JP2004522796A5 - - Google Patents

Download PDF

Info

Publication number
JP2004522796A5
JP2004522796A5 JP2002571030A JP2002571030A JP2004522796A5 JP 2004522796 A5 JP2004522796 A5 JP 2004522796A5 JP 2002571030 A JP2002571030 A JP 2002571030A JP 2002571030 A JP2002571030 A JP 2002571030A JP 2004522796 A5 JP2004522796 A5 JP 2004522796A5
Authority
JP
Japan
Prior art keywords
weight
alkaline salt
fine particles
microparticles
acid labile
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.)
Pending
Application number
JP2002571030A
Other languages
English (en)
Japanese (ja)
Other versions
JP2004522796A (ja
Filing date
Publication date
Priority claimed from SE0100822A external-priority patent/SE0100822D0/xx
Application filed filed Critical
Publication of JP2004522796A publication Critical patent/JP2004522796A/ja
Publication of JP2004522796A5 publication Critical patent/JP2004522796A5/ja
Pending legal-status Critical Current

Links

JP2002571030A 2001-03-09 2002-03-06 H+,k+−atpアーゼ阻害剤を含む微粒子の製造方法 Pending JP2004522796A (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
SE0100822A SE0100822D0 (sv) 2001-03-09 2001-03-09 Method II to obtain microparticles
PCT/SE2002/000400 WO2002072071A1 (en) 2001-03-09 2002-03-06 Method to obtain microparticles containing a h+, k+ -atp-ase inhibitor

Publications (2)

Publication Number Publication Date
JP2004522796A JP2004522796A (ja) 2004-07-29
JP2004522796A5 true JP2004522796A5 (enExample) 2005-12-22

Family

ID=20283293

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2002571030A Pending JP2004522796A (ja) 2001-03-09 2002-03-06 H+,k+−atpアーゼ阻害剤を含む微粒子の製造方法

Country Status (21)

Country Link
US (2) US20040101565A1 (enExample)
EP (1) EP1370243B1 (enExample)
JP (1) JP2004522796A (enExample)
KR (1) KR20030081506A (enExample)
CN (1) CN1507343A (enExample)
AT (1) ATE400253T1 (enExample)
AU (1) AU2002235101B8 (enExample)
BR (1) BR0207827A (enExample)
CA (1) CA2440163A1 (enExample)
DE (1) DE60227488D1 (enExample)
DK (1) DK1370243T3 (enExample)
ES (1) ES2307722T3 (enExample)
IL (1) IL157467A0 (enExample)
MX (1) MXPA03007887A (enExample)
NO (1) NO20033966L (enExample)
NZ (1) NZ527997A (enExample)
PT (1) PT1370243E (enExample)
SE (1) SE0100822D0 (enExample)
SI (1) SI1370243T1 (enExample)
WO (1) WO2002072071A1 (enExample)
ZA (1) ZA200306614B (enExample)

Families Citing this family (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20060159756A1 (en) * 1999-09-10 2006-07-20 Brita Sjoblom Method to obtain microparticles containing an H+,K+-ATP-ASE inhibitor
SE0100823D0 (sv) * 2001-03-09 2001-03-09 Astrazeneca Ab Method I to obtain microparticles
US8067032B2 (en) 2000-12-22 2011-11-29 Baxter International Inc. Method for preparing submicron particles of antineoplastic agents
US6977085B2 (en) 2000-12-22 2005-12-20 Baxter International Inc. Method for preparing submicron suspensions with polymorph control
US6607784B2 (en) 2000-12-22 2003-08-19 Baxter International Inc. Microprecipitation method for preparing submicron suspensions
US9700866B2 (en) 2000-12-22 2017-07-11 Baxter International Inc. Surfactant systems for delivery of organic compounds
US6884436B2 (en) 2000-12-22 2005-04-26 Baxter International Inc. Method for preparing submicron particle suspensions
US6951656B2 (en) 2000-12-22 2005-10-04 Baxter International Inc. Microprecipitation method for preparing submicron suspensions
US7193084B2 (en) 2000-12-22 2007-03-20 Baxter International Inc. Polymorphic form of itraconazole
SE0100824D0 (sv) * 2001-03-09 2001-03-09 Astrazeneca Ab Method III to obtain microparticles
SE0100822D0 (sv) * 2001-03-09 2001-03-09 Astrazeneca Ab Method II to obtain microparticles
CN1558755A (zh) 2001-09-26 2004-12-29 ���ع��ʹ�˾ 通过分散和除去溶剂或液相制备亚微米大小的纳米颗粒
US20060003012A9 (en) 2001-09-26 2006-01-05 Sean Brynjelsen Preparation of submicron solid particle suspensions by sonication of multiphase systems
US7112340B2 (en) 2001-10-19 2006-09-26 Baxter International Inc. Compositions of and method for preparing stable particles in a frozen aqueous matrix
CA2518780C (en) 2003-03-12 2014-05-13 Takeda Pharmaceutical Company Limited Drug composition having active ingredient adhered at high concentration to spherical core
DE10325989A1 (de) * 2003-06-07 2005-01-05 Glatt Gmbh Verfahren zur Herstellung von und daraus resultierende Mikropellets sowie deren Verwendung
US20050181052A1 (en) * 2004-02-17 2005-08-18 Patel Satishkumar A. Lansoprazole microtablets
WO2007095376A2 (en) * 2006-02-15 2007-08-23 Kennametal Inc. Method and apparatus for coating particulates utilizing physical vapor deposition
CH698658B1 (de) * 2006-04-24 2009-09-30 Mepha Ag Orale pharmazeutische Formulierung mit schneller Freisetzung für Pyridylmethylsulfinyl-Benzimidazole.
US20090087569A1 (en) * 2007-09-27 2009-04-02 Fenchem Enterprises Ltd. Methods for Preparing Highly Stable Hyaluronic Acid
IT1401284B1 (it) * 2010-08-06 2013-07-18 Valpharma S P A Nuove formulazioni farmaceutiche idonee per la somministrazione orale di esomeprazolo magnesio diidrato, in forma di compresse mups (multi unit pellets system).
WO2017145146A1 (en) 2016-02-25 2017-08-31 Dexcel Pharma Technologies Ltd. Compositions comprising proton pump inhibitors
US10076494B2 (en) 2016-06-16 2018-09-18 Dexcel Pharma Technologies Ltd. Stable orally disintegrating pharmaceutical compositions
WO2021153525A1 (ja) * 2020-01-27 2021-08-05 東和薬品株式会社 エソメプラゾール経口製剤およびその製造方法

Family Cites Families (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3565475D1 (en) * 1984-04-07 1988-11-17 Bayer Ag Process and apparatus for the production of granules
IL75400A (en) * 1984-06-16 1988-10-31 Byk Gulden Lomberg Chem Fab Dialkoxypyridine methyl(sulfinyl or sulfonyl)benzimidazoles,processes for the preparation thereof and pharmaceutical compositions containing the same
GB2189698A (en) * 1986-04-30 1987-11-04 Haessle Ab Coated omeprazole tablets
DE3909455A1 (de) * 1989-03-22 1990-09-27 Hoechst Ag Verfahren zur herstellung von wasserdispergierbaren granulaten
WO1996001623A1 (en) * 1994-07-08 1996-01-25 Astra Aktiebolag Multiple unit tableted dosage form i
FR2725623A1 (fr) * 1994-10-18 1996-04-19 Flamel Tech Sa Microcapsules medicamenteuses et/ou nutritionnelles pour administration per os
DE19613395A1 (de) * 1996-04-03 1997-10-09 Basf Ag Granulate hygroskopischer, wasserlöslicher Produkte
DE19733094A1 (de) * 1997-07-31 1999-02-04 Merck Patent Gmbh Formulierung auf der Basis von Ascorbinsäure mit verbesserter Farbstabilität
WO1999018935A1 (de) * 1997-10-15 1999-04-22 Merck Patent Gmbh Herstellung eines direkt verpressbaren tablettierhilfsstoffes
US6174548B1 (en) * 1998-08-28 2001-01-16 Andrx Pharmaceuticals, Inc. Omeprazole formulation
HUP0100065A2 (hu) * 1997-12-08 2001-08-28 Byk Gulden Lomberg Chemische Fabrik Gmbh. Savérzékeny vegyületet tartalmazó új kúp gyógyszerforma
SE9903236D0 (sv) * 1999-09-10 1999-09-10 Astra Ab Method to obtain microparticles
SE0100823D0 (sv) * 2001-03-09 2001-03-09 Astrazeneca Ab Method I to obtain microparticles
US20060159756A1 (en) * 1999-09-10 2006-07-20 Brita Sjoblom Method to obtain microparticles containing an H+,K+-ATP-ASE inhibitor
SE0100822D0 (sv) * 2001-03-09 2001-03-09 Astrazeneca Ab Method II to obtain microparticles
SE0100824D0 (sv) * 2001-03-09 2001-03-09 Astrazeneca Ab Method III to obtain microparticles

Similar Documents

Publication Publication Date Title
JP2004522796A5 (enExample)
JP2004527505A5 (enExample)
RU2170090C2 (ru) Способ получения фармацевтической лекарственной формы, способ ингибирования секреции кислоты в желудке у млекопитающих и человека
CA2323680C (en) Orally disintegrable tablets
JP3509105B2 (ja) 活性物質をポリマーで被覆したマイクロカプセルの製法と特にこの方法で得られる新規マイクロカプセル
JP4612184B2 (ja) 酸不安定な活性化合物を含有する新規の投与形
JP2001513752A (ja) 迅速崩壊ペレット
JP2008525433A5 (enExample)
JP2003504324A5 (enExample)
JP2009525300A5 (enExample)
CN104606146B (zh) 一种埃索美拉唑镁肠溶微丸制剂及其制备方法
JP7482182B2 (ja) プロトンポンプ阻害剤を含む経口用固形製剤組成物、それを含む経口用固形製剤及びその製造方法
JP4234427B2 (ja) 活性成分をベースとする微小顆粒およびその製造方法
Olayemi et al. Formulation and evaluation of Cyperus esculentus (Tiger Nut) starch-alginate microbeads in the oral delivery of ibuprofen
TW201532635A (zh) 口腔內崩解錠
JP2004522798A5 (enExample)
JPS62111916A (ja) 一定の放出性を保持した薬物粒子
CA2648538C (en) Oral rapid release pharmaceutical formulation for pyridylmethylsulfinyl-benzimidazoles
CN101827584A (zh) N-芳基脲基药物的固态分散体产品
JP2002529497A (ja) 改善された化学的方法および医薬処方物
WO2010018175A2 (en) Oral pharmaceutical formulation for omeprazole comprising a specific separation layer
JP2007515456A (ja) コーティング方法
JP4339685B2 (ja) ペクチン及びアスコルビン酸を含む組成物
EP1928408B1 (fr) Comprimes orodispersibles de principes actifs amers
WO2007015270A2 (en) Novel controlled release compositions of selective serotonin reuptake inhibitors