TY - JOUR
T1 - Organic electronic transmembrane device for hosting and monitoring 3D cell cultures
AU - Pitsalidis, Charalampos
AU - Van Niekerk, Douglas
AU - Moysidou, Chrysanthi Maria
AU - Boys, Alexander J.
AU - Withers, Aimee
AU - Vallet, Romane
AU - Owens, Róisín M.
N1 - Funding Information:
We wish to acknowledge funding from the European Research Council (ERC) under the European Union’s Horizon 2020 research and innovation program (grant agreement no. 723951 to R.M.O.). This material is based upon work supported by the Air Force Office of Scientific Research under award number FA8655-20-1-7021 to R.M.O. D.v.N. is funded by the W.D Armstrong Trust Fund and the Oppenheimer Memorial Trust. This work was supported by the European Research Council (ERC) under the European Union’s Horizon 2020 (grant agreement no. 723951 to R.M.O.), the Air Force Office of Scientific Research (award number FA8655-20-1-7021 to R.M.O.), and the Armstrong Trust Fund and the Oppenheimer Memorial Trust (to D.v.N.).
Publisher Copyright:
Copyright © 2022 The Authors, some rights reserved.
PY - 2022/9
Y1 - 2022/9
N2 - 3D cell models have made strides in the past decades in response to failures of 2D cultures to translate targets during the drug discovery process. Here, we report on a novel multiwell plate bioelectronic platform, namely, the e-transmembrane, capable of supporting and monitoring complex 3D cell architectures. Scaffolds made of PEDOT:PSS [poly(3,4-ethylenedioxythiophene):polystyrene sulfonate] are microengineered to function as separating membranes for compartmentalized cell cultures, as well as electronic components for real-time in situ recordings of cell growth and function. Owing to the high surface area–to–volume ratio, the e-transmembrane allows generation of deep, stratified tissues within the porous bulk and cell polarization at the apico-basal domains. Impedance spectroscopy measurements carried out throughout the tissue growth identified signatures from different cellular systems and allowed extraction of critical functional parameters. This platform has the potential to become a universal tool for biologists for the next generation of high-throughput drug screening assays.
AB - 3D cell models have made strides in the past decades in response to failures of 2D cultures to translate targets during the drug discovery process. Here, we report on a novel multiwell plate bioelectronic platform, namely, the e-transmembrane, capable of supporting and monitoring complex 3D cell architectures. Scaffolds made of PEDOT:PSS [poly(3,4-ethylenedioxythiophene):polystyrene sulfonate] are microengineered to function as separating membranes for compartmentalized cell cultures, as well as electronic components for real-time in situ recordings of cell growth and function. Owing to the high surface area–to–volume ratio, the e-transmembrane allows generation of deep, stratified tissues within the porous bulk and cell polarization at the apico-basal domains. Impedance spectroscopy measurements carried out throughout the tissue growth identified signatures from different cellular systems and allowed extraction of critical functional parameters. This platform has the potential to become a universal tool for biologists for the next generation of high-throughput drug screening assays.
UR - https://www.scopus.com/pages/publications/85138209486
U2 - 10.1126/sciadv.abo4761
DO - 10.1126/sciadv.abo4761
M3 - Article
C2 - 36112689
AN - SCOPUS:85138209486
SN - 2375-2548
VL - 8
JO - Science Advances
JF - Science Advances
IS - 37
M1 - eabo4761
ER -