April 7 - 11, 2025
Seattle, Washington
Symposium Supporters
2025 MRS Spring Meeting & Exhibit
SB11.04.05

A Novel 3D Transmembrane Organic Electrochemical Transistor for Monitoring Growth of Fibroblast Cells

When and Where

Apr 9, 2025
4:15pm - 4:30pm
Summit, Level 3, Room 331

Presenter(s)

Co-Author(s)

Rachana Acharya1,Douglas Niekerk1,Maria Lopez Cavestany1,Roisin Owens1

University of Cambridge1

Abstract

Rachana Acharya1,Douglas Niekerk1,Maria Lopez Cavestany1,Roisin Owens1

University of Cambridge1
Three-dimensional cell culture and in-vitro bioelectronic systems have made significant developments for monitoring and predicting biological activity for various applications. Bioelectronic devices such as have been extensively researched based on 2D films of electrically conducting or organic semiconductor films, while tissue engineering has developed 3D structures for cell culture, such as porous scaffolds, hydrogels and fibre meshes to better mimic human tissue physiology. In this work, we present a novel bioelectronic device encompassing the benefits of both domains and is based on a 3D microporous scaffold with the conducting polymer PEDOT:PSS integrated into an organic electrochemical transistor.
The 3D scaffold serves as the separator membrane to compartmentalize different cell cultures, the tissue-like cell growth medium as well as acts as an electronic element for recording cell growth and assessing tissue integrity. We demonstrate the design, fabrication and electrical characterization of the transmembrane 3D-OECT, which demonstrates up to 20 mA drain current and was characterized for 3D scaffolds with different thicknesses (100-500 µm), different polymers to show both p-type and n-type operation, gate electrodes with different materials and different contact electrode areas.
The device can be used to continuously monitor the growth of fibroblast cells and the growth of the surrounding ECM over 10 days, with a clear electrical signal change in the drain current for static characterization and the time constant extracted from the transient response of the 3D-OECT. We have monitored the difference in cell growth for different initial cell densities (125k, 250k and 500k cells) and distinctly show different patterns in cell growth, migration and ECM production depending on the density of the cells in the scaffold. The results have been well correlated with biological assays such as immunofluorescence imaging and DNA quantification.

Keywords

biomimetic (assembly)

Symposium Organizers

Jonathan Rivnay, Northwestern University
Roisin Owens, University of Cambridge
Dion Khodagholy, University of California, Irvine
Claudia Cea, Massachusetts Institute of Technology

Session Chairs

Alex Abramson
Dion Khodagholy

In this Session