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Proceedings
  • Extended Abstract
  • Open Access

9 November 2020

Different Approaches in Designing Sensitive Tools Based on Nanocomposite Materials for Biological Analytes Detection †

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1
National Institute for Research and Development in Chemistry and Petrochemistry-ICECHIM, 202 Spl. Independenţei, 060021 Bucharest, Romania
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EPI-SISTEM SRL, Bvd. Brasovului 145, Sacele, 505600 Brasov, Romania
*
Authors to whom correspondence should be addressed.
Presented at the 16th International Symposium “Priorities of Chemistry for a Sustainable Development” PRIOCHEM, Bucharest, Romania, 28–30 October 2020.
This article belongs to the Proceedings The 16th International Symposium “Priorities of Chemistry for a Sustainable Development” PRIOCHEM
Sensitive, stable and robust electrochemical sensors have been designed through modification of the working electrodes with different complex matrices based on carbon nanomaterials and metallic nanoparticles. Therefore, screen-printed electrodes were modified with complex matrices of hybrid nanomaterials using physical deposition or entrapment in polymeric film. The designed sensors allowed a fast and sensitive detection of some important biological analytes involved in the degradation process of several food products [1], as well as in the electrocatalytic activity toward oxidation of some phenolic compounds found to be environmental pollutants [2]. Electrochemical sensitive platforms have been designed by modification of the carbon screen-printed electrodes with a hybrid nanocomposite matrix, through entrapment into a polymeric film of 2,6-dihydroxinaphtalene and 2-(4-aminophenyl)-ethylamine. The functionalization of carbon nanomaterials with metallic nanoparticles leads to obtaining multifunctional materials with uniform structures and improved electrocatalytic behavior, allowing the acceleration of the electron transfer to the electrode surface and further sensitive detection of the analyte of interest. The functionalized sensors were characterized by electrochemical studies and the kinetics of the electron transfer were investigated by electrochemical impedance spectroscopy, while the morphology of the surface was determined by SEM, TEM and FTIR spectroscopy. The FTIR spectroscopy studies showed that a dispersion of carbon nanomaterials and metallic nanoparticles into the polymeric matrix leads to the formation of a stable film. The electron transfer resistance recorded for unmodified and modified sensors revealed that the presence of carbon nanomaterials together with platinum nanoparticles considerably decreases the resistance to electron transfer. This decrease shows that the nanocomposite materials pose high conductivity, accelerating the electron transfer and demonstrating the synergy of the materials used and the increase in the electrocatalytic capacity of the sensor surface. Further, amperometric detection of hydrogen peroxide has been performed at an applied working potential of +0.15 V vs. Ag/AgCl, in a concentration range of 0.01 to 5 mM. The modification of sensors with hybrid nanomaterials provides an electroconductive network and a large active surface of the sensors, thus accelerating the transfer of electrons, allowing a sensitive detection of some biological analytes without the need of a bioreceptor.

Acknowledgments

The authors acknowledge the support from Ministry of Research and Innovation of Romania through Program 1—Development of the National Research and Development System, Subprogram 1.2—Institutional Performance—Projects of Excellence Financing in RDI, project number PFE no 31/2018, from the NUCLEU program through the project PN 19.23.03.02/2019 and 5PS/2019.

References

  1. Vanegas, D.C.; Patiño, L.; Mendez, C.; de Oliveira, D.A.; Torres, A.M.; Gomes, C.L.; McLamore, E.S. Scribed Graphene Biosensor for Detection of Biogenic Amines in Food Samples Using Locally Sourced Materials. Biosensors 2018, 8, 42. [Google Scholar] [CrossRef] [PubMed]
  2. U.S. Environmental Protection Agency. Chemicals-in-Commerce Information System. In Chemical Update System Database; Environmental Protection Agency: Washington, DC, USA, 1998. [Google Scholar]
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