Voltammetric characteristics of diazinon on carbon paste electrode modified with tris(ethylenediamine) cobalt(II) iodide

In this study, cyclic and differential pulse voltammetric methods were used to investigate the electrochemical behavior of diazinon at carbon paste electrode modified with tris(ethylenediamine) cobalt(II) iodide ([Co(en)₃]I₂). Cobalt complex showed an anodic peak at 620 mV (vs. Ag/AgCl, in KNO₃ 0.1 M as supporting electrolyte) at carbon paste modified electrode. In the presence of diazinon, anodic peak intensity increased with increasing concentration of diazinon that confirmed electrocatalytic activity of cobalt complex for oxidation of diazinon (EC’ mechanism). Under optimized conditions, a linear calibration curve for diazinon was obtained in the range from 0.05 to 27 mg/L with detection limit 0.0075 mg/L (3S _b /m). Applications of the modified electrode to the determination of diazinon in different water samples were also tested. The results showed a very good precision (RSD < 0.04%) and very stable voltammetric response towards diazinon.     

Determination of fluoxetine in pharmaceutical preparations and biological samples using potentiometric sensors based on polymeric membranes

The construction and general performance of four novel potentiometric membrane sensors for the determination of fluoxetine have been described. The sensors are based on the formation of the ion association complex of fluoxetine with sodium tetraphenylborate and phosphotungstic acid as electroactive materialles, dispersed in a PVC matrix with dibuthyl sebacate (or diethyl sebacate) as a plasticizer. These sensors exhibit fast, stable and near-Nernstian response for the monocharged fluoxetine cation over wide concentration range from 3.0 × 10^?6 to 1.2 × 10^?2 M and pH 4.0–7.5. No interferences are caused by many inorganic and organic species. Direct potentiometric determinations of 5–100 μg/mL of fluoxetine in drug and urine samples show good recovery of fluoxetine. The developed membrane electrodes have been used as an end point indicator electrode; the potentiometric titration of fluoxetine with sodium tetraphenylborate as a titrant has been monitored.     

Nanostructured Screen Printed Graphite Electrode for the Development of a Novel Electrochemical Genosensor

The aim of this work is the preparation of DNA‐sensing architectures based on gold nanoparticles (AuNPs) in conjunction with an enzyme‐amplified detection to improve the analytical properties of genosensor. In order to assess the utility of study as DNA‐sensing devices, a thiolated DNA capture probe sequence was immobilized on the gold nanoparticle modified surface. After labeling of the biotinylated hybrid with a streptavidin‐alkaline phosphatase conjugate, the electrochemical detection of the enzymatic product was performed on the surface of a disposable electrode. Two different enzymatic substrates to detect the hybridization event were studied. In the first case, the enzyme catalyzed the hydrolysis of α‐naphthyl phosphate; the product is electroactive and has been detected by means of differential pulse voltammetry (DPV). In the second one, the enzyme catalyzed the precipitation of an insoluble and insulating product on the sensing interface. In this case, the electrochemical transduction of the hybridization process was performed by electrochemical impedance spectroscopy (EIS).     

Ion-selective electrode for aluminum determination in pharmaceutical substances, tea leaves and water samples

A novel ion-selective PVC membrane sensor for Al(III) ions based on 6-(4-nitrophenyl)-2-phenyl-4-(thiophen-2-yl)-3,5-diaza-bicyclo[3.1.0]hex-2-ene (NTDH) as a new ionophore has been prepared and studied. The electrode exhibit a good response for aluminum ion over concentration range of 1.0x10(-6) to 1.0x10(-1) mol L(-1) with a Nernstian slope of 19.6+/-0.4 mV per decade and low detection limit of 6.3x10(-7) mol L(-1). The best performance was obtained with membrane composition 30% poly(vinyl chloride), 62% acetophenone, 5% oleic acid, 3% ionophore and 2 ml tetrahydrofuran. NTDH-based electrode was suitable for aqueous solutions of pH 3. It has relatively fast response time (approximately 10 s) and can be used at least for 3 months without any considerable divergence in potentials. The proposed membrane electrode revealed good selectivity for Al(III) ions over a wide variety of other cations. The standard electrode potentials were determined at different temperatures and used to calculate the isothermal coefficient of the electrode. The formation constant and stoichiometry ratio of ionophore-Al(III) complex were calculated at 25 degrees C by using segmented sandwich membrane method. It was used in non-aqueous solvents and also as indicator electrode in potentiometric determination of Al(III) ions in some real samples.     

Electrochemical behavior and differential pulse voltammetric detection of thiobencarb on 2-(4-((4-ethoxyphenyl)diazenyl)phenylamino)ethanol-modified carbon paste electrode

Cyclic voltammetry, chronoamperometry, and rotating disk electrode voltammetry were used to investigate the electrochemical behavior of thiobencarb (TB) at carbon paste electrode modified with an azo dye, 2-(4-((4-ethoxyphenyl)diazenyl)phenylamino)ethanol (EDPE), EDPE/modified carbon paste electrode (MCPE). The modified electrode showed high electrocatalytic activity toward thiobencarb. The current was enhanced significantly relative to the situation prevailing when a bare glassy carbon electrode was used. The kinetics parameters of this process were calculated, the apparent electron transfer rate constant k _s and α (charge transfer coefficient between electrode and EDPE) were 14.6 s⁻¹ and 0.48, respectively. The experimental parameters were optimized, and the mechanism of the catalytic process was discussed. The best defined cathodic peak was obtained with 0.1 M acetate buffer (pH 3.0). The response of the sensor was very quick, and response time was approximately 5 s. The differential pulse voltammetry response of the MCPE was linear against the concentration of TB in the range of 0.96 to 106 μg L⁻¹. The limit of detection was found to be 0.025 μg L⁻¹. The precision was examined by carrying out eight replicate measurements at a concentration of 25 μg L⁻¹ TB; the relative standard deviation was 2.9%.     

Enhanced Electrocatalytic Reduction of Oxadiargyl and Its Determination on 2‐(4‐((4‐Acetylphenyl)diazenyl)phenylamino)‐ethanol Modified Graphene‐Paste Electrode

The electrochemical behavior of oxadiargyl at a graphene‐paste electrode modified with an azo dye, 2‐(4‐((4‐acetylphenyl)diazenyl)phenylamino)ethanol (ADPE), ADPE/MGRPE was investigated. The modified electrode showed high electrocatalytic activity toward oxadiargyl. The apparent electron transfer rate constant (k_s) and charge transfer coefficient (α) between electrode and ADPE were 1.16 s^?1 and 0.41, respectively. The differential pulse voltammetry response of the modified graphene‐paste electrode was linear against the concentration of oxadiargyl in the range from 0.03 to 1.4 mg L^?1. The limit of detection was found to be 1.3 µg L^?1 (S/N=3). The practical analytical utility of this electrode was demonstrated by measurement of oxadiargyl in river water, soil and rice samples.     

Fluorinated Analogues to the Pentuloses of the Pentose Phosphate Pathway

Fluorinated carbohydrates are valuable tools for enzymological studies due to their increased metabolic stability compared to their non-fluorinated analogues. Replacing different hydroxyl groups within the same monosaccharide by fluorine allows to influence a wide range of sugar–receptor interactions and enzymatic transformations. In the past, this principle was frequently used to study the metabolism of highly abundant carbohydrates, while the metabolic fate of rare sugars is still poorly studied. Rare sugars, however, are key intermediates of many metabolic routes, such as the pentose phosphate pathway (PPP). Here we present the design and purely chemical synthesis of a set of three deoxyfluorinated analogues of the rare sugars d -xylulose and d -ribulose: 1-deoxy-1-fluoro-d -ribulose ( 1DFRu ), 3-deoxy-3-fluoro-d -ribulose ( 3DFRu ) and 3-deoxy-3-fluoro-d -xylulose ( 3DFXu ). Together with a designed set of potential late-stage radio-fluorination precursors, they have the potential to become useful tools for studies on the complex equilibria of the non-oxidative PPP.