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水在 LiPCDA 单体晶体结构中的作用及 EBT-3 胶片放射治疗剂量响应。

Role of water in the crystal structure of LiPCDA monomer and the radiotherapy dose response of EBT-3 film.

机构信息

Department of Physics and Astronomy, York University, Toronto, Canada.

TECHNA Institute, University Health Network, Toronto, Canada.

出版信息

Med Phys. 2022 May;49(5):3470-3480. doi: 10.1002/mp.15597. Epub 2022 Mar 29.

Abstract

PURPOSE

Radiochromic material used in recent commercial films has been suggested as a candidate for in vivo dosimetry because of its dose sensitivity, real-time response, and atomic composition. It was observed that its sensitive material, lithium pentacosa-10,12-diynoate (LiPCDA), can have two distinct forms, with main absorbance peaks at ∼635 and ∼674 nm. The spectrum of the latter is similar to that of pentacosa-10,12-diynoic acid (PCDA) used in the commercial predecessor, obtained through desiccation of the commercial film. Water was suggested to be a part of the crystal structure and thus its presence or absence would affect dosimetric parameters. The objective of this study is to: (a) investigate how desiccated commercial films compared to the native form in terms of macroscopic crystal structure, dose-response, signal linearity, and post-exposure kinetics; (b) demonstrate proof-of-concept that the two versions can be combined into one optical dosimeter and measured simultaneously.

METHODS

Commercial radiochromic film, EBT-3, was desiccated for 10 days at 45°C. Using a 6 MV LINAC beam and standard setup of 100 Source to Axis Distance (SAD), 10 cm × 10 cm field size, and 1.5 cm depth, commercial and desiccated films were irradiated to 50, 100, 200, 500, 1000, 2000, 3000 cGy and the latter to 4000, 5000, and 7000 cGy. A custom phantom equipped with optical fibers for real-time read-out was used for all measurements. Absorbance spectra were collected at ∼1 Hz before, during, and after irradiation. Data were collected for ∼1 h after the end of irradiation for 200 cGy experiments. The radiation-induced change in optical density (∆OD) was calculated with a 10 nm band around the primary absorbance peak. The post-exposure percent optical density change was calculated and compared to ∆OD at the end of irradiation. Both commercial and desiccated films were also irradiated and measured simultaneously as proof-of-concept for using two materials within one optical path. For electron microscopy imaging, active materials from commercial and desiccated films were imaged on a scanning electron microscope at an accelerating voltage of 10 kV.

RESULTS

Scanning electron microscope images showed that desiccated film was similar in topographical structure to the commercial EBT-3 form. It maintained a non-linear ∆OD with dose but resulted in ∼1/3 signal compared to the commercial film. Evaluation of post-exposure response showed significantly lower percent increase in ∆OD for desiccated film initially, with no statistically significant difference at 1 h after the end of irradiation. Combining both films and simultaneously measuring their absorbance illustrated that the two absorbance peaks were identifiable and resolvable to allow for an independent determination of dose from each.

CONCLUSIONS

Water is implicated in the crystal structure of the EBT-3 radiochromic film, with its removal through desiccation affecting both dosimetric and spectroscopic characteristics of the material. The two forms of radiochromic material (with and without water) are spectrally resolvable allowing for independent dose determination from each, opening up possibilities for dose measurements at different locations along a single fiber.

摘要

目的

由于其剂量敏感性、实时响应和原子组成,最近商业胶片中使用的放射性变色材料被认为是体内剂量测定的候选材料。有人观察到,其敏感材料,五倍半-10,12-二炔酸锂(LiPCDA),可以有两种不同的形式,主要吸收峰在约 635nm 和 674nm。后者的光谱类似于商业前体中使用的五倍半-10,12-二炔酸(PCDA),通过商业胶片的干燥获得。有人认为水是晶体结构的一部分,因此其存在与否会影响剂量学参数。本研究的目的是:(a)研究干燥的商业胶片与天然形式在宏观晶体结构、剂量响应、信号线性和曝光后动力学方面的差异;(b)证明这两种形式可以结合到一个光学剂量计中并同时测量。

方法

将商用放射性变色胶片 EBT-3 在 45°C 下干燥 10 天。使用 6MV LINAC 光束和标准设置(100 源至轴距离(SAD)、10cm×10cm 射野大小和 1.5cm 深度),对商用和干燥胶片进行 50、100、200、500、1000、2000、3000cGy 的照射,并对后者进行 4000、5000 和 7000cGy 的照射。使用配备光纤的定制体模进行所有测量,以进行实时读取。在照射前后约 1Hz 时收集吸光度谱。在照射结束后约 1 小时内收集数据,以进行 200cGy 实验。用 10nm 带宽围绕主要吸收峰计算辐射引起的光密度变化(∆OD)。计算曝光后的光密度变化百分比,并与照射结束时的 ∆OD 进行比较。还同时对商用和干燥胶片进行了照射和测量,以证明在一个光学路径中同时使用两种材料的可行性。对于电子显微镜成像,用 10kV 加速电压在扫描电子显微镜上对商用和干燥胶片的活性材料进行成像。

结果

扫描电子显微镜图像显示,干燥的胶片在形貌结构上与商用 EBT-3 形式相似。它保持了与剂量的非线性 ∆OD,但与商用胶片相比,信号降低了约 1/3。对曝光后响应的评估表明,干燥胶片的初始 ∆OD 百分比增加明显较低,照射结束后 1 小时后无统计学差异。同时测量两种胶片并同时测量它们的吸光度表明,两个吸收峰是可分辨的,允许从每个峰独立确定剂量。

结论

水被认为是 EBT-3 放射性变色胶片晶体结构的一部分,通过干燥去除水会影响材料的剂量学和光谱特性。两种形式的放射性变色材料(有和没有水)在光谱上是可分辨的,允许从每个峰独立确定剂量,为在单个光纤的不同位置进行剂量测量开辟了可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f74/9314119/bb7c45c9d56a/MP-49-3470-g005.jpg

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