It has been suggested that the observed retention of carbonyl compounds could be explained by keto-enol tautomerism, i.e. interactions of surface silanols with aliphatic -OH groups of the enols. We do not find this to be likely, since the tauto-~7 1 ## [I81 [19] meric equilibrium very strongly fa
On-line automatic SPE-CE coupling for the determination of biological markers in urine
✍ Scribed by José Ruiz-Jiménez; José M. Mata-Granados; Maria Dolores Luque de Castro
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 436 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0173-0835
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Automatic SPE has been coupled on‐line to CE by a transfer tube and the replenishment system of the CE instrument. The approach allows the target analytes (viz. creatinine, creatine, xanthine, hypoxanthine, uric acid, p‐aminohippuric acid and ascorbic acid in urine samples) to be removed from the sample matrix, cleaned up, preconcentrated and injected into the capillary. The detection limits range between 0.14 and 4.50 μg/mL, the quantification limits between 0.45 and 15.0 μg/mL, and linear dynamic ranges – which include the reference healthy human values – from the quantification limits to 1332 μg/mL. The precision, expressed as RSD, ranges between 0.38 and 2.22% for repeatability and between 1.79 and 7.61% for within‐laboratory reproducibility. The errors, expressed as RSD for all compounds, range between 0.20 and 6.90%. The time for automatic SPE and that necessary for the individual separation–detection of the target analytes are 13 and 12 min, respectively; the analysis frequency is 5 h^−1^. The accuracy of the method and potential matrix effects were studied by using spiked samples and recoveries between 96.00 and 103.07 % were obtained. The proposed method was applied to samples from healthy young students.
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