Weronika Mazur1,2, Anna Stefańska-Bernatowicz2, Ewa Stodolak-Zych3, and Artur Tadeusz Krzyżak2
1Faculty of Physics and Applied Computer Science, AGH University of Science and Technology, Kraków, Poland, 2Faculty of Geology, Geophysics and Environmental Protection, AGH University of Science and Technology, Kraków, Poland, 3Faculty of Materials Science and Ceramics, AGH University of Science and Technology, Kraków, Poland
Synopsis
Anisotropic hydrogels has been attracting attention for biomedical purposes. These highly-hydrated materials have potential for tissue-mimicking and then, may serve for advanced medical imaging studies. In the work, we present two types of anisotropic hydrogels made from sodium alginate (NA) and polyvinyl alcohol (PVA) in the form of fiber bundle- a single component for larger phantom. We investigated their potential for diffusion-weighted imaging. NA-based phantoms are characterized by highly uniform diffusivity distribution, even higher then water. Single component turned out to be insufficient for the accurate quantification of the microstructure. PVA-based phantom exhibited desirable diffusion properties for tissue-mimicking.
INTRODUCTION
Hydrogels are highly hydrated polymers that has
been widely applied in biomedical engineering, in the isotropic and anisotropic
form as medium for cell culture or tissue engineering and potential use as
tissue substitute [1]. In recent years,
anisotropic hydrogels attracted attention in biomedical sciences, namely as
promising material to mimic anisotropic tissues [1]–[5]. Realistic, tissue-mimicking
phantoms, as well as periodic anisotropic phantoms are essential for
calibration procedures in medical imaging and protocol testing [2],[6]–[8]. Previously, we
presented several types of anisotropic phantoms with well-defined, capillary
and planar structures and their significant role in magnetic gradient field
calibration in diffusion-weighted (DWI) and diffusion tensor imaging (DTI) [6],[8],[9]. Although meaningful
and innovative, they bear a major drawback of advanced technology requirement
for their manufacturing from SiO2 and photonic fibers. This imposes
very high production costs. Here, we present a prototype of anisotropic,
biopolymer-based and polyvinyl alcohol-based phantoms for magnetic resonance
imaging applications. We investigated diffusion properties of polymeric fiber
bundle constituting a single component for a large, tissue-mimicking (e.g.
nervous or muscle) anisotropic phantom for the purpose of DWI/DTI calibration
and also for other MRI modalities.METHODS
Sodium alginate (NA;
NovaMatrix, Sandvika, Sweden) was chosen based on the test DWI experiments on
isotropic hydrogels samples (images not shown). Second phantom was made from
polyvinyl alcohol (PVA). Thin fibers were then obtained by wet-drawing method from
2%wt. NA crosslinked with calcium chloride and 6 wt.% polyvinyl alcohol (VRM
International PTE.LTD, India). Directional fiber alignment was obtained by
inserting a fiber bundle into a polypropylene tube to achieve tight filling.
The model was filled with ethyl alcohol (96%, POCh). Biopolymer fibers made
from NA showed smaller single fiber diameter (10-12 μm) and lower material
stiffness (E=0.54 MPa) than PVA fibers (fiber diameter of 15-18 μm and E=1.82 MPa).
The degree of crosslinking for biopolymer and PVA fibers equal to 40-60% and 65%,
respectively. Parallel arrangement of the fiber bundle allows the diameter of
the tube (to 92%) into which the medium in the form of ethanol has been
infiltrated to be filled for better durability of the fiber systems. DWI was
conducted on 0.6 T laboratory tomography system (Magritek, Aachen, Germany) using
spin-echo two-dimensional DWI in three orthogonal directions x, y, z (repetition time/echo time, TR/TE=10 s/56 ms; number
of scans, NoS=16 and FOV=40x60 mm2 for NA-based and NoS=8 and FOV=40x100
mm2 for PVA-based phantoms; slice thickness, ST= 2 mm; matrix=128x128; b-value=1000
s mm-1).RESULTS
We tested series of isotropic hydrogel samples and
chose 1% NA in the water medium, since having uniform and almost as high as
water’s diffusion coefficient (diffusion coefficients of water and 1% NA
hydrogel were Dwater=2.44±0.11∙10-3
mm2s-1 and D1% NA=2.272±0.059∙10-3
mm2s-1, respectively). NA-based component was very thin
and exhibited poor anisotropic properties in conducted DWI experiments (longitudinal
diffusivity did not stand out; Table 1,
Fig. 2). PVA-based phantom (Fig. 2) had significantly higher cross-section
diameter and revealed visibly demarked longitudinal (D||,PVA=Dz) and transversal component (D⊥,PVA=0.5(Dx+Dy); Table 1, Fig. 2).DISCUSSION
Isotropic
sample of 1% NA-water solution showed excellent diffusion coefficient uniformity
in the measured volume, slightly above two times higher than water. DWI was restricted
for anisotropic NA hydrogel by the very low resolution needed to capture such
small diameter of fiber bundle (Fig. 1). Thicker bundle or joined bundles will
be further considered. In PVA hydrogel D||,PVA/D⊥,PVA≈2.3 which meets the requirements for similarity to
tissues. Double mode in Dy may result from the placement method in
the black tube (bundle folded in half).CONCLUSION
Presented anisotropic hydrogels delivered
preliminary information on their microstructure visible in DWI. PVA-based phantom
is very stable in time and exhibit desirable diffusive properties. Considering
very high resolution used for NA-based phantom, it delivered reasonable data. Whereas
needs some manufacturing improvement, NA material seems to be promising
material for tissue-mimicking phantom with uniform properties. Presented data will serve for manufacturing methodology enhancement in order to approach an optimal setting for clinical applications.Acknowledgements
The work was financed by the Medical Research Agency (Contract No. 2020/ABM/01/00006-00). W.M. has been partly supported by the EU Project POWR.03.02.00-00-I004/16.References
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