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@ARTICLE{Heinrichs:845106,
author = {Heinrichs, Viktor and Dieluweit, Sabine and Stellbrink,
Jörg and Pyckhout-Hintzen, Wim and Hersch, Nils and
Richter, Dieter and Merkel, Rudolf},
title = {{C}hemically defined, ultrasoft {PDMS} elastomers with
selectable elasticity for mechanobiology},
journal = {PLoS one},
volume = {13},
number = {4},
issn = {1932-6203},
address = {Lawrence, Kan.},
publisher = {PLoS},
reportid = {FZJ-2018-02425},
pages = {e0195180 -},
year = {2018},
abstract = {Living animal cells are strongly influenced by the
mechanical properties of their environment. To model
physiological conditions ultrasoft cell culture substrates,
in some instances with elasticity (Young's modulus) of only
1 kPa, are mandatory. Due to their long shelf life
PDMS-based elastomers are a popular choice. However,
uncertainty about additives in commercial formulations and
difficulties to reach very soft materials limit their use.
Here, we produced silicone elastomers from few, chemically
defined and commercially available substances. Elastomers
exhibited elasticities in the range from 1 kPa to 55 kPa. In
detail, a high molecular weight (155 kg/mol),
vinyl-terminated linear silicone was crosslinked with a
multifunctional (f = 51) crosslinker (a copolymer of
dimethyl siloxane and hydrosilane) by a platinum catalyst.
The following different strategies towards ultrasoft
materials were explored: sparse crosslinking, swelling with
inert silicone polymers, and, finally, deliberate
introduction of dangling ends into the network (inhibition).
Rheological experiments with very low frequencies led to
precise viscoelastic characterizations. All strategies
enabled tuning of stiffness with the lowest stiffness of ~1
kPa reached by inhibition. This system was also most
practical to use. Biocompatibility of materials was tested
using primary cortical neurons from rats. Even after several
days of cultivation no adverse effects were found.},
cin = {ICS-7 / Neutronenstreuung ; JCNS-1},
ddc = {500},
cid = {I:(DE-Juel1)ICS-7-20110106 / I:(DE-Juel1)JCNS-1-20110106},
pnm = {552 - Engineering Cell Function (POF3-552)},
pid = {G:(DE-HGF)POF3-552},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:29624610},
UT = {WOS:000429379600017},
doi = {10.1371/journal.pone.0195180},
url = {https://juser.fz-juelich.de/record/845106},
}