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49 条记录 (耗时 0.034 秒)

    TABLET COMPUTER CASE AND ASSOCIATED METHODS
    42.
    发明申请
    TABLET COMPUTER CASE AND ASSOCIATED METHODS 有权
    平板计算机及相关方法

    公开(公告)号：US20110267757A1

    公开(公告)日：2011-11-03

    申请号：US13097043

    申请日：2011-04-28

    申请人： Brian Hullinger Probst ,  David W. Osborne

    发明人： Brian Hullinger Probst ,  David W. Osborne

    IPC分类号： G06F1/16

    CPC分类号： G06F1/1654 ,  G06F1/1616 ,  G06F1/1632 ,  G06F1/1681 ,  Y10T29/49002 ,  Y10T29/4984

    摘要： Tablet computer cases and associated methods are disclosed and described. In one embodiment, a tablet computer case may include a first panel configured to releasably engage and hold a tablet computer of a predetermined size and shape, a second panel having a keyboard a hinge rotatably attaching the two panels, and a communication connector that allows the keyboard to communicate with the tablet computer.

    摘要翻译： 公开并描述了平板电脑机箱和相关方法。 在一个实施例中，平板计算机外壳可以包括构造成可释放地接合和保持具有预定尺寸和形状的平板计算机的第一面板，具有键盘的第二面板，铰链可旋转地连接两个面板，以及通信连接器， 键盘与平板电脑进行通信。

    Protectant for UV-Induced Skin Damage
    44.
    发明申请
    Protectant for UV-Induced Skin Damage 审中-公开
    紫外线诱发皮肤损伤的保护剂

    公开(公告)号：US20080262095A1

    公开(公告)日：2008-10-23

    申请号：US12133977

    申请日：2008-07-01

    申请人： David W. Osborne

    发明人： David W. Osborne

    IPC分类号： A61K31/145 ,  A61P17/00

    CPC分类号： A61K31/136 ,  A61K8/46 ,  A61Q17/04

    摘要： The present invention provides a method for protecting against UV radiation-induced skin damage. Specifically, compositions including dapsone are administered to provide UV protection. The dapsone compositions may be administered orally, or by other parenteral routes, such as topically, transdermally, by inhalation, and the like.

    摘要翻译： 本发明提供一种防止紫外线辐射诱导的皮肤损伤的方法。 具体地，施用包含氨苯砜的组合物以提供UV保护。 氨苯砜酮组合物可以口服给药或通过其它肠胃外途径给药，例如局部，透皮，吸入等。

    PHARMACEUTICAL CARRIER DEVICE SUITABLE FOR DELIVERY OF PHARMACEUTICAL COMPOUNDS TO MUCOSAL SURFACES
    45.
    发明申请
    PHARMACEUTICAL CARRIER DEVICE SUITABLE FOR DELIVERY OF PHARMACEUTICAL COMPOUNDS TO MUCOSAL SURFACES 审中-公开
    适用于向肉眼表面递送药物化合物的药物载体装置

    公开(公告)号：US20080254105A1

    公开(公告)日：2008-10-16

    申请号：US12141858

    申请日：2008-06-18

    申请人： Gilles H. Tapolsky ,  David W. Osborne

    发明人： Gilles H. Tapolsky ,  David W. Osborne

    IPC分类号： A61F13/02 ,  A61K9/00

    CPC分类号： A61K9/006 ,  A61K9/7023

    摘要： The present invention relates to a pharmaceutical delivery device for application of a pharmaceutical to mucosal surfaces. The device comprises an adhesive layer and a non-adhesive backing layer, and the pharmaceutical may be provided in either or both layers. Upon application, the device adheres to the mucosal surface, providing localized drug delivery and protection to the treatment site. The kinetics of erodability are easily adjusted by varying the number of layers and/or the components.

    摘要翻译： 本发明涉及用于将药物施用于粘膜表面的药物递送装置。 该装置包括粘合剂层和非粘性背衬层，并且药物可以在两层或两层中提供。 应用后，该装置粘附于粘膜表面，为治疗部位提供局部药物输送和保护。 可以通过改变层数和/或组分来容易地调节可蚀性的动力学。

    System for percutaneous delivery of opioid analgesics
    46.
    发明授权
    System for percutaneous delivery of opioid analgesics 有权
    用于经皮输送阿片样镇痛药的系统

    公开(公告)号：US06355657B1

    公开(公告)日：2002-03-12

    申请号：US09475094

    申请日：1999-12-30

    申请人： David W. Osborne

    发明人： David W. Osborne

    IPC分类号： A61K3147

    CPC分类号： A61K47/18 ,  A61K9/0014 ,  A61K31/451 ,  A61K47/10 ,  A61K47/12

    摘要： Compositions and methods for the topical delivery of loperamide hydrochloride are disclosed. Novel solvent mixtures have been found to be beneficial in enhancing the penetration of loperamide hydrochloride through the skin.

    摘要翻译： 公开了用于局部递送盐酸洛哌丁胺的组合物和方法。 已经发现新的溶剂混合物有利于增强盐酸洛哌丁胺通过皮肤的渗透。

    Pharmaceutical gel preparation applicable to mucosal surfaces and body tissues
    47.
    发明授权
    Pharmaceutical gel preparation applicable to mucosal surfaces and body tissues 失效
    适用于粘膜表面和身体组织的药物凝胶制剂

    公开(公告)号：US6103266A

    公开(公告)日：2000-08-15

    申请号：US64433

    申请日：1998-04-22

    申请人： Gilles H. Tapolsky ,  David W. Osborne

    发明人： Gilles H. Tapolsky ,  David W. Osborne

    IPC分类号： A61K9/70 ,  A61K9/14 ,  A01N25/00 ,  A61K47/00

    CPC分类号： A61K9/7015

    摘要： The present invention relates to a non water-soluble pharmaceutical carrier gel which adheres to mucosal surfaces and body tissues upon application and forms a film, providing protection and delivery of pharmaceutical to the site of application, surrounding body tissues, and bodily fluids. The gel comprises a volatile or diffusing nonaqueous solvent and at least one non-water-soluble alkyl cellulose or hydroxyalkyl cellulose. A bioadhesive polymer may also be added. The gel provides an effective residence time with ease of use. The residence time may be adjusted by adding a component which acts to adjust the kinetics of erodability of the carrier.

    摘要翻译： 本发明涉及一种非水溶性药物载体凝胶，其在施用时粘附于粘膜表面和身体组织并形成膜，从而提供药物到施用部位，周围身体组织和体液的保护和递送。 凝胶包含挥发性或扩散性非水溶剂和至少一种非水溶性烷基纤维素或羟烷基纤维素。 还可以加入生物粘附聚合物。 凝胶提供有效的停留时间，易于使用。 可以通过添加用于调节载体的可侵蚀性的动力学的成分来调整停留时间。

    Pharmaceutical preparation applicable to mucosal surfaces and body tissues
    48.
    发明授权
    Pharmaceutical preparation applicable to mucosal surfaces and body tissues 失效
    适用于粘膜表面和身体组织的药物制剂

    公开(公告)号：US5955097A

    公开(公告)日：1999-09-21

    申请号：US733454

    申请日：1996-10-18

    申请人： Gilles H. Tapolsky ,  David W. Osborne

    发明人： Gilles H. Tapolsky ,  David W. Osborne

    IPC分类号： A61K9/00 ,  A61K9/70 ,  A61K47/38 ,  A61F13/00 ,  A61K9/14

    CPC分类号： A61K9/7015 ,  A61K9/006

    摘要： The present invention relates to a non water-soluble pharmaceutical carrier gel which adheres to mucosal surfaces and body tissues upon application and forms a film, providing protection and delivery of pharmaceutical to the site of application, surrounding body tissues, and bodily fluids. The gel comprises a volatile or diffusing nonaqueous solvent and at least one non-water-soluble alkyl cellulose or hydroxyalkyl cellulose. A bioadhesive polymer may also be added. The gel provides an effective residence time with ease of use.

    摘要翻译： 本发明涉及一种非水溶性药物载体凝胶，其在施用时粘附于粘膜表面和身体组织并形成膜，从而提供药物到施用部位，周围身体组织和体液的保护和递送。 凝胶包含挥发性或扩散性非水溶剂和至少一种非水溶性烷基纤维素或羟烷基纤维素。 还可以加入生物粘附聚合物。 凝胶提供有效的停留时间，易于使用。