Characterization of supermacroporous monolithic polyacrylamide based matrices designed for chromatography of bioparticles

被引:155
作者
Plieva, FM
Savina, IN
Deraz, S
Andersson, J
Galaev, IY
Mattiasson, B
机构
[1] Lund Univ, Dept Biotechnol, Ctr Chem & Chem Engn, SE-22100 Lund, Sweden
[2] Protista Int AB, SE-26722 Bjuv, Sweden
[3] Russian Acad Sci, AN Nesmeyanov Organoelement Cpds Inst, Moscow 119991, Russia
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2004年 / 807卷 / 01期
关键词
monolithic column; bioparticles; cryogel; supermacroporous polyacrylamide;
D O I
10.1016/j.jchromb.2004.01.050
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Supermacroporous monolithic acrylamide (AAm)-based cryogels were prepared by radical cryo-polymerizaton (polymerization in the moderately frozen system) of AAm with functional monomers and cross-linker N,N'-methylene-bis-acrylamide (MBAAm). Electron microscopy studies revealed supermacroporous structure of the developed cryogels with pore size of 5-100 mum. Cryogel porosity depended on cryo-polymerization conditions. More than 90% of the monolithic bed volume is the interconnected supermacropores filled with water and less than 10% of the monolithic volume is pore walls. The total protein binding capacity (lysozyme in the case of immobilized metal affinity chromatography (IMAC) column and bovine serum albumin (BSA) in the case of anion-exchange (AE) column) was independent of the flow rates till 600 cm/h. Chromatographic behavior of E. coli cells when a cell suspension was applied to ion-exchange cryogel columns depended on both the density of functional ligand and the porosity of the cryogel. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:129 / 137
页数:9
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