
Proceedings Paper
Multimode optical imaging of small animals: development and applicationsFormat | Member Price | Non-Member Price |
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Paper Abstract
We present an optical system for small animal imaging that can combine various in vivo imaging modalities, including
fluorescence (intensity and lifetime), spectral, and trans-illumination imaging. This system consists of light-tight box
with ultrafast pulsed or cw laser light excitation, motorized translational and rotational stages, a telecentric lens for
detection, and a cooled CCD camera that can be coupled to an ultrafast time-gated intensifier. All components are
modular, making possible laser excitation at various wavelengths and pulse lengths, and signal detection in a variety of
ways (multimode). Results of drug nanoconjugate carrier delivery studies in mice are presented. Conventional and
spectrally-resolved fluorescence images reveal details of in vivo drug nanoconjugate carrier accumulation within the
tumor region and several organs in real time. By multi-spectral image analysis of ex vivo specimens from the same mice,
we were able to evaluate the extent and topology of drug nanoconjugate carrier distribution into specific organs and the
tumor itself.
Paper Details
Date Published: 19 February 2007
PDF: 10 pages
Proc. SPIE 6441, Imaging, Manipulation, and Analysis of Biomolecules, Cells, and Tissues V, 644105 (19 February 2007); doi: 10.1117/12.711582
Published in SPIE Proceedings Vol. 6441:
Imaging, Manipulation, and Analysis of Biomolecules, Cells, and Tissues V
Daniel L. Farkas; Robert C. Leif; Dan V. Nicolau, Editor(s)
PDF: 10 pages
Proc. SPIE 6441, Imaging, Manipulation, and Analysis of Biomolecules, Cells, and Tissues V, 644105 (19 February 2007); doi: 10.1117/12.711582
Show Author Affiliations
J. Y. Hwang, Univ. of Southern California, Los Angeles (United States)
Cedars-Sinai Medical Ctr. (United States)
C. Moffatt-Blue, Cedars-Sinai Medical Ctr. (United States)
O. Equils, Cedars-Sinai Medical Ctr. (United States)
M. Fujita, Cedars-Sinai Medical Ctr. (United States)
J. Jeong, Univ. of Southern California, Los Angeles (United States)
Cedars-Sinai Medical Ctr. (United States)
N. M. Khazenzon, Cedars-Sinai Medical Ctr. (United States)
Cedars-Sinai Medical Ctr. (United States)
C. Moffatt-Blue, Cedars-Sinai Medical Ctr. (United States)
O. Equils, Cedars-Sinai Medical Ctr. (United States)
M. Fujita, Cedars-Sinai Medical Ctr. (United States)
J. Jeong, Univ. of Southern California, Los Angeles (United States)
Cedars-Sinai Medical Ctr. (United States)
N. M. Khazenzon, Cedars-Sinai Medical Ctr. (United States)
E. Lindsley, Cedars-Sinai Medical Ctr. (United States)
J. Ljubimova, Cedars-Sinai Medical Ctr. (United States)
A. G. Nowatzyk, Univ. of Southern California, Los Angeles (United States)
Cedars-Sinai Medical Ctr. (United States)
D. L. Farkas, Univ. of Southern California, Los Angeles (United States)
Cedars-Sinai Medical Ctr. (United States)
S. Wachsmann-Hogiu, Cedars-Sinai Medical Ctr. (United States)
J. Ljubimova, Cedars-Sinai Medical Ctr. (United States)
A. G. Nowatzyk, Univ. of Southern California, Los Angeles (United States)
Cedars-Sinai Medical Ctr. (United States)
D. L. Farkas, Univ. of Southern California, Los Angeles (United States)
Cedars-Sinai Medical Ctr. (United States)
S. Wachsmann-Hogiu, Cedars-Sinai Medical Ctr. (United States)
Published in SPIE Proceedings Vol. 6441:
Imaging, Manipulation, and Analysis of Biomolecules, Cells, and Tissues V
Daniel L. Farkas; Robert C. Leif; Dan V. Nicolau, Editor(s)
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