scholarly journals Modification of Electrode Using Arrowroot Starch Membrane for Uric Acid Determination

Molekul ◽  
2021 ◽  
Vol 16 (3) ◽  
pp. 186
Author(s):  
Elvian Eka Krisnaniningrum ◽  
Ani Mulyasuryani ◽  
Hermin Sulistyarti

Arrowroot starch membrane-modified glassy carbon electrode were constructed for the determination of uric acid. The membrane consist of arrowroot starch, polyvinyl alcohol, uric acid, and crosslinker. The crosslinker used was sodium tripolyphosphate, citric acid, and glutaraldehyde. Carbon material was added to increase the sensitivity. The composition of membrane influences the electrodes sensitivity. The best composition of arrowroot starch membrane is UA1 using 0.1% uric acid in membrane and STPP as crosslinker. The linearity concentration, sensitivity, and detection limit were 100-500 µM, 0.0509 A/M and 76 µM, respectively.

2018 ◽  
Vol 42 (18) ◽  
pp. 14796-14804 ◽  
Author(s):  
Xiaohui Gao ◽  
Rijun Gui ◽  
Kendrick Qizhou Xu ◽  
Huijun Guo ◽  
Hui Jin ◽  
...  

A novel and facile ratiometric electrochemical sensor was developed for sensitive determination of uric acid.


1979 ◽  
Vol 25 (4) ◽  
pp. 619-621 ◽  
Author(s):  
K Bartl ◽  
M Brandhuber ◽  
J Ziegenhorn

Abstract The enzymatic determination of serum uric acid by use of uricase, catalase, and aldehyde dehydrogenase according to Haeckel [J. Clin. Chem. Clin Biochem. 14, 101 (1976)] showed interferences from ethanol-converting enzymes, which are present in some patients' sera. We have identified these enzymes as alcohol dehydrogenase isoenzymes. Among other substances, a mixture of pyrazole and oxalate can be used to eliminate these interferences. This inhibitor system gives good results when used in the automated kinetic uric acid determination, as is shown by a comparison with the manual assay for uric acid according to Kageyama [Clin. Chim. Acta 31, 421 (1971)].


2008 ◽  
Vol 62 (3) ◽  
Author(s):  
Suling Feng ◽  
Xueping Liu

AbstractA novel kinetic spectrofluorimetric method for the determination of uric acid based on the activation effect of uric acid on the Cu(II) ion catalyzed oxidation of pyronine Y by hydrogen peroxide was developed. The influence of different buffer solutions was tested and the Britton-Robinson buffer solution with pH 2.2 was found to be the optimum. The detection limit and the linear range for uric acid are 0.09 μg mL−1 and 0.3–3.0 μg mL−1, respectively. The RSD for eleven determinations of 1.6 μg mL−1 uric acid was 1.6 %. Satisfactory results were obtained when using this method of uric acid determination in human urine.


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