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从生物制药制剂中去除宿主细胞蛋白:迈向质量源于设计的实现。

Host cell protein removal from biopharmaceutical preparations: Towards the implementation of quality by design.

机构信息

Department of Chemical Engineering, Imperial College London, London, United Kingdom.

出版信息

Biotechnol Adv. 2018 Jul-Aug;36(4):1223-1237. doi: 10.1016/j.biotechadv.2018.03.021. Epub 2018 Apr 11.

Abstract

Downstream processing of protein products of mammalian cell culture currently accounts for the largest fraction of the total production cost. A major challenge is the removal of host cell proteins, which are cell-derived impurities. Host cell proteins are potentially immunogenic and can compromise product integrity during processing and hold-up steps. There is an increasing body of evidence that the type of host cell proteins present in recombinant protein preparations is a function of cell culture conditions and handling of the harvest cell culture fluid. This, in turn, can affect the performance of downstream purification steps as certain species are difficult to remove and may require bespoke process solutions. Herein, we review recent research on the interplay between upstream process conditions, host cell protein composition and their downstream removal in antibody production processes, identifying opportunities for increasing process understanding and control. We further highlight advances in analytical and computational techniques that can enable the application of quality by design.

摘要

目前,哺乳动物细胞培养的蛋白质产物的下游处理占据了总成本的最大部分。主要的挑战是去除宿主细胞蛋白,这些是细胞衍生的杂质。宿主细胞蛋白具有潜在的免疫原性,并且在处理和滞留步骤中可能会影响产品的完整性。越来越多的证据表明,重组蛋白制剂中存在的宿主细胞蛋白的类型是细胞培养条件和收获细胞培养液处理的函数。这反过来又会影响下游纯化步骤的性能,因为某些物种难以去除,可能需要定制的工艺解决方案。本文综述了近年来关于抗体生产过程中上游工艺条件、宿主细胞蛋白组成及其下游去除之间相互作用的研究,确定了提高工艺理解和控制的机会。我们还进一步强调了分析和计算技术的进步,这些技术可以实现基于质量的设计的应用。

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