Resumo (PT):
This paper describes the use of a FIA system for the automatic determination of uric
acid in urine, using a tubular amperometric detector. In this system, glassy carbon
electrodes of tubular configuration were activated by successive cyclical scans from
- 0.30 to 2.00 V versus Ag/AgCl reference electrode in 0.50 mol.L-1 sulphuric acid
solution. Samples were diluted in supporting electrolyte before analysis and no other
pre-treatment was employed. Such dilution enabled the matrix effects to be reduced and
therefore improving the sensitivity provided by the activation step that allows the uric
acid (UA) to be detected at lower concentration levels after dilution. Uric acid
determination was performed in a single channel FIA manifold, which provided
reproducibility of sample transport to the detector and enabled a sampling rate of 120
samples per hour to be achieved. The tubular configuration of the cell offered
robustness to the system since it was rigidly fixed to the manifold, allowing the
manifold to be generalised for routine analysis application. The results obtained with the
FIA system for UA determination in urine were compared with those from the
enzymatic method used in clinical analysis laboratories. No statistical difference
between methods was found at the 95% confidence level. Relative deviations between
both methods were within ± 4% and the proposed system showed good repeatability
(about 3%, n = 10).
<br>
<br>
Keywords: uric acid, amperometric detection, tubular electrodes, FIA.
<br>
<a target="_blank" href="http://www.scielo.oces.mctes.pt/scielo.php?script=sci_arttext&pid=S0872-19042004000300006&lng=en&nrm=iso&tlng=en"> Texto integral </a>
<br>
<br>
Abstract (EN):
This paper describes the use of a FIA system for the automatic determination of uric
acid in urine, using a tubular amperometric detector. In this system, glassy carbon
electrodes of tubular configuration were activated by successive cyclical scans from
- 0.30 to 2.00 V versus Ag/AgCl reference electrode in 0.50 mol.L-1 sulphuric acid
solution. Samples were diluted in supporting electrolyte before analysis and no other
pre-treatment was employed. Such dilution enabled the matrix effects to be reduced and
therefore improving the sensitivity provided by the activation step that allows the uric
acid (UA) to be detected at lower concentration levels after dilution. Uric acid
determination was performed in a single channel FIA manifold, which provided
reproducibility of sample transport to the detector and enabled a sampling rate of 120
samples per hour to be achieved. The tubular configuration of the cell offered
robustness to the system since it was rigidly fixed to the manifold, allowing the
manifold to be generalised for routine analysis application. The results obtained with the
FIA system for UA determination in urine were compared with those from the
enzymatic method used in clinical analysis laboratories. No statistical difference
between methods was found at the 95% confidence level. Relative deviations between
both methods were within ± 4% and the proposed system showed good repeatability
(about 3%, n = 10).
<br>
<br>
Keywords: uric acid, amperometric detection, tubular electrodes, FIA.
<br>
<a target="_blank" href="http://www.scielo.oces.mctes.pt/scielo.php?script=sci_arttext&pid=S0872-19042004000300006&lng=en&nrm=iso&tlng=en"> Full text </a>
<br>
<br>
Language:
Portuguese
Type (Professor's evaluation):
Scientific