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Modular operation of microfluidic chips for highly parallelized cell culture and liquid dosing via a fluidic circuit board.
Vollertsen, A R; de Boer, D; Dekker, S; Wesselink, B A M; Haverkate, R; Rho, H S; Boom, R J; Skolimowski, M; Blom, M; Passier, R; van den Berg, A; van der Meer, A D; Odijk, M.
Afiliación
  • Vollertsen AR; BIOS Lab on Chip Group, MESA+ Institute for Nanotechnology, University of Twente, Enschede, The Netherlands.
  • de Boer D; Mesoscale Chemical Systems, MESA+ Institute for Nanotechnology, University of Twente, Enschede, The Netherlands.
  • Dekker S; BIOS Lab on Chip Group, MESA+ Institute for Nanotechnology, University of Twente, Enschede, The Netherlands.
  • Wesselink BAM; BIOS Lab on Chip Group, MESA+ Institute for Nanotechnology, University of Twente, Enschede, The Netherlands.
  • Haverkate R; BIOS Lab on Chip Group, MESA+ Institute for Nanotechnology, University of Twente, Enschede, The Netherlands.
  • Rho HS; Institute for Technology-Inspired Regenerative Medicine, Maastricht University, Maastricht, The Netherlands.
  • Boom RJ; Micronit Microtechnologies, Enschede, The Netherlands.
  • Skolimowski M; Micronit Microtechnologies, Enschede, The Netherlands.
  • Blom M; Micronit Microtechnologies, Enschede, The Netherlands.
  • Passier R; Applied Stem Cell Technologies, TechMed Centre, University of Twente, Enschede, The Netherlands.
  • van den Berg A; BIOS Lab on Chip Group, MESA+ Institute for Nanotechnology, University of Twente, Enschede, The Netherlands.
  • van der Meer AD; Applied Stem Cell Technologies, TechMed Centre, University of Twente, Enschede, The Netherlands.
  • Odijk M; BIOS Lab on Chip Group, MESA+ Institute for Nanotechnology, University of Twente, Enschede, The Netherlands.
Microsyst Nanoeng ; 6: 107, 2020.
Article en En | MEDLINE | ID: mdl-34567716
ABSTRACT
Microfluidic systems enable automated and highly parallelized cell culture with low volumes and defined liquid dosing. To achieve this, systems typically integrate all functions into a single, monolithic device as a "one size fits all" solution. However, this approach limits the end users' (re)design flexibility and complicates the addition of new functions to the system. To address this challenge, we propose and demonstrate a modular and standardized plug-and-play fluidic circuit board (FCB) for operating microfluidic building blocks (MFBBs), whereby both the FCB and the MFBBs contain integrated valves. A single FCB can parallelize up to three MFBBs of the same design or operate MFBBs with entirely different architectures. The operation of the MFBBs through the FCB is fully automated and does not incur the cost of an extra external footprint. We use this modular platform to control three microfluidic large-scale integration (mLSI) MFBBs, each of which features 64 microchambers suitable for cell culturing with high spatiotemporal control. We show as a proof of principle that we can culture human umbilical vein endothelial cells (HUVECs) for multiple days in the chambers of this MFBB. Moreover, we also use the same FCB to control an MFBB for liquid dosing with a high dynamic range. Our results demonstrate that MFBBs with different designs can be controlled and combined on a single FCB. Our novel modular approach to operating an automated microfluidic system for parallelized cell culture will enable greater experimental flexibility and facilitate the cooperation of different chips from different labs.
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Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Microsyst Nanoeng Año: 2020 Tipo del documento: Article País de afiliación: Países Bajos

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Microsyst Nanoeng Año: 2020 Tipo del documento: Article País de afiliación: Países Bajos