An innovative dual-signal electrochemical ratiometric determination of creatinine based on silver nanoparticles with intrinsic self-calibration property for bimetallic Prussian blue analogues
An ultrasensitive dual-signal ratiometric electrochemical sensor was developed for creatinine detection utilizing silver nanoparticles (Ag) with intrinsic self-calibration afforded by iron-nickel bimetallic Prussian blue (FeNiPBA) analogues. The Ag@FeNiPBA exhibits two redox signals corresponding to...
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Veröffentlicht in: | Analytical and bioanalytical chemistry 2023-10, Vol.415 (25), p.6247-6256 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | An ultrasensitive dual-signal ratiometric electrochemical sensor was developed for creatinine detection utilizing silver nanoparticles (Ag) with intrinsic self-calibration afforded by iron-nickel bimetallic Prussian blue (FeNiPBA) analogues. The Ag@FeNiPBA exhibits two redox signals corresponding to the Ag
+
/Ag and Fe
3+
/Fe
2+
systems. Adding chloride (Cl
−
) solution increases the anodic current of the Ag/Ag system significantly due to the formation of silver chloride through solid-state electrochemistry. While the anodic current of the Ag/Ag system decreases in the presence of creatinine due to the competitive reaction, the Fe/Fe system's anodic current remains the same, which enables a ratiometric response. Under optimized conditions, the response ratio (I
Ag
/I
Fe
) decreases while the creatinine concentration increases linearly between 0.015 and 140 μM, with 0.004 μM as a good detection limit (S/N = 3). These results demonstrate superior performance over previously reported methods for electrochemical creatinine determination. The high sensitivity arises from the signal amplification of the Ag/AgCl solid-state electrochemistry, while the selectivity originates from the specific interaction between Ag
+
and creatinine. The Ag@FeNiPBA hybrid can quantify creatinine in real samples with good recoveries. This work opens up new opportunities for applying dual-signal nanostructures to develop electrochemical sensors for (bio)molecule detection. |
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ISSN: | 1618-2642 1618-2650 |
DOI: | 10.1007/s00216-023-04901-6 |