Molinos Cesar, Sasser Todd, Salmon Phil, Gsell Willy, Viertl David, Massey James C, Mińczuk Krzysztof, Li Jie, Kundu Bijoy K, Berr Stuart, Correcher Carlos, Bahadur Ali, Attarwala Ali A, Stark Simon, Junge Sven, Himmelreich Uwe, Prior John O, Laperre Kjell, Van Wyk Sonica, Heidenreich Michael
Bruker BioSpin, Preclinical Imaging, Ettlingen, Germany.
MoSAIC, KU Leuven, Leuven, Belgium.
Front Med (Lausanne). 2019 May 3;6:88. doi: 10.3389/fmed.2019.00088. eCollection 2019.
Ionizing radiation constitutes a health risk to imaging scientists and study animals. Both PET and CT produce ionizing radiation. CT doses in pre-clinical imaging typically range from 50 to 1,000 mGy and biological effects in mice at this dose range have been previously described. [F]FDG body doses in mice have been estimated to be in the range of 100 mGy for [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.
电离辐射对影像科学家和实验动物构成健康风险。正电子发射断层扫描(PET)和计算机断层扫描(CT)都会产生电离辐射。临床前成像中的CT剂量通常在50至1000毫戈瑞之间,此前已描述过该剂量范围内小鼠的生物学效应。小鼠体内[F]FDG的剂量估计在100毫戈瑞左右。据报道,PET技术人员每年因处理放射性活度而受到的平均全身剂量为3 - 8毫希沃特。本文介绍了一种临床前PET/CT系统,其设计特点使其适用于小动物低剂量成像。CT子系统使用了针对小动物成像优化的X射线源功率。该系统设计集成了一个空间束整形器,与一个高灵敏度平板探测器以及非常快速的采集(<10秒)相结合,这使得全身扫描的剂量可低至3毫戈瑞。小鼠全身PET子系统采用基于连续晶体的探测器架构,与硅光电倍增管(SiPM)阵列耦合,并基于行和列进行读出。PET视野轴向为150毫米,横向为80毫米。样品的高立体角覆盖以及连续晶体的使用实现了9%(美国电气和电子工程师协会标准)的灵敏度,可用于低示踪剂剂量和/或进行快速扫描。全身PET子系统的低剂量成像能力通过美国电气和电子工程师协会标准体模、肿瘤模型、小鼠骨代谢扫描和大鼠心脏动态扫描进行了测试。CT成像能力在小鼠和低对比度体模中进行了测试。PET低剂量体模和动物实验证明,可获得适用于临床前PET研究的图像质量。此外,使用低剂量扫描设置的CT图像对比度适合作为PET扫描的参考。全身小鼠PET/CT研究可以在总剂量<10毫戈瑞的情况下完成。