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@MASTERSTHESIS{Glass:875396,
author = {Glass, Manuel},
title = {{M}olecular layer deposition and protein interface
patterning for guided cell growth},
volume = {215},
school = {Universität Köln},
type = {Masterarbeit},
address = {Jülich},
publisher = {Forschungszentrum Jülich GmbH Zentralbibliothek, Verlag},
reportid = {FZJ-2020-02005},
isbn = {978-3-95806-463-8},
series = {Schriften des Forschungszentrums Jülich. Reihe
Schlüsseltechnologien / Key Technologies},
pages = {IV, 81 S.},
year = {2020},
note = {Universität Köln, Masterarbeit, 2020},
abstract = {This thesis describes the design, assembly and structural
and functional characterization, of bio-(medical) applicable
interfacial layers with molecular controlled architectures
on solid substrates. The interaction between the living
world of cells, tissue, or whole organisms and the (organic
orinorganic) materials world of technical devices such as
implants, sensors, or medical parts requires a proper
construction and detailed structural (and functional)
control of this organism-machine interface. Therefore, a
possible way how to get from an optimal molecular layer
deposition (MLD) to guided cell growth is developed in this
work. By integrating a heater to an already existing MLD
setup and an optimization of the deposition temperature we
could improve the gas phase deposition process of GLYMO
(3-Glycidyloxypropyl)-trimethoxysilane) yielding a faster
formation of self-assembled monolayers(SAMs) and a better
quality of GLYMO SAMs. This was confirmed by ex-situ
analysis, e.g. fluorescence microscopy, referenced
ellipsometry, and surface potential measurements. With the
gas phase MLD, lithography, and lift-off processes
functionalization of SiO$_{2}$ surfaces with GLYMO SAMs and
patterned ploy-L-lysine proteins (PLL) could be achieved.
This enables to generate various micropatterns that support
cell adhesion, neurite outgrowth, and the formation of a
geometrically defined networks of neurons. Finally, guided
growth was demonstrated via rat cortical neuron cultures on
the GLYMO-PLL patterned surfaces. On first sight, the neuron
growth was clearly guided, i.e. neurons grow on PLL but not
on GLYMO. However, we also noticed that on certain areas
which should be coated with PLL, no cells were present. It
seemed that in these areas during the lithography PMMA is
cracked due to the e-beam exposure and partially binds to
the GLYMO. This cracked PMMA hinders the PLL to bind to
GLYMO and therefore only in places, where PLL dries out
during the coating, PLL is present in the GLYMO-PLL pattern.
These effects are observed via fluorescence imaging for the
PLL coating and for the cell growth. In conclusion, the
modified deposition process at elevated temperatures in
combination with the developed interface pattering process
via a combination of a molecular layer of GLYMO and the
protein PLL might be suitable for guidance of neuronal
growth, despite the problem of a PMMA blocking layer which
seem to be generated during the lithography. This
shortcoming could be overcome by an additional step in which
the blocking layer is remove.},
cin = {ICS-8},
cid = {I:(DE-Juel1)ICS-8-20110106},
pnm = {899 - ohne Topic (POF3-899)},
pid = {G:(DE-HGF)POF3-899},
typ = {PUB:(DE-HGF)3 / PUB:(DE-HGF)19},
urn = {urn:nbn:de:0001-2020060521},
url = {https://juser.fz-juelich.de/record/875396},
}