Brodin N Patrik, Chen Yong, Yaparpalvi Ravindra, Guha Chandan, Tomé Wolfgang A
*Institute for Onco-Physics, Albert Einstein College of Medicine, Bronx, NY 10461; †Department of Radiation Oncology, Montefiore Medical Center, Bronx, NY 10461.
Health Phys. 2016 Feb;110(2 Suppl 1):S26-38. doi: 10.1097/HP.0000000000000462.
Shielded Cs irradiators are routinely used in pre-clinical radiation research to perform in vitro or in vivo investigations. Without appropriate dosimetry and irradiation protocols in place, there can be large uncertainty in the delivered dose of radiation between irradiated subjects that could lead to inaccurate and possibly misleading results. Here, a dosimetric evaluation of the JL Shepard Mark I-68A Cs irradiator and an irradiation technique for whole-body irradiation of small animals that allows one to limit the between subject variation in delivered dose to ±3% are provided. Mathematical simulation techniques and Gafchromic EBT film were used to describe the region within the irradiation cavity with homogeneous dose distribution (100% ± 5%), the dosimetric impact of varying source-to-subject distance, and the variation in attenuation thickness due to turntable rotation. Furthermore, an irradiation protocol and dosimetry formalism that allows calculation of irradiation time for whole-body irradiation of small animals is proposed that is designed to ensure a more consistent dose delivery between irradiated subjects. To compare this protocol with the conventional irradiation protocol suggested by the vendor, high-resolution film dosimetry measurements evaluating the dose difference between irradiation subjects and the dose distribution throughout subjects was performed using phantoms resembling small animals. Based on these results, there can be considerable variation in the delivered dose of > ± 5% using the conventional irradiation protocol for whole-body irradiation doses below 5 Gy. Using the proposed irradiation protocol this variability can be reduced to within ±3% and the dosimetry formalism allows for more accurate calculation of the irradiation time in relation to the intended prescription dose.
屏蔽式铯辐照仪常用于临床前辐射研究,以进行体外或体内研究。如果没有适当的剂量测定和辐照方案,辐照对象之间所接受的辐射剂量可能存在很大的不确定性,从而导致结果不准确甚至可能产生误导。本文提供了对JL Shepard Mark I - 68A铯辐照仪的剂量学评估以及一种用于小动物全身辐照的辐照技术,该技术可将辐照对象之间所接受剂量的变化限制在±3%以内。使用数学模拟技术和Gafchromic EBT薄膜来描述辐照腔内剂量分布均匀(100%±5%)的区域、源与对象距离变化的剂量学影响以及由于转台旋转导致的衰减厚度变化。此外,还提出了一种辐照方案和剂量学形式,用于计算小动物全身辐照的辐照时间,旨在确保辐照对象之间的剂量传递更加一致。为了将该方案与供应商建议的传统辐照方案进行比较,使用类似小动物的体模进行了高分辨率薄膜剂量学测量,评估辐照对象之间的剂量差异以及整个对象的剂量分布。基于这些结果,对于低于5 Gy的全身辐照剂量,使用传统辐照方案时,所传递的剂量可能存在>±5%的显著变化。使用所提出的辐照方案,这种变异性可降低至±3%以内,并且剂量学形式允许更准确地计算与预期处方剂量相关的辐照时间。