Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Henkel, Thomas, Mayer, Günter, Hampl, Jörg, Cao, Jialan, Ehrhardt, Linda, Schober, Andreas, Groß, Gregor Alexander
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
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
_version_ 1784754822829834240
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
work_keys_str_mv AT henkelthomas frommicrotiterplatestodropletsthereandbackagain
AT mayergunter frommicrotiterplatestodropletsthereandbackagain
AT hampljorg frommicrotiterplatestodropletsthereandbackagain
AT caojialan frommicrotiterplatestodropletsthereandbackagain
AT ehrhardtlinda frommicrotiterplatestodropletsthereandbackagain
AT schoberandreas frommicrotiterplatestodropletsthereandbackagain
AT großgregoralexander frommicrotiterplatestodropletsthereandbackagain