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A readily usable two‐photon fluorescence lifetime microendoscope
Author(s) -
Hage CharlesHenri,
Leclerc Pierre,
Fabert Marc,
Bardet Sylvia M.,
Brevier Julien,
Ducourthial Guillaume,
Mansuryan Tigran,
Leray Aymeric,
Kudlinski Alexandre,
Louradour Frédéric
Publication year - 2019
Publication title -
journal of biophotonics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.877
H-Index - 66
eISSN - 1864-0648
pISSN - 1864-063X
DOI - 10.1002/jbio.201800276
Subject(s) - two photon excitation microscopy , fluorescence , autofluorescence , materials science , fluorescence lifetime imaging microscopy , microscopy , optics , microscope , lens (geology) , fluorescence microscope , resolution (logic) , optical fiber , usable , optoelectronics , computer science , physics , artificial intelligence , world wide web
A two‐photon fluorescence lifetime (2P‐FLIM) microendoscope, capable of energetic metabolism imaging through the intracellular nicotinamide adenine dinucleotide (NADH) autofluorescence, at sub‐cellular resolution, is demonstrated. It exhibits readily usable characteristics such as convenient endoscope probe diameter (≈2 mm), fiber length (>5 m) and data accumulation rate (16 frames per second (fps)), leading to a FLIM refreshing rate of ≈0.1 to 1 fps depending on the sample. The spiral scanning image formation does not influence the instrument response function (IRF) characteristics of the system. Near table‐top microscope performances are achieved through a comprehensive system including a home‐designed spectro‐temporal pulse shaper and a custom air‐silica double‐clad photonic crystal fiber, which enables to reach up to 40 mW of ≈100 fs pulses @ 760 nm with a 80 MHz repetition rate. A GRadient INdex (GRIN) lens provides a lateral resolution of 0.67 μm at the focus of the fiber probe. Intracellular NADH fluorescence lifetime data are finally acquired on cultured cells at 16 fps.