Toward the Development of an On-Chip Acoustic Focusing Fluorescence Lifetime Flow Cytometer

Conventional flow cytometry is a valuable quantitative tool. Flow cytometers reveal physical and biochemical information from cells at a high throughput, which is quite valuable for many biomedical, biological, and diagnostic research fields. Flow cytometers range in complexity and typically provide...

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Main Authors: Jesus Sambrano, Felicia Rodriguez, John Martin, Jessica P. Houston
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-05-01
Series:Frontiers in Physics
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fphy.2021.647985/full
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spelling doaj-0c71948c3f79482d8b6c064613b80dd62021-05-14T07:27:57ZengFrontiers Media S.A.Frontiers in Physics2296-424X2021-05-01910.3389/fphy.2021.647985647985Toward the Development of an On-Chip Acoustic Focusing Fluorescence Lifetime Flow CytometerJesus Sambrano0Felicia Rodriguez1John Martin2Jessica P. Houston3Department of Chemical and Materials Engineering, New Mexico State University, Las Cruces, NM, United StatesDepartment of Chemical and Materials Engineering, New Mexico State University, Las Cruces, NM, United StatesTiber Plasma Diagnostics, Las Cruces, NM, United StatesDepartment of Chemical and Materials Engineering, New Mexico State University, Las Cruces, NM, United StatesConventional flow cytometry is a valuable quantitative tool. Flow cytometers reveal physical and biochemical information from cells at a high throughput, which is quite valuable for many biomedical, biological, and diagnostic research fields. Flow cytometers range in complexity and typically provide multiparametric data for the user at rates of up to 50,000 cells measured per second. Cytometry systems are configured such that fluorescence or scattered light signals are collected per-cell, and the integrated optical signal at a given wavelength range indicates a particular cellular feature such as phenotype or morphology. When the timing of the optical signal is measured, the cytometry system becomes “time-resolved.” Time-resolved flow cytometry (TRFC) instruments can detect fluorescence decay kinetics, and such measurements are consequential for Förster Resonance Energy Transfer (FRET) studies, multiplexing, and metabolic mapping, to name a few. TRFC systems capture fluorescence lifetimes at rates of thousands of cells per-second, however the approach is challenged at this throughput by terminal cellular velocities. High flow rates limit the total number of photons integrated per-cell, reducing the reliability of the average lifetime as a cytometric parameter. In this contribution, we examine an innovative approach to address this signal-to-noise issue. The technology merges time-resolved hardware with microfluidics and acoustics. We present an “acoustofluidic” time-resolved flow cytometer so that cellular velocities can be adjusted on the fly with a standing acoustic wave (SAW). Our work shows that acoustic control can be combined with time-resolved features to appropriately balance the throughput with the optical signals necessary for lifetime data.https://www.frontiersin.org/articles/10.3389/fphy.2021.647985/fullflow cytometryFRETtime-resolved flow cytometryfluorescence lifetimeacoustofluidic
collection DOAJ
language English
format Article
sources DOAJ
author Jesus Sambrano
Felicia Rodriguez
John Martin
Jessica P. Houston
spellingShingle Jesus Sambrano
Felicia Rodriguez
John Martin
Jessica P. Houston
Toward the Development of an On-Chip Acoustic Focusing Fluorescence Lifetime Flow Cytometer
Frontiers in Physics
flow cytometry
FRET
time-resolved flow cytometry
fluorescence lifetime
acoustofluidic
author_facet Jesus Sambrano
Felicia Rodriguez
John Martin
Jessica P. Houston
author_sort Jesus Sambrano
title Toward the Development of an On-Chip Acoustic Focusing Fluorescence Lifetime Flow Cytometer
title_short Toward the Development of an On-Chip Acoustic Focusing Fluorescence Lifetime Flow Cytometer
title_full Toward the Development of an On-Chip Acoustic Focusing Fluorescence Lifetime Flow Cytometer
title_fullStr Toward the Development of an On-Chip Acoustic Focusing Fluorescence Lifetime Flow Cytometer
title_full_unstemmed Toward the Development of an On-Chip Acoustic Focusing Fluorescence Lifetime Flow Cytometer
title_sort toward the development of an on-chip acoustic focusing fluorescence lifetime flow cytometer
publisher Frontiers Media S.A.
series Frontiers in Physics
issn 2296-424X
publishDate 2021-05-01
description Conventional flow cytometry is a valuable quantitative tool. Flow cytometers reveal physical and biochemical information from cells at a high throughput, which is quite valuable for many biomedical, biological, and diagnostic research fields. Flow cytometers range in complexity and typically provide multiparametric data for the user at rates of up to 50,000 cells measured per second. Cytometry systems are configured such that fluorescence or scattered light signals are collected per-cell, and the integrated optical signal at a given wavelength range indicates a particular cellular feature such as phenotype or morphology. When the timing of the optical signal is measured, the cytometry system becomes “time-resolved.” Time-resolved flow cytometry (TRFC) instruments can detect fluorescence decay kinetics, and such measurements are consequential for Förster Resonance Energy Transfer (FRET) studies, multiplexing, and metabolic mapping, to name a few. TRFC systems capture fluorescence lifetimes at rates of thousands of cells per-second, however the approach is challenged at this throughput by terminal cellular velocities. High flow rates limit the total number of photons integrated per-cell, reducing the reliability of the average lifetime as a cytometric parameter. In this contribution, we examine an innovative approach to address this signal-to-noise issue. The technology merges time-resolved hardware with microfluidics and acoustics. We present an “acoustofluidic” time-resolved flow cytometer so that cellular velocities can be adjusted on the fly with a standing acoustic wave (SAW). Our work shows that acoustic control can be combined with time-resolved features to appropriately balance the throughput with the optical signals necessary for lifetime data.
topic flow cytometry
FRET
time-resolved flow cytometry
fluorescence lifetime
acoustofluidic
url https://www.frontiersin.org/articles/10.3389/fphy.2021.647985/full
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