Katz R, Cucinotta F A, Zhang C X
University of Nebraska, Lincoln 68588-0111, USA.
Nucl Instrum Methods Phys Res B. 1996 Feb;107(1-4):287-91. doi: 10.1016/0168-583x(95)01011-4.
The track structure model of heavy ion cross sections was developed by Katz and co-workers in the 1960s. In this model the action cross section is evaluated by mapping the dose-response of a detector to gamma rays (modeled from biological target theory) onto the radial dose distribution from delta rays about the path of the ion. This is taken to yield the radial distribution of probability for a "hit" (an interaction leading to an observable end-point). Radial integration of the probability yields the cross section. When different response from ions of different Z having the same stopping power is observed this model may be indicated. Since the 1960s there have been several developments in the computation of the radial dose distribution, in the measurement of these distributions, and in new radiobiological data against which to test the model. The earliest model, by Butts and Katz made use of simplified delta ray distribution functions, of simplified electron range-energy relations, and neglected angular distributions. Nevertheless it made possible the calculation of cross sections for the inactivation of enzymes and viruses, and allowed extension to tracks in nuclear emulsions and other detectors and to biological cells. It set the pattern for models of observable effects in the matter through which the ion passed. Here we outline subsequent calculations of radial dose which make use of improved knowledge of the electron emission spectrum, the electron range-energy relation, the angular distribution, and some considerations of molecular excitation, of particular interest both close to the path of the ion and the outer limits of electron penetration. These are applied to the modeling of action cross sections for the inactivation of several strains of E-coli and B. subtilis spores where extensive measurements in the "thin-down" region have been made with heavy ion beams. Such calculations serve to test the radial dose calculations at the outer limit of electron penetration. We lack data from which to test these calculations in regions close to the path of the ion aside from our earliest work on latent tracks in plastics, though it appears that the criterion then suggested for the threshold of track formation, of a minimal dose at a minimal distance (of about 20 angstroms, in plastics), remains valid.
重离子截面的径迹结构模型是由卡茨及其同事在20世纪60年代开发的。在这个模型中,作用截面是通过将探测器对伽马射线的剂量响应(根据生物靶理论建模)映射到围绕离子路径的δ射线的径向剂量分布上来评估的。这被用来得出“命中”(导致可观察到的终点的相互作用)的概率的径向分布。概率的径向积分得出截面。当观察到具有相同阻止本领的不同Z值离子有不同响应时,可能表明需要这个模型。自20世纪60年代以来,在径向剂量分布的计算、这些分布的测量以及用于检验该模型的新的放射生物学数据方面都有了一些进展。最早的模型,由巴茨和卡茨提出,使用了简化的δ射线分布函数、简化的电子射程-能量关系,并且忽略了角分布。然而,它使得计算酶和病毒失活的截面成为可能,并允许扩展到核乳胶和其他探测器以及生物细胞中的径迹。它为离子穿过的物质中可观察到的效应模型设定了模式。在这里,我们概述了随后对径向剂量的计算,这些计算利用了对电子发射光谱、电子射程-能量关系、角分布以及分子激发的一些考虑的改进知识,这些知识在离子路径附近和电子穿透的外极限处都特别重要。这些被应用于几种大肠杆菌和枯草芽孢杆菌孢子失活的作用截面建模,在“变薄”区域已经用重离子束进行了广泛的测量。这样的计算有助于检验电子穿透外极限处的径向剂量计算。除了我们最早关于塑料中潜径迹的工作外,我们缺乏在离子路径附近区域检验这些计算的数据,不过当时提出的关于径迹形成阈值的标准,即在最小距离(在塑料中约为20埃)处的最小剂量,似乎仍然有效。