PORTABLE MOBILE LIGHT STAGE
    3.
    发明申请
    PORTABLE MOBILE LIGHT STAGE 有权
    便携式手提灯

    公开(公告)号:US20130314502A1

    公开(公告)日:2013-11-28

    申请号:US13830665

    申请日:2013-03-14

    IPC分类号: H04N7/18

    摘要: A subject is imaged using imaging equipment arranged on portable, wireless vehicles. The vehicles are positioned in a pattern in proximity to the subject and illuminate the subject in order to collect image data. The image data can be collected by cameras carried by the vehicles in addition to or instead of external high speed cameras.

    摘要翻译: 使用布置在便携式无线车辆上的成像设备对被摄体进行成像。 车辆定位在靠近被摄体的图案中并照亮被摄体以便收集图像数据。 图像数据可以由除了外部高速摄像机之外的车辆或由外部高速摄像机代替的车辆携带的摄像机来收集。

    Method and device for the iontophoretic delivery of a drug
    6.
    发明申请
    Method and device for the iontophoretic delivery of a drug 有权
    药物离子电渗疗法的方法和装置

    公开(公告)号:US20070100317A1

    公开(公告)日:2007-05-03

    申请号:US11586818

    申请日:2006-10-25

    IPC分类号: A61N1/30 A61M31/00

    摘要: An iontophoretic drug delivery device storage apparatus and a method of using that device is disclosed. The device comprises a fluid reservoir, an electrode assembly and a tray apparatus. The fluid reservoir is capable of retaining a medicament and has a sealed fluid chamber defined by at least one seal. The seal includes a weaker region and a pinch-like configuration associated with that region such that application of pressure to the fluid reservoir breaks the weaker region of the seal, releasing the retained medicament. The electrode assembly comprises an active electrode, at least two passive electrodes a medicament carrying region, and a moat region around the medicament carrying region so that once fluid is delivered from the fluid reservoir to the electrode assembly the fluid is substantially retained in the medicament carrying means.

    摘要翻译: 公开了一种离子电渗药物输送装置的储存装置及其使用方法。 该装置包括流体储存器,电极组件和托盘装置。 流体储存器能够保持药物并且具有由至少一个密封件限定的密封流体室。 密封件包括与该区域相关联的较弱区域和夹紧形状,使得向流体储存器施加压力破坏密封件的较弱区域,释放保留的药剂。 电极组件包括有源电极,至少两个钝化电极,药物承载区域,以及围绕药物承载区域的护城河区域,使得一旦流体从流体储存器输送到电极组件,流体基本上保留在携带 手段。

    Indole, azaindole and related heterocyclic N-substituted piperazine derivatives
    8.
    发明授权
    Indole, azaindole and related heterocyclic N-substituted piperazine derivatives 有权
    吲哚,氮杂吲哚和相关杂环N-取代的哌嗪衍生物

    公开(公告)号:US08039486B2

    公开(公告)日:2011-10-18

    申请号:US12028189

    申请日:2008-02-08

    IPC分类号: A61K31/04 C07D215/38

    摘要: This invention provides compounds of Formula I, including pharmaceutically acceptable salts thereof, having drug and bio-affecting properties, their pharmaceutical compositions and method of use. These compounds possess unique antiviral activity, whether used alone or in combination with other antivirals, antiinfectives, immunomodulators or HIV entry inhibitors. More particularly, the present invention relates to the treatment of HIV and AIDS. The compounds of Formula I have the formula wherein: Z is Q is selected from the group consisting of m is 2; A is selected from the group consisting of cinnolinyl, napthyridinyl, quinoxalinyl, pyridinyl, pyrimidinyl, quinolinyl, isoquinolinyl, quinazolinyl, azabenzofuryl, and phthalazinyl each of which may be optionally substituted with one or two groups independently selected from methyl, methoxy, hydroxy, amino and halogen; and —W— is

    摘要翻译: 本发明提供具有药物和生物影响性质的式I化合物,包括其药学上可接受的盐,其药物组合物和使用方法。 这些化合物具有独特的抗病毒活性,无论是单独使用还是与其他抗病毒药,抗感染剂,免疫调节剂或HIV进入抑制剂组合使用。 更具体地说,本发明涉及艾滋病毒和艾滋病的治疗。 式I的化合物具有下式:其中:Z为Q选自m为2; A选自噌啉基,萘啶基,喹喔啉基,吡啶基,嘧啶基,喹啉基,异喹啉基,喹唑啉基,氮杂苯并呋喃基和酞嗪基,其各自可以任选被一个或两个独立地选自甲基,甲氧基,羟基,氨基 和卤素; 和-W-是

    Indole, azaindole and related heterocyclic ureido and thioureido piperazine derivatives
    9.
    发明申请
    Indole, azaindole and related heterocyclic ureido and thioureido piperazine derivatives 审中-公开
    吲哚,氮杂吲哚和相关杂环脲基和硫脲基哌嗪衍生物

    公开(公告)号:US20060094717A1

    公开(公告)日:2006-05-04

    申请号:US11304183

    申请日:2005-12-15

    摘要: This invention provides compounds having drug and bio-affecting properties, their pharmaceutical compositions and method of use. In particular, the invention is concerned with ureido and thioureido piperazine derivatives of Formula I. These compounds possess unique antiviral activity, whether used alone or in combination with other antivirals, antiinfectives, immunomodulators or HIV entry inhibitors. More particularly, the present invention relates to the treatment of HIV and AIDS. The compounds of Formula I are wherein: Y is O or S; Q is selected from the group consisting of m is 2; A is NR13R14; and —W— is

    摘要翻译: 本发明提供具有药物和生物影响性质的化合物,其药物组合物和使用方法。 特别地,本发明涉及式I的脲基和硫脲基哌嗪衍生物。这些化合物具有独特的抗病毒活性,无论是单独使用还是与其它抗病毒剂,抗感染剂,免疫调节剂或HIV进入抑制剂组合使用。 更具体地说,本发明涉及艾滋病毒和艾滋病的治疗。 式I的化合物是其中:Y是O或S; Q选自m为2; A是NR 13 R 14; 和-W-是