Presentation + Paper
15 February 2017 Spectral and lifetime endomicroscopic measurements using one and two-photon excitation
A. Ibrahim, F. Poulon, M. Zanello, R. Habert, P. Varlet, B. Devaux, A. Kudlinski, D. Abi Haidar
Author Affiliations +
Proceedings Volume 10040, Endoscopic Microscopy XII; 100400A (2017) https://doi.org/10.1117/12.2249670
Event: SPIE BiOS, 2017, San Francisco, California, United States
Abstract
Current surgical biopsy needs several days for the analysis process to be finished. Anatomopathologists provide analysis reports to the surgeon a few days after the surgical intervention, which makes it a lengthy decision making practice. In addition, the lack of precise guidance often leads to inaccuracies in the selection of tissue regions for biopsy and so necessitates repeating the operation sometimes. Our project aims at reducing this time as well as patient discomfort. In this context, we propose to develop a multimodal nonlinear endomicroscope providing several means of contrast. Among these contrast that are useful in the detection of tumor regions, we note imaging by linear and non-linear fluorescence, by second and third harmonic generation and by reflectance. In addition, this technique allows fluorescence lifetime and spectral measurements. Our endomicroscopic system is based on a new homemade customized double-clad photonic crystal fiber (DC-PCF). Finally, this double-clad micro structured optical fiber insures visible and near infrared excitation. This system was tested by measuring fluorescence lifetime and the spectral shape of a fixed tumoral brain sample in one and two photon excitations.
Conference Presentation
© (2017) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
A. Ibrahim, F. Poulon, M. Zanello, R. Habert, P. Varlet, B. Devaux, A. Kudlinski, and D. Abi Haidar "Spectral and lifetime endomicroscopic measurements using one and two-photon excitation", Proc. SPIE 10040, Endoscopic Microscopy XII, 100400A (15 February 2017); https://doi.org/10.1117/12.2249670
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KEYWORDS
Luminescence

GRIN lenses

Optical fibers

Tumors

Tissues

Cladding

Biopsy

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