Bridged polysilsesquioxane-based wide-bore monolithic capillary columns for hydrophilic interaction chromatography
Language English Country Netherlands Media print-electronic
Document type Journal Article
PubMed
27939871
DOI
10.1016/j.chroma.2016.11.062
PII: S0021-9673(16)31611-9
Knihovny.cz E-resources
- Keywords
- HILIC, Nucleosides, Oligosaccharides, Silica monolithic column,
- MeSH
- Chromatography, Liquid instrumentation methods MeSH
- Ethane analogs & derivatives chemistry MeSH
- Spectrometry, Mass, Electrospray Ionization MeSH
- Hydrophobic and Hydrophilic Interactions MeSH
- Immunoglobulin G metabolism MeSH
- Humans MeSH
- Methacrylates chemistry MeSH
- Microscopy, Electron, Scanning MeSH
- Oligosaccharides analysis isolation & purification MeSH
- Organosilicon Compounds chemistry MeSH
- Silicon Dioxide chemistry MeSH
- Ribonucleases metabolism MeSH
- Cattle MeSH
- Trimethylsilyl Compounds chemistry MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Cattle MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- 3-(trimethoxysilyl)propyl methacrylate MeSH Browser
- bis(trimethoxysilyl)ethane MeSH Browser
- Ethane MeSH
- Immunoglobulin G MeSH
- Methacrylates MeSH
- Oligosaccharides MeSH
- Organosilicon Compounds MeSH
- Silicon Dioxide MeSH
- polysilsesquioxane MeSH Browser
- ribonuclease B MeSH Browser
- Ribonucleases MeSH
- Trimethylsilyl Compounds MeSH
The synthesis and characterization of large-bore silica-based monolithic capillary columns (0.32mm×150mm) are presented. Columns were prepared by acidic hydrolysis of a mixture containing tetramethoxysilane (TMOS) and 1,2-bis(trimethoxysilyl)ethane (BTME) in different molar ratios in the presence of polyethylene glycol and urea. The monoliths were modified by zwitterionic monomer [2-(methacryloyloxy)ethyl]-dimethyl-(3-sulfopropyl)-ammonium hydroxide via 3-(trimethoxysilyl)propyl methacrylate. Prepared stationary phases were evaluated by scanning electron microscopy and chromatographic separation of nucleobases and their derivatives in the HILIC mode. The best chromatographic results were obtained with the column prepared from the reaction mixture containing BTME and TMOS in a 1:4 molar ratio. The permeability of such column reached 1.68×10-14m2 and the efficiency, expressed as a height equivalent of the theoretical plate, did not exceed 10.5μm for the tested compounds. The columns were successfully applied to HILIC separation of native and labeled oligosaccharides and glycans released from bovine ribonuclease B and human immunoglobulin G.
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