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An effective nanocomposite sensor for selective electroanalytical dopamine (DA) determination using overoxidized conducting polymer of poly‐1,5‐diaminonaphthalene (OPoly‐1,5‐DAN) functionalized graphene nanosheets (GNS) was achieved. The OPoly‐1,5‐DAN/GNS nanocomposite polymer was prepared via an electropolymerization of 1,5‐DAN on GNS/GCE after 7 cycles of potential scan (−0.2 V to +0.9 V), followed by an electrooveroxidation of the nanocomposite Poly‐1,5‐DAN/GNS by the potential cycle (0.0 V to +1.8 V) for 2 scans. The OPoly‐1,5‐DAN was effectively designed by GNS as a uniformly distribution of nanocomposite that caused more accumulations of analyte due to large electrocatalytic active positions created on electrode surface. The high specific and sensitive performance of the OPoly‐1,5‐DAN/GNS nanocomposite polymer was conducted to greater effective electrons transferring behavior for DA with copresent of vitamin C (VC). The stable and suitable formation of OPoly‐1,5‐DAN/GNS nanocomposite polymer showed rapid charge transport voltammogram and obvious electrocatalytic activity to DA and eliminated VC response. Moreover, the OPoly‐1,5‐DAN/GNS displays an excellent responses to DA determination with wide linear range (LR) 1.0–150 μM and lower detection limit (DL) 8.82±0.1 nM as comparing with other studies. Additionally, the excellent reproducibility of OPoly‐1,5‐DAN/GNS as well as long‐term stability indicated that it is an excellent and effective electrochemical DA sensor. Finally, the electroanalytical application of the OPoly‐1,5‐DAN/GNS nanocomposite polymer was employed for the electroanalysis of DA in human urine. [ABSTRACT FROM AUTHOR]

A new nanocomposite based on ruthenium nanoparticles (RuNPs) uniformly designed at chemically treated graphene oxide nanosheets (CTGONS) was prepared as active electrode for simultaneously sensing of dopamine (DA) and acetaminophen (AC) in the presence of high concentration of ascorbic acid (AA). The RuNPs actively decorates the CTGONS with uniform dispersion like pump sputtering of paints. The CTGONS of hexagonal nanosheets, 2D orientation, chemically treated to the reduced forms and active decoration by RuNPs lead to formation of high catalytic active sites and high loading of targets at the electrode surface. The suitable accommodation of RuNPs/CTGONS to fast response of targets ascertains a high catalytic activity, and fast charge transport. The RuNPs/CTGONS nanocomposite shows an obvious catalytic oxidation signal for DA and AC. The highly sensitive and selective electrode was designed based on RuNPs/CTGONS due to the large peak potentials separation of DA to AC of 0.22 V with sufficient electron mediating behavior. Moreover, the nanocomposite electrode shows individual and simultaneous determination of DA and AC with linear calibration plots from 5–120 μM and 10–120 μM, where their detection limits were calculated to be 0.018±0.002 and 0.023±0.003 μM, respectively. Finally, the analytical application of the RuNPs/CTGONS electrode was applied for the determination of DA and AC in the serum of human blood. [ABSTRACT FROM AUTHOR]

Nonenzymatic sensors based on a metals nanocomposite with high sensitivity, selectivity, and stability has been received considerable interest. In this study, a novel electrochemical nanocomposite sensor based on palladium nanoclusters (PdNCs) decorated electrochemically activated graphene (EAGr) was established for highly sensitive nonenzymatic H2O2 sensor. The PdNCs/EAGr nanocomposite was fabricated via an electrochemical activation of Gr by the potential cycling in the range of +0.6 to −1.8 V, followed by the electrodeposition of PdNCs at −0.4 V applied potential. The homogeneous dispersion of PdNCs/EAGr nanocomposite were characterized by scanning electron microscopy (SEM), X‐ray photoelectron spectroscopy (XPS), cyclic voltammetry (CV), and linear sweep voltammetry (LSV). The PdNCs/EAGr nanocomposite electrode showed higher electrocatalytic activity towards the reduction of H2O2 in pH 7.0 of 0.1 M PBS by significantly enhancing the reduction peak current and reduced the reduction overpotential as well as eliminated other interfering species responses. The PdNCs/EAGr electrode displayed a wide linear range for H2O2 reduction from 1.0 to 1100 μM with limit of detection 0.02±0.01 μM. The higher sensitivity and selectivity as well as long‐time stability and excellent reproducibility obtained, indicating the proposed sensor is an effective H2O2 based sensor. In addition, the analytical application of the nancomposite sensor was successfully examined for the determination of H2O2 in the real sample of human urine indicating that the appreciable practicality of the nonenzymatic sensor for the determination of H2O2 in physiological fluids. [ABSTRACT FROM AUTHOR]

A new analytical strategy based on potentiostatically pretreated graphene/CNT nanocomposite encapsulated Au nanoparticles (AuNPs/PPG/CNT) for the fabrication of H2O2 sensor was developed. The PPG/CNT nanocomposite was obtained through the potentiostatical of G and CNT mixture solution at an applied potential of −1.8 V, while AuNPs were immobilized on the PPG/CNT film via the produced active sites in the nanocomposite structure. The morphology and structure of the AuNPs/PPG/CNT nanocomposite were investigated by transmission electronic microscopy (TEM), UV-visible spectroscopy, scanning electron microscopy (SEM) and electrochemical impedance spectroscopy (EIS). The nanocomposite displays intensive electrocatalytic activity towards the reduction of H2O2 by enhancing the cathodic peak current and completely eliminating the interference of other species. The AuNPs/PPG/CNT sensor showed an excellent amperometric response to H2O2 reduction with linear range from 1.0-150 µM and detection limit of 0.017 µM. Moreover, the sensor showed good reproducibility as well as anti-interfering ability and long term stability. In addition, the proposed sensor was further applied for analytical determination of H2O2 in human urine real samples. [ABSTRACT FROM AUTHOR]

A simple detection method of ascorbic acid (AA) through selective catalytic oxidation has been developed using a novel conducting polymer poly-3′-(2-aminopyrimidyl)-2,2′:5′,2'-terthiophene (pAPTT). The pAPTT electrode showed an excellent selectivity in facilitating the electron transfer of AA and blocked the interferences of cationic species due to the positively charged pAPTT film. This method proved to be effective in the determination of AA in the presence of various biological interfering species. The dynamic range of AA detection was from 10 to 200 µM and the detection limit was 1.4±0.06 µM. [ABSTRACT FROM AUTHOR]

Herein, we have developed highly sensitive and selective non‐enzymatic bioinspired polydopamine derived nitrogen rich carbon (NC) coated bimetallic zeolitic imidazolate framework (BM‐ZIF) electrochemical sensor via simple hydrothermal approach for monitoring adrenaline (AD) from COVID‐19 quarantined person blood and pharmaceutical sample. The designed NC‐BM‐ZIF electrode shows excellent sensitive and selective performance towards AD monitoring with detection limit (LOD) of 0.01 nM and 0.1931 μA/nM/cm2 sensitivity over a wide linear range of 50–1625 nM. To the best of our knowledge, this is the first study of using of NC‐BM‐ZIF electrode for the electrochemical sensing of AD from quarantined person blood and pharmaceutical sample. [ABSTRACT FROM AUTHOR]