Two-Photon Endoscopy
Investigators:
Wanrong Gao, Peter So
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Two-photon
fluorescence microscopic imaging has been demonstrated to be a new
way to produce optical sectioned images in highly scattering medium
such as tissues (ref.1 to 6). The development of a two-photon endoscope
will be a critical step toward realizing non-invasive
optical biopsy. It is clear that the
imaging of intra-vessel structural morphology is of great clinical
importance, especially the techniques that can image the tissue structural
morphology beneath the surfaces of the internal biological vessels.
However, the endoscope
should be as small as possible because it would be used to image
the internal human organ systems. A promising way is to use single-mode
and multi-mode fiber as well as GRIN lens
for light delivering, focusing, scanning and collecting. To do this,
one should solved the following challenge problems.
(1)
Group-Velocity Dispersion,
(2) Scan methods,
(3) Small Size,
(4) High signal-to-noise
ratio.
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1
- Denk W., Strickler J.H., Webb W.W. (1990) Two-phone laser scanning
fluorescence microscop. Science, 248: 73-76.
2 - Bird D., Gu M. (2002) Resolution improvement in two-photon fluorescence
microscopy with a single-mode fiber. Applied Optics,
41, No.10: 1852-1857.
3 - Wolleschensky R., Feurer T., Sauerbrey R., Simon U. (1998) Characterization
and optimization of a laser-scanning microscope. Applied Physics,
B67: 87-94.
4 - Tearney G.J., Boppart S.A., Bouma B.E., Brezinski M.E., Weissman
N.J., Southern J.F., Fujimoto J.G. (1996) Scanning single-mode fiber
optic catheter-endiscope for optical coherence tomography. Optics
Letters, 21, No. 7: 543-545.
5 - So P.T.C., Dong C.Y., Masters B.R. (2000) Two-photon excitation
fluorescence microscopy.Annu. Rev. Biomed. Eng. 02:
399-429.
6 - Winfried Denk W., David W. Piston D.W., and Watt W. Webb W.W.
Two-photon molecular excitation in laser scanning microscopy. Edited
by James B. Plenum, New York, 1995:445-458
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