Nanoparticles for immunotherapy
    1.
    发明申请
    Nanoparticles for immunotherapy 有权
    用于免疫治疗的纳米颗粒

    公开(公告)号:US20080031899A1

    公开(公告)日:2008-02-07

    申请号:US11707627

    申请日:2007-02-19

    IPC分类号: A61K39/00 A61K9/14 A61P43/00

    摘要: Nanoparticles that activate complement in the absence of biological molecules are described. The nanoparticles are shown to specifically target antigen presenting cells in specifically in lymph nodes, without the use of a biological molecule for targeting. These particles are useful vehicles for delivering immunotherapeutics.

    摘要翻译: 描述了在不存在生物分子的情况下激活补体的纳米颗粒。 显示了纳米颗粒特异性靶向抗原呈递细胞,特别是在淋巴结中,而不用生物分子进行靶向。 这些颗粒是用于递送免疫治疗剂的有用载体。

    Surface for the immobilisation of nucleic acids
    7.
    发明申请
    Surface for the immobilisation of nucleic acids 审中-公开
    用于固定核酸的表面

    公开(公告)号:US20050009026A1

    公开(公告)日:2005-01-13

    申请号:US10487915

    申请日:2002-08-24

    摘要: The invention relates to a surface for the immobilization of one or several first nucleic acids as recognition elements (“immobilization surface”), for the production of a recognition surface for the detection of one or several second nucleic acids in one or more samples which are brought into contact with the recognition surface, the first nucleic acids being applied to a layer of the graft copolymer poly(L-lysine)-g-poly(ethyleneglycol) (PLL-g-PEG) as surface for immobilization, characterized in that the grafting ratio g, in other words the ratio between the number of lysine units and the number of polyethylene glycol side chains (“PEG” side chains) has an average value between 7 and 13. The invention also relates to a method for the qualitative and/or quantitative detection of one or more second nucleic acids in one or more samples, characterized in that said samples and optionally further reagents are brought into contact with an immobilization surface according to the invention, upon which one or several first nucleic acids are immobilized as recognition elements for specific binding/hybridization with said second nucleic acids and changes in optical or electronic signals resulting from the binding/hybridization of said second nucleic acid, or further, resulting from applied tracer substances applied for analyte detection, are measured.

    摘要翻译: 本发明涉及用于将一个或几个第一核酸作为识别元件(“固定表面”)固定的表面,用于产生用于检测一个或多个样品中一个或多个第二核酸的识别表面,所述一个或多个第二核酸是 与识别表面接触,将第一核酸施加到作为用于固定的表面的接枝共聚物聚(L-赖氨酸)-g-聚(乙二醇)(PLL-g-PEG)的层上,其特征在于, 接枝率g,换句话说,赖氨酸单元数与聚乙二醇侧链(“PEG”侧链)的数量之间的平均值为7-13之间。本发明还涉及一种定性和 /或一个或多个样品中一种或多种第二核酸的定量检测,其特征在于所述样品和任选的其它试剂与根据本发明的固定化表面接触,u pon,其中一个或几个第一核酸被固定为用于与所述第二核酸特异性结合/杂交的识别元件,以及由所述第二核酸的结合/杂交产生的光学或电子信号的变化,或者进一步由施用的示踪物质 应用于分析物检测。

    DRUG DELIVERY MATRICES TO ENHANCE WOUND HEALING
    8.
    发明申请
    DRUG DELIVERY MATRICES TO ENHANCE WOUND HEALING 审中-公开
    药物递送矩阵,以加强伤口愈合

    公开(公告)号:US20070202178A1

    公开(公告)日:2007-08-30

    申请号:US11739607

    申请日:2007-04-24

    IPC分类号: A61K9/00

    摘要: Bioactive molecules are entrapped within a matrix for the controlled delivery of these compounds for therapeutic healing applications. The matrix may be formed of natural or synthetic compounds. The primary method of entrapment of the bioactive molecule is through precipitation of the bioactive molecule during gelation of the matrix, either in vitro or in vivo. The bioactive molecule may be modified to reduce its effective solubility in the matrix to retain it more effectively within the matrix, such as through the deglycosylation of members within the cystine knot growth factor superfamily and particularly within the TGFβ superfamily. The matrix may be modified to include sites with binding affinity for different bioactive molecules, for example, for heparin binding.

    摘要翻译: 生物活性分子被包埋在基质内,用于受控递送这些化合物用于治疗性愈合应用。 基质可以由天然或合成的化合物形成。 捕获生物活性分子的主要方法是通过体外或体内在基质凝胶化过程中沉淀生物活性分子。 可以修饰生物活性分子以降低其在基质中的有效溶解度,从而更有效地将其保留在基质内,例如通过胱氨酸结生长因子超家族内,特别是在TGFbeta超家族内的成员的去糖基化。 可以修饰基质以包括对不同生物活性分子具有结合亲和力的位点,例如用于肝素结合的位点。

    Methods and apparatus for selective, oxidative patterning of a surface

    公开(公告)号:US20060127595A1

    公开(公告)日:2006-06-15

    申请号:US11333090

    申请日:2006-01-17

    IPC分类号: B41M5/00 C08F2/46

    摘要: The present invention provides methods and apparatus for selectively patterning surfaces using radical species generated with a photocatalyst. The photocatalyst may comprise a photocatalytic semiconductor or a photosensitizer. The radical species are brought into contact with an oxidizable coating disposed on the surface, thereby locally oxidizing and selectively patterning the surface. The photocatalyst is preferably disposed on a delivery device, such as a stamp, mask, or scanning probe, that is brought into close proximity or contact with the coated surface. The photocatalyst is then excited in a manner capable of generating radical species, for example, oxygen-containing radical species, in appropriate media. It is expected that these radical species will be transferred to the coated surface along a substantially shortest distance path, thereby locally oxidizing and patterning the surface.