Bitar A, Lisbona A, Thedrez P, Sai Maurel C, Le Forestier D, Barbet J, Bardies M
INSERM, U601, Nantes, F-44093, France.
Phys Med Biol. 2007 Feb 21;52(4):1013-25. doi: 10.1088/0031-9155/52/4/010. Epub 2007 Jan 23.
Murine models are useful for targeted radiotherapy pre-clinical experiments. These models can help to assess the potential interest of new radiopharmaceuticals. In this study, we developed a voxel-based mouse for dosimetric estimates. A female nude mouse (30 g) was frozen and cut into slices. High-resolution digital photographs were taken directly on the frozen block after each section. Images were segmented manually. Monoenergetic photon or electron sources were simulated using the MCNP4c2 Monte Carlo code for each source organ, in order to give tables of S-factors (in Gy Bq-1 s-1) for all target organs. Results obtained from monoenergetic particles were then used to generate S-factors for several radionuclides of potential interest in targeted radiotherapy. Thirteen source and 25 target regions were considered in this study. For each source region, 16 photon and 16 electron energies were simulated. Absorbed fractions, specific absorbed fractions and S-factors were calculated for 16 radionuclides of interest for targeted radiotherapy. The results obtained generally agree well with data published previously. For electron energies ranging from 0.1 to 2.5 MeV, the self-absorbed fraction varies from 0.98 to 0.376 for the liver, and from 0.89 to 0.04 for the thyroid. Electrons cannot be considered as 'non-penetrating' radiation for energies above 0.5 MeV for mouse organs. This observation can be generalized to radionuclides: for example, the beta self-absorbed fraction for the thyroid was 0.616 for I-131; absorbed fractions for Y-90 for left kidney-to-left kidney and for left kidney-to-spleen were 0.486 and 0.058, respectively. Our voxel-based mouse allowed us to generate a dosimetric database for use in preclinical targeted radiotherapy experiments.
小鼠模型对于靶向放射治疗的临床前实验很有用。这些模型有助于评估新放射性药物的潜在价值。在本研究中,我们开发了一种基于体素的小鼠用于剂量估算。将一只30克的雌性裸鼠冷冻后切成薄片。每切完一片后,直接在冷冻块上拍摄高分辨率数码照片。手动对图像进行分割。使用MCNP4c2蒙特卡罗代码为每个源器官模拟单能光子或电子源,以便给出所有靶器官的S因子表(单位为Gy Bq-1 s-1)。然后将从单能粒子获得的结果用于生成靶向放射治疗中几种潜在感兴趣的放射性核素的S因子。本研究考虑了13个源区域和25个靶区域。对于每个源区域,模拟了十六种光子能量和十六种电子能量。计算了靶向放射治疗中16种感兴趣的放射性核素的吸收分数、比吸收分数和S因子。所获得的结果总体上与先前发表的数据吻合良好。对于能量范围在0.1至2.5 MeV的电子,肝脏的自吸收分数在0.98至0.376之间变化,甲状腺的自吸收分数在0.89至0.04之间变化。对于小鼠器官,能量高于0.5 MeV的电子不能被视为“非穿透性”辐射。这一观察结果可以推广到放射性核素:例如,I-131的甲状腺β自吸收分数为0.616;Y-90从左肾到左肾以及从左肾到脾脏的吸收分数分别为0.486和0.058。我们基于体素的小鼠使我们能够生成一个剂量学数据库,用于临床前靶向放射治疗实验。