-15 | Medicem Institute s.r.o. | Light-adjustable hydrogel and bioanalogic intraocular lens |
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| JP2025009288A (ja) * | 2023-07-07 | 2025-01-20 | 信越化学工業株式会社 | 分子鎖中に第3級アミノ基または第4級アンモニウムカチオン部位を有する両末端(メタ)アクリル変性シリコーンマクロマーおよびその製造方法 |
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-
2006
- 2006-04-13 US US11/403,393 patent/US7960447B2/en not_active Expired - Fee Related
-
2007
- 2007-04-03 JP JP2009505539A patent/JP2009533532A/ja active Pending
- 2007-04-03 WO PCT/US2007/065851 patent/WO2007121084A1/en not_active Ceased
- 2007-04-03 AT AT07760018T patent/ATE438677T1/de not_active IP Right Cessation
- 2007-04-03 EP EP07760018A patent/EP2004729B1/en not_active Not-in-force
- 2007-04-03 DE DE602007001881T patent/DE602007001881D1/de active Active
- 2007-04-03 CN CNA2007800132441A patent/CN101421335A/zh active Pending
- 2007-04-03 ES ES07760018T patent/ES2329197T3/es active Active
-
2013
- 2013-02-05 JP JP2013020229A patent/JP2013100539A/ja active Pending
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