Pile-up free fluorescence lifetime imaging with a SPAD-based single pixel camera
In the last years, single-pixel imaging (SPI) has been extensively utilized in fluorescence lifetime imaging (FLIM) experiments. In this context, to attain high temporal resolution, time-correlated single photon counting (TCSPC) is typically adopted, with the major drawback of the pile-up phenomenon...
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| Published in | Optics express Vol. 33; no. 11; p. 22296 |
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| Main Authors | , , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
United States
02.06.2025
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| Online Access | Get full text |
| ISSN | 1094-4087 1094-4087 |
| DOI | 10.1364/OE.555297 |
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| Abstract | In the last years, single-pixel imaging (SPI) has been extensively utilized in fluorescence lifetime imaging (FLIM) experiments. In this context, to attain high temporal resolution, time-correlated single photon counting (TCSPC) is typically adopted, with the major drawback of the pile-up phenomenon, that limits the photon count rate to 1–5% of the laser excitation rate. This clearly hinders the possibility of monitoring a wide variety of biological phenomena in real-time. In this paper, to the best of our knowledge, we apply for the first time to a single-pixel camera (SPC) a hardware-based method, that allows to completely avoid the onset of pile-up by matching the dead time of the employed single-photon avalanche diode (SPAD) detector to an integer multiple of the laser period. We therefore demonstrate that undistorted and high-fidelity lifetime maps can be acquired at count rates (40%) well above the classic pile-up limitation, even in the presence of computational imaging algorithms. These results are supported by a thorough analysis of both the raw data prior to the reconstruction process and the final reconstructed lifetime maps. |
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| AbstractList | In the last years, single-pixel imaging (SPI) has been extensively utilized in fluorescence lifetime imaging (FLIM) experiments. In this context, to attain high temporal resolution, time-correlated single photon counting (TCSPC) is typically adopted, with the major drawback of the pile-up phenomenon, that limits the photon count rate to 1–5% of the laser excitation rate. This clearly hinders the possibility of monitoring a wide variety of biological phenomena in real-time. In this paper, to the best of our knowledge, we apply for the first time to a single-pixel camera (SPC) a hardware-based method, that allows to completely avoid the onset of pile-up by matching the dead time of the employed single-photon avalanche diode (SPAD) detector to an integer multiple of the laser period. We therefore demonstrate that undistorted and high-fidelity lifetime maps can be acquired at count rates (40%) well above the classic pile-up limitation, even in the presence of computational imaging algorithms. These results are supported by a thorough analysis of both the raw data prior to the reconstruction process and the final reconstructed lifetime maps. In the last years, single-pixel imaging (SPI) has been extensively utilized in fluorescence lifetime imaging (FLIM) experiments. In this context, to attain high temporal resolution, time-correlated single photon counting (TCSPC) is typically adopted, with the major drawback of the pile-up phenomenon, that limits the photon count rate to 1-5% of the laser excitation rate. This clearly hinders the possibility of monitoring a wide variety of biological phenomena in real-time. In this paper, to the best of our knowledge, we apply for the first time to a single-pixel camera (SPC) a hardware-based method, that allows to completely avoid the onset of pile-up by matching the dead time of the employed single-photon avalanche diode (SPAD) detector to an integer multiple of the laser period. We therefore demonstrate that undistorted and high-fidelity lifetime maps can be acquired at count rates (40%) well above the classic pile-up limitation, even in the presence of computational imaging algorithms. These results are supported by a thorough analysis of both the raw data prior to the reconstruction process and the final reconstructed lifetime maps.In the last years, single-pixel imaging (SPI) has been extensively utilized in fluorescence lifetime imaging (FLIM) experiments. In this context, to attain high temporal resolution, time-correlated single photon counting (TCSPC) is typically adopted, with the major drawback of the pile-up phenomenon, that limits the photon count rate to 1-5% of the laser excitation rate. This clearly hinders the possibility of monitoring a wide variety of biological phenomena in real-time. In this paper, to the best of our knowledge, we apply for the first time to a single-pixel camera (SPC) a hardware-based method, that allows to completely avoid the onset of pile-up by matching the dead time of the employed single-photon avalanche diode (SPAD) detector to an integer multiple of the laser period. We therefore demonstrate that undistorted and high-fidelity lifetime maps can be acquired at count rates (40%) well above the classic pile-up limitation, even in the presence of computational imaging algorithms. These results are supported by a thorough analysis of both the raw data prior to the reconstruction process and the final reconstructed lifetime maps. |
| Author | Farina, Serena D’Andrea, Cosimo Farina, Andrea Rech, Ivan Acconcia, Giulia Ghezzi, Alberto Labanca, Ivan |
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| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/40515223$$D View this record in MEDLINE/PubMed |
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| Title | Pile-up free fluorescence lifetime imaging with a SPAD-based single pixel camera |
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