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Microfabricated tuneable and transferable porous PDMS membranes for Organs-on-Chips

  • W. F. Quirós-Solano
  • , N. Gaio
  • , Oscar Stassen
  • , Y. B. Arik
  • , C. Silvestri
  • , Nicole van Engeland
  • , A. Van der Meer
  • , R. Passier
  • , Cecilia Sahlgren
  • , C. V. C. Bouten
  • , A. van den Berg
  • , R. Dekker
  • , P. M. Sarro

Research output: Contribution to journalArticleScientificpeer-review

87 Citations (Scopus)
128 Downloads (Pure)

Abstract

We present a novel and highly reproducible process to fabricate transferable porous PDMS membranes for PDMS-based Organs-on-Chips (OOCs) using microelectromechanical systems (MEMS) fabrication technologies. Porous PDMS membranes with pore sizes down to 2.0 mu m in diameter and a wide porosity range (2-65%) can be fabricated. To overcome issues normally faced when using replica moulding and extend the applicability to most OOCs and improve their scalability and reproducibility, the process includes a sacrificial layer to easily transfer the membranes from a silicon carrier to any PDMS-based OOC. The highly reliable fabrication and transfer method does not need of manual handling to define the pore features (size, distribution), allowing very thin (< 10 mu m) functional membranes to be transferred at chip level with a high success rate (85%). The viability of cell culturing on the porous membranes was assessed by culturing two different cell types on transferred membranes in two different OOCs. Human umbilical endothelial cells (HUVEC) and MDA-MB-231 (MDA) cells were successfully cultured confirming the viability of cell culturing and the biocompatibility of the membranes. The results demonstrate the potential of controlling the porous membrane features to study cell mechanisms such as transmigrations, monolayer formation, and barrier function. The high control over the membrane characteristics might consequently allow to intentionally trigger or prevent certain cellular responses or mechanisms when studying human physiology and pathology using OOCs.
Original languageUndefined/Unknown
Pages (from-to)
Number of pages11
JournalScientific Reports
Volume8
DOIs
Publication statusPublished - 2018
MoE publication typeA1 Journal article-refereed

Funding

This work was part of the NanoInside project Organs-on-Chips Technology Platform, a subsidy promoted by human organ and disease model technologies (hDMT) and granted by NanoNextNL. William F. Quirós-Solano is partially financed by Instituto Tecnológico de Costa Rica. Nikolas Gaio is financed by Electronic Components and Systems for European Leadership (ECSEL) InForMed (No. 2014-2-662155). Yusuf B. Arik is financed by Stichting Toegepast Wetenschappelijk Instituut voor Neuromodulatie (TWIN) project “Inflammation and Edema in an Organ-on-a-Chip Model of Wet Age-Related Macular Degeneration”. Oscar M.J.A. Stassen was financed by the European Union’s Seventh Framework Programme for research, technological development and demonstration under grant agreement No. 604514 (ImaValve).

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