Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2016 Aug 22:6:31715.
doi: 10.1038/srep31715.

Optical coherence microscopy in 1700 nm spectral band for high-resolution label-free deep-tissue imaging

Affiliations

Optical coherence microscopy in 1700 nm spectral band for high-resolution label-free deep-tissue imaging

Masahito Yamanaka et al. Sci Rep. .

Abstract

Optical coherence microscopy (OCM) is a label-free, high-resolution, three-dimensional (3D) imaging technique based on optical coherence tomography (OCT) and confocal microscopy. Here, we report that the 1700-nm spectral band has the great potential to improve the imaging depth in high-resolution OCM imaging of animal tissues. Recent studies to improve the imaging depth in OCT revealed that the 1700-nm spectral band is a promising choice for imaging turbid scattering tissues due to the low attenuation of light in the wavelength region. In this study, we developed high-resolution OCM by using a high-power supercontinuum source in the 1700-nm spectral band, and compared the attenuation of signal-to-noise ratio between the 1700-nm and 1300-nm OCM imaging of a mouse brain under the condition of the same sensitivity. The comparison clearly showed that the 1700-nm OCM provides larger imaging depth than the 1300-nm OCM. In this 1700-nm OCM, the lateral resolution of 1.3 μm and the axial resolution of 2.8 μm, when a refractive index was assumed to be 1.38, was achieved.

PubMed Disclaimer

Figures

Figure 1
Figure 1
(A) Optical setup of the optical coherence microscopy using the SC source in the 1700-nm spectral band and (B) optical spectrum of the SC source.
Figure 2
Figure 2
(A) Interference signal obtained with the developed OCM, (B) the logarithmically demodulated signal, (C) OCM image of a single polystyrene bead with a diameter of 200 nm in x-y plane (en-face) and the intensity profile spanning the white dotted line in the image, and (D) OCM image of a pig thyroid gland at a depth of 150 μm. (E) Sample observation configuration in this experiment. Scale bar: (C) 5 μm and (D) 50 μm.
Figure 3
Figure 3
Cross-sectional images of a mouse brain obtained with (A) the 1700-nm OCM and (B) the 1300-nm OCM. The lateral and axial width of the images were 100 and 1700 μm, respectively. (C) SNR of each OCM at difference depths. The dotted lines are exponential fits.
Figure 4
Figure 4
OCM images (x-y plane (en-face)) of (A) a pig thyroid grand and (B) a mouse brain at different imaging depths. Scale bar: 20 μm.

Similar articles

Cited by

References

    1. Soares C. P. et al.. 2D and 3D-Organized Cardiac Cells Shows Differences in Cellular Morphology, Adhesion Junctions, Presence of Myofibrils and Protein Expression. PLoS ONE 7, e38147 (2012). - PMC - PubMed
    1. Nyga A., Cheema U. & Loizidou M. 3D tumour models: novel in vitro approaches to cancer studies. J. Cell Commun. Signal. 5, 239–248 (2011). - PMC - PubMed
    1. Shamir E. R. & Ewald A. J. Three-dimensional organotypic culture: experimental models of mammalian biology and disease. Nat. Rev. Mol. Cell Biol. 15, 647–664 (2014). - PMC - PubMed
    1. Murphy S. V. & Anthony A. 3D bioprinting of tissues and organs, Nat. Biotechnol. 32, 773–785 (2014). - PubMed
    1. Pampaloni F. Reynaud E. G. & Stelzer E. H. K. The third dimension bridges the gap between cell culture and live tissue. Nat. Rev. Mol. Cell Biol. 8, 839–845 (2007). - PubMed

LinkOut - more resources