|
ES2287971T3
(es)
|
1997-08-11 |
2007-12-16 |
Pfizer Products Inc. |
Dispersiones farmaceuticas solidas con biodisponibilidad incrementada.
|
|
EP1741424B1
(en)
*
|
1997-08-11 |
2018-10-03 |
Pfizer Products Inc. |
Solid pharmaceutical dispersions with enhanced bioavailabilty
|
|
JPH11130698A
(ja)
*
|
1997-10-31 |
1999-05-18 |
Freunt Ind Co Ltd |
アルギン酸多価金属塩球状微粒子集合体、該球状微粒子集合体に難溶性薬剤を担持した放出制御製剤及びそれらの製造方法
|
|
IE980115A1
(en)
*
|
1998-02-16 |
2000-02-09 |
Biovail Internat Ltd |
Solubilizing delivery systems and method of manufacture
|
|
ATE400251T1
(de)
|
1999-02-09 |
2008-07-15 |
Pfizer Prod Inc |
Zusammensetzungen basischer arzneistoffe mit verbesserter bioverfügbarkeit
|
|
ATE404178T1
(de)
*
|
1999-02-10 |
2008-08-15 |
Pfizer Prod Inc |
Vorrichtung mit matrixgesteuerter wirkstofffreisetzung
|
|
ES2251985T3
(es)
|
1999-03-24 |
2006-05-16 |
R.P. Scherer Technologies, Inc. |
Particula granulada para mejorar la solubilidad acuosa de farmacos, y su procedimiento de preparacion.
|
|
GB9920558D0
(en)
*
|
1999-08-31 |
1999-11-03 |
Bradford Particle Design Ltd |
Methods for particle formation and their products
|
|
EP1175205B1
(en)
|
1999-11-12 |
2006-06-14 |
Abbott Laboratories |
Solid dispersion comprising ritonavir, fenofibrate or griseofulvin
|
|
US7364752B1
(en)
|
1999-11-12 |
2008-04-29 |
Abbott Laboratories |
Solid dispersion pharamaceutical formulations
|
|
CN1402629A
(zh)
|
1999-12-23 |
2003-03-12 |
辉瑞产品公司 |
提供提高的药物浓度的药物组合物
|
|
DE10013289A1
(de)
*
|
2000-03-17 |
2001-09-20 |
Knoll Ag |
Torasemid enthaltende pharmazeutische Zubereitungen
|
|
DE10026698A1
(de)
*
|
2000-05-30 |
2001-12-06 |
Basf Ag |
Selbstemulgierende Wirkstoffformulierung und Verwendung dieser Formulierung
|
|
US7115279B2
(en)
*
|
2000-08-03 |
2006-10-03 |
Curatolo William J |
Pharmaceutical compositions of cholesteryl ester transfer protein inhibitors
|
|
US20030086972A1
(en)
*
|
2000-08-09 |
2003-05-08 |
Appel Leah E. |
Hydrogel-driven drug dosage form
|
|
CA2418490A1
(en)
*
|
2000-08-11 |
2002-02-21 |
Eisai Co., Ltd. |
Drug-containing solid dispersion having improved solubility
|
|
KR20020014570A
(ko)
*
|
2000-08-18 |
2002-02-25 |
김충섭 |
고체분산화시킨 무정형 이프리플라본의 제조방법
|
|
WO2002024168A1
(fr)
*
|
2000-09-25 |
2002-03-28 |
Nippon Shinyaku Co., Ltd. |
Procede de production d'une dispersion solide medicinale
|
|
US6482847B2
(en)
*
|
2000-10-03 |
2002-11-19 |
Hoffmann-La Roche Inc. |
Amorphous form of cell cycle inhibitor having improved solubility and bioavailability
|
|
JP4057418B2
(ja)
*
|
2000-11-07 |
2008-03-05 |
久光製薬株式会社 |
経皮吸収型製剤
|
|
US7037528B2
(en)
|
2000-12-22 |
2006-05-02 |
Baxter International Inc. |
Microprecipitation method for preparing submicron suspensions
|
|
US8067032B2
(en)
|
2000-12-22 |
2011-11-29 |
Baxter International Inc. |
Method for preparing submicron particles of antineoplastic agents
|
|
US6977085B2
(en)
|
2000-12-22 |
2005-12-20 |
Baxter International Inc. |
Method for preparing submicron suspensions with polymorph control
|
|
US7193084B2
(en)
|
2000-12-22 |
2007-03-20 |
Baxter International Inc. |
Polymorphic form of itraconazole
|
|
US9700866B2
(en)
|
2000-12-22 |
2017-07-11 |
Baxter International Inc. |
Surfactant systems for delivery of organic compounds
|
|
US6951656B2
(en)
|
2000-12-22 |
2005-10-04 |
Baxter International Inc. |
Microprecipitation method for preparing submicron suspensions
|
|
US6884436B2
(en)
*
|
2000-12-22 |
2005-04-26 |
Baxter International Inc. |
Method for preparing submicron particle suspensions
|
|
US20050048126A1
(en)
|
2000-12-22 |
2005-03-03 |
Barrett Rabinow |
Formulation to render an antimicrobial drug potent against organisms normally considered to be resistant to the drug
|
|
WO2002083101A1
(de)
*
|
2001-04-11 |
2002-10-24 |
Bayer Aktiengesellschaft |
Nimodipin-tablette mit kontrollierter freisetzung und verfahren zu deren herstellung
|
|
JP2004534812A
(ja)
|
2001-06-22 |
2004-11-18 |
ファイザー・プロダクツ・インク |
薬物および中性ポリマーの分散物の医薬組成物
|
|
EP1269994A3
(en)
|
2001-06-22 |
2003-02-12 |
Pfizer Products Inc. |
Pharmaceutical compositions comprising drug and concentration-enhancing polymers
|
|
BR0212833A
(pt)
|
2001-09-26 |
2004-10-13 |
Baxter Int |
Preparação de nanopartìculas de tamanho submìcron através de dispersão e de remoção de solvente ou de fase lìquida
|
|
US20060003012A9
(en)
|
2001-09-26 |
2006-01-05 |
Sean Brynjelsen |
Preparation of submicron solid particle suspensions by sonication of multiphase systems
|
|
US7112340B2
(en)
|
2001-10-19 |
2006-09-26 |
Baxter International Inc. |
Compositions of and method for preparing stable particles in a frozen aqueous matrix
|
|
ITMI20012749A1
(it)
|
2001-12-21 |
2003-06-21 |
Chiesi Farma Spa |
Procedimento per la preparazione mediante trattamento con microonde di composti di inclusione tra farmaco e ciclodestrine e prodotti ottenut
|
|
EP1469827B1
(en)
*
|
2002-01-09 |
2017-12-27 |
Emisphere Technologies, Inc. |
Polymorphs of sodium 4- (4-chloro-2-hydroxybenzoyl)amino butanoate
|
|
DE60320940D1
(de)
|
2002-02-01 |
2008-06-26 |
Pfizer Prod Inc |
Pharmazeutische zusammensetzungen amorpher dispersionen von wirkstoffen und lipophiler mikrophasenbildender materialien
|
|
MY128945A
(en)
*
|
2002-04-16 |
2007-03-30 |
Kowa Co |
Solid dispersion composition
|
|
DE10224170A1
(de)
*
|
2002-05-31 |
2003-12-11 |
Desitin Arzneimittel Gmbh |
Pharmazeutische Zusammensetzung mit verzögerter Wirkstofffreisetzung
|
|
GB0216700D0
(en)
*
|
2002-07-18 |
2002-08-28 |
Astrazeneca Ab |
Process
|
|
US20040132771A1
(en)
*
|
2002-12-20 |
2004-07-08 |
Pfizer Inc |
Compositions of choleseteryl ester transfer protein inhibitors and HMG-CoA reductase inhibitors
|
|
ITMI20022748A1
(it)
*
|
2002-12-23 |
2004-06-24 |
Eurand Int |
Dispersioni solide stabilizzate di farmaco in un carrier organico e procedimento per la loro preparazione.
|
|
BRPI0413277A
(pt)
|
2003-08-04 |
2006-10-10 |
Pfizer Prod Inc |
composições farmacêuticas de adsorvatos de medicamentos amorfos e materiais que formam microfases lipofìlicas
|
|
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
|
|
CN100563658C
(zh)
*
|
2003-11-14 |
2009-12-02 |
味之素株式会社 |
苯丙氨酸衍生物的固体分散体或固体分散体医药制剂
|
|
US8535716B2
(en)
*
|
2004-04-01 |
2013-09-17 |
Tsrl, Inc. |
Methods and composition of extended delivery of water insoluble drugs
|
|
BRPI0509381A
(pt)
*
|
2004-04-08 |
2007-09-18 |
Wyeth Corp |
dispersão sólida, métodos de preparar a dispersão sólida, de tratar um mamìfero tendo uma doença ou sìndrome associadas com a deficiência ou o excesso de estrogênio, uma doença ou distúrbio associados com a proliferação ou desenvolvimento anormal de tecidos endometrais, de tratar cáncer de mamas de um mamìfero, e uma mulher pós-menopáusica quanto a um ou mais distúrbios vasomotores, de reduzir colesterol, e de inibir perda óssea em um mamìfero, composição, forma de dosagem, e, uso de uma dispersão sólida
|
|
US7507823B2
(en)
|
2004-05-06 |
2009-03-24 |
Bristol-Myers Squibb Company |
Process of making aripiprazole particles
|
|
AR049297A1
(es)
*
|
2004-06-08 |
2006-07-12 |
Vertex Pharma |
Una composicion farmaceutica y dispersiones solidas de vx-950 (inhibidor de la proteasa de hcv ns3/4a) y proceso de obtencion
|
|
JP2006028130A
(ja)
*
|
2004-07-21 |
2006-02-02 |
Toa Eiyo Ltd |
ピモベンダン経口投与製剤
|
|
US7576216B2
(en)
|
2004-07-30 |
2009-08-18 |
Abbott Laboratories |
Preparation of pyridonecarboxylic acid antibacterials
|
|
FR2875409B1
(fr)
*
|
2004-09-17 |
2010-05-07 |
Sanofi Aventis |
Composition pharmaceutique comprenant une dispersion solide a matrice polymere comprenant une phase continue de polydextrose et une phase continue d'un polymere autre que du polydextrose
|
|
US20080095841A1
(en)
*
|
2004-10-06 |
2008-04-24 |
Eisai R&D Management Co., Ltd. |
Pharmaceutical Composition, Method for Producing the Same, and Method for Stabilizing Dihydropyridine Compound in the Pharmaceutical Composition
|
|
EP1830824B1
(en)
*
|
2004-12-31 |
2016-01-13 |
Iceutica Pty Ltd. |
Nanoparticle composition and methods for synthesis thereof
|
|
JP4913030B2
(ja)
|
2005-01-31 |
2012-04-11 |
株式会社バイオセレンタック |
経皮吸収製剤、経皮吸収製剤保持シート、及び経皮吸収製剤保持用具
|
|
ES2384333T3
(es)
*
|
2005-04-11 |
2012-07-03 |
Abbott Laboratories |
Composiciones farmacéuticas que tienen perfiles de disolución mejorados para fármacos poco solubles
|
|
US9205047B2
(en)
*
|
2005-04-25 |
2015-12-08 |
The Governing Council Of The University Of Toronto |
Tunable sustained release of a sparingly soluble hydrophobic therapeutic agent from a hydrogel matrix
|
|
US9205046B2
(en)
*
|
2005-04-25 |
2015-12-08 |
The Governing Council Of The University Of Toronto |
Enhanced stability of inverse thermal gelling composite hydrogels
|
|
WO2006118210A1
(ja)
*
|
2005-04-28 |
2006-11-09 |
Eisai R & D Management Co., Ltd. |
ジヒドロピリジン系化合物の分解を防止する方法
|
|
AU2006254675A1
(en)
*
|
2005-06-02 |
2006-12-07 |
Thallion Pharmaceuticals Inc. |
Formulation comprising farnesyl dibenzodiazepinone and a pharmaceutically acceptable surfactant
|
|
US20070026073A1
(en)
*
|
2005-07-28 |
2007-02-01 |
Doney John A |
Amorphous efavirenz and the production thereof
|
|
JP4974018B2
(ja)
*
|
2005-08-24 |
2012-07-11 |
オリンパステルモバイオマテリアル株式会社 |
生体材料とその製造方法
|
|
CN101272767B
(zh)
*
|
2005-08-29 |
2012-08-29 |
赛诺菲-安万特美国有限责任公司 |
7-氯-N,N,5-三甲基-4-氧-3-苯基-3,5-二氢-4H-哒嗪并[4,5-b]吲哚-1-乙酰胺的无定形固体分散体
|
|
WO2007108463A1
(ja)
|
2006-03-23 |
2007-09-27 |
Shionogi & Co., Ltd. |
溶解性が改善された固形製剤
|
|
US20080085315A1
(en)
*
|
2006-10-10 |
2008-04-10 |
John Alfred Doney |
Amorphous ezetimibe and the production thereof
|
|
US20080152717A1
(en)
*
|
2006-12-14 |
2008-06-26 |
Isp Investments, Inc. |
Amorphous valsartan and the production thereof
|
|
US8613946B2
(en)
*
|
2006-12-21 |
2013-12-24 |
Isp Investment Inc. |
Carotenoids of enhanced bioavailability
|
|
WO2008092046A2
(en)
*
|
2007-01-26 |
2008-07-31 |
Isp Investments Inc. |
Amorphous oxcarbazepine and the production thereof
|
|
JP5508859B2
(ja)
*
|
2007-01-26 |
2014-06-04 |
アイエスピー インヴェストメンツ インコーポレイテッド |
噴霧乾燥製品を製造するための調剤処理方法
|
|
WO2008120724A1
(ja)
*
|
2007-03-30 |
2008-10-09 |
Ajinomoto Co., Inc. |
固体分散体製剤
|
|
US8309129B2
(en)
|
2007-05-03 |
2012-11-13 |
Bend Research, Inc. |
Nanoparticles comprising a drug, ethylcellulose, and a bile salt
|
|
US8703204B2
(en)
|
2007-05-03 |
2014-04-22 |
Bend Research, Inc. |
Nanoparticles comprising a cholesteryl ester transfer protein inhibitor and anon-ionizable polymer
|
|
US8722736B2
(en)
|
2007-05-22 |
2014-05-13 |
Baxter International Inc. |
Multi-dose concentrate esmolol with benzyl alcohol
|
|
US8426467B2
(en)
|
2007-05-22 |
2013-04-23 |
Baxter International Inc. |
Colored esmolol concentrate
|
|
EP2162120B1
(en)
|
2007-06-04 |
2016-05-04 |
Bend Research, Inc |
Nanoparticles comprising a non-ionizable cellulosic polymer and an amphiphilic non-ionizable block copolymer
|
|
WO2008149230A2
(en)
|
2007-06-04 |
2008-12-11 |
Pfizer Products Inc. |
Nanoparticles comprising drug, a non-ionizable cellulosic polymer and tocopheryl polyethylene glycol succinate
|
|
JP5325779B2
(ja)
*
|
2007-06-14 |
2013-10-23 |
株式会社ポーラファルマ |
医薬組成物
|
|
EP2030613A1
(en)
|
2007-08-17 |
2009-03-04 |
Abbott GmbH & Co. KG |
Preparation of compositions with essentially noncrystalline embedded macrolide antibiotics
|
|
US20100240711A1
(en)
*
|
2007-09-21 |
2010-09-23 |
Shionogi & Co., Ltd. |
Solid preparation comprising npyy5 receptor antagonist
|
|
EP2231169B1
(en)
|
2007-12-06 |
2016-05-04 |
Bend Research, Inc. |
Pharmaceutical compositions comprising nanoparticles and a resuspending material
|
|
WO2009073216A1
(en)
|
2007-12-06 |
2009-06-11 |
Bend Research, Inc. |
Nanoparticles comprising a non-ionizable polymer and an amine-functionalized methacrylate copolymer
|
|
US20110065800A1
(en)
|
2008-05-14 |
2011-03-17 |
Haihong Fan |
Formulations for cathepsin k inhibitors
|
|
US20100159001A1
(en)
*
|
2008-12-19 |
2010-06-24 |
Cardinal John R |
Extended-Release Pharmaceutical Formulations
|
|
US20100160363A1
(en)
*
|
2008-12-19 |
2010-06-24 |
Aaipharma Services Corp. |
Extended-release pharmaceutical formulations
|
|
JPWO2010107040A1
(ja)
*
|
2009-03-19 |
2012-09-20 |
塩野義製薬株式会社 |
Npyy5受容体拮抗剤を含有する固形製剤
|
|
CN102438594A
(zh)
|
2009-04-24 |
2012-05-02 |
伊休蒂卡有限公司 |
吲哚美辛的新剂型
|
|
CN101618012B
(zh)
*
|
2009-07-10 |
2012-07-04 |
东华大学 |
一种难溶性药物固体分散体制备方法
|
|
FR2954771B1
(fr)
*
|
2010-04-23 |
2013-09-13 |
Mohamed Skiba |
Nouveau procede de synthese de copolymeres, terpolymeres et tetrapolymeres de cyclodextrines et leurs utilisations
|
|
JP2014503470A
(ja)
*
|
2010-10-14 |
2014-02-13 |
アボット ゲーエムベーハー ウント カンパニー カーゲー |
クルクミノイド固体分散製剤
|
|
WO2013058751A1
(en)
*
|
2011-10-19 |
2013-04-25 |
Virginia Tech Intellectual Properties, Inc. |
Cellulose derivatives for enhancing bioavailability of flavonoids
|
|
JP5909796B2
(ja)
|
2012-03-02 |
2016-04-27 |
株式会社サンギ |
難溶性物質の水溶解性改善方法
|
|
EP2874613A1
(en)
*
|
2012-07-23 |
2015-05-27 |
Dow Global Technologies, Inc. |
Film composition for hard capsule shells
|
|
KR101986683B1
(ko)
*
|
2012-12-13 |
2019-06-10 |
한미약품 주식회사 |
테트라졸 유도체를 활성 성분으로 포함하는 용해도가 개선된 고체 분산체
|
|
CN103191077B
(zh)
*
|
2013-04-18 |
2014-08-20 |
广东彼迪药业有限公司 |
一种格列齐特片及其制备方法
|
|
EP2832723B1
(en)
*
|
2013-07-29 |
2017-02-15 |
Zentiva, a.s. |
Stabilised amorphous forms of Saxagliptin
|
|
JP2015189677A
(ja)
*
|
2014-03-27 |
2015-11-02 |
テバ製薬株式会社 |
ソリフェナシン非晶質体を含有する医薬組成物
|
|
JPWO2015174475A1
(ja)
|
2014-05-15 |
2017-04-20 |
株式会社セラバリューズ |
経口摂取用組成物
|
|
US9526734B2
(en)
|
2014-06-09 |
2016-12-27 |
Iceutica Pty Ltd. |
Formulation of meloxicam
|
|
WO2016031651A1
(ja)
*
|
2014-08-29 |
2016-03-03 |
花王株式会社 |
難溶解性ポリフェノール類を含有する固体分散体の製造方法
|
|
WO2016145132A1
(en)
*
|
2015-03-12 |
2016-09-15 |
Fmc Corporation |
Solid dispersions
|
|
AR105887A1
(es)
*
|
2015-09-04 |
2017-11-22 |
Sumitomo Chemical Co |
Composición, método de producción para la composición, y composición agroquímica
|
|
KR101912224B1
(ko)
*
|
2017-02-20 |
2018-10-26 |
충남대학교산학협력단 |
타다라필 함유 고체 분산체, 이를 포함하는 약제학적 조성물 및 이의 제조방법
|
|
WO2019172420A1
(ja)
*
|
2018-03-09 |
2019-09-12 |
協和発酵キリン株式会社 |
医薬組成物
|
|
CN111184692B
(zh)
*
|
2020-02-14 |
2021-10-26 |
南京大渊医美生物技术有限公司 |
一种白藜芦醇的制剂及其制备方法
|
|
CN111803447B
(zh)
*
|
2020-06-22 |
2022-08-09 |
三明学院 |
一种制备无定形药物的方法
|
|
WO2022090295A1
(en)
*
|
2020-10-28 |
2022-05-05 |
Merck Patent Gmbh |
Method for producing an amorphous solid dispersion and pharmaceutical composition for stabilizing active pharmaceutical ingredients
|
|
CN113350309B
(zh)
*
|
2021-08-09 |
2021-11-12 |
北京五和博澳药业股份有限公司 |
一种难溶性药物渗透泵控释片剂及其制备方法
|
|
CN117257964B
(zh)
*
|
2023-10-25 |
2024-04-02 |
苏州大学 |
基于碳酸氢铵的微波诱导吲哚美辛原位无定形化增溶技术
|
|
CN121044616B
(zh)
*
|
2025-11-05 |
2026-02-13 |
北京大学 |
一种氨基酸介导的非晶态稀土氧化物的合成方法
|