Metal oxide nanoparticle based electrochemical sensor for total antioxidant capacity (TAC) detection in wine samples

A single-use electrochemical screen-printed electrode is reported based on biomimetic properties of nanoceria particles (CeNPs). The developed tool showed an easy approach compared to the classical spectrophotometric methods reported in literature in terms of ease of use, cost, portability, and unnecessary secondary reagents. The sensor allowed the detection of the total antioxidant capacity (TAC) in wine samples. The sensor has been optimized and characterized electrochemically and then tested with antioxidant compounds occurred in wine samples. The electrochemical CeNPs modified sensor has been used for detection of TAC in white and red commercial wines and the data compared to the 2,2'-azino-bis(3-ethylbenzthiazoline-6-sulphonic acid (ABTS)-based spectrophotometric method. Finally, the obtained results have demonstrated that the proposed sensor was suitable for the simple and quick evaluation of TAC in beverage samples

Catalase-based modified graphite electrode for hydrogen peroxide detection in different beverages

A catalase-based (NAF/MWCNTs) nanocomposite film modified glassy carbon electrode for hydrogen peroxide (H2O2) detection was developed. The developed biosensor was characterized in terms of its bioelectrochemical properties. Cyclic voltammetry (CV) technique was employed to study the redox features of the enzyme in the absence and in the presence of nanomaterials dispersed in Nafion polymeric solution. The electron transfer coefficient, , and the electron transfer rate constant, , were found to be 0.42 and 1.71 s−1, at pH 7.0, respectively. Subsequently, the same modification steps were applied to mesoporous graphite screenprinted electrodes. Also, these electrodes were characterized in terms of their main electrochemical and kinetic parameters. The biosensor performances improved considerably after modification with nanomaterials. Moreover, the association of Nafion with carbon nanotubes retained the biological activity of the redox protein. The enzyme electrode response was linear in the range 2.5– 1150 mol L−1, with LOD of 0.83 mol L−1. From the experimental data, we can assess the possibility of using the modified biosensor as a useful tool for H2O2 determination in packaged beverages

Inhibition-based first-generation electrochemical biosensors: theoretical aspects and application to 2,4-dichlorophenoxy acetic acid detection

In this work, several theoretical aspects involved in the first-generation inhibition-based electrochemical biosensor measurements have been discussed. In particular, we have developed a theoretical-methodological approach for the characterization of the kinetic interaction between alkaline phosphatase (AlP) and 2,4- dichlorophenoxy acetic acid (2,4-D) as representative inhibitor studied by means of cyclic voltammetry and amperometry. Based on these findings, a biosensor for the fast, simple, and inexpensive determination of 2,4-D has been developed. The enzyme has been immobilized on screen-printed electrodes (SPEs). To optimize the biosensor performances, several carbon-based SPEs, namely graphite (G), graphene (GP), and multiwalled carbon nanotubes (MWCNTs), have been evaluated. AlP was immobilized on the electrode surface by means of polyvinyl alcohol with styryl-pyridinium groups (PVA-SbQ) as cross-linking agent. In the presence of ascorbate 2-phosphate (A2P) as substrate, the herbicide has been determined, thanks to its inhibition activity towards the enzyme catalyzing the oxidation of A2P to ascorbic acid (AA). Under optimum experimental conditions, the best performance in terms of catalytic efficiency has been demonstrated by MWCNTs SPE-based biosensor. The inhibition biosensor shows a linearity range towards 2,4-D within 2.1–110 ppb, a LOD of 1 ppb, and acceptable repeatability and stability. This analysis method was applied to fortified lake water samples with recoveries above 90 %. The low cost of this device and its good analytical performances suggest its application for the screening and monitoring of 2,4-D in real matrices

Nanoparticles modified screen printed electrode for electrochemical determination of COD

The Chemical Oxygen Demand (COD) is a parameter widely used to determine organic pollutants in water and is defined as the number of oxygen equivalents necessary to oxidize the organic compounds. The standard method for COD measurement (the dichromate titration) suffers from several inherent drawbacks such as the long time of the process and the consumption of toxic chemicals. Hence, interest is growing towards those methods employing electrochemical oxidation of organic compounds, as they allow to dispense with toxic reagents and above all to perform a continuous determination. In this work a new electrochemical method for COD measurement has been developed based on direct oxidation of organic molecules on suitably modified electrodic surfaces. In particular, we have developed various sensors based on modified working electrode surfaces obtained by electrodepositing copper and/or nickel oxide nanoparticles onto several commercial screen printed electrodes. Glucose was used as the standard compound for COD measurements: C6H12O6 + 6O2 → 6CO2 + 6H2O The metallic nanoparticles catalyze the oxidation of the glucose, as well as of different organic pollutants, and make the detection possible at relatively low potential, also in presence of chloride as interferent. The analytical parameters were optimized and the results obtained highlight how the electrodeposition of different metallic nanoparticles onto several screen printed electrode surfaces can influence the selectivity and sensitivity towards the COD detection in real matrices, via electrochemical method. The results were compared with those obtained by the standard method and showed a good agreement. These findings provide an interesting strategy to obtain a simple, cheap, portable and eventually continuous sensor for COD measurement

Evaluation of new cholinium-amino acids based room temperature ionic liquids (RTILs) as immobilization matrix for electrochemical biosensor development: proof-of-concept with trametes versicolor laccase

In this work, we present new cholinium-amino acids room temperature ionic liquids (ChAARTILs) that can be used as an efficient immobilization matrix for electrochemical biosensor development. The ideal immobilization strategy should be able to ensure the highest enzyme loading and a tight enzymatic immobilization, preserving its native structure and biological activity. In this regard, ChAARTILs present different side chains on the amino acids giving rise to van der Waals, π-π stacking and hydrogen bonding interactions. All these interactions can affect the nanomaterial organization onto the electrode surface. To this aim, we have evaluated the main electrochemical parameters, namely electroactive area (AEA) and the heterogeneous electron transfer rate constant (k0), showing how both cations and anions of room temperature ionic liquids (RTILs) can independently affect multi-walled carbon nanotubes (MWCNTs) organization. In particular, [Ch][Phe] showed the best performance in terms of AEA (3.432 cm2) and k0 (4.71·10−3 cm s−1) with a homogeneous distribution of MWCNTs bundles onto the electrodes and a faster electron transfer rate

Electrochemical biosensors for environmental monitoring

The challenge for the monitoring of environmental hazards such as pollutants, herbicides, pesticides and toxins caused by expanding industrialisation and application of new intensive agricultural technologies is to develop efficient tools that offer precision, sensitivity, and speed and ease of operation in situ and avoid consequently risks for both human and environmental health. In this context, electrochemical biosensors appear as excellent analytical devices alternative or complementary to conventional systems for environmental monitoring purposes. This paper presents a review about the use of electrochemical biosensors for environmental analysis, taking into particular account the general principles and characteristics as well as some representative applications of enzymatic, antibody and aptamer-based biosensors. This review covers several papers published in the last 15 years putting in evidence the improvement reached in this field of research. Copyright © 2012 Inderscience Enterprises Ltd

Microneedle-based electrochemical devices for transdermal biosensing: a review

Many research efforts over the last decade have been devoted to the development of microneedle-based diagnostic devices for minimally invasive transdermal biosensing and for long-term health monitoring. Transdermal biosensing via microneedle allows the development of minimally invasive easy-to-use point-of-care biodevices. The main objective of this short review is to provide a general overview of the most immediate and relevant progress in microneedle-based transdermal biosensing in the last five years. A critical analysis of the recent literature is finally presented