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Absorbed dose in target cell nuclei and dose conversion coefficient of radon progeny in the human lung

机译:人肺中靶细胞核的吸收剂量和of子体的剂量转换系数

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摘要

To calculate the absorbed dose in the human lung due to inhaled radon progeny, ICRP focussed on the layers containing the target cells, i.e., the basal and secretory cells. Such an approach did not consider details of the sensitive cells in the layers. The present work uses the microdosimetric approach and determines the absorbed alpha-particle energy in non-spherical nuclei of target cells (basal and secretory cells). The absorbed energy for alpha particles emitted by radon progeny in the human respiratory tract was calculated in basal- and secretory-cell nuclei, assuming conical and ellipsoidal forms for these cells. Distributions of specific energy for different combinations of alpha-particle sources, energies and targets are calculated and shown. The dose conversion coefficient for radon progeny is reduced for about 2 mSv/WLM when conical and ellipsoidal cell nuclei are considered instead of the layers. While changes in the geometry of secretory-cell nuclei do not have significant effects on their absorbed dose, changes from spherical to conical basal-cell nuclei have significantly reduced their absorbed dose from ~4 to ~3 mGy/WLM. This is expected because basal cells are situated close to the end of the range of 6 MeV alpha particles. This also underlines the significance of better and more precise information on targets in the T-B tree. A further change in the dose conversion coefficient can be achieved if a different weighting scheme is adopted for the doses for the cells. The results demonstrate the necessity for better information on the target cells for more accurate dosimetry for radon progeny.
机译:为了计算由于吸入ra子气而在人肺中吸收的剂量,ICRP着眼于包含靶细胞(即基底细胞和分泌细胞)的层。这种方法没有考虑层中敏感单元的细节。本工作使用微剂量法,并确定了靶细胞(基础细胞和分泌细胞)的非球形核中吸收的α粒子能量。假设ra细胞子代呈圆锥形和椭圆形,计算ra气后代在人呼吸道中释放的α粒子的吸收能。计算并显示了α粒子源,能量和目标的不同组合的比能分布。当考虑使用圆锥形和椭圆形细胞核代替层时,ra子代的剂量转换系数降低约2 mSv / WLM。尽管分泌细胞核的几何形状变化对其吸收剂量没有显着影响,但从球形基底细胞到圆锥形基底细胞核的变化已将其吸收剂量从约4 mGy / WLM显着降低。这是可以预期的,因为基础细胞位于6 MeVα粒子范围的末端附近。这也强调了在T-B树中获得更好,更精确的目标信息的重要性。如果对细胞的剂量采用不同的加权方案,则可以实现剂量转换系数的进一步变化。结果证明有必要在靶细胞上获得更好的信息,以更准确地测定ra子体的剂量。

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