期刊论文详细信息
Frontiers in Medicine
Low-Dose Imaging in a New Preclinical Total-Body PET/CT Scanner
article
Cesar Molinos1  Stuart Berr2  Carlos Correcher1  Ali Bahadur1  Ali A. Attarwala1  Simon Stark1  Sven Junge1  Uwe Himmelreich3  John O. Prior4  Kjell Laperre1  Sonica Van Wyk1  Todd Sasser1  Michael Heidenreich1  Phil Salmon1  Willy Gsell3  David Viertl4  James C. Massey2  Krzysztof Mińczuk2  Jie Li2  Bijoy K. Kundu2 
[1] Bruker BioSpin;Department of Radiology and Medical Imaging, University of Virginia, United States;MoSAIC;Department of Nuclear Medicine and Molecular Imaging, Lausanne University Hospital
关键词: preclinical;    imaging;    PET;    CT;    low dose;    [ 18 F]FDG;    oncology;    total-body;   
DOI  :  10.3389/fmed.2019.00088
学科分类:社会科学、人文和艺术(综合)
来源: Frontiers
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【 摘 要 】

Ionizing radiation constitutes a health risk to imaging scientists and study animals. Both PET and CT produce ionizing radiation. CT doses in pre-clinical in vivo imaging typically range from 50 to 1,000 mGy and biological effects in mice at this dose range have been previously described. [ 18 F]FDG body doses in mice have been estimated to be in the range of 100 mGy for [ 18 F]FDG. Yearly, the average whole body doses due to handling of activity by PET technologists are reported to be 3–8 mSv. A preclinical PET/CT system is presented with design features which make it suitable for small animal low-dose imaging. The CT subsystem uses a X-source power that is optimized for small animal imaging. The system design incorporates a spatial beam shaper coupled with a highly sensitive flat-panel detector and very fast acquisition (<10 s) which allows for whole body scans with doses as low as 3 mGy. The mouse total-body PET subsystem uses a detector architecture based on continuous crystals, coupled to SiPM arrays and a readout based in rows and columns. The PET field of view is 150 mm axial and 80 mm transaxial. The high solid-angle coverage of the sample and the use of continuous crystals achieve a sensitivity of 9% (NEMA) that can be leveraged for use of low tracer doses and/or performing rapid scans. The low-dose imaging capabilities of the total-body PET subsystem were tested with NEMA phantoms, in tumor models, a mouse bone metabolism scan and a rat heart dynamic scan. The CT imaging capabilities were tested in mice and in a low contrast phantom. The PET low-dose phantom and animal experiments provide evidence that image quality suitable for preclinical PET studies is achieved. Furthermore, CT image contrast using low dose scan settings was suitable as a reference for PET scans. Total-body mouse PET/CT studies could be completed with total doses of <10 mGy.

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