Felix Schrank1, Heiko Tzschätzsch1, Angela Ariza de Schellenberger1, Paul Janmey2, Jürgen Braun3, and Ingolf Sack1
1Department of Radiology, Charité - Universitätsmedizin Berlin, Berlin, Germany, 2Institute for Medicine and Engineering, University of Pennsylvania, Philadelphia, PA, United States, 3Institute of Medical Informatics, Charité - Universitätsmedizin Berlin, Berlin, Germany
Synopsis
Shear
rheometry was combined with magnetic resonance elastography (MRE) in
a 1.5-T clinical system and a 0.5-T tabletop MRE system to
investigate the viscoelastic powerlaw behavior of heparin and
polyacrylamide
(PAAm) over more than three orders of magnitude dynamic range.
While heparin has softer properties than encountered in soft in-vivo
tissues, crosslinked PAAm has similar stiffness as measured for
in-vivo tissues, however, with lower dispersive properties. Overall
both materials are good candidates for the use as standard phantom
materials in MRE due to their well predictable springpot properties
across the full frequency range relevant for MRE investigations.
Introduction
The
viscoelastic
springpot
model
is
a
powerlaw
which
describes
the
mechanical
properties
of
many
biological
tissues
across
a
wide
range
of
frequencies.
The
model
provides
two
independent
parameters,
the
shear
modulus μ
(Pa)
and
a
powerlaw
exponent α
(dimensionless),
which
are
related
to
the
stiffness
and
dispersion
of
biological
soft
tissue,
respectively.
Springpot-based
viscoelastic
constants
have
been
reported
in-vivo
for
human
liver
with μ
= 4.63±0.91kPa
and α
= 0.27±0.01
and
human
brain
with μ
= 5.58±0.90kPa
and α
= 0.29±0.01.
1
This
study
is
motivated
by
the
need
for
phantom
materials
in
MRE
which
reproduce
the
viscoelastic
powerlaw
behavior
of
soft
tissue
in
a
wide
dynamic
range.
We
investigated
heparin
gel
and
polyacrylamide
as
viscoelastic
phantom-materials,
analyze
their
powerlaw
behavior
over
a
wide
frequency
range
and
compare
our
findings
with
a
commercially
available
phantom.
Methods
We
investigated heparin gel (180000 i.e./100g heparin-sodium,
Ratiopharm, Ulm, Germany) and two polymer network samples made of
polyacrylamides (PAAm): (i) linear PAAm, i.e. purely linear
polymerized PAAm (10 weight percent) and, (ii) crosslinked PAAm, i.e.
a composite gel, prepared from crosslinked PAAm polymerized in a
solution of linear polymerized PAAm (5%) and water (15, 64, and 14
weight percent, respectively). In
addition,
a
commercially
available
phantom,
CIRS
Model-049
phantom
(CIRS,
Norfolk,
Virginia,
USA)
was
investigated
for
its
matrix
stiffness,
neglecting
inclusions.
To
obtain
data
in
a
wide
dynamic
range
we
investigated
heparin
and
both
PAAm
samples
by
combining
experiments
from
three
modalities:
(i)
oscillatory
shear
rheometer
(MCR
301, Anton
Paar,
Austria)
for
0.08 to
80Hz,
(ii)
1.5-T-MRE
(Siemens
Sonata,
Siemens
Erlangen,
Germany)
for
50 to
200Hz
and,
(iii)
0.5-T
compact
tabletop
MRE,2,
for
200 up
to
3000Hz
dynamic
range.
Overall
a
wide
frequency
range
of
more
than
11 octaves
and three orders of magnitude was
covered.
For
both
MRE
systems,
harmonic
vibrations
were
excited
by
an
external
piezoelectric
driver
and
captured
by
motion
sensitive
phase-contrast
MRI
(see
figure
1). MRE
postprocessing
was
based
on
analytical
fits
of
shear
waves
in
order
to
avoid
discretization
artifacts
and
noise
biases
frequently
encountered
in
direct-inversion
MRE.3
The
complex
shear
modulus
G*
was
obtained
as
a
function
of
frequency
which
was
fitted
by
the
springpot
model.Results
Figures
2,3 show
the
measured shear modulus dispersion functions for heparin gel and both
PAAm polymer network samples including springpot fits demonstrating
the wide range of powerlaw behavior of heparin and crosslinked PAAm.
Deviations from the powerlaw at very low frequencies (< 1 Hz) are
expected since the springpot does not support static stress. In
contrast to heparin and crosslinked PAAm, linear PAAm, does not obey
a powerlaw since there G' and G'' intersect at approximately 100Hz.
The CIRS phantom (matrix) showed almost perfect elastic behavior with μ
= 5.82±0.20kPa and very low α
of 0.02±0.01. The measured viscoelastic constants are summarized in
table 1.Discussion
To
the
best
of
our
knowledge,
this
study
combines
for
the
first
time
low-dynamic
mechanical
tests
with
high-frequency
MRE
at
two
different
MRI
systems
in
order
to
investigate
the
viscoelastic
powerlaw
behavior
of
generic
gel
samples
over
more
than
11 octaves
and three orders of magnitude frequency
range.
While
heparin
and
crosslinked PAAm
feature
solid
powerlaw
behavior
from
10 to
1200Hz
and
1 to
3000Hz,
respectively,
linear PAAm
has
more
fluid
than
solid
properties
up
to
100Hz.
In contrast, the
CIRS-matrix
is
an
almost
perfect
rubber-like
solid
without
significant
loss
and
cannot
mimic
biological
soft
tissue
properties.
Deviations
from
the
powerlaw
behavior
at
very
low
frequencies
(< 1Hz)
are
expected
since
the
springpot
model
does
not
support
static
stress.
Ideally,
a
phantom
material
should
obey
perfect
powerlaw
behavior
with
an α-parameter
similar
to
that
observed
in
biological
tissues.
This
requirement
is
best
fulfilled
for
heparin
in
our
study.
However,
heparin
has
softer
properties
than
encountered
in
soft
in-vivo
tissues
such
as
the
liver
or
brain.
On
the
contrary,
crosslinked
PAAm
covers
a
similar
range
of
stiffness
as
measured
for
in-vivo
tissues,
however,
with
lower
dispersive
properties.
Nevertheless,
both
materials
are
good
candidates
for
the
use
as
standard
phantom
materials
in
MRE
since
both
have
well
predictable
springpot
properties
over
the
entire
frequency
range
relevant
for
MRE
investigations.
Conclusion
We
analyze
heparin,
PAAm
polymer
samples
and
a
standardized
CIRS
elastography
phantom
by
combining
shear
rheometry
with
MRE
in
a
clinical
system
and
a
benchtop
lab
system.
Dispersion
functions
in
a
wide
dynamic
range
up
to
11.8 octaves,
were
measured
and
analyzed
by
the
springpot
powerlaw
model.
Both,
heparin
and
crosslinked
PAAm
feature
solid
powerlaw
properties
with
suitable μ-
and α-parameter
ranges
for
comparison
to
soft
biological
matter.
Acknowledgements
No acknowledgement found.References
1.
Sack, I., et al.,
Structure-sensitive elastography: on the viscoelastic powerlaw behavior
of in vivo human tissue in health and disease. Soft Matter 2013, 9(24), 5672-5680
2.
Braun, J.,et al., A compact 0.5 T MR
elastography device and its application for studying viscoelasticity
changes in biological tissues during progressive formalin fixation. Magnetic Resonance in Medicine 2017.
3.
Yasar TK, Royston TJ, Magin RL., Wideband MR elastography for
viscoelasticity model identification. Magnetic resonance in medicine
2013;70(2):479-489.