Effects of resin ligand density on yield and impurity clearance in preparative cation exchange chromatography. II. Process characterization

被引:25
作者
Fogle, Jace [1 ]
Persson, Josefine [1 ]
机构
[1] Genentech Pharma Tech Dev, San Francisco, CA 94080 USA
关键词
Cation exchange chromatography; Monoclonal antibodies; Ligand density; SP Sepharose (TM) Fast Flow; Design of experiments; High-throughput screening; WEAK ACID GROUPS; ION-EXCHANGE; HYDROPHOBIC INTERACTION; PH TRANSITIONS; PROTEIN; SEPARATIONS; COLUMNS;
D O I
10.1016/j.chroma.2011.12.049
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Ion exchange resins are key raw materials in biopharmaceutical manufacturing processes, and variability in ligand density has the potential to compromise process robustness if not controlled within appropriate ranges. In this study, yield and impurity clearance were evaluated for several preparative cation exchange chromatography steps using SP Sepharose (TM) Fast Flow resins at the high, low, and center of the commercial ligand density specification range. This was accomplished using a design of experiments (DoE) approach coupled to high-throughput screening in 96-well plate format, as well as column chromatography experiments with gradient elution. Results of the DoE study indicated that ligand density variation within the commercial specification range of SP Sepharose (TM) Fast Flow had no effect on yield, HCP clearance, aggregate clearance, or distribution of charge variants. However, results from the column experiments showed that ligand density has the potential to influence protein elution profiles which can lead to small changes in impurity clearance in some cases. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:70 / 78
页数:9
相关论文
共 20 条
[1]  
Cecchini D., 2009, APPL DESIGN SPACE BI, P138
[2]   High-throughput screening of chromatographic separations: I. Method development and column modeling [J].
Coffman, Jonathan L. ;
Kramarczyk, Jack F. ;
Kelley, Brian D. .
BIOTECHNOLOGY AND BIOENGINEERING, 2008, 100 (04) :605-618
[3]   Determinants of protein retention characteristics on cation-exchange adsorbents [J].
DePhillips, P ;
Lenhoff, AM .
JOURNAL OF CHROMATOGRAPHY A, 2001, 933 (1-2) :57-72
[4]   Effects of resin ligand density on yield and impurity clearance in preparative cation exchange chromatography. I. Mechanistic evaluation [J].
Fogle, Jace ;
Mohan, Nina ;
Cheung, Eric ;
Persson, Josefine .
JOURNAL OF CHROMATOGRAPHY A, 2012, 1225 :62-69
[5]   Understanding and mitigating conductivity transitions in weak cation exchange chromatography [J].
Fogle, Jace ;
Hsiung, Jenny .
JOURNAL OF CHROMATOGRAPHY A, 2010, 1217 (05) :660-666
[6]   Factorial screening of antibody purification processes using three chromatography steps without protein A [J].
Follman, DK ;
Farner, RL .
JOURNAL OF CHROMATOGRAPHY A, 2004, 1024 (1-2) :79-85
[7]   Role of the ligand density in cation exchange materials for the purification of proteins [J].
Franke, Agnes ;
Forrer, Nicola ;
Butte, Alessandro ;
Cvijetic, Bozidar ;
Morbidelli, Massimo ;
Joehnck, Matthias ;
Schulte, Michael .
JOURNAL OF CHROMATOGRAPHY A, 2010, 1217 (15) :2216-2225
[8]   pH transitions in ion-exchange systems: Role in the development of a cation-exchange process for a recombinant protein [J].
Ghose, S ;
McNerney, TM ;
Hubbard, B .
BIOTECHNOLOGY PROGRESS, 2002, 18 (03) :530-537
[9]   Ion exchange chromatography of monoclonal antibodies: Effect of resin ligand density on dynamic binding capacity [J].
Hardin, Ann Marie ;
Harinarayan, Chithkala ;
Malmquist, Gunnar ;
Axen, Andreas ;
van Reis, Robert .
JOURNAL OF CHROMATOGRAPHY A, 2009, 1216 (20) :4366-4371
[10]   An exclusion mechanism in ion exchange chromatography [J].
Harinarayan, C. ;
Mueller, J. ;
Ljunglof, A. ;
Fahrner, R. ;
Van Alstine, J. ;
van Reis, R. .
BIOTECHNOLOGY AND BIOENGINEERING, 2006, 95 (05) :775-787