TY - JOUR
T1 - Compressive confocal microscopy imaging at the single-photon level with ultra-low sampling ratios
AU - Liu, Shuai
AU - Chen, Bin
AU - Zou, Wenzhen
AU - Sha, Hao
AU - Feng, Xiaochen
AU - Han, Sanyang
AU - Li, Xiu
AU - Yao, Xuri
AU - Zhang, Jian
AU - Zhang, Yongbing
N1 - Publisher Copyright:
© The Author(s) 2024.
PY - 2024/12
Y1 - 2024/12
N2 - Laser-scanning confocal microscopy serves as a critical instrument for microscopic research in biology. However, it suffers from low imaging speed and high phototoxicity. Here we build a novel deep compressive confocal microscope, which employs a digital micromirror device as a coding mask for single-pixel imaging and a pinhole for confocal microscopic imaging respectively. Combined with a deep learning reconstruction algorithm, our system is able to achieve high-quality confocal microscopic imaging with low phototoxicity. Our imaging experiments with fluorescent microspheres demonstrate its capability of achieving single-pixel confocal imaging with a sampling ratio of only approximately 0.03% in specific sparse scenarios. Moreover, the deep compressive confocal microscope allows single-pixel imaging at the single-photon level, thus reducing the excitation light power requirement for confocal imaging and suppressing the phototoxicity. We believe that our system has great potential for long-duration and high-speed microscopic imaging of living cells.
AB - Laser-scanning confocal microscopy serves as a critical instrument for microscopic research in biology. However, it suffers from low imaging speed and high phototoxicity. Here we build a novel deep compressive confocal microscope, which employs a digital micromirror device as a coding mask for single-pixel imaging and a pinhole for confocal microscopic imaging respectively. Combined with a deep learning reconstruction algorithm, our system is able to achieve high-quality confocal microscopic imaging with low phototoxicity. Our imaging experiments with fluorescent microspheres demonstrate its capability of achieving single-pixel confocal imaging with a sampling ratio of only approximately 0.03% in specific sparse scenarios. Moreover, the deep compressive confocal microscope allows single-pixel imaging at the single-photon level, thus reducing the excitation light power requirement for confocal imaging and suppressing the phototoxicity. We believe that our system has great potential for long-duration and high-speed microscopic imaging of living cells.
UR - http://www.scopus.com/inward/record.url?scp=85201641912&partnerID=8YFLogxK
U2 - 10.1038/s44172-024-00236-x
DO - 10.1038/s44172-024-00236-x
M3 - Article
AN - SCOPUS:85201641912
SN - 2731-3395
VL - 3
JO - Communications Engineering
JF - Communications Engineering
IS - 1
M1 - 88
ER -