Microscopic Imaging of Alpha Particle Trajectory and Its Application for Radionuclide Distribution Measurement in Cell

IF 2.1 3区 工程技术 Q2 ANATOMY & MORPHOLOGY Microscopy Research and Technique Pub Date : 2025-03-18 DOI:10.1002/jemt.24855
Pingping Kong, Changran Geng, Xiaowen Tian, Haichao Zhuang, Xiaobin Tang
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Abstract

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.

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粒子轨迹显微成像及其在细胞内放射性核素分布测量中的应用。
在放射性同位素成像和中子能谱测量等高能物理实验中,对α粒子轨迹的成像和分析是研究α粒子分布的关键。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分布的新方法。提出了一种基于粒子轨迹上的像素灰度值分布来确定粒子初始位置的重建技术。通过固定入射α粒子的成像实验验证了该技术的有效性。系统地研究了关键成像参数,包括帧、曝光时间和光学参数(如放大倍率)对成像质量的影响。结果表明,增大分束值可提高检测灵敏度,但降低空间分辨率。缩短曝光时间有效地防止了轨迹重叠,有助于轨迹识别、计数和分析。较高的物镜放大倍率提高了整个系统的空间分辨率,但对样品平面度和相机灵敏度的要求更高。进一步开发了一个测量平台,以探索靶向α治疗中放射性药物的细胞分布。使用外部Ra-223源和A549单元实现了轨迹和细胞图像的耦合配准。这种轨迹测量技术广泛适用于靶向治疗中放射性药物的细胞分布分析。
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来源期刊
Microscopy Research and Technique
Microscopy Research and Technique 医学-解剖学与形态学
CiteScore
5.30
自引率
20.00%
发文量
233
审稿时长
4.7 months
期刊介绍: Microscopy Research and Technique (MRT) publishes articles on all aspects of advanced microscopy original architecture and methodologies with applications in the biological, clinical, chemical, and materials sciences. Original basic and applied research as well as technical papers dealing with the various subsets of microscopy are encouraged. MRT is the right form for those developing new microscopy methods or using the microscope to answer key questions in basic and applied research.
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