Development of a stacking-CZE method for the analysis of phenolic acids
Language English Country Great Britain, England Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
16488099
DOI
10.1016/j.jpba.2006.01.025
PII: S0731-7085(06)00063-X
Knihovny.cz E-resources
- MeSH
- alpha-Cyclodextrins chemistry MeSH
- Electrophoresis, Capillary methods MeSH
- Hydroxybenzoates analysis MeSH
- Calibration MeSH
- Hydrogen-Ion Concentration MeSH
- Reproducibility of Results MeSH
- Sensitivity and Specificity MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- alpha-Cyclodextrins MeSH
- alpha-cyclodextrin MeSH Browser
- Hydroxybenzoates MeSH
- phenolic acid MeSH Browser
Eight phenolic acids were analyzed by capillary zone electrophoresis. On-line analyte preconcentration was carried out by hydrodynamic injection of large volume of sample followed by removal of the bulk of the low conductivity sample matrix by polarity switching. The optimal electrolyte system consisted of 50mM sodium tetraborate of pH 9.0 (adjusted with 0.1 M phosphoric acid) containing 2% of alpha-cyclodextrin. The separations were carried out with a fused silica capillary (effective length 50 cm, i.d. 50 microm) and monitored at 200 nm. Under optimized preconcentration conditions (sample injection 99 s at 100 mbar and the polarity switching time 1.0 min) linear calibration ranges (0.1-2.0 microg/ml, R=0.9979-0.9995), favourable limits of detection (0.01-0.025 microg/ml) and good repeatability of the peak areas (R.S.D.: 2.76-5.69%, n=6) were achieved.
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