O'Reilly Shannon E, DeWeese Lindsay S, Maynard Matthew R, Rajon Didier A, Wayson Michael B, Marshall Emily L, Bolch Wesley E
J Crayton Pruitt Family Department of Biomedical Engineering, University of Florida, Gainesville, FL, USA.
Department of Radiology, University of Florida, Gainesville, FL, USA.
Phys Med Biol. 2016 Dec 21;61(24):8794-8824. doi: 10.1088/1361-6560/61/24/8794. Epub 2016 Nov 29.
An image-based skeletal dosimetry model for internal electron sources was created for the ICRP-defined reference adult female. Many previous skeletal dosimetry models, which are still employed in commonly used internal dosimetry software, do not properly account for electron escape from trabecular spongiosa, electron cross-fire from cortical bone, and the impact of marrow cellularity on active marrow self-irradiation. Furthermore, these existing models do not employ the current ICRP definition of a 50 µm bone endosteum (or shallow marrow). Each of these limitations was addressed in the present study. Electron transport was completed to determine specific absorbed fractions to both active and shallow marrow of the skeletal regions of the University of Florida reference adult female. The skeletal macrostructure and microstructure were modeled separately. The bone macrostructure was based on the whole-body hybrid computational phantom of the UF series of reference models, while the bone microstructure was derived from microCT images of skeletal region samples taken from a 45 years-old female cadaver. The active and shallow marrow are typically adopted as surrogate tissue regions for the hematopoietic stem cells and osteoprogenitor cells, respectively. Source tissues included active marrow, inactive marrow, trabecular bone volume, trabecular bone surfaces, cortical bone volume, and cortical bone surfaces. Marrow cellularity was varied from 10 to 100 percent for active marrow self-irradiation. All other sources were run at the defined ICRP Publication 70 cellularity for each bone site. A total of 33 discrete electron energies, ranging from 1 keV to 10 MeV, were either simulated or analytically modeled. The method of combining skeletal macrostructure and microstructure absorbed fractions assessed using MCNPX electron transport was found to yield results similar to those determined with the PIRT model applied to the UF adult male skeletal dosimetry model. Calculated skeletal averaged absorbed fractions for each source-target combination were found to follow similar trends of more recent dosimetry models (image-based models) but did not follow results from skeletal models based upon assumptions of an infinite expanse of trabecular spongiosa.
针对国际辐射防护委员会(ICRP)定义的参考成年女性,创建了一个基于图像的内部电子源骨骼剂量学模型。许多先前的骨骼剂量学模型,仍被用于常用的内部剂量学软件中,没有恰当地考虑电子从小梁骨松质中的逸出、皮质骨的电子交叉照射以及骨髓细胞密度对活跃骨髓自身照射的影响。此外,这些现有模型没有采用ICRP当前对50微米骨内膜(或浅骨髓)的定义。本研究解决了上述每一个局限性。通过电子传输来确定佛罗里达大学参考成年女性骨骼区域对活跃骨髓和浅骨髓的特定吸收分数。分别对骨骼的宏观结构和微观结构进行建模。骨骼宏观结构基于UF系列参考模型的全身混合计算体模,而骨骼微观结构则源自取自一名45岁女性尸体的骨骼区域样本的显微CT图像。活跃骨髓和浅骨髓通常分别被用作造血干细胞和骨祖细胞的替代组织区域。源组织包括活跃骨髓、非活跃骨髓、小梁骨体积、小梁骨表面、皮质骨体积和皮质骨表面。对于活跃骨髓自身照射,骨髓细胞密度在10%至100%之间变化。所有其他源在每个骨部位按照ICRP第70号出版物定义的细胞密度运行。总共模拟或解析建模了33种离散电子能量,范围从1 keV到10 MeV。结果发现,使用MCNPX电子传输评估的结合骨骼宏观结构和微观结构吸收分数的方法,产生的结果与应用于UF成年男性骨骼剂量学模型的PIRT模型所确定的结果相似。发现每个源 - 靶组合的计算骨骼平均吸收分数遵循与最近的剂量学模型(基于图像的模型)相似的趋势,但不遵循基于小梁骨松质无限延伸假设的骨骼模型的结果。