Intravenous immunoglobulin composition
    1.
    发明申请
    Intravenous immunoglobulin composition 有权
    静脉内免疫球蛋白组成

    公开(公告)号:US20070037170A1

    公开(公告)日:2007-02-15

    申请号:US11201282

    申请日:2005-08-11

    IPC分类号: C12Q1/70 C12Q1/68

    摘要: A method for preparing a concentrated, immunoglobulin composition for treating subjects vaccinated against or infected with a pathogenic microorganism, comprising: (a) selecting a population of individuals previously vaccinated against one or more antigens associated with the pathogenic microorganism; (b) determining the level of specific antibodies immunoreactive with the pathogenic microorganism in a blood or blood component of the individuals to identify very high titre individuals having a very high titre of the specific antibodies; (c) combining blood or blood components comprising immunoglobulins from the very high titre individuals; and (d) purifying and/or concentrating the product of step (c), thereby obtaining a concentrated immunoglobulin composition. Also disclosed is a concentrated immunoglobulin composition comprising specific antibodies immunoreactive with a pathogenic microorganism, characterized in that the titre of specific antibodies of the composition is at least 5 times higher than the average titre of specific antibodies of a population of individuals previously vaccinated against one or more antigens associated with the pathogenic microorganism. The composition has a relatively high protein concentration and a low percentage of protein aggregates, and is therefore suitable for both iv and im administration. In a preferred embodiment, the pathogenic microorganism is smallpox virus or vaccinia virus.

    摘要翻译: 一种制备用于治疗接种疫苗或感染病原微生物的受试者的浓缩免疫球蛋白组合物的方法,包括:(a)选择先前针对与病原微生物相关的一种或多种抗原接种的个体群体; (b)确定在个体的血液或血液成分中与病原微生物免疫反应的特异性抗体的水平,以鉴定具有非常高的特异性抗体滴度的极高滴度的个体; (c)从非常高的滴度个体组合包含免疫球蛋白的血液或血液成分; 和(d)纯化和/或浓缩步骤(c)的产物,由此获得浓缩的免疫球蛋白组合物。 还公开了包含与病原微生物免疫反应性的特异性抗体的浓缩免疫球蛋白组合物,其特征在于组合物的特异性抗体滴度比先前接种于一种或多种疫苗的个体群体的特异性抗体的平均滴度高至少5倍 更多与病原微生物相关的抗原。 该组合物具有相对高的蛋白质浓度和低百分比的蛋白质聚集体,因此适用于iv和im施用。 在优选的实施方案中,致病微生物是天花病毒或痘苗病毒。

    Intravenous immunoglobulin composition
    2.
    发明授权
    Intravenous immunoglobulin composition 有权
    静脉内免疫球蛋白组成

    公开(公告)号:US09365635B2

    公开(公告)日:2016-06-14

    申请号:US13619011

    申请日:2012-09-14

    摘要: A concentrated, immunoglobulin composition for treating subjects vaccinated against or infected with a pathogenic microorganism, is made by (a) selecting a population of individuals previously vaccinated against antigens associated with the pathogenic microorganism; (b) identifying very high titer individuals by determining the level of specific antibodies immunoreactive with the pathogenic microorganism in the blood of the individuals; (c) combining blood from the very high titer individuals; and (d) purifying and/or concentrating the product of step (c). A concentrated immunoglobulin composition can include specific antibodies immunoreactive with a pathogenic microorganism, wherein the titer of specific antibodies is at least 5 times higher than the average titer of specific antibodies of a population of individuals previously vaccinated against antigens associated with the pathogenic microorganism. The composition has a relatively high protein concentration and a low percentage of protein aggregates. The pathogenic microorganism is preferably smallpox virus or vaccinia virus.

    摘要翻译: 用于治疗接种疫苗或感染致病微生物的受试者的浓缩的免疫球蛋白组合物是通过(a)选择先前针对与病原微生物相关的抗原进行接种的个体群体; (b)通过确定与个体血液中的病原微生物免疫反应的特异性抗体的水平来鉴定非常高的滴度个体; (c)结合来自极高滴度个体的血液; 和(d)纯化和/或浓缩步骤(c)的产物。 浓缩的免疫球蛋白组合物可以包括与病原微生物免疫反应的特异性抗体,其中特异性抗体的滴度比先前接种抗原与病原微生物相关抗原的个体群体的特异性抗体的平均滴度高至少5倍。 该组合物具有相对高的蛋白质浓度和低百分比的蛋白质聚集体。 病原微生物优选为天花病毒或痘苗病毒。

    INTRAVENOUS IMMUNOGLOBULIN COMPOSITION
    3.
    发明申请
    INTRAVENOUS IMMUNOGLOBULIN COMPOSITION 有权
    内脏免疫组织化学

    公开(公告)号:US20130011388A1

    公开(公告)日:2013-01-10

    申请号:US13619011

    申请日:2012-09-14

    摘要: A concentrated, immunoglobulin composition for treating subjects vaccinated against or infected with a pathogenic microorganism, is made by (a) selecting a population of individuals previously vaccinated against antigens associated with the pathogenic microorganism; (b) identifying very high titre individuals by determining the level of specific antibodies immunoreactive with the pathogenic microorganism in the blood of the individuals; (c) combining blood from the very high titre individuals; and (d) purifying and/or concentrating the product of step (c). A concentrated immunoglobulin composition can include specific antibodies immunoreactive with a pathogenic microorganism, wherein the titre of specific antibodies is at least 5 times higher than the average titre of specific antibodies of a population of individuals previously vaccinated against antigens associated with the pathogenic microorganism. The composition has a relatively high protein concentration and a low percentage of protein aggregates. The pathogenic microorganism is preferably smallpox virus or vaccinia virus.

    摘要翻译: 用于治疗接种疫苗或感染致病微生物的受试者的浓缩的免疫球蛋白组合物是通过(a)选择先前针对与病原微生物相关的抗原进行接种的个体群体; (b)通过确定与个体血液中的病原微生物免疫反应的特异性抗体的水平来鉴定非常高的滴度个体; (c)结合极高滴度个体的血液; 和(d)纯化和/或浓缩步骤(c)的产物。 浓缩的免疫球蛋白组合物可以包括与病原微生物免疫反应的特异性抗体,其中特异性抗体的滴度比先前接种抗原与病原微生物相关抗原的个体群体的特异性抗体的平均滴度高至少5倍。 该组合物具有相对高的蛋白质浓度和低百分比的蛋白质聚集体。 病原微生物优选为天花病毒或痘苗病毒。

    Intravenous immunoglobulin composition
    4.
    发明授权
    Intravenous immunoglobulin composition 有权
    静脉内免疫球蛋白组成

    公开(公告)号:US08354249B2

    公开(公告)日:2013-01-15

    申请号:US11201282

    申请日:2005-08-11

    IPC分类号: C12P21/04

    摘要: A method for preparing a concentrated, immunoglobulin composition for treating subjects vaccinated against or infected with a pathogenic microorganism, comprising: (a) selecting a population of individuals previously vaccinated against one or more antigens associated with the pathogenic microorganism; (b) determining the level of specific antibodies immunoreactive with the pathogenic microorganism in a blood or blood component of the individuals to identify very high titre individuals having a very high titre of the specific antibodies; (c) combining blood or blood components comprising immunoglobulins from the very high titre individuals; and (d) purifying and/or concentrating the product of step (c), thereby obtaining a concentrated immunoglobulin composition. Also disclosed is a concentrated immunoglobulin composition comprising specific antibodies immunoreactive with a pathogenic microorganism, characterized in that the titre of specific antibodies of the composition is at least 5 times higher than the average titre of specific antibodies of a population of individuals previously vaccinated against one or more antigens associated with the pathogenic microorganism. The composition has a relatively high protein concentration and a low percentage of protein aggregates, and is therefore suitable for both iv and im administration. In a preferred embodiment, the pathogenic microorganism is smallpox virus or vaccinia virus.

    摘要翻译: 一种制备用于治疗接种疫苗或感染病原微生物的受试者的浓缩免疫球蛋白组合物的方法,包括:(a)选择先前针对与病原微生物相关的一种或多种抗原接种的个体群体; (b)确定在个体的血液或血液成分中与病原微生物免疫反应的特异性抗体的水平,以鉴定具有非常高的特异性抗体滴度的极高滴度的个体; (c)从非常高的滴度个体组合包含免疫球蛋白的血液或血液成分; 和(d)纯化和/或浓缩步骤(c)的产物,由此获得浓缩的免疫球蛋白组合物。 还公开了包含与病原微生物免疫反应性的特异性抗体的浓缩免疫球蛋白组合物,其特征在于组合物的特异性抗体滴度比先前接种于一种或多种疫苗的个体群体的特异性抗体的平均滴度高至少5倍 更多与病原微生物相关的抗原。 该组合物具有相对高的蛋白质浓度和低百分比的蛋白质聚集体,因此适用于iv和im施用。 在优选的实施方案中,致病微生物是天花病毒或痘苗病毒。

    Removal of plasmin or plasminogen from cryoprecipitate
    7.
    发明授权
    Removal of plasmin or plasminogen from cryoprecipitate 有权
    从冷沉淀物中去除纤溶酶或纤溶酶原

    公开(公告)号:US08563288B2

    公开(公告)日:2013-10-22

    申请号:US12289499

    申请日:2008-10-29

    IPC分类号: C12N9/66 A61K35/16

    摘要: A method for specifically removing or isolating plasmin(ogen) or plasmin in presence of fibrinogen from a mixture containing plasmin(ogen) or plasmin by contacting the mixture with a rigid amino acid wherein the amino group of the amino acid and the carboxylic group of the amino acid are about 6-8 Angstroms, preferably about 7 Angstroms apart and the rigid amino acid is covalently bound to the support via the amino group of the amino acid.

    摘要翻译: 一种通过使混合物与刚性氨基酸接触的方法,其特征在于从含有纤维蛋白溶酶(ogen)或纤溶酶的混合物中除去或分离纤维蛋白原(纤维蛋白原)存在下的纤维蛋白溶酶或纤溶酶,其中氨基酸和羧基的氨基 氨基酸约6-8埃,优选约7埃,刚性氨基酸通过氨基酸的氨基与载体共价结合。

    Device for administering an at least two-component substance
    9.
    发明申请
    Device for administering an at least two-component substance 审中-公开
    用于施用至少两种组分物质的装置

    公开(公告)号:US20100217231A1

    公开(公告)日:2010-08-26

    申请号:US12708453

    申请日:2010-02-18

    IPC分类号: A61M5/31 A61B17/03 A61M35/00

    摘要: The device for administering an at least two-component substance comprises a concentric lumen arrangement including (i) an inner cannula having a lumen with an inlet opening at a first end and a tip with an outlet opening at a second end opposite its first end, and (ii) an outer sheath having opposite first and second ends facing the respective first and second ends of the inner cannula, and surrounding the inner cannula along an axial length between the first and second ends of the inner cannula, wherein the outer sheath at its second end is sealingly and fixedly connected to the inner cannula and defining an outer lumen around the inner cannula, and wherein the inner cannula is provided with at least one opening for providing fluid communication between the outer lumen around the inner cannula and the lumen of the inner cannula.

    摘要翻译: 用于施用至少两种组分物质的装置包括同心的腔排列,其包括(i)具有在第一端具有入口开口的内腔和在其第一端相对的第二端处具有出口开口的末端的内套管, 和(ii)外护套,其具有相对的第一和第二端面向所述内套管的相应的第一和第二端,并且沿着所述内套管的第一和第二端之间的轴向长度包围所述内套管,其中, 其第二端密封地和固定地连接到内套管并且围绕内插管限定外腔,并且其中内插管设置有至少一个开口,用于提供围绕内插管的外腔与内套管之间的流体连通 内套管。

    Removal of plasmin(ogen) from protein solutions
    10.
    发明申请
    Removal of plasmin(ogen) from protein solutions 有权
    从蛋白质溶液中去除纤溶酶(ogen)

    公开(公告)号:US20090176293A1

    公开(公告)日:2009-07-09

    申请号:US12289499

    申请日:2008-10-29

    IPC分类号: C12N9/68

    摘要: A method for specifically removing or isolating plasmin(ogen) or plasmin in presence of fibrinogen from a mixture containing plasmin(ogen) or plasmin by contacting the mixture with a rigid amino acid wherein the amino group of the amino acid and the carboxylic group of the amino acid are about 6-8 Angstroms, preferably about 7 Angstroms apart and the rigid amino acid is covalently bound to the support via the amino group of the amino acid.

    摘要翻译: 一种通过使混合物与刚性氨基酸接触的方法,其特征在于从含有纤维蛋白溶酶(ogen)或纤溶酶的混合物中除去或分离纤维蛋白原(纤维蛋白原)存在下的纤维蛋白溶酶或纤溶酶,其中氨基酸和羧基的氨基 氨基酸约6-8埃,优选约7埃,刚性氨基酸通过氨基酸的氨基与载体共价结合。