Advancements in fluorescence lifetime imaging microscopy Instrumentation: Towards high speed and 3D

被引:10
作者
Park, Jongchan [1 ]
Gao, Liang [1 ]
机构
[1] Univ Calif Los Angeles, Dept Bioengn, Los Angeles, CA 90025 USA
基金
美国国家卫生研究院;
关键词
Fluorescence lifetime; Bioimaging; High speed imaging; 3D imaging; Microscopy; METABOLIC DYNAMICS; TIME-DOMAIN; TOMOGRAPHY; APOPTOSIS;
D O I
10.1016/j.cossms.2024.101147
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Fluorescence lifetime imaging microscopy (FLIM) is a powerful imaging tool offering molecular specific insights into samples through the measurement of fluorescence decay time, with promising applications in diverse research fields. However, to acquire two-dimensional lifetime images, conventional FLIM relies on extensive scanning in both the spatial and temporal domain, resulting in much slower acquisition rates compared to intensity-based approaches. This problem is further magnified in three-dimensional imaging, as it necessitates additional scanning along the depth axis. Recent advancements have aimed to enhance the speed and threedimensional imaging capabilities of FLIM. This review explores the progress made in addressing these challenges and discusses potential directions for future developments in FLIM instrumentation.
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页数:9
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