AR055398A1 - PHARMACEUTICAL COMPOSITION OF SOLID DISPERSION OF PRANLUKAST WITH BETTER RATE OF INITIAL DISSOLUTION AND METHOD TO PREPARE THE COMPOSITION - Google Patents
PHARMACEUTICAL COMPOSITION OF SOLID DISPERSION OF PRANLUKAST WITH BETTER RATE OF INITIAL DISSOLUTION AND METHOD TO PREPARE THE COMPOSITIONInfo
- Publication number
- AR055398A1 AR055398A1 ARP060103719A ARP060103719A AR055398A1 AR 055398 A1 AR055398 A1 AR 055398A1 AR P060103719 A ARP060103719 A AR P060103719A AR P060103719 A ARP060103719 A AR P060103719A AR 055398 A1 AR055398 A1 AR 055398A1
- Authority
- AR
- Argentina
- Prior art keywords
- pranlukast
- solid dispersion
- pharmaceutical composition
- solid
- initial dissolution
- Prior art date
Links
Classifications
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- 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
-
- 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
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
-
- 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
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2022—Organic macromolecular compounds
- A61K9/2031—Organic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyethylene glycol, polyethylene oxide, poloxamers
-
- 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
- A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
- A61K9/50—Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/16—Otologicals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Landscapes
- Health & Medical Sciences (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pulmonology (AREA)
- Immunology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Composicion farmacéutica de una dispersion solida de pranlukast con una mejor tasa de disolucion inicial y método para su preparacion. Más específicamente, se describe una composicion farmacéutica de una dispersion solida de pranlukast preparada mezclando una dispersion solida de pranlukast con un agente anticoagulante con un rango determinado de HLB a una temperatura elevada, que puede ser procesada como gránulos y encapsulada, posibilitando un mejoramiento de la tasa inicial de disolucion del pranlukast. Se soluciona el grave problema de la adherencia de las dispersiones solidas de pranlukast a las paredes de la cápsula y se mejora la biodisponibilidad al presentar valores de Cmax y AUC más elevados comparados, en base a la misma dosis de administracion, con las composiciones farmacéuticas comerciales de pranlukast formuladas con los métodos convencionales; y método de preparacion. Reivindicacion 1: Una composicion farmacéutica de dispersion solida de pranlukast caracterizada porque comprende 100 partes en peso de dispersion solida de pranlukast y entre 0,1 y 10 partes en peso de agente de anticoagulacion, el cual está en estado solido o semi-solido a temperatura ambiente y tiene 10-40 de HLB.Pharmaceutical composition of a solid dispersion of pranlukast with a better initial dissolution rate and method for its preparation. More specifically, a pharmaceutical composition of a solid dispersion of pranlukast prepared by mixing a solid dispersion of pranlukast with an anticoagulant agent with a determined range of HLB at an elevated temperature, which can be processed as granules and encapsulated, enabling an improvement of the pharmaceutical composition is described. initial dissolution rate of pranlukast. The serious problem of the adhesion of solid dispersions of pranlukast to the capsule walls is solved and the bioavailability is improved by presenting higher Cmax and AUC values compared, based on the same administration dose, with the commercial pharmaceutical compositions of pranlukast formulated with conventional methods; and method of preparation. Claim 1: A pharmaceutical composition of solid dispersion of pranlukast characterized in that it comprises 100 parts by weight of solid dispersion of pranlukast and between 0.1 and 10 parts by weight of anticoagulation agent, which is in solid or semi-solid state at temperature environment and has 10-40 of HLB.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020050078535A KR101233235B1 (en) | 2005-08-26 | 2005-08-26 | Pharmaceutical composition of pranlukast solid-dispersion with improved early dissolution rate and the method of preparing the composition |
Publications (1)
Publication Number | Publication Date |
---|---|
AR055398A1 true AR055398A1 (en) | 2007-08-22 |
Family
ID=37771823
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP060103719A AR055398A1 (en) | 2005-08-26 | 2006-08-25 | PHARMACEUTICAL COMPOSITION OF SOLID DISPERSION OF PRANLUKAST WITH BETTER RATE OF INITIAL DISSOLUTION AND METHOD TO PREPARE THE COMPOSITION |
Country Status (5)
Country | Link |
---|---|
JP (1) | JP5297194B2 (en) |
KR (1) | KR101233235B1 (en) |
CN (1) | CN101282716B (en) |
AR (1) | AR055398A1 (en) |
WO (1) | WO2007024123A1 (en) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100981751B1 (en) * | 2005-10-28 | 2010-09-10 | 주식회사유한양행 | Granules containing Franlukast and preparation method thereof |
WO2016198983A1 (en) | 2015-06-09 | 2016-12-15 | Bend Research Inc. | Formulations to achieve rapid dissolution of drug from spray-dried dispersions in capsules |
US10653690B1 (en) | 2019-07-09 | 2020-05-19 | Orexo Ab | Pharmaceutical composition for nasal delivery |
US10729687B1 (en) | 2019-07-09 | 2020-08-04 | Orexo Ab | Pharmaceutical composition for nasal delivery |
BR112022023307A2 (en) | 2020-05-18 | 2022-12-20 | Orexo Ab | PHARMACEUTICAL COMPOSITION FOR DELIVERY OF DRUGS |
CA3238850A1 (en) | 2021-11-25 | 2023-06-01 | Jonas Savmarker | Pharmaceutical composition comprising adrenaline |
WO2025018777A1 (en) * | 2023-07-18 | 2025-01-23 | 삼아제약 주식회사 | Method for preparing pharmaceutical composition containing pranlukast and pharmaceutical composition prepared thereby |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1996019239A1 (en) * | 1994-12-21 | 1996-06-27 | Yamanouchi Pharmaceutical Co., Ltd. | Solid composition with improved solubility and absorbability |
WO1996041628A1 (en) * | 1995-06-12 | 1996-12-27 | Ono Pharmaceutical Co., Ltd. | Granules containing pranlukast, process for producing the granules, and method of lowering cohesiveness of pranlukast |
JP2958863B2 (en) * | 1995-06-12 | 1999-10-06 | 小野薬品工業株式会社 | Granulated product containing pranlukast, method for producing the same, and method for improving adhesion and cohesion of pranlukast |
TW486370B (en) * | 1996-12-25 | 2002-05-11 | Yamanouchi Pharma Co Ltd | Rapidly disintegrable pharmaceutical composition |
US6248363B1 (en) * | 1999-11-23 | 2001-06-19 | Lipocine, Inc. | Solid carriers for improved delivery of active ingredients in pharmaceutical compositions |
AUPQ583600A0 (en) * | 2000-02-24 | 2000-03-16 | Cds Worldwide Pty Ltd | Vehicle parking system |
KR100381834B1 (en) * | 2000-05-20 | 2003-04-26 | 이상득 | Solid dispersion system of pranlukast with improved dissolution, and the method thereof |
WO2004073692A1 (en) * | 2003-02-18 | 2004-09-02 | Yamashita, Shinji | Hard capsule of hardly water-soluble drug |
US20050096365A1 (en) * | 2003-11-03 | 2005-05-05 | David Fikstad | Pharmaceutical compositions with synchronized solubilizer release |
JP4544856B2 (en) * | 2003-12-25 | 2010-09-15 | 日医工株式会社 | Formulation containing pranlukast hydrate |
KR101086254B1 (en) * | 2004-11-04 | 2011-11-24 | 에스케이케미칼주식회사 | Franlukast solid dispersion composition with improved bioavailability and method for preparing the solid dispersion |
-
2005
- 2005-08-26 KR KR1020050078535A patent/KR101233235B1/en active IP Right Grant
-
2006
- 2006-08-25 CN CN2006800374107A patent/CN101282716B/en not_active Expired - Fee Related
- 2006-08-25 AR ARP060103719A patent/AR055398A1/en unknown
- 2006-08-25 JP JP2008527854A patent/JP5297194B2/en not_active Expired - Fee Related
- 2006-08-25 WO PCT/KR2006/003368 patent/WO2007024123A1/en active Application Filing
Also Published As
Publication number | Publication date |
---|---|
CN101282716B (en) | 2012-05-23 |
JP2009506027A (en) | 2009-02-12 |
JP5297194B2 (en) | 2013-09-25 |
KR101233235B1 (en) | 2013-02-15 |
CN101282716A (en) | 2008-10-08 |
KR20070024047A (en) | 2007-03-02 |
WO2007024123A1 (en) | 2007-03-01 |
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