Cationic polymer precipitation for enhanced impurity removal in downstream processing

色谱法 降水 化学 下游加工 等电点 大小排阻色谱法 蛋白质沉淀 超滤(肾) 质谱法 过滤(数学) 错流过滤 生物化学 物理 气象学 统计 数学
作者
Zhao Li,Justin Chen,Kirby Martinez‐Fonts,Michael A. Rauscher,Shannon Rivera,John P. Welsh,Sunitha Kandula
出处
期刊:Biotechnology and Bioengineering [Wiley]
卷期号:120 (7): 1902-1913 被引量:5
标识
DOI:10.1002/bit.28416
摘要

Abstract Precipitation can be used for the removal of impurities early in the downstream purification process of biologics, with the soluble product remaining in the filtrate through microfiltration. The objective of this study was to examine the use of polyallylamine (PAA) precipitation to increase the purity of product via higher host cell protein removal to enhance polysorbate excipient stability to enable a longer shelf life. Experiments were performed using three monoclonal antibodies (mAbs) with different properties of isoelectric point and IgG subclass. High throughput workflows were established to quickly screen precipitation conditions as a function of pH, conductivity and PAA concentrations. Process analytical tools (PATs) were used to evaluate the size distribution of particles and inform the optimal precipitation condition. Minimal pressure increase was observed during depth filtration of the precipitates. The precipitation was scaled up to 20L size and the extensive characterization of precipitated samples after protein A chromatography showed >75% reduction of host cell protein (HCP) concentrations (by ELISA), >90% reduction of number of HCP species (by mass spectrometry), and >99.8% reduction of DNA. The stability of polysorbate containing formulation buffers for all three mAbs in the protein A purified intermediates was improved at least 25% after PAA precipitation. Mass spectrometry was used to obtain additional understanding of the interaction between PAA and HCPs with different properties. Minimal impact on product quality and <5% yield loss after precipitation were observed while the residual PAA was <9 ppm. These results expand the toolbox in downstream purification to solve HCP clearance issues for programs with purification challenges, while also providing important insights into the integration of precipitation–depth filtration and the current platform process for the purification of biologics.
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