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两段式切向流微滤连续集成抗体沉淀,实现恒质量流。

Continuous integrated antibody precipitation with two-stage tangential flow microfiltration enables constant mass flow.

机构信息

Department of Biotechnology, University of Natural Resources and Life Sciences,, Vienna, Austria.

Austrian Centre of Industrial Biotechnology (ACIB), Vienna, Austria.

出版信息

Biotechnol Bioeng. 2019 May;116(5):1053-1065. doi: 10.1002/bit.26922. Epub 2019 Jan 23.

DOI:10.1002/bit.26922
PMID:30636284
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6667901/
Abstract

Continuous precipitation is a new unit operation for the continuous capture of antibodies. The capture step is based on continuous precipitation with PEG6000 and Zn in a tubular reactor integrated with a two-stage continuous tangential flow filtration unit. The precipitate cannot be separated with centrifugation, because a highly compressed sediment results in poor resolubilization. We developed a new two-stage tangential flow microfiltration method, where part of the concentrated retentate of the first stage was directly fed to the second stage, together with the wash buffer. Thus, the precipitate was concentrated and washed in a continuous process. We obtained 97% antibody purity, a 95% process yield during continuous operation, and a fivefold reduction in pre-existing high-molecular-weight impurities. For other unit operations, surge tanks are often required, due to interruptions in the product mass flow out of the unit operation (e.g., the bind/elute mode in periodic counter-current chromatography). Our setup required no surge tanks; thus, it provided a truly continuous antibody capture operation with uninterrupted product mass flow. Continuous virus inactivation and other flow-through unit operations can be readily integrated downstream of the capture step to create truly continuous, integrated, downstream antibody processing without the need for hold tanks.

摘要

连续沉淀是一种用于连续捕获抗体的新型单元操作。捕获步骤基于在管状反应器中使用 PEG6000 和 Zn 进行连续沉淀,该反应器与两级连续切向流过滤单元集成在一起。沉淀不能通过离心分离,因为高度压缩的沉淀物导致难以重新溶解。我们开发了一种新的两级切向流微滤方法,其中第一级的部分浓缩保留液与洗涤缓冲液一起直接进料到第二级。因此,沉淀在连续过程中被浓缩和洗涤。我们在连续操作中获得了 97%的抗体纯度、95%的过程收率,以及五倍减少了预先存在的高分子量杂质。对于其他单元操作,由于产品质量流量从单元操作中断(例如周期性逆流色谱中的结合/洗脱模式),通常需要缓冲罐。我们的设置不需要缓冲罐;因此,它提供了真正连续的抗体捕获操作,产品质量流量不间断。连续病毒灭活和其他直通式单元操作可以很容易地在捕获步骤的下游集成,从而创建真正连续、集成的下游抗体处理,而无需使用储罐。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1196/6667901/091c51591f65/BIT-116-1053-g008.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1196/6667901/0a5a7c1b542e/BIT-116-1053-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1196/6667901/091c51591f65/BIT-116-1053-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1196/6667901/92d7777978cd/BIT-116-1053-g001.jpg
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