Analytically useful pentafluoro ketone derivatives of fatty acids are described. The gas chromatographic/ mass spectrometric characteristics of these new derivatives are compared with those of methyl, trimethylsilyl and pentafluorobenzyl esters. Pentafluoro ketones exhibit excellent chromatographic
Sensitivity enhancement by on-line preconcentration and in-capillary derivatization for the electrophoretic determination of amino acids
✍ Scribed by Rosa M. Latorre; Javier Saurina; Santiago Hernández-Cassou
- Publisher
- John Wiley and Sons
- Year
- 2001
- Tongue
- English
- Weight
- 488 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0173-0835
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✦ Synopsis
Sensitivity enhancement by on-line preconcentration and in-capillary derivatization for the electrophoretic determination of amino acids
This study describes an application of on-line preconcentration by large-volume stacking in combination with in-capillary derivatization for enhancing spectrophotometric detection sensitivity in capillary electrophoresis. The method is illustrated by an example dealing with the determination of amino acids with 1,2-naphthoquinone-4-sulfonate as a labelling agent. Samples are dissolved in water in order to create a stacking process based on differences in the conductivity between this medium and a concentrated running buffer. The in-capillary derivatization is accomplished following a sandwich procedure in which the sample is inserted between two segments of reagent. Amino acid derivatives are obtained and separated in a fused-silica capillary with a sodium borate electrolyte buffer using 2-propanol as an organic modifier. The method is applied to the analysis of amino acids in pharmaceutical and feed samples. A good concordance between the predicted values and those obtained with the standard method is observed, with overall quantification error below 5%. The proposed procedure allows the detection limits sensitivity to be enhanced in 1000-fold with respect to conventional precapillary derivatization.
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