Percutaneous absorption composition

    公开(公告)号:US10588973B2

    公开(公告)日:2020-03-17

    申请号:US15960392

    申请日:2018-04-23

    申请人: MEDRx CO., LTD

    摘要: The embodiments provide a percutaneous absorption composition for a basic medicament having improved transdermal absorbability. The percutaneous absorption composition comprises a sorbic acid and/or a metal sorbate as a percutaneous absorption promotor. The molar ration of the sorbic acid and/or the metal sorbate to the basic medicament is 0.5-2.5. The composition of the present disclosure may further comprise a basic component.

    Laminated Type Patch
    4.
    发明申请

    公开(公告)号:US20220370376A1

    公开(公告)日:2022-11-24

    申请号:US17769944

    申请日:2020-10-14

    申请人: MEDRX CO., LTD.

    摘要: The present disclosure, for example, can include a laminated type patch A, comprising a release layer 1, a drug layer 2, a drug support layer 3 having elasticity, an adhesive layer 4, and an adhesive support layer 5 laminated in this order, wherein the outer edges of the release layer, the adhesive layer, and the adhesive support layer are all outside the outer edges of both the drug layer and the drug support layer; wherein the portion surrounded by the outer edges of the drug layer and the drug support layer, and the inner sides of the release layer and the adhesive layer has a space; and wherein the cross-sectional area of the space is 0.3 mm2 or more, at least when cut along the longitudinal centerline and the transverse centerline on the plane surfaces of the drug layer and the drug support layer.

    PERCUTANEOUS ABSORPTION COMPOSITION
    5.
    发明申请

    公开(公告)号:US20200171156A1

    公开(公告)日:2020-06-04

    申请号:US16782988

    申请日:2020-02-05

    申请人: MEDRx CO., LTD

    摘要: The embodiments provide a percutaneous absorption composition for a basic medicament having improved transdermal absorbability. The percutaneous absorption composition comprises a sorbic acid and/or a metal sorbate as a percutaneous absorption promotor. The molar ration of the sorbic acid and/or the metal sorbate to the basic medicament is 0.5-2.5. The composition of the present disclosure may further comprise a basic component.

    PERCUTANEOUS ABSORPTION COMPOSITION
    7.
    发明申请

    公开(公告)号:US20180236082A1

    公开(公告)日:2018-08-23

    申请号:US15960392

    申请日:2018-04-23

    申请人: MEDRx CO., LTD

    摘要: The embodiments provide a percutaneous absorption composition for a basic medicament having improved transdermal absorbability. The percutaneous absorption composition comprises a sorbic acid and/or a metal sorbate as a percutaneous absorption promotor. The molar ration of the sorbic acid and/or the metal sorbate to the basic medicament is 0.5-2.5. The composition of the present disclosure may further comprise a basic component.

    PERCUTANEOUS ABSORPTION COMPOSITION
    8.
    发明申请
    PERCUTANEOUS ABSORPTION COMPOSITION 有权
    PERCUTANEOUS吸收组合物

    公开(公告)号:US20170056502A1

    公开(公告)日:2017-03-02

    申请号:US15279210

    申请日:2016-09-28

    申请人: MEDRx CO., LTD

    摘要: The embodiments provide a percutaneous absorption composition for a basic medicament having improved transdermal absorbability. The percutaneous absorption composition comprises a sorbic acid and/or a metal sorbate as a percutaneous absorption promotor. The molar ration of the sorbic acid and/or the metal sorbate to the basic medicament is 0.5-2.5. The composition of the present disclosure may further comprise a basic component.

    摘要翻译: 实施方案提供了具有改善的经皮吸收能力的碱性药物的经皮吸收组合物。 经皮吸收组合物包含作为经皮吸收促进剂的山梨酸和/或金属山梨酸酯。 山梨酸和/或金属山梨酸盐对碱性药物的摩尔比为0.5-2.5。 本公开的组合物还可以包含基本组分。

    Tizanidine therapy system
    10.
    发明授权

    公开(公告)号:US11559519B2

    公开(公告)日:2023-01-24

    申请号:US16965758

    申请日:2019-01-31

    申请人: MEDRx Co., Ltd.

    IPC分类号: A61K31/433 A61K9/70 A61K47/12

    摘要: An object of the present invention is to provide a method for the treatment of a patient suffering from spasticity comprising administering to said patient a modified release dosage form comprising tizanidine or a pharmaceutically acceptable salt thereof.
    The present invention relates to a method of administering a transdermal patch preparation comprising tizanidine or a pharmaceutically acceptable salt thereof to a subject in need thereof, wherein the transdermal patch preparation releases about 4 mg to about 36 mg of tizanidine or a pharmaceutically acceptable salt thereof for at least about 24 hours.