Canadian Nuclear Laboratories, Chalk River, Canada.
McGill University, Montreal, Canada.
Radiat Res. 2023 Aug 1;200(2):162-175. doi: 10.1667/RADE-23-00023.1.
Previous publications describe the estimation of the dose from ionizing radiation to the whole lens or parts of it but have not considered other eye tissues that are implicated in cataract development; this is especially critical for low-dose, low-ionizing-density exposures. A recent review of the biological mechanisms of radiation-induced cataracts showed that lenticular oxidative stress can be increased by inflammation and vascular damage to non-lens tissues in the eye. Also, the radiation oxygen effect indicates different radiosensitivities for the vascular retina and the severely hypoxic lens. Therefore, this study uses the Monte Carlo N-Particle simulations to quantify dose conversion coefficients for several eye tissues for incident antero-posterior exposure to electrons, photons, and neutrons (and the tertiary electron component of neutron exposure). A stylized, multi-tissue eye model was developed by modifying a model by Behrens etal. (2009) to include the retina, uvea, sclera, and lens epithelial cell populations. Electron exposures were simulated as a single eye, whereas photon and neutron exposures were simulated employing two eyes embedded in the ADAM-EVA phantom. For electrons and photons, dose conversion coefficients are highest for either anterior tissues for low-energy incident particles or posterior tissues for high-energy incident particles. Neutron dose conversion coefficients generally increase with increasing incident energy for all tissues. The ratio of the absorbed dose delivered to each tissue to the absorbed dose delivered to the whole lens demonstrated the considerable deviation of non-lens tissue doses from lens doses, depending on particle type and its energy. These simulations demonstrate that there are large variations in the dose to various ocular tissues depending on the incident radiation dose coefficients; this large variation will potentially impact cataract development.
先前的出版物描述了对整个晶状体或其部分的电离辐射剂量的估计,但没有考虑到其他与白内障发展有关的眼部组织;这对于低剂量、低电离密度的辐射暴露尤其重要。最近对辐射诱导白内障的生物学机制的综述表明,晶状体的氧化应激可以通过眼部非晶状体组织的炎症和血管损伤而增加。此外,辐射氧效应表明,血管视网膜和严重缺氧的晶状体对辐射的敏感性不同。因此,本研究使用蒙特卡罗 N-粒子模拟来量化几种眼部组织对前-后向电子、光子和中子(以及中子暴露的三级电子成分)入射的剂量转换系数。通过修改 Behrens 等人的模型(2009 年),开发了一种多组织的眼部简化模型,该模型包括视网膜、葡萄膜、巩膜和晶状体上皮细胞群体。模拟电子暴露时,采用单个眼睛;而模拟光子和中子暴露时,则采用嵌入 ADAM-EVA 体模中的两个眼睛。对于电子和光子,低能入射粒子的前组织或高能入射粒子的后组织的剂量转换系数最高。对于所有组织,中子剂量转换系数通常随入射能量的增加而增加。每个组织的吸收剂量与整个晶状体的吸收剂量之比表明,非晶状体组织的剂量与晶状体剂量存在很大偏差,这取决于粒子类型及其能量。这些模拟表明,根据入射辐射剂量系数,各种眼部组织的剂量存在很大差异;这种大的变化可能会影响白内障的发展。