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In this study, we report a facile and effective production process of palladium nanoparticles supported on polypyrrole/reduced graphene oxide (rGo/pd@ppy nps). A novel electrochemical sensor was fabricated by incorporation of the prepared nps onto glassy carbon electrode (Gce) for the simultaneous detection of ascorbic acid (AA), dopamine (DA) and uric acid (UA). the electrodes modified with rGO/Pd@PPy NPs were well decorated on the GCE and exhibited superior catalytic activity and conductivity for the detection of these molecules with higher current and oxidation peak intensities. Simultaneous detection of these molecules was achieved due to the high selectivity and sensitivity of rGo/pd@ppy nps. for each biomolecule, well-separated voltammetric peaks were obtained at the modified electrode in cyclic voltammetry (CV) and differential pulse voltammetry (DPV) measurements. Additionally, the detection of these molecules was performed in blood serum samples with satisfying results. the detection limits and calibration curves for AA, DA, and UA were found to be 4.9 × 10 −8 , 5.6 × 10 −8 , 4.7 × 10 −8 M (S/n = 3) and ranging from 1 × 10 −3 to 1.5 × 10 −2 M (in 0.1 M PBS, pH 3.0), respectively. Hereby, the fabricated rGO/Pd@PPy NPs can be used with high reproducibility, selectivity, and catalytic activity for the development of electrochemical applications for the simultaneous detection of these biomolecules.

In this work, highly monodispersed palladium-nickel (Pd-Ni) nanoparticles supported on reduced graphene oxide (rGO) were synthesized by the microwave-assisted methodology. The synthesized nanoparticles were used for modification of a glassy carbon electrode (GCE) to produce our final product as PdNi@rGO/GCE, which were utilized for non-enzymatic detecting of glucose. In the present study, electrochemical impedance spectroscopy (EIS), chronoamperometry (CA) and, cyclic voltammetry (CV) methods were implemented to investigate the sensing performance of the developed glucose electrode. The modified electrode, PdNi@rGO/GCE, exhibited very noticeable results with a linear working range of 0.05–1.1 mM. Moreover, an ultralow detection limit of 0.15 μM was achieved. According to the results of amperometric signals of the electrodes, no significant change was observed, even after 250 h of operation period. In addition, the highly monodisperse PdNi@rGO/GCE was utilized to electrochemical detection of glucose in real serum samples. In light of the results, PdNi@rGO/GCE has shown an excellent sensing performance and can be used successfully in serum samples for glucose detection and it is suitable for practical and clinical applications.

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