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1.
Analyst ; 148(13): 3087-3096, 2023 Jun 26.
Artículo en Inglés | MEDLINE | ID: mdl-37310360

RESUMEN

This paper presents a novel approach for the fabrication of low cost Electrochemical-Surface Enhanced Raman Scattering (EC-SERS) sensing platforms. Laser Induced Graphene (LIG) electrodes were readily fabricated by direct laser writing of polyimide tapes and functionalized with silver nanoparticles (Ag NPs) to obtain hybrid Ag NPs - LIG electrodes suitable for EC-SERS analysis. Detection was achieved by coupling a handheld potentiostat with a Raman spectrograph, enabling measurement of SERS spectra of target analytes generated during voltage sweeps in the 0.0 to -1.0 V interval range. The sensing capabilities of the fabricated system were first tested with model molecule 4-aminobenzenethiol (4-ABT). Following sensitive detection of 4-ABT, EC-SERS analysis of food contaminant melamine in milk and antibiotic difloxacin hydrochloride (DIF) in river water was demonstrated, achieving sensitive detection of both analytes without pre-treatment steps. The easiness of fabrication, versatility of design, rapid analysis time and potential miniaturization of the system make Ag NPs - LIG electrodes suitable for a large range of in situ applications in the field of food monitoring and for environmental analysis.

2.
Anal Bioanal Chem ; 411(9): 1905-1913, 2019 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-30397760

RESUMEN

In this study, we report the simultaneous use of gold and silver nanoparticles to set a multicolor multiplex lateral flow immunoassay (xLFIA). Silver nanoparticles (AgNPs), spherical in shape and characterized by a brilliant yellow color, were obtained by a new viable one-step synthetic protocol. AgNPs were stable over time and acceptably robust to conditions used for fabricating LFIA devices. These AgNPs were employed as a colorimetric probe in combination with two different kinds of gold nanoparticles (AuNPs) to set a visual xLFIA for detecting allergens. Surface plasmon resonance peaks of probes (AgNPs, spherical and desert rose-like AuNPs) were centered at 420, 525, and 620 nm, respectively. Therefore, the xLFIA output was easily interpreted through a "yellow magenta cyan (YMC)" color code. The prospect of the YMC xLFIA was demonstrated by simultaneously detecting three major allergens in bakery products. Antibodies directed towards casein, ovalbumin, and hazelnut allergenic proteins were individually adsorbed onto metal nanoparticles to produce three differently colored specific probes. These were inserted in a LFIA comprising three lines, each responsive for one allergen. The trichromatic xLFIA was able to detect allergenic proteins at levels as low as 0.1 mg/l and enabled the easy identification of the allergens in commercial biscuits based on the color of the probes. Graphical Abstract.


Asunto(s)
Alérgenos/análisis , Colorimetría/métodos , Hipersensibilidad a los Alimentos/diagnóstico , Oro/química , Nanopartículas del Metal/química , Sondas Moleculares/química , Plata/química
3.
Nanoscale Adv ; 6(5): 1524-1534, 2024 Feb 27.
Artículo en Inglés | MEDLINE | ID: mdl-38419877

RESUMEN

Direct pen writing offers versatile opportunities for development of low-cost tests for point-of-care applications. In this work a lateral flow immunoassay (LFIA) test was fabricated by hand "writing" immunoprobes onto hand-cut nitrocellulose strips with a commercial fountain pen. The qualitative capabilities of the test were extended by addition of a Raman reporter and consequent design and fabrication of a Surface Enhanced Resonant Raman Scattering (SERRS)-LFIA test. As proof-of-concept, dual detection of penicillin G was achieved in milk with a visual LOD of 20 ppm and a dynamic range of 0.03-97.5 ppm. Evaluation against equivalent tests performed with conventionally prepared LFIA strips showed comparable results, thus demonstrating the validity of the test. These results demonstrate the potential for further decrease in cost and consequent broader use of LFIA tests in remote regions and resource-limited environments.

4.
ACS Sustain Chem Eng ; 12(41): 15063-15076, 2024 Oct 14.
Artículo en Inglés | MEDLINE | ID: mdl-39421636

RESUMEN

In this work, we demonstrate chemiresistive volatile organic compound (VOC) sensors prepared by drop-cast assembly of layered tin monoxide mesoflowers (SnO-MFs) on additively produced laser-induced graphene-like carbon (LIG). The SnO-MFs were synthesized below 100 °C at ambient pressure and offer a low fabrication energy alternative route to typical furnace-prepared metal-oxide materials. The additive dropcast assembly of room-temperature operating metal oxide active material allows the substitution of LIG for metal current collectors and glass for alumina, reducing the environmental footprint of the sensor. The sensors can detect methanol (150-4000 ppm) at room temperature and humidity (∼18 °C, ∼55% RH), with response and recovery times (150 ppm methanol) of t 90,resp ≈ 50 ± 10 s and t 90,rec ≈ 5 ± 0.5 s, respectively. The sensors demonstrated a limit of detection (170 ± 40 ppm) below 8 h worker safety exposure levels (200 ppm) and stable DC resistance responses ΔR/R = 9 ± 2% to 710 ppm of methanol for over 21 days in ambient laboratory conditions, n = 4. First-principles density functional theory simulations were used to elucidate the interactions of VOC species on the SnO surfaces. LIG-SnO hybrid sensors thus present a resource-efficient route to develop chemiresistive sensors for low-power applications, although with cross-selectivity to other alcohol species.

5.
Talanta ; 240: 123155, 2022 Apr 01.
Artículo en Inglés | MEDLINE | ID: mdl-34942474

RESUMEN

The foot-and-mouth disease (FMD) is the most important transboundary viral disease of livestock in the international context, because of its extreme contagiousness, widespread diffusion, and severe impact on animal trade and animal productions. The rapid and on-field detection of the virus responsible for the FMD represents an urgent demand to efficiently control the diffusion of the infection, especially in low resource setting where the FMD is endemic. Colorimetric lateral flow immunoassay (LFIA) is largely used for the development of rapid tests, due to the extreme simplicity, cost-effectiveness, and on-field operation. In this work, two multiplex LFIA devices were designed for the diagnosis of FMD and the simultaneous identification of major circulating serotypes of the FMD virus. The LFIAs relied on the sandwich-type immunoassay and combined a set of well-characterised monoclonal antibodies (mAb) pairs. One LFIA aimed at detecting and identifying O, A and Asia-1 serotypes, the second device enabled the detection and differentiation of the SAT 1 and SAT 2 serotypes. Both devices also incorporated a broad-specific test line reporting on infection from FMDV, regardless the strain and the serotype involved. Accordingly, five and four reactive zones were arranged in the two devices to achieve a total of six simultaneous analyses. The development of the two multiplex systems highlighted for the first time the relevance of the mAb positioning along the LFIA strip in connection with the use of the same or different mAb as capture and detector ligands. In fact, the excess of detector mAb typically employed for increasing the sensitivity of sandwich immunoassay induced a new type of hook effect when combined with the same ligand used as the capture. This effect strongly impacted assay sensitivity, which could be improved by an intelligent alignment of the mAb pairs along the LFIA strip. The analytical and diagnostic performances of the two LFIAs were studied by testing reference FMDV strains grown in cell cultures and some representative field samples (epithelium homogenates). Almost equivalent sensitivity and specificity to those of a reference Ag-ELISA kit were shown, except for the serotype SAT 2. These simple devices are suitable in endemic regions for in-field diagnosis of FMD accompanied by virus serotyping and, moreover, could be deployed and used for rapid confirmation of secondary outbreaks after FMD incursions in free-areas, thus contributing to promptly implement control measures.


Asunto(s)
Virus de la Fiebre Aftosa , Fiebre Aftosa , Animales , Anticuerpos Monoclonales , Anticuerpos Antivirales , Fiebre Aftosa/diagnóstico , Inmunoensayo , Serogrupo
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