单克隆抗体工艺开发集成微尺度平台的自动化,采用深度过滤器模拟。

IF 2.5 3区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Paras Sharma, Petra Sebastian, Lars Robbel, Michael Schmitt, Daniel G Bracewell
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引用次数: 0

摘要

高通量工艺开发(HTPD)被广泛用于单克隆抗体(mAb)纯化色谱操作的高效开发和优化。然而,非色谱单元操作的整合,特别是蛋白质A层析后的深度过滤,对于在离子交换层析(IEX)操作之前去除工艺和产品相关杂质至关重要,由于缺乏商用的微尺度深度过滤工具,仍然是一个挑战。这限制了该单元操作在净化序列中的整合,限制了过程相互作用的分析和整体过程的理解。在本研究中,设计并评估了一个微型HTPD平台,以实现深度过滤模拟物Sartobind®Q阴离子交换吸附剂在单抗纯化序列中的集成。这是通过使用工作流程设计工具将实验室规模的协议转换为微观规模,并在自动化液体处理系统上执行而实现的。对步骤收率和杂质净除率进行了评估,以确认缩小比例的等效性。Sartobind®Q膜实现了宿主细胞DNA (hcDNA)的有效去除,而随后的IEX操作去除宿主细胞蛋白(HCPs)和高分子量组分(HMWC),满足目标产品质量标准。该平台在不同的杂质概况中表现出鲁棒性,支持其适用于不同的工艺中间体。与实验室规模操作的对比分析证实了微尺度系统的性能和可扩展性,将总运行时间缩短了50%以上。集成的HTPD平台为综合mAb纯化工艺开发提供了一种资源高效、可扩展的方法,适用于开发早期的可开发性评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Automation of an integrated micro-scale platform for monoclonal antibody process development by incorporation of a depth filter mimic.

High throughput process development (HTPD) has been widely adopted for efficient development and optimization of chromatographic operations in monoclonal antibody (mAb) purification. However, the integration of non-chromatographic unit operations, particularly depth filtration following protein A chromatography, which is essential for the removal of process- and product-related impurities prior to the ion exchange chromatography (IEX) operations, remains a challenge due to the absence of commercially available micro-scale depth filtration tools. This limits the integration of this unit operation within the purification sequence, restricting the analysis of process interactions and overall process understanding. In this study, a micro-scale HTPD platform was designed and evaluated to enable integration of a depth filtration mimic, Sartobind® Q anion exchange adsorber, within a mAb purification sequence. This was achieved by translating laboratory-scale protocols to the micro-scale using workflow design tools and executed on an automated liquid handling system. Step yields and impurity clearance were assessed to confirm the equivalence of scale-down. The Sartobind® Q membrane achieved effective removal of host cell DNA (hcDNA), while subsequent IEX operations removed host cell proteins (HCPs) and high molecular weight components (HMWC), meeting target product quality specifications. The platform demonstrated robustness across varying impurity profiles, supporting its applicability for diverse process intermediates. Comparative analysis with laboratory-scale operations confirmed the performance and scalability of the micro-scale system, reducing the total run time by greater than 50%. The integrated HTPD platform offers a resource-efficient, scalable approach for comprehensive mAb purification process development and is suitable for developability assessments during early-stage development.

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来源期刊
Biotechnology Progress
Biotechnology Progress 工程技术-生物工程与应用微生物
CiteScore
6.50
自引率
3.40%
发文量
83
审稿时长
4 months
期刊介绍: Biotechnology Progress , an official, bimonthly publication of the American Institute of Chemical Engineers and its technological community, the Society for Biological Engineering, features peer-reviewed research articles, reviews, and descriptions of emerging techniques for the development and design of new processes, products, and devices for the biotechnology, biopharmaceutical and bioprocess industries. Widespread interest includes application of biological and engineering principles in fields such as applied cellular physiology and metabolic engineering, biocatalysis and bioreactor design, bioseparations and downstream processing, cell culture and tissue engineering, biosensors and process control, bioinformatics and systems biology, biomaterials and artificial organs, stem cell biology and genetics, and plant biology and food science. Manuscripts concerning the design of related processes, products, or devices are also encouraged. Four types of manuscripts are printed in the Journal: Research Papers, Topical or Review Papers, Letters to the Editor, and R & D Notes.
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