Kong Pingping, Geng Changran, Tian Xiaowen, Zhuang Haichao, Tang Xiaobin
Department of Nuclear Science and Technology, Nanjing University of Aeronautics and Astronautics, Nanjing, China.
Key Laboratory of Advanced Nuclear Technology and Radiation Protection, Ministry of Industry and Information Technology, Nanjing, China.
Microsc Res Tech. 2025 Aug;88(8):2232-2240. doi: 10.1002/jemt.24855. Epub 2025 Mar 18.
Imaging and analyzing alpha-particle trajectories are crucial for studying alpha-particle distributions in high-energy physics experiments, such as radioisotope imaging and neutron energy spectrum measurements. This study introduces a novel method that combines an electron-multiplying charge-coupled device (EMCCD) camera, a gadolinium aluminum gallium garnet (GAGG) scintillator film, and a fluorescent microscope to measure the micro-distribution of radionuclides. A reconstruction technique was developed to determine the initial positions of alpha particles based on the pixel gray-value distributions along their trajectories. The effectiveness of this technique was validated through imaging experiments using fixed incident alpha particles. Key imaging parameters, including binning, exposure time, and optical parameters such as magnification, were systematically investigated for their impacts on imaging quality. Results indicated that increasing the binning value improved detection sensitivity but reduced spatial resolution. Shortening exposure times effectively prevented track overlap, aiding trajectory identification, counting, and analysis. Higher magnification of objective lenses enhanced the spatial resolution of the whole system but required greater sample flatness and camera sensitivity. A measurement platform was further developed to explore the cellular distribution of radioactive drugs in targeted alpha therapy. Coupled registration of trajectory and cellular images was achieved using an external Ra-223 source and A549 cells. This trajectory measurement technique is broadly applicable for analyzing the cellular distribution of radioactive drugs in targeted alpha therapy.
在高能物理实验中,如放射性同位素成像和中子能谱测量,对α粒子轨迹进行成像和分析对于研究α粒子分布至关重要。本研究介绍了一种结合电子倍增电荷耦合器件(EMCCD)相机、钆铝镓石榴石(GAGG)闪烁体薄膜和荧光显微镜来测量放射性核素微观分布的新方法。开发了一种重建技术,以根据α粒子轨迹上的像素灰度值分布来确定其初始位置。通过使用固定入射α粒子的成像实验验证了该技术的有效性。系统研究了包括像素合并、曝光时间等关键成像参数以及放大倍数等光学参数对成像质量的影响。结果表明,增加像素合并值可提高检测灵敏度,但会降低空间分辨率。缩短曝光时间有效防止了轨迹重叠,有助于轨迹识别、计数和分析。更高放大倍数的物镜提高了整个系统的空间分辨率,但需要样品具有更高的平整度和相机具有更高的灵敏度。进一步开发了一个测量平台,以探索放射性药物在靶向α治疗中的细胞分布。使用外部Ra-223源和A549细胞实现了轨迹图像与细胞图像的耦合配准。这种轨迹测量技术广泛适用于分析放射性药物在靶向α治疗中的细胞分布。