...
首页> 外文期刊>Physics in medicine and biology. >A cell-based dosimetry model for radium-223 dichloride therapy using bone micro-CT images and GATE simulations
【24h】

A cell-based dosimetry model for radium-223 dichloride therapy using bone micro-CT images and GATE simulations

机译:使用骨微型CT图像和浇口模拟的镭-223二氯化钠治疗的基于细胞的剂量测定模型

获取原文
获取原文并翻译 | 示例
           

摘要

Dosimetry at the cellular level has outperformed macrodosimetry in terms of agreement with toxicity effects in clinical studies. This fact has encouraged dosimetry studies aiming to quantify the absorbed doses needed to reach radiotoxicity at the cellular level and to inform recommendations on the administration of radium-223. The aim of this work is to qualitatively and quantitatively evaluate the absorbed doses of radium-223 and the interactions of the doses at the cellular level. The analysis was performed by Monte Carlo simulations in GATE using micro-CT image of a mouse. Two physics lists available in the GATE code were tested. The influence of single and multiple scattering models on the absorbed dose distribution and number of particle hits was also studied. In addition, the fuzzy c-means clustering method was used for data segmentation. The segmentation method was suitable for these analyses, particularly given that it was unsupervised. There was no significant difference in the estimated absorbed dose between the two proposed physics lists. The absorbed dose values were not significantly influenced by scattering, although single scattering resulted in twice as many interactions as multiple scattering. The absorbed dose histogram at the voxel level shows heterogeneous absorbed dose values within each shell, but the observations from the graph of the medians were comparable to those in the literature. The interaction histogram indicates 104 events, although some voxels had no interactions with alpha particles. However, the voxels did not show absorbed doses capable of deterministic effects in the deepest part of the bone marrow. The absorbed dose distribution in images of mouse trabecular bone was compatible with simple geometric models, with absorbed doses capable of deterministic effects near the bone surface. The interaction distributions need to be correlated with in vivo studies for better interpretation.
机译:在临床研究中的毒性效应方面,细胞水平的剂量率在临床研究中的一致性方面表现优于宏观分子。这一事实鼓励了旨在量化在细胞水平下达到无抗毒性所需的吸收剂量的剂量测量的研究,并为镭〜223的施用提供信息。这项工作的目的是定性和定量地评估吸收的镭-223和剂量在细胞水平上的相互作用。使用鼠标的微型CT图像,通过蒙特卡罗模拟进行分析。测试栅极代码中可用的两个物理列表。还研究了单一散射模型对吸收剂量分布和颗粒命中​​数的影响。此外,模糊C-Means聚类方法用于数据分割。分段方法适用于这些分析,特别是考虑到它是无监督的分析。两种拟议物理列表之间的估计吸收剂量没有显着差异。由于单次散射导致多个散射产生两倍的相互作用,所吸收的剂量值没有显着影响。体素水平的吸收剂量直方图显示了每个壳体内的非均相吸收剂量值,但从中位数图的观察结果与文献中的相当。相互作用直方图表示104个事件,尽管一些体素没有与α粒子的相互作用。然而,体素没有显示出能够在骨髓最深部分中的确定性效果的吸收剂量。小梁骨骼图像中的吸收剂量分布与简单的几何模型相容,吸收剂量能够在骨表面附近的确定性效果。相互作用分布需要与体内研究相关,以便更好地解释。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号