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在一个完全基于膜的过程中,将灌注反应器与连续沉淀相结合用于抗体捕获。

Integration of a perfusion reactor and continuous precipitation in an entirely membrane-based process for antibody capture.

作者信息

Recanati Gabriele, Pappenreiter Magdalena, Gstoettner Christoph, Scheidl Patrick, Vega Elena Domínguez, Sissolak Bernhard, Jungbauer Alois

机构信息

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

Innovation Management Bilfinger Life Science GmbH Salzburg Austria.

出版信息

Eng Life Sci. 2023 Sep 7;23(10):e2300219. doi: 10.1002/elsc.202300219. eCollection 2023 Oct.

Abstract

Continuous precipitation coupled with continuous tangential flow filtration is a cost-effective alternative for the capture of recombinant antibodies from crude cell culture supernatant. The removal of surge tanks between unit operations, by the adoption of tubular reactors, maintains a continuous harvest and mass flow of product with the advantage of a narrow residence time distribution (RTD). We developed a continuous process implementing two orthogonal precipitation methods, CaCl precipitation for removal of host-cell DNA and polyethylene glycol (PEG) for capturing the recombinant antibody, with no influence on the glycosylation profile. Our lab-scale prototype consisting of two tubular reactors and two stages of tangential flow microfiltration was continuously operated for up to 8 days in a truly continuous fashion and without any product flow interruption, both as a stand-alone capture and as an integrated perfusion-capture. Furthermore, we explored the use of a negatively charged membrane adsorber for flow-through anion exchange as first polishing step. We obtained a product recovery of approximately 80% and constant product quality, with more than two logarithmic reduction values (LRVs) for both host-cell proteins and host-cell DNA by the combination of the precipitation-based capture and the first polishing step.

摘要

连续沉淀结合连续切向流过滤是从粗细胞培养上清液中捕获重组抗体的一种经济高效的替代方法。通过采用管式反应器去除单元操作之间的缓冲罐,可保持产品的连续收获和质量流,具有窄停留时间分布(RTD)的优势。我们开发了一种连续工艺,采用两种正交沉淀方法,即氯化钙沉淀去除宿主细胞DNA,聚乙二醇(PEG)捕获重组抗体,且对糖基化谱无影响。我们的实验室规模原型由两个管式反应器和两级切向流微滤组成,以真正连续的方式连续运行长达8天,且无任何产品流中断,既作为独立捕获,也作为集成灌注捕获。此外,我们探索了使用带负电荷的膜吸附剂进行流通阴离子交换作为第一步精制步骤。通过基于沉淀的捕获和第一步精制步骤的组合,我们获得了约80%的产品回收率和恒定的产品质量,宿主细胞蛋白和宿主细胞DNA的对数减少值均超过两个对数。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/051f/10545976/269731973cd9/ELSC-23-e2300219-g007.jpg

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