Fluorescence lifetime imaging microscopy (FLIM) is a powerful technique for probing molecular environments and biological interactions through fluorescence decay measurements. We present a fast FLIM system based on compressive sensing (CS) and a single-pixel camera (SPC) for real-time imaging of biological dynamic processes. The system employs a silicon photomultiplier (SiPM) detection module that allows high-throughput FLIM measurements. We achieve acquisition rates up to 10 frames per second (fps). This acquisition speed makes it possible to follow in real time the dynamics of most biological processes, enabling more accurate and specific analyses for new biomedical studies.

Computational fast FLIM for imaging of biological dynamic processes

Federico Simoni;Shivaprasad Varakkoth;Gennaro Fratta;Piergiorgio Daniele;Giulia Acconcia;Ivan Rech;Cosimo D'Andrea
2026-01-01

Abstract

Fluorescence lifetime imaging microscopy (FLIM) is a powerful technique for probing molecular environments and biological interactions through fluorescence decay measurements. We present a fast FLIM system based on compressive sensing (CS) and a single-pixel camera (SPC) for real-time imaging of biological dynamic processes. The system employs a silicon photomultiplier (SiPM) detection module that allows high-throughput FLIM measurements. We achieve acquisition rates up to 10 frames per second (fps). This acquisition speed makes it possible to follow in real time the dynamics of most biological processes, enabling more accurate and specific analyses for new biomedical studies.
2026
Fluorescence, Single pixel camera, Compressive sensing, Film, Lifetime, Chlorophyll
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11311/1331128
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