Medicament form for the delivery of collagenase to wounds and process
for the preparation thereof
    4.
    发明授权
    Medicament form for the delivery of collagenase to wounds and process for the preparation thereof 失效
    用于将胶原酶递送至伤口的药物形式及其制备方法

    公开(公告)号:US6074664A

    公开(公告)日:2000-06-13

    申请号:US875723

    申请日:1997-11-17

    摘要: An administration form for the release of collagenase to wounds is characterised in that it exhibits a combination of specific properties as hereinbelow:a. it is coherent, flat-shaped and deformable;b. it has a superficial extension that is equal to or smaller than the wound surface to be treated;c. it comprises collagenase in defined amounts in homogeneously distributed form;d. it is designed for the controlled release of collagenase.

    摘要翻译: PCT No.PCT / EP96 / 00294 Sec。 371日期:1997年11月17日 102(e)1997年11月17日PCT PCT 1996年1月25日PCT公布。 WO96 / 23487 PCT公开号 日本1996年8月8日将胶原酶释放到伤口上的给药形式的特征在于其具有以下具体特性的组合:a。 它是连贯的,平坦的和可变形的; b。 它具有等于或小于待治疗的伤口表面的表面延伸; C。 它以均匀分布的形式包含限定量的胶原酶; d。 它被设计用于胶原酶的控制释放。

    Impeding the extraction of active ingredients out of tablets
    6.
    发明授权
    Impeding the extraction of active ingredients out of tablets 有权
    阻止从片剂中提取活性成分

    公开(公告)号:US06197314B1

    公开(公告)日:2001-03-06

    申请号:US09156538

    申请日:1998-09-17

    申请人: Heinz Einig

    发明人: Heinz Einig

    IPC分类号: A61K920

    摘要: Solid oral administration forms from which the active ingredients can be isolated only with difficulty are described and comprise, besides conventional ingredients, as addition a mixture of pharmacologically suitable fats or gel formers with surfactants. Addition of the mixtures impedes extraction of the active ingredients out of the administration forms.

    摘要翻译: 除了常规成分之外,还描述了固体口服给药形式,其中仅能很难分离活性成分,除了药理学上合适的脂肪或凝胶形成剂与表面活性剂的混合物外,还包括其它成分。 添加混合物阻碍了从给药形式中提取活性成分。

    Pharmaceutical dosage forms with impeded extractability of a sympathomimetic
    8.
    发明申请
    Pharmaceutical dosage forms with impeded extractability of a sympathomimetic 审中-公开
    具有阻碍的交感神经的可提取性的药物剂型

    公开(公告)号:US20060062847A1

    公开(公告)日:2006-03-23

    申请号:US11225176

    申请日:2005-09-14

    IPC分类号: A61K9/20 C07C67/36

    摘要: A solid oral pharmaceutical dosage form of a sympathomimetic with impeded extractability of the sympathomimetic, comprising I) a sympathomimetic (component I) II) an excipient mixture (component II) composed of a) 5 to 50% by weight of hydroxyalkylcelluloses or alkylcelluloses or mixtures thereof b) 5 to 70% by weight of xanthan c) 5 to 50% by weight of an alkaline earth metal salt of a C10-C30 fatty acid d) 10 to 70% by weight of an alkali metal or alkaline earth metal salt of a mineral acid, of a sulfonic acid or of a C2-C6 carboxylic acid or mixtures thereof, where the total of components a) to d) is 100% by weight, where the ratio of active ingredient to excipient mixture II) is from 1:2 to 3:1 by weight.

    摘要翻译: 包含I)拟交感神经元(组分I)II)赋形剂混合物(组分II)的固体口服药物剂型,其具有妨碍所述交感神经活性的可提取性,其包含a)5至50重量%的羟烷基纤维素或烷基纤维素或混合物 b)5〜70重量%的呫吨