@inproceedings{6ebd8a796e5f43549f8d608e8431b16c,
title = "Widefiled multiphoton excited florescence microcopy for animal study in vivo",
abstract = "Unlike conventional multiphoton excited microscopy according to pixel-by-pixel point scanning, a widefield multiphoton excited microscopy based on spatiotemporal focusing has been developed to construct three-dimensional (3D) multiphoton fluorescence images only with the need of an axial scanning. By implementing a 4.0 W 10 kHz femtosecond laser amplifier with an instant strong peak power and a fast TE-cooled EMCCD camera with an ultra-sensitive fluorescence detection, the multiphoton excited fluorescence images with the excitation area over 100 μm × 100 μm can be achieved at a frame rate up to 80 Hz. A mechanical shutter is utilized to control the exposure time of 1 ms, i.e. average ten laser pulses reach the fluorescent specimen, and hence an uniform enough multiphoton excited fluorescence image can be attained with less photobleaching. The Brownian motion of microbeads and 3D neuron cells of a rat cerebellum have been observed with a lateral spatial resolution of 0.24 μm and an axial resolution of 2.5 μm. Therefore, the developed widefield multiphoton microscopy can provide fast and high-resolution multiphoton excited fluorescence images for animal study in vivo.",
keywords = "Multiphoton excited fluorescence microscopy, Neural cell, Temporal focusing, Widefield",
author = "Cheng, {L. C.} and Chang, {C. Y.} and Lin, {C. H.} and Su, {Y. D.} and Huang, {T. Y.} and Shean-Jen Chen",
year = "2010",
doi = "10.1117/12.864107",
language = "English",
isbn = "9780819482617",
series = "Proceedings of SPIE - The International Society for Optical Engineering",
booktitle = "Nanobiosystems",
note = "Nanobiosystems: Processing, Characterization, and Applications III ; Conference date: 04-08-2010 Through 05-08-2010",
}