Hanne Vanduffel1, Nick Arango2, Willy Gsell1, Uwe Himmelreich3, Wim Vanduffel1, Cesar Parra1, Berkin Bilgic4, Clarissa Cooley4, Dimitios Sakellariou1, Rodrigo de Oliviera SIlva1, Lawrence Wald4, Rob Ameloot1, and Jason Stockmann4
1KULeuven, Leuven, Belgium, 2MIT, Cambridge, MA, United States, 3KULeuven, 3000, Belgium, 4Martinos Center, Charlestown, MA, United States
Synopsis
Keywords: Shims, High-Field MRI
We present a new method for passive shimming based on 3D printed ferromagnetic inks that are fully compatible with the scanner RF coils. We show simulated B0 shim performance for designs that are optimized to shim the human brain for both a subject-specific passive shim insert and a robust general insert.
Introduction
Subject-specific local B0
inhomogeneities degrade the geometric fidelity of MR images and introduce
signal voids, banding, and other artifacts.[1]-[6] Active shims, which use sets of coils
driven by typically, can only compensate B0 field up to 2nd
order.[7] Dedicated multi-coil shim arrays have
been shown to effectively shim up to 6th-order inhomogeneities.[8]-[12] However, these approaches can potentially interfere with the performance of RF Tx and Rx coils
and take up scarce bore space. Alternatively, passive B0 shimming exploits the
strategic placement of ferro-, dia- and paramagnetic materials for field
shaping purposes.[13-[19] But the fabrication of
subject-specific passive shim configurations is a manually intensive,
error-prone and time-consuming process with limited efficacy for field
correction, leading to limited adoption in the MR community. Ideally, a method can
be developed that allows for the fully-automated fabrication of passive shim
inserts that do not interfere with RF performance but have enough magnetic
susceptibility to compensate for nuisance B0 fields in the brain.
Our research explores the use of binder-jetting
3D printing to overcome the limitations of traditional passive shim
configurations for brain imaging.[20] We embed small amounts of iron oxide
nanoparticles in 3D-printed housing materials. The iron oxide is coated in a
surfactant that limits the conductivity of the finished material, thus reducing
interactions with RF fields. Methods
3D printing
A binder-jetting 3D printer (10"x15"x8"
build volume, 600x540dpi, 0.004" layer resolution, 0.020" minimum
feature size; DOD-thermal HP11-printheads;
Projet 660 3DSystems) was modified to allow the printing
of custom inks and build material (Figure 1). A polymer-powder-polymethyl-methacrylate
(dp= 50 μm BS150N) was used as build material in combination with a magnetic
ink (MICR, VersaInk-Nano Black, dp = 50 nm, containing 30 wt% of magnetite
nanoparticles). The binder ink consists of a 2:1 volume ratio of acetophenone and butanone and 25 mg mL−1 of N-octadecylsuccinic
anhydride (TCI Europe).
The passive shim geometry was
designed as a close-fitting helmet-liner that fits inside a 1Tx/32Rx
7T Nova Medical coil (Figure 2). A quadratic programming algorithm minimizes
the RMSE of the predicted B0 field and input in vivo B0
maps using the sensitivity matrix (including 0th-2nd-order
scanner shims and 2144 3x3x3mm passive shim voxels), under the constraints that
0-100% of ferromagnetic ink can be printed per CAD voxel. The calculated
correction values are converted to a printable VRML CAD format that contains the
RGB grayscale value required in each CAD voxel to achieve the targeted B0
distribution in the brain (Figure 3). To make the passive shim design robust across
different subjects, the optimized grayscale RGB distribution within the CAD
geometry is determined by the RGB average of shim geometries derived from 5 in
vivo shimmed B0 maps (obtained from the open-source Human Connectome
database).[21][22]
To test RF performance, a felt liner
was homogeneously impregnated with 5 ml of the ferromagnetic ink (corresponding
to three times more ink than the calculated CAD PS helmet ink volume). The
liner was placed inside Nova Medical RF
array to image an anthropomorphic head phantom. SNR maps and flip angle maps were
acquired on the phantom before with and without the
liner.[23][24][25] The unloaded quality factor (Qu)
of a tuned RF receive loop for the two cases was measured on the lab bench with
a double probe. Finally, a spin echo
sequence was run at 100% SAR for 10 minutes, and an infrared camera was used to
measure the temperature before and after.Results
Figure 4 shows minimal impact of the
felt liner on RF Rx and Tx performance. Bench measurements of Qu of Rx loop
show insignificant changes on the order of 1-3%. No temperature change was detected
during the heating test.
B0 simulations comparing the baseline 0th-2nd shims
to the subject-specific 3D printed passive shim insert for 5 subjects show a
45% average improvement in the standard deviation of B0. Figure 5 shows the simulated
B0 maps for the baseline, subject-specific passive and general passive shim cases
for subject #1. Discussion
RF evaluation suggests
that the low conducitivity of the ferromagnetic ink make it minimally disruptive
to the scanner’s RF performance. The preliminary B0 shimming simulations show
significant gains for 3D printed subject-specific passive shim inserts. In
future work we will explore the possibility of using the 3D printed passive
shim insert as the inner helmet surface of the RF coil itself, to economize on space
close to the head. To make this approach to shimming clinically relevant, we will
refine our optimization methods to imrpove robustness of the shim design across
a broad range of subject brains. Optimization and CAD design software are available at https://rflab.martinos.org/.Acknowledgements
The authors acknowledge the support of
NIH (R01EB028797), the KULeuven (Project. No. IDN/20/016, C14/21/111 and C3/21/027),
the Research Foundation—Flanders (FWO SB Grant No. 1SB8519N), the European
Commission for H2020 INSPiRE-Med (Grant No. 813120) and Innovation Human Brain
Project SGA3 (Grant No. 945539).
Data were provided in part by the
Human Connectome Project, WU-Minn Consortium (Principal Investigators: David
Van Essen and Kamil Ugurbil; 1U54MH091657).References
[1] K. Wachowicz, Res.
Reports Nucl. Med. 2014, 1.
[2] J. P. Stockmann, L. L.
Wald, Neuroimage 2018, 168, 71.
[3] C. Juchem, R. A. de Graaf,
Anal. Biochem. 2017, 529, 17.
[4] P. Jezzard, F. Centre, J.
R. Hospital, O. Ox, n.d., 0.
[5] K. M. Koch, X.
Papademetris, D. L. Rothman, R. A. De Graaf, Phys. Med. Biol. 2006,
51, 6381.
[6] D. F. Hillenbrand, K. M.
Lo, W. F. B. Punchard, T. G. Reese, Rev. Lit. Arts Am. 2005, 4.
[7] C. J. Wiggins, C. Choi, Y.
Li, A. P. Lin, S. B. Thakur, E. M. Ratai, Magn. Reson. Mater. Physics, Biol.
Med. 2021, 34, 179.
[8] B. Pinho Meneses, J. P.
Stockmann, N. Arango, P. F. Gapais, E. Giacomini, F. Mauconduit, V. Gras, N.
Boulant, A. Vignaud, M. Luong, A. Amadon, Neuroimage 2022, 261,
119498.
[9] B. P. Meneses, A. Amadon, Phys.
Med. Biol. 2021, 66, DOI 10.1088/1361-6560/abc810.
[10] F. Jia, H. Elshatlawy, A.
Aghaeifar, Y. H. Chu, Y. C. Hsu, S. Littin, S. Kroboth, H. Yu, P. Amrein, X.
Gao, W. Yang, P. LeVan, K. Scheffler, M. Zaitsev, Magn. Reson. Med. 2020,
83, 1442.
[11] N. Arango, J. Stockmann, E.
Adalsteinsson, J. White, Int. Soc. Magn. Reson. Med. 2019, 1462.
[12] J. P. Stockmann, T. Witzel,
B. Keil, J. R. Polimeni, A. Mareyam, C. Lapierre, K. Setsompop, L. L. Wald, Magn.
Reson. Med. 2016, 75, 441.
[13] F. Liu, J. Zhu, L. Xia, S.
Crozier, 2011, 21, 60.
[14] K. M. Koch, P. B. Brown, D.
L. Rothman, R. A. de Graaf, J. Magn. Reson. 2006, 182, 66.
[15] K. M. Koch, P. M. Brown, D.
L. Rothman, R. A. De Graaf, 2006, 972, 2006.
[16] A. Bungert, C. D. Chambers,
M. Phillips, C. J. Evans, Neuroimage 2012, 59, 2167.
[17] M. Bekiesińska-Figatowska, Polish
J. Radiol. 2015, 80, 93.
[18] J. L. Wilson, P. Jezzard, 2003,
1094, 1089.
[19] Jesmanowicz, 2001, 9,
2001.
[20] T. D. Ngo, A. Kashani, G.
Imbalzano, K. T. Q. Nguyen, D. Hui, Compos. Part B Eng. 2018, 143,
172.
[21] D. C. Van Essen, K.
Ugurbil, E. Auerbach, D. Barch, T. E. J. Behrens, R. Bucholz, A. Chang, L.
Chen, M. Corbetta, S. W. Curtiss, S. Della Penna, D. Feinberg, M. F. Glasser,
N. Harel, A. C. Heath, L. Larson-Prior, D. Marcus, G. Michalareas, S. Moeller,
R. Oostenveld, S. E. Petersen, F. Prior, B. L. Schlaggar, S. M. Smith, A. Z.
Snyder, J. Xu, E. Yacoub, Neuroimage 2012, 62, 2222.
[22] D. S. Marcus, J. Harwell,
T. Olsen, M. Hodge, M. F. Glasser, F. Prior, M. Jenkinson, T. Laumann, S. W.
Curtiss, D. C. Van Essen, Front. Neuroinform. 2011, 5, 1.
[23] P. Kellman, E. R. McVeigh, Magn.
Reson. Med. 2005, 54, 1439.
[24] S. Chung, D. Kim, E.
Breton, L. Axel, Magn. Reson. Med. 2010, 64, 439.
[25] B. Guérin, J. P. Stockmann,
M. Baboli, A. Torrado-Carvajal, A. V. Stenger, L. L. Wald, Magn. Reson. Med.
2016, 76, 540.