Methacrylate-based short monolithic columns: enabling tools for rapid and efficient analyses of biomolecules and nanoparticles.

This review describes the novel chromatography stationary phase--a porous monolithic methacrylate-based polymer--in terms of the design of the columns and some of the features that make these columns attractive for the purification of large biomolecules. We first start with a brief summary of the characteristics of these large molecules (more precisely large proteins like immunoglobulins G and M, plasmid deoxyribonucleic acid (DNA), and viral particles), and a list of some of the problems that were encountered during the development of efficient purification processes. We then briefly describe the structure of the methacrylate-based monolith and emphasize the features which make them more than suitable for dealing with large entities. The highly efficient structure on a small scale can be transferred to a large scale without the need of making column modifications, and the various approaches of how this is accomplished are briefly presented in this paper. This is followed by presenting some of the examples from the bioprocess development schemes, where the implementation of the methacrylate-based monolithic columns has resulted in a very efficient and productive process. Following this, we move back to the analytical scale and demonstrate the efficiency of the monolithic column--where the mass transfer between the stationary and mobile phase is greatly enhanced--for the in-process and final control of the new therapeutics. The combination of an efficient structure and the appropriate hardware results in separations of proteins with residence time less than 0.1 s.

[1]  A. Jungbauer,et al.  Polymethacrylate monoliths for preparative and industrial separation of biomolecular assemblies. , 2008, Journal of chromatography. A.

[2]  A. Podgornik,et al.  Purification and concentration of bacteriophage T4 using monolithic chromatographic supports. , 2008, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

[3]  A. Podgornik,et al.  Influence of the methacrylate monolith structure on genomic DNA mechanical degradation, enzymes activity and clogging. , 2007, Journal of chromatography. A.

[4]  David R. Latulippe,et al.  Flux-dependent transmission of supercoiled plasmid DNA through ultrafiltration membranes , 2007 .

[5]  M. Peterka,et al.  Short monolithic columns--a breakthrough in purification and fast quantification of tomato mosaic virus. , 2007, Journal of chromatography. A.

[6]  A. Podgornik,et al.  Fast and efficient separation of immunoglobulin M from immunoglobulin G using short monolithic columns. , 2007, Journal of chromatography. A.

[7]  A. Jungbauer,et al.  Dispersion effects in preparative polymethacrylate monoliths operated in radial-flow columns. , 2007, Journal of biochemical and biophysical methods.

[8]  Uwe Gottschalk,et al.  New Q membrane scale-down model for process-scale antibody purification. , 2006, Journal of chromatography. A.

[9]  D. Roper,et al.  Adenovirus type 5 intrinsic adsorption rates measured by surface plasmon resonance. , 2006, Analytical biochemistry.

[10]  Joe X. Zhou,et al.  Basic Concepts in Q Membrane Chromatography for Large‐Scale Antibody Production , 2006, Biotechnology progress.

[11]  W. Buchinger,et al.  Industrial Scale cGMP Purification of Pharmaceutical Grade Plasmid‐DNA , 2005 .

[12]  Ales Podgornik,et al.  Convective interaction media short monolithic columns: enabling chromatographic supports for the separation and purification of large biomolecules. , 2005, Journal of separation science.

[13]  Ales Podgornik,et al.  Application of monoliths for plasmid DNA purification development and transfer to production. , 2005, Journal of chromatography. A.

[14]  A. Podgornik,et al.  Convective Interaction Media (CIM)--short layer monolithic chromatographic stationary phases. , 2005, Biotechnology annual review.

[15]  Jochen Urthaler,et al.  Improved downstream process for the production of plasmid DNA for gene therapy. , 2005, Acta biochimica Polonica.

[16]  A. Podgornik,et al.  Large-scale methacrylate monolithic columns: design and properties. , 2004, Journal of biochemical and biophysical methods.

[17]  A. Jungbauer,et al.  Mass transfer characteristics of plasmids in monoliths. , 2004, Journal of separation science.

[18]  A. Podgornik,et al.  Chapter 3 - Short Monolithic Columns ­ Rigid Disks , 2003 .

[19]  A. Podgornik,et al.  Transfer of gradient chromatographic methods for protein separation to Convective Interaction Media monolithic columns. , 2003, Journal of chromatography. A.

[20]  I. Mihelič,et al.  Temperature distribution effects during polymerization of methacrylate‐based monoliths , 2003 .

[21]  Hiroshi Kobayashi,et al.  Chapter 8 – Monolithic Silica Columns for Capillary Liquid Chromatography , 2003 .

[22]  I. Mihelič,et al.  Chapter 4 – Tubes , 2003 .

[23]  F. Švec,et al.  Monolithic materials : preparation, properties and applications , 2003 .

[24]  D. Josić,et al.  Very fast analysis of impurities in immunoglobulin concentrates using conjoint liquid chromatography on short monolithic disks. , 2002, Journal of immunological methods.

[25]  A. Podgornik,et al.  APPLICATION OF VERY SHORT MONOLITHIC COLUMNS FOR SEPARATION OF LOW AND HIGH MOLECULAR MASS SUBSTANCES , 2002 .

[26]  G. Carta,et al.  Protein adsorption on novel acrylamido-based polymeric ion-exchangers. IV. Effects of protein size on adsorption capacity and rate. , 2002, Journal of chromatography. A.

[27]  R. Hahn,et al.  Mass transfer properties of monoliths , 2002 .

[28]  A. Podgornik,et al.  Short monolithic columns as stationary phases for biochromatography. , 2002, Advances in biochemical engineering/biotechnology.

[29]  I. Mihelič,et al.  Kinetic model of a methacrylate-based monolith polymerization , 2001 .

[30]  A. Podgornik,et al.  The effect of agitation and nitrogen concentration on lignin peroxidase (LiP) isoform composition during fermentation of Phanerochaete chrysosporium. , 2001, Journal of biotechnology.

[31]  D. Josić,et al.  Monoliths as stationary phases for separation of proteins and polynucleotides and enzymatic conversion. , 2001, Journal of chromatography. B, Biomedical sciences and applications.

[32]  R L Fahrner,et al.  Membrane ion-exchange chromatography for process-scale antibody purification. , 2001, Journal of chromatography. A.

[33]  D. Josić,et al.  Application of monoliths for downstream processing of clotting factor IX. , 2000, Journal of chromatography. A.

[34]  E. Klein Affinity membranes: a 10-year review , 2000 .

[35]  A. Podgornik,et al.  Application of Convective Interaction Media (CIM) disk monolithic columns for fast separation and monitoring of organic acids. , 2000, Journal of chromatographic science.

[36]  D. Josić,et al.  Construction of large-volume monolithic columns. , 2000, Analytical chemistry.

[37]  J J Meyers,et al.  Network modeling of the convective flow and diffusion of molecules adsorbing in monoliths and in porous particles packed in a chromatographic column. , 1999, Journal of chromatography. A.

[38]  A. Podgornik,et al.  Isocratic separations on thin glycidyl methacrylate–ethylenedimethacrylate monoliths , 1999 .

[39]  D. Josić,et al.  Application of Membranes and Compact, Porous Units for the Separation of Biopolymers , 1999 .

[40]  F. Švec,et al.  Effect of porous structure of macroporous polymer supports on resolution in high-performance membrane chromatography of proteins. , 1998, Journal of chromatography. A.

[41]  J. Fréchet,et al.  Preparation of Large-Diameter “Molded” Porous Polymer Monoliths and the Control of Pore Structure Homogeneity , 1997 .

[42]  D. Josić,et al.  Application of compact porous tubes for preparative isolation of clotting factor VIII from human plasma. , 1997, Journal of chromatography. A.

[43]  K. Nakanishi,et al.  Octadecylsilylated porous silica rods as separation media for reversed-phase liquid chromatography. , 1996, Analytical chemistry.

[44]  D. Josić,et al.  Application of compact porous disks for fast separations of biopolymers and in-process control in biotechnology. , 1996, Analytical chemistry.

[45]  Jean M. J. Fréchet,et al.  New Designs of Macroporous Polymers and Supports: From Separation to Biocatalysis , 1996, Science.

[46]  Jacob H. Masliyah,et al.  SINGLE FLUID FLOW IN POROUS MEDIA , 1996 .

[47]  J. Fréchet,et al.  Monolithic, “Molded”, Porous Materials with High Flow Characteristics for Separations, Catalysis, or Solid-Phase Chemistry: Control of Porous Properties during Polymerization , 1996 .

[48]  E. Lightfoot,et al.  Estimating plate heights in stacked-membrane chromatography by flow reversal , 1995 .

[49]  Jean M. J. Fréchet,et al.  Kinetic Control of Pore Formation in Macroporous Polymers. Formation of "Molded" Porous Materials with High Flow Characteristics for Separations or Catalysis , 1995 .

[50]  F. Švec,et al.  High-performance membrane chromatography: Highly efficient separation method for proteins in ion-exchange, hydrophobic interaction and reversed-phase modes , 1993 .

[51]  Jean M. J. Fréchet,et al.  Continuous rods of macroporous polymer as high-performance liquid chromatography separation media , 1992 .

[52]  F. Švec,et al.  High-Performance Membrane Chromatography. A Novel Method of Protein Separation , 1990 .

[53]  S. Hjertén,et al.  High-performance liquid chromatography on continuous polymer beds , 1989 .

[54]  I. Pilz,et al.  Small-angle X-ray studies of a human immunoglobulin M. , 1978, European journal of biochemistry.