Department of Physics, University of Surrey, Guildford, Surrey, UK.
Phys Med Biol. 2013 Sep 21;58(18):6279-97. doi: 10.1088/0031-9155/58/18/6279. Epub 2013 Aug 22.
Previous research on optical computed tomography (CT) microscopy in the context of the synchrotron microbeam has shown the potential of the technique and demonstrated high quality images, but has left two questions unanswered: (i) are the images suitably quantitative for 3D dosimetry? and (ii) what is the impact on the spatial resolution of the system of the limited depth-of-field of the microscope optics? Cuvette and imaging studies are reported here that address these issues. Two sets of cuvettes containing the radiochromic plastic PRESAGE® were irradiated at the ID17 biomedical beamline of the European Synchrotron Radiation facility over the ranges 0-20 and 0-35 Gy and a third set of cuvettes was irradiated over the range 0-20 Gy using a standard medical linac. In parallel, three cylindrical PRESAGE® samples of diameter 9.7 mm were irradiated with test patterns that allowed the quantitative capabilities of the optical CT microscope to be verified, and independent measurements of the imaging modulation transfer function (MTF) to be made via two different methods. Both spectrophotometric analysis and imaging gave a linear dose response, with gradients ranging from 0.036-0.041 cm(-1) Gy(-1) in the three sets of cuvettes and 0.037 (optical CT units) Gy(-1) for the imaging. High-quality, quantitative imaging results were obtained throughout the 3D volume, as illustrated by depth-dose profiles. These profiles are shown to be monoexponential, and the linear attention coefficient of PRESAGE® for the synchrotron-generated x-ray beam is measured to be (0.185 ± 0.02) cm(-1) in excellent agreement with expectations. Low-level (<5%) residual image artefacts are discussed in detail. It was possible to resolve easily slit patterns of width 37 µm (which are smaller than many of the microbeams used on ID-17), but some uncertainty remains as to whether the low values of MTF for the higher spatial frequencies are scanner related or a result of genuine (but non-ideal) dose distributions. We conclude that microscopy images from our scanner do indeed have intensities that are proportional to spectrophotometric optical density and can thus be used as the basis for accurate dosimetry. However, further investigations are necessary before the microscopy images can be used to make the quantitative measures of peak-to-valley ratios for small-diameter microbeams. We suggest various strategies for moving forward and are optimistic about the future potential of this system.
先前的基于同步辐射微束的光学计算层析成像(CT)显微镜研究表明了该技术的潜力,并展示了高质量的图像,但仍有两个问题没有得到解答:(i) 这些图像是否适合用于 3D 剂量测定?(ii) 显微镜光学器件的有限景深对系统的空间分辨率有什么影响?本文报道了针对这些问题的微腔和成像研究。两组含有放射性塑料 PRESAGE®的微腔在欧洲同步辐射设施的 ID17 生物医学光束线上进行照射,照射范围分别为 0-20 和 0-35 Gy,第三组微腔使用标准医用直线加速器在 0-20 Gy 范围内进行照射。同时,三个直径为 9.7 毫米的 PRESAGE®圆柱体样本用测试图案进行照射,这些测试图案验证了光学 CT 显微镜的定量能力,并通过两种不同的方法独立测量了成像调制传递函数(MTF)。分光光度分析和成像均得到了线性剂量响应,三组微腔中的梯度范围为 0.036-0.041 cm-1 Gy-1,成像的梯度为 0.037(光学 CT 单位)Gy-1。整个 3D 体积都获得了高质量、定量的成像结果,如图像深度剂量分布所示。这些分布呈单指数分布,同步辐射产生的 X 射线束对 PRESAGE®的线性吸收系数测量值为(0.185 ± 0.02)cm-1,与预期结果非常吻合。详细讨论了低水平(<5%)的残留图像伪影。很容易分辨宽度为 37 µm 的狭缝图案(比 ID-17 上使用的许多微束还要小),但对于更高空间频率的 MTF 值较低的情况,仍然存在一些不确定性,这是由于扫描仪的原因还是由于真实(但非理想)剂量分布的原因。我们得出的结论是,我们的扫描仪的显微镜图像的强度确实与分光光度光密度成正比,因此可以用作准确剂量测定的基础。然而,在显微镜图像可以用于对小直径微束的峰谷比进行定量测量之前,还需要进行进一步的研究。我们提出了各种推进的策略,并对该系统的未来潜力持乐观态度。