Patch
    1.
    发明授权
    Patch 有权
    补丁

    公开(公告)号:US09173855B2

    公开(公告)日:2015-11-03

    申请号:US13882565

    申请日:2011-11-02

    摘要: Disclosed is a patch which is a formulation including deposited clonidine crystals and provides stable transdermal absorbability even after storage at varying temperatures. The patch disclosed includes a backing and a medicated layer integrally superposed on one surface of the backing. The medicated layer contains: 5 to 30% by weight of clonidine including clonidine in a crystallized state; 25 to 90% by weight of a macromolecular base (A) having a viscosity-average molecular weight of 800,000 or larger; and 5 to 60% by weight of a liquid additive capable of dissolving the clonidine. The weight ratio of the liquid additive to the macromolecular base (A) [the liquid additive/the macromolecular base (A)] is 0.1 to 2.0.

    摘要翻译: 公开了一种贴剂,其是包含沉积的可乐定晶体的制剂,并且即使在变化的温度下储存后也能提供稳定的经皮吸收能力。 所公开的贴剂包括一体地叠置在背衬的一个表面上的背衬和药物层。 含药层含有5〜30重量%的可乐定,包括结晶状态下的可乐定; 25〜90重量%的粘均分子量为80万以上的高分子基(A) 和5〜60重量%的能够溶解可乐定的液体添加剂。 液体添加剂与大分子基质(A)[液体添加剂/大分子基(A)]的重量比为0.1〜2.0。

    PATCH
    2.
    发明申请
    PATCH 有权
    补丁

    公开(公告)号:US20130261572A1

    公开(公告)日:2013-10-03

    申请号:US13882565

    申请日:2011-11-02

    IPC分类号: A61K9/70 A61K31/4168

    摘要: Disclosed is a patch which is a formulation including deposited clonidine crystals and provides stable transdermal absorbability even after storage at varying temperatures. The patch disclosed includes a backing and a medicated layer integrally superposed on one surface of the backing. The medicated layer contains: 5 to 30% by weight of clonidine including clonidine in a crystallized state; 25 to 90% by weight of a macromolecular base (A) having a viscosity-average molecular weight of 800,000 or larger; and 5 to 60% by weight of a liquid additive capable of dissolving the clonidine. The weight ratio of the liquid additive to the macromolecular base (A) [the liquid additive/the macromolecular base (A)] is 0.1 to 2.0.

    摘要翻译: 公开了一种贴剂,其是包含沉积的可乐定晶体的制剂,并且即使在变化的温度下储存后也能提供稳定的经皮吸收能力。 所公开的贴剂包括一体地叠置在背衬的一个表面上的背衬和药物层。 含药层含有5〜30重量%的可乐定,包括结晶状态下的可乐定; 25〜90重量%的粘均分子量为80万以上的高分子基(A) 和5〜60重量%的能够溶解可乐定的液体添加剂。 液体添加剂与大分子基质(A)[液体添加剂/大分子基(A)]的重量比为0.1〜2.0。