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Transient microfluidic compartmentalization using actionable microfilaments for biochemical assays, cell culture and organs-on-chip.
Yamada, Ayako; Renault, Renaud; Chikina, Aleksandra; Venzac, Bastien; Pereiro, Iago; Coscoy, Sylvie; Verhulsel, Marine; Parrini, Maria Carla; Villard, Catherine; Viovy, Jean-Louis; Descroix, Stéphanie.
Afiliación
  • Yamada A; Laboratoire Physico Chimie Curie, Institut Curie, PSL Research University, CNRS UMR168, 75005, Paris, France. ayako.yamada@curie.fr stephanie.descroix@curie.fr and Sorbonne Universités, UPMC Univ Paris 06, 75005, Paris, France and Institut Pierre-Gilles de Gennes, 75005, Paris, France.
  • Renault R; Laboratoire Physico Chimie Curie, Institut Curie, PSL Research University, CNRS UMR168, 75005, Paris, France. ayako.yamada@curie.fr stephanie.descroix@curie.fr and Sorbonne Universités, UPMC Univ Paris 06, 75005, Paris, France and Institut Pierre-Gilles de Gennes, 75005, Paris, France.
  • Chikina A; Laboratoire Physico Chimie Curie, Institut Curie, PSL Research University, CNRS UMR168, 75005, Paris, France. ayako.yamada@curie.fr stephanie.descroix@curie.fr and Sorbonne Universités, UPMC Univ Paris 06, 75005, Paris, France and Institut Pierre-Gilles de Gennes, 75005, Paris, France.
  • Venzac B; Laboratoire Physico Chimie Curie, Institut Curie, PSL Research University, CNRS UMR168, 75005, Paris, France. ayako.yamada@curie.fr stephanie.descroix@curie.fr and Sorbonne Universités, UPMC Univ Paris 06, 75005, Paris, France and Institut Pierre-Gilles de Gennes, 75005, Paris, France.
  • Pereiro I; Laboratoire Physico Chimie Curie, Institut Curie, PSL Research University, CNRS UMR168, 75005, Paris, France. ayako.yamada@curie.fr stephanie.descroix@curie.fr and Sorbonne Universités, UPMC Univ Paris 06, 75005, Paris, France and Institut Pierre-Gilles de Gennes, 75005, Paris, France.
  • Coscoy S; Laboratoire Physico Chimie Curie, Institut Curie, PSL Research University, CNRS UMR168, 75005, Paris, France. ayako.yamada@curie.fr stephanie.descroix@curie.fr and Sorbonne Universités, UPMC Univ Paris 06, 75005, Paris, France.
  • Verhulsel M; Laboratoire Physico Chimie Curie, Institut Curie, PSL Research University, CNRS UMR168, 75005, Paris, France. ayako.yamada@curie.fr stephanie.descroix@curie.fr and Sorbonne Universités, UPMC Univ Paris 06, 75005, Paris, France and Institut Pierre-Gilles de Gennes, 75005, Paris, France.
  • Parrini MC; Institut Curie, Centre de Recherche, PSL Research University, 75005, Paris, France and ART group, Inserm U830, 75248 Paris, France.
  • Villard C; Laboratoire Physico Chimie Curie, Institut Curie, PSL Research University, CNRS UMR168, 75005, Paris, France. ayako.yamada@curie.fr stephanie.descroix@curie.fr and Sorbonne Universités, UPMC Univ Paris 06, 75005, Paris, France and Institut Pierre-Gilles de Gennes, 75005, Paris, France.
  • Viovy JL; Laboratoire Physico Chimie Curie, Institut Curie, PSL Research University, CNRS UMR168, 75005, Paris, France. ayako.yamada@curie.fr stephanie.descroix@curie.fr and Sorbonne Universités, UPMC Univ Paris 06, 75005, Paris, France and Institut Pierre-Gilles de Gennes, 75005, Paris, France.
  • Descroix S; Laboratoire Physico Chimie Curie, Institut Curie, PSL Research University, CNRS UMR168, 75005, Paris, France. ayako.yamada@curie.fr stephanie.descroix@curie.fr and Sorbonne Universités, UPMC Univ Paris 06, 75005, Paris, France and Institut Pierre-Gilles de Gennes, 75005, Paris, France.
Lab Chip ; 16(24): 4691-4701, 2016 11 29.
Article en En | MEDLINE | ID: mdl-27797384
ABSTRACT
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.
Asunto(s)
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Citoesqueleto de Actina / Técnicas de Cultivo de Célula / Dispositivos Laboratorio en un Chip Límite: Animals Idioma: En Revista: Lab Chip Asunto de la revista: BIOTECNOLOGIA / QUIMICA Año: 2016 Tipo del documento: Article País de afiliación: Francia
Buscar en Google
Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Citoesqueleto de Actina / Técnicas de Cultivo de Célula / Dispositivos Laboratorio en un Chip Límite: Animals Idioma: En Revista: Lab Chip Asunto de la revista: BIOTECNOLOGIA / QUIMICA Año: 2016 Tipo del documento: Article País de afiliación: Francia