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公开(公告)号:US20130323309A1
公开(公告)日:2013-12-05
申请号:US14000264
申请日:2012-02-07
申请人: Pravin Meghrajji Bhutada , Ashish Ashokrao Deshmukh , Sajeev Chandran , Vineeth Raghavan , Shirishkumar Kulkarni
发明人: Pravin Meghrajji Bhutada , Ashish Ashokrao Deshmukh , Sajeev Chandran , Vineeth Raghavan , Shirishkumar Kulkarni
CPC分类号: A61K9/5073 , A61K9/1676 , A61K9/5047 , A61K9/5078 , A61K31/13
摘要: A sustained release pharmaceutical composition comprising; a core including memantine or its pharmaceutically acceptable salts and one or more pharmaceutical acceptable excipients, and a sustained release coating comprising a water insoluble substance and a water soluble substance where the ratio of the water insoluble substance to the water soluble substance is from about 1:0 to about 3:5:1, optionally containing an immediate release coating having memantine where the immediate release coating is applied over the sustained release coating.
摘要翻译: 一种缓释药物组合物,其包含: 包括美金刚或其药学上可接受的盐和一种或多种药学上可接受的赋形剂的核心,以及包含水不溶性物质和水溶性物质的持续释放包衣,其中水不溶性物质与水溶性物质的比例为约1: 0至约3:5:1,任选地包含具有美金刚的速释涂层,其中速释涂层施用于缓释涂层上。
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公开(公告)号:US20130022654A1
公开(公告)日:2013-01-24
申请号:US13638239
申请日:2011-02-07
IPC分类号: A61K31/137 , A61K9/00 , A61P25/00 , C07C215/54
CPC分类号: A61K9/209 , A61K9/0004 , A61K9/0065 , A61K9/1617 , A61K9/1635 , A61K9/1652 , A61K9/1676 , A61K9/2054 , A61K9/2077 , A61K9/5026 , A61K9/5042 , A61K31/137 , A61K45/06 , A61K2300/00
摘要: A once daily controlled release pharmaceutical compositions comprising tapentadol, wherein preferably the mean Tmax of tapentadol is reached after 10 hours of administration of the composition. The composition comprises tapentadol, such that it maintains serum concentration of tapentadol of at least about 20 ng/ml for at least about 17 hours after oral administration of the composition. According to one embodiment the controlled release pharmaceutical composition comprises tapentadol, which is gastroretentive.
摘要翻译: 包含他喷他多的每日一次的控释药物组合物,其中优选在施用组合物10小时后达到他喷他多的平均T max。 组合物包含他喷他多,使得其在口服给药组合物后至少约17小时维持至少约20ng / ml的他喷他多的血清浓度。 根据一个实施方案,控释药物组合物包含胃酸滞留的他喷他多。
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公开(公告)号:US20120283252A1
公开(公告)日:2012-11-08
申请号:US13513335
申请日:2010-12-02
IPC分类号: A61K31/542 , A61P27/02
CPC分类号: A61K9/0048 , A61K47/10 , A61K47/26 , A61K47/32 , A61K47/38
摘要: Pharmaceutical ophthalmic compositions comprising active ingredient(s) such as carbonic anhydrase inhibitor (CAI) or combinations and processes for making such compositions and the use of these compositions in patient populations including pediatric populations. A process for preparing an ophthalmic composition comprising a carbonic anhydrase inhibitor, which comprises a) preparing a slurry comprising a carbonic anhydrase inhibitor and a surfactant; b) preparing a polymer slurry comprising a polymer and water; c) preparing a solution comprising tonicity and preservative agents; d) mixing the polymer slurry of step b and the solution of step c, to form a vehicle concentrate and adjusting pH; e) adding the slurry of step a, to the vehicle concentrate of step d and mixing to homogenize; f) autoclaving the mixture of step e; g) sizing the mixture of step f, under aseptic condition.
摘要翻译: 包含活性成分如碳酸酐酶抑制剂(CAI)或组合的药物眼用组合物和用于制备此类组合物的方法以及这些组合物在包括儿科人群的患者群体中的用途。 一种制备包含碳酸酐酶抑制剂的眼用组合物的方法,其包括:a)制备包含碳酸酐酶抑制剂和表面活性剂的浆液; b)制备包含聚合物和水的聚合物浆料; c)制备包含张力和防腐剂的溶液; d)将步骤b的聚合物浆料和步骤c的溶液混合,形成载体浓缩物并调节pH值; e)将步骤a的浆料加入到步骤d的车辆浓缩物中并混合均匀; f)高压灭菌步骤e的混合物; g)在无菌条件下调整步骤f的混合物的尺寸。
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公开(公告)号:US09421165B2
公开(公告)日:2016-08-23
申请号:US13982561
申请日:2012-02-03
IPC分类号: A61K9/00 , A61K9/20 , A61K9/24 , A61K9/28 , A61K31/4545
CPC分类号: A61K9/0053 , A61K9/0004 , A61K9/2018 , A61K9/2054 , A61K9/2072 , A61K9/2086 , A61K9/209 , A61K9/2846 , A61K9/2866 , A61K31/4545
摘要: The present invention relates to oral controlled release pharmaceutical compositions comprising Bepotastine. The oral controlled release pharmaceutical composition comprises Bepotastine or pharmaceutically acceptable salts thereof and at least one release controlling agent. The present invention also provides the use of oral controlled release pharmaceutical compositions of Bepotastine for the treatment of allergic rhinitis and for the treatment of pruritus caused by urticaria.
摘要翻译: 本发明涉及包含布替沙星的口服控释药物组合物。 口服释放药物组合物包含布替托汀或其药学上可接受的盐和至少一种释放控制剂。 本发明还提供了布替斯汀的口服控释药物组合物用于治疗过敏性鼻炎和治疗由荨麻疹引起的瘙痒的用途。
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公开(公告)号:US20130317063A1
公开(公告)日:2013-11-28
申请号:US13982561
申请日:2012-02-03
IPC分类号: A61K9/00 , A61K31/4545
CPC分类号: A61K9/0053 , A61K9/0004 , A61K9/2018 , A61K9/2054 , A61K9/2072 , A61K9/2086 , A61K9/209 , A61K9/2846 , A61K9/2866 , A61K31/4545
摘要: The present invention relates to oral controlled release pharmaceutical compositions comprising Bepotastine. The oral controlled release pharmaceutical composition comprises Bepotastine or pharmaceutically acceptable salts thereof and at least one release controlling agent. The present invention also provides the use of oral controlled release pharmaceutical compositions of Bepotastine for the treatment of allergic rhinitis and for the treatment of pruritus caused by urticaria.
摘要翻译: 本发明涉及包含布替沙星的口服控释药物组合物。 口服释放药物组合物包含布替托汀或其药学上可接受的盐和至少一种释放控制剂。 本发明还提供了布替斯汀的口服控释药物组合物用于治疗过敏性鼻炎和治疗由荨麻疹引起的瘙痒的用途。
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公开(公告)号:US20130143897A1
公开(公告)日:2013-06-06
申请号:US13816342
申请日:2011-08-10
IPC分类号: A61K31/496
CPC分类号: A61K31/496 , A61K9/2054 , A61K9/2072 , A61K9/2077 , A61K9/2081 , A61K9/209 , A61K9/2846 , A61K9/2853 , A61K9/2866 , A61K9/4866 , A61K9/5026 , A61K9/5078 , A61K31/519
摘要: An oral controlled release pharmaceutical composition comprising Blonanserin and release controlling agent(s) and optionally pharmaceutically acceptable excipients is provided. The present invention further relates to a controlled release pharmaceutical composition comprising Blonanserin and release controlling agent(s) such that the composition releases not less than about 80% of Blonanserin within 20 hours, when dissolution is carried out in 900 ml, 0.1 N HCl, USP apparatus Type II (Paddle) at 50 rpm for 20 hrs. The controlled release pharmaceutical composition of the invention releases 50% of Blonanserin between about 4 to 14 hours, when dissolution is carried out in 900 ml, 0.1 N HCl, USP apparatus Type II (Paddle) at 50 rpm.
摘要翻译: 提供了包含布兰宁素和释放控制剂和任选的药学上可接受的赋形剂的口服控释药物组合物。 本发明还涉及包含布兰宁素和释放控制剂的控释药物组合物,使得当在900ml,0.1N HCl中溶解时,组合物在20小时内释放不少于约80%的布兰宁素, USP装置II型(桨)在50rpm下20小时。 当在900rpm,0.1N HCl,USP装置II型(桨式)中以50rpm进行溶解时,本发明的控释药物组合物释放出约4至14小时的布朗宁素50%。
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公开(公告)号:US20130004545A1
公开(公告)日:2013-01-03
申请号:US13518102
申请日:2010-12-23
IPC分类号: A61K31/454 , A61P25/18 , A61K9/00
CPC分类号: A61K9/2866 , A61K9/0004 , A61K9/0007 , A61K9/0065 , A61K9/2013 , A61K9/2027 , A61K9/2031 , A61K9/2054 , A61K9/2086 , A61K9/209 , A61K9/2846 , A61K9/5078 , A61K31/454
摘要: A slow release pharmaceutical composition comprising iloperidone or its active metabolites and a slow release agent is described. Also disclosed is slow release pharmaceutical composition comprising iloperidone or its active metabolites, wherein the slow release composition is a combination of a controlled release composition and an immediate release composition.
摘要翻译: 描述了包含伊潘立酮或其活性代谢物和缓释剂的缓释药物组合物。 还公开了包含伊潘立酮或其活性代谢物的缓释药物组合物,其中缓释组合物是控释组合物和速释组合物的组合。
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公开(公告)号:US08614210B2
公开(公告)日:2013-12-24
申请号:US13513335
申请日:2010-12-02
IPC分类号: A61P27/02 , A61K31/542
CPC分类号: A61K9/0048 , A61K47/10 , A61K47/26 , A61K47/32 , A61K47/38
摘要: Pharmaceutical ophthalmic compositions comprising active ingredient(s) such as carbonic anhydrase inhibitor (CAI) or combinations and processes for making such compositions and the use of these compositions in patient populations including pediatric populations. A process for preparing an ophthalmic composition comprising a carbonic anhydrase inhibitor, which comprises a) preparing a slurry comprising a carbonic anhydrase inhibitor and a surfactant; b) preparing a polymer slurry comprising a polymer and water; c) preparing a solution comprising tonicity and preservative agents; d) mixing the polymer slurry of step b and the solution of step c, to form a vehicle concentrate and adjusting pH; e) adding the slurry of step a, to the vehicle concentrate of step d and mixing to homogenize; f) autoclaving the mixture of step e; g) sizing the mixture of step f, under aseptic condition.
摘要翻译: 包含活性成分如碳酸酐酶抑制剂(CAI)或组合的药物眼用组合物和用于制备此类组合物的方法以及这些组合物在包括儿科人群的患者群体中的用途。 一种制备包含碳酸酐酶抑制剂的眼用组合物的方法,其包括:a)制备包含碳酸酐酶抑制剂和表面活性剂的浆液; b)制备包含聚合物和水的聚合物浆料; c)制备包含张力和防腐剂的溶液; d)将步骤b的聚合物浆料和步骤c的溶液混合,形成载体浓缩物并调节pH值; e)将步骤a的浆料加入到步骤d的车辆浓缩物中并混合均匀; f)高压灭菌步骤e的混合物; g)在无菌条件下调整步骤f的混合物的尺寸。
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公开(公告)号:US09884022B2
公开(公告)日:2018-02-06
申请号:US13638239
申请日:2011-02-07
IPC分类号: A61K31/137 , A61K9/00 , A61P25/00 , C07C215/54 , A61K9/24 , A61K9/16 , A61K9/20 , A61K9/50 , A61K45/06
CPC分类号: A61K9/209 , A61K9/0004 , A61K9/0065 , A61K9/1617 , A61K9/1635 , A61K9/1652 , A61K9/1676 , A61K9/2054 , A61K9/2077 , A61K9/5026 , A61K9/5042 , A61K31/137 , A61K45/06 , A61K2300/00
摘要: A once daily controlled release pharmaceutical compositions comprising tapentadol, wherein preferably the mean Tmax of tapentadol is reached after 10 hours of administration of the composition. The composition comprises tapentadol, such that it maintains serum concentration of tapentadol of at least about 20 ng/ml for at least about 17 hours after oral administration of the composition. According to one embodiment the controlled release pharmaceutical composition comprises tapentadol, which is gastroretentive.
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公开(公告)号:US20130142849A1
公开(公告)日:2013-06-06
申请号:US13817169
申请日:2011-08-13
CPC分类号: A61K47/38 , A61K9/0004 , A61K9/0065 , A61K9/2054 , A61K9/2072 , A61K9/2081 , A61K9/2086 , A61K9/209 , A61K9/2853 , A61K9/2866 , A61K9/2886 , A61K9/4808 , A61K9/5026 , A61K9/5047 , A61K9/5073 , A61K9/5084 , A61K31/343
摘要: The present invention relates to controlled release formulation of dronedarone or pharmaceutically acceptable salts, esters, metabolites, prodrugs or enantiomers thereof and controlled release polymers. The use of controlled release formulations of Dronedarone would improve the bioavailability and the patient compliance with reduction in number of dosages to be taken per day.
摘要翻译: 本发明涉及决奈达隆或其药学上可接受的盐,酯,代谢物,前药或其对映体和控制释放聚合物的控制释放制剂。 使用决奈达隆的控释制剂将提高生物利用度和患者对每日服用剂量减少的依从性。
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