This proposal is aimed at the preparation and application of novel advanced bead polymers for use as packing materials in the high performance liquid chromatography of organic and biological fluids. The new monosized polymer beads would complement, and in some cases replace, existing silica-based materials by providing increased chemical stability as well as added functionality and versatility. In particular, new approaches to polymer beads that can perform several analyses in a single column are sought. These unprecedented truly """"""""multimodal"""""""" chromatographic media would be able to separate several classes of compounds such as proteins, drugs, and metabolites in a single column through a simple change in eluting solvent between each mode of chromato- graphic separation. To achieve this goal, important targets include the control of porous structures of the uniformly sized polymer beads, the control of the chemistry at the surface of their pores through a site selective separation process or a pore size-selective modification technique. For example, a bimodal column for the direct analysis of blood plasma might contain large hydrophilic pores for the analysis of proteins by aqueous size-exclusion chromatography, and small hydrophobic pores for the analysis of drugs and metabolites by reversed-phase chromatography. Several other types of bimodal as well as trimodal columns will be designed and prepared. The advantages of these multimodal columns are numerous: they facilitate analysis by eliminating steps of sample preparation or precolumn treatment, they provide a complete view of the contents of the biological fluid rather than a restricted view of one type of component only, and they reduce the complexity of instrumentation needed for the analysis. Similarly, great versatility is achieved as a vast array of monomers with reactive groups useful for advanced separations will be introduced in the new bead materials. In addition to direct applications to the analysis of biological and organic solutions, the new media can find applications in classical high performance liquid chromatography as they are extremely rugged and can operate in a broad spectrum of solvents over the entire pH range. Finally, tests on artificial samples will be carried out to evaluate their applicability to the determination of trace amounts of materials such as N-acetylneuraminic acid (for cancer diagnosis) or hemoperfusion. This study will also provide a fundamental understanding of the requirements for optimal porous particulate separation media for use in the analysis of biological samples.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM044885-05
Application #
2182837
Study Section
Metallobiochemistry Study Section (BMT)
Project Start
1990-07-01
Project End
1997-06-30
Budget Start
1994-07-01
Budget End
1995-06-30
Support Year
5
Fiscal Year
1994
Total Cost
Indirect Cost
Name
Cornell University
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
City
Ithaca
State
NY
Country
United States
Zip Code
14850
Slater, Michael D; Fréchet, Jean M J; Svec, Frantisek (2009) In-column preparation of a brush-type chiral stationary phase using click chemistry and a silica monolith. J Sep Sci 32:21-8
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Geiser, Laurent; Eeltink, Sebastiaan; Svec, Frantisek et al. (2008) In-line system containing porous polymer monoliths for protein digestion with immobilized pepsin, peptide preconcentration and nano-liquid chromatography separation coupled to electrospray ionization mass spectroscopy. J Chromatogr A 1188:88-96
Augustin, Violaine; Stachowiak, Timothy; Svec, Frantisek et al. (2008) CEC separation of peptides using a poly(hexyl acrylate-co-1,4-butanediol diacrylate-co-[2-(acryloyloxy)ethyl]trimethyl ammonium chloride) monolithic column. Electrophoresis 29:3875-86
Eeltink, Sebastiaan; Geiser, Laurent; Svec, Frantisek et al. (2007) Optimization of the porous structure and polarity of polymethacrylate-based monolithic capillary columns for the LC-MS separation of enzymatic digests. J Sep Sci 30:2814-20
Geiser, Laurent; Eeltink, Sebastiaan; Svec, Frantisek et al. (2007) Stability and repeatability of capillary columns based on porous monoliths of poly(butyl methacrylate-co-ethylene dimethacrylate). J Chromatogr A 1140:140-6
Xu, M; Brahmachary, E; Janco, M et al. (2001) Preparation of highly selective stationary phases for high-performance liquid chromatographic separation of enantiomers by direct copolymerization of monomers with single or twin chiral ligands. J Chromatogr A 928:25-40
Hosoya, K; Kishii, Y; Kimata, K et al. (1995) Uniform-size hydrophobic polymer-based separation media selectively modified with a hydrophilic external polymeric layer. J Chromatogr A 690:21-8

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