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Microfluidic bead encapsulation above 20 kHz with triggered drop formation

Microsphere beads are functionalized with oligonucleotides, antibodies, and other moieties to enable specific detection of analytes. Droplet microfluidics leverages this for single-molecule or -cell analysis by pairing beads and targets in water-in-oil droplets. Pairing is achieved with devices oper...

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Detalles Bibliográficos
Autores principales: Clark, Iain C., Abate, Adam R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6251341/
https://www.ncbi.nlm.nih.gov/pubmed/30362490
http://dx.doi.org/10.1039/c8lc00514a
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author Clark, Iain C.
Abate, Adam R.
author_facet Clark, Iain C.
Abate, Adam R.
author_sort Clark, Iain C.
collection PubMed
description Microsphere beads are functionalized with oligonucleotides, antibodies, and other moieties to enable specific detection of analytes. Droplet microfluidics leverages this for single-molecule or -cell analysis by pairing beads and targets in water-in-oil droplets. Pairing is achieved with devices operating in the dripping regime, limiting throughput. Here, we describe a pairing method that uses beads to trigger the breakup of a jet into monodispersed droplets. We use the method to pair 10(5) Human T cells with polyacrylamide beads ten times faster than methods operating in the dripping regime. Our method improves the throughput of bead-based droplet workflows, enabling analysis of large populations and the detection of rare events.
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spelling pubmed-62513412018-12-19 Microfluidic bead encapsulation above 20 kHz with triggered drop formation Clark, Iain C. Abate, Adam R. Lab Chip Chemistry Microsphere beads are functionalized with oligonucleotides, antibodies, and other moieties to enable specific detection of analytes. Droplet microfluidics leverages this for single-molecule or -cell analysis by pairing beads and targets in water-in-oil droplets. Pairing is achieved with devices operating in the dripping regime, limiting throughput. Here, we describe a pairing method that uses beads to trigger the breakup of a jet into monodispersed droplets. We use the method to pair 10(5) Human T cells with polyacrylamide beads ten times faster than methods operating in the dripping regime. Our method improves the throughput of bead-based droplet workflows, enabling analysis of large populations and the detection of rare events. Royal Society of Chemistry 2018-12-07 2018-10-26 /pmc/articles/PMC6251341/ /pubmed/30362490 http://dx.doi.org/10.1039/c8lc00514a Text en This journal is © The Royal Society of Chemistry 2018 http://creativecommons.org/licenses/by-nc/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported Licence (CC BY-NC 3.0)
spellingShingle Chemistry
Clark, Iain C.
Abate, Adam R.
Microfluidic bead encapsulation above 20 kHz with triggered drop formation
title Microfluidic bead encapsulation above 20 kHz with triggered drop formation
title_full Microfluidic bead encapsulation above 20 kHz with triggered drop formation
title_fullStr Microfluidic bead encapsulation above 20 kHz with triggered drop formation
title_full_unstemmed Microfluidic bead encapsulation above 20 kHz with triggered drop formation
title_short Microfluidic bead encapsulation above 20 kHz with triggered drop formation
title_sort microfluidic bead encapsulation above 20 khz with triggered drop formation
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6251341/
https://www.ncbi.nlm.nih.gov/pubmed/30362490
http://dx.doi.org/10.1039/c8lc00514a
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