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Connected flow-through chromatography processes as continuous downstream processing of proteins

机译:连接的流通色谱法可作为蛋白质的连续下游加工

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Continuous manufacturing is expected to increase the productivity of protein drug production. However, it is not easy to build the continuous process especially for downstream processing as many unit operations (chromatography and membrane filtration) are involved. An operation method known as flow-through chromatography (FTC) is considered to be an efficient method for separating two components as the flow is continuous. In FTC, a target protein is eluted from the chromatography column without adsorption whereas contaminants are strongly bound. Since at least two different modes of chromatography are needed in order to remove contaminants, two FTC columns have to be connected in order to build the continuous process. This is not an easy task since the mobile phase properties (pH, salt, buffer ions) are different for the two columns. In this paper, we investigated how connected FTC columns can remove impurities efficiently from the cell culture broth containing monoclonal antibody. It was found that the sequence (activated carbon - anion exchange chromatography - cation exchange chromatography) is most efficient when the mobile phase pH and conductivity were properly chosen.
机译:连续生产有望提高蛋白质药物生产的生产率。但是,建立连续过程并不容易,特别是对于下游过程而言,因为涉及许多单元操作(色谱和膜过滤)。由于流是连续的,一种称为流通色谱(FTC)的操作方法被认为是分离两种组分的有效方法。在FTC中,目标蛋白从色谱柱上洗脱下来而没有吸附,而污染物则被牢固地结合在一起。由于至少需要两种不同的色谱模式才能去除污染物,因此必须连接两个FTC色谱柱才能建立连续过程。这不是一件容易的事,因为两个色谱柱的流动相特性(pH,盐,缓冲离子)不同。在本文中,我们研究了连接的FTC色谱柱如何从含有单克隆抗体的细胞培养液中有效去除杂质。据发现,所述序列(活性炭 - 阴离子交换色谱 - 阳离子交换色谱法)是最有效的,当移动相的pH和电导率分别适当选择。

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