High resolution 3D in vivo mouse brain imaging at 9.4 T bruker MRI system

Author(s):  
C.S. Hamilton ◽  
Y. Ma ◽  
S.D. Smith ◽  
H. Benveniste
NeuroImage ◽  
2013 ◽  
Vol 83 ◽  
pp. 18-26 ◽  
Author(s):  
Dan Wu ◽  
Jiadi Xu ◽  
Michael T. McMahon ◽  
Peter C.M. van Zijl ◽  
Susumu Mori ◽  
...  

2008 ◽  
Vol 60 (2) ◽  
pp. 449-456 ◽  
Author(s):  
Niels Braakman ◽  
Thomas Oerther ◽  
Huub J.M. de Groot ◽  
A. Alia

2021 ◽  
Vol 8 (1) ◽  
Author(s):  
Julia G. Mannheim ◽  
Ju-Chieh (Kevin) Cheng ◽  
Nasim Vafai ◽  
Elham Shahinfard ◽  
Carolyn English ◽  
...  

Abstract Background The Siemens high-resolution research tomograph (HRRT - a dedicated brain PET scanner) is to this day one of the highest resolution PET scanners; thus, it can serve as useful benchmark when evaluating performance of newer scanners. Here, we report results from a cross-validation study between the HRRT and the whole-body GE SIGNA PET/MR focusing on brain imaging. Phantom data were acquired to determine recovery coefficients (RCs), % background variability (%BG), and image voxel noise (%). Cross-validation studies were performed with six healthy volunteers using [11C]DTBZ, [11C]raclopride, and [18F]FDG. Line profiles, regional time-activity curves, regional non-displaceable binding potentials (BPND) for [11C]DTBZ and [11C]raclopride scans, and radioactivity ratios for [18F]FDG scans were calculated and compared between the HRRT and the SIGNA PET/MR. Results Phantom data showed that the PET/MR images reconstructed with an ordered subset expectation maximization (OSEM) algorithm with time-of-flight (TOF) and TOF + point spread function (PSF) + filter revealed similar RCs for the hot spheres compared to those obtained on the HRRT reconstructed with an ordinary Poisson-OSEM algorithm with PSF and PSF + filter. The PET/MR TOF + PSF reconstruction revealed the highest RCs for all hot spheres. Image voxel noise of the PET/MR system was significantly lower. Line profiles revealed excellent spatial agreement between the two systems. BPND values revealed variability of less than 10% for the [11C]DTBZ scans and 19% for [11C]raclopride (based on one subject only). Mean [18F]FDG ratios to pons showed less than 12% differences. Conclusions These results demonstrated comparable performances of the two systems in terms of RCs with lower voxel-level noise (%) present in the PET/MR system. Comparison of in vivo human data confirmed the comparability of the two systems. The whole-body GE SIGNA PET/MR system is well suited for high-resolution brain imaging as no significant performance degradation was found compared to that of the reference standard HRRT.


2008 ◽  
Vol 35 (9) ◽  
pp. 3972-3978 ◽  
Author(s):  
M. W. DiFrancesco ◽  
J. M. Rasmussen ◽  
W. Yuan ◽  
R. Pratt ◽  
S. Dunn ◽  
...  
Keyword(s):  

2002 ◽  
Vol 120 (2) ◽  
pp. 203-209 ◽  
Author(s):  
O Natt ◽  
T Watanabe ◽  
S Boretius ◽  
J Radulovic ◽  
J Frahm ◽  
...  

1999 ◽  
Vol 7 (5) ◽  
pp. 526-532 ◽  
Author(s):  
R Frank Kooy ◽  
Edwin Reyniers ◽  
Marleen Verhoye ◽  
Jan Sijbers ◽  
Cathy E Bakker ◽  
...  

2020 ◽  
Vol 6 (15) ◽  
pp. eaaz9664 ◽  
Author(s):  
Wu Yuan ◽  
Defu Chen ◽  
Rachel Sarabia-Estrada ◽  
Hugo Guerrero-Cázares ◽  
Dawei Li ◽  
...  

Current minimally invasive optical techniques for in vivo deep-brain imaging provide a limited resolution, field of view, and speed. These limitations prohibit direct assessment of detailed histomorphology of various deep-seated brain diseases at their native state and therefore hinder the potential clinical utilities of those techniques. Here, we report an ultracompact (580 μm in outer diameter) theranostic deep-brain microneedle combining 800-nm optical coherence tomography imaging with laser ablation. Its performance was demonstrated by in vivo ultrahigh-resolution (1.7 μm axial and 5.7 μm transverse), high-speed (20 frames per second) volumetric imaging of mouse brain microstructures and optical attenuation coefficients. Its translational potential was further demonstrated by in vivo cancer visualization (with an imaging depth of 1.23 mm) and efficient tissue ablation (with a 1448-nm continuous-wave laser at a 350-mW power) in a deep mouse brain (with an ablation depth of about 600 μm).


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