RADIOTRACER COMPOSITIONS
    4.
    发明申请
    RADIOTRACER COMPOSITIONS 有权
    放射性组合物

    公开(公告)号:US20130259804A1

    公开(公告)日:2013-10-03

    申请号:US13992800

    申请日:2011-12-09

    Abstract: The present invention relates to improved radiotracer imaging agent compositions, which comprises 18F-labelled biological targeting moieties, wherein impurities which affect imaging in vivo are identified and suppressed. Also provided are radiopharmaceuticals comprising said improved compositions, together with radiofluorinated aldehyde compositions useful in preparing said radiotracer compositions. The invention also includes methods of imaging and/or diagnosis using the radiopharmaceutical compositions described.

    Abstract translation: 本发明涉及改进的放射性示踪剂成像剂组合物,其包含18F标记的生物靶向部分,其中鉴定和抑制影响体内成像的杂质。 还提供了包含所述改进的组合物的放射性药物,以及可用于制备所述放射性示踪剂组合物的放射性氟化醛组合物。 本发明还包括使用所述放射性药物组合物进行成像和/或诊断的方法。

    Synthesis of a PEG-6 moiety from commercial low-cost chemicals
    9.
    发明授权
    Synthesis of a PEG-6 moiety from commercial low-cost chemicals 失效
    从商业低成本化学品合成PEG-6部分

    公开(公告)号:US08415510B2

    公开(公告)日:2013-04-09

    申请号:US12918391

    申请日:2009-02-10

    Applicant: Torgrim Engell

    Inventor: Torgrim Engell

    Abstract: The present invention provides novel synthesis's for obtaining a protecting group aminoxy PEG-6 linker from cost effective, and readily available starting materials and chemicals or modified polyethylene glycols. More specifically, a novel synthesis of obtaining a modified Boc-protected aminoxy PEG-6 linker was achieved so that said linker may be attached to a vector such as a peptide based fragment.

    Abstract translation: 本发明提供了从成本有效的和容易得到的原料和化学品或改性聚乙二醇获得保护基团氨基PEG-6连接体的新型合成方法。 更具体地,获得获得修饰的Boc-保护的氨基羟基PEG-6接头的新合成,使得所述接头可以连接到载体如基于肽的片段上。

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