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From Microtiter Plates to Droplets—There and Back Again †
Droplet-based microfluidic screening techniques can benefit from interfacing established microtiter plate-based screening and sample management workflows. Interfacing tools are required both for loading preconfigured microtiter-plate (MTP)-based sample collections into droplets and for dispensing th...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9316479/ https://www.ncbi.nlm.nih.gov/pubmed/35888839 http://dx.doi.org/10.3390/mi13071022 |
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author | Henkel, Thomas Mayer, Günter Hampl, Jörg Cao, Jialan Ehrhardt, Linda Schober, Andreas Groß, Gregor Alexander |
author_facet | Henkel, Thomas Mayer, Günter Hampl, Jörg Cao, Jialan Ehrhardt, Linda Schober, Andreas Groß, Gregor Alexander |
author_sort | Henkel, Thomas |
collection | PubMed |
description | Droplet-based microfluidic screening techniques can benefit from interfacing established microtiter plate-based screening and sample management workflows. Interfacing tools are required both for loading preconfigured microtiter-plate (MTP)-based sample collections into droplets and for dispensing the used droplets samples back into MTPs for subsequent storage or further processing. Here, we present a collection of Digital Microfluidic Pipetting Tips (DMPTs) with integrated facilities for droplet generation and manipulation together with a robotic system for its operation. This combination serves as a bidirectional sampling interface for sample transfer from wells into droplets (w2d) and vice versa droplets into wells (d2w). The DMPT were designed to fit into 96-deep-well MTPs and prepared from glass by means of microsystems technology. The aspirated samples are converted into the channel-confined droplets’ sequences separated by an immiscible carrier medium. To comply with the demands of dose-response assays, up to three additional assay compound solutions can be added to the sample droplets. To enable different procedural assay protocols, four different DMPT variants were made. In this way, droplet series with gradually changing composition can be generated for, e.g., 2D screening purposes. The developed DMPT and their common fluidic connector are described here. To handle the opposite transfer d2w, a robotic transfer system was set up and is described briefly. |
format | Online Article Text |
id | pubmed-9316479 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-93164792022-07-27 From Microtiter Plates to Droplets—There and Back Again † Henkel, Thomas Mayer, Günter Hampl, Jörg Cao, Jialan Ehrhardt, Linda Schober, Andreas Groß, Gregor Alexander Micromachines (Basel) Article Droplet-based microfluidic screening techniques can benefit from interfacing established microtiter plate-based screening and sample management workflows. Interfacing tools are required both for loading preconfigured microtiter-plate (MTP)-based sample collections into droplets and for dispensing the used droplets samples back into MTPs for subsequent storage or further processing. Here, we present a collection of Digital Microfluidic Pipetting Tips (DMPTs) with integrated facilities for droplet generation and manipulation together with a robotic system for its operation. This combination serves as a bidirectional sampling interface for sample transfer from wells into droplets (w2d) and vice versa droplets into wells (d2w). The DMPT were designed to fit into 96-deep-well MTPs and prepared from glass by means of microsystems technology. The aspirated samples are converted into the channel-confined droplets’ sequences separated by an immiscible carrier medium. To comply with the demands of dose-response assays, up to three additional assay compound solutions can be added to the sample droplets. To enable different procedural assay protocols, four different DMPT variants were made. In this way, droplet series with gradually changing composition can be generated for, e.g., 2D screening purposes. The developed DMPT and their common fluidic connector are described here. To handle the opposite transfer d2w, a robotic transfer system was set up and is described briefly. MDPI 2022-06-28 /pmc/articles/PMC9316479/ /pubmed/35888839 http://dx.doi.org/10.3390/mi13071022 Text en © 2022 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 Henkel, Thomas Mayer, Günter Hampl, Jörg Cao, Jialan Ehrhardt, Linda Schober, Andreas Groß, Gregor Alexander From Microtiter Plates to Droplets—There and Back Again † |
title | From Microtiter Plates to Droplets—There and Back Again † |
title_full | From Microtiter Plates to Droplets—There and Back Again † |
title_fullStr | From Microtiter Plates to Droplets—There and Back Again † |
title_full_unstemmed | From Microtiter Plates to Droplets—There and Back Again † |
title_short | From Microtiter Plates to Droplets—There and Back Again † |
title_sort | from microtiter plates to droplets—there and back again † |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9316479/ https://www.ncbi.nlm.nih.gov/pubmed/35888839 http://dx.doi.org/10.3390/mi13071022 |
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