Affiliated with Université Laval & CERVO Research Centre

Extended depth of field microscopy for rapid volumetric two-photon imaging.

TitleExtended depth of field microscopy for rapid volumetric two-photon imaging.
Publication TypeJournal Article
Year of Publication2013
AuthorsThériault G, De Koninck Y, McCarthy N
JournalOpt Express
Volume21
Issue8
Pagination10095-104
Date Published2013 Apr 22
ISSN1094-4087
KeywordsAnimals, Equipment Design, Equipment Failure Analysis, Image Enhancement, Imaging, Three-Dimensional, Lenses, Mice, Microscopy, Fluorescence, Multiphoton, Neurons
Abstract

Two-photon fluorescence microscopy is an influential tool in biology, providing valuable information on the activity of cells deep inside the tissue. However, it is limited by its low speed for imaging volume samples. Here we present the design of a two-photon scanning microscope with an extended and adjustable depth of field, which improves the temporal resolution for sampling thick samples. Moreover, this method implies no loss of optical power and resolution, and can be easily integrated into most commercial laser-scanning microscopy systems. We demonstrate experimentally the gain in performance of the system by comparing volumetric scans of neuronal structures with a standard versus an extended depth of field system.

DOI10.1364/OE.21.010095
Alternate JournalOpt Express
PubMed ID23609714
Grant List / / Canadian Institutes of Health Research / Canada