Chimeric recombinant antigens of Toxoplasma gondii
    31.
    发明授权
    Chimeric recombinant antigens of Toxoplasma gondii 失效
    弓形虫的嵌合重组抗原

    公开(公告)号:US07867503B2

    公开(公告)日:2011-01-11

    申请号:US11899754

    申请日:2007-09-06

    IPC分类号: A61K39/012

    摘要: A method for treatment or prevention of Toxoplasma gondii infections pharmaceutical composition comprising an antigen fragments of Toxoplasma gondii in the form of a chimeric fusion product or a nucleotide sequence coding for the chimeric fusion product and a method of using the chimeric fusion product or nucleotide sequence coding therefor.

    摘要翻译: 用于治疗或预防弓形虫感染药物组合物的方法,其包含嵌合融合产物形式的弓形体的抗原片段或编码嵌合融合物的核苷酸序列的方法,以及使用嵌合融合产物或核苷酸序列编码 因此。

    Deglycosylated and desialidated long pentraxin PTX3
    35.
    发明授权
    Deglycosylated and desialidated long pentraxin PTX3 有权
    去糖基化和去极化的长pentraxin PTX3

    公开(公告)号:US07833981B2

    公开(公告)日:2010-11-16

    申请号:US12710559

    申请日:2010-02-23

    IPC分类号: C07K14/00 A61K38/00

    CPC分类号: C07K14/71 A61K38/00

    摘要: Deglycosylated long pentraxin PTX3 and desialidated long pentraxin PTX3 are disclosed, as well as processes for their preparation, pharmacological compositions containing them, and their use for the preparation of a medicament for the treatment of diseases in which the use of the long pentraxin PTX is indicated, particularly infectious and inflammatory diseases and female fertility disorders. These proteins are endowed with therapeutic activity superior to that of glycosylated pentraxin.

    摘要翻译: 公开了脱糖基化的长五倍体PTX3和去离子的长五聚蛋白PTX3,以及其制备方法,含有它们的药理学组合物及其用于制备用于治疗其中使用长五倍素PTX的疾病的药物的用途 ,特别是感染性和炎性疾病和女性生殖障碍。 这些蛋白质具有优于糖基化五肽的治疗活性。

    Method for inhibiting bacterial growth in a leuko-reduced platelet concentrate by adding L-carnitine
    36.
    发明授权
    Method for inhibiting bacterial growth in a leuko-reduced platelet concentrate by adding L-carnitine 失效
    通过加入左旋肉碱来抑制白细胞减少的血小板浓缩物中的细菌生长的方法

    公开(公告)号:US07816073B2

    公开(公告)日:2010-10-19

    申请号:US10756368

    申请日:2004-01-14

    IPC分类号: A01N1/02

    摘要: Cell membrane maintenance of red blood cells and platelet concentrates is improved by the addition of 1 mM-10 mM L-carnitine and derivatives. This improvement allows extension of the period of viability of packed red blood cells and platelet concentrations beyond current periods. Additionally, the materials so treated exhibit extended circulation half life upon transfusion to a patient. Improvements in membrane maintenance achieved by this method permit irradiation of sealed containers of blood products so as to substantially sterilize and destroy leukocytes in the same.

    摘要翻译: 通过加入1mM-10mM左旋肉碱及其衍生物来改善红细胞和血小板浓缩物的细胞膜维持。 这种改善使得包装的红血细胞和血小板浓度的生存期延长超过当前时期。 此外,如此处理的材料在输血时显示延长的循环半衰期。 通过该方法实现的膜维持改进允许照射血液制品的密封容器,从而基本上消毒和破坏其中的白细胞。

    OXIDIZED AVIDIN WITH HIGH RESIDENCY TIME IN THE TREATED TISSUES
    37.
    发明申请
    OXIDIZED AVIDIN WITH HIGH RESIDENCY TIME IN THE TREATED TISSUES 有权
    在处理组织中具有高停留时间的氧化物

    公开(公告)号:US20100239497A1

    公开(公告)日:2010-09-23

    申请号:US12670925

    申请日:2008-07-16

    CPC分类号: A61K51/08

    摘要: The present invention describes chemically modified avidins that have higher permanence in treated tissues compared to wild type avidin. Avidin oxidation is performed by periodate incubation in the presence of the low affinity ligand HABA which, occupying the biotin binding sites, prevents protein denaturation during the oxidation step. Periodate oxidation generates CHO groups from avidin mannose ring opening that, once injected, react with tissue NH2 residues to form stable Schiff's bases. The anchored avidins maintain the ability to bind biotinylated agents endowed of therapeutic activity, like radiolabeled biotins, stem cells and somatic cells, useful for brachytherapies like Intraoperative Avidination Radionuclide Therapy (IART®) or degenerative or genetic diseases.

    摘要翻译: 本发明描述了与野生型抗生物素蛋白相比,在处理组织中具有更高持久性的化学修饰的avidins。 在低亲和性配体HABA存在下,通过高碘酸盐温育进行抗生物素蛋白氧化,其占据生物素结合位点,防止氧化步骤期间的蛋白质变性。 高碘酸氧化从抗生物素蛋白甘露糖开环产生CHO基团,一旦注射,与组织NH2残留物反应形成稳定的席夫碱。 锚定的avidins保持结合具有治疗活性的生物素化试剂的能力,如放射性标记的生物素,干细胞和体细胞,可用于诸如术中放射性放射性核素治疗(IART)或退行性或遗传性疾病之类的近程疗法。

    SYNTHESIS OF DEOXYBIOTINYL HEXAMETHYLENEDIAMINE-DOTA
    40.
    发明申请
    SYNTHESIS OF DEOXYBIOTINYL HEXAMETHYLENEDIAMINE-DOTA 有权
    脱氧胆碱合成十四酰胺胺-DTA

    公开(公告)号:US20100184972A1

    公开(公告)日:2010-07-22

    申请号:US11993185

    申请日:2006-05-31

    IPC分类号: C07D495/04

    CPC分类号: C07D495/04

    摘要: A process for the synthesis of deoxybiotinyl hexamethylenediamine0-DOTA is herein described. Said process comprises reacting biotinyl hexamithylenediamine with tri-t-butyl DOTA in the presence of benzotriazol-1-yl-oxytripyrrolidinophosphonium hexafluorophosphate, as the condensing agent, and triethylamine, as a base.

    摘要翻译: 本文描述了合成脱氧生物基六亚甲基二胺-ODTA的方法。 所述方法包括在苯并三唑-1-基 - 氧三吡咯烷鏻六氟磷酸盐作为缩合剂和作为碱的三乙胺存在下,将生物素基六亚甲基二胺与三叔丁基DOTA反应。