Recent advances in the fabrication and application of screen-printed electrochemical (bio)sensors based on carbon materials for biomedical, agri-food and environmental analyses

This review describes recent advances in the fabrication of electrochemical (bio)sensors based on screen-printing technology involving carbon materials and their application in biomedical, agri-food and environmental analyses. It will focus on the various strategies employed in the fabrication of screen-printed (bio)sensors, together with their performance characteristics; the application of these devices for the measurement of selected naturally occurring biomolecules, environmental pollutants and toxins will be discussed

Electrochemical and Optical Methods for the Quantification of Lead and Other Heavy Metal Ions in Liquid Samples

Minerals and elementary compounds of heavy metals are part of the ecosystem. Because of their high density and property to accumulate in stable forms, they are considered to be highly toxic to animals, plants and humans. Continuous mining activities and industrial effluents are the major sources which are adding toxic heavy metal ions into ecosystem and biota. Hence it is of utmost importance to quantify the levels of heavy metal ions in environmental and biological samples. On the other hand, it is equally important to remove the heavy metal ions and their compounds from the environmental and biological samples. That facilitates the environmental samples to be fit for using, consumption. In this regard, promising quantification methods such as electrochemical, spectrophotometric, naked eye sensing, test strips for spot analysis of heavy metal ions are considered for discussion. The main objective of this chapter is to give the overview of the most practiced quantification approaches available in the literature. Please note that reader cannot find the pin to pin publications regarding the same and that is not the aim of this book chapter

Electrochemical studies of metal-ligand interactions and of metal binding proteins

Electrochemical methods were researched for the analysis of metals, proteins and the identification of metal binding proteins. Adsorptive cathodic stripping voltamrnetry for metal analysis combines the inherent sensitivity of electrochemical techniques with the specificity of ligands for the nonfaradaic preconcentration of analytes at the electrode. The utility of catechol, resorcinol, 4-methylcatechol and 4-t-butylcatechol as ligands was explored for the sensitive analysis of copper, bismuth, cadmium and lead on a mercury film glassy carbon electrode. Metal complexes of lead, copper and bismuth with resorcinol showed the largest increase in current with increase in metal concentration, whereas complexes of these metals with 4-t-butylcatechol showed the lowest current response. Cadmium showed the highest current responses with 4-methylcatechol. The four metals could be determined simultaneously in the presence of resorcinol, although considerable interference was observed between bismuth and copper. The electroanalysis of cysteine and cysteine containing proteins at carbon electrodes are impaired by slow electron transfer rates at carbon electrodes, exhibiting high overpotentials, greater than 1 V vs Ag! Agel. Metallophthalocyanines have been shown to promote the electrocatalysis of cysteine at lowered potentials. Chemical modification of electrodes with appropriate modifiers is a means of incorporating specificity into electroanalysis, with applications in electrocatalysis. A glassy carbon electrode was modified by electrodeposition of cobalt (II) tetrasulphophthalocyanine [Co(II)TSPct to produce a chemically modified glassy carbon electrode (CMGCE). The CoTSPc-CMGCE catalysed the oxidation of cysteine in the pH range 1 to 10. The significance of this electrode is an application for analysis of proteins at biological pH's. A biscyanoruthenium(II) phthalocyanine CMGCE catalysed the oxidation of cysteine at 0.43 V vs Ag/AgCl a significant lowering in the overpotential for the oxidation of cysteine. Metallothionein, a metal binding protein, is believed to be involved in metal homeostasis and detoxification in the peripheral organs of living systems. A method for the quantitative determination of this protein utilising its high cysteine content was presented. At pH 8.4 Tris-HCl buffer, and using a CoTSPc-CMGCE modified by electrodeposition of the modifier, the anodic peaks for the oxidation of metallothionein was observed at 0. 90 V vs Ag/ AgCI. Ferredoxin is a simple iron-sulphur protein. One tenth of its residues are cysteine. Ferredoxin is involved in simple electron transfer processes during photosynthesis and respiration. Electrochemical studies of spinach ferredoxin were conducted at a CoTSPc-CMGCE. Anodic currents for the oxidation of the cysteine fragment of ferredoxin was observed at 0.85 V vs Ag/AgCl in HEPES buffer at pH 7.4, representing a new method for analysis of this protein. Voltammetric studies of its ferric/ferrous transition have shown quasi-reversible waves atE~ -0.62 V vs Ag/AgCl only in the presence of promoters. At a CoTSPc-CMGCE, a cathodic wave attributed to the reduction of Fe(III)/Fe(II) was observed at Epc -0.34 V vs Ag/AgCl. This represents an alternative method for voltammetric studies of the ferric/ferrous transition at significantly lowered potentials. Melatonin, a pineal gland hormone functions m setting and entraining circadian rhythms and in neuroprotection as a free radical scavenger and general antioxidant. Using adsorptive cathodic stripping voltammetry, the binding affinities of melatonin, serotonin and tryptophan for metals, were measured. The results showed that the following metal complexes were formed: aluminium with melatonin, serotonin and tryptophan; cadmium with melatonin and tryptophan; copper with melatonin and serotonin; iron (III) with melatonin and serotonin; lead with melatonin, tryptophan and serotonin, zinc with melatonin and tryptophan and iron (II) with tryptophan. The studies suggest a further role for melatonin in the reduction of free radical generation and in metal detoxification and may explain the accumulation of aluminium in Alzheimer's disease

Recent advances in chemical sensors for soil analysis: a review

The continuously rising interest in chemical sensors' applications in environmental monitoring, for soil analysis in particular, is owed to the sufficient sensitivity and selectivity of these analytical devices, their low costs, their simple measurement setups, and the possibility to perform online and in-field analyses with them. In this review the recent advances in chemical sensors for soil analysis are summarized. The working principles of chemical sensors involved in soil analysis; their benefits and drawbacks; and select applications of both the single selective sensors and multisensor systems for assessments of main plant nutrition components, pollutants, and other important soil parameters (pH, moisture content, salinity, exhaled gases, etc.) of the past two decades with a focus on the last 5 years (from 2017 to 2021) are overviewed

Electrochemical studies of metal-ligand interactions and of metal binding proteins

Electrochemical methods were researched for the analysis of metals, proteins and the identification of metal binding proteins. Adsorptive cathodic stripping voltamrnetry for metal analysis combines the inherent sensitivity of electrochemical techniques with the specificity of ligands for the nonfaradaic preconcentration of analytes at the electrode. The utility of catechol, resorcinol, 4-methylcatechol and 4-t-butylcatechol as ligands was explored for the sensitive analysis of copper, bismuth, cadmium and lead on a mercury film glassy carbon electrode. Metal complexes of lead, copper and bismuth with resorcinol showed the largest increase in current with increase in metal concentration, whereas complexes of these metals with 4-t-butylcatechol showed the lowest current response. Cadmium showed the highest current responses with 4-methylcatechol. The four metals could be determined simultaneously in the presence of resorcinol, although considerable interference was observed between bismuth and copper. The electroanalysis of cysteine and cysteine containing proteins at carbon electrodes are impaired by slow electron transfer rates at carbon electrodes, exhibiting high overpotentials, greater than 1 V vs Ag! Agel. Metallophthalocyanines have been shown to promote the electrocatalysis of cysteine at lowered potentials. Chemical modification of electrodes with appropriate modifiers is a means of incorporating specificity into electroanalysis, with applications in electrocatalysis. A glassy carbon electrode was modified by electrodeposition of cobalt (II) tetrasulphophthalocyanine [Co(II)TSPct to produce a chemically modified glassy carbon electrode (CMGCE). The CoTSPc-CMGCE catalysed the oxidation of cysteine in the pH range 1 to 10. The significance of this electrode is an application for analysis of proteins at biological pH's. A biscyanoruthenium(II) phthalocyanine CMGCE catalysed the oxidation of cysteine at 0.43 V vs Ag/AgCl a significant lowering in the overpotential for the oxidation of cysteine. Metallothionein, a metal binding protein, is believed to be involved in metal homeostasis and detoxification in the peripheral organs of living systems. A method for the quantitative determination of this protein utilising its high cysteine content was presented. At pH 8.4 Tris-HCl buffer, and using a CoTSPc-CMGCE modified by electrodeposition of the modifier, the anodic peaks for the oxidation of metallothionein was observed at 0. 90 V vs Ag/ AgCI. Ferredoxin is a simple iron-sulphur protein. One tenth of its residues are cysteine. Ferredoxin is involved in simple electron transfer processes during photosynthesis and respiration. Electrochemical studies of spinach ferredoxin were conducted at a CoTSPc-CMGCE. Anodic currents for the oxidation of the cysteine fragment of ferredoxin was observed at 0.85 V vs Ag/AgCl in HEPES buffer at pH 7.4, representing a new method for analysis of this protein. Voltammetric studies of its ferric/ferrous transition have shown quasi-reversible waves atE~ -0.62 V vs Ag/AgCl only in the presence of promoters. At a CoTSPc-CMGCE, a cathodic wave attributed to the reduction of Fe(III)/Fe(II) was observed at Epc -0.34 V vs Ag/AgCl. This represents an alternative method for voltammetric studies of the ferric/ferrous transition at significantly lowered potentials. Melatonin, a pineal gland hormone functions m setting and entraining circadian rhythms and in neuroprotection as a free radical scavenger and general antioxidant. Using adsorptive cathodic stripping voltammetry, the binding affinities of melatonin, serotonin and tryptophan for metals, were measured. The results showed that the following metal complexes were formed: aluminium with melatonin, serotonin and tryptophan; cadmium with melatonin and tryptophan; copper with melatonin and serotonin; iron (III) with melatonin and serotonin; lead with melatonin, tryptophan and serotonin, zinc with melatonin and tryptophan and iron (II) with tryptophan. The studies suggest a further role for melatonin in the reduction of free radical generation and in metal detoxification and may explain the accumulation of aluminium in Alzheimer's disease

Electrochemical method for the rapid in situ screening of heavy metals in soil and water samples

The aim of this work has been to develop a field-based electrochemical sensor for the detection of cadmium (Cd), lead (Pb), copper (Cu), zinc (Zn), arsenic (As) and mercury (Hg) in soil and water samples. In situ analysis, using rapid sample screening tools, can facilitate monitoring and remediation processes by minimising delays and substantially reducing costs. Disposable screen-printed electrodes (SPEs) have been fabricated using low-cost thick film technology. Carbon SPEs, coupled with anodic stripping voltammetry (ASV), provided a rapid, inexpensive in situ electrochemical screening sensor capable of simultaneously detecting Cd, Pb and Cu in soil and water samples in the microgram per liter range (pg I*1). A simplified soil extraction procedure, using 1 mol I'1 aqua regia and a three minute ultrasonic sample agitation, was developed for use with the sensor, addressing the lack of existing field-based soil extraction protocol. Extraction efficiency was evaluated using a soil certified reference material (CRM). Recoveries of 64%, 52% and 57% for Cd, Pb and Cu respectively were obtained, with a relative standard deviation (RSD) of <8% for all analytes (n=10). 82 soil samples were tested using the combined extraction + ASV sensor and compared against standard ICP-MS analysis. Correlation coefficients of 0.9782, 0.9728 and 0.9869 for Cd, Pb and Cu, respectively, indicated a good linear relationship between the two methods. A novel gold (Au) SPE, fabricated using a curable Au ink, was next evaluated for the detection of As and Hg. This is an improvement in the current state-of the-art as no surface modification or subsequent electrode adulteration to facilitate metal analyte depositioning is required. Furthermore, the Au ink can be cured at a low temperature (130°C), permitting electrode fabrication using disposable, cheap, plastic substrates. A patent has been filed. A limit of detection (LOD) of 2.7 pg I"1 and 1 pg I"1 for As3+ and Hg2+, respectively, was obtained following a 30 s depositioning. Speciation measurements for As were performed by reducing As5+ effectively over a short (10 min) reduction time using cysteine. An LOD of 42 pg f 1 following a 30 s depositioning was obtained. Initial studies also indicated the possibility of using the Au SPEs for measuring Cd, Pb and Cu, providing an alterative Hg-free procedure.Ph

Ultrasensitive electrochemical sensors based on Cu and Cu@Ag nanorods for simultaneous heavy metal detection

This work reports the development of ultrasensitive miniaturized electrochemical device for heavy metal sensing. A laser engraver based patterning of fluorine-doped tin oxide (FTO) sheet was done to draw an etched pattern forming a miniaturized 3-electrode configuration. A layer of Ag/AgCl ink served as pseudo-reference electrode. The sensing electrode was coated using low-cost Cu nanorods (CuNRs) grown radially along the {110} surface with aspect ratio of 8.0 and Cu@Ag core-shell nanorods (Cu@AgNRs) formed via galvanic displacement for simultaneous electrocatalytic detection of heavy metal ions (Pb(II), Cd(II), Hg(II), and Zn(II)) present in water. The electroactive surface area of the prepared devices is 0.026, 0.093 and 0.125 cm2 for bare FTO, CuNRs/FTO and Cu@AgNRs/FTO, respectively. Bimetal Cu@AgNRs/FTO sensor exhibited the lowest limit of detection of 1, 2, 5 and 6 nM, respectively, detecting Cd(II), Pb(II), Zn(II), and Hg(II) ions, and it was 2, 2, 3 and 4 nM, respectively, for simultaneous detection of Zn(II), Pb(II), Cd(II) and Hg(II). The Cu@AgNRs/FTO based device showed distinct peak-to-peak separation by 0.40, 0.25 and 0.51 V for Zn(II)-Cd(II), Cd(II)-Pb(II) and Pb(II)-Hg(II), respectively. This device was highly sensitive (583.6–1261.8 μA․μM−1․cm−2) for heavy metal detection over CuNRs/FTO (15.9–107.4 μA․μM−1․cm−2). The Cu@AgNRs/FTO based sensors demonstrated good reproducibility (relative standard deviation ≤ 5%) with recovery (>90%) in the case of all target heavy metals simultaneously present in environmental water samples. Hence, the Cu nanorods based miniaturized sensing platforms developed in the present study for simultaneous heavy metal detection are potential low-cost alternatives providing a repeatability of upto 4 cycles unlike the commercial screen-printed electrodes

Voltammetric determination of metal ions beyond mercury electrodes. A review

For a long time mercury electrodes have been the main choice for the analysis of metal ions and some metalloids. However, in the last years, safety and environmental considerations have restricted their use and encouraged the search for alternative materials more environmentally friendly and with more possibilities for in-situ and flow analysis. This research has been reinforced by the popularisation of nanomaterials, biomolecules and screen-printed electrodes, as well as for the new advances in sensor miniaturization and integration of the electrodes in multi-sensor platforms and electronic tongues. The present review critically summarizes and discusses the progress made since 2010 in the development and application of new electrodes for the analysis of metals and metalloids

Desenvolupament de sensors i llengües electròniques voltamperomètriques per a la determinació d’ions metàl·lics en mostres d’interès ambientals

[cat] La problemàtica mediambiental associada a la contaminació per ions metàl·lics és mundialment coneguda. En les últimes dècades hi ha hagut un enduriment de la legislació associada a aquests contaminants que ha permès disminuir les seves emissions al medi ambient però, degut a la seva elevada persistència i al seu caràcter no biodegradable, les concentracions dels ions metàl·lics en mostres mediambientals són encara preocupants. Actualment, tot i que existeixen diverses tècniques analítiques per a la determinació d’ions metàl·lics, encara és necessari el desenvolupament de noves metodologies analítiques que permetin determinar-los on-site i a nivell traça. En aquest sentit, les tècniques voltamperomètriques de redissolució són una bona opció ja que són tècniques sensibles i reproduïbles que proporcionen anàlisis ràpides sense requerir instrumentació voluminosa o excessivament costosa. A més, el caràcter portàtil d’aquestes tècniques s’ha vist afavorit amb la introducció dels elèctrodes serigrafiats, que són dispositius compactes, miniaturitzats, versàtils i que es poden produir en massa. Un dels avantatges que proporcionen els elèctrodes serigrafiats és la possibilitat de modificar el seu elèctrode de treball per tal de millorar la seva sensibilitat i selectivitat o permetre treballar a diferents condicions experimentals. En aquest sentit, una primera part d’aquesta tesi doctoral s’ha centrat en el desenvolupament de nous elèctrodes serigrafiats voltamperomètrics per a la determinació d’ions metàl·lics a nivell traça en mostres mediambientals. Concretament, s’han estudiat diferents estratègies de modificació com la modificació química, la formació de pel·lícules metàl·liques i l’ús de diversos nanomaterials (nanopartícules metàl·liques, nanoal·lòtrops de carboni i silici porós). Per a cada estratègia s’han estudiat diferents aspectes del procés de modificació i s’ha avaluat l’aplicabilitat del sensor que proporciona millors resultats en mostres reals. Sovint però, en l’anàlisi de mostres reals trobem mescles complexes on els ions metàl·lics s’interfereixen entre si o donen lloc a pics solapats. En aquests casos l’ús d’un sol sensor no permet determinar correctament la concentració dels diferents ions i cal recórrer a altres estratègies d’anàlisi més sofisticades. Aquest és el cas de les llengües voltamperomètriques, on es combinen diversos sensors no específics amb un tractament de dades multivariant. Així, la segona part d’aquesta tesi doctoral s’ha centrat en el desenvolupament de llengües voltamperomètriques per a l’anàlisi de mostres complexes d’ions metàl·lics. Concretament s’han estudiat el sistema Tl(I) i In(III) i el sistema Cd(II), Pb(II), Tl(I) i Bi(III) en presència de Zn(II) i In(III), que es caracteritzen, respectivament, per la presència de dos metalls que donen lloc a senyals fortament solapats i per la presència d’un elevat nombre de metalls. Concretament, s’ha estudiat la selecció dels sensors que componen la llengua voltamperomètrica, la seva disposició i el disseny experimental. Un altre aspecte crucial en el desenvolupament de les llengües voltamperomètriques és el tractament de dades. Així, en la segona part d’aquesta tesi doctoral també s’ha fet èmfasi en aquest tema, on s’han estudiat diversos pretractaments i s’han construït diversos models quimiomètrics basats en la regressió per mínims quadrats parcials (PLS). A més, s’han estudiat també dos sistemes de calibratge multivariant, el calibratge multivariant extern i l’addició estàndard multivariant, per a la qual s’ha desenvolupat una nova estratègia basada en l’ús de PLS i la simulació del blanc de la mostra a partir de l’omissió de l’etapa de preconcentració de la mesura voltamperomètrica. Aquest segon mètode de calibratge proporciona prediccions més acurades per a mostres amb un fort efecte matriu. Els resultats obtinguts a partir dels estudis realitzats al llarg d’aquesta tesi doctoral han donat lloc a 12 articles, 9 d’ells referents a la part de desenvolupament de sensors voltamperomètrics i 3 referents al desenvolupament de llengües voltamperomètriques.[eng] On-site monitoring of metal ions at trace levels is crucial for safety and environmental reasons. In this sense, stripping voltammetry is a good option due to its high sensitivity and reproducibility and the fact that it provides fast analysis with relatively low cost and portable equipment. These last features are further enhanced by the coupling of stripping voltammetry with screen-printed electrodes, which are compact, miniaturized and versatile devices that can be mass-produced in a reproducible manner. A first part of this PhD thesis has focused on the development of new screen-printed voltammetric sensors for the determination of metal ions at trace levels in environmental samples. Particularly, several modification strategies (chemical modification, metal films and nanomaterials) have been studied. For each strategy, some aspects of the modification process were evaluated and their applicability to real samples was tested for the sensor that provided better results. Frequently though, the analysis of real samples involves complex mixtures where metal ions interact with each other or give rise to highly overlapped peaks. In these scenarios, it is necessary to resort to more sophisticated analytical strategies like voltammetric electronic tongues. Thus, the second part of this PhD thesis has focused on the development of voltammetric tongues for the analysis of complex mixtures of metal ions. In particular, two systems have been studied: Tl(I) and In(III), two metals that give rise to highly overlapped peaks, and Cd(II), Pb(II), Tl(I) and Bi(III) in the presence of Zn(II) and In(III). In both cases, several studies involving the selection of sensors, their arrangement and the experimental design were performed. The second part of this PhD thesis has also focused on data treatment, a key aspect in the development of voltammetric tongues. Two multivariate calibration systems were studied, multivariate external calibration and multivariate standard addition, for which a new strategy based on PLS and the simulation of a blank signal by skipping the deposition step of stripping voltammetry was developed. The results achieved throughout this PhD thesis have resulted in 12 articles, 9 related to the development of voltammetric sensors and 3 related to the development of voltammetric electronic tongues