System and method for optimizing tissue barrier transfer of compounds
    4.
    发明授权
    System and method for optimizing tissue barrier transfer of compounds 失效
    用于优化化合物组织阻挡转移的系统和方法

    公开(公告)号:US06758099B2

    公开(公告)日:2004-07-06

    申请号:US09904725

    申请日:2001-07-13

    IPC分类号: G01F100

    摘要: The present invention relates to high-throughput systems and methods to prepare a large number of component combinations, at varying concentrations and identities, at the same time, and high-throughput methods to test tissue barrier transfer, such as transdermal transfer, of components in each combination. The methods of the present invention allow determination of the effects of inactive components, such as solvents, excipients, enhancers, adhesives and additives, on tissue barrier transfer of active components, such as pharmaceuticals. The invention thus encompasses the high-throughput testing of pharmaceutical compositions or formulations in order to determine the overall optimal composition or formulation for improved tissue transport, such as transdermal transport.

    摘要翻译: 本发明涉及高通量系统和方法,以同时以不同的浓度和同一性制备大量组分组合,以及高通量方法来测试组织屏障转移,例如透皮转移 每个组合。 本发明的方法允许测定非活性组分如溶剂,赋形剂,增强剂,粘合剂和添加剂对活性组分如药物的组织屏障转移的影响。 因此,本发明包括药物组合物或制剂的高通量测试,以便确定用于改善组织转运的总体最佳组合物或制剂,例如透皮转运。

    Transdermal assay with magnetic clamp
    5.
    发明授权
    Transdermal assay with magnetic clamp 失效
    用磁夹进行透皮测定

    公开(公告)号:US06852526B2

    公开(公告)日:2005-02-08

    申请号:US10282505

    申请日:2002-10-28

    摘要: The transdermal assay apparatus includes first, second, and third members. The first member has one or more sample surfaces, each of which is configured to receive a sample thereon. The second member defines one or more reservoirs, each of which has an opening on a surface of the second member. Each sample surface is substantially the same size as each opening. The transdermal assay apparatus also includes a magnetic clamp configured to clamp a tissue specimen between the sample surface and the opening. The magnetic clamp preferably includes a magnet having a strength that is selected based on the clamping force required between the first member and the second member. The invention also provides a method for using a transdermal assay apparatus.

    摘要翻译: 透皮测定装置包括第一,第二和第三构件。 第一构件具有一个或多个样品表面,每个样品表面被配置为在其上接收样品。 第二构件限定一个或多个储存器,每个储存器在第二构件的表面上具有开口。 每个样品表面的大小与每个开口大致相同。 透皮测定装置还包括构造成在样品表面和开口之间夹持组织样本的磁性夹具。 磁夹具优选地包括具有基于第一构件和第二构件之间所需的夹紧力选择的强度的磁体。 本发明还提供了一种使用透皮测定装置的方法。

    System and method for optimizing tissue barrier transfer of compounds
    6.
    发明授权
    System and method for optimizing tissue barrier transfer of compounds 失效
    用于优化化合物组织阻挡转移的系统和方法

    公开(公告)号:US07172859B2

    公开(公告)日:2007-02-06

    申请号:US10371372

    申请日:2003-02-20

    IPC分类号: C12Q1/00

    CPC分类号: G01N33/5088 G01N13/00

    摘要: The present invention relates to high-throughput systems and methods to prepare a large number of component combinations, at varying concentrations and identities, at the same time, and high-throughput methods to test tissue barrier transfer, such as transdermal transfer, of components in each combination. The methods of the present invention allow determination of the effects of inactive components, such as solvents, excipients, enhancers, adhesives and additives, on tissue barrier transfer of active components, such as pharmaceuticals. The invention thus encompasses the high-throughput testing of pharmaceutical compositions or formulations in order to determine the overall optimal composition or formulation for improved tissue transport, such as transdermal transport.

    摘要翻译: 本发明涉及高通量系统和方法,以同时以不同的浓度和同一性制备大量组分组合,以及高通量方法来测试组织屏障转移,例如透皮转移 每个组合。 本发明的方法允许测定非活性组分如溶剂,赋形剂,增强剂,粘合剂和添加剂对活性组分如药物的组织屏障转移的影响。 因此,本发明包括药物组合物或制剂的高通量测试,以便确定用于改善组织转运的总体最佳组合物或制剂,例如透皮转运。

    Implantable device for controlled drug delivery
    8.
    发明授权
    Implantable device for controlled drug delivery 有权
    用于受控药物输送的可植入装置

    公开(公告)号:US09017312B2

    公开(公告)日:2015-04-28

    申请号:US12851494

    申请日:2010-08-05

    摘要: Implantable devices and methods for delivery of lidocaine or other drugs to a patient are provided. In one embodiment, the device includes a first drug portion which has a first drug housing which contains a first drug formulation in a solid form which includes a pharmaceutically acceptable salt of lidocaine; and a second drug portion which includes a second drug housing which contains a second drug formulation which includes lidocaine base. In another embodiment, the device includes a drug reservoir component which has an elastic tube having at least one lumen bounded by a porous sidewall having an open-cell structure, a closed-cell structure, or a combination thereof; and a drug formulation contained within the at least one lumen, wherein the device is deformable between a low-profile deployment shape and a relatively expanded retention shape.

    摘要翻译: 提供了用于将利多卡因或其他药物递送给患者的可植入装置和方法。 在一个实施方案中,该装置包括第一药物部分,其具有第一药物外壳,其包含固体形式的第一药物制剂,其包含利多卡因的药学上可接受的盐; 和第二药物部分,其包括含有包含利多卡因碱的第二药物制剂的第二药物外壳。 在另一个实施方案中,该装置包括药物储存器部件,该药物储存器部件具有弹性管,该弹性管具有由具有开孔结构,闭孔结构或其组合的多孔侧壁限定的至少一个内腔; 以及包含在所述至少一个内腔内的药物制剂,其中所述装置可在低轮廓展开形状和相对扩张的保留形状之间变形。

    Time-selective bioresorbable or collapsible drug delivery systems and methods
    10.
    发明授权
    Time-selective bioresorbable or collapsible drug delivery systems and methods 有权
    时间选择性生物可吸收或可折叠药物递送系统和方法

    公开(公告)号:US08690840B2

    公开(公告)日:2014-04-08

    申请号:US13267560

    申请日:2011-10-06

    IPC分类号: A61M31/00

    摘要: Implantable medical devices and treatment methods are provided, particularly for use in the bladder. The device is configured for retention in the bladder for at least a portion of the drug delivery period and includes at least one biodegradable component such that following a biodegradation at a selected time, the retention function is lost and the device or portions thereof are resorbed and/or excreted. The method may include deploying into the bladder of a patient a device having a device structure housing a drug formulation comprising at a drug; releasing drug from the device structure into the bladder; and then, changing the composition of urine in the bladder, e.g., by altering the pH, to trigger degradation of at least part of the device structure to enable the device structure or parts thereof to be excreted from the bladder.

    摘要翻译: 提供了可植入的医疗装置和治疗方法,特别用于膀胱。 该装置构造成在膀胱中保留药物递送期的至少一部分,并且包括至少一种可生物降解的组分,使得在选定时间内经过生物降解后,保留功能丧失并且其装置或部分被吸收, /或排泄。 该方法可以包括向患者的膀胱中部署具有容纳包含药物的药物制剂的装置结构的装置; 将药物从装置结构释放到膀胱中; 然后,例如通过改变pH来改变膀胱中尿液的组成,以触发装置结构的至少一部分的降解,使装置结构或其部分能够从膀胱排出。