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迈向CoPACaPAnA:在端到端一次性GMP下游制造工艺中实施用于抗体应用的连续蛋白A捕获工艺。

Moving to CoPACaPAnA: Implementation of a continuous protein A capture process for antibody applications within an end-to-end single-use GMP manufacturing downstream process.

作者信息

Ötes Ozan, Bernhardt Cathrin, Brandt Kevin, Flato Hendrik, Klingler Otmar, Landrock Katharina, Lohr Verena, Stähler Ralf, Capito Florian

机构信息

Purification Development, Industriepark Höchst, Sanofi-Aventis Deutschland GmbH, 65926 Frankfurt am Main, Germany.

Drug Substance Manufacturing Biologics, Industriepark Höchst, Sanofi-Aventis Deutschland GmbH, 65926 Frankfurt am Main, Germany.

出版信息

Biotechnol Rep (Amst). 2020 May 4;26:e00465. doi: 10.1016/j.btre.2020.e00465. eCollection 2020 Jun.

Abstract

For the first time to our knowledge the implementation of a continuous protein A capture process for antibody applications (CoPACaPAnA) embedded in an end-to-end single-use 500 L GMP manufacturing downstream process of a multispecific monoclonal antibody (mAb) using a single-use SMB system was conducted. Throughout the last years, a change concerning the pipelines in pharmaceutical industry could be observed, moving to a more heterogeneous portfolio of antibodies, fusion proteins and nanobodies. Trying to adjust purification processes to these new modalities, a higher degree of flexibility and lower operational and capital expenditure is desired. The implementation of single-use equipment is a favored solution for increasing manufacturing agility and it has been demonstrated that continuous processing can be beneficial concerning processing cost and time. Reducing protein A resin resulted in 59% cost reduction for the protein A step, with additional cost reduction also for the intermediate and polishing step due to usage of disposable technology. The downstream process applied here consisted of three chromatography steps that were all conducted on a single-use SMB system, with the capture step being run in continuous mode while intermediate and polishing was conducted in batch mode. Further, two steps dedicated to virus inactivation/ removal and three filtration steps were performed, yielding around 100 g of drug substance going into clinical phase I testing. Therefore, in this study it has been demonstrated that employing a continuous capture within a GMP single-use downstream processing chain is feasible and worthy of consideration among the biotech industry for future application to modality-diverse pipelines.

摘要

据我们所知,首次使用一次性模拟移动床(SMB)系统,在多特异性单克隆抗体(mAb)的端到端一次性500L GMP生产下游工艺中,实施了用于抗体应用的连续蛋白A捕获工艺(CoPACaPAnA)。在过去几年中,可以观察到制药行业管道方面的变化,转向了抗体、融合蛋白和纳米抗体等更多样化的产品组合。为了使纯化工艺适应这些新模式,需要更高的灵活性以及更低的运营和资本支出。一次性设备的应用是提高生产灵活性的理想解决方案,并且已经证明连续加工在加工成本和时间方面是有益的。减少蛋白A树脂使用量使蛋白A步骤的成本降低了59%,由于使用了一次性技术,中间步骤和精制步骤的成本也有所降低。此处应用的下游工艺包括三个色谱步骤,所有步骤均在一次性SMB系统上进行,捕获步骤以连续模式运行,而中间步骤和精制步骤以分批模式进行。此外,还进行了两个病毒灭活/去除步骤和三个过滤步骤,得到约100g进入I期临床试验的药物原料。因此,在本研究中已证明,在GMP一次性下游加工链中采用连续捕获是可行的,并且在生物技术行业中值得考虑用于未来多样化模式的产品线。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/872a/7218147/d2c9c0f4563d/gr1.jpg

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