Development of Membrane Selective Electrode for Determination of the Antipsychotic Sulpiride in Pharmaceuticals and Urine

The construction and electrochemical response characteristics of a poly(vinyl chloride) (PVC) membrane selective electrode for the determination of sulpiride (SPD) are described. The sensing membrane comprised an ion-exchanger formed between the protonated drug and tetraphenylborate (TPB-) in a plasticized PVC matrix. The influence of membrane composition on the electrode response was studied. The electrode showed a fast, stable and Nernstian response over a sulpiride concentration range (1 × 10-4 – 1 × 10-2 M) with a mean slope of 58.4 ± 0.9 mV dec-1 of concentration, a mean detection limit of 4.2 × 10-5 ± 1.2 × 10-5 M, a wide working pH range (2 – 8) and a fast response time (< 15 s). The electrode showed good selectivity towards sulpiride with respect to some inorganic and organic compounds. When the electrode was applied to the determination of sulpiride in pharmaceuticals and human urine, a high percentage of recovery was attained with no need for sample pretreatment procedures because of the lack of interfering matrix effects

Voltammetric Determination of the Herbicide Linuron Using a Tricresyl Phosphate-Based Carbon Paste Electrode

This paper summarises the results of voltammetric studies on the herbicide 3-(3,4-dichlorophenyl)-1-methoxy-1-methylurea (Linuron), using a carbon paste electrode containing tricresyl phosphate (TCP-CPE) as liquid binder. The principal experimental conditions, such as the pH effect, investigated in Britton-Robinson buffer solutions (pH 2.0–7.0), the peak characteristics for the analyte of interest, or instrumental parameters for the differential pulse voltammetric mode were optimized for the method. As found out, the best electroanalytical performance of the TCP-CPE was achieved at pH 2.0, whereby the oxidation peak of Linuron appeared at ca. +1.3 V vs. SCE. The analytical procedure developed offers good linearity in the concentration range of 1.25–44.20 μg mL−1 (1.77 × 10−4–5.05 × 10−6 mol L−1), showing—for the first time—the applicability of the TCP-CPE for anodic oxidations in direct voltammetry (without accumulation). The method was then verified by determining Linuron in a spiked river water sample and a commercial formulation and the results obtained agreed well with those obtained by the reference HPLC/UV determination

Metallic modified (bismuth, antimony, tin and combinations thereof) film carbon electrodes.

In this paper in situ bismuth, antimony, tin modified electrodes and combinations thereof are explored towards the model target analytes cadmium(II) and lead(II), chosen since they are the most widely studied, to explore the role of the underlying electrode substrate with respect to boron-doped diamond, glassy carbon, and screen-printed graphite electrodes. It is found that differing electrochemical responses are observed, dependent upon the underlying electrode substrate. The electrochemical response using the available range of metallic modifications is only ever observed when the underlying electrode substrate exhibits relatively slow electron transfer properties; in the case of fast electron transfer properties, no significant advantages are evident. Furthermore these bismuth modified systems which commonly employ a pH 4 acetate buffer, reported to ensure the bismuth(III) stability upon the electrode surface can create create a problem when sensing at low concentrations of heavy metals due to its high background current. It is demonstrated that a simple change of pH can allow the detection of the target analytes (cadmium(II) and lead(II)) at levels below that set by the World Health Organisation (WHO) using bare graphite screen-printed electrodes

Porous electrodes for bioanalytical applications

Dans cette mémoire nous discutons l élaboration d électrodes poreuses par un processus de type template et leur application potentielle dans le domaine de l analyse environnementale et neurobiologique. La première partie de ce travail est dédiée à l'élaboration d électrodes poreuses de bismuth et d'antimoine. Ces électrodes montrent des limites de détection améliorées par rapport à des électrodes non poreuses, ouvrant ainsi des applications prometteuses dans le domaine de l'analyse de trace. La deuxième partie vise à surmonter des facteurs limitants de micro-électrodes dans le cadre de l'enregistrement de signaux extracellulaires et la stimulation de réseaux neuronaux en culture, qui peut donner des informations sur des interactions et des phénomènes synergétiques dans les systèmes nerveux.In the present dissertation thesis the elaboration of porous electrodes via templating methods and their potential application in the field of environmental and neurobiological analysis are discussed. The electrodes of controlled porosity are characterized by an increased internal electroactive area and thus they can be used to enhance significantly the electrochemical performance. High surface area materials are promising for biosensing and more generally in electrochemical experiments. The first part of this work is focused on the elaboration of porous bismuth and antimony film electrodes. These porous electrodes show improved detection limits compared to non-porous one and thus open up promising applications in the field of trace analysis. The second part deals with overcoming limiting factors of microelectrode arrays in the context of extracellular recording and stimulating cellular neuronal networks or neural tissues in culture that can reveal information about interactions and synergetic features of nervous systems.BORDEAUX1-Bib.electronique (335229901) / SudocSudocFranceF