2009 APS March Meeting
Volume 54, Number 1
Monday–Friday, March 16–20, 2009;
Pittsburgh, Pennsylvania
Session Y2: Advances in Optical Microscopy
8:00 AM–11:00 AM,
Friday, March 20, 2009
Room: Spirit of Pittsburgh Ballroom BC
Sponsoring
Unit:
DCMP
Chair: David Weitz, Harvard University
Abstract ID: BAPS.2009.MAR.Y2.4
Abstract: Y2.00004 : New techniques for fluorescence background rejection in microscopy and endoscopy
9:48 AM–10:24 AM
Preview Abstract
Abstract
Author:
Cathie Ventalon
(Laboratory of Neurophysiology and New Microscopies, CNRS UMR 8154, INSERM S603, University Paris Descartes - 45 rue des Saints P\`eres - 75006 Paris)
Confocal microscopy is a popular technique in the bioimaging
community,
mainly because it provides optical sectioning. However, its standard
implementation requires 3-dimensional scanning of focused
illumination
throughout the sample. Efficient non-scanning alternatives have been
implemented, among which the simple and well-established incoherent
structured illumination microscopy (SIM) [1]. We recently
proposed a similar
technique, called Dynamic Speckle Illumination (DSI) microscopy,
wherein the
incoherent grid illumination pattern is replaced with a coherent
speckle
illumination pattern from a laser, taking advantage of the fact
that speckle
contrast is highly maintained in a scattering media, making the
technique
well adapted to tissue imaging [2].
DSI microscopy relies on the illumination of a sample with a
sequence of
dynamic speckle patterns and an image processing algorithm based
only on an
a priori knowledge of speckle statistics. The choice of this
post-processing
algorithm is crucial to obtain a good sectioning strength: in
particular, we
developed a novel post-processing algorithm based one wavelet
pre-filtering
of the raw images and obtained near-confocal fluorescence
sectioning in a
mouse brain labeled with GFP, with a good image quality maintained
throughout a depth of $\sim $100 $\mu $m [3].
In the purpose of imaging fluorescent tissue at higher depth, we
recently
applied structured illumination to endoscopy. We used a similar
set-up
wherein the illumination pattern (a one-dimensional grid) is
transported to
the sample with an imaging fiber bundle with miniaturized
objective and the
fluorescence image is collected through the same bundle. Using a
post-processing algorithm similar to the one previously described
[3], we
obtained high-quality images of a fluorescein-labeled rat colonic
mucosa
[4], establishing the potential of our endomicroscope for bioimaging
applications.
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\underline {Ref:}
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[1] M. A. A. Neil \textit{et al}, Opt. Lett. 22, 1905 (1997)
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[2] C. Ventalon \textit{et al}, Opt. Lett. \textbf{30}, 3350 (2005)
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[3] C. Ventalon \textit{et al}, Opt. Lett. \textbf{32,} 1417 (2007)
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[4] N. Bozinovic \textit{et al}, Opt. Express \textbf{16}, 8016
(2008)
To cite this abstract, use the following reference: http://meetings.aps.org/link/BAPS.2009.MAR.Y2.4