JP2011525536A - 多方向性粘膜送達装置および使用法 - Google Patents
多方向性粘膜送達装置および使用法 Download PDFInfo
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Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2014035219A1 (ko) * | 2012-08-31 | 2014-03-06 | 동국대학교 산학협력단 | 유동적 위장관점막 부착성 경구투여용 제형 |
| JP2023533774A (ja) * | 2020-07-07 | 2023-08-04 | オクルジェル | ブプレノルフィンを送達するための親水性分解性マイクロスフェア |
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| US5968547A (en) | 1997-02-24 | 1999-10-19 | Euro-Celtique, S.A. | Method of providing sustained analgesia with buprenorphine |
| US8900497B2 (en) | 2001-10-12 | 2014-12-02 | Monosol Rx, Llc | Process for making a film having a substantially uniform distribution of components |
| US7357891B2 (en) | 2001-10-12 | 2008-04-15 | Monosol Rx, Llc | Process for making an ingestible film |
| US8900498B2 (en) | 2001-10-12 | 2014-12-02 | Monosol Rx, Llc | Process for manufacturing a resulting multi-layer pharmaceutical film |
| US20070281003A1 (en) | 2001-10-12 | 2007-12-06 | Fuisz Richard C | Polymer-Based Films and Drug Delivery Systems Made Therefrom |
| US20190328679A1 (en) | 2001-10-12 | 2019-10-31 | Aquestive Therapeutics, Inc. | Uniform films for rapid-dissolve dosage form incorporating anti-tacking compositions |
| US8765167B2 (en) | 2001-10-12 | 2014-07-01 | Monosol Rx, Llc | Uniform films for rapid-dissolve dosage form incorporating anti-tacking compositions |
| US8603514B2 (en) | 2002-04-11 | 2013-12-10 | Monosol Rx, Llc | Uniform films for rapid dissolve dosage form incorporating taste-masking compositions |
| US10285910B2 (en) | 2001-10-12 | 2019-05-14 | Aquestive Therapeutics, Inc. | Sublingual and buccal film compositions |
| US11207805B2 (en) | 2001-10-12 | 2021-12-28 | Aquestive Therapeutics, Inc. | Process for manufacturing a resulting pharmaceutical film |
| US20110033542A1 (en) | 2009-08-07 | 2011-02-10 | Monosol Rx, Llc | Sublingual and buccal film compositions |
| RS54764B1 (sr) | 2006-07-21 | 2016-10-31 | Biodelivery Sciences Int Inc | Sredstvo za transmukozalnu isporuku sa povećanim nakupljanjem |
| US8475832B2 (en) | 2009-08-07 | 2013-07-02 | Rb Pharmaceuticals Limited | Sublingual and buccal film compositions |
| US9149959B2 (en) | 2010-10-22 | 2015-10-06 | Monosol Rx, Llc | Manufacturing of small film strips |
| US8939943B2 (en) | 2011-01-26 | 2015-01-27 | Kaleo, Inc. | Medicament delivery device for administration of opioid antagonists including formulations for naloxone |
| US8627816B2 (en) | 2011-02-28 | 2014-01-14 | Intelliject, Inc. | Medicament delivery device for administration of opioid antagonists including formulations for naloxone |
| US8601691B2 (en) | 2011-04-27 | 2013-12-10 | General Electric Company | Component and methods of fabricating a coated component using multiple types of fillers |
| JP6158810B2 (ja) | 2011-08-18 | 2017-07-05 | バイオデリバリー サイエンシズ インターナショナル,インコーポレーテッド | ブプレノルフィンの乱用抵抗性粘膜付着性送達デバイス |
| US20130086784A1 (en) | 2011-10-06 | 2013-04-11 | General Electric Company | Repair methods for cooled components |
| US9901539B2 (en) | 2011-12-21 | 2018-02-27 | Biodelivery Sciences International, Inc. | Transmucosal drug delivery devices for use in chronic pain relief |
| KR20210003313A (ko) * | 2011-12-21 | 2021-01-11 | 바이오딜리버리 사이언시스 인터내셔널 인코포레이티드 | 만성 통증 완화에 이용되는 점막 관통 약물 전달 장치 |
| US9435208B2 (en) | 2012-04-17 | 2016-09-06 | General Electric Company | Components with microchannel cooling |
| WO2013171146A1 (en) * | 2012-05-15 | 2013-11-21 | Lts Lohmann Therapie-Systeme Ag | Oral film containing enteric release opiate resinate |
| US11931227B2 (en) | 2013-03-15 | 2024-03-19 | Cook Medical Technologies Llc | Bimodal treatment methods and compositions for gastrointestinal lesions with active bleeding |
| US9839611B2 (en) | 2013-09-10 | 2017-12-12 | Insys Development Company, Inc. | Sublingual buprenorphine spray |
| US9918981B2 (en) | 2013-09-10 | 2018-03-20 | Insys Development Company, Inc. | Liquid buprenorphine formulations |
| US9867818B2 (en) | 2013-09-10 | 2018-01-16 | Insys Development Company, Inc. | Sublingual buprenorphine spray |
| JP2016529328A (ja) | 2013-09-10 | 2016-09-23 | インシス・ファーマ・インコーポレーテッド | 舌下ブプレノルフィンスプレー |
| US10617686B2 (en) | 2014-07-08 | 2020-04-14 | Hikma Pharmaceuticals Usa Inc. | Liquid naloxone spray |
| CA2954370A1 (en) | 2014-07-08 | 2016-01-14 | Insys Pharma, Inc. | Sublingual naloxone spray |
| US10722510B2 (en) | 2014-07-08 | 2020-07-28 | Hikma Pharmaceuticals Usa Inc. | Liquid naloxone spray |
| US9517307B2 (en) | 2014-07-18 | 2016-12-13 | Kaleo, Inc. | Devices and methods for delivering opioid antagonists including formulations for naloxone |
| US9956323B2 (en) | 2014-12-18 | 2018-05-01 | Cook Medical Technologies Llc | Medical devices for local bioactive delivery |
| US12433850B2 (en) | 2016-05-05 | 2025-10-07 | Aquestive Therapeutics, Inc. | Enhanced delivery epinephrine and prodrug compositions |
| US12427121B2 (en) | 2016-05-05 | 2025-09-30 | Aquestive Therapeutics, Inc. | Enhanced delivery epinephrine compositions |
| US11273131B2 (en) | 2016-05-05 | 2022-03-15 | Aquestive Therapeutics, Inc. | Pharmaceutical compositions with enhanced permeation |
| KR20230137362A (ko) | 2016-05-05 | 2023-10-04 | 어퀘스티브 테라퓨틱스, 아이엔씨. | 강화된 전달 에프네프린 조성물 |
| CN110913912A (zh) | 2017-09-22 | 2020-03-24 | 株式会社医药处方 | 不可再贴的贴剂 |
| US11452798B2 (en) | 2017-09-27 | 2022-09-27 | Cook Medical Technologies Llc | Crosslinking submucosal injectate system |
| GB2574878A (en) * | 2018-06-22 | 2019-12-25 | Biofilm Ltd | Oral compositions and mucoadhesive thin films formed therefrom |
| CN109276333B (zh) * | 2018-10-25 | 2021-02-26 | 杭州口腔医院集团有限公司 | 用于口腔种植修复附着龈增宽的装置及方法 |
| CN115151336B (zh) * | 2019-10-02 | 2025-02-11 | 海德奥克赛斯控股有限公司 | 耐用膜及其制备和用途 |
| WO2023076281A1 (en) | 2021-10-25 | 2023-05-04 | Aquestive Therapeutics, Inc. | Oral and nasal compositions and methods of treatment |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2001506640A (ja) * | 1996-12-16 | 2001-05-22 | エルティエス ローマン テラピー−ズュステーメ アーゲー | ブプレノルフィンまたは薬理学上同等物質の口腔における投与及び放出用の平らな製剤、並びにその製造方法 |
| WO2008025791A1 (en) * | 2006-08-30 | 2008-03-06 | Euro-Celtique S.A. | Buprenophine-wafer for drug substitution therapy |
| WO2008068471A1 (en) * | 2006-12-04 | 2008-06-12 | Orexo Ab | New non-abusable pharmaceutical composition comprising opioids |
| WO2008104737A1 (en) * | 2007-03-01 | 2008-09-04 | Reckitt Benckiser Healthcare (Uk) Limited | Improved medicinal compositions comprising buprenorphine and naloxone |
Family Cites Families (38)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5562012A (en) * | 1978-11-06 | 1980-05-10 | Teijin Ltd | Slow-releasing preparation |
| JPS5770816A (en) * | 1980-10-17 | 1982-05-01 | Ono Pharmaceut Co Ltd | Multilayered film preparation of prostagladin of prolonged action |
| US4582384A (en) | 1984-05-04 | 1986-04-15 | Amp Incorporated | Overmolded shielded connector |
| JPS61280423A (ja) * | 1985-06-05 | 1986-12-11 | Kiyuukiyuu Yakuhin Kogyo Kk | 口腔内粘膜貼付剤 |
| US4713243A (en) * | 1986-06-16 | 1987-12-15 | Johnson & Johnson Products, Inc. | Bioadhesive extruded film for intra-oral drug delivery and process |
| US5047244A (en) * | 1988-06-03 | 1991-09-10 | Watson Laboratories, Inc. | Mucoadhesive carrier for delivery of therapeutical agent |
| US5236714A (en) * | 1988-11-01 | 1993-08-17 | Alza Corporation | Abusable substance dosage form having reduced abuse potential |
| JP2656338B2 (ja) * | 1989-01-31 | 1997-09-24 | 日東電工株式会社 | 口腔粘膜貼付製剤 |
| JP3197035B2 (ja) * | 1991-12-10 | 2001-08-13 | 積水化学工業株式会社 | 口腔粘膜適用製剤 |
| US5346701A (en) * | 1993-02-22 | 1994-09-13 | Theratech, Inc. | Transmucosal delivery of macromolecular drugs |
| EP0750905B1 (en) * | 1995-06-27 | 2003-01-02 | Kao Corporation | Patch comprising water soluble adhesive sheet |
| US5800832A (en) | 1996-10-18 | 1998-09-01 | Virotex Corporation | Bioerodable film for delivery of pharmaceutical compounds to mucosal surfaces |
| DE19646392A1 (de) * | 1996-11-11 | 1998-05-14 | Lohmann Therapie Syst Lts | Zubereitung zur Anwendung in der Mundhöhle mit einer an der Schleimhaut haftklebenden, Pharmazeutika oder Kosmetika zur dosierten Abgabe enthaltenden Schicht |
| US5968547A (en) * | 1997-02-24 | 1999-10-19 | Euro-Celtique, S.A. | Method of providing sustained analgesia with buprenorphine |
| ATE314092T1 (de) * | 1997-09-26 | 2006-01-15 | Noven Pharma | Biologische kleber und verfahren zur topischen verabreichung von wirkstoffen |
| CN1204890C (zh) * | 1997-12-22 | 2005-06-08 | 欧罗赛铁克股份有限公司 | 防止阿片样物质滥用的方法 |
| ES2412409T3 (es) * | 1997-12-22 | 2013-07-11 | Euro-Celtique S.A. | Forma farmacéutica para dosificación oral que comprende una combinación de un agonista opiáceo y un antagonista opiáceo |
| US6200604B1 (en) * | 1998-03-27 | 2001-03-13 | Cima Labs Inc. | Sublingual buccal effervescent |
| US6227384B1 (en) | 1999-04-30 | 2001-05-08 | Haworth, Inc. | Slotted divider arrangement |
| US6264981B1 (en) * | 1999-10-27 | 2001-07-24 | Anesta Corporation | Oral transmucosal drug dosage using solid solution |
| DE19960154A1 (de) * | 1999-12-14 | 2001-07-12 | Lohmann Therapie Syst Lts | Flache Arzneizubereitung zur transmucosalen Verabreichung von Oxycodon oder einem vergleichbaren Wirkstoff in der Mundhöhle, für die Anwendung in der Schmerztherapie und Suchttherapie |
| US20020022048A1 (en) * | 2000-05-26 | 2002-02-21 | Bromberg Lev E. | Composite wafer for controlled drug delivery |
| JP4850346B2 (ja) * | 2001-03-15 | 2012-01-11 | 救急薬品工業株式会社 | 粘膜貼付剤 |
| US6585997B2 (en) * | 2001-08-16 | 2003-07-01 | Access Pharmaceuticals, Inc. | Mucoadhesive erodible drug delivery device for controlled administration of pharmaceuticals and other active compounds |
| US20030194420A1 (en) * | 2002-04-11 | 2003-10-16 | Richard Holl | Process for loading a drug delivery device |
| DE10252726B4 (de) * | 2002-11-13 | 2008-05-08 | Lts Lohmann Therapie-Systeme Ag | Mehrschichtiges transmucosales therapeutisches System |
| SE0302947D0 (sv) * | 2003-01-24 | 2003-11-07 | Magle Ab | A composition material for transmucosal delivery |
| SE0300187D0 (sv) * | 2003-01-24 | 2003-01-24 | Magle Ab | A smokeless tobacco substitute material |
| US8790689B2 (en) * | 2003-04-30 | 2014-07-29 | Purdue Pharma L.P. | Tamper resistant transdermal dosage form |
| DE10328942A1 (de) * | 2003-06-27 | 2005-01-27 | Lts Lohmann Therapie-Systeme Ag | Transmukosale Darreichungsformen mit verminderter Schleimhautirritation |
| US8173840B2 (en) * | 2003-07-29 | 2012-05-08 | Signature R&D Holdings, Llc | Compounds with high therapeutic index |
| US20050042281A1 (en) * | 2003-08-21 | 2005-02-24 | Singh Nikhilesh N. | Compositions for delivering therapeutic agents across the oral mucosa |
| WO2005040228A2 (en) * | 2003-10-24 | 2005-05-06 | Adhesives Research, Inc. | Disintegratable films for diagnostic devices |
| EP2269606A3 (en) * | 2003-10-30 | 2012-04-25 | ALZA Corporation | Transdermal analgesic systems having reduced abuse potential |
| US8529939B2 (en) * | 2003-12-08 | 2013-09-10 | Gel-Del Technologies, Inc. | Mucoadhesive drug delivery devices and methods of making and using thereof |
| JP4727499B2 (ja) * | 2005-07-13 | 2011-07-20 | 日本電子株式会社 | 走査型プローブ顕微鏡及びその動作方法 |
| EP1968539A2 (en) * | 2005-12-13 | 2008-09-17 | Biodelivery Sciences International, Inc. | Abuse resistant transmucosal drug delivery device |
| RS54764B1 (sr) * | 2006-07-21 | 2016-10-31 | Biodelivery Sciences Int Inc | Sredstvo za transmukozalnu isporuku sa povećanim nakupljanjem |
-
2009
- 2009-06-23 WO PCT/US2009/048325 patent/WO2010008863A1/en not_active Ceased
- 2009-06-23 CA CA2728912A patent/CA2728912C/en active Active
- 2009-06-23 ES ES09798502.2T patent/ES2663777T3/es active Active
- 2009-06-23 US US12/996,101 patent/US20110189259A1/en not_active Abandoned
- 2009-06-23 CN CN201610218221.5A patent/CN105833420A/zh active Pending
- 2009-06-23 CN CN200980121458XA patent/CN102056578A/zh active Pending
- 2009-06-23 EP EP09798502.2A patent/EP2293751B1/en not_active Not-in-force
- 2009-06-23 JP JP2011516543A patent/JP2011525536A/ja active Pending
- 2009-06-23 BR BRPI0915386A patent/BRPI0915386B8/pt not_active IP Right Cessation
- 2009-06-23 AU AU2009271271A patent/AU2009271271A1/en not_active Abandoned
-
2014
- 2014-11-13 JP JP2014230432A patent/JP2015052003A/ja active Pending
-
2015
- 2015-05-18 US US14/714,574 patent/US20150246003A1/en not_active Abandoned
-
2016
- 2016-05-18 US US15/157,497 patent/US20170231977A1/en not_active Abandoned
- 2016-11-04 JP JP2016215881A patent/JP2017019878A/ja active Pending
-
2018
- 2018-03-22 US US15/928,957 patent/US20180369234A1/en not_active Abandoned
-
2019
- 2019-07-02 JP JP2019123542A patent/JP2019156859A/ja active Pending
- 2019-09-05 US US16/561,505 patent/US20200061052A1/en not_active Abandoned
-
2020
- 2020-04-30 US US16/863,807 patent/US20200360368A1/en not_active Abandoned
-
2021
- 2021-05-31 JP JP2021090747A patent/JP2021121639A/ja active Pending
-
2022
- 2022-02-07 US US17/666,304 patent/US20220226309A1/en not_active Abandoned
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2001506640A (ja) * | 1996-12-16 | 2001-05-22 | エルティエス ローマン テラピー−ズュステーメ アーゲー | ブプレノルフィンまたは薬理学上同等物質の口腔における投与及び放出用の平らな製剤、並びにその製造方法 |
| WO2008025791A1 (en) * | 2006-08-30 | 2008-03-06 | Euro-Celtique S.A. | Buprenophine-wafer for drug substitution therapy |
| WO2008068471A1 (en) * | 2006-12-04 | 2008-06-12 | Orexo Ab | New non-abusable pharmaceutical composition comprising opioids |
| WO2008104737A1 (en) * | 2007-03-01 | 2008-09-04 | Reckitt Benckiser Healthcare (Uk) Limited | Improved medicinal compositions comprising buprenorphine and naloxone |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2014035219A1 (ko) * | 2012-08-31 | 2014-03-06 | 동국대학교 산학협력단 | 유동적 위장관점막 부착성 경구투여용 제형 |
| JP2023533774A (ja) * | 2020-07-07 | 2023-08-04 | オクルジェル | ブプレノルフィンを送達するための親水性分解性マイクロスフェア |
Also Published As
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| JP2019156859A (ja) | 2019-09-19 |
| CN102056578A (zh) | 2011-05-11 |
| BRPI0915386B1 (pt) | 2021-05-18 |
| ES2663777T3 (es) | 2018-04-17 |
| AU2009271271A1 (en) | 2010-01-21 |
| US20110189259A1 (en) | 2011-08-04 |
| CA2728912C (en) | 2018-04-10 |
| US20180369234A1 (en) | 2018-12-27 |
| US20200061052A1 (en) | 2020-02-27 |
| EP2293751B1 (en) | 2018-01-10 |
| BRPI0915386B8 (pt) | 2022-02-22 |
| US20170231977A1 (en) | 2017-08-17 |
| CN105833420A (zh) | 2016-08-10 |
| US20220226309A1 (en) | 2022-07-21 |
| US20200360368A1 (en) | 2020-11-19 |
| BRPI0915386A2 (pt) | 2015-11-03 |
| EP2293751A1 (en) | 2011-03-16 |
| JP2015052003A (ja) | 2015-03-19 |
| US20150246003A1 (en) | 2015-09-03 |
| CA2728912A1 (en) | 2010-01-21 |
| EP2293751A4 (en) | 2013-05-08 |
| WO2010008863A1 (en) | 2010-01-21 |
| JP2017019878A (ja) | 2017-01-26 |
| JP2021121639A (ja) | 2021-08-26 |
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