Noise reduction technique for fluorescence imaging in multifocal multiphoton microscopy

被引:0
|
作者
Ryu, Inkeon [1 ]
Park, Eunwoo [2 ]
Kim, Eunbin [1 ]
Kim, Daekeun [1 ]
机构
[1] Dankook Univ, Dept Mech Engn, Yongin, South Korea
[2] Pohang Univ Sci & Technol POSTECH, Dept Convergence IT Engn, Pohang, South Korea
关键词
Multifocal multiphoton microscopy; Crosstalk; Noise reduction; Beam shaper;
D O I
10.1117/12.2624203
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Multifocal multiphoton microscopy (MMM) by forming multifocal created with a lenslet array enables high-speed imaging than single-focal multiphoton microscopy. However, most multifocal multiphoton microscopy has a problem of degrading image quality compared to single-focal microscopes. In order to solve this problem, it is necessary to equalize the intensity of the multifocal incident light. The fluorescence signal emitted from the fluorescence material is determined by the intensity of the incident light, but compared to the single-focal multiphoton microscope, the incident light passing through the lenslet array not only causes problems in acquiring fluorescence images but also limits the field of view ( FOV). This problem was overcome by using a specially designed beam shaper to equalize the multifocal incident light intensity. Another problem with MMM is that typical biopsy samples are opaque, so light scattering occurs when light is irradiated onto the sample. This is a cause of the noise that degrades image quality by generating crosstalk in which fluorescence signals emitted from each focus deviate from the focal plane and interfere with each other. For the minimization of crosstalk, we set up the algorithm technology to correct the sensitivity non-uniformity between channels of multi-channel photomultiplier tubes (PMT). And to minimize crosstalk between PMT circuits, an independent short-channel photon discriminator was designed to expand the number of focal points of the MMM system. Among the problems of MMM, two techniques were introduced, and it was confirmed that the noise of the fluorescence image was reduced.
引用
收藏
页数:4
相关论文
共 50 条
  • [1] Multiphoton, multifocal fluorescence lifetime imaging
    Hogan, Hank
    PHOTONICS SPECTRA, 2007, 41 (12) : 110 - 111
  • [2] Multiphoton, multifocal fluorescence lifetime imaging
    Hogan, Hank
    Biophoton Int, 2007, 12 (54-55): : 54 - 55
  • [3] Live cell imaging by multifocal multiphoton microscopy
    Straub, M
    Lodemann, P
    Holroyd, P
    Jahn, R
    Hell, SW
    EUROPEAN JOURNAL OF CELL BIOLOGY, 2000, 79 (10) : 726 - 734
  • [4] Multifocal multiphoton microscopy: a fast and efficient tool for 3-D fluorescence imaging
    Straub, M
    Hell, SW
    BIOIMAGING, 1998, 6 (04) : 177 - 185
  • [5] Fast Noise Reduction Approach in Multifocal Multiphoton Microscopy Based on Monte-Carlo Simulation
    Kim, Dongmok
    Shin, Younghoon
    Kwon, Hyuk-Sang
    CURRENT OPTICS AND PHOTONICS, 2021, 5 (04) : 421 - 430
  • [6] Multifocal multiphoton microscopy
    Bewersdorf, J
    Pick, R
    Hell, SW
    OPTICS LETTERS, 1998, 23 (09) : 655 - 657
  • [7] Review Multiphoton fluorescence microscopy for in vivo imaging
    Xu, Chris
    Nedergaard, Maiken
    Fowell, Deborah J.
    Friedl, Peter
    Ji, Na
    CELL, 2024, 187 (17) : 4458 - 4487
  • [8] Deep tissue imaging with multiphoton fluorescence microscopy
    Miller, David R.
    Jarrett, Jeremy W.
    Hassan, Ahmed M.
    Dunn, Andrew K.
    CURRENT OPINION IN BIOMEDICAL ENGINEERING, 2017, 4 : 32 - 39
  • [9] Scanless volumetric imaging by selective access multifocal multiphoton microscopy
    Xue, Yi
    Berry, Kalen P.
    Boivin, Josiah R.
    Rowlands, Christopher J.
    Takiguchi, Yu
    Nedivi, Elly
    So, Peter T. C.
    OPTICA, 2019, 6 (01) : 76 - 83
  • [10] Widefield multiphoton and temporally decorrelated multifocal multiphoton microscopy
    Fittinghoff, DN
    Wiseman, PW
    Squier, JA
    OPTICS EXPRESS, 2000, 7 (08): : 273 - 279