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Coupling Capillary-Driven Microfluidics with Lateral Flow Immunoassay for Signal Enhancement

Microfluidics has emerged as a versatile technology that is applied to enhance the performance of analytical techniques, among others. Pursuing this, we present a capillary-driven microfluidic device that improves the sensitivity of lateral flow immunoassay rapid tests thanks to offering an automate...

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Autores principales: Azizian, Pooya, Casals-Terré, Jasmina, Guerrero-SanVicente, Elena, Grinyte, Ruta, Ricart, Jordi, Cabot, Joan M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10452194/
https://www.ncbi.nlm.nih.gov/pubmed/37622918
http://dx.doi.org/10.3390/bios13080832
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author Azizian, Pooya
Casals-Terré, Jasmina
Guerrero-SanVicente, Elena
Grinyte, Ruta
Ricart, Jordi
Cabot, Joan M.
author_facet Azizian, Pooya
Casals-Terré, Jasmina
Guerrero-SanVicente, Elena
Grinyte, Ruta
Ricart, Jordi
Cabot, Joan M.
author_sort Azizian, Pooya
collection PubMed
description Microfluidics has emerged as a versatile technology that is applied to enhance the performance of analytical techniques, among others. Pursuing this, we present a capillary-driven microfluidic device that improves the sensitivity of lateral flow immunoassay rapid tests thanks to offering an automated washing step. A novel multilevel microfluidic chip was 3D-printed with a photocurable black resin, sealed by an optically clear pressure-sensitive adhesive, and linked to the lateral flow strip. To depict the efficacy of microfluidics and the washing step, cortisol was measured quantitatively within the proposed device. Measuring cortisol levels is a way to capture physiological stress responses. Among biofluids, saliva is less infectious and easier to sample than others. However, higher sensitivity is demanded because the salivary cortisol concentrations are much lower than in blood. We carried out a competitive lateral flow immunoassay protocol with the difference that the microfluidic device applies an automated washing step after the sample is drained downstream. It washes the trapped quantum-dot-labeled antibodies out from nitrocellulose, diminishing background noise as these are bonded to cortisols and not to the immobilized receptors. Fluorescence spectroscopy, as a high-precision analysis, was successfully applied to determine clinically relevant salivary cortisol concentrations within a buffer quantitatively. The microfluidic design relied on a 3D valve that avoids reagent cross-contamination. This cross-contamination could make the washing buffer impure and undesirably dilute the sample. The proposed device is cost-effective, self-powered, robust, and ideal for non-expert users.
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spelling pubmed-104521942023-08-26 Coupling Capillary-Driven Microfluidics with Lateral Flow Immunoassay for Signal Enhancement Azizian, Pooya Casals-Terré, Jasmina Guerrero-SanVicente, Elena Grinyte, Ruta Ricart, Jordi Cabot, Joan M. Biosensors (Basel) Article Microfluidics has emerged as a versatile technology that is applied to enhance the performance of analytical techniques, among others. Pursuing this, we present a capillary-driven microfluidic device that improves the sensitivity of lateral flow immunoassay rapid tests thanks to offering an automated washing step. A novel multilevel microfluidic chip was 3D-printed with a photocurable black resin, sealed by an optically clear pressure-sensitive adhesive, and linked to the lateral flow strip. To depict the efficacy of microfluidics and the washing step, cortisol was measured quantitatively within the proposed device. Measuring cortisol levels is a way to capture physiological stress responses. Among biofluids, saliva is less infectious and easier to sample than others. However, higher sensitivity is demanded because the salivary cortisol concentrations are much lower than in blood. We carried out a competitive lateral flow immunoassay protocol with the difference that the microfluidic device applies an automated washing step after the sample is drained downstream. It washes the trapped quantum-dot-labeled antibodies out from nitrocellulose, diminishing background noise as these are bonded to cortisols and not to the immobilized receptors. Fluorescence spectroscopy, as a high-precision analysis, was successfully applied to determine clinically relevant salivary cortisol concentrations within a buffer quantitatively. The microfluidic design relied on a 3D valve that avoids reagent cross-contamination. This cross-contamination could make the washing buffer impure and undesirably dilute the sample. The proposed device is cost-effective, self-powered, robust, and ideal for non-expert users. MDPI 2023-08-21 /pmc/articles/PMC10452194/ /pubmed/37622918 http://dx.doi.org/10.3390/bios13080832 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Azizian, Pooya
Casals-Terré, Jasmina
Guerrero-SanVicente, Elena
Grinyte, Ruta
Ricart, Jordi
Cabot, Joan M.
Coupling Capillary-Driven Microfluidics with Lateral Flow Immunoassay for Signal Enhancement
title Coupling Capillary-Driven Microfluidics with Lateral Flow Immunoassay for Signal Enhancement
title_full Coupling Capillary-Driven Microfluidics with Lateral Flow Immunoassay for Signal Enhancement
title_fullStr Coupling Capillary-Driven Microfluidics with Lateral Flow Immunoassay for Signal Enhancement
title_full_unstemmed Coupling Capillary-Driven Microfluidics with Lateral Flow Immunoassay for Signal Enhancement
title_short Coupling Capillary-Driven Microfluidics with Lateral Flow Immunoassay for Signal Enhancement
title_sort coupling capillary-driven microfluidics with lateral flow immunoassay for signal enhancement
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10452194/
https://www.ncbi.nlm.nih.gov/pubmed/37622918
http://dx.doi.org/10.3390/bios13080832
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