用于生物工艺开发的宿主细胞蛋白杂质高通量定量的微流体方法

J. Heo, X. Mou, Fengqiang Wang, J. Troisi, Christopher W Sandifer, S. Kirby, D. Driscoll, Suzanne Mercorelli, D. Pollard
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引用次数: 8

摘要

背景:过程相关杂质的分析对生物制药过程的控制和最终生物制品的质量至关重要。宿主细胞蛋白(HCPs)等单克隆抗体产品中的残留杂质增加了免疫原性的风险,并可能直接影响药物效力。常用的HCP酶联免疫吸附法样品制备复杂,操作时间长,试剂量大。为了克服这些挑战,使用微流控平台(MFP)系统开发了全自动CHO HCP测定方法,并与现有的基于平板的ELISA法进行了比较,用于单克隆抗体纯化中间体中HCP的定量。结果:与基于Tecan板的ELISA相比,基于MFP的自动化检测方法提高了吞吐量(快5 - 10倍),更宽的动态范围(100倍),减少了样品消耗、手工时间和检测开发持续时间。结论:新开发的微流控法比常规方法更具有优势。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A microfluidic approach to high throughput quantification of host cell protein impurities for bioprocess development
Background: Analysis of process-related impurities is critical for the control of biopharmaceutical processes and the quality of final biological products. Residual impurities in monoclonal antibody products such as host cell proteins (HCPs) increase the risk of immunogenicity and may directly affect drug potency. Commonly used HCP ELISA often involves complicated sample preparation, lengthy operation, and large volumes of reagent. To overcome these challenges, a fully automated CHO HCP assay was developed using a microfluidic platform (MFP) system and compared with existing plate-based ELISA for quantification of HCP in monoclonal antibody purification intermediates. Results: The automated MFP based assay approach enabled an improved throughput (5–10-times faster), broader dynamic range (100-times) and decreased sample consumption, hands on time and duration for assay development compared with Tecan plate-based ELISA. Conclusion: The newly developed microfluidic assay demonstrated its advantages over pla...
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