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December 6, 2025Chemosensors4 citationsOpen Access

Carbon Quantum Dot–Supported Nickel Nanoparticles as a Synergistic Interface for Electrochemical Creatinine Sensing

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VOVelia OsunaEZErasto Armando Zaragoza‐Contreras

Key Points

  • The sensor demonstrates a low detection limit of 5 µM for creatinine, ensuring accurate measurements.
  • Electrochemical characterization using ferricyanide/ferrocyanide confirms enhanced performance via composite materials.
  • This non-enzymatic sensing approach leverages carbon quantum dots and nickel nanoparticles to optimize linearity in detection.
  • Significantly, the architecture provides a stable platform for reliable creatinine detection with minimal interference.

Abstract

We report a non-enzymatic electrochemical sensing platform for creatinine based on a nickel-nanoparticle/carbon-quantum-dot (NiNP–CQD) hybrid interface. In this system, the analytical signal originates from the direct electrocatalytic oxidation of creatinine mediated by the Ni(II)/Ni(III) redox couple (Ni(OH)2/NiOOH), which forms during electrochemical activation of nickel in alkaline media. These redox centers act as catalytic sites that oxidize creatinine without requiring enzymes or biomolecular labels. The CQDs provide a conductive sp2-rich network with abundant oxygenated groups that promote homogeneous nucleation and dispersion of NiNPs, enhancing both surface area and electron-transfer efficiency. Electrochemical characterization of the modified electrodes was performed using the ferricyanide/ferrocyanide redox couple as the electron-transfer probe. Structural and microscopic characterization confirms uniform NiNP deposition on the CQD layer, while electrochemical studies demonstrates that the composite outperforms CQDs or NiNPs alone in current density, linearity, and resistance to active-site saturation. The resulting sensor exhibits a wide linear range (10–1000 µM), high area-normalized sensitivity (1.41 µA µM−1 cm−2), and a low detection limit of 5 µM. Selectivity tests reveal minimal interference from common physiological species. By explicitly leveraging a catalyst-driven, enzyme-free oxidation pathway, this NiNP–CQD architecture provides a robust, stable, and scalable platform for clinically relevant creatinine detection.

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Cite This Study

Osuna et al. (2025) studied this question.

synapsesocial.com/papers/69337cfbb3f947a0a125a6afhttps://doi.org/10.3390/chemosensors13120416
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