{"title":"Microscopic Imaging of Alpha Particle Trajectory and Its Application for Radionuclide Distribution Measurement in Cell.","authors":"Pingping Kong, Changran Geng, Xiaowen Tian, Haichao Zhuang, Xiaobin Tang","doi":"10.1002/jemt.24855","DOIUrl":null,"url":null,"abstract":"<p><p>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.</p>","PeriodicalId":18684,"journal":{"name":"Microscopy Research and Technique","volume":" ","pages":""},"PeriodicalIF":2.0000,"publicationDate":"2025-03-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Microscopy Research and Technique","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1002/jemt.24855","RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ANATOMY & MORPHOLOGY","Score":null,"Total":0}
引用次数: 0
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.
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.