用蒙特卡罗模拟测定脑癌硼中子俘获治疗中的中子通量

F. Arianto, Liska Tri Handayani, W. Budi, P. Basuki
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引用次数: 0

摘要

硼中子俘获疗法(BNCT)是一种相对安全的杀死癌细胞的技术,其中一种是多形性胶质母细胞瘤。BNCT设备的主要组成部分之一是准直器,它作为超热中子粒子撞击癌细胞的出口点。除了实验方法外,BNCT的研究还可以通过建模进行,包括使用基于蒙特卡罗方法的MCNPX软件。本研究旨在确定ORNL MIRD幻象头中快中子和超热中子的通量分布以及快中子和γ击中靶癌细胞的剂量率。使用MCNPX软件建模有三个主要部分:单元卡、表面卡和数据卡。在数据卡上使用计数来计算中子通量。根据模拟结果计算,超热中子的通量为2.87 × 109 n/cm2.s。超热中子与快中子的剂量比为2.29 × 10-14 Gy.cm2/n。那么,低温辐射对γ的剂量率平衡为1.64 x 10-14 Gy。Cm2 /n,超热中子通量与热中子通量之比为0.004。在本研究中,细胞靶中击中靶癌细胞的超热中子通量在4 cm处减慢,在8 cm深度处能量转化为热中子。根据对结果的分析,可以得出结论,与癌组织相互作用的中子通量是热中子,而不是超热中子通量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Determination of Neutron Flux in Brain Cancer Boron Neutron Capture Therapy Using Monte Carlo Simulation
Boron Neutron Capture Therapy (BNCT) is a relatively safer technology for killing cancer cells, one of which is the Glioblastoma multiforme. One of the main components of the BNCT equipment is the collimator which functions as an exit point for epithermal neutron particles that hit cancer cells. In addition to the experimental method, BNCT research can be carried out by modeling, including using the MCNPX software based on the Monte Carlo Method. This research aimed to determine the flux distribution of fast and epithermal neutrons and the dose rate of fast neutrons and gamma that hit the target cancer cells in the phantom head of ORNL MIRD. Modeling using the MCNPX software has three main parts: cell cards, surface cards, and data cards. A tally is used on the data card to calculate the neutron flux. Based on the calculation of the modeling results, the flux of epithermal neutron is 2.87 x 109 n/cm2.s. The dose ratio of the epithermal to the fast neutron flux is 2.29 x 10-14 Gy.cm2/n. Then, the balance of the dose rate of the epithermal to the gamma is 1.64 x 10-14 Gy.cm2/n, and the ratio of epithermal to thermal neutron flux is 0.004. In this study, the epithermal neutron flux hitting the target cancer cells in cell target was moderated at 4 cm so that at a depth of 8 cm, the energy was converted into thermal neutrons. Based on the analysis of the results, it can be concluded that the neutron flux that will interact with cancer tissue is thermal neutrons, not epithermal neutron flux.
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