A Modular Microfluidic Organoid Platform Using LEGO®‐like Bricks

Author:

Carvalho Daniel J.1ORCID,Kip Anna M.2,Tegel Andreas3,Stich Matthias3,Krause Christian3,Romitti Mírian4,Branca Carlotta2,Verhoeven Bart5,Costagliola Sabine4,Moroni Lorenzo2,Giselbrecht Stefan1ORCID

Affiliation:

1. Department of Instructive Biomaterials Engineering MERLN Institute for Technology‐Inspired Regenerative Medicine Maastricht University Maastricht 6229 The Netherlands

2. Department of Complex Tissue Regeneration MERLN Institute for Technology‐Inspired Regenerative Medicine Maastricht University Maastricht 6229 ER The Netherlands

3. PreSens Precision Sensing GmbH Am Biopark 11 93053 Regensburg Germany

4. Institute of Interdisciplinary Research in Molecular Human Biology (IRIBHM) Université Libre de Bruxelles 808 route de Lennik Anderlecht 1070 Belgium

5. IDEE Instrument Development Engineering & Evaluation – Research Engineering Universiteitssingel 50 Maastricht 6200 MD The Netherlands

Abstract

AbstractThe convergence of organoid and organ‐on‐a‐chip (OoC) technologies is urgently needed to overcome limitations of current 3D in vitro models. However, integrating organoids in standard OoCs faces several technical challenges as it is typically laborious, lacks flexibility and often results in even more complex and less efficient cell culture protocols. Therefore, specifically adapted and more flexible microfluidic platforms need to be developed to facilitate the incorporation of complex 3D in vitro models. Here, we developed a modular, tubeless fluidic circuit board (FCB) coupled with reversibly sealed cell culture bricks for dynamic culture of embryonic stem cell (ESC)‐derived thyroid follicles. The FCB was fabricated by milling channels in a polycarbonate (PC) plate followed by thermal bonding against another PC plate. LEGO®‐like fluidic interconnectors allowed plug‐and‐play connection between a variety of cell culture bricks and the FCB. Lock‐and‐play (LnP) clamps were integrated in the organoid brick to enable easy (un)loading of organoids. A multiplexed perfusion experiment was conducted with six FCBs, where thyroid organoids were transferred on‐chip within minutes and cultured up to 10 days without losing their structure and functionality, thus validating this system as a flexible, easy‐to‐use platform, capable of synergistically combining organoids with advanced microfluidic platforms.This article is protected by copyright. All rights reserved

Publisher

Wiley

Subject

Pharmaceutical Science,Biomedical Engineering,Biomaterials

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