Aqueous pharmaceutical compositions
    1.
    发明授权
    Aqueous pharmaceutical compositions 有权
    水性药物组合物

    公开(公告)号:US07612115B2

    公开(公告)日:2009-11-03

    申请号:US11374450

    申请日:2006-03-13

    摘要: The present invention has an object to provide an antibacterial aqueous pharmaceutical composition and an aqueous pharmaceutical composition which have a sufficiently low gelation temperature even when new quinolone antibacterial agents such as ofloxacin as the active ingredient and can be retained at the administration site for a long time by virtue of rapid viscosity increase after administration in spite of their being liquid at administration and thereby attain high availability of pharmaceutical agent.The present invention relates to an antibacterial aqueous pharmaceutical composition which comprises: 2.8 to 4 w/v % of methylcellulose, the 2 w/v % aqueous solution of which has a viscosity of 12 mPa·s or below at 20° C.; 1.5 to 2.3 w/v % of citric acid; 2 to 4 w/v % of polyethylene glycol; and 0.1 to 0.5 w/v % of ofloxacin.

    摘要翻译: 本发明的目的在于提供一种抗菌水性药物组合物和含水药物组合物,即使新的喹诺酮类抗菌剂如氧氟沙星作为活性成分,也能够在施用部位长时间保留,具有足够低的凝胶化温度 由于施用后的粘度快速增加,尽管它们在施用时是液体,从而获得药剂的高可用性。 本发明涉及一种抗菌水性药物组合物,其包含:2.8〜4w / v%的甲基纤维素,其2w / v%水溶液在20℃下的粘度为12mPa·s或更低。 1.5至2.3w / v%的柠檬酸; 2至4w / v%的聚乙二醇; 和0.1至0.5w / v%的氧氟沙星。

    Aqueous pharmaceutical compositions

    公开(公告)号:US20060172969A1

    公开(公告)日:2006-08-03

    申请号:US11374450

    申请日:2006-03-13

    IPC分类号: A61K31/717 A61K31/496

    摘要: The present invention has an object to provide an antibacterial aqueous pharmaceutical composition and an aqueous pharmaceutical composition which have a sufficiently low gelation temperature even when new quinolone antibacterial agents such as ofloxacin as the active ingredient and can be retained at the administration site for a long time by virtue of rapid viscosity increase after administration in spite of their being liquid at administration and thereby attain high availability of pharmaceutical agent. The present invention relates to an antibacterial aqueous pharmaceutical composition which comprises: 2.8 to 4 w/v % of methylcellulose, the 2 w/v % aqueous solution of which has a viscosity of 12 mPa·s or below at 20° C.; 1.5 to 2.3 w/v % of citric acid; 2 to 4 w/v % of polyethylene glycol; and 0.1 to 0.5 w/v % of ofloxacin.

    Method for Producing Genetically Modified Plant Expressing Miraculin
    6.
    发明申请
    Method for Producing Genetically Modified Plant Expressing Miraculin 审中-公开
    生产转基因植物表达Miraculin的方法

    公开(公告)号:US20090205068A1

    公开(公告)日:2009-08-13

    申请号:US11659342

    申请日:2005-08-04

    IPC分类号: A01H5/00 A61K38/16

    摘要: The present invention relates to: a method for producing a transgenic plant expressing miraculin, comprising introducing a miraculin gene into a useful plant that can be easily produced and cultivated throughout the year using plant molecular breeding technology; a transgenic plant expressing miraculin, which is produced by the method; and the use thereof. The present invention also relates to a food additive, a food or drink, or an antidiabetic drug, which contains miraculin that is produced by the transgenic plant.

    摘要翻译: 本发明涉及:用于生产表达miraculin的转基因植物的方法,包括将miraculin基因引入可利用植物分子育种技术在一年中容易地生产和培育的有用植物中; 通过该方法生产表达miraculin的转基因植物; 及其用途。 本发明还涉及包含由转基因植物产生的miraculin的食品添加剂,食品或饮料或抗糖尿病药物。