WO2008035376A3 - A novel bio-erodible insert for ophthalmic applications and a process for the preparation thereof - Google Patents
A novel bio-erodible insert for ophthalmic applications and a process for the preparation thereof Download PDFInfo
- Publication number
- WO2008035376A3 WO2008035376A3 PCT/IN2007/000374 IN2007000374W WO2008035376A3 WO 2008035376 A3 WO2008035376 A3 WO 2008035376A3 IN 2007000374 W IN2007000374 W IN 2007000374W WO 2008035376 A3 WO2008035376 A3 WO 2008035376A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- insert
- preparation
- erodible
- conditions
- bio
- Prior art date
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0019—Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/10—Dispersions; Emulsions
- A61K9/127—Liposomes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/19—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles lyophilised, i.e. freeze-dried, solutions or dispersions
Abstract
The present invention provides a novel bio-erodible ophthalmic insert a process for the preparation of the said bio-erodible insert. In the said process collagen is treated with organic polar solvents, hydrophilic polymers and therapeutically active substances under controlled conditions. The resulting solution is air dried in a dust free chamber to make collagen film. This film is cut into shape to obtain insert, which is subjected to cross-linking with UV irradiation followed by conventional sterilization. The prepared inserts are very effective for temporary punctal occlusion in various corneal conditions and are very effective to treat dry eye syndrome due to occupational conditions.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IN2064DE2006 | 2006-09-19 | ||
IN2064/DEL/2006 | 2006-09-19 |
Publications (3)
Publication Number | Publication Date |
---|---|
WO2008035376A2 WO2008035376A2 (en) | 2008-03-27 |
WO2008035376A3 true WO2008035376A3 (en) | 2008-11-20 |
WO2008035376A4 WO2008035376A4 (en) | 2009-01-29 |
Family
ID=39092185
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/IN2007/000374 WO2008035376A2 (en) | 2006-09-19 | 2007-08-30 | A novel bio-erodible insert for ophthalmic applications and a process for the preparation thereof |
Country Status (1)
Country | Link |
---|---|
WO (1) | WO2008035376A2 (en) |
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ES2700433T3 (en) | 2005-12-13 | 2019-02-15 | Incyte Holdings Corp | Derivatives of pyrrolo [2,3-d] pyrimidine as inhibitors of Janus kinases |
HUE029236T2 (en) | 2007-06-13 | 2017-02-28 | Incyte Holdings Corp | Crystalline salts of the janus kinase inhibitor (r)-3-(4-(7h-pyrrolo[2,3-d]pyrimidin-4-yl)-1h-pyrazol-1-yl)-3-cyclopentylpropanenitrile |
CN101683538B (en) * | 2008-09-28 | 2013-01-02 | 上海市第十人民医院 | Lacrimal passage stopper and preparation method thereof |
JP5890182B2 (en) | 2009-02-12 | 2016-03-22 | インセプト エルエルシー | Drug delivery with hydrogel plugs |
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WO2010135621A1 (en) | 2009-05-22 | 2010-11-25 | Incyte Corporation | 3-[4-(7h-pyrrolo[2,3-d]pyrimidin-4-yl)-1h-pyrazol-1-yl]octane- or heptane-nitrile as jak inhibitors |
TW201113285A (en) | 2009-09-01 | 2011-04-16 | Incyte Corp | Heterocyclic derivatives of pyrazol-4-yl-pyrrolo[2,3-d]pyrimidines as janus kinase inhibitors |
ES2662588T3 (en) | 2010-03-10 | 2018-04-09 | Incyte Holdings Corporation | Piperidin-4-IL azetidine derivatives as JAK1 inhibitors |
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WO2012068440A1 (en) | 2010-11-19 | 2012-05-24 | Incyte Corporation | Heterocyclic-substituted pyrrolopyridines and pyrrolopyrimidines as jak inhibitors |
AU2011329734B2 (en) | 2010-11-19 | 2015-05-28 | Incyte Holdings Corporation | Cyclobutyl substituted pyrrolopyridine and pyrrolopyrimidine derivatives as JAK inhibitors |
MY165963A (en) | 2011-06-20 | 2018-05-18 | Incyte Holdings Corp | Azetidinyl phenyl, pyridyl or pyrazinyl carboxamide derivatives as jak inhibitors |
TW201313721A (en) | 2011-08-18 | 2013-04-01 | Incyte Corp | Cyclohexyl azetidine derivatives as JAK inhibitors |
UA111854C2 (en) | 2011-09-07 | 2016-06-24 | Інсайт Холдінгс Корпорейшн | METHODS AND INTERMEDIATE COMPOUNDS FOR JAK INHIBITORS |
US10226417B2 (en) | 2011-09-16 | 2019-03-12 | Peter Jarrett | Drug delivery systems and applications |
US9193733B2 (en) | 2012-05-18 | 2015-11-24 | Incyte Holdings Corporation | Piperidinylcyclobutyl substituted pyrrolopyridine and pyrrolopyrimidine derivatives as JAK inhibitors |
EA201590930A1 (en) | 2012-11-15 | 2015-08-31 | Инсайт Корпорейшн | DOSAGE FORMS OF RUXOLITINIB WITH Slow Release. |
CN105189509B (en) | 2013-03-06 | 2017-12-19 | 因赛特公司 | For preparing the method and intermediate of JAK inhibitor |
SI3030227T1 (en) | 2013-08-07 | 2020-08-31 | Incyte Corporation | Sustained release dosage forms for a jak1 inhibitor |
WO2015184305A1 (en) | 2014-05-30 | 2015-12-03 | Incyte Corporation | TREATMENT OF CHRONIC NEUTROPHILIC LEUKEMIA (CNL) AND ATYPICAL CHRONIC MYELOID LEUKEMIA (aCML) BY INHIBITORS OF JAK1 |
TW201924683A (en) | 2017-12-08 | 2019-07-01 | 美商英塞特公司 | Low dose combination therapy for treatment of myeloproliferative neoplasms |
MX2020007973A (en) | 2018-01-30 | 2020-12-07 | Incyte Corp | Processes for preparing (1 -(3-fluoro-2-(trifluoromethyl)isonicot inyl)piperidine-4-one). |
CN113768934A (en) | 2018-03-30 | 2021-12-10 | 因赛特公司 | Treatment of hidradenitis suppurativa with JAK inhibitors |
US11833155B2 (en) | 2020-06-03 | 2023-12-05 | Incyte Corporation | Combination therapy for treatment of myeloproliferative neoplasms |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4164559A (en) * | 1977-09-21 | 1979-08-14 | Cornell Research Foundation, Inc. | Collagen drug delivery device |
US5185152A (en) * | 1990-01-10 | 1993-02-09 | Peyman Gholam A | Method and apparatus for controlled release drug delivery to the cornea and anterior chamber of the eye |
WO2000059420A1 (en) * | 1999-04-01 | 2000-10-12 | The Uab Research Foundation | Improved conjunctival inserts for topical delivery of medication or lubrication |
WO2006031658A2 (en) * | 2004-09-10 | 2006-03-23 | Allergan, Inc. | Therapeutic lacrimal canalicular inserts and related methods |
-
2007
- 2007-08-30 WO PCT/IN2007/000374 patent/WO2008035376A2/en active Application Filing
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4164559A (en) * | 1977-09-21 | 1979-08-14 | Cornell Research Foundation, Inc. | Collagen drug delivery device |
US5185152A (en) * | 1990-01-10 | 1993-02-09 | Peyman Gholam A | Method and apparatus for controlled release drug delivery to the cornea and anterior chamber of the eye |
WO2000059420A1 (en) * | 1999-04-01 | 2000-10-12 | The Uab Research Foundation | Improved conjunctival inserts for topical delivery of medication or lubrication |
WO2006031658A2 (en) * | 2004-09-10 | 2006-03-23 | Allergan, Inc. | Therapeutic lacrimal canalicular inserts and related methods |
Also Published As
Publication number | Publication date |
---|---|
WO2008035376A2 (en) | 2008-03-27 |
WO2008035376A4 (en) | 2009-01-29 |
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