Improving impurities clearance by amino acids addition to buffer solutions for chromatographic purifications of monoclonal antibodies

被引:15
作者
Ishihara, Takashi [1 ]
Hosono, Mareto [1 ]
机构
[1] Kyowa Hakko Kirin Co Ltd, Prod Div, Bioproc Res & Dev Labs, Takasaki, Gunma 3700013, Japan
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2015年 / 995卷
关键词
Protein separation; Biopharmaceutical; Cell cultures; Chromatography resins; CATION-EXCHANGE CHROMATOGRAPHY; PROTEIN-A; THERMAL-STABILITY; ARGININE; ELUTION; AGGREGATION; FORMULATION; STABILIZATION; MECHANISM; HISTIDINE;
D O I
10.1016/j.jchromb.2015.05.018
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The performance of amino acids in Protein A affinity chromatography, anion exchange chromatography and cation exchange chromatography for monoclonal antibody purification was investigated. Glycine, threonine, arginine, glutamate, and histidine were used as buffer components in the equilibration, washing, and elution steps of these chromatographies. Improved clearance of impurity, high molecular weight species (HMW) and host cell proteins (HCP) was observed in the purification processes when using the amino acids as base-buffer constituents, additives or eluents compared with that of buffers without these amino acids. In addition, we designed a buffer system in which the mobile phases were composed of only a single amino acid, histidine, and applied it to the above three chromatographies. Effective HMW and HCP clearance was also obtained in this manner. These results suggest that amino acids may enhance impurity clearance during the purification of monoclonal antibodies. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:107 / 114
页数:8
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