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A novel electrochemical biosensor is reported for simultaneous detection of two of the most common food-borne pathogens: Listeria monocytogenes and Staphylococcus aureus . The biosensor is composed of an array of gold nanoparticles-modified screen-printed carbon electrodes on which magnetic nanoparticles coupled to specific peptides were immobilized via streptavidin-biotin interaction. Taking advantage of the proteolytic activities of the protease enzymes produced from the two bacteria on the specific peptides, the detection was achieved in 1 min. The detection was realized by measuring the percentage increase of the square wave voltammetric peak current at 0.1 V versus a Ag/AgCl reference electrode in ferro/ferricyanide redox couple after incubation with the bacteria protease. The integration of the specificity of the bacterial enzymes towards their peptide substrates with the sensitivity of the electrochemical detection on the sensor array allows the rapid, sensitive and selective quantification of the two bacteria. Outstanding sensitivities were achieved using this biosensor array platform with limit of detection of 9 CFU mL −1 for Listeria monocytogenes and 3 CFU mL −1 for Staphylococcus aureus . The multiplexing capability and selectivity of the array voltammetric biosensor were demonstrated by analysing samples of Staphylococcus aureus , Listeria monocytogenes or E. coli and also containing a mixture of two or three bacteria. Using this biosensor, the two bacteria were successfully quantified simultaneously in one step without the need for DNA extraction or amplification techniques. This platform offers promise for rapid, simple and cost-effective simultaneous detection of various bacteria. Graphical abstract

A method is described for the simultaneous voltammetric determination of the heavy metal ions cadmium(II), lead(II), mercury(II), zinc(II), and copper(II) using a glassy carbon electrode (GCE) modified with magnetite (Fe 3 O 4 ) nanoparticles and fluorinated multiwalled carbon nanotubes (Fe 3 O 4 /F-MWCNTs). The Fe 3 O 4 /F-MWCNT composite was synthesized by a hydrothermal method and characterized by X-ray photoelectron spectroscopy, X-ray diffraction, transmission electron microscopy, scanning electron microscopy, elemental mapping, electrochemical impedance spectroscopy, and square wave stripping voltammetry. Under the optimum conditions, the electrode displays excellent response to the ions. Figures of merit for Cd(II), Pb(II), Hg(II), Zn(II), and Cu(II), respectively, include (a) high electrochemical sensitivity (29.88, 43.50, 120.86, 47.34 and 90.31 (μA μM −1  cm −2 ), (b) well separated peaks (at −0.70, −0.53, +0.37, −1.11 and + 0.01 V vs. Ag/AgCl); (c) low limits of detection (0.014, 0.0084, 0.0039, 0.012, and 0.0053 μM); and (d) wide linear ranges (0.048–30.0, 0.028–30.0, 0.013–32.5, 0.039–32.5, and 0.017–31.5 μM). The modified GCE displays satisfying selectivity in the presence of potentially interfering other metal ions, stability for 30 days, and reproducibility of electrodes (with a relative standard deviation between 1.2 and 4.8% for n  = 6). The modified GCE was applied to the determination of several heavy metal ions in (spiked) water and rice samples, and the results agreed well with data obtained by atomic fluorescence spectrometry or inductively coupled plasma-mass spectrometry. The dramatic performance probably result from the semi-ionic C-F bond on F-MWCNTs surface with a strong negative charge, the good electrical conductivity of the F-MWCNTs and Fe 3 O 4 , the synergistic interaction between Fe 3 O 4 and F-MWCNTs, and the nafion conductive membrane improving the stability of the modified layer and enhanced cation adsorption. Graphical abstract An environmentally-friendly, low-cost, high-throughput Fe 3 O 4 /fluorinated multi-walled carbon nanotube composite (Fe 3 O 4 /F-MWCNTs) modified glassy carbon electrode is described. It was applied to simultaneous electrochemical determination of Cd(II), Pb(II), Hg(II), Zn(II), and Cu(II) by square wave stripping voltammetry

Liquid biopsy analysis represents a suitable alternative analysis procedure in several cases where no tumor tissue is available or in poor patient conditions. Amino acids can play a crucial role in aiding cancer diagnosis. Monitoring of tryptophan (Trp) catabolism can aid in tracking cancer progression. Therefore, a novel nanocomposite was fabricated using overoxidized polypyrrole film doped with nano-carbon dots (nano-CDs) on the pencil graphite electrode (PGE) surface for sensitive evaluation of Trp in human serum. Using square wave voltammetry (SWV), the overoxidized polypyrrole/carbon dots/pencil graphite electrode (Ov-Ox PPy/CDs/PGE) achieved excellent electrochemical catalytic activity for evaluating Trp. The modified electrode, known as Ov-Ox PPy/CDs/PGE, demonstrated superior electrochemical catalytic activity compared to bare PGE, CDs/PGE, PPy/PGE, and PPy/CDs/PGE for evaluation of Trp. The method’s excellent sensitivity was confirmed by the low limits of detection (LOD = 0.003 μmol L −1 ) and limit of quantitation (LOQ = 0.009 μmol L − 1 ). The biosensor that was developed can measure tryptophan (Trp) levels in the serum of both healthy individuals and female breast cancer patients with high accuracy and sensitivity. The results indicate that there is a significant difference, as shown by the F -test, between healthy individuals and those with breast cancer. This suggests that Trp amino acid could be an essential biomarker for cancer diagnosis. Consequently, liquid biopsy analysis presents a valuable opportunity for early disease detection, particularly for cancer. Graphical abstract

A glassy carbon electrode (GCE) modified with electrochemically reduced graphene oxide (ErGO) and gold nanorods (AuNRs) (GCE/ErGO/AuNRs) was prepared for determining As(III) in bivalve mollusks samples ( Mytilus chilensis ). The modified electrode was characterized by cyclic voltammetry, scanning electron microscopy (SEM), and atomic force microscopy (AFM). Chemical and electrochemical parameters were optimized, observing that the presence of AuNRs provides selectivity, while the incorporation of ErGO improves the sensitivity of the modified electrode for the detection of As(III). Using square wave anodic stripping voltammetry (SWASV), a linear range of 2.0–60.0 µg L −1 with a detection limit (LOD) of 0.21 µg L −1 was obtained. The validation was made using water and mussel tissue-certified reference materials (TMDA-64.2 and ERM ® -CE278k, respectively), showing good accuracy and reproducibility. The methodology allowed the determination of As(III) in real samples of marine resources, with excellent results (RSD < 2%). Graphical abstract

A rapid and sensitive electrochemical sensing platform is reported based on bimetallic gold-platinum nanoclusters (AuPtNCs) dispersed on reduced graphene oxide (rGO) for the simultaneous detection of guanine and adenine using square wave voltammetry (SWV). The synthesis of AuPtNCs-rGO nanocomposite was achieved by a simultaneous reduction of graphene oxide (GO) and metal ions (Au 3+ and Pt 4+ ) in an aqueous solution. The developed AuPtNCs-rGO electrochemical sensor with the optimized 50:50 bimetallic (Au:Pt) nanoclusters exhibited an outstanding electrocatalytic performance towards the simultaneous oxidation of guanine and adenine without the aid of any enzymes or mediators in physiological pH. The electrochemical sensor platform showed low detection limits of 60 nM and 100 nM (S/ N  = 3) for guanine and adenine, respectively, with high sensitivity and an extensive linear range from 1.0 μM to 0.2 mM for both guanine and adenine. The interference from the most common electrochemically active interferents, including ascorbic acid, uric acid, and dopamine, was almost negligible. The simultaneous sensing of guanine and adenine in denatured Salmon Sperm DNA sample was successfully achieved using the proposed platform, showing that the AuPtNCs-rGO nanocomposite could provide auspicious clinical diagnosis and biomedical applications. Graphical abstract

An electrochemical aptasensor is described for determination of the phytohormone of zearalenone (ZEA). The gold electrode was modified with ZEA via covalent attachment using cysteamine-hydrochloride and 1,4-phenylene diisocyanate linker. A truncated ZEA aptamer with a dissociation constant of 13.4 ± 2.1 nM was used in an aptasensor. The electrochemical property was investigated using square wave voltammetry for monitoring the change in the electron transfer using the ferro/ferricyanide system as redox probe. Under optimal experimental conditions, the response was best measured at a potential of 0.20 V (vs. Ag/AgCl). The signals depended on the competitive mechanism between the immobilised ZEA and free ZEA for the aptamer binding site. The aptasensor works in the range 0.01 to 1000 ng·mL −1 ZEA concentration, with a detection limit of 0.017 ng·mL −1 . High degree of cross-reactivity with the other analogues of ZEA was observed, whereas none towards other mycotoxins. The aptasensor was further applied for the determination of ZEA in the extract of maize grain and showed good recovery percentages between 87 and 110%. Graphical abstract Schematic representation of the electrochemical determination of zearalenone based on indirect competitive assay. Step a Immobilisation of ZEA on the surface of gold electrode via covalent attachment, b competition for the ZEA aptamer binding site between immobilised and free ZEA, and c current signal of the binding event based on SWV technique.

This work describes the development of an electroanalytical methodology for the direct determination of Aflatoxin B1 using a surface-modified vitreous carbon electrode with a bismuth film and gold nanoparticles. Cyclic voltammetry was used to determine the electrochemical behavior of Aflatoxin B1 on the working electrode. A well-defined cathodic peak was observed in the voltammogram which is associated with the direct reduction of Aflatoxin B1, so this signal was selected as the analytical response. To maximize this response, Square Wave Voltammetry was selected as the quantitative technique; then, pulse frequency, pulse amplitude, and potential step were optimized using a Box-Behnken surface design. A calibration curve was constructed by measuring different Aflatoxin B1 standard concentrations from 1 to 200 ng L −1 ; with the proper statistical analysis, it was found a linear range from 19.01 to 100 ng L −1 , with a limit of detection of 5.71 ng L −1 , and a sensitivity of 0.033 μA ng L −1 . A relative standard deviation percentage of 4.28 was obtained in the repeatability study. Finally, the proposed methodology was successfully used to analyze commercial milk samples. Graphical abstract

A carbon paste electrode was modified with a Ce(III)-imprinted polymer (Ce-IP) and used for voltammetric determination of Ce(III) ions in real water samples. Precipitation polymerization was used for synthesis of the nano-sized Ce-IP from vinylpyridine and methacrylic acid (acting as the complexing ligands and functional monomers), divinylbenzene (cross-linker) and AIBN as the radical starter. The Ce-IP was characterized by scanning electron microscopy and zeta potentials. A carbon paste electrode (CPE) was then impregnated with the Ce-IP and used for the extraction and subsequent determination of Ce(III). Oxidative square wave voltammetry showed the electrode to give a significantly better response than an electrode modified with the non-imprinted polymer. The addition of multiwalled carbon nanotubes to the Ce-IP-modified electrode further improves the signal, thereby increasing the sensitivity of the method. The effects of electrode composition, extraction pH value, volume and time were optimized. The electrode, if operated at a voltage of 1.05 V (vs. Ag/AgCl), displays a linear response to Ce(III) in the 1.0 μM to 25 pM concentration range, and the detection limit is 10 pM (at an S/N ratio of 3). The relative standard deviation of 5 separate determinations is 3.1 %. The method was successfully applied to the determination of Ce(III) in the spiked samples of drinking water and sea water. Graphical abstract A carbon paste electrode was modified with Ce-imprinted polymer and multiwalled carbon nanotube (Ce-IP-CNT-CP), and then utilized for the extraction of Ce(III) prior to its electroanalysis by square wave voltammety (SWV).

A carbon paste electrode (CPE) was modified with Pt-Co nanoparticles and 2-(3,4-dihydroxyphenethyl)isoindoline-1,3-dione (3,4-DHPID) and then used for determination of N -acetylcysteine ( N -AC) in the presence of paracetamol (PC) and folic acid (FA). The Pt-Co nanoparticles were synthesized by the polyol method and characterized by X-ray diffraction, energy dispersive X-ray analysis and transmission electron microscopy. The modified CPE displays good electrocatalytic activity towards the electrooxidation of N-AC in solution of pH 7.0. It was applied to the determination of N -AC in the presence of PC and FA (with well separated signals peaking at 0.2, 0.55 and 0.86 V vs. Ag/AgCl) by using square wave voltammetry. The peak currents are linearly dependent on the concentrations of N-AC, PC and FA in the respective ranges from 0.07 to 500, 1.0 to 850, and 2.0 to 550 μmol·L −1 , with detection limits of 0.009, 0.6 and 0.8 μmol·L −1 . The modified CPE was applied to the determination of N -AC, PC and FA in (spiked) pharmaceutical and biological samples. Graphical abstract Pt-Co nanoparticles and 2-(3,4-dihydroxyphenethyl)isoindoline-1,3-dione were used for modification of a carbon paste electrode which then was used for sensitive determination of N -actylcysteine in the presence of paracetamol and folic acid.

Abstract A gold nanoparticle–modified copper-based metal organic framework (Au NPs@Cu-BDC) was fabricated for the electrochemical determination of cysteine (Cys-SH). The nanocomposites were characterized using different techniques such as scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy-dispersive X-ray spectroscopy (EDX), powder X-ray spectroscopy (PXRD), thermogravimetry (TGA), nitrogen adsorption–desorption isotherms, and Fourier transform infrared spectroscopy (FTIR). Formation of a new anodic peak of Cu(II)-Cys complex at + 0.43 V was used to detect Cys-SH. Cyclic and square wave voltammetric studies proved that the Au NPs enhanced the conductivity of Cu-BDC. The proposed electrode exhibited a linear range of 0.0015–10.5 μM and low detection limit of 0.0004 μM with a good sensitivity of 0.78 ± 0.01 μA μM. The as-fabricated electrode was successfully used for the estimation of Cys-SH in real samples (human plasma, urine, and saliva) with recovery % of 99–100% and RSD % of 2.7–3.6%, respectively.