Very fast analysis of impurities in immunoglobulin concentrates using conjoint liquid chromatography on short monolithic disks

被引:37
作者
Branovic, K
Lattner, G
Barut, M
Strancar, A
Josic, D
Buchacher, A
机构
[1] Octapharm Pharmazeut Produktionsges MBH, A-1100 Vienna, Austria
[2] Inst Immunol Inc, Zagreb, Croatia
[3] BIA Separat Doo, Ljubljana, Slovenia
关键词
monolithic column; CLC; conjoint liquid chromatography; immunoglobulin; albumin; transferrin; quantification; validation;
D O I
10.1016/S0022-1759(02)00339-3
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Transferrin and albumin are often present in immunoglobulin G (IgG) concentrates and are considered as impurities. Therefore, it is important to determine their concentration in order to obtain a well-characterized biological product. Here, we describe their determination based on conjoint liquid chromatography (CLC). The established method combines two different chromatographic modes in one step: affinity and ion-exchange chromatography (IEC) combined in one column. Therefore, two CIM Protein G and one CIM quaternary amine (QA) monolithic disks were placed in series in one housing, forming a CLC monolithic column. Binding conditions were optimized in a way that immunoglobulins were captured on the CIM Protein G disks, while transferrin and albumin were bound on the CIM QA disks. Subsequently, transferrin and albumin were eluted separately by a stepwise gradient with sodium chloride, whereas immunoglobulins were released from the Protein G ligands by applying low pH. A complete separation of all three proteins was achieved in less than 5 min. The method permits the quantification of albumin and transferrin in IgG concentrates and has been successfully validated. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:47 / 58
页数:12
相关论文
共 29 条
[1]  
AKERSTROM B, 1985, J IMMUNOL, V135, P2589
[2]  
BJORCK L, 1984, J IMMUNOL, V133, P969
[3]   PREPARATION AND PROPERTIES OF SERUM AND PLASMA PROTEINS .4. A SYSTEM FOR THE SEPARATION INTO FRACTIONS OF THE PROTEIN AND LIPOPROTEIN COMPONENTS OF BIOLOGICAL TISSUES AND FLUIDS [J].
COHN, EJ ;
STRONG, LE ;
HUGHES, WL ;
MULFORD, DJ ;
ASHWORTH, JN ;
MELIN, M ;
TAYLOR, HL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1946, 68 (03) :459-475
[4]  
Curling J., 1980, METHODS PLASMA PROTE
[5]  
Dickler HB, 1996, ADV INTERNAL MED, V41, P641
[6]   Real-time isoform analysis by two-dimensional chromatography of a monoclonal antibody during bioreactor fermentations [J].
Fang, Y ;
Dumont, L ;
Larsen, B .
JOURNAL OF CHROMATOGRAPHY A, 1998, 816 (01) :39-47
[7]   COLUMN ION-EXCHANGE CHROMATOGRAPHIC PRODUCTION OF HUMAN IMMUNE SERUM GLOBULIN FOR INTRAVENOUS USE [J].
FRIESEN, AD ;
BOWMAN, JM ;
BEES, WCH .
VOX SANGUINIS, 1985, 48 (04) :201-212
[8]   Quantitative investigation of the affinity properties of different recombinant forms of protein G by means of high-performance monolithic chromatography [J].
Gupalova, TV ;
Lojkina, OV ;
Pàlàgnuk, VG ;
Totolian, AA ;
Tennikova, TB .
JOURNAL OF CHROMATOGRAPHY A, 2002, 949 (1-2) :185-193
[9]  
HAGE DS, 1987, J CHROMATOGR, V386, P37
[10]   Control method for integrity of continuous beds [J].
Hahn, R ;
Jungbauer, A .
JOURNAL OF CHROMATOGRAPHY A, 2001, 908 (1-2) :179-184