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    • 3. 发明申请
    • TRANSDERMAL DELIVERY OF LASOFOXIFENE
    • LASOFOXIFENE的透皮递送
    • WO0191724A3
    • 2002-05-30
    • PCT/US0117567
    • 2001-05-31
    • WATSON PHARMACEUTICALS INCFIKSTAD DAVIDQUAN DANYI
    • FIKSTAD DAVIDQUAN DANYI
    • A61K9/00A61K9/70A61K31/40A61K31/445A61K31/46A61K47/10A61K47/14A61P5/30
    • A61K9/7061A61K9/7084A61K31/40
    • The present invention to provide methods, pharmaceutical formulations, and devices for the transdermal delivery of 5-substituted-6-cyclic-5,6,7,8,-tetrahydronaphthalene2-o1 compounds ("lasofoxifene" or "CP-336,156") and pharmaceutically acceptable salts thereof. The invention also provides transdermal compositions of CP-336,156 or its salts dissolved or dispersed in a suitable carrier vehicle, optionally containing permeation enhancers and other excipients. The carrier vehicle may be a pressure sensitive adhesive, polymeric reservoir, or a fluid of controlled viscosity. The carrier vehicle may be contained in a device for purposes of holding the composition against the skin surface. Such devices may be in the form of matrix patches (drug in adhesive) or reservoir patches (drug in a liquid or polymeric reservoir with peripheral, in-line, or over-layed pressure sensitive adhesive). Further provided by this invention are methods for treating pathologies associated with the binding of lasofoxifene with the human estrogen receptor-alpha. For example, the invention formulations and devices are useful to treat or prevent bone loss, obesity, breast cancer, endometriosis, cardiovascular disease and prostatic disease.
    • 本发明提供5-取代-6-环-5,6,7,8-四氢萘-2-基化合物(“拉索昔芬”或“CP-336,156”)的透皮递送的方法,药物制剂和装置,以及 其药学上可接受的盐。 本发明还提供CP-336,156或其盐溶解或分散在合适的载体载体中的透皮组合物,任选地含有渗透促进剂和其它赋形剂。 载体载体可以是压敏粘合剂,聚合物储存器或具有可控粘度的流体。 载体载体可以容纳在用于将组合物保持在皮肤表面上的装置中。 这样的装置可以是基质贴片(粘合剂中的药物)或储存器贴片(液体中的药物或具有外围,在线或过度叠加的压敏粘合剂的聚合物储存器)的形式。 本发明进一步提供的是用于治疗与拉索非昔芬与人雌激素受体-α的结合相关的病理学的方法。 例如,本发明的制剂和装置可用于治疗或预防骨丢失,肥胖,乳腺癌,子宫内膜异位症,心血管疾病和前列腺疾病。
    • 4. 发明申请
    • BEVERAGE SYSTEMS
    • 饮料系统
    • WO2007075433A3
    • 2007-12-13
    • PCT/US2006047941
    • 2006-12-14
    • XEL HERBACEUTICALS INCQUAN DANYIXIONG WADE W
    • QUAN DANYIXIONG WADE W
    • A23K1/175
    • A23L2/52
    • A beverage and supplement system includes a beverage container (12) having: i) a liquid contained therein; and ii) a dispensive opening (14). A removable envelope (18) is in communication with the dispensive opening of the container, and has a first side (20) sealed to a second side (22) with the supplement (24) being contained therebetween. The second side of the envelope is rupturable upon application of force to the first side in an amount sufficient to rupture the second side without rupturing the first side, in order to dispense the supplement from the envelope without contacting the supplement with an external object.
    • 饮料和补充系统包括饮料容器(12),其具有:i)容纳在其中的液体; 和ii)昂贵的开口(14)。 可拆卸的外壳(18)与容器的昂贵的开口连通,并且具有密封到第二侧(22)的第一侧(20),其间包含有补充物(24)。 信封的第二面在向第一面施加足够的力以使第二面破裂而不破坏第一面的情况下是可破裂的,以便从信封中分配补充物而不会使补充物与外部物体接触。
    • 5. 发明申请
    • GREEN TEA FORMULATIONS AND METHODS OF PREPARATION
    • 绿茶配方和制备方法
    • WO2006012238A3
    • 2006-07-13
    • PCT/US2005022328
    • 2005-06-24
    • XEL HERBACEUTICALS INCQUAN DANYIXIONG WADE W
    • QUAN DANYIXIONG WADE W
    • A23F3/00A23F3/16A23F3/18
    • A23F3/18A23F3/163
    • Green tea formulations and methods for the preparation thereof are disclosed and described. Generally speaking, the method of preparation includes the mixing of fresh tea leaves in an amount of cold water, followed by pulverization of the leaves to release their intracellular material from the cells of the green tea leaves into the water and form an aqueous extract component. The remaining cellular material forms a leaf residue component which is removed from the mixture. Once the leaf residue is removed, the aqueous extract component is collected and may be dried or further processed to produce a final tea extract that has good natural color, robust natural flavor, and pleasant organoleptic properties, which also is high in polyphenol content, and may be used for various purposes such as the creation of a green tea beverage.
    • 公开并描述了绿茶制剂及其制备方法。 一般而言,制备方法包括将新鲜茶叶在一定量的冷水中混合,然后粉碎叶片以将它们的细胞内物质从绿茶叶的细胞释放到水中并形成水性提取物组分。 剩余的细胞材料形成从混合物中除去的叶渣组分。 一旦叶渣被除去,收集含水提取物组分并且可以干燥或进一步加工以产生具有良好的天然色泽,坚固的天然风味和令人愉快的感官特性(其也具有高的多酚含量)的最终茶提取物,以及 可用于各种目的,例如创建绿茶饮料。