CO6270206A2 - SOLID DISPERSION PRODUCT OF DRUGS BASED ON N-ARIL UREA - Google Patents

SOLID DISPERSION PRODUCT OF DRUGS BASED ON N-ARIL UREA

Info

Publication number
CO6270206A2
CO6270206A2 CO10049271A CO10049271A CO6270206A2 CO 6270206 A2 CO6270206 A2 CO 6270206A2 CO 10049271 A CO10049271 A CO 10049271A CO 10049271 A CO10049271 A CO 10049271A CO 6270206 A2 CO6270206 A2 CO 6270206A2
Authority
CO
Colombia
Prior art keywords
solid dispersion
dispersion product
pharmaceutically acceptable
agent
matrix forming
Prior art date
Application number
CO10049271A
Other languages
Spanish (es)
Inventor
Rudolf Schroeder
Tanja Heitermann
Original Assignee
Abbot Gmbh & Co Kg
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Abbot Gmbh & Co Kg filed Critical Abbot Gmbh & Co Kg
Publication of CO6270206A2 publication Critical patent/CO6270206A2/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/14Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/16Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
    • A61K9/1605Excipients; Inactive ingredients
    • A61K9/1629Organic macromolecular compounds
    • A61K9/1635Organic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyvinyl pyrrolidone, poly(meth)acrylates
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/335Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/337Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having four-membered rings, e.g. taxol
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/14Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/16Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
    • A61K9/1605Excipients; Inactive ingredients
    • A61K9/1617Organic compounds, e.g. phospholipids, fats
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/14Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/16Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
    • A61K9/1605Excipients; Inactive ingredients
    • A61K9/1629Organic macromolecular compounds
    • A61K9/1652Polysaccharides, e.g. alginate, cellulose derivatives; Cyclodextrin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Epidemiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Organic Chemistry (AREA)
  • Biophysics (AREA)
  • Molecular Biology (AREA)
  • Medicinal Preparation (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

1.- Un producto de dispersion solida que comprende al menos un agente con actividad farmacéutica, que se obtiene a) preparando una mezcla liquida que contiene el al menos un agente activo, al menos un agente formador de matriz farmacéuticamente aceptable, al menos un agente tensioactivo farmacéuticamente aceptable y al menos un solvente, y b) eliminando el o los solventes de la mezcla liquida para obtener el producto de dispersion solida.2.- El producto de dispersion solida de la reivindicacion 1, donde se agrega al menos un relleno a la mezcla liquida antes de eliminar el o los solventes. 3.- El producto de dispersion solida de la reivindicacion 1, donde la relacion de masa entre el agente activo y el agente formador de matriz farmacéuticamente aceptable es de entre 0,01:1 y 1:3. 4.- El producto de dispersion solida de la reivindicacion 1, donde la relacion de masa entre el agente activo y el agente tensioactivo farmacéuticamente aceptable es de entre 0,1:1 y 1:7. 5.- El producto de dispersion solida de la reivindicacion 1, donde el agente formador de matriz farmacéuticarnente aceptable se selecciona del grupo que consiste en ciclodextrinas, polimeros farmacéuticamente aceptables, lipidos o combinaciones de dos o mas de los anteriores. 6.- El producto de dispersion solida de la reivindicacion 1, donde dicho agente formador de matriz farmacéuticamente aceptable se selecciona del grupo que consiste en ésteres de celulosa, éteres de celulosa, rnaltodextrinas, homopolimeros de N-vinil pirrolidona, copolimeros de N-vinil pirrolidona y combinaciones de dos o mas de los anteriores. 7.- El producto de dispersion solida de la reivindicacion 1, donde dicho agente formador de matriz farmacéuticamente aceptable se selecciona del grupo que consiste en poli N-vinilpirrolidonas, copolimeros de N-vinil pirrolidona y acetato de vinilo y combinaciones de los anteriores.1. A solid dispersion product comprising at least one agent with pharmaceutical activity, which is obtained a) preparing a liquid mixture containing the at least one active agent, at least one pharmaceutically acceptable matrix forming agent, at least one agent pharmaceutically acceptable surfactant and at least one solvent, and b) removing the solvent (s) from the liquid mixture to obtain the solid dispersion product. 2. The solid dispersion product of claim 1, wherein at least one filler is added to the liquid mixture before removing the solvent (s). 3. The solid dispersion product of claim 1, wherein the mass ratio between the active agent and the pharmaceutically acceptable matrix forming agent is between 0.01: 1 and 1: 3. 4. The solid dispersion product of claim 1, wherein the mass ratio between the active agent and the pharmaceutically acceptable surfactant is between 0.1: 1 and 1: 7. 5. The solid dispersion product of claim 1, wherein the pharmaceutically acceptable matrix forming agent is selected from the group consisting of cyclodextrins, pharmaceutically acceptable polymers, lipids or combinations of two or more of the foregoing. 6. The solid dispersion product of claim 1, wherein said pharmaceutically acceptable matrix forming agent is selected from the group consisting of cellulose esters, cellulose ethers, rnaltodextrins, N-vinyl pyrrolidone homopolymers, N-vinyl copolymers pyrrolidone and combinations of two or more of the above. 7. The solid dispersion product of claim 1, wherein said pharmaceutically acceptable matrix forming agent is selected from the group consisting of poly N-vinyl pyrrolidones, copolymers of N-vinyl pyrrolidone and vinyl acetate and combinations of the foregoing.

CO10049271A 2007-10-19 2010-04-27 SOLID DISPERSION PRODUCT OF DRUGS BASED ON N-ARIL UREA CO6270206A2 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US99961807P 2007-10-19 2007-10-19

Publications (1)

Publication Number Publication Date
CO6270206A2 true CO6270206A2 (en) 2011-04-20

Family

ID=40089463

Family Applications (1)

Application Number Title Priority Date Filing Date
CO10049271A CO6270206A2 (en) 2007-10-19 2010-04-27 SOLID DISPERSION PRODUCT OF DRUGS BASED ON N-ARIL UREA

Country Status (18)

Country Link
EP (1) EP2197425A2 (en)
JP (1) JP2011500649A (en)
KR (1) KR20100087170A (en)
CN (1) CN101827584A (en)
AU (1) AU2008313622A1 (en)
BR (1) BRPI0818340A2 (en)
CA (1) CA2699301A1 (en)
CO (1) CO6270206A2 (en)
CR (1) CR11442A (en)
DO (1) DOP2010000117A (en)
EC (1) ECSP10010183A (en)
GT (1) GT201000102A (en)
MX (1) MX2010004291A (en)
PA (1) PA8800101A1 (en)
RU (1) RU2010119929A (en)
UA (1) UA100865C2 (en)
WO (1) WO2009050291A2 (en)
ZA (1) ZA201002095B (en)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20090203709A1 (en) * 2008-02-07 2009-08-13 Abbott Laboratories Pharmaceutical Dosage Form For Oral Administration Of Tyrosine Kinase Inhibitor
JO3002B1 (en) 2009-08-28 2016-09-05 Irm Llc Compounds and compositions as protein kinase inhibitors
TW201202234A (en) * 2010-06-09 2012-01-16 Abbott Lab Solid dispersions containing kinase inhibitors
MX354725B (en) 2011-11-11 2018-03-16 Novartis Ag Method of treating a proliferative disease.
JP6216325B2 (en) 2011-11-23 2017-10-18 ノバルティス アーゲー Pharmaceutical formulation
WO2014003677A1 (en) * 2012-06-28 2014-01-03 Xspray Microparticles Ab Pharmaceutical compositions comprising solid dispersion particles containing tadalafil
WO2014003678A1 (en) * 2012-06-28 2014-01-03 Xspray Microparticles Ab Pharmaceutical compositions comprising ambrisentan and solid dispersion particles containing tadalafil

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2626579A1 (en) * 2005-10-25 2007-05-03 Abbott Laboratories Formulation comprising a drug of low water solubility and method of use thereof
WO2007066189A2 (en) * 2005-12-09 2007-06-14 Pfizer Products Inc. Salts, prodrugs and formulations of 1-[5-(4-amino-7-isopropyl-7h-pyrrolo[2,3-d]pyrimidine-5-carbonyl)-2-methoxy-phenyl]-3-(2,4-dichloro-phenyl)-urea
KR20090094815A (en) * 2006-11-09 2009-09-08 애보트 게엠베하 운트 콤파니 카게 Pharmaceutical dosage form for oral administration of tyrosine kinase inhibitor

Also Published As

Publication number Publication date
GT201000102A (en) 2012-03-12
ZA201002095B (en) 2011-11-30
BRPI0818340A2 (en) 2015-04-22
CA2699301A1 (en) 2009-04-23
AU2008313622A1 (en) 2009-04-23
KR20100087170A (en) 2010-08-03
DOP2010000117A (en) 2010-05-15
EP2197425A2 (en) 2010-06-23
CN101827584A (en) 2010-09-08
ECSP10010183A (en) 2010-06-29
WO2009050291A2 (en) 2009-04-23
UA100865C2 (en) 2013-02-11
RU2010119929A (en) 2011-11-27
PA8800101A1 (en) 2009-05-15
MX2010004291A (en) 2010-08-02
CR11442A (en) 2010-09-06
WO2009050291A3 (en) 2010-04-08
JP2011500649A (en) 2011-01-06

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