Malaroda A, Flux G D, Buffa F M, Ott R J
Joint Dept. of Physics, Institute of Cancer Research and Royal Marsden Hospital, London, UK.
Cancer Biother Radiopharm. 2003 Jun;18(3):451-61. doi: 10.1089/108497803322285215.
A software package to investigate absorbed doses and dose-rates at the cellular and multicellular scale has been developed that considers two- and three-dimensional activity distributions and makes use of analytical representations of the point-dose kernels for (131)I, (32)P, and (90)Y. This software allows cell assemblies to be simulated by definition of the number, size, and geometry of cells and their nuclei, and radionuclide uptake can be specified to occur within the nucleus, the cytoplasm, at the membrane, or within the extracellular space. The software has been validated at a cellular scale by comparison with results obtained using spherical geometry, as found in the literature. At a multicellular scale, comparisons were made with a Monte Carlo simulation in voxel geometry. The software has been designed to work within a user-defined voxel geometry. This geometry is useful not only to simulate complex cell assemblies and realistic heterogeneous radionuclide distributions, but will also allow the use of histological and autoradiographic data. Absorbed dose distributions for a single cell calculated using this code varied significantly with activity localization within the cell, and to a lesser extent, with the cellular geometry. At a multicellular level, a two-dimensional heterogeneous activity distribution inferred from a two-dimensional image of a slice throughout a spheroid was used to calculate a dose-rate distribution. This resulted in a heterogeneous dose-rate delivery even for longer-range radionuclides such as (90)Y and (32)P.
已开发出一个软件包,用于研究细胞和多细胞尺度下的吸收剂量和剂量率。该软件包考虑二维和三维活度分布,并利用针对(131)I、(32)P和(90)Y的点剂量核的解析表达式。通过定义细胞及其细胞核的数量、大小和几何形状,该软件可以模拟细胞集合,并且可以指定放射性核素在细胞核、细胞质、细胞膜或细胞外空间内摄取。通过与文献中使用球形几何形状获得的结果进行比较,该软件已在细胞尺度上得到验证。在多细胞尺度上,与体素几何形状的蒙特卡罗模拟进行了比较。该软件设计为在用户定义的体素几何形状内运行。这种几何形状不仅有助于模拟复杂的细胞集合和实际的异质放射性核素分布,还将允许使用组织学和放射自显影数据。使用此代码计算的单个细胞的吸收剂量分布随细胞内活度定位的变化很大,在较小程度上也随细胞几何形状而变化。在多细胞水平上,从整个球体切片的二维图像推断出的二维异质活度分布用于计算剂量率分布。即使对于诸如(90)Y和(32)P等长程放射性核素,这也会导致剂量率传递的不均匀性。