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PMID: 15645812 Published · ppublish English Evaluation Study Journal Article Research Support, Non-U.S. Gov't

Fluorescence-lifetime imaging with a multifocal two-photon microscope.

Optics letters ·Vol. 29 ·No. 24 ·2004-12-15 ·Pages 2884-6

Lévêque-Fort S, Fontaine-Aupart MP, Roger G, Georges P

Abstract

Two-photon microscopy is a powerful tool for imaging of cells or tissues. However, it presents the drawback of being a laser-scanning technique that involves a long acquisition time for fluorescence-lifetime imaging. Thus it is commonly limited to intensity images that give only indications of the location of fluorophores but do not identify the physicochemical properties and interactions between cells' components. To protect biological samples from experiments that are too long and to provide a more comprehensive spectroscopic tool we have developed a time-resolved multifocal multiphoton microscope. This setup allows us to speed up the acquisition while retaining the possibility of measuring both intensity and lifetime images of the sample.

MeSH Terms
Equipment Design Equipment Failure Analysis Feasibility Studies Image Enhancement/instrumentation,methods Image Interpretation, Computer-Assisted/instrumentation,methods Microscopy, Fluorescence, Multiphoton/instrumentation,methods Reproducibility of Results Sensitivity and Specificity
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Lévêque-Fort S
Laboratoire de Photophysique Moléculaire, Centre National de la Recherche Scientifique, Unité Propre de Recherche 3361, Centre Universitaire, Batiment 210, 91405 Orsay, France. sandrine.fort@ppm.u-psud.fr
Fontaine-Aupart M P
Roger G
Georges P
Article Info
Journal
Optics letters
Abbr.
Opt Lett
ISSN
0146-9592
Published
2004-12-15
Pages
2884-6
Language
English
Region
United States
NLM ID
7708433
Subset
IM
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