Disposable Potentiometric Sensor Research Articles

Touch–based potentiometric sensors for simultaneous detection of urea and ammonium from fingertip sweat

Urea is a biomarker for diagnosis and management of multiple disorders. The measurement of urea could help in the diagnosis of patients with kidney dysfunction. Despite their attractive analytical performances, the existing urea measurement methods are still limited to sophisticated and time–consuming or require invasive blood sampling. Herein, a reliable noninvasive, simple, and disposable touch–based potentiometric sensor is fabricated for rapid monitoring of fingertip sweat urea. Novel touch–based urea detection relies on immobilized urease recognition and a solid–contact ammonium–ion–selective electrode, along with a screen–printed carbon working electrode modified carboxylated carbon nanotubes for enhancing sensor’s sensitivity. The fingertip sweat under sedentary rest conditions can be instantaneously collected on customized porous polyvinyl alcohol hydrogel transporting sweat to working electrode surface where the hydrolysis of urea is catalyzed, generating bicarbonate and ammonium. The resulting ammonium can be detected with ion–selective transducer, enabling indirect monitoring of sweat urea. Potential interference from co–existing ammonium in human sweat is addressed by developing a dual disposable potentiometric sensor, consisting of urea and ammonium sensors on a single strip platform allowing for simultaneous touch–based detection of sweat urea and ammonium. The resulting dual disposable sensing system offers rapid urea and ammonium monitoring within a group of healthy human subjects, along with a good correlation with R2 = 0.974 between the sweat urea and capillary blood urea levels. Additional confirmation among a broad sample of individuals along with the validation of sensor data through centralized laboratory tests will establish the practicality of simultaneously monitoring urea and ammonium levels.

Decentralized ORP Measurements for Gut Redox Status Monitoring: Toward Personalized Gut Microbiota Balance.

Gut microbiome targeting has emerged as a new generation of personalized medicine and a potential wellness and disease driver. Specifically, the gut redox balance plays a key role in shaping the gut microbiota and its link with the host, immune system, and disease evolution. In this sense, precise and personalized nutrition has proven synergy and capability to modulate the gut microbiome environment through the formulation of dietary interventions, such as vitamin support. Accordingly, there are urgent demands for simple and effective analytical platforms for understanding the relationship between the tailored vitamin administration and the gut microbiota balance by rapid noninvasive on-the-spot oxidation/reduction potential monitoring for frequent and close surveillance of the gut redox status and targeting by personalized nutrition interventions. Herein, we present a disposable potentiometric sensor chip and a homemade multiwell potentiometric array to address the interplay of vitamin levels with the oxidation/reduction potential in human feces and saliva. The potentiometric ORP sensing platforms have been successfully validated and scaled up for the setup of a multiapplication prototype for cross-talk-free simple screening of many specimens. The interpersonal variability of the gut microbiota environment illustrates the potential of feces and saliva samples for noninvasive, frequent, and decentralized monitoring of the gut redox status to support timely human microbiota surveillance and guide precise dietary intervention toward restoring and promoting personalized gut redox balance.

Point-of-care diagnostics for rapid determination of prostate cancer biomarker sarcosine: application of disposable potentiometric sensor based on oxide-conductive polymer nanocomposite

One of the most important reasons for an increased mortality rate of cancer is late diagnosis. Point-of-care (POC) diagnostic sensors can provide rapid and cost-effective diagnosis and monitoring of cancer biomarkers. Portable, disposable, and sensitive sarcosine solid-contact ion-selective potentiometric sensors (SC-ISEs) were fabricated as POC analyzers for the rapid determination of the prostate cancer biomarker sarcosine. Tungsten trioxide nanoparticles (WO3 NPs), polyaniline nanoparticles (PANI NPs), and PANI-WO3 nanocomposite were used as ion-to-electron transducers on screen-printed sensors. WO3 NPs and PANI-WO3 nanocomposite have not been investigated before as ion-to-electron transducer layers in potentiometric SC sensors. The designated sensors were characterized using SEM, XRD, FTIR, UV-VIS spectroscopy, and EIS. The inclusion of WO3 and PANI in SC sensors enhanced the transduction at the interface between the screen-printed SC and the ion-selective membrane, offering lower potential drift, a longer lifetime, shorter response time, and better sensitivity. The proposed sarcosine sensors exhibited Nernstian slopes over linear response ranges 10−3–10−7 M, 10−3–10−8 M, 10−5–10−9 M, and 10−7–10−12 M for control, WO3 NPs, PANI NPs, and PANI-WO3 nanocomposite-based sensors, respectively. From a comparative point of view between the four sensors, PANI-WO3 nanocomposite inclusion offered the lowest potential drift (0.5 mV h−1), the longest lifetime (4 months), and the best LOD (9.95 × 10−13 M). The proposed sensors were successfully applied to determine sarcosine as a potential prostate cancer biomarker in urine without prior sample treatment steps. The WHO ASSURED criteria for point-of-care diagnostics are met by the proposed sensors.Graphical abstract

3D-Drawn Supports for Ion-Selective Electrodes.

A new concept of easy to make, potentially disposable potentiometric sensors is presented. A thermoprocessable carbon black-loaded, electronically conducting, polylactide polymer composite was used to prepare substrate electrodes of user’s defined shape/arrangement applying a 3D pen in a hot melt process. Covering of the carbon black-loaded polylactide 3D-drawn substrate electrode with a PVC-based ion-selective membrane cocktail results in spontaneous formation of a zip-lock structure with a large contact area. Thus, obtained ion-selective electrodes offer sensors of excellent performance, including potential stability expressed by SD of the mean value of potential recorded equal to ±1.0 mV (n = 6) within one day and ±1.5 mV (n = 6) between five days. The approach offers also high device-to-device potential reproducibility: SD of mean value of E0 equal to ±1.5 mV (n = 5).

Continuous Manufacturing of Graphene-Contact Ion-Selective Electrodes Using Roll-to-Roll Processes: The Case for Nitrate Sensors

Soil contains various species of nitrogen, which is crucial for plant growth. Nitrate ion (NO3 -) is essential for promoting high crop yields and is widely used in fertilizers, however groundwater can be polluted by the overuse of nitrate. “Smart agriculture” can be supported by monitoring NO3 - in ground-soil using a distributed network of disposable potentiometric sensors. We have found the performance of such sensors to be enhanced by adding graphene nanoplatelets (GrNPs) as a conductive yet hydrophobic solid contact between the electrode and ion-selective membrane. Exfoliated GrNPs can be stably dispersed in ethyl acetate by liquid-assisted ball-milling, then deposited using methods compatible with the scalable roll-to-roll (R2R) production of ion-selective electrodes (ISEs). Ultra thin layers of GrNPs were formed by spray-coating onto a moving web of screen-printed Ag electrodes on polyethylene terephthalate (PET), followed by in-line deposition of a NO3 - selective membrane and silicone sealant then oven drying. Multiple electrodes from each production run were conditioned in aqueous KNO3 solutions and potentiometric characterizations of sensitivity, selectivity and stability were completed using an 80-channel analyzer. The GrNP layer serves as a hydrophobic transducer of ion adsorption and provides a high capacitance for stable potentiometric signals while also protecting SC-ISEs from damage caused by water permeation. We find that R2R processes can successfully produce graphene-contact NO3 - ISEs for agricultural applications, with extended operational lifetimes and high levels of quality control.

A Sensitive Potentiometric Sensor for Isothermal Amplification-Coupled Detection of Nucleic Acids.

A disposable potentiometric sensor was newly developed for the amplification-coupled detection of nucleic acids. The hydrogen-ion is generally released during isothermal amplification of nucleic acids. The surface potential on the oxide-functionalized electrode of the extended gate was directly measured using full electrical circuits with the commercial metal-oxide semiconductor field-effect transistors (MOSFETs) and ring oscillator components, which resulted in cost-effective, portable and scalable real-time nucleic acid analysis. The current-starved ring oscillator changes surface potential to its frequency depending on the square of the variation in pH with a high signal-to-noise ratio during isothermal amplification. The device achieves a conversion rate of 20.5 kHz/mV and a detection resolution of 200 µV for the surface potential. It is demonstrated that the sensor successfully monitors in real-time isothermal amplification of the extracted nucleic acids from Salmonella pathogenic bacteria. The in situ variations in the frequency of the pH-sensitive sensor were compared with the results of both a conventional optical device and pH-meter during isothermal amplification.

Disposable potentiometric citrate sensor based on polypyrrole‐doped films for indirect determination of sildenafil in pharmaceuticals formulations

ABSTRACTA new sensitive and selective disposable potentiometric sensor based on polypyrrole (PPy) films for determination of sildenafil citrate (SC) was proposed. The pyrrole polymerization was performed in presence of citrate ions under galvanostatic conditions which resulted in a membrane of PPy doped with citrate anion at graphite pencil electrode surface. Experimental conditions (e.g., pH and conditioning time) and instrumental parameters (e.g., current density and electrical charge) were evaluated in order to reach the best potentiometric response for the proposed sensor. Under optimized conditions, the device presented a linear dynamic range (LDR) for citrate ions concentrations varying from 0.034 to 1.7 mmol L−1 with a Nernstian slope of 57.2 mV dec−1 and a limit of detection (LOD) of 30 µmol L−1. The developed potentiometric sensor was applied for sildenafil citrate (SC) determination (pharmaceutical formulations) and results compared with an official spectrophotometric method indicating a good agreement for a confidence level of 95%. Effect of concomitants species on the potentiometric response of the proposed device and morphologic characterization using microscopy of atomic force (AFM) were realized. The surface roughness of PPy films (synthesized in citrate solution and chloride) showed poorly affected by changing the doping anion, probably because the polypyrrole nodules grow three‐dimensionally simultaneously. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016, 133, 43762.

Filmes de polipirrol aplicados no desenvolvimento de eletrodos descartáveis seletivos a íons fluoreto

O presente manuscrito descreve o desenvolvimento de um sensor descartável sensível e seletivo baseado em filmes de polipirrol dopados (PPy) para determinação íons fluoreto. Os íons fluoretos foram incorporados na matriz PPy durante a polimerização eletroquímica realizada em condições galvanostáticas em um eletrodo compósito etileno vinil acetato e negro de fumo. Parâmetros experimentais envolvidos na preparação de película PPy tais como densidade de corrente elétrica, carga elétrica, o pH e a concentração de eletrólito foram otimizados de forma a maximizar a resposta potenciométrica. A resposta do sensor para íons de flúor foi linear no intervalo de concentração de 1,00 × 10- 5 a 1,08 × 10- 2 mol L- 1, com uma inclinação de ~ 40 mV / pF e foi estável suficiente para várias determinações. O método foi aplicado com sucesso na determinação de íons fluoreto em amostras comerciais farmacêuticas. Os resultados demonstraram que o sensor proposto pode ser utilizado como uma alternativa interessante aos métodos analíticos tradicionais para determinação de íons fluoreto.

Performance of a portable biosensor for the analysis of ethion residues

Sensitive disposable potentiometric sensors for determination of the organophosphorus pesticide (OPs), ethion and its degradation residues have been constructed. The fabricated screen printed sensors are based on multi-walled carbon nanotube-polyvinyl chloride (MWNT-PVC) composite incorporated with α-cyclodextrin (α-CD) ionophore for butyrylcholine (BuCh) determination. Butyrylcholinesterase (BuChE) activity was measured through monitoring the BuCh hydrolysis using the fabricated sensors. The electrode potential changes linearly with BuChE concentration over the range from 0.04 to 0.4 U in phosphate buffer solution. This approach can also be used to analyze ethion and its degradation products in the concentration range from 0 to 330 ng mL(-1) by measuring the relative inhibition percentage of BuChE. From different ethion degradation products, inhibition by dioxon and monooxon were more potent than the parent pesticide. The proposed method was applied for determination of ethion in different samples with good accuracy and precision. The relative simple fabrication protocol of biosensor, high sensitivity and stability represents a promising approach for determination of environmental pollutants in field conditions.

Simple and disposable potentiometric sensors based on graphene or multi-walled carbon nanotubes – carbon–plastic potentiometric sensors

A simple procedure leading to disposable potentiometric sensors using as a supporting electrode - electrical lead and transducer - a layer of carbon nanostructured material, either graphene or multi-walled nanotubes, is proposed, and the effect of the material used on the properties of the sensor is discussed. The obtained layers were partially covered with a conventional poly(vinyl chloride) (PVC) based ion-selective membrane to result in simple, planar, and disposable potentiometric sensors. The analytical performance of the thus obtained electrodes was compared with that of classical macroscopic all-solid-state ion-selective electrodes (e.g. employing poly(octylthiophene) as a solid contact and a similar ion-selective membrane). It was superior (taking into account detection limits or selectivity towards Na(+) ions) compared to that of other disposable sensors proposed recently. The observed excellent analytical performance was attributed to the applied method of preparation of carbon nanostructured materials, which does not require addition of a surfactant to obtain a stable suspension (ink) used to prepare the electrical lead and the transducer of the sensor. Although the proposed sensors are predominantly intended for disposable use, pronounced stability of potential readings was obtained in within-day experiments. Moreover, due to their high conductivity carbon-plastic electrodes can be also applied in polarized potentiometric measurements.

Paper-Based Ion-Selective Potentiometric Sensors

A new approach to develop ultra low-cost, robust, rugged, and disposable potentiometric sensors is presented. A suspension of carbon nanotubes in a water-surfactant mixture (carbon nanotubes ink) is applied on conventional filter papers to turn them into conductive papers, which are then used as a substrate to build ion-selective electrodes. The electrodes are made by drop casting a membrane on a small circular area of the conductive paper. In this way, the carbon nanotubes act as both electric conductors and ion-to-electron transducers of the potentiometric signal. Electrodes for sensing K(+), NH(4)(+), and pH were built and tested using this approach, and the results were compared with classical solid-state ion selective electrodes using carbon nanotubes as transducers and glassy carbon as a substrate. In all cases, the analytical performance (sensitivity, linear ranges, limits of detection, selectivity, etc.) of these disposable paper electrodes was similar to that obtained for the more conventional type of ion-selective-electrodes. This opens new avenues for very low-cost platforms for generation of chemical information.

Disposable potentiometric sensors for monitoring cholinesterase activity

A highly sensitive disposable screen-printed butyrylcholine (BuCh) potentiometric sensor, based on heptakis (2,3,6-tri-o-methyl)-β-cyclodextrin (β-CD) as ionophore, was developed for butyrylcholinesterase (BuChE) activity monitoring. The proposed sensors have been characterized and optimized according to the constituents of homemade printing carbon ink including β-CD, anionic sites, and plasticizer. The fabricated sensor showed Nernstian responses from 10 −6 to 10 −2 mol L −1 with detection limit of 8 × 10 −7 mol L −1, fast response time (1.6 s) and adequate shelf-life (6 months). Improved selectivity towards BuCh with minimal interference from choline (Ch) was achieved and the sensor was used for determination of 0.06–1.25 U mL −1 BuChE. The developed disposable sensors have been successfully applied for real-time intoxication monitoring through assaying cholinesterases (ChEs) activity in human serum. Determination of organophosphate pesticide was conducted by measuring their inhibition of BuChE with successful assaying of malathion in insecticide samples with high accuracy and precision.

Screen-printed sensor for batch and flow injection potentiometric chromium(VI) monitoring

A disposable screen-printed electrode was designed and evaluated for direct detection of chromium(VI) in batch and flow analysis. The carbon screen-printed electrode was modified with a graphite-epoxy composite. The optimal graphite-epoxy matrix contains 37.5% graphite powder, 12.5% diphenylcarbohydrazide, a selective compound for chromium(VI), and 50% epoxy resin. The principal analytical parameters of the potentiometric response in batch and flow analysis were optimized and calculated. The screen-printed sensor exhibits a response time of 20 +/- 1 s. In flow analysis, the analytical frequency of sampling is 70 injections per hour using 0.1 M NaNO(3) solution at pH 3 as the carrier, a flow rate of 2.5 mL.min(-1), and an injection sample volume of 0.50 mL. The sensor shows potentiometric responses that are very selective for chromium(VI) ions and optimal detection limits in both static mode (2.1 x 10(-7) M) and online analysis (9.4 x 10(-7) M). The disposable potentiometric sensor was employed to determine toxicity levels of chromium(VI) in mineral, tap, and river waters by flow-injection potentiometry and batch potentiometry. Chromium(VI) determination was also carried out with successful results in leachates from municipal solid waste landfills.

POTENTIOMETRIC THICK-FILM GRAPHITE ELECTRODES WITH IMPROVED RESPONSE TO COPPER IONS

Thick-film graphite electrodes produced by screen-printing have been investigated as inexpensive disposable potentiometric sensors for determination of heavy metal ions. The modification of graphite paste with copper sulfides caused an improvement of the analytical characteristics of the sensors. The electrodes based on Cu2S-doped graphite film are useful for reproducible, fast, and selective determination of copper ions with Nernstian sensitivity in a wide range of concentration.