University of North Florida
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Stuart Chalk, Ph.D.
Department of Chemistry
University of North Florida
Phone: 1-904-620-1938
Fax: 1-904-620-3535
Email: schalk@unf.edu
Website: @unf

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Electrode

Classification: Electrode -> carbon -> open tubular

Citations 2

"Biamperometric Determination Of Glycerol And Triglycerides With Open Tubular Carbon Electrodes In Flow Streams"
Anal. Chim. Acta 1979 Volume 106, Issue 2 Pages 225-231

Notice (8): Undefined variable: uid [APP/View/Elements/citation.ctp, line 40]
Abdulrahman S. Attiyat and Gary D. Christian

Abstract: Biamperometric measurements, with open tubular carbon electrodes in flowing streams, are used to monitor the concentration of hexacyanoferrate(II) produced by the diaphorase-catalyzed reaction between NADH and hexacyanoferrate(III). NADH produced by the glycerol dehydrogenase-catalyzed reaction between glycerol and NAD can be measured in this manner to determine glycerol concentrations; linear calibration plots are obtained in the range 5 x 10^-5 - 6 x 10^-1 M glycerol. Triglycerides are hydrolyzed by lipase and the glycerol liberated is measured similarly. Glycerol and triglycerides are determined in serum control samples by the standard addition technique.
Glycerol Triglycerides Enzyme

"Continuous-flow Determination Of Blood Alcohol Using Biamperometric Monitoring Of Enzymatic Reaction"
Anal. Lett. 1987 Volume 20, Issue 7 Pages 1099-1113

Notice (8): Undefined variable: uid [APP/View/Elements/citation.ctp, line 40]
Attiyat, A.S.;Christian, G.D.

Abstract: A three-channel flow system was used, the first channel pumping NAD+ and dihydrolipoamide dehydrogenase(I), the second alcohol dehydrogenase(II) and K3Fe(CN)6 and the third diluted blood samples, all at the same flow rate. The three channels merged at a single point, thence passing through a flow cell containing two open-tubular carbon electrodes, with a potential difference of 200 mV. In the presence of ethanol and II, NAD+ was reduced to NADH; this was oxidized back to NAD+ by Fe(CN)63- in the presence of I. The Fe(CN)64- formed was detected at the electrodes. Blood samples were initially diluted 100-fold with 0.1 M Tris buffer (pH 8.5). The detection limit was 0.15 µg mL-1 of ethanol in blood and coefficient of variation were 4%. On eleven samples, correlation with a GC method was good (r = 0.98).
Ethanol Whole Method comparison