Abstract
Fentanyl is a powerful synthetic opioid used to treat severe pain. New administration routes toward its illegal consumption for recreational purposes pose a growing threat to public health, either due to misuse or abuse of this substance. As a result, the rapid qualitative and quantitative determination of fentanyl in biofluids is of great interest. A novel enzymatic biosensor based on adsorptive-stripping cyclic voltammetry is proposed as a cost-effective, reliable, and efficient device for fentanyl determination in urine samples. Disposable screen-printed carbon electrodes modified with multi-walled carbon nanotubes and cytochrome c were used to develop the testing platform. The electrochemical behavior of fentanyl exhibited a well-defined anodic wave around 0.66 V vs. pseudo reference electrode. The experimental conditions were optimized to obtain the best analytical response, and linear regression analysis of increasing concentration standards was applied to estimate the performance parameters. The results suggest a simple method with a wide linearity range, high sensitivity, low limits of detection (0.086 μg/mL) and quantification, and satisfactory precision (2.9% RSD). The feasibility and applicability of the voltammetric approach were assessed by fentanyl-spiked urine samples by standard additions calibration curves in two levels of enrichment with an accuracy of 92% and 100%.
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Acknowledgements
J. González-Hernández would like to thank CELEQ and Sistema de Estudios de Posgrado de la Universidad de Costa Rica for supporting and financing the internship at Universidad de Burgos and J. García for digital images processing.
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The work was funded by Vicerrectoría de Investigación de la Universidad de Costa Rica (project N° 804-C2-070) and CELEQ.
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González-Hernández, J., Moya-Alvarado, G., Alvarado-Gámez, A.L. et al. Electrochemical biosensor for quantitative determination of fentanyl based on immobilized cytochrome c on multi-walled carbon nanotubes modified screen-printed carbon electrodes. Microchim Acta 189, 483 (2022). https://doi.org/10.1007/s00604-022-05578-x
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DOI: https://doi.org/10.1007/s00604-022-05578-x