This work describes fully integrated multifolding electrochemical paper-based devices (ePADs) for enhanced multiplexed voltammetric determination of heavy metals (Zn(II), Cd(II), and Pb(II)) using tunable passive preconcentration. The paper devices integrate five circular sample preconcentration layers and a 3-electrode electrochemical cell. The hydrophobic barriers of the devices are drawn by pen-plotting with hydrophobic ink, while the electrodes are deposited by screen-printing. The devices exploit the wicking ability of cellulose paper to perform passive preconcentration of the target analytes, resulting in a ∼6-fold signal enhancement. For this purpose, drops of the sample are placed at the five sample pads of the preconcentration layers, the device is folded, and the target metals are eluted in a vertical-flow mode to the electrochemical cell, where they are measured directly by anodic stripping voltammetry (ASV). The working electrode of the ePADs is bulk-modified with bismuth citrate; during the ASV measurements, the bismuth precursor is converted to nanodomains of metallic bismuth at the surface of the working electrode. By combining the triplex signal amplification through passive preconcentration, electrochemical preconcentration, and judicious working electrode modification with generated bismuth nanoparticles, ultrasensitive and multiplexed heavy metal assays can be achieved. Due to their high degree of integration, low cost, easy and fast fabrication, and sensitivity, the multifolding ePADs are particularly suitable for on-site heavy metals' monitoring applications.
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http://dx.doi.org/10.1021/acs.analchem.4c06982 | DOI Listing |
Anal Chem
January 2025
Laboratory of Analytical Chemistry, Department of Chemistry, University of Athens, Athens 157 71, Greece.
This work describes fully integrated multifolding electrochemical paper-based devices (ePADs) for enhanced multiplexed voltammetric determination of heavy metals (Zn(II), Cd(II), and Pb(II)) using tunable passive preconcentration. The paper devices integrate five circular sample preconcentration layers and a 3-electrode electrochemical cell. The hydrophobic barriers of the devices are drawn by pen-plotting with hydrophobic ink, while the electrodes are deposited by screen-printing.
View Article and Find Full Text PDFAnal Methods
July 2024
National Institute for Research and Development of Optoelectronics INOE 2000, Research Institute for Analytical Instrumentation, Donath 67, 400293, Cluj-Napoca, Romania.
The determination of rare earth element (REE) content in different natural minerals is of high interest due to their extensive use in modern and sustainable technologies. The REEs occurring in natural zeolites are specific to each deposit. This study presents the validation and evaluation of the measurement uncertainty for the determination of REEs (Ce, Dy, Er, Eu, Gd, La, Lu, Nd, Pr, Sm, Y, and Yb) in natural zeolites using microwave-assisted acid digestion and inductively coupled plasma optical emission spectrometry (ICP-OES) after diffusive gradients in thin-film preconcentration.
View Article and Find Full Text PDFBiosensors (Basel)
June 2024
Columbia Environmental Research Center, U.S. Geological Survey, 4200 New Haven Road, Columbia, MO 65201, USA.
The scope of this study was to apply advances in materials science, specifically the use of organosilicate nanoparticles as a high surface area platform for passive sampling of chemicals or pre-concentration for active sensing in multiple-phase complex environmental media. We have developed a novel nanoporous organosilicate (NPO) film as an extraction phase and proof of concept for application in adsorbing hydrophobic compounds in water and sediment. We characterized the NPO film properties and provided optimization for synthesis and coatings in order to apply the technology in environmental media.
View Article and Find Full Text PDFDiagnostics (Basel)
April 2024
Department of Cell and Chemical Biology, Leiden University Medical Center, 2300 RC Leiden, The Netherlands.
A laboratory-based lateral flow (LF) test that utilizes up-converting reporter particles (UCP) for ultrasensitive quantification of circulating anodic antigen (CAA) in urine is a well-accepted test to identify active infection. However, this UCP-LF CAA test requires sample pre-treatment steps not compatible with field applications. Flow, a new low-cost disposable, allows integration of large-volume pre-concentration of urine analytes and LF detection into a single field-deployable device.
View Article and Find Full Text PDFJ Hazard Mater
May 2024
Lancaster Environment Centre, Lancaster University, Lancaster LA1 4YQ, United Kingdom. Electronic address:
Polycyclic aromatic hydrocarbons (PAHs) are priority pollutants and need to be measured reliably in waters and other media, to understand their sources, fate, behaviour and to meet regulatory monitoring requirements. Conventional water sampling requires large water volumes, time-consuming pre-concentration and clean-up and is prone to analyte loss or contamination. Here, for the first time, we developed and validated a novel diffusive gradients in thin-films (DGT) passive sampler for PAHs.
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