Countercurrent staged diafiltration for formulation of high value proteins

被引:29
作者
Nambiar, Anirudh M. K. [1 ]
Li, Ying [1 ]
Zydney, Andrew L. [1 ]
机构
[1] Penn State Univ, Dept Chem Engn, University Pk, PA 16802 USA
关键词
antibody; continuous processing; diafiltration; formulation; ultrafiltration; OPTIMIZATION; PURIFICATION; CASCADE;
D O I
10.1002/bit.26441
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
A number of groups have studied the application of continuous bioreactors and continuous chromatographic systems as part of efforts to develop an integrated continuous biomanufacturing process. The objective of this study was to examine the feasibility of using a countercurrent staged diafiltration process for continuous protein formulation with reduced buffer requirements. Experiments were performed using a polyclonal immunoglobulin (IgG) with Cadence Inline Concentrators. Model equations were developed for the product yield, impurity removal, and buffer requirements as a function of the number of stages and the stage conversion (ratio of permeate to feed flow rate). Data from a countercurrent two-stage system were in excellent agreement with model calculations, demonstrating the potential of using countercurrent staged diafiltration for protein formulation. Model simulations demonstrated the importance of the countercurrent staging on both the extent of buffer exchange and the amount of buffer required per kg of formulated product. The staged diafiltration process not only provides for continuous buffer exchange, it could also provide significant reductions in the number of pump passes while providing opportunities for reduced buffer requirements.
引用
收藏
页码:139 / 144
页数:6
相关论文
共 17 条
[1]   Protein concentration with single-pass tangential flow filtration (SPTFF) [J].
Casey, Catherine ;
Gallos, Tina ;
Alekseev, Yana ;
Ayturk, Engin ;
Pearl, Steven .
JOURNAL OF MEMBRANE SCIENCE, 2011, 384 (1-2) :82-88
[2]  
Cheryan M., 1998, Ultrafiltration and microfiltration handbook
[3]   Purification of monoclonal antibodies from clarified cell culture fluid using Protein A capture continuous countercurrent tangential chromatography [J].
Dutta, Amit K. ;
Tran, Travis ;
Napadensky, Boris ;
Teella, Achyuta ;
Brookhart, Gary ;
Ropp, Philip A. ;
Zhang, Ada W. ;
Tustian, Andrew D. ;
Zydney, Andrew L. ;
Shinkazh, Oleg .
JOURNAL OF BIOTECHNOLOGY, 2015, 213 :54-64
[4]   Periodic counter-current chromatography - design and operational considerations for integrated and continuous purification of proteins [J].
Godawat, Rahul ;
Brower, Kevin ;
Jain, Sujit ;
Konstantinov, Konstantin ;
Riske, Frank ;
Warikoo, Veena .
BIOTECHNOLOGY JOURNAL, 2012, 7 (12) :1496-1508
[5]  
Harrison R.G., 2002, Bioseparations Science and Engineering
[6]  
Kang J., 2016, BioProcess Int, V14, P40
[7]   The "push-to-low" approach for optimization of high-density perfusion cultures of animal cells [J].
Konstantinov, Konstantin ;
Goudar, Chetan ;
Ng, Maria ;
Meneses, Renato ;
Thrift, John ;
Chuppa, Sandy ;
Matanguihan, Cary ;
Michaels, Jim ;
Naveh, David .
CELL CULTURE ENGINEERING, 2006, 101 :75-98
[8]  
Lacki K., 2011, U.S. Pat., Patent No. [7901581, 7,901,581]
[9]   Nanofiltration membrane cascade for continuous solvent exchange [J].
Lin, Justin Chun-Te ;
Livingston, Andrew G. .
CHEMICAL ENGINEERING SCIENCE, 2007, 62 (10) :2728-2736
[10]   Concepts of industrial-scale diafiltration systems [J].
Lipnizki, F ;
Boelsmand, J ;
Madsen, RF .
DESALINATION, 2002, 144 (1-3) :179-184