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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2018
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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. |
format | Online Article Text |
id | pubmed-6251341 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
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
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title_full | Microfluidic bead encapsulation above 20 kHz with triggered drop formation
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title_fullStr | Microfluidic bead encapsulation above 20 kHz with triggered drop formation
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title_full_unstemmed | Microfluidic bead encapsulation above 20 kHz with triggered drop formation
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title_short | Microfluidic bead encapsulation above 20 kHz with triggered drop formation
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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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