Injectable depot formulation comprising crystals of iloperidone
    2.
    发明申请
    Injectable depot formulation comprising crystals of iloperidone 审中-公开
    包含伊潘立酮晶体的可注射贮库制剂

    公开(公告)号:US20050250813A1

    公开(公告)日:2005-11-10

    申请号:US10521064

    申请日:2003-07-14

    摘要: An injectable depot formulation comprising crystals having Structure (I) wherein R is (FII) and the X50 value of the crystals is from 1 to 200 microns. Depot formulations containing crystals of iloperidone or its metabolite have the following advantages: (i) release of the crystals in plasma can be correlated with the size of the crystals; (ii) absorption of the crystals in plasma can be correlated with the size of the crystals; (iii) the particle size of the crystals can be controlled by crystal engineering and/or milling; and (iv) the crystals are stable upon storage, and stable to sterilization procedures, such as gamma irradiation.

    摘要翻译: 包含具有结构(I)的晶体的可注射贮库制剂,其中R为(FII)且晶体的X 50值为1至200微米。 含有伊洛哌啶或其代谢物晶体的储备制剂具有以下优点:(i)等离子体中晶体的释放可与晶体尺寸相关; (ii)等离子体中的晶体的吸收可以与晶体的大小相关; (iii)可以通过晶体工程和/或研磨来控制晶体的粒度; 和(iv)晶体在储存时是稳定的,并且对灭菌过程如γ辐射是稳定的。

    Injectable depot formulation comprising crystals of iloperidone
    3.
    发明授权
    Injectable depot formulation comprising crystals of iloperidone 有权
    包含伊潘立酮晶体的可注射贮库制剂

    公开(公告)号:US08293765B2

    公开(公告)日:2012-10-23

    申请号:US13106417

    申请日:2011-05-12

    摘要: An injectable depot formulation comprising crystals having structure (I) wherein R is (FII) and the X50 value of the crystals is from 1 to 200 microns. Depot formulations containing crystals of iloperidone or its metabolites have the following advantages: (i) release of the crystals in plasma can be correlated with the size of the crystals; (ii) absorption of the crystals in plasma can be correlated with the size of the crystals; (iii) the particle size of the crystals can be controlled by crystal engineering and/or milling; and (iv) the crystals are stable upon storage, and stable to sterilization procedures, such as gamma irradiation.

    摘要翻译: 包含具有结构(I)的晶体的可注射贮库制剂,其中R为(FII)且晶体的X 50值为1至200微米。 含有伊立替康或其代谢物晶体的储备制剂具有以下优点:(i)等离子体中晶体的释放可与晶体尺寸相关; (ii)等离子体中的晶体的吸收可以与晶体的大小相关; (iii)可以通过晶体工程和/或研磨来控制晶体的粒度; 和(iv)晶体在储存时是稳定的,并且对灭菌过程如γ辐射是稳定的。

    INJECTABLE DEPOT FORMULATION COMPRISING CRYSTALS OF ILOPERIDONE
    5.
    发明申请
    INJECTABLE DEPOT FORMULATION COMPRISING CRYSTALS OF ILOPERIDONE 有权
    包含ILOPERIDONE晶体的注射剂配方

    公开(公告)号:US20110212141A1

    公开(公告)日:2011-09-01

    申请号:US13106417

    申请日:2011-05-12

    IPC分类号: A61K9/14 A61K31/454 A61P25/18

    摘要: An injectable depot formulation comprising crystals having structure (I) wherein R is (FII) and the X50 value of the crystals is from 1 to 200 microns. Depot formulations containing crystals of iloperidone or its metabolites have the following advantages: (i) release of the crystals in plasma can be correlated with the size of the crystals; (ii) absorption of the crystals in plasma can be correlated with the size of the crystals; (iii) the particle size of the crystals can be controlled by crystal engineering and/or milling; and (iv) the crystals are stable upon storage, and stable to sterilization procedures, such as gamma irradiation.

    摘要翻译: 包含具有结构(I)的晶体的可注射贮库制剂,其中R为(FII)且晶体的X 50值为1至200微米。 含有伊立替康或其代谢物晶体的储备制剂具有以下优点:(i)等离子体中晶体的释放可与晶体尺寸相关; (ii)等离子体中的晶体的吸收可以与晶体的大小相关; (iii)可以通过晶体工程和/或研磨来控制晶体的粒度; 和(iv)晶体在储存时是稳定的,并且对灭菌过程如γ辐射是稳定的。

    Injectable depot formulation comprising crystals of iloperidone
    6.
    发明授权
    Injectable depot formulation comprising crystals of iloperidone 有权
    包含伊潘立酮晶体的可注射贮库制剂

    公开(公告)号:US08614232B2

    公开(公告)日:2013-12-24

    申请号:US13618753

    申请日:2012-09-14

    摘要: An injectable depot formulation comprising crystals having structure (I) wherein R is (FII) and the X50 value of the crystals is from 1 to 200 microns. Depot formulations containing crystals of iloperidone or its metabolites have the following advantages: (i) release of the crystals in plasma can be correlated with the size of the crystals; (ii) absorption of the crystals in plasma can be correlated with the size of the crystals; (iii) the particle size of the crystals can be controlled by crystal engineering and/or milling; and (iv) the crystals are stable upon storage, and stable to sterilization procedures, such as gamma irradiation.

    摘要翻译: 包含具有结构(I)的晶体的可注射贮库制剂,其中R为(FII)且晶体的X 50值为1至200微米。 含有伊立替康或其代谢物晶体的储备制剂具有以下优点:(i)等离子体中晶体的释放可与晶体尺寸相关; (ii)等离子体中的晶体的吸收可以与晶体的大小相关; (iii)可以通过晶体工程和/或研磨来控制晶体的粒度; 和(iv)晶体在储存时是稳定的,并且对灭菌过程如γ辐射是稳定的。

    INJECTABLE DEPOT FORMULATION COMPRISING CRYSTALS OF ILOPERIDONE
    7.
    发明申请
    INJECTABLE DEPOT FORMULATION COMPRISING CRYSTALS OF ILOPERIDONE 有权
    包含ILOPERIDONE晶体的注射剂配方

    公开(公告)号:US20120156264A1

    公开(公告)日:2012-06-21

    申请号:US13401310

    申请日:2012-02-21

    摘要: An injectable depot formulation comprising crystals having structure (I) wherein R is (FII) and the X50 value of the crystals is from 1 to 200 microns. Depot formulations containing crystals of iloperidone or its metabolites have the following advantages: (i) release of the crystals in plasma can be correlated with the size of the crystals; (ii) absorption of the crystals in plasma can be correlated with the size of the crystals; (iii) the particle size of the crystals can be controlled by crystal engineering and/or milling; and (iv) the crystals are stable upon storage, and stable to sterilization procedures, such as gamma irradiation.

    摘要翻译: 包含具有结构(I)的晶体的可注射贮库制剂,其中R为(FII)且晶体的X 50值为1至200微米。 含有伊立替康或其代谢物晶体的储备制剂具有以下优点:(i)等离子体中晶体的释放可与晶体尺寸相关; (ii)等离子体中的晶体的吸收可以与晶体的大小相关; (iii)可以通过晶体工程和/或研磨来控制晶体的粒度; 和(iv)晶体在储存时是稳定的,并且对灭菌过程如γ辐射是稳定的。

    INJECTABLE DEPOT FORMULATION COMPRISING CRYSTALS OF ILOPERIDONE
    8.
    发明申请
    INJECTABLE DEPOT FORMULATION COMPRISING CRYSTALS OF ILOPERIDONE 审中-公开
    包含ILOPERIDONE晶体的注射剂配方

    公开(公告)号:US20090099232A1

    公开(公告)日:2009-04-16

    申请号:US12254925

    申请日:2008-10-21

    IPC分类号: A61K31/454

    摘要: An injectable depot formulation comprising crystals having structure (I) wherein R is (FII) and the X50 value of the crystals is from 1 to 200 microns. Depot formulations containing crystals of iloperidone or its metabolites have the following advantages: (i) release of the crystals in plasma can be correlated with the size of the crystals; (ii) absorption of the crystals in plasma can be correlated with the size of the crystals; (iii) the particle size of the crystals can be controlled by crystal engineering and/or milling; and (iv) the crystals are stable upon storage, and stable to sterilization procedures, such as gamma irradiation.

    摘要翻译: 包含具有结构(I)的晶体的可注射贮库制剂,其中R为(FII)且晶体的X 50值为1至200微米。 含有伊立替康或其代谢物晶体的储备制剂具有以下优点:(i)等离子体中晶体的释放可与晶体尺寸相关; (ii)等离子体中的晶体的吸收可以与晶体的大小相关; (iii)可以通过晶体工程和/或研磨来控制晶体的粒度; 和(iv)晶体在储存时是稳定的,并且对灭菌过程如γ辐射是稳定的。

    Process for modifying drug crystal formation
    9.
    发明授权
    Process for modifying drug crystal formation 有权
    改变药物晶体形成的方法

    公开(公告)号:US08124795B2

    公开(公告)日:2012-02-28

    申请号:US13198022

    申请日:2011-08-04

    IPC分类号: C07D307/78

    摘要: A process for modifying the crystal habit of acicular drug substances, crystals obtained by such a process, and particular crystal forms or modifications of mycophenolic acid or mycophenolate sodium are provided, as well as pharmaceutical compositions comprising the crystals, methods of treatment and uses thereof.

    摘要翻译: 提供了一种改变针状药物晶体习性的方法,通过这种方法获得的晶体,以及特定的霉酚酸或霉酚酸钠的晶型或改性物,以及包含晶体,治疗方法及其用途的药物组合物。

    PROCESS FOR MODIFYING DRUG CRYSTAL FORMATION
    10.
    发明申请
    PROCESS FOR MODIFYING DRUG CRYSTAL FORMATION 有权
    改造药物结晶的方法

    公开(公告)号:US20110288313A1

    公开(公告)日:2011-11-24

    申请号:US13198022

    申请日:2011-08-04

    IPC分类号: C07D307/88

    摘要: A process for modifying the crystal habit of acicular drug substances, crystals obtained by such a process, and particular crystal forms or modifications of mycophenolic acid or mycophenolate sodium are provided, as well as pharmaceutical compositions comprising the crystals, methods of treatment and uses thereof.

    摘要翻译: 提供了一种改变针状药物晶体习性的方法,通过这种方法获得的晶体,以及特定的霉酚酸或霉酚酸钠的晶型或改性物,以及包含晶体,治疗方法及其用途的药物组合物。