COMPOSITION AND METHOD FOR DELIVERY OF HYDROPHOBIC ACTIVE AGENTS
    94.
    发明申请
    COMPOSITION AND METHOD FOR DELIVERY OF HYDROPHOBIC ACTIVE AGENTS 有权
    用于输送疏水活性剂的组合物和方法

    公开(公告)号:US20170072057A1

    公开(公告)日:2017-03-16

    申请号:US15357496

    申请日:2016-11-21

    Abstract: Disclosed herein is a delivery composition for administering a hydrophobic active agent. In one embodiment, a delivery composition for local administration of a hydrophobic active agent to a tissue or organ of a patient is disclosed. In one embodiment, the delivery composition includes a cationic delivery agent, a therapeutically effective amount of a hydrophobic active agent and a pharmaceutically acceptable aqueous carrier. In one embodiment, the cationic delivery agent includes polyethyleneimine (PEI). In a more specific embodiment, the cationic delivery agent includes branched PEI. Methods of making the delivery composition, as well as kits and methods of use are also disclosed.

    Abstract translation: 本文公开了用于施用疏水性活性剂的递送组合物。 在一个实施方案中,公开了用于向患者的组织或器官局部施用疏水性活性剂的递送组合物。 在一个实施方案中,递送组合物包括阳离子递送剂,治疗有效量的疏水活性剂和药学上可接受的水性载体。 在一个实施方案中,阳离子递送剂包括聚乙烯亚胺(PEI)。 在更具体的实施方案中,阳离子递送剂包括支链PEI。 还公开了制备递送组合物的方法,以及试剂盒和使用方法。

    LUBRICIOUS MEDICAL DEVICE COATING WITH LOW PARTICULATES
    96.
    发明申请
    LUBRICIOUS MEDICAL DEVICE COATING WITH LOW PARTICULATES 有权
    具有低颗粒度的润滑性医疗器械涂层

    公开(公告)号:US20160271300A1

    公开(公告)日:2016-09-22

    申请号:US15165650

    申请日:2016-05-26

    Inventor: David E. Babcock

    Abstract: Embodiments of the invention include lubricious medical device coatings. In an embodiment the invention includes a coating for a medical device including a first layer comprising polyvinylpyrrolidone derivatized with a photoreactive group; anda first cross-linking agent comprising at least two photoreactive groups; a second layer disposed on the first layer comprising polyvinylpyrrolidone derivatized with a photoreactive group; a second cross-linking agent comprising at least two photoreactive groups; and a polymer comprising polyacrylamide, the polymer derivatized with at least one photoreactive group. Other embodiments are included herein.

    Abstract translation: 包含至少两个光反应性基团的第一交联剂; 设置在第一层上的第二层包含用光反应性基团衍生的聚乙烯吡咯烷酮; 包含至少两个光反应性基团的第二交联剂; 和包含聚丙烯酰胺的聚合物,所述聚合物用至少一种光反应性基团衍生化。 本文还包括其它实施例。

    SOLVENT METHODS FOR PREPARING CRYSTALLINE MACROLIDE PARTICULATES, COMPOSITIONS, AND ARTICLES CONTAINING PARTICULATES
    100.
    发明申请
    SOLVENT METHODS FOR PREPARING CRYSTALLINE MACROLIDE PARTICULATES, COMPOSITIONS, AND ARTICLES CONTAINING PARTICULATES 有权
    用于制备晶体结构的颗粒,组合物和含有颗粒物的制品的溶剂方法

    公开(公告)号:US20150017219A1

    公开(公告)日:2015-01-15

    申请号:US14303309

    申请日:2014-06-12

    Abstract: The invention provides therapeutic particulates including a macrolide, such as rapamycin, in solid state crystalline form, having a size of 20 μm or less, or 10 μm or less. The particulates are formed in one method by preparing a composition with a macrolide and first (e.g., xylene) and second (e.g., an alcohol, acetone, or acetonitrile) solvents. In the composition a maximum solubility for the macrolide that is greater than a maximum solubility of the macrolide dissolved in either the first or second solvent individually. The first and second solvents are then evaporated from the composition to provide the macrolide particulates. In another method, the particulates can be formed by a method including sonication and stirring/evaporation steps, and the particulates can be obtained from a supersaturated solution, formed during the process. Particulates display desirable low polydispersity, and can be used in therapeutic compositions, or can be associated with an implantable or insertable medical device for the treatment of a subject.

    Abstract translation: 本发明提供治疗性微粒,其包括固体状结晶形式的大环内酯如雷帕霉素,其尺寸为20μm或更小或10μm或更小。 通过制备具有大环内酯和第一(例如二甲苯)和第二(例如醇,丙酮或乙腈)溶剂的组合物来形成颗粒。 在组合物中,大环内酯的最大溶解度大于单独溶解在第一或第二溶剂中的大环内酯的最大溶解度。 然后将第一和第二溶剂从组合物中蒸发以提供大环内酯颗粒。 在另一种方法中,颗粒可以通过包括超声处理和搅拌/蒸发步骤的方法形成,并且颗粒可以从在过程中形成的过饱和溶液获得。 颗粒显示出期望的低多分散性,并且可以用于治疗组合物,或者可以与用于治疗受试者的可植入或可插入的医疗装置相关联。

Patent Agency Ranking