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Optofluidic Flow Cytometer with In-Plane Spherical Mirror for Signal Enhancement

Statistical analysis of the properties of single microparticles, such as cells, bacteria or plastic slivers, has attracted increasing interest in recent years. In this regard, field flow cytometry is considered the gold standard technique, but commercially available instruments are bulky, expensive,...

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Autores principales: Zorzi, Filippo, Bonfadini, Silvio, Aloisio, Ludovico, Moschetta, Matteo, Storti, Filippo, Simoni, Francesco, Lanzani, Guglielmo, Criante, Luigino
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10675696/
https://www.ncbi.nlm.nih.gov/pubmed/38005576
http://dx.doi.org/10.3390/s23229191
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author Zorzi, Filippo
Bonfadini, Silvio
Aloisio, Ludovico
Moschetta, Matteo
Storti, Filippo
Simoni, Francesco
Lanzani, Guglielmo
Criante, Luigino
author_facet Zorzi, Filippo
Bonfadini, Silvio
Aloisio, Ludovico
Moschetta, Matteo
Storti, Filippo
Simoni, Francesco
Lanzani, Guglielmo
Criante, Luigino
author_sort Zorzi, Filippo
collection PubMed
description Statistical analysis of the properties of single microparticles, such as cells, bacteria or plastic slivers, has attracted increasing interest in recent years. In this regard, field flow cytometry is considered the gold standard technique, but commercially available instruments are bulky, expensive, and not suitable for use in point-of-care (PoC) testing. Microfluidic flow cytometers, on the other hand, are small, cheap and can be used for on-site analyses. However, in order to detect small particles, they require complex geometries and the aid of external optical components. To overcome these limitations, here, we present an opto-fluidic flow cytometer with an integrated 3D in-plane spherical mirror for enhanced optical signal collection. As a result, the signal-to-noise ratio is increased by a factor of six, enabling the detection of particle sizes down to 1.5 µm. The proposed optofluidic detection scheme enables the simultaneous collection of particle fluorescence and scattering using a single optical fiber, which is crucial to easily distinguishing particle populations with different optical properties. The devices have been fully characterized using fluorescent polystyrene beads of different sizes. As a proof of concept for potential real-world applications, signals from fluorescent HEK cells and Escherichia coli bacteria were analyzed.
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spelling pubmed-106756962023-11-15 Optofluidic Flow Cytometer with In-Plane Spherical Mirror for Signal Enhancement Zorzi, Filippo Bonfadini, Silvio Aloisio, Ludovico Moschetta, Matteo Storti, Filippo Simoni, Francesco Lanzani, Guglielmo Criante, Luigino Sensors (Basel) Article Statistical analysis of the properties of single microparticles, such as cells, bacteria or plastic slivers, has attracted increasing interest in recent years. In this regard, field flow cytometry is considered the gold standard technique, but commercially available instruments are bulky, expensive, and not suitable for use in point-of-care (PoC) testing. Microfluidic flow cytometers, on the other hand, are small, cheap and can be used for on-site analyses. However, in order to detect small particles, they require complex geometries and the aid of external optical components. To overcome these limitations, here, we present an opto-fluidic flow cytometer with an integrated 3D in-plane spherical mirror for enhanced optical signal collection. As a result, the signal-to-noise ratio is increased by a factor of six, enabling the detection of particle sizes down to 1.5 µm. The proposed optofluidic detection scheme enables the simultaneous collection of particle fluorescence and scattering using a single optical fiber, which is crucial to easily distinguishing particle populations with different optical properties. The devices have been fully characterized using fluorescent polystyrene beads of different sizes. As a proof of concept for potential real-world applications, signals from fluorescent HEK cells and Escherichia coli bacteria were analyzed. MDPI 2023-11-15 /pmc/articles/PMC10675696/ /pubmed/38005576 http://dx.doi.org/10.3390/s23229191 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
Zorzi, Filippo
Bonfadini, Silvio
Aloisio, Ludovico
Moschetta, Matteo
Storti, Filippo
Simoni, Francesco
Lanzani, Guglielmo
Criante, Luigino
Optofluidic Flow Cytometer with In-Plane Spherical Mirror for Signal Enhancement
title Optofluidic Flow Cytometer with In-Plane Spherical Mirror for Signal Enhancement
title_full Optofluidic Flow Cytometer with In-Plane Spherical Mirror for Signal Enhancement
title_fullStr Optofluidic Flow Cytometer with In-Plane Spherical Mirror for Signal Enhancement
title_full_unstemmed Optofluidic Flow Cytometer with In-Plane Spherical Mirror for Signal Enhancement
title_short Optofluidic Flow Cytometer with In-Plane Spherical Mirror for Signal Enhancement
title_sort optofluidic flow cytometer with in-plane spherical mirror for signal enhancement
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10675696/
https://www.ncbi.nlm.nih.gov/pubmed/38005576
http://dx.doi.org/10.3390/s23229191
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