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@ARTICLE{Zhou:891002,
author = {Zhou, Chen and Bette, Sebastian and Babendreyer, Aaron and
Hoffmann, Christina and Gerlach, Sven and Kremers, Tom and
Ludwig, Andreas and Hoffmann, Bernd and Merkel, Rudolf and
Uhlig, Stefan and Schnakenberg, Uwe},
title = {{S}tretchable electrical cell-substrate impedance sensor
platform for monitoring cell monolayers under strain},
journal = {Sensors and actuators / B},
volume = {336},
issn = {0925-4005},
address = {Amsterdam [u.a.]},
publisher = {Elsevier Science},
reportid = {FZJ-2021-01307},
pages = {129656 -},
year = {2021},
abstract = {Stretchable microelectrodes paired with an ultra-elastic
substrate can be used for electrical sensing of mechanically
stretched cells and cell monolayers. Here, we present the
development of a cell-stretching platform with thin-film
interdigitated microelectrodes. Up to 35 $\%$ cyclic stretch
are feasible with a novel interlaced meander design
connected to the microelectrodes and using
Poly(dimethylsiloxane) (PDMS) with a Young’s modulus of 50
kPa as an ultra-elastic substrate. Reliable electrical
contacting of the microelectrodes under stretch was achieved
by perforation of the contact pads. The novel platform
enables label-free, real-time electrical cell-substrate
impedance (ECIS) monitoring of cell monolayers.
Proof-of-concept experiments indicated that electrical
impedance of Madin-Darby canine kidney (MDCK) cell
monolayers increased sharply by uniaxial mechanical strain
above 20 $\%.$ For comparison, human alveolar basal
epithelial adenocarcinoma (A549) cell monolayers, which are
known to lack mature cell junctions, showed a continuous
decrease of electrical impedance over the whole applied
strain range of 35 $\%.$ The data reveal that impedance
changes upon stretching depend on epithelial cell types and
existence of tight cellular junctions. The system provides
the basis for reliable continuous long-term monitoring of
electrical properties of cell monolayers under strain by
electrical impedance spectroscopy, e.g., to monitor
epithelial permeability changes in real time and under
label-free conditions to screen the influence of
pharmacological substances.},
cin = {IBI-2},
ddc = {620},
cid = {I:(DE-Juel1)IBI-2-20200312},
pnm = {311 - Zellbiologie und Tumorbiologie (POF4-311) / DFG
project 273723265 - Mechanosensation und Mechanoreaktion in
epidermalen Systemen (273723265) / 5243 - Information
Processing in Distributed Systems (POF4-524)},
pid = {G:(DE-HGF)POF4-311 / G:(GEPRIS)273723265 /
G:(DE-HGF)POF4-5243},
typ = {PUB:(DE-HGF)16},
UT = {WOS:000639153300007},
doi = {10.1016/j.snb.2021.129656},
url = {https://juser.fz-juelich.de/record/891002},
}