JP6379043B2 - カンデサルタンシレキセチル含有医薬組成物 - Google Patents
カンデサルタンシレキセチル含有医薬組成物 Download PDFInfo
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- JP6379043B2 JP6379043B2 JP2014559742A JP2014559742A JP6379043B2 JP 6379043 B2 JP6379043 B2 JP 6379043B2 JP 2014559742 A JP2014559742 A JP 2014559742A JP 2014559742 A JP2014559742 A JP 2014559742A JP 6379043 B2 JP6379043 B2 JP 6379043B2
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- candesartan cilexetil
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- 239000000196 tragacanth Substances 0.000 description 1
- 229940116362 tragacanth Drugs 0.000 description 1
- 229940074410 trehalose Drugs 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- 229940078499 tricalcium phosphate Drugs 0.000 description 1
- 235000019731 tricalcium phosphate Nutrition 0.000 description 1
- 229910000391 tricalcium phosphate Inorganic materials 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Classifications
-
- 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
- A61K31/4164—1,3-Diazoles
- A61K31/4184—1,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
-
- 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
- A61K47/08—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
- A61K47/10—Alcohols; Phenols; Salts thereof, e.g. glycerol; Polyethylene glycols [PEG]; Poloxamers; PEG/POE alkyl ethers
-
- 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
- A61K47/30—Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
- A61K47/36—Polysaccharides; Derivatives thereof, e.g. gums, starch, alginate, dextrin, hyaluronic acid, chitosan, inulin, agar or pectin
- A61K47/38—Cellulose; Derivatives thereof
-
- 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
- A61K9/10—Dispersions; Emulsions
-
- 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
- A61K9/1682—Processes
- A61K9/1694—Processes resulting in granules or microspheres of the matrix type containing more than 5% of excipient
-
- 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
- A61K9/2013—Organic compounds, e.g. phospholipids, fats
- A61K9/2018—Sugars, or sugar alcohols, e.g. lactose, mannitol; Derivatives thereof, e.g. polysorbates
-
- 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
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2022—Organic macromolecular compounds
- A61K9/205—Polysaccharides, e.g. alginate, gums; Cyclodextrin
- A61K9/2054—Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
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- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
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- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Molecular Biology (AREA)
- Biophysics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- Dispersion Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
Description
上述したように、本発明に係るカンデサルタンシレキセチル含有医薬組成物は、カンデサルタンシレキセチルを溶剤に分散させた分散液を用いて粉体の添加物とともに湿式造粒することにより製造することができる。
精製水848.75gに、D−マンニトール65g、ヒドロキシプロピルセルロース(HPC)0.75g及びラウロマクロゴール0.5gを添加して、攪拌機(プライミクス社製)を用いて、2000rpmで20分撹拌して、溶解させた。続いて、分散機(プライミクス社製)に溶液を移し、カンデサルタンシレキセチル60gを添加して8000rpmで20分撹拌して、カンデサルタンシレキセチルを溶液中に分散させた。
精製水908.75gに、D−マンニトール65g、ヒドロキシプロピルセルロース(HPC)0.75g及びラウロマクロゴール0.5gを添加して、攪拌機(プライミクス社製)を用いて、2000rpmで20分撹拌して、溶解させた。カンデサルタンシレキセチル60g、D−マンニトール367.25g、低置換度ヒドロキシプロピルセルロース(L−HPC)70g、粉末還元麦芽糖水アメ2g及びスクラロース3gを30号篩で分級し、流動層造粒機(パウレック(株)製)に投入し、得られた溶液を添加して流動層造粒を行った。得られた造粒物を乾燥後、22号篩で整粒し、得られた整粒物、ステアリン酸40g、結晶セルロース32.5g、メタケイ酸アルミン酸マグネシウム(ノイシリンUFL2)6.5g及びステアリン酸マグネシウム2.5gをV型混合機(不二パウダル(株)製)にて混合し、得られた混合末をロータリー式打錠機(菊水製作所(株)製)で、1錠当たりの重量130.0mg、厚み3.30mmとなるよう打錠し、錠剤を得た。
実施例及び比較例について、溶出性を検討した。カンデサルタンシレキセチルの溶出性は、後発医薬品の生物学的同等性試験ガイドラインに準じて溶出試験を実施し、0.1% Tween pH6.8の溶液を用いて、50回転/分の条件で120分後までのカンデサルタンシレキセチルの溶出率(%)を求めた。実施例及び比較例のカンデサルタンシレキセチルの溶出性の測定結果を図1に示す。図1から明らかなように、本実施例においては比較例に比して優れた溶出性が認められた。
Claims (4)
- 水溶性高分子及びマンニトールを含むカンデサルタンシレキセチルの分散液を用いて粉体の添加物とともに湿式造粒することを特徴とするカンデサルタンシレキセチル含有医薬組成物の製造方法。
- 前記水溶性高分子はヒドロキシプロピルセルロースであることを特徴とする請求項1に記載のカンデサルタンシレキセチル含有医薬組成物の製造方法。
- 前記分散液は安定化剤をさらに含むことを特徴とする請求項1に記載のカンデサルタンシレキセチル含有医薬組成物の製造方法。
- 前記安定化剤はラウロマクロゴールであることを特徴とする請求項3に記載のカンデサルタンシレキセチル含有医薬組成物の製造方法。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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JP2013015099 | 2013-01-30 | ||
JP2013015099 | 2013-01-30 | ||
PCT/JP2014/052126 WO2014119667A1 (ja) | 2013-01-30 | 2014-01-30 | カンデサルタンシレキセチル含有医薬組成物 |
Publications (2)
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JPWO2014119667A1 JPWO2014119667A1 (ja) | 2017-01-26 |
JP6379043B2 true JP6379043B2 (ja) | 2018-08-22 |
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JP2014559742A Active JP6379043B2 (ja) | 2013-01-30 | 2014-01-30 | カンデサルタンシレキセチル含有医薬組成物 |
Country Status (4)
Country | Link |
---|---|
US (2) | US20150335621A1 (ja) |
EP (1) | EP2952187A4 (ja) |
JP (1) | JP6379043B2 (ja) |
WO (1) | WO2014119667A1 (ja) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2928468A4 (en) * | 2012-12-05 | 2016-07-27 | Sawai Seiyaku Kk | PREPARATION CONTAINING CANDÉSARTAN CILEXÉTIL |
WO2017209216A1 (ja) * | 2016-05-31 | 2017-12-07 | 協和発酵キリン株式会社 | 難溶性薬物の微粒子を含有する医薬組成物の製造方法 |
CN117442577B (zh) * | 2023-12-21 | 2024-03-15 | 山东则正医药技术有限公司 | 一种坎地沙坦酯微片及制备方法和应用 |
Family Cites Families (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2682353B2 (ja) * | 1991-11-20 | 1997-11-26 | 武田薬品工業株式会社 | 経口用医薬組成物およびその製造法 |
PL187160B1 (pl) * | 1994-01-31 | 2004-05-31 | Yamanouchi Pharma Co Ltd | Sposób wytwarzania rozpuszczalnej wewnątrzustnie formowanej tłocznie wypraski |
SI1100469T1 (ja) * | 1998-07-28 | 2005-08-31 | Takeda Pharmaceutical | |
JP2006070046A (ja) * | 1999-06-18 | 2006-03-16 | Takeda Chem Ind Ltd | 速崩壊性固形製剤 |
KR20080042039A (ko) | 2005-04-18 | 2008-05-14 | 루비콘 리서치 피브이티. 엘티디. | 생물학적으로 강화된 조성물 |
EP1763525A2 (en) | 2005-05-10 | 2007-03-21 | Teva Pharmaceutical Industries Ltd. | Stable micronized candesartan cilexetil and methods for preparing thereof |
JP2007137802A (ja) * | 2005-11-16 | 2007-06-07 | Takeda Chem Ind Ltd | 錠剤の製造法 |
JP2010502698A (ja) | 2006-09-05 | 2010-01-28 | アストラゼネカ アクチボラグ | カンデサルタンシレキセチルを含む医薬組成物 |
WO2008068727A2 (en) * | 2006-12-06 | 2008-06-12 | Ranbaxy Laboratories Limited | Pharmaceutical composition comprising candesartan cilexetil |
AU2008235790B2 (en) | 2007-03-28 | 2013-06-06 | Takeda Pharmaceutical Company Limited | Solid pharmaceutical composition comprising a benzimidazole-7-carboxylate derivative and a pH control agent |
EP2182927A2 (en) * | 2007-08-01 | 2010-05-12 | Teva Pharmaceutical Industries Ltd. | Pharmaceutical compositions of candesartan |
EP2165702B1 (en) * | 2008-09-17 | 2011-11-16 | Helm AG | Stable and readily dissolved compositions of candesartan cilexetil prepared with wet granulation |
JP6072539B2 (ja) * | 2009-05-27 | 2017-02-01 | アルカーメス ファーマ アイルランド リミテッド | ナノ粒子活性物質組成物におけるフレーク状凝集の軽減 |
JP2012025715A (ja) * | 2010-07-27 | 2012-02-09 | Ohara Yakuhin Kogyo Kk | カンデサルタンシレキセチル含有錠剤 |
JP5367735B2 (ja) | 2011-01-25 | 2013-12-11 | 大原薬品工業株式会社 | 錠剤の製造方法 |
-
2014
- 2014-01-30 EP EP14746787.2A patent/EP2952187A4/en not_active Withdrawn
- 2014-01-30 WO PCT/JP2014/052126 patent/WO2014119667A1/ja active Application Filing
- 2014-01-30 JP JP2014559742A patent/JP6379043B2/ja active Active
-
2015
- 2015-07-30 US US14/813,486 patent/US20150335621A1/en not_active Abandoned
-
2016
- 2016-05-06 US US15/148,181 patent/US20160250192A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
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US20150335621A1 (en) | 2015-11-26 |
WO2014119667A1 (ja) | 2014-08-07 |
US20160250192A1 (en) | 2016-09-01 |
EP2952187A1 (en) | 2015-12-09 |
JPWO2014119667A1 (ja) | 2017-01-26 |
EP2952187A4 (en) | 2016-08-17 |
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