Dartmouth College, Thayer School of Engineering, Hanover, New Hampshire, United States.
Dartmouth College, Geisel School of Medicine, Department of Medicine, Hanover, New Hampshire, United States.
J Biomed Opt. 2023 Mar;28(3):036005. doi: 10.1117/1.JBO.28.3.036005. Epub 2023 Mar 13.
High-energy x-ray delivery from a linear accelerator results in the production of spectrally continuous broadband Cherenkov light inside tissue. In the absence of attenuation, there is a linear relationship between Cherenkov emission and deposited dose; however, scattering and absorption result in the distortion of this linear relationship. As Cherenkov emission exits the absorption by tissue dominates the observed Cherenkov emission spectrum. Spectroscopic interpretation of this effects may help to better relate Cherenkov emission to ionizing radiation dose delivered during radiotherapy.
In this study, we examined how color Cherenkov imaging intensity variations are caused by absorption from both melanin and hemoglobin level variations, so that future Cherenkov emission imaging might be corrected for linearity to delivered dose.
A custom, time-gated, three-channel intensified camera was used to image the red, green, and blue wavelengths of Cherenkov emission from tissue phantoms with synthetic melanin layers and varying blood concentrations. Our hypothesis was that spectroscopic separation of Cherenkov emission would allow for the identification of attenuated signals that varied in response to changes in blood content versus melanin content, because of their different characteristic absorption spectra.
Cherenkov emission scaled with dose linearly in all channels. Absorption in the blue and green channels increased with increasing oxy-hemoglobin in the blood to a greater extent than in the red channel. Melanin was found to absorb with only slight differences between all channels. These spectral differences can be used to derive dose from measured Cherenkov emission.
Color Cherenkov emission imaging may be used to improve the optical measurement and determination of dose delivered in tissues. Calibration for these factors to minimize the influence of the tissue types and skin tones may be possible using color camera system information based upon the linearity of the observed signals.
从线性加速器发射的高能 X 射线会在组织内产生连续光谱宽带切伦科夫光。在没有衰减的情况下,切伦科夫发射与沉积剂量之间存在线性关系;然而,散射和吸收会导致这种线性关系发生扭曲。由于切伦科夫发射离开组织的吸收,因此观察到的切伦科夫发射光谱主要由组织的吸收主导。对这种效应的光谱解释可能有助于更好地将切伦科夫发射与放射治疗期间传递的电离辐射剂量联系起来。
在这项研究中,我们研究了颜色切伦科夫成像强度变化是如何由黑色素和血红蛋白水平变化引起的吸收引起的,以便未来的切伦科夫发射成像可以针对传递剂量进行线性校正。
使用定制的、门控的、三通道增强型相机来成像组织体模中红色、绿色和蓝色波长的切伦科夫发射,这些体模具有合成黑色素层和不同的血液浓度。我们的假设是,切伦科夫发射的光谱分离将允许识别因血液含量变化而变化的衰减信号,而不是黑色素含量变化,因为它们具有不同的特征吸收光谱。
所有通道中的切伦科夫发射都与剂量呈线性比例。在蓝色和绿色通道中,随着血液中氧合血红蛋白的增加,吸收增加的程度大于红色通道。黑色素的吸收在所有通道之间几乎没有差异。这些光谱差异可用于从测量的切伦科夫发射中得出剂量。
颜色切伦科夫发射成像可用于改善组织中光学测量和剂量传递的确定。通过使用基于观察到的信号的线性度的彩色相机系统信息,对这些因素进行校准以最小化组织类型和肤色的影响可能是可行的。