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Monte Carlo simulations of absorbed dose in a mouse phantom from 18-fluorine compounds

机译:蒙特卡洛模拟小鼠幻影中18种氟化合物的吸收剂量

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摘要

The purpose of this study was to calculate internal absorbed dose distribution in mice from preclinical small animal PET imaging procedures with fluorine-18 labeled compounds (18FDG, 18FLT, and fluoride ion). The GATE Monte Carlo software and a realistic, voxel-based mouse phantom that included a subcutaneous tumor were used to perform simulations. Discretized time-activity curves obtained from dynamic in vivo studies with each of the compounds were used to set the activity concentration in the simulations. For 18FDG, a realistic range of uptake ratios was considered for the heart and tumor. For each simulated time frame, the biodistribution of the radionuclide in the phantom was considered constant, and a sufficient number of decays were simulated to achieve low statistical uncertainty. Absorbed dose, which was scaled to take into account radioactive decay, integration with time, and changes in biological distribution was reported in mGy per MBq of administered activity for several organs and uptake scenarios. The mean absorbed dose ranged from a few mGy/MBq to hundreds of mGy/MBq. Major organs receive an absorbed dose in a range for which biological effects have been reported. The effects on a given investigation are hard to predict; however, investigators should be aware of potential perturbations especially when the studied organ receives high absorbed dose and when longitudinal imaging protocols are considered.
机译:这项研究的目的是通过使用氟18标记的化合物( 18 FDG, 18 FLT和氟化物)从临床前小动物PET成像程序计算小鼠体内的吸收剂量分布离子)。使用GATE Monte Carlo软件和包括皮下肿瘤的逼真的基于体素的小鼠体模进行模拟。从每种化合物的动态体内研究获得的离散时间-活性曲线用于在模拟中设置活性浓度。对于 18 FDG,考虑到心脏和肿瘤的实际摄取率范围。对于每个模拟的时间范围,人体模型中放射性核素的生物分布被认为是恒定的,并且模拟了足够数量的衰减以实现较低的统计不确定性。报告了吸收剂量,该吸收剂量被缩放以考虑到放射性衰变,与时间的积分以及生物分布的变化,在几个器官和摄取情况下,以每MBq施用活性的mGy为单位。平均吸收剂量范围从几mGy / MBq到数百mGy / MBq。主要器官接受的吸收剂量在报道的生物学效应范围内。对给定调查的影响很难预测。然而,研究人员应意识到潜在的干扰,特别是当被研究器官接受高吸收剂量并考虑纵向成像方案时。

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