AU2001242328A1 - Formulations of active components in the form of a solid dispersion - Google Patents
Formulations of active components in the form of a solid dispersionInfo
- Publication number
- AU2001242328A1 AU2001242328A1 AU2001242328A AU4232801A AU2001242328A1 AU 2001242328 A1 AU2001242328 A1 AU 2001242328A1 AU 2001242328 A AU2001242328 A AU 2001242328A AU 4232801 A AU4232801 A AU 4232801A AU 2001242328 A1 AU2001242328 A1 AU 2001242328A1
- Authority
- AU
- Australia
- Prior art keywords
- solid dispersion
- formulations
- active components
- solid
- carrier
- 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.)
- Abandoned
Links
- 239000000203 mixture Substances 0.000 title abstract 3
- 239000007962 solid dispersion Substances 0.000 title abstract 3
- 238000009472 formulation Methods 0.000 title abstract 2
- 239000002202 Polyethylene glycol Substances 0.000 abstract 2
- 229920001223 polyethylene glycol Polymers 0.000 abstract 2
- 229920000036 polyvinylpyrrolidone Polymers 0.000 abstract 2
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 abstract 2
- 239000001267 polyvinylpyrrolidone Substances 0.000 abstract 2
- 239000007787 solid Substances 0.000 abstract 2
- 150000001875 compounds Chemical class 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
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/141—Intimate drug-carrier mixtures characterised by the carrier, e.g. ordered mixtures, adsorbates, solid solutions, eutectica, co-dried, co-solubilised, co-kneaded, co-milled, co-ground products, co-precipitates, co-evaporates, co-extrudates, co-melts; Drug nanoparticles with adsorbed surface modifiers
- A61K9/146—Intimate drug-carrier mixtures characterised by the carrier, e.g. ordered mixtures, adsorbates, solid solutions, eutectica, co-dried, co-solubilised, co-kneaded, co-milled, co-ground products, co-precipitates, co-evaporates, co-extrudates, co-melts; Drug nanoparticles with adsorbed surface modifiers with organic macromolecular compounds
-
- 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4422—1,4-Dihydropyridines, e.g. nifedipine, nicardipine
-
- 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
- A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
- A61K9/1605—Excipients; Inactive ingredients
- A61K9/1629—Organic macromolecular compounds
- A61K9/1635—Organic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyvinyl pyrrolidone, poly(meth)acrylates
-
- 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
- A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
- A61K9/1605—Excipients; Inactive ingredients
- A61K9/1629—Organic macromolecular compounds
- A61K9/1641—Organic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyethylene glycol, poloxamers
Landscapes
- Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Preparation (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Formulations of active compounds in the form of a solid dispersion, where the solid dispersion is formed from at least one active component and a carrier characterized in that the carrier is a mixture of polyvinylpyrrolidone (PVP) with a weight average molecular weight of ≰1 500 000 Da and of a polyethylene glycol (PEG) which is semi-solid or solid at temperatures of 17 to 22° C. and has an average molar mass of 950 to 3300 Da.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE10000792A DE10000792A1 (en) | 2000-01-11 | 2000-01-11 | Formulations of active substances in the form of a solid dispersion |
DE10000792 | 2000-01-11 | ||
PCT/EP2001/000224 WO2001051025A2 (en) | 2000-01-11 | 2001-01-10 | Formulations of active components in the form of a solid dispersion |
Publications (1)
Publication Number | Publication Date |
---|---|
AU2001242328A1 true AU2001242328A1 (en) | 2001-07-24 |
Family
ID=7627157
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AU2001242328A Abandoned AU2001242328A1 (en) | 2000-01-11 | 2001-04-10 | Formulations of active components in the form of a solid dispersion |
Country Status (9)
Country | Link |
---|---|
US (1) | US8021688B2 (en) |
EP (1) | EP1246611B1 (en) |
AT (1) | ATE373470T1 (en) |
AU (1) | AU2001242328A1 (en) |
CA (1) | CA2396722C (en) |
DE (2) | DE10000792A1 (en) |
DK (1) | DK1246611T3 (en) |
ES (1) | ES2293982T3 (en) |
WO (1) | WO2001051025A2 (en) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE10026698A1 (en) | 2000-05-30 | 2001-12-06 | Basf Ag | Self-emulsifying active ingredient formulation and use of this formulation |
US8377952B2 (en) | 2003-08-28 | 2013-02-19 | Abbott Laboratories | Solid pharmaceutical dosage formulation |
US8025899B2 (en) | 2003-08-28 | 2011-09-27 | Abbott Laboratories | Solid pharmaceutical dosage form |
AU2005321346B2 (en) * | 2004-12-30 | 2011-06-23 | Pierre Fabre Medicament | Stable solid dispersion of a derivative of vinca alkaloid and process for manufacturing it |
FR2880274B1 (en) * | 2004-12-30 | 2007-04-13 | Pierre Fabre Medicament Sa | STABLE SOLID DISPERSION OF VINCA ALKALOID DERIVATIVE AND PROCESS FOR PRODUCING THE SAME |
CN104023710A (en) | 2011-12-21 | 2014-09-03 | 拜耳知识产权有限责任公司 | Preparations containing amorphous emodepside |
CN103271902B (en) * | 2013-05-07 | 2015-11-11 | 西安交通大学 | A kind of insoluble medicine solid dispersoid and preparation method thereof |
CN109481411B (en) * | 2017-09-13 | 2021-02-02 | 亚宝药业集团股份有限公司 | Hot-melt extrusion solid dispersion of nimodipine and preparation method of tablet thereof |
CN114699373B (en) * | 2022-03-30 | 2023-03-17 | 山东新时代药业有限公司 | Metoclopramide solid dispersion and preparation method thereof |
Family Cites Families (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4291015A (en) * | 1979-08-14 | 1981-09-22 | Key Pharmaceuticals, Inc. | Polymeric diffusion matrix containing a vasodilator |
US4292104A (en) * | 1979-09-13 | 1981-09-29 | Corning Glass Works | Decalcomania manufacture |
US4321263A (en) * | 1980-09-30 | 1982-03-23 | Rowell Laboratories, Inc. | Psyllium compositions |
US4764378A (en) * | 1986-02-10 | 1988-08-16 | Zetachron, Inc. | Buccal drug dosage form |
DE3839825A1 (en) * | 1988-11-25 | 1990-06-13 | Henning Berlin Gmbh | SOLIDS DISPERSIONS CONTAIN OXIPURINOL AND / OR ITS ALKALI OR EARTH ALKALISALZE |
US5368864A (en) * | 1988-11-25 | 1994-11-29 | Henning Berlin Gmbh Chemie- Und Pharmawerk | Formulation of oxypurinol and/or its alkali and alkaline earth salts |
US5080471A (en) * | 1990-04-06 | 1992-01-14 | Eic Laboratories, Inc. | Electrochromic material and electro-optical device using same |
JP2696438B2 (en) * | 1991-04-22 | 1998-01-14 | 富士写真フイルム株式会社 | Photothermographic material |
AU671811B2 (en) * | 1991-12-18 | 1996-09-12 | Warner-Lambert Company | A process for the preparation of a solid dispersion |
US5294615A (en) * | 1993-04-29 | 1994-03-15 | Abbott Laboratories | Terazosin polymorph and pharmaceutical composition |
US5599583A (en) * | 1994-05-27 | 1997-02-04 | Micro Flo Company | Encapsulation with water soluble polymer |
KR100239799B1 (en) * | 1995-01-21 | 2000-02-01 | 손경식 | Cyclosporin a solid micelle dispersion for oral administration, the preparation method thereof and its solid dosage form |
US5637319A (en) * | 1995-03-01 | 1997-06-10 | Takada; Kanji | Controlled-release preparations |
US6391338B1 (en) * | 1995-09-07 | 2002-05-21 | Biovail Technologies Ltd. | System for rendering substantially non-dissoluble bio-affecting agents bio-available |
DE19701949A1 (en) * | 1997-01-13 | 1998-07-16 | Jenapharm Gmbh | Transdermal therapeutic system |
US5955475A (en) * | 1997-06-30 | 1999-09-21 | Endo Pharmaceuticals Inc. | Process for manufacturing paroxetine solid dispersions |
US6086915A (en) * | 1998-04-01 | 2000-07-11 | Bioresponse L.L.C. | Compositions and methods of adjusting steroid hormone metabolism through phytochemicals |
US6168805B1 (en) * | 1998-05-07 | 2001-01-02 | Endo Pharmaceuticals, Inc. | Aqueous process for manufacturing paroxetine solid dispersions |
-
2000
- 2000-01-11 DE DE10000792A patent/DE10000792A1/en not_active Ceased
-
2001
- 2001-01-10 DE DE50113030T patent/DE50113030D1/en not_active Expired - Lifetime
- 2001-01-10 US US10/169,665 patent/US8021688B2/en not_active Expired - Fee Related
- 2001-01-10 CA CA002396722A patent/CA2396722C/en not_active Expired - Lifetime
- 2001-01-10 AT AT01915129T patent/ATE373470T1/en active
- 2001-01-10 ES ES01915129T patent/ES2293982T3/en not_active Expired - Lifetime
- 2001-01-10 WO PCT/EP2001/000224 patent/WO2001051025A2/en active IP Right Grant
- 2001-01-10 EP EP01915129A patent/EP1246611B1/en not_active Expired - Lifetime
- 2001-01-10 DK DK01915129T patent/DK1246611T3/en active
- 2001-04-10 AU AU2001242328A patent/AU2001242328A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
US20030109639A1 (en) | 2003-06-12 |
CA2396722C (en) | 2008-08-19 |
EP1246611B1 (en) | 2007-09-19 |
DE10000792A1 (en) | 2001-07-19 |
DE50113030D1 (en) | 2007-10-31 |
CA2396722A1 (en) | 2001-07-19 |
DK1246611T3 (en) | 2008-01-28 |
US8021688B2 (en) | 2011-09-20 |
WO2001051025A2 (en) | 2001-07-19 |
ATE373470T1 (en) | 2007-10-15 |
EP1246611A2 (en) | 2002-10-09 |
WO2001051025A3 (en) | 2002-04-18 |
ES2293982T3 (en) | 2008-04-01 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
PT1073470E (en) | Pharmaceutical compositions containing active compounds capable of improving the absorption of active ingredients | |
CA2420874A1 (en) | Active ingredient combinations with insecticidal and acaricidal properties | |
CA2259780A1 (en) | Alcohol based anti-microbial compositions with cosmetic appearance | |
DE69307977D1 (en) | Stabilized derivatives of pharmaceutical compositions containing vitamin D2 and D3 | |
WO1999039694A3 (en) | Compositions containing organic compounds | |
EP1432408B8 (en) | Pharmaceutical compositions comprising colloidal silicon dioxide | |
CA2338684A1 (en) | Injectable propofol formulations | |
EP1059333A4 (en) | Aqueous polytetrafluoroethylene dispersion composition | |
WO2002017870A3 (en) | Clear antiperspirants and deodorants made with siloxane-based polyamides | |
CA2407621A1 (en) | High efficacy, low residue antiperspirant stick compositions | |
AU2001289438A1 (en) | Pharmaceutical semi-solid composition of isotretinoin | |
CO4890854A1 (en) | NON-AQUEOUS PROTIC PEPTIDE FORMULATIONS | |
EP0882450A3 (en) | Cholesterol-lowering composition comprising coenzyme Q | |
WO2001072125A8 (en) | Active substance combinations having insecticidal and acaricidal properties | |
AU2001242328A1 (en) | Formulations of active components in the form of a solid dispersion | |
WO2002047657A3 (en) | Composition containing heteropolymers and oil-soluble polymers | |
NZ511085A (en) | Oral pharmaceutical compositions containing buprenorphin | |
CA2022177A1 (en) | Arginine deiminase, its manufacturing method, and an anti-cancer agent containing this enzyme as an effective ingredient | |
WO2001078682A3 (en) | Sustained release drug compositions | |
AU2001267560A1 (en) | Antistatic polyoxymethylene molding compounds | |
WO1998009608A3 (en) | Personal care compositions | |
HUP0000818A2 (en) | Aqueous compositions and their use | |
IL148193A0 (en) | Hard candy with improved storage stability | |
WO2003020265A3 (en) | Compositions comprising pectin and ascorbic acid | |
WO2003065803A3 (en) | Use of a solvent/antifoam substance mixture in aqueous formulations and resulting formulations |