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An Automated Microfluidic Multiplexer for Fast Delivery of C. elegans Populations from Multiwells

Automated biosorter platforms, including recently developed microfluidic devices, enable and accelerate high-throughput and/or high-resolution bioassays on small animal models. However, time-consuming delivery of different organism populations to these systems introduces a major bottleneck to execut...

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Autores principales: Ghorashian, Navid, Gökçe, Sertan Kutal, Guo, Sam Xun, Everett, William Neil, Ben-Yakar, Adela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3775957/
https://www.ncbi.nlm.nih.gov/pubmed/24069313
http://dx.doi.org/10.1371/journal.pone.0074480
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author Ghorashian, Navid
Gökçe, Sertan Kutal
Guo, Sam Xun
Everett, William Neil
Ben-Yakar, Adela
author_facet Ghorashian, Navid
Gökçe, Sertan Kutal
Guo, Sam Xun
Everett, William Neil
Ben-Yakar, Adela
author_sort Ghorashian, Navid
collection PubMed
description Automated biosorter platforms, including recently developed microfluidic devices, enable and accelerate high-throughput and/or high-resolution bioassays on small animal models. However, time-consuming delivery of different organism populations to these systems introduces a major bottleneck to executing large-scale screens. Current population delivery strategies rely on suction from conventional well plates through tubing periodically exposed to air, leading to certain disadvantages: 1) bubble introduction to the sample, interfering with analysis in the downstream system, 2) substantial time drain from added bubble-cleaning steps, and 3) the need for complex mechanical systems to manipulate well plate position. To address these concerns, we developed a multiwell-format microfluidic platform that can deliver multiple distinct animal populations from on-chip wells using multiplexed valve control. This Population Delivery Chip could operate autonomously as part of a relatively simple setup that did not require any of the major mechanical moving parts typical of plate-handling systems to address a given well. We demonstrated automatic serial delivery of 16 distinct C. elegans worm populations to a single outlet without introducing any bubbles to the samples, causing cross-contamination, or damaging the animals. The device achieved delivery of more than 90% of the population preloaded into a given well in 4.7 seconds; an order of magnitude faster than delivery modalities in current use. This platform could potentially handle other similarly sized model organisms, such as zebrafish and drosophila larvae or cellular micro-colonies. The device’s architecture and microchannel dimensions allow simple expansion for processing larger numbers of populations.
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spelling pubmed-37759572013-09-25 An Automated Microfluidic Multiplexer for Fast Delivery of C. elegans Populations from Multiwells Ghorashian, Navid Gökçe, Sertan Kutal Guo, Sam Xun Everett, William Neil Ben-Yakar, Adela PLoS One Research Article Automated biosorter platforms, including recently developed microfluidic devices, enable and accelerate high-throughput and/or high-resolution bioassays on small animal models. However, time-consuming delivery of different organism populations to these systems introduces a major bottleneck to executing large-scale screens. Current population delivery strategies rely on suction from conventional well plates through tubing periodically exposed to air, leading to certain disadvantages: 1) bubble introduction to the sample, interfering with analysis in the downstream system, 2) substantial time drain from added bubble-cleaning steps, and 3) the need for complex mechanical systems to manipulate well plate position. To address these concerns, we developed a multiwell-format microfluidic platform that can deliver multiple distinct animal populations from on-chip wells using multiplexed valve control. This Population Delivery Chip could operate autonomously as part of a relatively simple setup that did not require any of the major mechanical moving parts typical of plate-handling systems to address a given well. We demonstrated automatic serial delivery of 16 distinct C. elegans worm populations to a single outlet without introducing any bubbles to the samples, causing cross-contamination, or damaging the animals. The device achieved delivery of more than 90% of the population preloaded into a given well in 4.7 seconds; an order of magnitude faster than delivery modalities in current use. This platform could potentially handle other similarly sized model organisms, such as zebrafish and drosophila larvae or cellular micro-colonies. The device’s architecture and microchannel dimensions allow simple expansion for processing larger numbers of populations. Public Library of Science 2013-09-17 /pmc/articles/PMC3775957/ /pubmed/24069313 http://dx.doi.org/10.1371/journal.pone.0074480 Text en © 2013 Ghorashian et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Ghorashian, Navid
Gökçe, Sertan Kutal
Guo, Sam Xun
Everett, William Neil
Ben-Yakar, Adela
An Automated Microfluidic Multiplexer for Fast Delivery of C. elegans Populations from Multiwells
title An Automated Microfluidic Multiplexer for Fast Delivery of C. elegans Populations from Multiwells
title_full An Automated Microfluidic Multiplexer for Fast Delivery of C. elegans Populations from Multiwells
title_fullStr An Automated Microfluidic Multiplexer for Fast Delivery of C. elegans Populations from Multiwells
title_full_unstemmed An Automated Microfluidic Multiplexer for Fast Delivery of C. elegans Populations from Multiwells
title_short An Automated Microfluidic Multiplexer for Fast Delivery of C. elegans Populations from Multiwells
title_sort automated microfluidic multiplexer for fast delivery of c. elegans populations from multiwells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3775957/
https://www.ncbi.nlm.nih.gov/pubmed/24069313
http://dx.doi.org/10.1371/journal.pone.0074480
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