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Method of manufacturing fibrinogen of very high — purity, fibrinogen of very high — purity obtained as well as a pharmaceutical composition containing.

机译:制备非常高纯度的纤维蛋白原的方法,获得的非常高纯度的纤维蛋白原以及包含其的药物组合物。

摘要

The invention relates to a process for the production of high-purity fibrinogen. This process is characterized in that it comprises, from blood plasma cryoprecipitate of animal or human origin, an aqueous solution, the treatment of this solution in order to bring it to an ionic force equal to that of a buffer solution which has the following composition: & br / (see appended drawing in bopi) & br / & & br / is passed through this solution of ionic force adjusted on an anion exchange column comprising a gel of the anion exchange, for example in the form of balls, based on agarose crosslinked comprising quaternary amine groups, in particular at the end of a spacer arm, for example alkylene type c1 - c6 connected to the agarose beads, in particular to approximately 6% agarose and then an elution with a first solution of elution of the same ionic strength, these conditions, making it possible to selectively adsorb the fibrinogen on said column, which is desorbed by elution solution of ionic strength higher at approximately 200 mm nacl. & br / it is possible to obtain a high-purity fibrinogen.
机译:本发明涉及生产高纯度纤维蛋白原的方法。该方法的特征在于,它包含来自动物或人的血浆低温沉淀物的水溶液,对该溶液进行处理以使其离子强度等于具有以下组成的缓冲溶液的离子强度: & br />(请参见bopi中的附图)& br /& &使br>通过在包含阴离子交换凝胶的阴离子交换柱上调节的离子力溶液,该阴离子交换柱例如呈球状,基于包含季胺基的琼脂糖交联,特别是在间隔基末端臂,例如连接到琼脂糖珠,特别是大约6%的琼脂糖的c1-c6亚烷基,然后用这些具有相同离子强度的第一溶液洗脱,在这些条件下,可以选择性地吸附纤维蛋白原所述柱,其通过离子强度较高的洗脱溶液在约200 mm氯化钠下解吸。 &可以得到高纯度的纤维蛋白原。

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