Presentation
5 March 2021 Real-time phasor analysis of fast FLIM for visualizing metabolic dynamics
Author Affiliations +
Abstract
Fluorescence lifetime imaging microscopy (FLIM) of reduced nicotinamide adenine dinucleotide and reduced nicotinamide adenine dinucleotide phosphate, together termed NAD(P)H, is often used to analyze and characterize the metabolic state of biological samples. The use of photon counting in FLIM of NAD(P)H often leads to long accumulation times which average out sub-second dynamics. This challenge is overcome with the presented two-photon fast FLIM system that uses an analog detection system and fast digitizer, enabling imaging up to 20 frames per second. Furthermore, GPU processing is used for real-time phasor analysis and visualization of collected data.
Conference Presentation
© (2021) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Janet E. Sorrells, Rishyashring R. Iyer, Lingxiao Yang, Andrew J. Bower, Marina Marjanovic, and Stephen A. Boppart "Real-time phasor analysis of fast FLIM for visualizing metabolic dynamics", Proc. SPIE 11655, Label-free Biomedical Imaging and Sensing (LBIS) 2021, 1165503 (5 March 2021); https://doi.org/10.1117/12.2576001
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KEYWORDS
Fluorescence lifetime imaging

Visualization

Visual analytics

Imaging systems

Luminescence

Biological research

Data acquisition

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