Monoliths for fast bioseparation and bioconversion and their applications in biotechnology

被引:147
作者
Jungbauer, A
Hahn, R
机构
[1] Univ Nat Resources & Appl Life Sci, Dept Biotechnol, A-1190 Vienna, Austria
[2] Austrian Ctr Biopharmaceut Technol, Vienna, Austria
关键词
macropores; gigapores; poly(glycidyl methacrylate-co-ethylene dimethacrylate); cryogel; poly(vinyl alcohol); polyacrylamide; monolith; bioseparation;
D O I
10.1002/jssc.200401812
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Monoliths have consolidated their position in bioseparation. More than 200 different applications have been reported in the past two decades and their advantages compared to conventional chromatography demonstrated. These include the high mass transfer efficiency due to the convective flow enabled by the macroporous character of the matrix. Recently plasmid DNA and viruses were separated with high efficiency and cryogels and monolithic superporous agarose were developed for capture of proteins from crude homogenates and separation of microorganisms or lymphocytes. Currently four companies manufacture monoliths mainly for analytical applications although monoliths with a volume of 0.8 liter are commercially available and 8 L are available as prototypes. A book entitled "Monolithic materials: preparation, properties and applications" was published in 2003 [1] and became standard reference of the status of this area. This review focuses on the progress in monoliths that goes beyond the scope of this reference book. Less progress has been made in the field of bioconversions in spite of the fact that monolithic supports exhibit better performance than beads in enzymatic processing of macromolecules. It appears that the scientific community has not yet realized that supports for these applications are readily available. In addition, monoliths will further substantially advance bioseparations of both small and large molecules in the future.
引用
收藏
页码:767 / 778
页数:12
相关论文
共 115 条
[1]  
Amatschek K, 2000, HRC-J HIGH RES CHROM, V23, P47
[2]  
[Anonymous], 1989, POLYM SCI USSR
[3]   Direct chromatographic capture of enzyme from crude homogenate using immobilized metal affinity chromatography on a continuous supermacroporous adsorbent [J].
Arvidsson, P ;
Plieva, FM ;
Lozinsky, VI ;
Galaev, IY ;
Mattiasson, B .
JOURNAL OF CHROMATOGRAPHY A, 2003, 986 (02) :275-290
[4]   Chromatography of microbial cells using continuous supermacroporous affinity and ion-exchange columns [J].
Arvidsson, P ;
Plieva, FM ;
Savina, IN ;
Lozinsky, VI ;
Fexby, S ;
Bülow, L ;
Galaev, IY ;
Mattiasson, B .
JOURNAL OF CHROMATOGRAPHY A, 2002, 977 (01) :27-38
[5]   Protein separation by monolithic capillary electrochromatography [J].
Bandilla, D ;
Skinner, CD .
JOURNAL OF CHROMATOGRAPHY A, 2003, 1004 (1-2) :167-179
[6]   Comparison of antibody binding to immobilized group specific affinity ligands in high performance monolith affinity chromatography [J].
Berruex, LG ;
Freitag, R ;
Tennikova, TB .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2000, 24 (01) :95-104
[7]   Application of short monolithic columns for fast purification of plasmid DNA [J].
Branovic, K ;
Forcic, D ;
Ivancic, J ;
Strancar, A ;
Barut, M ;
Gulija, TK ;
Zgorelec, R ;
Mazuran, R .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2004, 801 (02) :331-337
[8]   Application of short monolithic columns for improved detection of viruses [J].
Branovic, K ;
Forcic, D ;
Ivancic, J ;
Strancar, A ;
Barut, M ;
Kosutic-Gulija, T ;
Zgorelec, R ;
Mazuran, R .
JOURNAL OF VIROLOGICAL METHODS, 2003, 110 (02) :163-171
[9]   Very fast analysis of impurities in immunoglobulin concentrates using conjoint liquid chromatography on short monolithic disks [J].
Branovic, K ;
Lattner, G ;
Barut, M ;
Strancar, A ;
Josic, D ;
Buchacher, A .
JOURNAL OF IMMUNOLOGICAL METHODS, 2002, 271 (1-2) :47-58
[10]   FAST PROTEIN CHROMATOGRAPHY ON ANALYTICAL AND PREPARATIVE SCALE USING MODIFIED MICROPOROUS MEMBRANES [J].
BRIEFS, KG ;
KULA, MR .
CHEMICAL ENGINEERING SCIENCE, 1992, 47 (01) :141-149