Presentation
26 March 2020 Ultrafast fluorescence lifetime imaging microscopy by frequency-division multiplexing (Conference Presentation)
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Abstract
We demonstrate ultrafast fluorescence lifetime imaging microscopy (FLIM) based on frequency-division multiplexing. As a proof-of-concept demonstration, we obtained images with fluorescence intensity and lifetime contrasts of MCF-7 breast cancer cells stained by SYTO16 at a record high frame rate of 16,000 fps, which is 100 times higher than that of previously reported FLIM techniques. Our method is expected to expand the utility of FLIM to quantitative analysis of rapid intracellular dynamics and high-throughput cell screening based on fluorescence lifetime images.
Conference Presentation
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Hiroshi Kanno, Hideharu Mikami, and Keisuke Goda "Ultrafast fluorescence lifetime imaging microscopy by frequency-division multiplexing (Conference Presentation)", Proc. SPIE 11246, Single Molecule Spectroscopy and Superresolution Imaging XIII, 112460D (26 March 2020); https://doi.org/10.1117/12.2550427
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KEYWORDS
Fluorescence lifetime imaging

Microscopy

Frequency division multiplexing

Ultrafast imaging

Luminescence

Confocal microscopy

Calcium

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