Method of producing solid shape forms containing an active ingredient
    3.
    发明授权
    Method of producing solid shape forms containing an active ingredient 有权
    制备含有活性成分的固体形状的方法

    公开(公告)号:US07014810B2

    公开(公告)日:2006-03-21

    申请号:US10149762

    申请日:2000-12-15

    IPC分类号: B29C45/03 B29C45/72

    摘要: The present invention relates to an apparatus for producing solid active ingredient-containing forms from an active ingredient-containing formulation which comprises at least one polymeric binder. The apparatus according to the invention has at least one extruder 1 for continuous plastication of the formulation and at least two injection units 2 which are provided separate from one another, each of which is connected to the extruder 1, and through which the formulation can be injected into at least one mold 3. In the process according to the invention for producing solid active ingredient-containing forms from an active ingredient-containing formulation which comprises at least one binder, the active ingredient-containing formulation is continuously plasticated, the plasticated formulation is fed into an injection unit 21, and the formulation present in this injection unit 21 is injected into a mold 3, and plasticated formulation is fed into another injection molding unit 22, and the formulation present in the other injection molding unit 22 is injected into the mold 3 or another mold.

    摘要翻译: 本发明涉及包含至少一种聚合物粘合剂的含活性成分的制剂的含固体活性成分的形式的装置。 根据本发明的装置具有至少一个用于制剂的连续塑化的挤出机1和至少两个彼此分离的注射单元2,每个注射单元2彼此连接到挤出机1,并且制剂可以通过该挤出机1 注入至少一个模具3。 在根据本发明的用于由含有至少一种粘合剂的含活性成分的制剂生产含固体活性成分的制剂的方法中,含有活性成分的制剂被连续塑化,所述塑化的制剂进料到注射单元2' SUB> 1,并且将存在于该注射单元2 1中的制剂注射到模具3中,并且将塑化的制剂进料到另一个注射成型单元2 2 / >,并且存在于另一个注射成型单元2 2中的配方被注入到模具3或另一个模具中。

    Composition and Dosage Form Comprising a Solid or Semi-Solid Matrix
    6.
    发明申请
    Composition and Dosage Form Comprising a Solid or Semi-Solid Matrix 审中-公开
    包含固体或半固体基质的组合物和剂型

    公开(公告)号:US20090220596A1

    公开(公告)日:2009-09-03

    申请号:US11922609

    申请日:2006-06-22

    IPC分类号: A61K9/20 A61K9/10

    摘要: A composition which comprises a solid or semi-solid matrix having at least one active ingredient uniformly dispersed therein, the matrix comprising at least one pharmaceutically acceptable matrix-forming agent and a 1,3-bis(lactamyl)-butane compound, in particular 1,3-bis(pyrrolidon-1-yl)-butane. The active ingredient is preferably dispersed in the matrix in a state of a solid solution. The matrix-forming agent is preferably a pharmaceutically acceptable polymer. The composition is useful for the manufacture of pharmaceutical dosage forms.

    摘要翻译: 一种组合物,其包含固体或半固体基质,其具有均匀分散于其中的至少一种活性成分,所述基质包含至少一种药学上可接受的基质形成剂和1,3-双(内酰胺基) - 丁烷化合物,特别是1 ,3-双(吡咯烷酮-1-基) - 丁烷。 活性成分优选以固体状态分散在基质中。 基质形成剂优选为药学上可接受的聚合物。 该组合物可用于制备药物剂型。

    Formulation based on heparin, glycosaminoglycan or heparinoid, use of the formulation and the formulation base
    10.
    发明授权
    Formulation based on heparin, glycosaminoglycan or heparinoid, use of the formulation and the formulation base 失效
    基于肝素,糖胺聚糖或类肝素的制剂,使用制剂和制剂基础

    公开(公告)号:US07393840B2

    公开(公告)日:2008-07-01

    申请号:US10296441

    申请日:2001-05-29

    IPC分类号: A61N31/747

    摘要: The present invention relates to formulations based on at least one heparin, glycosaminoglycan or heparinoid and on a formulation base with a lipid component and a polymer component. The use of this formulation as drug form for oral administration of at least one heparin, glycosaminoglycan or heparinoid, and also a process for producing the formulations by mixing the formulation components to form a plastic mixture and, where appropriate, to manufacture the formulations as drug form, advantageously using melt extrusion, are described. The lipid component advantageously has active ingredient-promoting properties, while the polymer component is soluble or swellable. At least parts of the lipid component are embedded in a polymer matrix, preferably in the form of a molecular dispersion. The formulations can form emulsions in water or aqueous liquids.

    摘要翻译: 本发明涉及基于至少一种肝素,糖胺聚糖或类肝素的制剂,以及具有脂质组分和聚合物组分的制剂基质。 使用这种制剂作为口服给药至少一种肝素,糖胺聚糖或类肝素的药物形式,以及通过混合制剂组分以形成塑料混合物并在适当时制备制剂作为药物来制备制剂的方法 描述了有利地使用熔体挤出的形式。 脂质组分有利地具有活性成分促进性质,而聚合物组分是可溶的或可溶胀的。 至少部分脂质组分嵌入聚合物基质中,优选以分子分散体的形式。 制剂可以在水或含水液体中形成乳液。