Analytic and Monte Carlo calculations of dose-mean lineal energy for 1 MeV-1 GeV protons with application to radiation protection quality factor.

IF 1.5 4区 环境科学与生态学 Q3 BIOLOGY
Radiation and Environmental Biophysics Pub Date : 2025-03-01 Epub Date: 2025-02-10 DOI:10.1007/s00411-025-01110-w
Alexis Papadopoulos, Ioanna Kyriakou, Yusuke Matsuya, Miguel Antonio Cortés-Giraldo, Miguel Galocha-Oliva, Ianik Plante, Robert D Stewart, Ngoc Hoang Tran, Weibo Li, Ioannis A Daglis, Giovanni Santin, Petteri Nieminen, Sebastien Incerti, Dimitris Emfietzoglou
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引用次数: 0

Abstract

Radiation quality for determining biological effects is commonly linked to the microdosimetric quantity lineal energy ( y ) and to the dose-mean lineal energy ( y D ). Calculations of y D are typically performed by specialised Monte Carlo track-structure (MCTS) codes, which can be time-intensive. Thus, microdosimetry-based analytic models are potentially useful for practical calculations. Analytic model calculations of proton y D and radiation protection quality factor ( Q ) values in sub-micron liquid water spheres (diameter 10-1000 nm) over a broad energy range (1 MeV-1 GeV) are compared against MCTS simulations by PHITS, RITRACKS, and Geant4-DNA. Additionally, an improved analytic microdosimetry model is proposed. The original analytic model of Xapsos is refined and model parameters are updated based on Geant4-DNA physics model. Direct proton energy deposition is described by an alternative energy-loss straggling distribution and the contribution of secondary electrons is calculated using the dielectric formulation of the relativistic Born approximation. MCTS simulations of proton y D values using the latest versions of the PHITS, RITRACKS, and Geant4-DNA are reported along with the Monte Carlo Damage Simulation (MCDS) algorithm. The y D datasets are then used within the Theory of Dual Radiation Action (TDRA) to illustrate variations in Q with proton energy. By a careful selection of parameters, overall differences at the ~ 10% level between the proposed analytic model and the MCTS codes can be attained, significantly improving upon existing models. MCDS estimates of y D are generally much lower than estimates from MCTS simulations. The differences of Q among the examined methods are somewhat smaller than those of y D . Still, estimates of proton Q values by the present model are in better agreement with MCTS-based estimates than the existing analytic models. An improved microdosimetry-based analytic model is presented for calculating proton y D values over a broad range of proton energies (1 MeV-1 GeV) and target sizes (10-1000 nm) in very good agreement with state-of-the-art MCTS simulations. It is envisioned that the proposed model might be used as an alternative to CPU-intensive MCTS simulations and advance practical microdosimetry and quality factor calculations in medical, accelerator, and space radiation applications.

1 MeV-1 GeV质子剂量-平均线性能量的解析和蒙特卡罗计算及其辐射防护质量因子的应用。
用于确定生物效应的辐射质量通常与微剂量量线性能量(y)和剂量-平均线性能量(y D)有关。y - D的计算通常由专门的蒙特卡罗轨道结构(MCTS)代码执行,这可能会耗费大量时间。因此,基于微剂量学的分析模型在实际计算中具有潜在的实用性。分析模型计算了亚微米液态水球(直径10-1000 nm)在宽能量范围(1 MeV-1 GeV)下的质子y D和辐射防护质量因子(Q)值,并与PHITS、RITRACKS和Geant4-DNA的MCTS模拟结果进行了比较。此外,提出了一种改进的分析微剂量学模型。基于Geant4-DNA物理模型,对Xapsos原始分析模型进行了细化,并更新了模型参数。直接质子能量沉积用替代能量损失离散分布来描述,二次电子的贡献用相对论玻恩近似的介电公式来计算。使用最新版本的PHITS, RITRACKS和Geant4-DNA进行质子y -D值的MCTS模拟,并报道了蒙特卡罗损伤模拟(MCDS)算法。然后在双辐射作用理论(TDRA)中使用y D数据集来说明Q随质子能量的变化。通过仔细选择参数,所提出的分析模型与MCTS规范之间的总体差异在10%左右,显著改善了现有模型。MCDS对y D的估计值通常远低于MCTS模拟的估计值。检验方法之间Q的差异略小于y D的差异。尽管如此,与现有的分析模型相比,目前模型对质子Q值的估计更符合基于mcts的估计。提出了一种改进的基于微剂量学的分析模型,用于计算质子能量(1 MeV-1 GeV)和目标尺寸(10-1000 nm)范围内的质子y D值,与最先进的MCTS模拟非常吻合。设想所提出的模型可作为cpu密集型MCTS模拟的替代方案,并在医疗、加速器和空间辐射应用中推进实际微剂量学和质量因子计算。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.00
自引率
5.90%
发文量
53
审稿时长
>36 weeks
期刊介绍: This journal is devoted to fundamental and applied issues in radiation research and biophysics. The topics may include: Biophysics of ionizing radiation: radiation physics and chemistry, radiation dosimetry, radiobiology, radioecology, biophysical foundations of medical applications of radiation, and radiation protection. Biological effects of radiation: experimental or theoretical work on molecular or cellular effects; relevance of biological effects for risk assessment; biological effects of medical applications of radiation; relevance of radiation for biosphere and in space; modelling of ecosystems; modelling of transport processes of substances in biotic systems. Risk assessment: epidemiological studies of cancer and non-cancer effects; quantification of risk including exposures to radiation and confounding factors Contributions to these topics may include theoretical-mathematical and experimental material, as well as description of new techniques relevant for the study of these issues. They can range from complex radiobiological phenomena to issues in health physics and environmental protection.
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