Cargando…
Nanofluidic-Based Accumulation of Antigens for Miniaturized Immunoassay
The continuous advances of Nanofluidics have been stimulating the development of novel nanostructures and strategies to accumulate very diluted analytes, for implementing a new class of high sensitivity miniaturized polymeric sensors. We take advantage of the electrokinetic properties of these struc...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7146560/ https://www.ncbi.nlm.nih.gov/pubmed/32183234 http://dx.doi.org/10.3390/s20061615 |
_version_ | 1783520229367742464 |
---|---|
author | Pezzuoli, Denise Angeli, Elena Repetto, Diego Ferrera, Francesca Guida, Patrizia Firpo, Giuseppe Repetto, Luca |
author_facet | Pezzuoli, Denise Angeli, Elena Repetto, Diego Ferrera, Francesca Guida, Patrizia Firpo, Giuseppe Repetto, Luca |
author_sort | Pezzuoli, Denise |
collection | PubMed |
description | The continuous advances of Nanofluidics have been stimulating the development of novel nanostructures and strategies to accumulate very diluted analytes, for implementing a new class of high sensitivity miniaturized polymeric sensors. We take advantage of the electrokinetic properties of these structures, which allow accumulating analytes inside asymmetric microfluidic structures to implement miniaturized sensors able to detect diluted solutions down to nearly 1.2 pg/mL. In particular, exploiting polydimethylsiloxane devices, fabricated by using the junction gap breakdown technique, we concentrate antigens inside a thin microfunnel functionalized with specific antibodies to favor the interaction and, if it is the case, the recognition between antigens in solution and antibodies anchored to the surface. The transduction mechanism consists in detecting the fluorescence signal of labeled avidin when it binds to biotinylated antigens. Here, we demonstrate that exploiting these electrokinetic phenomena, typical of nanofluidic structures, we succeeded in concentrating biomolecules in correspondence of a 1 pL sensing region, a strategy that grants to the device performance comparable to standard immunoassays. |
format | Online Article Text |
id | pubmed-7146560 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-71465602020-04-20 Nanofluidic-Based Accumulation of Antigens for Miniaturized Immunoassay Pezzuoli, Denise Angeli, Elena Repetto, Diego Ferrera, Francesca Guida, Patrizia Firpo, Giuseppe Repetto, Luca Sensors (Basel) Article The continuous advances of Nanofluidics have been stimulating the development of novel nanostructures and strategies to accumulate very diluted analytes, for implementing a new class of high sensitivity miniaturized polymeric sensors. We take advantage of the electrokinetic properties of these structures, which allow accumulating analytes inside asymmetric microfluidic structures to implement miniaturized sensors able to detect diluted solutions down to nearly 1.2 pg/mL. In particular, exploiting polydimethylsiloxane devices, fabricated by using the junction gap breakdown technique, we concentrate antigens inside a thin microfunnel functionalized with specific antibodies to favor the interaction and, if it is the case, the recognition between antigens in solution and antibodies anchored to the surface. The transduction mechanism consists in detecting the fluorescence signal of labeled avidin when it binds to biotinylated antigens. Here, we demonstrate that exploiting these electrokinetic phenomena, typical of nanofluidic structures, we succeeded in concentrating biomolecules in correspondence of a 1 pL sensing region, a strategy that grants to the device performance comparable to standard immunoassays. MDPI 2020-03-13 /pmc/articles/PMC7146560/ /pubmed/32183234 http://dx.doi.org/10.3390/s20061615 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Pezzuoli, Denise Angeli, Elena Repetto, Diego Ferrera, Francesca Guida, Patrizia Firpo, Giuseppe Repetto, Luca Nanofluidic-Based Accumulation of Antigens for Miniaturized Immunoassay |
title | Nanofluidic-Based Accumulation of Antigens for Miniaturized Immunoassay |
title_full | Nanofluidic-Based Accumulation of Antigens for Miniaturized Immunoassay |
title_fullStr | Nanofluidic-Based Accumulation of Antigens for Miniaturized Immunoassay |
title_full_unstemmed | Nanofluidic-Based Accumulation of Antigens for Miniaturized Immunoassay |
title_short | Nanofluidic-Based Accumulation of Antigens for Miniaturized Immunoassay |
title_sort | nanofluidic-based accumulation of antigens for miniaturized immunoassay |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7146560/ https://www.ncbi.nlm.nih.gov/pubmed/32183234 http://dx.doi.org/10.3390/s20061615 |
work_keys_str_mv | AT pezzuolidenise nanofluidicbasedaccumulationofantigensforminiaturizedimmunoassay AT angelielena nanofluidicbasedaccumulationofantigensforminiaturizedimmunoassay AT repettodiego nanofluidicbasedaccumulationofantigensforminiaturizedimmunoassay AT ferrerafrancesca nanofluidicbasedaccumulationofantigensforminiaturizedimmunoassay AT guidapatrizia nanofluidicbasedaccumulationofantigensforminiaturizedimmunoassay AT firpogiuseppe nanofluidicbasedaccumulationofantigensforminiaturizedimmunoassay AT repettoluca nanofluidicbasedaccumulationofantigensforminiaturizedimmunoassay |