Ocular implant with hydrogel expansion capabilities
    1.
    发明授权
    Ocular implant with hydrogel expansion capabilities 有权
    眼部植入物具有水凝胶扩张能力

    公开(公告)号:US09585789B2

    公开(公告)日:2017-03-07

    申请号:US13365175

    申请日:2012-02-02

    IPC分类号: A61F9/007

    摘要: An ocular implant includes an elongate member having an internal lumen forming a flow pathway that provides a fluid pathway between the anterior chamber and the suprachoroidal space of the eye. The implant includes a hydrogel member attached to the elongate member, wherein the hydrogel member is adapted to expand upon implantation of the elongate member in the eye. An attachment attaches the hydrogel member to the elongate member.

    摘要翻译: 眼部植入物包括细长构件,其具有形成流动路径的内部内腔,所述流动路径在眼睛的前房和脉管外空间之间提供流体通路。 所述植入物包括连接到所述细长构件的水凝胶构件,其中所述水凝胶构件适于在细长构件植入眼中时扩张。 附件将水凝胶构件附接到细长构件。

    Ocular implant with hydrogel expansion capabilities
    2.
    发明授权
    Ocular implant with hydrogel expansion capabilities 有权
    眼部植入物具有水凝胶扩张能力

    公开(公告)号:US08672870B2

    公开(公告)日:2014-03-18

    申请号:US12175294

    申请日:2008-07-17

    IPC分类号: A61M5/00 A61M35/00

    摘要: An ocular implant includes an elongate member having an internal lumen forming a flow pathway that provides a fluid pathway between the anterior chamber and the suprachoroidal space of the eye. The implant includes a hydrogel member attached to the elongate member, wherein the hydrogel member is adapted to expand upon implantation of the elongate member in the eye. An attachment attaches the hydrogel member to the elongate member.

    摘要翻译: 眼部植入物包括细长构件,其具有形成流动路径的内部内腔,所述流动路径在眼睛的前房和脉管外空间之间提供流体通路。 所述植入物包括连接到所述细长构件的水凝胶构件,其中所述水凝胶构件适于在细长构件植入眼中时扩张。 附件将水凝胶构件附接到细长构件。

    Drug cores for sustained release of therapeutic agents
    7.
    发明授权
    Drug cores for sustained release of therapeutic agents 有权
    用于持续释放治疗剂的药物核心

    公开(公告)号:US08628792B2

    公开(公告)日:2014-01-14

    申请号:US13367823

    申请日:2012-02-07

    IPC分类号: A61F2/00 B28B11/12

    摘要: A solid drug core insert can be manufactured by injecting a liquid mixture comprising a therapeutic agent and a matrix precursor into a sheath body. The injection can be conducted at subambient temperatures. The mixture is cured to form a solid drug-matrix core. The therapeutic agent can be a liquid at about room temperature that forms a dispersion of droplets in the matrix material. A surface of the solid drug core is exposed, for example by cutting the tube, and the exposed surface of the solid drug core releases therapeutic quantities of the therapeutic agent when implanted into the patient. In some embodiments, the insert body inhibits release of the therapeutic agent, for example with a material substantially impermeable to the therapeutic agent, such that the therapeutic quantities are released through the exposed surface, thereby avoiding release of the therapeutic agent to non-target tissues.

    摘要翻译: 可以通过将包含治疗剂和基质前体的液体混合物注入鞘体来制造固体药物核心插入物。 注射可以在低于环境温度下进行。 将混合物固化以形成固体药物基质核心。 治疗剂可以是在约室温下的液体,其形成液滴在基质材料中的分散体。 固体药物核心的表面例如通过切割管而暴露,并且固体药物核心的暴露表面在植入患者体内释放治疗剂量。 在一些实施方案中,插入体抑制治疗剂的释放,例如具有对治疗剂基本上不可渗透的材料,使得治疗量通过暴露表面释放,从而避免将治疗剂释放到非靶组织 。

    Method of preventing proliferation of retinal pigment epithelium by retinoic acid receptor agonists
    8.
    发明授权
    Method of preventing proliferation of retinal pigment epithelium by retinoic acid receptor agonists 失效
    视黄酸受体激动剂预防视网膜色素上皮细胞增生的方法

    公开(公告)号:US06372753B1

    公开(公告)日:2002-04-16

    申请号:US09536221

    申请日:2000-03-27

    IPC分类号: A61K31435

    摘要: Proliferation of retinal pigment epithelium following surgery or trauma or resulting in ocular diseases associated with choroidal neovascularization, such as age related macular degeneration and histoplasmosis syndrome, is prevented by contacting retinal pigment epithelium cells with a therapeutic amount of a retinoic acid receptor (RAR agonist, preferably one with specific activity for retinoic acid receptors. Preferably the RAR agonist is also a potent antagonist of AP1-dependent gene expression. Alternatively, the proliferation of retinal pigment epithelium is ameliorated with a therapeutic amount of an AP-1 antagonist, alone or in combination with an RAR agonist. The drug can be administered by bolus injection into the vitreous cavity using a dosage from about 50 to 150 &mgr;g. Or by slow release from liposomes or an oil tamponade injected into the vitreous cavity. Formulations for preventing proliferation of retinal pigment epithelium are also provided.

    摘要翻译: 通过使视网膜色素上皮细胞与治疗量的视黄酸受体(RAR激动剂,血管内皮细胞生长因子受体)接触,可防止手术或外伤后视网膜色素上皮细胞增生,或导致与脉络膜新生血管形成相关的眼部疾病,如年龄相关性黄斑变性和组织胞浆菌病综合征 优选地,具有比较活性的视黄酸受体,优选地,RAR激动剂也是AP1依赖性基因表达的有效拮抗剂,或者,视网膜色素上皮的增殖用治疗量的AP-1拮抗剂单独或在 与RAR激动剂组合,药物可以通过使用约50至150杯的剂量通过快速注射进入玻璃体腔,或通过从脂质体缓慢释放或注射到玻璃体腔中的油脂填充剂来制备。用于防止视网膜增殖的制剂 还提供了色素上皮。