ES2177022T3 - Un itraconazol que exhibe una solubilidad mejorada, un metodo para preparar el mismo y una composicion farmaceutica para administracion oral que comprende el mismo. - Google Patents
Un itraconazol que exhibe una solubilidad mejorada, un metodo para preparar el mismo y una composicion farmaceutica para administracion oral que comprende el mismo.Info
- Publication number
- ES2177022T3 ES2177022T3 ES98929878T ES98929878T ES2177022T3 ES 2177022 T3 ES2177022 T3 ES 2177022T3 ES 98929878 T ES98929878 T ES 98929878T ES 98929878 T ES98929878 T ES 98929878T ES 2177022 T3 ES2177022 T3 ES 2177022T3
- Authority
- ES
- Spain
- Prior art keywords
- same
- exhibits
- itraconazol
- understands
- preparing
- 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.)
- Expired - Lifetime
Links
- VHVPQPYKVGDNFY-ZPGVKDDISA-N itraconazole Chemical compound O=C1N(C(C)CC)N=CN1C1=CC=C(N2CCN(CC2)C=2C=CC(OC[C@@H]3O[C@](CN4N=CN=C4)(OC3)C=3C(=CC(Cl)=CC=3)Cl)=CC=2)C=C1 VHVPQPYKVGDNFY-ZPGVKDDISA-N 0.000 title 1
- 239000008194 pharmaceutical composition Substances 0.000 title 1
- VHVPQPYKVGDNFY-DFMJLFEVSA-N 2-[(2r)-butan-2-yl]-4-[4-[4-[4-[[(2r,4s)-2-(2,4-dichlorophenyl)-2-(1,2,4-triazol-1-ylmethyl)-1,3-dioxolan-4-yl]methoxy]phenyl]piperazin-1-yl]phenyl]-1,2,4-triazol-3-one Chemical compound O=C1N([C@H](C)CC)N=CN1C1=CC=C(N2CCN(CC2)C=2C=CC(OC[C@@H]3O[C@](CN4N=CN=C4)(OC3)C=3C(=CC(Cl)=CC=3)Cl)=CC=2)C=C1 VHVPQPYKVGDNFY-DFMJLFEVSA-N 0.000 abstract 3
- 229960004130 itraconazole Drugs 0.000 abstract 3
- 239000002245 particle Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/10—Antimycotics
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Un itraconazol que exhibe una disponibilidad mejorada, en donde el diámetro de las partículas de itraconazol está en el intervalo de 0,5 a 10 µm y el itraconazol tiene una forma amorfa.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1019970024938A KR19990001564A (ko) | 1997-06-16 | 1997-06-16 | 용해도를 개선한 아졸계 항진균제 및 이를 함유하는 제제 |
Publications (1)
Publication Number | Publication Date |
---|---|
ES2177022T3 true ES2177022T3 (es) | 2002-12-01 |
Family
ID=19509733
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES98929878T Expired - Lifetime ES2177022T3 (es) | 1997-06-16 | 1998-06-16 | Un itraconazol que exhibe una solubilidad mejorada, un metodo para preparar el mismo y una composicion farmaceutica para administracion oral que comprende el mismo. |
Country Status (17)
Country | Link |
---|---|
US (1) | US6346533B1 (es) |
EP (1) | EP0991646B1 (es) |
JP (1) | JP2002504930A (es) |
KR (1) | KR19990001564A (es) |
CN (1) | CN1129598C (es) |
AT (1) | ATE216699T1 (es) |
AU (1) | AU7939298A (es) |
BR (1) | BR9810124A (es) |
CA (1) | CA2294398A1 (es) |
DE (1) | DE69805070T2 (es) |
DK (1) | DK0991646T3 (es) |
ES (1) | ES2177022T3 (es) |
HU (1) | HUP0004050A3 (es) |
PL (1) | PL338631A1 (es) |
PT (1) | PT991646E (es) |
WO (1) | WO1998057967A1 (es) |
YU (1) | YU66799A (es) |
Families Citing this family (52)
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DE60023465T2 (de) | 1999-03-24 | 2006-07-20 | R.P. Scherer Technologies, Inc., Las Vegas | Pharmazeutische formulierungen mit verbesserter löslichkeit in wasser |
IT1312115B1 (it) * | 1999-06-24 | 2002-04-04 | Nicox Sa | Composti amorfi e relative composizioni farmaceutiche |
KR100694667B1 (ko) * | 1999-12-08 | 2007-03-14 | 동아제약주식회사 | 생체내이용률 향상과 개인간 및 개인내 흡수 편차를감소시킨 이트라코나졸 함유 항진균성 제제 |
KR20010097244A (ko) * | 2000-04-21 | 2001-11-08 | 유충식 | 위산도 비의존성 고용해도를 갖는 이트라코나졸 함유약학적 조성물 및 그 제조방법 |
KR100432949B1 (ko) * | 2000-06-13 | 2004-05-31 | 코오롱제약주식회사 | 생체이용율이 향상된 이트라코나졸의 분립체 조성물과이를 이용한 이트라코나졸 제제 및 그 제조방법 |
US8067032B2 (en) | 2000-12-22 | 2011-11-29 | Baxter International Inc. | Method for preparing submicron particles of antineoplastic agents |
US6884436B2 (en) * | 2000-12-22 | 2005-04-26 | Baxter International Inc. | Method for preparing submicron particle suspensions |
US20050048126A1 (en) * | 2000-12-22 | 2005-03-03 | Barrett Rabinow | Formulation to render an antimicrobial drug potent against organisms normally considered to be resistant to the drug |
US20030096013A1 (en) * | 2000-12-22 | 2003-05-22 | Jane Werling | Preparation of submicron sized particles with polymorph control |
BR0116377A (pt) * | 2000-12-22 | 2005-12-13 | Baxter Int | Métodos para preparar partìculas submicronicamente dimensionadas de um composto orgânico, e para preparar uma suspensão de um composto farmaceuticamente ativo, e, composição de matéria |
US6951656B2 (en) | 2000-12-22 | 2005-10-04 | Baxter International Inc. | Microprecipitation method for preparing submicron suspensions |
US20040256749A1 (en) * | 2000-12-22 | 2004-12-23 | Mahesh Chaubal | Process for production of essentially solvent-free small particles |
US9700866B2 (en) * | 2000-12-22 | 2017-07-11 | Baxter International Inc. | Surfactant systems for delivery of organic compounds |
US7193084B2 (en) * | 2000-12-22 | 2007-03-20 | Baxter International Inc. | Polymorphic form of itraconazole |
US20040173147A1 (en) * | 2001-06-07 | 2004-09-09 | Figueroa Iddys D. | Application of a bioactive agent to a delivery substrate |
US6962715B2 (en) * | 2001-10-24 | 2005-11-08 | Hewlett-Packard Development Company, L.P. | Method and dosage form for dispensing a bioactive substance |
US20040173146A1 (en) * | 2001-06-07 | 2004-09-09 | Figueroa Iddys D. | Application of a bioactive agent to a delivery substrate |
AU2002317063A (en) * | 2001-06-12 | 2002-12-23 | Smartrix Technologies Inc | Itraconazole granulations: pharmaceutical formulations for oral administration and method of preparing same |
US7163700B2 (en) | 2001-07-31 | 2007-01-16 | Capricorn Pharma, Inc. | Amorphous drug beads |
KR100438485B1 (ko) * | 2001-08-13 | 2004-07-09 | 한국디디에스제약 주식회사 | 아졸류 항진균제의 약제학적 조성물 |
MXPA04002446A (es) * | 2001-09-26 | 2004-07-23 | Baxter Int | Preparacion de nanoparticulas de tamano de submicras mediante dispersion y remocion de la fase liquida o solvente. |
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 |
CA2363376A1 (en) * | 2001-11-16 | 2003-05-16 | Bernard Charles Sherman | Solid pharmaceutical compositions for oral administration comprising itraconazole |
US7927613B2 (en) | 2002-02-15 | 2011-04-19 | University Of South Florida | Pharmaceutical co-crystal compositions |
US7446107B2 (en) | 2002-02-15 | 2008-11-04 | Transform Pharmaceuticals, Inc. | Crystalline forms of conazoles and methods of making and using the same |
US7790905B2 (en) | 2002-02-15 | 2010-09-07 | Mcneil-Ppc, Inc. | Pharmaceutical propylene glycol solvate compositions |
JP4906233B2 (ja) | 2002-03-01 | 2012-03-28 | ユニバーシティー オブ サウス フロリダ | 少なくとも1種の有効薬剤成分を含有する多構成要素固相 |
CA2480377A1 (en) * | 2002-03-26 | 2003-10-09 | Teva Pharmaceutical Industries Ltd. | Drug microparticles |
AU2003243354A1 (en) | 2002-05-31 | 2003-12-19 | Transform Pharmaceuticals, Inc. | Novel conazole crystalline forms and related processes, pharmaceutical compositions and methods |
MXPA05000232A (es) | 2002-06-21 | 2005-06-17 | Transform Pharmaceuticals Inc | Composiciones farmaceuticas con disolucion mejorada. |
KR100557680B1 (ko) * | 2002-11-23 | 2006-03-07 | 한국유나이티드제약 주식회사 | 이트라코나졸의 용해도 개선을 위한 펠렛제제 및 그제조방법 |
US8183290B2 (en) | 2002-12-30 | 2012-05-22 | Mcneil-Ppc, Inc. | Pharmaceutically acceptable propylene glycol solvate of naproxen |
DK1438960T4 (da) * | 2003-01-14 | 2013-03-25 | Cimex Pharma Ag | Sammensætning af itraconazol dispergeret i en hydrofil polymer med forhøjet biotilgængelighed |
GB0319797D0 (en) * | 2003-08-26 | 2003-09-24 | Leuven K U Res & Dev | Particle size reduction of poorly soluble drugs |
CN1905905B (zh) * | 2003-09-22 | 2011-06-08 | 巴克斯特国际公司 | 用于药物制剂和医药产品最终灭菌的高压灭菌 |
US20050118265A1 (en) * | 2003-11-28 | 2005-06-02 | Anandi Krishnan | Antifungal oral dosage forms and the methods for preparation |
WO2005082915A1 (en) * | 2004-02-26 | 2005-09-09 | Zentiva, A.S. | Amorphous forms of risedronate monosodium |
CN1294912C (zh) * | 2004-03-01 | 2007-01-17 | 上海医药工业研究院 | 伊曲康唑盐酸盐组合物及其冻干粉针 |
US20050202051A1 (en) * | 2004-03-15 | 2005-09-15 | Chinea Vanessa I. | Pharmaceutical vehicle |
US20050203482A1 (en) * | 2004-03-15 | 2005-09-15 | Chinea Vanessa I. | Pharmaceutical dispensing apparatus and method |
CA2598204C (en) | 2004-11-09 | 2015-01-13 | Board Of Regents, The University Of Texas System | Stabilized hme composition with small drug particles |
US20060182777A1 (en) * | 2005-02-15 | 2006-08-17 | Steve Kangas | Method of modulating drug release from a coated substrate |
MX2007015183A (es) * | 2005-06-14 | 2008-02-19 | Baxter Int | Formulaciones farmaceuticas para minimizar las interacciones farmaco-farmaco. |
US20070134341A1 (en) * | 2005-11-15 | 2007-06-14 | Kipp James E | Compositions of lipoxygenase inhibitors |
US20090152176A1 (en) * | 2006-12-23 | 2009-06-18 | Baxter International Inc. | Magnetic separation of fine particles from compositions |
US20080293814A1 (en) * | 2007-05-22 | 2008-11-27 | Deepak Tiwari | Concentrate esmolol |
US8426467B2 (en) * | 2007-05-22 | 2013-04-23 | Baxter International Inc. | Colored esmolol concentrate |
US8722736B2 (en) * | 2007-05-22 | 2014-05-13 | Baxter International Inc. | Multi-dose concentrate esmolol with benzyl alcohol |
GB0818403D0 (en) * | 2008-10-08 | 2008-11-12 | Univ Leuven Kath | Aqueous electrophoretic deposition |
WO2010040648A2 (en) * | 2008-10-06 | 2010-04-15 | Katholieke Universiteit Leuven, K.U.Leuven R&D | Functional layers of biomolecules and living cells, and a novel system to produce such |
CN104224687A (zh) * | 2014-09-28 | 2014-12-24 | 武汉药谷生物工程有限公司 | 硝酸异康唑阴道栓及其制备方法 |
Family Cites Families (15)
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US4368200A (en) | 1978-06-23 | 1983-01-11 | Janssen Pharmaceutica N.V. | Heterocyclic derivatives of (4-phenyl-piperazine-1-yl-aryloxymethyl-1,3-dioxolan-2-yl)-methyl-1H-imidazoles and 1H-1,2,4-triazoles |
US4267179A (en) * | 1978-06-23 | 1981-05-12 | Janssen Pharmaceutica, N.V. | Heterocyclic derivatives of (4-phenylpiperazin-1-yl-aryloxymethyl-1,3-dioxolan-2-yl)methyl-1H-imidazoles and 1H-1,2,4-triazoles |
US4490530A (en) | 1981-01-14 | 1984-12-25 | Janssen Pharmaceutica N.V. | Heterocyclic derivatives of (4-phenylpiperazin-1-yl-aryloxymethyl-1,3-dioxolan-2-yl)-methyl-1H-imidazoles and 1H-1,2,4-triazoles |
JPS60139688A (ja) * | 1983-12-28 | 1985-07-24 | Tokyo Tanabe Co Ltd | 無定形ジヒドロピリジン粉末製剤 |
GB8506792D0 (en) | 1985-03-15 | 1985-04-17 | Janssen Pharmaceutica Nv | Derivatives of y-cyclodextrin |
US4870060A (en) | 1985-03-15 | 1989-09-26 | Janssen Pharmaceutica | Derivatives of γ-cylodextrin |
PH30929A (en) * | 1992-09-03 | 1997-12-23 | Janssen Pharmaceutica Nv | Beads having a core coated with an antifungal and a polymer. |
WO1994016700A1 (en) * | 1993-01-27 | 1994-08-04 | Sepracor, Inc. | Method and composition employing (2r,4s) itraconazole |
IT1263831B (it) * | 1993-01-29 | 1996-09-04 | Paolo Chiesi | Complessi di inclusione multicomponente ad elevata solubilita' costituiti da un farmaco di tipo basico, un acido ed una ciclodestrina |
TW438601B (en) * | 1994-05-18 | 2001-06-07 | Janssen Pharmaceutica Nv | New mucoadhesive emulsion compositions and a process for the preparation thereof |
FR2722984B1 (fr) * | 1994-07-26 | 1996-10-18 | Effik Lab | Procede de preparation de formes pharmaceutiques seches et les compositions pharmaceutiques ainsi realisees |
US5750147A (en) * | 1995-06-07 | 1998-05-12 | Emisphere Technologies, Inc. | Method of solubilizing and encapsulating itraconazole |
EP0862463A1 (en) * | 1995-11-23 | 1998-09-09 | Janssen Pharmaceutica N.V. | Solid mixtures of cyclodextrins prepared via melt-extrusion |
US5686133A (en) * | 1996-01-31 | 1997-11-11 | Port Systems, L.L.C. | Water soluble pharmaceutical coating and method for producing coated pharmaceuticals |
EE03902B1 (et) * | 1996-05-20 | 2002-12-16 | Janssen Pharmaceutica N.V. | Osakesed, nende valmistamismeetod ja kasutamine, farmatseutiline doseerimisvorm ja selle valmistamismeetod, tahke dispersioon ning farmatseutiline pakend |
-
1997
- 1997-06-16 KR KR1019970024938A patent/KR19990001564A/ko not_active Application Discontinuation
-
1998
- 1998-06-16 PT PT98929878T patent/PT991646E/pt unknown
- 1998-06-16 HU HU0004050A patent/HUP0004050A3/hu unknown
- 1998-06-16 BR BR9810124-2A patent/BR9810124A/pt not_active IP Right Cessation
- 1998-06-16 AU AU79392/98A patent/AU7939298A/en not_active Abandoned
- 1998-06-16 PL PL98338631A patent/PL338631A1/xx unknown
- 1998-06-16 ES ES98929878T patent/ES2177022T3/es not_active Expired - Lifetime
- 1998-06-16 CN CN98806999A patent/CN1129598C/zh not_active Expired - Fee Related
- 1998-06-16 DK DK98929878T patent/DK0991646T3/da active
- 1998-06-16 US US09/445,886 patent/US6346533B1/en not_active Expired - Fee Related
- 1998-06-16 JP JP50419399A patent/JP2002504930A/ja not_active Ceased
- 1998-06-16 AT AT98929878T patent/ATE216699T1/de not_active IP Right Cessation
- 1998-06-16 EP EP98929878A patent/EP0991646B1/en not_active Expired - Lifetime
- 1998-06-16 CA CA002294398A patent/CA2294398A1/en not_active Abandoned
- 1998-06-16 DE DE69805070T patent/DE69805070T2/de not_active Expired - Fee Related
- 1998-06-16 YU YU66799A patent/YU66799A/sh unknown
- 1998-06-16 WO PCT/KR1998/000164 patent/WO1998057967A1/en not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
DK0991646T3 (da) | 2002-06-10 |
HUP0004050A3 (en) | 2003-03-28 |
KR19990001564A (ko) | 1999-01-15 |
PL338631A1 (en) | 2000-11-06 |
JP2002504930A (ja) | 2002-02-12 |
BR9810124A (pt) | 2000-08-08 |
DE69805070T2 (de) | 2002-11-07 |
CN1262682A (zh) | 2000-08-09 |
ATE216699T1 (de) | 2002-05-15 |
PT991646E (pt) | 2002-08-30 |
WO1998057967A1 (en) | 1998-12-23 |
HUP0004050A2 (hu) | 2001-06-28 |
CA2294398A1 (en) | 1998-12-23 |
US6346533B1 (en) | 2002-02-12 |
EP0991646B1 (en) | 2002-04-24 |
EP0991646A1 (en) | 2000-04-12 |
AU7939298A (en) | 1999-01-04 |
DE69805070D1 (de) | 2002-05-29 |
CN1129598C (zh) | 2003-12-03 |
YU66799A (sh) | 2002-06-19 |
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