The distinctive separation attributes of mixed-mode resins and their application in monoclonal antibody downstream purification process

被引:117
作者
Chen, Jie [1 ]
Tetrault, Jen [1 ]
Zhang, Yanyu [1 ]
Wasserman, Andy [1 ]
Conley, Greg [1 ]
DiLeo, Mike [1 ]
Haimes, Elliot [1 ]
Nixon, Andrew E. [1 ]
Ley, Arthur [1 ]
机构
[1] Dyax Corp, Proc Sci & Discovery Res, Cambridge, MA 02139 USA
关键词
Mixed-mode chromatography; MEP; CHT; Capto adhere; Aggregates removal; Monoclonal antibody purification process; CHARGE INDUCTION CHROMATOGRAPHY; PROTEIN-A;
D O I
10.1016/j.chroma.2009.09.047
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Increased upstream productivity and the continuous pressure to deliver high quality drug product have resulted in the development of new separation technologies and platform strategies for downstream purification processes of monoclonal antibodies (mAb). In this study, the separation attributes of three mixed-mode resins. Mercapto-Ethyl-Pyridine (MEP) hydrophobic charge induction resin, Capto adhere multi-modal anion exchange resin, and ceramic hydroxyapatite/fluoroapatite (CHT/CFT) resins, were investigated to define their roles in monoclonal antibody purification processes. We demonstrated that the multi-modal nature of ligands on mixed-mode resins allows the separation resolution to be honed, either through a single dominant mechanism or through mix-modal balanced purification strategies. in addition, the three mixed-mode resins present different purification powers for different types of impurities. We also demonstrated that besides enhancing chromatography separation and improve product quality. especially for high molecular weight (HMW) aggregate reduction. mixed-mode resins can also help to improve process efficiency in industrial-scale mAb drug manufacturing. Our results underscore the importance of selecting appropriate chromatography resins during DSP design to obtain the best overall process outcome. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:216 / 224
页数:9
相关论文
共 32 条
[1]   Scale-up of monoclonal antibody purification processes [J].
Aldington, Suzanne ;
Bonnerjea, Julian .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2007, 848 (01) :64-78
[2]  
[Anonymous], BIOPROCESS J
[3]  
*BIOR LAB, CHT CFT INSTR MAN
[4]   Antibody separation by hydrophobic charge induction chromatography [J].
Boschetti, E .
TRENDS IN BIOTECHNOLOGY, 2002, 20 (08) :333-337
[5]  
CHEN J, 2007, OCT PRES IBC INT BIO
[6]   Comparison of standard and new generation hydrophobic interaction chromatography resins in the monoclonal antibody purification process [J].
Chen, Jie ;
Tetrault, Jenifer ;
Ley, Arthur .
JOURNAL OF CHROMATOGRAPHY A, 2008, 1177 (02) :272-281
[7]   Where disease pathogenesis meets protein formulation: Renal deposition of immunoglobulin aggregates [J].
Demeule, B ;
Gumy, R ;
Arvinte, T .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2006, 62 (02) :121-130
[8]  
ERIKSSON K, 2009, BIOPROCESS INT, P52
[9]  
Ferreira GM, 2007, BIOPHARM INT, V20, P32
[10]  
FRANKLIN S, 2004, BIOPROCESS INT MAY, P56