Arginine–malate-based dual-emission carbon dots for uric acid determination in human serum with a miniaturized device

Author(s):  
Xiaoqiu Gan ◽  
Elvi Angelina ◽  
Fangyuan Gu ◽  
Kewen Zheng ◽  
Lei Cui
2016 ◽  
Vol 11 (2) ◽  
pp. 192
Author(s):  
Abdi Naufal Ramadhan ◽  
Luluil Maknun ◽  
Noerma Juli Azhari

The control of uric acid is important. A high level of uric acid can cause gout disease. Therefore a simple, fast, and accurate method for uric acid determination is required. In this research a conductometric biosensor has been developed by SPCE – Nata de coco for uric acid determination. The prepared biosensor was optimized to get a good performance of biosensor and it is applicable for human serum samples. The optimized variables were enzyme concentration, membrane thickness and pH solution. The various enzyme concentration were 6 μg/mL; 12 μg/mL; 18μg/mL; 24 μg/mL. The various membrane thickness were 5 μm; 10 μm; 15 μm. Meanwhile, the various pH solution were 7; 7.5; 8; 8.5; 9. The optimum enzime concentration was 18 µg/mL with the membrane thickness and pH were 5 µm and 8, respectively. The prepared biosensor can determine the uric acid concentration at range of 0 – 1.2 ppm with the sensitivity of 7.74 µS/ppm and the limit detection is 0 ppm. The biosensor was applied to uric acid detection in human serum with accuracy of 95 %.


2004 ◽  
Vol 17 (8) ◽  
pp. 701-705 ◽  
Author(s):  
R. F. Dutra ◽  
K. A. Moreira ◽  
M. I. P. Oliveira ◽  
A. N. Araújo ◽  
M. C. B. S. Montenegro ◽  
...  

2016 ◽  
Vol 11 (2) ◽  
pp. 192
Author(s):  
Abdi Naufal Ramadhan ◽  
Luluil Maknun ◽  
Noerma Juli Azhari

The control of uric acid is important. A high level of uric acid can cause gout disease. Therefore a simple, fast, and accurate method for uric acid determination is required. In this research a conductometric biosensor has been developed by SPCE – Nata de coco for uric acid determination. The prepared biosensor was optimized to get a good performance of biosensor and it is applicable for human serum samples. The optimized variables were enzyme concentration, membrane thickness and pH solution. The various enzyme concentration were 6 μg/mL; 12 μg/mL; 18μg/mL; 24 μg/mL. The various membrane thickness were 5 μm; 10 μm; 15 μm. Meanwhile, the various pH solution were 7; 7.5; 8; 8.5; 9. The optimum enzime concentration was 18 µg/mL with the membrane thickness and pH were 5 µm and 8, respectively. The prepared biosensor can determine the uric acid concentration at range of 0 – 1.2 ppm with the sensitivity of 7.74 µS/ppm and the limit detection is 0 ppm. The biosensor was applied to uric acid detection in human serum with accuracy of 95 %.


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)].


2015 ◽  
Vol 22 (10) ◽  
pp. 1212-1219 ◽  
Author(s):  
Mandy J. Schmella ◽  
Rebecca G. Clifton ◽  
Andrew D. Althouse ◽  
James M. Roberts

2006 ◽  
Vol 85 (5) ◽  
pp. 519-525 ◽  
Author(s):  
Jeltsje S. Cnossen ◽  
Hanna de Ruyter-Hanhijärvi ◽  
Joris A. M. van der Post ◽  
Ben W. J. Mol ◽  
Khalid S. Khan ◽  
...  

1980 ◽  
Vol 59 (3) ◽  
pp. 662-663 ◽  
Author(s):  
C. RUFFINI CASTROVILLI ◽  
M. RIGONI

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