METHOD FOR PRODUCING PARTICLES
    1.
    发明申请
    METHOD FOR PRODUCING PARTICLES 审中-公开
    生产颗粒的方法

    公开(公告)号:WO2017150692A1

    公开(公告)日:2017-09-08

    申请号:PCT/JP2017/008384

    申请日:2017-03-02

    Abstract: A method for producing particles, the method including: applying vibration to a liquid including a physiologically active substance and included in a liquid-column resonance liquid-chamber to form a standing wave based on liquid column resonance, to thereby discharge the liquid from at least one discharging port, which is formed in an amplitude direction of the standing wave, to at least one region corresponding to at least one anti-node of the standing wave; and drying the liquid discharged, to thereby form particles.

    Abstract translation: 一种制造颗粒的方法,所述方法包括:向包含生理活性物质的液体施加振动并将其包括在液柱共振液体室中以基于液柱共振形成驻波, 由此将液体从在驻波的振幅方向上形成的至少一个排出口排出到与驻波的至少一个波腹对应的至少一个区域; 干燥排出的液体,从而形成颗粒。

    Solid dispersion
    8.
    发明授权

    公开(公告)号:US11234984B2

    公开(公告)日:2022-02-01

    申请号:US16765575

    申请日:2018-11-28

    Abstract: The present invention relates to a solid dispersion containing a compound represented by General Formula (I): wherein R1 is an unsubstituted phenyl group or a phenyl group substituted with a substituent; the substituent is an alkyl group having 1 to 8 carbon atoms, an alkyl group having 1 to 8 carbon atoms substituted with a halogen atom, an alkoxy group having 1 to 8 carbon atoms, an alkoxycarbonyl group having 2 to 8 carbon atoms, a formyl group, a carboxyl group, a halogen atom, a phenyl group or a phenoxy group; R2 is a cyano group or a nitro group; R3 is a hydroxyl group; X is an oxygen atom or —S(O)n—; n is an integer of 0 to 2; Y is an oxygen atom or a sulfur atom, or a pharmaceutically acceptable salt thereof and a hypromellose derivative.

    SOLID DISPERSION
    9.
    发明申请
    SOLID DISPERSION 审中-公开

    公开(公告)号:US20200306251A1

    公开(公告)日:2020-10-01

    申请号:US16765575

    申请日:2018-11-28

    Abstract: The present invention relates to a solid dispersion containing a compound represented by General Formula (1): wherein R1 is an unsubstituted phenyl group or a phenyl group substituted with a substituent; the substituent is an alkyl group having 1 to 8 carbon atoms, an alkyl group having 1 to 8 carbon atoms substituted with a halogen atom, an alkoxy group having 1 to 8 carbon atoms, an alkoxycarbonyl group having 2 to 8 carbon atoms, a formyl group, a carboxyl group, a halogen atom, a phenyl group or a phenoxy group; R2 is a cyano group or a nitro group; R3 is a hydroxyl group; X is an oxygen atom or —S(O)n—; n is an integer of 0 to 2; Y is an oxygen atom or a sulfur atom, or a pharmaceutically acceptable salt thereof and a hypromellose derivative.

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