Composition containing medicine extremely slightly soluble in water and method for preparation thereof
    2.
    发明申请
    Composition containing medicine extremely slightly soluble in water and method for preparation thereof 失效
    含有极微溶于水的药物的组合物及其制备方法

    公开(公告)号:US20070128273A1

    公开(公告)日:2007-06-07

    申请号:US10551901

    申请日:2004-04-28

    IPC分类号: A61K9/20

    摘要: A composition containing a very low water-soluble drug, which composition is produced by treating, with a supercritical or subcritical carbon dioxide fluid, a mixture containing a very low water-soluble drug and a porous material (exclusive of a porous silica material characterized in that the material has an average pore diameter of 1 to 20 nm, the total pore volume of the material that have a diameter falling within a range of ±40% of the average pore diameter account for 60% or more the volume of all the pores of the material, and, when subjected to X-ray diffractometry, the material exhibits one or more peaks at a diffraction angle (2θ) corresponding to d of 1 nm or more); and a method for producing the composition. The very-low-water-soluble-drug-containing composition of the present invention ensures improved dissolution of the very low water-soluble drug.

    摘要翻译: 含有非常低水溶性药物的组合物,该组合物通过用超临界或亚临界二氧化碳流体处理含有非常低水溶性药物和多孔材料的混合物(不包括多孔二氧化硅材料 该材料的平均孔径为1〜20nm,直径在平均孔径的±40%范围内的材料的总孔体积占所有孔的体积的60%以上 的材料,并且当进行X射线衍射测定时,该材料在对应于d为1nm以上的衍射角(2θ)处表现出一个或多个峰); 以及该组合物的制造方法。 本发明的非常低水溶性药物的组合物确保极低水溶性药物的溶出度得到改善。

    Composition containing medicine extremely slightly soluble in water and method for preparation thereof
    3.
    发明授权
    Composition containing medicine extremely slightly soluble in water and method for preparation thereof 失效
    含有极微溶于水的药物的组合物及其制备方法

    公开(公告)号:US08101207B2

    公开(公告)日:2012-01-24

    申请号:US10551901

    申请日:2004-04-28

    摘要: A composition containing a very low water-soluble drug, which composition is produced by treating, with a supercritical or subcritical carbon dioxide fluid, a mixture containing a very low water-soluble drug and a porous material (exclusive of a porous silica material characterized in that the material has an average pore diameter of 1 to 20 nm, the total pore volume of the material that have a diameter falling within a range of ±40% of the average pore diameter account for 60% or more the volume of all the pores of the material, and, when subjected to X-ray diffractometry, the material exhibits one or more peaks at a diffraction angle (2θ) corresponding to d of 1 nm or more); and a method for producing the composition.The very-low-water-soluble-drug-containing composition of the present invention ensures improved dissolution of the very low water-soluble drug.

    摘要翻译: 含有非常低水溶性药物的组合物,该组合物通过用超临界或亚临界二氧化碳流体处理含有非常低水溶性药物和多孔材料的混合物(不包括多孔二氧化硅材料 该材料的平均孔径为1〜20nm,直径在平均孔径的±40%范围内的材料的总孔体积占所有孔的体积的60%以上 的材料,当进行X射线衍射测定时,该材料在对应于d的衍射角(2θ)为1nm以上)表现出一个以上的峰值。 以及该组合物的制造方法。 本发明的非常低水溶性药物的组合物确保极低水溶性药物的溶出度得到改善。

    Method for Producing Adsorptive Porous Body
    4.
    发明申请
    Method for Producing Adsorptive Porous Body 审中-公开
    生产吸附多孔体的方法

    公开(公告)号:US20090005384A1

    公开(公告)日:2009-01-01

    申请号:US11813968

    申请日:2006-01-24

    IPC分类号: A61K31/50

    摘要: The present invention relates to a method for producing a 2-benzyl-5-(4-chlorophenyl)-6-[4-(methylthio)phenyl]-2H-pyridazin-3-one adsorptive porous material characterized by treating a porous material with a halogen-containing organic solvent in which 2-benzyl-5-(4-chlorophenyl)-6-[4-(methylthio)phenyl]-2H-pyridazin-3-one is dissolved. The production method of the present invention is simple and easy, and the obtained adsorptive porous material is excellent in dissolution properties of 2-benzyl-5-(4-chlorophenyl)-6-[4-(methylthio)phenyl]-2H-pyridazin-3-one.

    摘要翻译: 本发明涉及2-苄基-5-(4-氯苯基)-6- [4-(甲硫基)苯基] -2H-哒嗪-3-酮吸附多孔材料的制备方法,其特征在于用 其中溶解2-苄基-5-(4-氯苯基)-6- [4-(甲硫基)苯基] -2H-哒嗪-3-酮的含卤素的有机溶剂。 本发明的制造方法简单易行,所得到的吸附性多孔体的2-苄基-5-(4-氯苯基)-6- [4-(甲硫基)苯基] -2H-哒嗪的溶解性优异 -3-one。

    Hollow granular medicine and its preparation
    8.
    发明授权
    Hollow granular medicine and its preparation 失效
    中空粒状药物及其制备

    公开(公告)号:US5057323A

    公开(公告)日:1991-10-15

    申请号:US367948

    申请日:1989-06-19

    IPC分类号: A61K9/00 A61K9/16

    CPC分类号: A61K9/0065 A61K9/1676

    摘要: A granular medicine with slow drug-release characteristics that is sufficiently absorbed in the intestines, in which the granular medicine has a hollow spherical structure, a drug is dispersed in the shell, which mainly consists of an enteron-soluble polymer. The method for preparing the medicine includes the steps of: (a) mixing a hydrophilic or hydrophobic drug with an enteron-soluble polymer in a mixture of an aliphatic alcohol and a chlorohydrocarbon; and (b) pouring this mixture into water or an aqueous medium, and stirring the solution to precipitate the medicine.

    摘要翻译: 具有缓慢的药物释放特性的颗粒药物在肠中充分吸收,其中颗粒药物具有中空球形结构,药物分散在壳中,其主要由肠溶性聚合物组成。 制备药物的方法包括以下步骤:(a)将亲水或疏水性药物与肠溶性聚合物混合在脂族醇和氯代烃的混合物中; 和(b)将该混合物倒入水或水性介质中,并搅拌该溶液以沉淀药物。