What is a 'low dose' of radiation?

V P Bond, L E Feinendegen, J Booz
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引用次数: 42

Abstract

Although the expression of radiation-induced biological effects and responses may be at either the cell, organ or organism level, induction of some of these phenomena (e.g. cancer of clastogenic and genetic effects) can have their origin in the interaction of a single charged particle with the target-containing volume (TCV) of the cell, e.g. the cell nucleus. However, the independent variable now used in both organ and cell population studies, the absorbed dose to the organ, provides no information directly on particle-TCV interactions. Even if calculated as a mean to an organized population of cells, the absorbed dose becomes a composite and confounded quantity, (FzN), in which F is the fraction of TCVs 'hit' by a particle during a given exposure, z is the mean value of z1, the energy absorbed in the TCV in a single hit, and N is the mean number of hits per affected TCV. Scientific precepts demand the avoidance of such confounded variables by achieving their isolation. The needed separation can be effected by the use of microdosimetric techniques, which make it possible to hold one component quantity constant while the others are varied. As an example, low-level radiation exposure (LLE) can be used to hold F at a constant value of 0.2 where, on average, there is but one hit per TCV. The probability of a cellular quantal response, as a function of z1 only, can then be determined by use of LLE to radiations covering a wide span of LETs. Conversely, the effect of varying only the fraction of cells hit can be studied by holding z constant. This can be accomplished by working within a narrow band of LET, but only in the LLE range. The effectiveness of preirradiation altering cell sensitivity as a function of the number of hits per TCV can be determined by working within, and somewhat above, the LLE range. In either risk assessment or the application of radiation as a pretreatment, minimal consequences can be assured only if very low-level exposure is employed in order that F will be small, and if the exposure is in a field of radiation of very low LET so that z1 will be as small as possible. That is to say, exposure conditions with low consequences cannot be specified in terms of any single quantity.

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什么是“低剂量”辐射?
虽然辐射诱导的生物效应和反应可能在细胞、器官或有机体水平上表达,但其中一些现象(如致裂癌和遗传效应)的诱导可能源于单个带电粒子与细胞(如细胞核)的靶体积(TCV)的相互作用。然而,目前在器官和细胞群体研究中使用的自变量,即器官的吸收剂量,并不能直接提供颗粒- tcv相互作用的信息。即使作为有组织细胞群体的平均值计算,吸收剂量也成为一个复合和混淆量(FzN),其中F是给定暴露期间粒子“击中”的TCV的分数,z是单次击中TCV中吸收的能量z1的平均值,N是每个受影响的TCV的平均击中数。科学规范要求通过隔离这些混杂变量来避免它们。所需的分离可以通过使用微剂量技术来实现,微剂量技术可以使一种成分的量保持不变,而其他成分的量是变化的。例如,低水平辐射暴露(LLE)可用于将F保持在0.2的恒定值,其中平均每个TCV只有一次撞击。细胞量子响应的概率仅作为z1的函数,然后可以通过使用LLE来确定覆盖宽let范围的辐射。相反,通过保持z恒定,可以研究仅改变被击中细胞的比例的影响。这可以通过在LET的窄频带内工作来实现,但只能在LLE范围内。通过在LLE范围内或略高于LLE范围内工作,可以确定辐照前改变细胞灵敏度的有效性作为每个TCV命中次数的函数。在风险评估或辐射作为预处理的应用中,只有采用极低水平的照射以使F变小,并且在极低LET的辐射场中照射以使z1尽可能小,才能保证最小的后果。也就是说,低后果的暴露条件不能用任何单一的量来表示。
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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