Zhang M, Qin S, Haffty B, Yue N
The Cancer Institute of New Jersey, New Brunswick, NJ.
The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China.
Med Phys. 2012 Jun;39(6Part9):3704. doi: 10.1118/1.4735064.
In megavoltage external beam radiotherapy, in vivo cell experiments suggest GNP could be used as a radiosensitizer by having radiation dose enhancement factor (DEF) significantly larger than 1. However, Monte Carlo (MC) simulations published in the literature failed to give prove, in which most of them only simulated the interactions between the radiation beams and a single GNP. In this study, we built a multi-GNPs model considering possible spatial arrangements of GNPs relative to a cell to calculate the DEFs of GNPs.
Geant4 MC code with G4DNA physics model which can trace electrons down to eV level was used. Two types of geometry models representing different GNP-cell binding were created with each GNP modeled individually: (1) shell model with GNPs randomly and sparsely distributed in a shell in water mimicking when the GNPs were binding to the cell membrane, and (2) sphere model with GNPs randomly and sparsely distributed in a sphere in water mimicking when GNPs were floating inside the cytoplasm. Photon and electron spectrum at 5 cm in depth in water from a Varian 6MV beam was used as the radiation source. Dose to water inside the shell or the sphere representing cytoplasm were scored and compared to situations without GNPs to calculate the DEF. We also looked into the variation of DEFs due to different GNP sizes and concentrations.
A 35 um water cubic were successfully built in Geant4 with spatial resolution of 100 nm. Preliminary results shown under 200 keV electron irradiation, 100 nm GNPs in the shell model shown increased dose to cell at the beam entrance (DEF = 1.08).
The computation is undergoing for different GNP sizes and concentrations. Meaningful results are expected on the completion of this study.
在兆伏级外照射放疗中,体内细胞实验表明,由于金纳米颗粒(GNP)的辐射剂量增强因子(DEF)显著大于1,它可作为一种放射增敏剂。然而,文献中发表的蒙特卡罗(MC)模拟未能给出证明,其中大多数仅模拟了辐射束与单个GNP之间的相互作用。在本研究中,我们构建了一个多GNP模型,考虑GNP相对于细胞的可能空间排列,以计算GNP的DEF。
使用具有G4DNA物理模型的Geant4 MC代码,该模型可以将电子追踪到电子伏特水平。创建了两种代表不同GNP-细胞结合的几何模型,每个GNP都单独建模:(1)壳模型,GNP随机且稀疏地分布在水中的一个壳层中,模拟GNP与细胞膜结合的情况;(2)球体模型,GNP随机且稀疏地分布在水中的一个球体中,模拟GNP漂浮在细胞质内的情况。使用瓦里安6MV束在水中深度5cm处的光子和电子能谱作为辐射源。对代表细胞质的壳层或球体内水的剂量进行评分,并与没有GNP的情况进行比较,以计算DEF。我们还研究了由于不同GNP尺寸和浓度导致的DEF变化。
在Geant4中成功构建了一个边长为35μm的水立方,空间分辨率为100nm。初步结果表明,在200keV电子照射下,壳模型中的100nm GNP在束流入口处显示出对细胞的剂量增加(DEF = 1.08)。
正在针对不同的GNP尺寸和浓度进行计算。预计本研究完成时会得到有意义的结果。