SALTS OF DASATINIB IN CRYSTALLINE FORM
    1.
    发明申请
    SALTS OF DASATINIB IN CRYSTALLINE FORM 审中-公开
    DASATINIB在结晶形式中的作用

    公开(公告)号:WO2015011120A3

    公开(公告)日:2015-04-16

    申请号:PCT/EP2014065675

    申请日:2014-07-22

    Applicant: BASF SE

    CPC classification number: C07D417/12 C07B2200/13 C07D275/06

    Abstract: The present invention primarily relates to molecular crystalline substances, preferably salts of Dasatinib in crystalline form, comprising a compound of formula 1, preferably a cation of a compound of formula 1, and a second compound selected from the group consisting of glutaric acid, nicotinic acid and saccharin, preferably an anion thereof. The invention is further related to pharmaceutical compositions comprising such a substance. Furthermore, the invention relates to processes for preparing said substances. The invention also relates to several aspects of using said substances or pharmaceutical compositions to treat a disease.

    Abstract translation: 本发明主要涉及分子结晶物质,优选结晶形式的达沙替尼盐,其包含式1化合物,优选式1化合物的阳离子和选自戊二酸,烟酸 和糖精,优选其阴离子。 本发明还涉及包含这种物质的药物组合物。 此外,本发明涉及制备所述物质的方法。 本发明还涉及使用所述物质或药物组合物治疗疾病的若干方面。

    SALTS OF DASATINIB IN AMORPHOUS FORM
    3.
    发明申请
    SALTS OF DASATINIB IN AMORPHOUS FORM 审中-公开
    非那西丁盐以非晶形式存在

    公开(公告)号:WO2015011119A2

    公开(公告)日:2015-01-29

    申请号:PCT/EP2014065674

    申请日:2014-07-22

    Applicant: BASF SE

    CPC classification number: C07D417/12 C07C55/12 C07D213/80 C07D275/06

    Abstract: The present invention primarily relates to salts of Dasatinib, wherein the salts are in amorphous form. The salts described herein preferably comprise a cation of a compound of formula 1 and an anion of a second compound selected from the group consisting of glutaric acid, nicotinic acid and saccharin. The invention is further related to pharmaceutical compositions comprising such a salt. Furthermore, the invention relates to processes for preparing said salts. The invention also relates to several aspects of using said salt or pharmaceutical composition to treat a disease.

    Abstract translation: 本发明主要涉及达沙替尼的盐,其中盐为无定形形式。 本文所述的盐优选包含式1化合物的阳离子和选自戊二酸,烟酸和糖精的第二化合物的阴离子。 本发明还涉及包含这种盐的药物组合物。 此外,本发明涉及制备所述盐的方法。 本发明还涉及使用所述盐或药物组合物治疗疾病的几个方面。

    HYDROPHOBINS AS SURFACE ACTIVE PROTEINS AS EXCIPIENTS IN SOLID PHARMACEUTICAL FORMULATIONS
    4.
    发明申请
    HYDROPHOBINS AS SURFACE ACTIVE PROTEINS AS EXCIPIENTS IN SOLID PHARMACEUTICAL FORMULATIONS 审中-公开
    作为表面活性蛋白的水解物作为固体药物制剂中的主要成分

    公开(公告)号:WO2010060811A3

    公开(公告)日:2010-10-21

    申请号:PCT/EP2009065100

    申请日:2009-11-13

    Abstract: The invention relates to a use of surface active hydrophobins for applications in pharmaceutical technology, in particular as excipients for galenic use. Provided is a method for either admixture of hydrophobins to galenic compositions or for treating the surface of pharmaceutical forms with a hydrophobin-containing solution to modify the pharmaceutical properties of the galenic form. In a preferred embodiment of the invention hydrophobins are used to improve the properties of a pharmaceutical composition, e. g. to act as a surfactant or to increase resistance to disintegration of the galenic forms to achieve a retarded drug release. The galenic form to be modified by the use of surface active proteins as excipients can be capsules, tablets, pills, microparticles, vesicles, and suppositories, although further galenic forms are envisioned. The surface active proteins used for the purpose of present invention can either be isolated from their respective natural source or prepared by recombinant techniques and expression in a suitable host.

    Abstract translation: 本发明涉及用于制药技术中的表面活性疏水蛋白的用途,特别是作为涂覆液使用的赋形剂。 提供了将疏水蛋白与盖仑组合物混合或用含疏水蛋白的溶液处理药物形式的表面以改变盖仑膜形式的药物性质的方法。 在本发明的优选实施方案中,疏水蛋白用于改善药物组合物的性质,例如, G。 作为表面活性剂或增加耐受霜冻形式的崩解以实现延缓药物释放。 通过使用表面活性蛋白质作为赋形剂来修饰的盖仑形式可以是胶囊,片剂,丸剂,微粒,囊泡和栓剂,尽管可以预见到更多的盖仑制剂形式。 用于本发明目的的表面活性蛋白质可以从它们各自的天然来源中分离或者通过重组技术制备并在合适的宿主中表达。

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