AR030382A1 - Formulacion oral de un inhibidor de ciclooxigenasa-2 de fusion rapida - Google Patents
Formulacion oral de un inhibidor de ciclooxigenasa-2 de fusion rapidaInfo
- Publication number
- AR030382A1 AR030382A1 ARP010103961A ARP010103961A AR030382A1 AR 030382 A1 AR030382 A1 AR 030382A1 AR P010103961 A ARP010103961 A AR P010103961A AR P010103961 A ARP010103961 A AR P010103961A AR 030382 A1 AR030382 A1 AR 030382A1
- Authority
- AR
- Argentina
- Prior art keywords
- drug
- agent
- inhibitor
- cyclloxygenasa
- granules
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title abstract 5
- 230000004927 fusion Effects 0.000 title abstract 2
- 238000009472 formulation Methods 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- 239000003814 drug Substances 0.000 abstract 4
- 229940079593 drug Drugs 0.000 abstract 4
- 238000000034 method Methods 0.000 abstract 4
- 150000001720 carbohydrates Chemical class 0.000 abstract 2
- 239000008187 granular material Substances 0.000 abstract 2
- 229940124639 Selective inhibitor Drugs 0.000 abstract 1
- 238000005054 agglomeration Methods 0.000 abstract 1
- 230000002776 aggregation Effects 0.000 abstract 1
- 239000011230 binding agent Substances 0.000 abstract 1
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 238000007906 compression Methods 0.000 abstract 1
- 230000006835 compression Effects 0.000 abstract 1
- 239000000796 flavoring agent Substances 0.000 abstract 1
- 235000013355 food flavoring agent Nutrition 0.000 abstract 1
- 235000003599 food sweetener Nutrition 0.000 abstract 1
- 239000000314 lubricant Substances 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 238000002844 melting Methods 0.000 abstract 1
- 239000007935 oral tablet Substances 0.000 abstract 1
- 239000003765 sweetening agent Substances 0.000 abstract 1
- 239000003826 tablet Substances 0.000 abstract 1
- 238000005550 wet granulation Methods 0.000 abstract 1
- 239000000080 wetting agent Substances 0.000 abstract 1
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
- A61K9/0053—Mouth and digestive tract, i.e. intraoral and peroral administration
- A61K9/0056—Mouth soluble or dispersible forms; Suckable, eatable, chewable coherent forms; Forms rapidly disintegrating in the mouth; Lozenges; Lollipops; Bite capsules; Baked products; Baits or other oral forms for animals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/63—Compounds containing para-N-benzenesulfonyl-N-groups, e.g. sulfanilamide, p-nitrobenzenesulfonyl hydrazide
- A61K31/635—Compounds containing para-N-benzenesulfonyl-N-groups, e.g. sulfanilamide, p-nitrobenzenesulfonyl hydrazide having a heterocyclic ring, e.g. sulfadiazine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/26—Carbohydrates, e.g. sugar alcohols, amino sugars, nucleic acids, mono-, di- or oligo-saccharides; Derivatives thereof, e.g. polysorbates, sorbitan fatty acid esters or glycyrrhizin
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Zoology (AREA)
- Nutrition Science (AREA)
- Physiology (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Medicinal Preparation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
Se describe un proceso para preparar una composicion oral de fusion rápida de una droga inhibidora selectiva de cilooxigensasa-2, donde dicho proceso comprende (a) un paso de granulacion humeda de la droga, junto con un agente aglutinante que comprende un sacárido de alta moldeabilidad, y (b) un paso que consiste en mezclar un sacárido de baja moldeabilidad con la droga donde los pasos anteriormente mencionados (a) y (b) se llevan a cabo en cualquier orden o simultáneamente para causar la formacion de gránulos. El proceso opcionalmente incorpora medios para inhibir la aglomeracion de la droga, por ejemplo la adicion de un agente de humedecimiento. Opcionalmente el proceso comprende además (c) un paso de mezclar los gránulos con por lo menos uno de un lubricante, un agente edulcorante y un agente saborizante para hacer una mezcla para formar tabletas, y (d) un paso de compresion de la mezcla para formar las tabletas orales de fusion rápida. También se proporciona una composicion preparada mediante un proceso con esas características.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US22634900P | 2000-08-18 | 2000-08-18 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR030382A1 true AR030382A1 (es) | 2003-08-20 |
Family
ID=37515865
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP010103961A AR030382A1 (es) | 2000-08-18 | 2001-08-17 | Formulacion oral de un inhibidor de ciclooxigenasa-2 de fusion rapida |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US20020119193A1 (es) |
| AR (1) | AR030382A1 (es) |
| PE (1) | PE20020322A1 (es) |
| TW (1) | TWI256305B (es) |
Families Citing this family (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19940740A1 (de) * | 1999-08-31 | 2001-03-01 | Gruenenthal Gmbh | Pharmazeutische Salze |
| US7790905B2 (en) * | 2002-02-15 | 2010-09-07 | Mcneil-Ppc, Inc. | Pharmaceutical propylene glycol solvate compositions |
| US7927613B2 (en) * | 2002-02-15 | 2011-04-19 | University Of South Florida | Pharmaceutical co-crystal compositions |
| AU2003213719A1 (en) | 2002-03-01 | 2003-09-16 | Regents Of The University Of Michigan | Multiple-component solid phases containing at least one active pharmaceutical ingredient |
| MXPA05000232A (es) * | 2002-06-21 | 2005-06-17 | Transform Pharmaceuticals Inc | Composiciones farmaceuticas con disolucion mejorada. |
| AU2003267231A1 (en) * | 2002-09-20 | 2004-04-08 | Transform Pharmaceuticals, Inc. | Pharmaceutical compositions with improved dissolution |
| RS20050390A (sr) * | 2002-11-26 | 2008-04-04 | Boehringer Ingelheim Pharma Gmbh. & Co.Kg., | Farmaceutska kompozicija koja obuhvata ltb4 antagonist i koks-2 inhibitor ili kombinovani koks1/2 inhibitor |
| GB0228465D0 (en) * | 2002-12-06 | 2003-01-08 | Univ Belfast | A method of treating disease |
| US8183290B2 (en) | 2002-12-30 | 2012-05-22 | Mcneil-Ppc, Inc. | Pharmaceutically acceptable propylene glycol solvate of naproxen |
| AT413944B (de) * | 2003-05-27 | 2006-07-15 | Binder Eva Dkfm | Verwendung von oxicam-verbindungen |
| CA2542277A1 (en) * | 2003-10-21 | 2005-05-12 | Pharmacia Corporation | Method for the treatment or prevention of respiratory inflammation with a cyclooxygenase-2 inhibitor in combination with a phosphodiesterase 4 inhibitor and compositions therewith |
| US20050113410A1 (en) * | 2003-11-03 | 2005-05-26 | Mark Tawa | Pharmaceutical salts of zafirlukast |
| AU2005238220A1 (en) * | 2004-04-29 | 2005-11-10 | Binder, Eva | Enantiomer-pure hexahydro- pyrrolocyclopenta- pyridine derivatives |
| EP1765296A2 (en) * | 2004-06-30 | 2007-03-28 | Albemarle Corporation | High ibuprofen content granules and their preparation and use |
| EP1808163A1 (en) * | 2005-12-22 | 2007-07-18 | Teva Pharmaceutical Industries Ltd. | Compressed solid dosage forms with drugs of low solubility and process for making the same |
| US20070148245A1 (en) * | 2005-12-22 | 2007-06-28 | Ilan Zalit | Compressed solid dosage forms with drugs of low solubility and process for making the same |
| WO2007073389A1 (en) * | 2005-12-22 | 2007-06-28 | Teva Pharmaceutical Industries Ltd. | Compressed solid dosage forms with drugs of low solubility and process for making the same |
| BRPI0717008A2 (pt) * | 2006-09-01 | 2014-01-21 | Usv Ltd | Processo para o preparo de cloridrato de sevelamer e formulação do mesmo |
| US7964182B2 (en) * | 2006-09-01 | 2011-06-21 | USV, Ltd | Pharmaceutical compositions comprising phosphate-binding polymer |
| MX2010003720A (es) * | 2007-10-08 | 2010-10-20 | Intrexon Corp | Celulas dendriticas creadas por ingenieria genetica y usos para el tratamiento de cancer. |
| RU2011134847A (ru) * | 2009-01-22 | 2013-02-27 | Юсв Лимитед | Фармацевтические композиции, содержащие фосфатсвязывающий полимер |
| CN104027319A (zh) * | 2014-06-25 | 2014-09-10 | 万特制药(海南)有限公司 | 一种塞来昔布分散片及其制备方法 |
| US10350171B2 (en) | 2017-07-06 | 2019-07-16 | Dexcel Ltd. | Celecoxib and amlodipine formulation and method of making the same |
| CN108057025A (zh) * | 2017-12-08 | 2018-05-22 | 佛山市弘泰药物研发有限公司 | 一种依托考昔口崩片及其制备方法 |
| CN111407733A (zh) * | 2020-03-19 | 2020-07-14 | 大桐制药(中国)有限责任公司 | 一种塞莱昔布片剂的制备方法 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6573290B1 (en) * | 1999-05-17 | 2003-06-03 | Ilex Oncology, Inc. | DFMO and celecoxib in combination for cancer chemoprevention and therapy |
| US6395300B1 (en) * | 1999-05-27 | 2002-05-28 | Acusphere, Inc. | Porous drug matrices and methods of manufacture thereof |
| US6964978B2 (en) * | 1999-12-08 | 2005-11-15 | Pharmacia Corporation | Solid-state form of celecoxib having enhanced bioavailability |
-
2001
- 2001-08-17 AR ARP010103961A patent/AR030382A1/es unknown
- 2001-08-17 TW TW090120287A patent/TWI256305B/zh not_active IP Right Cessation
- 2001-08-17 US US09/932,494 patent/US20020119193A1/en not_active Abandoned
- 2001-08-17 PE PE2001000821A patent/PE20020322A1/es not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| PE20020322A1 (es) | 2002-05-10 |
| US20020119193A1 (en) | 2002-08-29 |
| TWI256305B (en) | 2006-06-11 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FB | Suspension of granting procedure |