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Authors Shen Y, Yan L, Shao X, Zhao B, Bai J, Lu W, Wang DJJ
Received 1 April 2018
Accepted for publication 4 May 2018
Published 3 July 2018 Volume 2018:13 Pages 3839—3852
DOI http://doi.org/10.2147/IJN.S169860
Checked for plagiarism Yes
Review by Single-blind
Peer reviewers approved by Dr Thiruganesh Ramasamy
Peer reviewer comments 3
Editor who approved publication: Prof. Dr. Thomas J Webster
Purpose: The purpose of this study was to investigate the feasibility and
sensitivity of cellular magnetic resonance imaging (MRI) with ferumoxytol
nanocomplex-labeled macrophages at ultrahigh magnetic field of 7 T.
Materials and methods: THP-1-induced macrophages were labeled using
self-assembling heparin + protamine + ferumoxytol nanocomplexes which were
injected into a gelatin phantom visible on both microscope and MRI.
Susceptibility-weighted imaging (SWI) and balanced steady-state free precession
(bSSFP) pulse sequences were applied at 3 and 7 T. The average, maximum
intensity projection, and root mean square combined images were generated for
phase-cycled bSSFP images. The signal-to-noise ratio and contrast-to-noise
ratio (CNR) efficiencies were calculated. Ex vivo experiments were then
performed using a formalin-fixed pig brain injected with ~100 and ~1,000
labeled cells, respectively, at both 3 and 7 T.
Results: A high cell labeling efficiency (>90%) was
achieved with heparin + protamine + ferumoxytol nanocomplexes. Less than 100
cells were detectable in the gelatin phantom at both 3 and 7 T. The 7 T data
showed more than double CNR efficiency compared to the corresponding sequences
at 3 T. The CNR efficiencies of phase-cycled bSSFP images were higher compared to
those of SWI, and the root mean square combined bSSFP showed the highest CNR
efficiency with minimal banding. Following co-registration of microscope and MR
images, more cells (51/63) were detected by bSSFP at 7 T than at 3 T (36/63).
On pig brain, both ~100 and ~1,000 cells were detected at 3 and 7 T. While the
cell size appeared larger due to blooming effects on SWI, bSSFP allowed better
contrast to precisely identify the of the cells with higher
signal-to-noise ratio efficiency.
Conclusion: The proposed cellular MRI with ferumoxytol
nanocomplex-labeled macrophages at 7 T has a high sensitivity to detect <100
cells. The proposed method has great translational potential and may have broad
clinical applications that involve cell types with a primary phagocytic
phenotype.
Keywords: ultrasmall
superparamagnetic iron oxide nanoparticles, ultrahigh field, balanced
steady-state free precession, cellular magnetic resonance imaging,
self-assembling nanocomplexes, 7 T
摘要视频链接:Phase-cycled bSSFP of
ferumoxxytol nanocomplex-labeled macrophages at 7T