Monolithic poly(N-vinylcarbazole-co-1,4-divinylbenzene) capillary columns for the separation of biomolecules

• Published in: Analyst (London) Vol. 138; no. 17; pp. 589 - 598
• Main Authors: Koeck, Rainer, Bakry, Rania, Tessadri, Richard, Bonn, Guenther K
• Format: Journal Article
• Language: English
• Published: England 01.01.2013
• Subjects: Biomolecules; Capillarity; Chromatography, High Pressure Liquid - methods; Copolymerization; Elution; Free radicals; Mercury - chemistry; Nitrogen - chemistry; Oligonucleotides; Oligonucleotides - isolation & purification; Peptides - isolation & purification; Polyvinyls - chemistry; Porosity; Proteins - isolation & purification; Scanning electron microscopy; Separation; Vinyl Compounds - chemistry
• ISSN: 0003-2654; 1364-5528
• DOI: 10.1039/c3an00377a

Monolithic capillary columns were prepared by thermally initiated free radical copolymerization of N -vinylcarbazole (NVC) and 1,4-divinylbenzene (DVB) within the confines of 200 and 100 μm i.d. fused silica capillaries. The reaction was carried out under the influence of inert micro-(toluene) and macroporogen (1-decanol) and α,α′-azoisobutyronitrile (AIBN) as a free radical initiator. The material proved high mechanical stability applying water and acetonitrile as mobile phases. The morphological and porous properties were studied by scanning electron microscopy (SEM), nitrogen sorption (BET) and mercury intrusion porosimetry (MIP). The homogeneity of the copolymerization process was confirmed by elemental analysis and monomer conversion measurements. The newly developed NVC/DVB monolithic supports showed high separation efficiency towards biomolecules, applying reversed-phase (RP) and ion-pair reversed-phase (IP-RP) separation modes, which is exemplified by the separations of peptides, proteins and oligonucleotides. Furthermore the maximum loading capacity was evaluated. The chromatographic performance under isocratic elution was determined in terms of theoretical plate number and plate height, where up to 41 000 plates per column and a minimum plate height value of 1.7 μm were achieved, applying oligonucleotide separations. In gradient elution mode, peak capacities of 96 and 127 were achieved within a gradient time window of 60 min for protein and oligonucleotide separations, respectively. The material proved to have high permeability, good repeatability of the fabrication process and high surface areas in the range of 120-160 m 2 g −1 . A monolithic poly( N -vinylcarbazole- co -1,4-divinylbenzene) stationary phase with high separation efficiency towards biomolecules, high permeability, minimum plate height of 1.7 μm in 100 μm i.d. capillary column and surface areas of 120-160 m 2 g −1 is prepared.