JP2016516835A5 - - Google Patents
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- Publication number
- JP2016516835A5 JP2016516835A5 JP2015560340A JP2015560340A JP2016516835A5 JP 2016516835 A5 JP2016516835 A5 JP 2016516835A5 JP 2015560340 A JP2015560340 A JP 2015560340A JP 2015560340 A JP2015560340 A JP 2015560340A JP 2016516835 A5 JP2016516835 A5 JP 2016516835A5
- Authority
- JP
- Japan
- Prior art keywords
- cellulose ether
- esterified cellulose
- esterified
- mpa
- viscosity
- 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
- 229920003086 cellulose ether Polymers 0.000 claims description 34
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 12
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 9
- 239000000203 mixture Substances 0.000 claims description 7
- 239000004480 active ingredient Substances 0.000 claims description 5
- 125000001931 aliphatic group Chemical group 0.000 claims description 5
- 239000007788 liquid Substances 0.000 claims description 5
- 239000003085 diluting agent Substances 0.000 claims description 4
- 239000007962 solid dispersion Substances 0.000 claims description 4
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 3
- -1 aliphatic monocarboxylic acid Chemical class 0.000 claims description 3
- 239000002775 capsule Substances 0.000 claims description 3
- 239000002552 dosage form Substances 0.000 claims description 3
- 238000000034 method Methods 0.000 claims description 3
- 239000007894 caplet Substances 0.000 claims description 2
- 239000008187 granular material Substances 0.000 claims description 2
- 229920000639 hydroxypropylmethylcellulose acetate succinate Polymers 0.000 claims description 2
- 239000008188 pellet Substances 0.000 claims description 2
- 239000003826 tablet Substances 0.000 claims description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 2
- 150000002148 esters Chemical class 0.000 claims 3
- 150000008064 anhydrides Chemical class 0.000 claims 2
- 230000032050 esterification Effects 0.000 claims 1
- 238000005886 esterification reaction Methods 0.000 claims 1
- 239000007937 lozenge Substances 0.000 claims 1
- 239000000829 suppository Substances 0.000 claims 1
- 125000002252 acyl group Chemical group 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 125000002029 aromatic hydrocarbon group Chemical group 0.000 description 1
- 125000004063 butyryl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 239000011859 microparticle Substances 0.000 description 1
- 239000006187 pill Substances 0.000 description 1
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201361774161P | 2013-03-07 | 2013-03-07 | |
| US61/774,161 | 2013-03-07 | ||
| PCT/US2014/019266 WO2014137778A1 (en) | 2013-03-07 | 2014-02-28 | Novel esterified cellulose ethers of very low viscosity |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2016516835A JP2016516835A (ja) | 2016-06-09 |
| JP2016516835A5 true JP2016516835A5 (enExample) | 2016-11-04 |
| JP6267239B2 JP6267239B2 (ja) | 2018-01-24 |
Family
ID=50439471
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2015560340A Expired - Fee Related JP6267239B2 (ja) | 2013-03-07 | 2014-02-28 | 極めて低粘度の新規エステル化セルロースエーテル |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US9617351B2 (enExample) |
| EP (1) | EP2964204B1 (enExample) |
| JP (1) | JP6267239B2 (enExample) |
| KR (1) | KR101661952B1 (enExample) |
| CN (1) | CN105025887B (enExample) |
| BR (1) | BR112015015846A2 (enExample) |
| WO (1) | WO2014137778A1 (enExample) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP6356922B2 (ja) * | 2015-03-16 | 2018-07-11 | ダウ グローバル テクノロジーズ エルエルシー | 低い中和度を有する水溶性エステル化セルロースエーテル |
| US20180030157A1 (en) * | 2015-03-16 | 2018-02-01 | Dow Global Technologies Llc | Process for fractionating an esterified cellulose ether |
| KR20170128350A (ko) * | 2015-03-16 | 2017-11-22 | 다우 글로벌 테크놀로지스 엘엘씨 | 에스테르화된 셀룰로오스 에테르의 수용액 |
| EP3270970B1 (en) | 2015-03-16 | 2019-01-09 | Dow Global Technologies LLC | Gelling esterified cellulose ethers |
| BR112017018232A2 (pt) | 2015-03-16 | 2018-04-17 | Dow Global Technologies Llc | éteres de celulose esterificados solúveis em água |
| KR20170128349A (ko) * | 2015-03-16 | 2017-11-22 | 다우 글로벌 테크놀로지스 엘엘씨 | 지방족 카복실산의 존재하에서의 에스테르화된 셀룰로오스 에테르의 제조 방법 |
| KR20190013815A (ko) * | 2016-05-25 | 2019-02-11 | 다우 글로벌 테크놀로지스 엘엘씨 | 셀룰로스 에터 아세테이트의 수용액 |
| KR102490265B1 (ko) * | 2016-11-02 | 2023-01-20 | 신에쓰 가가꾸 고교 가부시끼가이샤 | 히프로멜로오스아세트산에스테르숙신산에스테르 및 제조 방법 |
| WO2018170083A1 (en) | 2017-03-17 | 2018-09-20 | Dow Global Technologies Llc | Process for recovering an esterified cellulose ether from a reaction product mixture |
| CN110366566B (zh) | 2017-03-17 | 2021-08-13 | 陶氏环球技术有限责任公司 | 用于从反应产物混合物中回收酯化纤维素醚的方法 |
| JP2020511572A (ja) | 2017-03-17 | 2020-04-16 | ダウ グローバル テクノロジーズ エルエルシー | 反応生成物混合物からのエステル化セルロースエーテルの回収方法 |
Family Cites Families (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS4819231B1 (enExample) * | 1970-03-06 | 1973-06-12 | ||
| US4226981A (en) * | 1977-09-28 | 1980-10-07 | Shin-Etsu Chemical Co., Ltd. | Ether-ester derivatives of cellulose and their applications |
| US4365060A (en) | 1979-04-28 | 1982-12-21 | Shin-Etsu Chemical Co. Ltd. | Enterosoluble capsules |
| JPS59167521A (ja) * | 1983-03-14 | 1984-09-21 | Shin Etsu Chem Co Ltd | 腸溶性コ−テイング剤組成物 |
| JPS6281402A (ja) * | 1985-10-07 | 1987-04-14 | Shin Etsu Chem Co Ltd | セルロ−スエ−テル酸性ジカルボン酸エステルの製造方法 |
| JP3149122B2 (ja) | 1994-11-07 | 2001-03-26 | 信越化学工業株式会社 | 固形腸溶製剤のコーティング用基剤 |
| JPH10167959A (ja) * | 1996-12-04 | 1998-06-23 | Zensei Yakuhin Kogyo Kk | ジクロフェナクナトリウムの徐放性カプセル製剤 |
| EP0872233A1 (en) | 1997-04-14 | 1998-10-21 | Janssen Pharmaceutica N.V. | Antiretroviral compositions with improved bioavailability |
| ES2287971T3 (es) | 1997-08-11 | 2007-12-16 | Pfizer Products Inc. | Dispersiones farmaceuticas solidas con biodisponibilidad incrementada. |
| KR100387126B1 (ko) * | 2001-04-19 | 2003-06-12 | 삼성정밀화학 주식회사 | 히드록시프로필메틸 셀룰로오스 프탈레이트의 분리정제방법 |
| DE10141680B4 (de) * | 2001-08-25 | 2004-02-26 | Clariant Gmbh | Verfahren zur Herstellung niederviskoser Celluloseether durch sauer-oxidativen Abbau von gemahlenen und getrockneten Celluloseethern |
| IL165043A0 (en) | 2002-05-17 | 2005-12-18 | Tibotec Pharm Ltd | broadspectrum substituted benzisoxazole sulfonamide hiv protease inhibitors |
| EP1530457B1 (en) | 2002-08-12 | 2009-09-09 | Bend Research, Inc. | Pharmaceutical compositions of drugs in semi-ordered form and polymers |
| CA2568007A1 (en) * | 2004-05-28 | 2005-12-08 | Pfizer Products Inc. | Pharmaceutical compositions with enhanced performance |
| US8920553B2 (en) | 2007-11-09 | 2014-12-30 | Dow Global Technologies Llc | Cellulose ether coating compositions and method |
| MX2010004931A (es) * | 2007-11-09 | 2010-06-11 | Union Carbide Chem Plastic | Metodo para preparar eter de celulosa de muy baja viscosidad y producto. |
| US8569364B2 (en) * | 2007-11-28 | 2013-10-29 | Sequoia Pharmaceuticals, Inc. | 5-substituted benzofurans as inhibitors of cytochrome P450 2D6 |
| JP5322740B2 (ja) | 2009-04-01 | 2013-10-23 | 国立大学法人東京農工大学 | 有害生物防除方法 |
| JP5792807B2 (ja) | 2010-06-14 | 2015-10-14 | ダウ グローバル テクノロジーズ エルエルシー | アセテートおよびサクシネートの置換が向上されたヒドロキシプロピルメチルセルロースアセテートサクシネート |
| US20120251588A1 (en) * | 2011-03-30 | 2012-10-04 | Miyuki Fukasawa | Coating Composition, Solid Preparation Coated Therewith, and Method for Preparing Solid Preparation |
| WO2013148154A1 (en) | 2012-03-27 | 2013-10-03 | Dow Global Technologies Llc | A process of preparing an ester of a cellulose ether |
| CN104427979B (zh) | 2012-04-11 | 2018-02-16 | 陶氏环球技术有限责任公司 | 具有特定的取代基分布的酯化的纤维素醚 |
| KR102138546B1 (ko) * | 2012-08-24 | 2020-07-28 | 다우 글로벌 테크놀로지스 엘엘씨 | 부분적으로 가교결합된 에스테르화된 셀룰로즈 에테르 |
| MX374548B (es) * | 2012-08-24 | 2025-03-06 | Dow Global Technologies Llc | Eteres de celulosa esterificados novedosos de alto peso molecular y homogeneidad. |
| MX2015002430A (es) * | 2012-08-24 | 2015-06-22 | Dow Global Technologies Llc | Acetato-succinatos de hidroxialquilmetilcelulosa. |
-
2014
- 2014-02-28 KR KR1020157026855A patent/KR101661952B1/ko not_active Expired - Fee Related
- 2014-02-28 CN CN201480011014.1A patent/CN105025887B/zh not_active Expired - Fee Related
- 2014-02-28 JP JP2015560340A patent/JP6267239B2/ja not_active Expired - Fee Related
- 2014-02-28 US US14/766,786 patent/US9617351B2/en not_active Expired - Fee Related
- 2014-02-28 WO PCT/US2014/019266 patent/WO2014137778A1/en not_active Ceased
- 2014-02-28 EP EP14715466.0A patent/EP2964204B1/en not_active Not-in-force
- 2014-02-28 BR BR112015015846A patent/BR112015015846A2/pt not_active Application Discontinuation
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