The Critical Role of Mobile Phase Composition in Size Exclusion Chromatography of Protein Pharmaceuticals

被引:176
作者
Arakawa, Tsutomu [1 ]
Ejima, Daisuke [2 ]
Li, Tiansheng [3 ]
Phil, John S. [1 ]
机构
[1] Alliance Prot Labs, Thousand Oaks, CA USA
[2] Ajinomoto Inc, Amino Sci Labs, Dept Appl Res, Kanagawa, Japan
[3] HTL Biosolut Inc, Newbury Pk, CA USA
关键词
size exclusion chromatography; nonspecific adsorption; cosolvent; organic solvent; arginine; negative binding; GEL-PERMEATION CHROMATOGRAPHY; FIELD-FLOW FRACTIONATION; PERFORMANCE LIQUID-CHROMATOGRAPHY; COLUMN CHROMATOGRAPHY; AMINO ACIDS; ANALYTICAL ULTRACENTRIFUGATION; GLOBULAR-PROTEINS; AMMONIUM-SULFATE; MOLECULAR-WEIGHT; PREFERENTIAL INTERACTIONS;
D O I
10.1002/jps.21974
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Size exclusion chromatography (SEC) is the most widely used method for aggregation analysis of pharmaceutical proteins. However SEC analysis has a number of limitations, and one of the most important ones is protein adsorption to the resin. This problem is particularly severe when using new columns, and often column preconditioning protocols are required. This review focuses on the role that addition of various cosolvents to the mobile phase plays in suppressing that protein adsorption. Cosolvents such as salt, amino acids, and organic solvents are often used for this purpose. Because the protein interaction with the resin surface is highly heterogeneous, different cosolvents affect the protein adsorption differently. We will summarize the various effects of cosolvents on protein adsorption and retention and describe the mechanism of the cosolvent effects. (C) 2009 Wiley-Liss, Inc. and the American Pharmacists Association J Pharm Sci 99:1674-1692, 2010
引用
收藏
页码:1674 / 1692
页数:19
相关论文
共 112 条
[81]   HYDROPHOBIC CHROMATOGRAPHY AND FRACTIONATION OF ENZYMES FROM EXTREMELY HALOPHILIC BACTERIA USING DECREASING CONCENTRATION GRADIENTS OF AMMONIUM-SULFATE [J].
MEVARECH, M ;
LEICHT, W ;
WERBER, MM .
BIOCHEMISTRY, 1976, 15 (11) :2383-2387
[82]   Production and crystallization of lobster muscle tropomyosin expressed in Sf9 cells [J].
Miegel, A ;
Sano, K ;
Yamamoto, K ;
Maeda, K ;
Maeda, Y ;
Taniguchi, H ;
Yao, M ;
Wakatsuki, S .
FEBS LETTERS, 1996, 394 (02) :201-205
[83]   Influence of macromolecular crowding upon the stability and state of association of proteins: Predictions and observations [J].
Minton, AP .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2005, 94 (08) :1668-1675
[84]   In situ analysis of protein chromatography and column efficiency using magnetic resonance imaging [J].
Mitchell, NS ;
Hagel, L ;
Fernandez, EJ .
JOURNAL OF CHROMATOGRAPHY A, 1997, 779 (1-2) :73-89
[85]   PREVENTION OF ADSORPTION OF PROTEIN ON CONTROLLED-PORE GLASS WITH AMINO-ACID BUFFER [J].
MIZUTANI, T ;
MIZUTANI, A .
JOURNAL OF CHROMATOGRAPHY, 1975, 111 (01) :214-216
[86]  
NOZAKI Y, 1970, J BIOL CHEM, V245, P1648
[87]  
NOZAKI Y, 1971, J BIOL CHEM, V246, P2211
[88]  
NOZAKI Y, 1965, J BIOL CHEM, V240, P3568
[89]  
NOZAKI Y, 1963, J BIOL CHEM, V238, P4074
[90]   NON-SIZE EXCLUSION EFFECTS DURING GEL-PERMEATION CHROMATOGRAPHY OF MILK PROTEIN HYDROLYSATES ON AN FPLC SUPEROSE-12 COLUMN [J].
OCALLAGHAN, DM ;
DONNELLY, WJ ;
SLATTERY, HM ;
MULVIHILL, DM .
JOURNAL OF LIQUID CHROMATOGRAPHY, 1995, 18 (08) :1543-1562