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
[11]   SIMPLIFIED METHOD FOR SILVER STAINING OF PROTEINS IN POLYACRYLAMIDE GELS AND THE MECHANISM OF SILVER STAINING [J].
HEUKESHOVEN, J ;
DERNICK, R .
ELECTROPHORESIS, 1985, 6 (03) :103-112
[12]   PREVENTION OF RH-IMMUNIZATION - MODIFIED PRODUCTION OF IGG ANTI-RH FOR INTRAVENOUS APPLICATION BY ION-EXCHANGE CHROMATOGRAPHY (IEC) [J].
HOPPE, HH ;
MESTER, T ;
HENNIG, W ;
KREBS, HJ .
VOX SANGUINIS, 1973, 25 (04) :308-316
[13]   Monoliths as stationary phases for separation of proteins and polynucleotides and enzymatic conversion [J].
Josic, D ;
Buchacher, A ;
Jungbauer, A .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2001, 752 (02) :191-205
[14]   Use of compact, porous units with immobilized ligands with high molecular masses in affinity chromatography and enzymatic conversion of substrates with high and low molecular masses [J].
Josic, D ;
Schwinn, H ;
Strancar, A ;
Podgornik, A ;
Barut, M ;
Lim, YP ;
Vodopivec, M .
JOURNAL OF CHROMATOGRAPHY A, 1998, 803 (1-2) :61-71
[15]   LARGE SCALE PRODUCTION OF HUMAN PLASMA FRACTIONS [J].
KISTLER, P ;
NITSCHMANN, H .
VOX SANGUINIS, 1962, 7 (04) :414-&
[16]   CLEAVAGE OF STRUCTURAL PROTEINS DURING ASSEMBLY OF HEAD OF BACTERIOPHAGE-T4 [J].
LAEMMLI, UK .
NATURE, 1970, 227 (5259) :680-+
[17]   SURFACE-MODIFIED MEMBRANES AS A MATRIX FOR PROTEIN-PURIFICATION [J].
LANGLOTZ, P ;
KRONER, KH .
JOURNAL OF CHROMATOGRAPHY, 1992, 591 (1-2) :107-113
[18]  
Mancini G, 1965, Immunochemistry, V2, P235, DOI 10.1016/0019-2791(65)90004-2
[19]  
NOURICHAFI N, 1993, BIOTECHNOL BLOOD PRO, V227, P207
[20]   Multifunctional fractionation of polyclonal antibodies by immunoaffinity high-performance monolithic disk chromatography [J].
Ostryanina, ND ;
Vlasov, GP ;
Tennikova, TB .
JOURNAL OF CHROMATOGRAPHY A, 2002, 949 (1-2) :163-171