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登陆火星任务:宇宙辐射剂量预测与宇航员剂量限制比较。

A Mission to Mars: Prediction of GCR Doses and Comparison with Astronaut Dose Limits.

机构信息

INFN, Sezione di Pavia, Via Bassi 6, 27100 Pavia, Italy.

Physics Department, University of Pavia, Via Bassi 6, 27100 Pavia, Italy.

出版信息

Int J Mol Sci. 2023 Jan 24;24(3):2328. doi: 10.3390/ijms24032328.

Abstract

Long-term human space missions such as a future journey to Mars could be characterized by several hazards, among which radiation is one the highest-priority problems for astronaut health. In this work, exploiting a pre-existing interface between the BIANCA biophysical model and the FLUKA Monte Carlo transport code, a study was performed to calculate astronaut absorbed doses and equivalent doses following GCR exposure under different shielding conditions. More specifically, the interface with BIANCA allowed us to calculate both the RBE for cell survival, which is related to non-cancer effects, and that for chromosome aberrations, related to the induction of stochastic effects, including cancer. The results were then compared with cancer and non-cancer astronaut dose limits. Concerning the stochastic effects, the equivalent doses calculated by multiplying the absorbed dose by the RBE for chromosome aberrations ("high-dose method") were similar to those calculated using the Q-values recommended by ICRP. For a 650-day mission at solar minimum (representative of a possible Mars mission scenario), the obtained values are always lower than the career limit recommended by ICRP (1 Sv), but higher than the limit of 600 mSv recently adopted by NASA. The comparison with the JAXA limits is more complex, since they are age and sex dependent. Concerning the deterministic limits, even for a 650-day mission at solar minimum, the values obtained by multiplying the absorbed dose by the RBE for cell survival are largely below the limits established by the various space agencies. Following this work, BIANCA, interfaced with an MC transport code such as FLUKA, can now predict RBE values for cell death and chromosome aberrations following GCR exposure. More generally, both at solar minimum and at solar maximum, shielding of 10 g/cm Al seems to be a better choice than 20 g/cm for astronaut protection against GCR.

摘要

长期载人航天任务,如未来的火星之旅,可能具有多种危害,其中辐射是宇航员健康的首要问题之一。在这项工作中,利用 BIANCA 生物物理模型和 FLUKA 蒙特卡罗输运代码之间现有的接口,研究了在不同屏蔽条件下 GCR 暴露后宇航员吸收剂量和当量剂量的计算。更具体地说,与 BIANCA 的接口允许我们计算细胞存活率的 RBE,这与非癌症效应有关,以及与随机效应诱导有关的染色体畸变的 RBE,包括癌症。然后将结果与癌症和非癌症宇航员剂量限制进行比较。关于随机效应,通过将吸收剂量乘以染色体畸变的 RBE 计算得到的当量剂量(“高剂量法”)与使用 ICRP 推荐的 Q 值计算得到的当量剂量相似。对于在太阳极小期(代表可能的火星任务场景)进行的 650 天任务,得到的值始终低于 ICRP 推荐的职业限制(1 Sv),但高于 NASA 最近采用的 600 mSv 限制。与 JAXA 限制的比较更为复杂,因为它们取决于年龄和性别。关于确定性限制,即使对于在太阳极小期进行的 650 天任务,通过将吸收剂量乘以细胞存活的 RBE 计算得到的值也大大低于各个空间机构设定的限制。在这项工作之后,BIANCA 与 FLUKA 等 MC 输运代码接口,现在可以预测 GCR 暴露后细胞死亡和染色体畸变的 RBE 值。更一般地说,无论是在太阳极小期还是太阳极大期,对于宇航员的 GCR 防护,10 g/cm Al 的屏蔽似乎比 20 g/cm Al 更好。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8eff/9916691/611e012f6f2e/ijms-24-02328-g001.jpg

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