A study on the characteristics of the Analog Mean Delay (AMD) method for high-speed Fluorescence Lifetime Imaging Microscopy (FLIM)

2016 ◽  
Author(s):  
Byungyeon Kim ◽  
Byungjun Park ◽  
Seungrag Lee ◽  
Youngjae Won
2011 ◽  
Vol 19 (4) ◽  
pp. 3396 ◽  
Author(s):  
Youngjae Won ◽  
Sucbei Moon ◽  
Wenzhong Yang ◽  
Donguk Kim ◽  
Won-Taek Han ◽  
...  

Optica ◽  
2018 ◽  
Vol 5 (10) ◽  
pp. 1290 ◽  
Author(s):  
Andrew J. Bower ◽  
Joanne Li ◽  
Eric J. Chaney ◽  
Marina Marjanovic ◽  
Darold R. Spillman ◽  
...  

2019 ◽  
Vol 10 (12) ◽  
pp. 6408 ◽  
Author(s):  
Andrew J. Bower ◽  
Janet E. Sorrells ◽  
Joanne Li ◽  
Marina Marjanovic ◽  
Ronit Barkalifa ◽  
...  

2020 ◽  
Author(s):  
Yayao Ma ◽  
Youngjae Lee ◽  
Catherine Best-Popescu ◽  
Liang Gao

AbstractWe present high-resolution, high-speed fluorescence lifetime imaging microscopy (FLIM) of live cells based on a compressed sensing scheme. By leveraging the compressibility of biological scenes in a specific domain, we simultaneously record the time-lapse fluorescence decay upon pulsed laser excitation within a large field of view. The resultant system, referred to as compressed FLIM, can acquire a widefield fluorescence lifetime image within a single camera exposure, eliminating the motion artifact and minimizing the photobleaching and phototoxicity. The imaging speed, limited only by the readout speed of the camera, is up to 100 Hz. We demonstrated the utility of compressed FLIM in imaging various transient dynamics at the microscopic scale.


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