Development of different comprehensive two dimensional systems for the separation of phenolic antioxidants
Language English Country Germany Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
- MeSH
- Electrophoresis, Gel, Two-Dimensional MeSH
- Food Analysis methods MeSH
- Antioxidants analysis chemistry isolation & purification MeSH
- Chemistry Techniques, Analytical instrumentation methods MeSH
- Chromatography, Liquid methods MeSH
- Chromatography methods MeSH
- Phenol analysis chemistry isolation & purification MeSH
- Kinetics MeSH
- Silicon Dioxide chemistry MeSH
- Beer MeSH
- Polyethylene Glycols chemistry MeSH
- Regression Analysis MeSH
- Carbon chemistry MeSH
- Chromatography, High Pressure Liquid methods MeSH
- Zirconium chemistry MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Antioxidants MeSH
- Phenol MeSH
- Silicon Dioxide MeSH
- Polyethylene Glycols MeSH
- Carbon MeSH
- zirconium oxide MeSH Browser
- Zirconium MeSH
Three different comprehensive 2-D HPLC systems for the separation of phenolic antioxidants have been developed on the basis of different selectivities of a PEG-silica column in the first dimension and a packed or monolithic C18 or a ZR-CARBON column, respectively, in the second dimension. Two-dimensional comprehensive liquid chromatography using a serially connected short PEG-silica column and a conventional C18-silica or a ZR-CARBON column in the second dimension was tested to improve the resolution of the earlier eluting compounds in the first dimension. Various types of interface were used to connect the columns in the first and in the second dimension: i) two injection sampling loops of 100 microL in conventional arrangement; ii) a 10-port 2-position valve equipped with two trapping X-Terra columns instead of loops; and iii) two analytical D2 columns in parallel. The mobile phase in the first dimension has a lower elution strength than in the second dimension, allowing band compression of the solutes transferred from the first to the second dimension. This effect was enhanced using trapping columns instead of sampling loops as the interface between the two dimensions, thus allowing a decrease in the time of analysis. These systems were used for the analysis of beer samples. The relative location of the components in the 2-D retention plane varied in relation to their chemical structure in each instrumental set-up and allowed positive peak identification.
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