HUP0004050A2 - Javított oldódású itrakonazol, eljárás ennek előállítására és ezt tartalmazó orális gyógyszerkészítmény - Google Patents
Javított oldódású itrakonazol, eljárás ennek előállítására és ezt tartalmazó orális gyógyszerkészítményInfo
- Publication number
- HUP0004050A2 HUP0004050A2 HU0004050A HUP0004050A HUP0004050A2 HU P0004050 A2 HUP0004050 A2 HU P0004050A2 HU 0004050 A HU0004050 A HU 0004050A HU P0004050 A HUP0004050 A HU P0004050A HU P0004050 A2 HUP0004050 A2 HU P0004050A2
- Authority
- HU
- Hungary
- Prior art keywords
- same
- itraconazole
- preparing
- pharmaceutical composition
- oral administration
- Prior art date
Links
- 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 title abstract 6
- 229960004130 itraconazole Drugs 0.000 title abstract 6
- 238000000034 method Methods 0.000 title abstract 2
- 230000001747 exhibiting effect Effects 0.000 title 1
- 239000008194 pharmaceutical composition Substances 0.000 title 1
- 239000002245 particle Substances 0.000 abstract 2
- 238000004090 dissolution Methods 0.000 abstract 1
- 238000001035 drying Methods 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 239000003960 organic solvent Substances 0.000 abstract 1
- 238000002360 preparation method Methods 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
Abstract
A találmány tárgya javított bioavailabilitást mutató itrakonazol, aholaz itrakonazol részecske átmérője 0,5-10 mm és amorf formávalrendelkezik. A találmány tárgya továbbá eljárás 0,5-10 mm részecskeátmérőjű, amorf formájú, javított tulajdonságú itrakonazolelőállítására oly módon, hogy az itrakonazolt valamely szervesoldószerben oldják és a keveréket oldás indukálta szárításnak vetikalá. A találmány a javított oldódású itrakonazolt tartalmazógyógyszerkészítményekre is vonatkozik. Ó
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1019970024938A KR19990001564A (ko) | 1997-06-16 | 1997-06-16 | 용해도를 개선한 아졸계 항진균제 및 이를 함유하는 제제 |
PCT/KR1998/000164 WO1998057967A1 (en) | 1997-06-16 | 1998-06-16 | An itraconazole exhibiting an improved solubility, a method of preparing the same and a pharmaceutical composition for oral administration comprising the same |
Publications (2)
Publication Number | Publication Date |
---|---|
HUP0004050A2 true HUP0004050A2 (hu) | 2001-06-28 |
HUP0004050A3 HUP0004050A3 (en) | 2003-03-28 |
Family
ID=19509733
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HU0004050A HUP0004050A3 (en) | 1997-06-16 | 1998-06-16 | Itraconazole exhibiting improved solubility, a method of preparing the same and pharmaceutical composition for oral administration comprising the same |
Country Status (17)
Country | Link |
---|---|
US (1) | US6346533B1 (hu) |
EP (1) | EP0991646B1 (hu) |
JP (1) | JP2002504930A (hu) |
KR (1) | KR19990001564A (hu) |
CN (1) | CN1129598C (hu) |
AT (1) | ATE216699T1 (hu) |
AU (1) | AU7939298A (hu) |
BR (1) | BR9810124A (hu) |
CA (1) | CA2294398A1 (hu) |
DE (1) | DE69805070T2 (hu) |
DK (1) | DK0991646T3 (hu) |
ES (1) | ES2177022T3 (hu) |
HU (1) | HUP0004050A3 (hu) |
PL (1) | PL338631A1 (hu) |
PT (1) | PT991646E (hu) |
WO (1) | WO1998057967A1 (hu) |
YU (1) | YU66799A (hu) |
Families Citing this family (52)
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BR0009176A (pt) | 1999-03-24 | 2001-12-18 | Fmc Corp | Partìcula granular, forma de dosagem, métodopara preparar uma partìcula granular, misturaseca, e, formulação granular |
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 |
US7193084B2 (en) * | 2000-12-22 | 2007-03-20 | Baxter International Inc. | Polymorphic form of itraconazole |
US20040256749A1 (en) * | 2000-12-22 | 2004-12-23 | Mahesh Chaubal | Process for production of essentially solvent-free small particles |
US6951656B2 (en) | 2000-12-22 | 2005-10-04 | Baxter International Inc. | Microprecipitation method for preparing submicron suspensions |
US20030096013A1 (en) * | 2000-12-22 | 2003-05-22 | Jane Werling | Preparation of submicron sized particles with polymorph control |
US8067032B2 (en) | 2000-12-22 | 2011-11-29 | Baxter International Inc. | Method for preparing submicron particles of antineoplastic agents |
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 |
US6884436B2 (en) * | 2000-12-22 | 2005-04-26 | Baxter International Inc. | Method for preparing submicron particle suspensions |
US9700866B2 (en) | 2000-12-22 | 2017-07-11 | Baxter International Inc. | Surfactant systems for delivery of organic compounds |
ES2260337T3 (es) * | 2000-12-22 | 2006-11-01 | Baxter International Inc. | Procedimiento para preparar suspensiones de particulas submicronicas de agentes farmaceuticos. |
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 |
US20040173147A1 (en) * | 2001-06-07 | 2004-09-09 | Figueroa Iddys D. | Application of a bioactive agent to a delivery substrate |
WO2002100407A1 (en) * | 2001-06-12 | 2002-12-19 | 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 |
US20060003012A9 (en) | 2001-09-26 | 2006-01-05 | Sean Brynjelsen | Preparation of submicron solid particle suspensions by sonication of multiphase systems |
IL160570A0 (en) * | 2001-09-26 | 2004-07-25 | Baxter Int | Preparation of submicron sized nanoparticles via dispersion and solvent or liquid phase removal |
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 |
CA2477923C (en) | 2002-03-01 | 2021-02-23 | University Of South Florida | Multiple-component solid phases containing at least one active pharmaceutical ingredient |
US20030224059A1 (en) | 2002-03-26 | 2003-12-04 | Lerner E. Itzhak | 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 |
ATE357234T1 (de) * | 2003-01-14 | 2007-04-15 | Cimex Pharma Ag | Zusammensetzung in form eines festen dispersion enthaltend itraconazol und ein hydrophilisches polymer mit einer verbesserten bioverfügbarkeit |
GB0319797D0 (en) * | 2003-08-26 | 2003-09-24 | Leuven K U Res & Dev | Particle size reduction of poorly soluble drugs |
ES2394208T3 (es) * | 2003-09-22 | 2013-01-23 | Baxter International Inc. | Esterilización a alta presión para la esterilización definitiva de preparaciones farmacéuticas y productos médicos |
US20050118265A1 (en) * | 2003-11-28 | 2005-06-02 | Anandi Krishnan | Antifungal oral dosage forms and the methods for preparation |
UA83900C2 (en) † | 2004-02-26 | 2008-08-26 | ЗЕНТИВА, а.с. | 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 |
US9504658B2 (en) * | 2004-11-09 | 2016-11-29 | 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. |
CA2628630A1 (en) * | 2005-11-15 | 2007-05-24 | Baxter International Inc. | Compositions of lipoxygenase inhibitors |
WO2008080047A2 (en) * | 2006-12-23 | 2008-07-03 | Baxter International Inc. | Magnetic separation of fine particles from compositions |
US8426467B2 (en) * | 2007-05-22 | 2013-04-23 | Baxter International Inc. | Colored esmolol concentrate |
US20080293814A1 (en) * | 2007-05-22 | 2008-11-27 | Deepak Tiwari | Concentrate esmolol |
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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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 |
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 |
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 |
SK67298A3 (en) | 1995-11-23 | 1998-11-04 | Janssen Pharmaceutica Nv | 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 |
CZ293841B6 (cs) * | 1996-05-20 | 2004-08-18 | Janssenápharmaceuticaán@Áv | Částice s obsahem itrakonazolu |
-
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 PL PL98338631A patent/PL338631A1/xx unknown
- 1998-06-16 EP EP98929878A patent/EP0991646B1/en not_active Expired - Lifetime
- 1998-06-16 AT AT98929878T patent/ATE216699T1/de not_active IP Right Cessation
- 1998-06-16 DK DK98929878T patent/DK0991646T3/da active
- 1998-06-16 BR BR9810124-2A patent/BR9810124A/pt not_active IP Right Cessation
- 1998-06-16 US US09/445,886 patent/US6346533B1/en not_active Expired - Fee Related
- 1998-06-16 HU HU0004050A patent/HUP0004050A3/hu unknown
- 1998-06-16 JP JP50419399A patent/JP2002504930A/ja not_active Ceased
- 1998-06-16 WO PCT/KR1998/000164 patent/WO1998057967A1/en not_active Application Discontinuation
- 1998-06-16 DE DE69805070T patent/DE69805070T2/de not_active Expired - Fee Related
- 1998-06-16 CN CN98806999A patent/CN1129598C/zh not_active Expired - Fee Related
- 1998-06-16 ES ES98929878T patent/ES2177022T3/es not_active Expired - Lifetime
- 1998-06-16 CA CA002294398A patent/CA2294398A1/en not_active Abandoned
- 1998-06-16 AU AU79392/98A patent/AU7939298A/en not_active Abandoned
- 1998-06-16 YU YU66799A patent/YU66799A/sh unknown
Also Published As
Publication number | Publication date |
---|---|
EP0991646A1 (en) | 2000-04-12 |
HUP0004050A3 (en) | 2003-03-28 |
CN1129598C (zh) | 2003-12-03 |
PL338631A1 (en) | 2000-11-06 |
US6346533B1 (en) | 2002-02-12 |
YU66799A (sh) | 2002-06-19 |
JP2002504930A (ja) | 2002-02-12 |
WO1998057967A1 (en) | 1998-12-23 |
DE69805070D1 (de) | 2002-05-29 |
DK0991646T3 (da) | 2002-06-10 |
CN1262682A (zh) | 2000-08-09 |
BR9810124A (pt) | 2000-08-08 |
ATE216699T1 (de) | 2002-05-15 |
AU7939298A (en) | 1999-01-04 |
KR19990001564A (ko) | 1999-01-15 |
ES2177022T3 (es) | 2002-12-01 |
EP0991646B1 (en) | 2002-04-24 |
DE69805070T2 (de) | 2002-11-07 |
PT991646E (pt) | 2002-08-30 |
CA2294398A1 (en) | 1998-12-23 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
FD9A | Lapse of provisional protection due to non-payment of fees |