Signal-to-background ratio and lateral resolution in deep tissue imaging by optical coherence microscopy in the 1700 nm spectral band

被引:9
作者
Yamanaka, Masahito [1 ]
Hayakawa, Naoki [1 ]
Nishizawa, Norihiko [1 ]
机构
[1] Nagoya Univ, Dept Elect, Chikusa Ku, Furo Cho, Nagoya, Aichi 4648603, Japan
关键词
1.7; MU-M; TOMOGRAPHY; SCATTERING; DEPTH;
D O I
10.1038/s41598-019-52175-9
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
We quantitatively investigated the image quality in deep tissue imaging with optical coherence microscopy (OCM) in the 1700 nm spectral band, in terms of the signal-to-background ratio (SBR) and lateral resolution. In this work, to demonstrate the benefits of using the 1700 nm spectral band for OCM imaging of brain samples, we compared the imaging quality of OCM en-face images obtained at the same position by using a hybrid 1300 nm/1700 nm spectral domain (SD) OCM system with shared sample and reference arms. By observing a reflective resolution test target through a 1.5 mm-thick tissue phantom, which had a similar scattering coefficient to brain cortex tissue, we confirmed that 1700 nm OCM achieved an SBR about 6-times higher than 1300 nm OCM, although the lateral resolution of the both OCMs was similarly degraded with the increase of the imaging depth. Finally, we also demonstrated high-contrast deep tissue imaging of a mouse brain at a depth up to 1.8 mm by using high-resolution 1700 nm SD-OCM.
引用
收藏
页数:8
相关论文
共 29 条
  • [1] High-resolution optical coherence microscopy for high-speed, in vivo cellular imaging
    Aguirre, AD
    Hsiung, P
    Ko, TH
    Hartl, I
    Fujimoto, JG
    [J]. OPTICS LETTERS, 2003, 28 (21) : 2064 - 2066
  • [2] Swept source optical coherence microscopy using a 1310 nm VCSEL light source
    Ahsen, Osman O.
    Tao, Yuankai K.
    Potsaid, Benjamin M.
    Sheikine, Yuri
    Jiang, James
    Grulkowski, Ireneusz
    Tsai, Tsung-Han
    Jayaraman, Vijaysekhar
    Kraus, Martin F.
    Connolly, James L.
    Hornegger, Joachim
    Cable, Alex
    Fujimoto, James G.
    [J]. OPTICS EXPRESS, 2013, 21 (15): : 18021 - 18033
  • [3] Swept-source optical coherence tomography powered by a 1.3-μm vertical cavity surface emitting laser enables 2.3-mm-deep brain imaging in mice in vivo
    Choi, Woo June
    Wang, Ruikang K.
    [J]. JOURNAL OF BIOMEDICAL OPTICS, 2015, 20 (10)
  • [4] Noninvasive, in vivo imaging of subcortical mouse brain regions with 1.7 μm optical coherence tomography
    Chong, Shau Poh
    Merkle, Conrad W.
    Cooke, Dylan F.
    Zhang, Tingwei
    Radhakrishnan, Harsha
    Krubitzer, Leah
    Srinivasan, Vivek J.
    [J]. OPTICS LETTERS, 2015, 40 (21) : 4911 - 4914
  • [5] Deep tissue two-photon microscopy
    Helmchen, F
    Denk, W
    [J]. NATURE METHODS, 2005, 2 (12) : 932 - 940
  • [6] The effect of water dispersion and absorption on axial resolution in ultrahigh-resolution optical coherence tomography
    Hillman, TR
    Sampson, DD
    [J]. OPTICS EXPRESS, 2005, 13 (06): : 1860 - 1874
  • [7] Horton NG, 2013, NAT PHOTONICS, V7, P205, DOI [10.1038/NPHOTON.2012.336, 10.1038/nphoton.2012.336]
  • [8] Quantitative comparison of contrast and imaging depth of ultrahigh-resolution optical coherence tomography images in 800-1700 nm wavelength region
    Ishida, Shutaro
    Nishizawa, Norihiko
    [J]. BIOMEDICAL OPTICS EXPRESS, 2012, 3 (02): : 282 - 294
  • [9] Ultrahigh-Resolution Optical Coherence Tomography in 1.7 μm Region with Fiber Laser Supercontinuum in Low-Water-Absorption Samples
    Ishida, Shutaro
    Nishizawa, Norihiko
    Ohta, Takefumi
    Itoh, Kazuyoshi
    [J]. APPLIED PHYSICS EXPRESS, 2011, 4 (05)
  • [10] OPTICAL COHERENCE MICROSCOPY IN SCATTERING MEDIA
    IZATT, JA
    HEE, MR
    OWEN, GM
    SWANSON, EA
    FUJIMOTO, JG
    [J]. OPTICS LETTERS, 1994, 19 (08) : 590 - 592