High throughput compressive fluorescence lifetime imaging with a silicon photomultiplier detector

被引:0
|
作者
Ghezzi, Alberto [1 ,2 ]
Avanzi, Elisabetta [1 ]
Fleitas, A. R. I. E. L. GARCiA [1 ,3 ]
DI Sieno, Laura [1 ]
Dalla Mora, Alberto [1 ]
Santabarbara, Stefano [4 ]
Bassi, Andrea [1 ,2 ]
Valentini, Gianluca [1 ,2 ]
Farina, Andrea [2 ]
D'andrea, Cosimo [1 ,3 ]
机构
[1] Politecn Milan, Dipartimento Fis, Piazza L da Vinci 32, I-20133 Milan, Italy
[2] Ist Foton & Nanotecnol, Consiglio Nazl Ric, Piazza L da Vinci 32, I-20133 Milan, Italy
[3] Ist Italiano Tecnol, Ctr Nano Sci & Technol, Via Raffaele Rubattino 81, I-20134 Milan, Italy
[4] Ist Biol & Biotecnol Agr, Consiglio Nazl Ric, Via Bassini 15a, I-20133 Milan, Italy
来源
OPTICS EXPRESS | 2024年 / 32卷 / 14期
关键词
CHLOROPHYLL FLUORESCENCE; TIME; CELLS;
D O I
10.1364/OE.519995
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
Fluorescence lifetime imaging microscopy (FLIM) is a powerful technique for studying biological processes. There exists a growing interest in developing strategies to enhance throughput and reduce acquisition time of FLIM systems, which commonly employ laser scanning excitation and time-correlated single-photon counting (TCSPC) detection. In this work, we propose a wide-field FLIM microscope based on compressive sensing and high photon rate detection (beyond pile-up limit) based on a high-efficiency silicon photomultiplier detector as a single-pixel camera. We experimentally validate the capabilities of this design achieving 20 frames per second FLIM images on free-moving green algae sample. (c) 2024 Optica Publishing Group under the terms of the Optica Open Access Publishing Agreement
引用
收藏
页码:24553 / 24562
页数:10
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