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Transient microfluidic compartmentalization using actionable microfilaments for biochemical assays, cell culture and organs-on-chip

Authors :
Ayako Yamada
Aleksandra Chikina
Stéphanie Descroix
Jean-Louis Viovy
Bastien Venzac
Iago Pereiro
Renaud Renault
Catherine Villard
Sylvie Coscoy
Marine Verhulsel
Maria Carla Parrini
Physico-Chimie-Curie ( PCC )
Centre National de la Recherche Scientifique ( CNRS ) -INSTITUT CURIE-Université Pierre et Marie Curie - Paris 6 ( UPMC )
Institut Pierre-Gilles de Gennes pour la Microfluidique
Institut Curie
Unité de génétique et biologie des cancers ( U830 )
Université Paris Descartes - Paris 5 ( UPD5 ) -Institut Curie-Institut National de la Santé et de la Recherche Médicale ( INSERM )
Physico-Chimie-Curie (PCC)
Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut Curie [Paris]-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)
Institut Curie [Paris]
Unité de génétique et biologie des cancers (U830)
Université Paris Descartes - Paris 5 (UPD5)-Institut Curie [Paris]-Institut National de la Santé et de la Recherche Médicale (INSERM)
HAL-UPMC, Gestionnaire
Centre National de la Recherche Scientifique (CNRS)-Institut Curie [Paris]-Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut de Chimie du CNRS (INC)
Source :
Lab on a Chip, Lab on a Chip, Royal Society of Chemistry, 2016, 〈10.1039/c6lc01143h〉, Lab on a Chip, 2016, ⟨10.1039/c6lc01143h⟩, Lab on a Chip, Royal Society of Chemistry, 2016, ⟨10.1039/c6lc01143h⟩
Publication Year :
2016
Publisher :
HAL CCSD, 2016.

Abstract

International audience; We report here a simple yet robust transient compartmentalization system for microfluidic platforms. Cylindrical microfilaments made of commercially available fishing lines are embedded in a microfluidic chamber and employed as removable walls, dividing the chamber into several compartments. These partitions allow tight sealing for hours, and can be removed at any time by longitudinal sliding with minimal hydrodynamic perturbation. This allows the easy implementation of various functions, previously impossible or requiring more complex instrumentation. In this study, we demonstrate the applications of our strategy, firstly to trigger chemical diffusion, then to make surface co-coating or cell co-culture on a two-dimensional substrate, and finally to form multiple cell-laden hydrogel compartments for three-dimensional cell co-culture in a microfluidic device. This technology provides easy and low-cost solutions, without the use of pneumatic valves or external equipment, for constructing well-controlled microenvironments for biochemical and cellular assays.

Details

Language :
English
ISSN :
14730197 and 14730189
Database :
OpenAIRE
Journal :
Lab on a Chip, Lab on a Chip, Royal Society of Chemistry, 2016, 〈10.1039/c6lc01143h〉, Lab on a Chip, 2016, ⟨10.1039/c6lc01143h⟩, Lab on a Chip, Royal Society of Chemistry, 2016, ⟨10.1039/c6lc01143h⟩
Accession number :
edsair.doi.dedup.....591d87274ae7e240b84f50d0bfee1a4e
Full Text :
https://doi.org/10.1039/c6lc01143h〉