Application of graphite screen printed electrode modified with dysprosium tungstate nanoparticles in voltammetric determination of epinephrine in the presence of acetylcholine

The current work focuses on the development of a sensitive and selective electrochemical device based on a graphite screen printed electrode modified with Dy2（WO4）3 nanoparticles（DWO/SPE） for the analysis of epinephrine in samples also containing acetylcholine. The study proves that the sensor has excellent electron-mediating behavior in the oxidation of epinephrine in a 0.1 mol/L phosphate buffer solution（PBS）（pH 7.0）. The application of the DWO/SPE in differential pulse voltammetry（DPV） is found to lead to distinct response for the oxidation of epinephrine and acetylcholine, with the potentials of the epinephrine and acetylcholine peaks（△Ep） to be 550 mV apart. The detection limits of the method for epinephrine and acetylcholine are 0.5 and 0.7 μmol/L（S/N = 3） and the responses are found to be linear in the concentration ranges of 1.0-900.0 μmol/L and 1.0-1200.0 μmol/L in a PBS buffer（pH = 7.0）respectively. The modified electrode was used for the detection of epinephrine and acetylcholine in real samples and found to produce satisfactory results. These results can be a proof that Dy2（WO4）3 nanoparticles can find promising applications in electrochemical sensors to be used for the analysis of（bio）chemical species.

Immobilisation of electrochemically active bacteria on screen-printed electrodes for rapid in situ toxicity biosensing

are time-consuming and not sensitive enough.However,bacteria typically connect to electrodes through biofilm formation,leading to problems due to lack of uniformity or long device production times.A suitable immobilisation technique can overcome these challenges.Still,they may respond more slowly than biofilm-based electrodes because bacteria gradually adapt to electron transfer during biofilm formation.In this study,we propose a controlled and reproducible way to fabricate bacteria-modified electrodes.The method consists of an immobilisation step using a cellulose matrix,followed by an electrode polarization in the presence of ferricyanide and glucose.Our process is short,reproducible and led us to obtain ready-to-use electrodes featuring a high-current response.An excellent shelf-life of the immobilised electrochemically active bacteria was demonstrated for up to one year.After an initial 50% activity loss in the first month,no further declines have been observed over the following 11 months.We implemented our bacteria-modified electrodes to fabricate a lateral flow platform for toxicity monitoring using formaldehyde(3%).Its addition led to a 59% current decrease approximately 20 min after the toxic input.The methods presented here offer the ability to develop a high sensitivity,easy to produce,and long shelf life bacteria-based toxicity detectors.

Microfibrillated Cellulose Based Ink for Eco-Sustainable Screen Printed Flexible Electrodes in Lithium Ion Batteries

Free organic solvent ink containing graphite, carboxymethyl cellulose and microfibrillated cellulose as active material, dispersing and binder, respectively, has been formulated to produce flexible and eco- sustainable electrodes for lithium ion batteries. Content ratio of components and dispersion protocol were tailored in order to have theological properties suitable for a large and cheap manufacturing process as well as screen printing. The bio-sourced printed electrodes exhibit a high porosity value of 70% that limits the electrochemical performances. However, the calendering process enhances electrode performances by increasing the reversible capacity from 85 until 315 mAh/g and reducing porosity to an optimal value of 34%. Moreover the introduction of 2% w/w of monofluoro-ethylene carbonate in the electrolyte reduced their reversible capacity loss of 11% in the printed electrode.

Development of new potentiometric sensors for the determination of proguanil hydrochloride in serum and urine

Potentiometric electrodes were developed for the rapid determination of proguanil hydrochloride in pure samples, pharmaceutical preparations and spiked serum and urine samples using PVC membrane,screen printed（SPE）, coated wired（CWE）, carbon paste（CPE） and modified carbon paste（MCPE）electrodes based on the ion-exchanger of proguanil with phosphotungestic acid（Pr-PT） as a chemical modifier. The prepared electrodes showed Nernestian slopes of 59.7, 58.1, 58.5, 58.5 and 57.0 for the PVC,SPE, CWE, CPE and MCPE for the proguanil ions in a wide concentration range of 1.0 ＊ 10^-5–1.0 ＊ 10^-2mol L^-1 at 25°C with detection limits of 7.94 ＊ 10^-6, 1.0 ＊ 10^-5, 1.0 ＊ 10^-6, 7.07 ＊ 10^-6 and 2.5 ＊ 10^-6 mol L^-1, respectively. The prepared electrodes exhibited high proguanil selectivity in relation to several inorganic ions and sugars and they could be successfully utilized for its determination in pure solutions, pharmaceutical preparations and serum and urine samples using the direct potentiometry and standard addition methods with very good recovery values.