2019
DOI: 10.1016/j.electacta.2019.01.096
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Electrochemical method of pyrophosphate determination by quinone reduction

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Cited by 10 publications
(4 citation statements)
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“…32,33 In addition, the peak potential of the new peak was dependent on the proton donor (pK a of the acid). [32][33][34] As ATP (pK a2 6.95), 35 ADP (pK a2 6.88), 35 and CTP (pK a2 6.4) 36 were hydrolyzed to produce H 2 PO 4 − (pK a 7.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…32,33 In addition, the peak potential of the new peak was dependent on the proton donor (pK a of the acid). [32][33][34] As ATP (pK a2 6.95), 35 ADP (pK a2 6.88), 35 and CTP (pK a2 6.4) 36 were hydrolyzed to produce H 2 PO 4 − (pK a 7.…”
Section: Resultsmentioning
confidence: 99%
“…When the protons provided by ATP, ADP and CTP were depleted, the pH of the electrode surface increased abruptly, which caused the formation of the peaks A 2 , A 3 , B 2 , B 3 , C 2 , and C 3 . Wang 27,28,34 revealed that the peak current was dependent on the proton donor concentration.…”
Section: Resultsmentioning
confidence: 99%
“…The correlation coefficient (R 2 ) is fairly good (R 2 = 0.993), favorable to attain an impressive LOD of 0.68 nM for PPi. The analytical efficiency of the coffee-Tryp-CuNCs-based fluorescence sensor is compared to the reported approaches [38][39][40][41][42][43][44][45][46][47][48][49][50][51] for detecting of OH and PPi, as shown in Tables 1 and 2.…”
Section: Sensitivity Of Coffee-tryp-cuncs Towards Oh and Ppimentioning
confidence: 99%
“…Therefore, measuring PPi levels is of great significance for the effective diagnosis of diseases. In recent years, the detection methods of PPi include liquid chromatography [11], ultraviolet-visible absorption spectrometry [12], capillary electrophoresis [13], and electrochemical analysis [14]. However, these methods may suffer from complex and time-consuming sample pretreatment, high cost, low sensitivity, and poor repeatability.…”
Section: Introductionmentioning
confidence: 99%