AI Article Synopsis

  • Manganese-56 was a significant neutron-activated radionuclide released during the atomic bombings, contributing to radiation exposure in nearby areas.
  • The study focused on the spatial microdistribution of radiation doses in lung tissues exposed to 56Mn, highlighting the potential for elevated irradiation of alveoli and ducts.
  • Using the Monte Carlo simulation, researchers found a significant gradient in the absorbed dose in lung epithelial cells, indicating that low-energy electrons from 56Mn decay preferentially irradiate these cells.

Article Abstract

Manganese-56 (56Mn) was one of the dominant neutron-activated radionuclides during the first hours following the atomic-bombing of Hiroshima and Nagasaki. The radiation spectrum of 56Mn and the radiation emission from excited levels of 56Fe following 56Mn beta-decay include gamma-quanta, beta-particles, Auger electrons and X-rays. The dispersion of neutron activated 56Mn in the air can lead to entering of radioactive microparticles into the lungs. The investigation of spatial microdistribution of an internal dose in biological tissue exposed to 56Mn is an important matter with regards to the possible elevated irradiation of the lung alveoli and alveolar ducts. The Monte Carlo code (MCNP-4C) was used for the calculation of absorbed doses in biological tissue around 56Mn dioxide microparticles. The estimated absorbed dose has a very essential gradient in the epithelium cells of lung alveoli and alveolar duct: from 61 mGy/decay on the surface of simple squamous cells of epithelium to 0.15 mGy/decay at distance of 0.3 μm, which is maximal cell thickness. It has been concluded that epithelial cells of these pulmonary microstructures are selectively irradiated by low-energy electrons: short-range component of beta-particles spectrum and Auger electrons. The data obtained are important for the interpretation of biological experiments implementing dispersed neutron-activated 56Mn dioxide powder.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9377032PMC
http://dx.doi.org/10.1093/jrr/rrac023DOI Listing

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