Towards two-photon excited endogenous ...
Type de document :
Compte-rendu et recension critique d'ouvrage
DOI :
Titre :
Towards two-photon excited endogenous fluorescence lifetime imaging microendoscopy
Auteur(s) :
Hage, C.H. [Auteur]
XLIM [XLIM]
Leclerc, P. [Auteur]
XLIM [XLIM]
Brevier, J. [Auteur]
XLIM [XLIM]
Fabert, M. [Auteur]
XLIM [XLIM]
Nézet, C. Le [Auteur]
Laboratoire de Physique des Lasers, Atomes et Molécules - UMR 8523 [PhLAM]
Kudlinski, A. [Auteur]
Laboratoire de Physique des Lasers, Atomes et Molécules - UMR 8523 [PhLAM]
Héliot, L. [Auteur]
Laboratoire de Physique des Lasers, Atomes et Molécules - UMR 8523 [PhLAM]
Louradour, D F. [Auteur]
XLIM [XLIM]
XLIM [XLIM]
Leclerc, P. [Auteur]
XLIM [XLIM]
Brevier, J. [Auteur]
XLIM [XLIM]
Fabert, M. [Auteur]
XLIM [XLIM]
Nézet, C. Le [Auteur]
Laboratoire de Physique des Lasers, Atomes et Molécules - UMR 8523 [PhLAM]
Kudlinski, A. [Auteur]
Laboratoire de Physique des Lasers, Atomes et Molécules - UMR 8523 [PhLAM]
Héliot, L. [Auteur]
Laboratoire de Physique des Lasers, Atomes et Molécules - UMR 8523 [PhLAM]
Louradour, D F. [Auteur]
XLIM [XLIM]
Titre de la revue :
Biomedical optics express
Pagination :
921 - 930
Éditeur :
Optical Society of America - OSA Publishing
Date de publication :
2017
ISSN :
2156-7085
Discipline(s) HAL :
Sciences de l'ingénieur [physics]/Optique / photonique
Résumé en anglais : [en]
In situ fluorescence lifetime imaging microscopy (FLIM) in an endoscopic configuration of the endogenous biomarker nicotinamide adenine dinucleotide (NADH) has a great potential for malignant tissue diagnosis. Moreover, ...
Lire la suite >In situ fluorescence lifetime imaging microscopy (FLIM) in an endoscopic configuration of the endogenous biomarker nicotinamide adenine dinucleotide (NADH) has a great potential for malignant tissue diagnosis. Moreover, two-photon nonlinear excitation provides intrinsic optical sectioning along with enhanced imaging depth. We demonstrate, for the first time to our knowledge, nonlinear endogenous FLIM in a fibered microscope with proximal detection, applied to NADH in cultured cells, as a first step to a nonlinear endomicroscope, using a double-clad microstructured fiber with convenient fiber length (> 3 m) and excitation pulse duration (≈50 fs). Fluorescence photons are collected by the fiber inner cladding and we show that its contribution to the impulse response function (IRF), which originates from its intermodal and chromatic dispersions, is small (< 600 ps) and stable for lengths up to 8 m and allows for short lifetime measurements. We use the phasor representation as a quick visualization tool adapted to the endoscopy speed requirements.Lire moins >
Lire la suite >In situ fluorescence lifetime imaging microscopy (FLIM) in an endoscopic configuration of the endogenous biomarker nicotinamide adenine dinucleotide (NADH) has a great potential for malignant tissue diagnosis. Moreover, two-photon nonlinear excitation provides intrinsic optical sectioning along with enhanced imaging depth. We demonstrate, for the first time to our knowledge, nonlinear endogenous FLIM in a fibered microscope with proximal detection, applied to NADH in cultured cells, as a first step to a nonlinear endomicroscope, using a double-clad microstructured fiber with convenient fiber length (> 3 m) and excitation pulse duration (≈50 fs). Fluorescence photons are collected by the fiber inner cladding and we show that its contribution to the impulse response function (IRF), which originates from its intermodal and chromatic dispersions, is small (< 600 ps) and stable for lengths up to 8 m and allows for short lifetime measurements. We use the phasor representation as a quick visualization tool adapted to the endoscopy speed requirements.Lire moins >
Langue :
Anglais
Vulgarisation :
Non
Source :
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