| Literature DB >> 15295637 |
Dan Elson1, Jose Requejo-Isidro, Ian Munro, Fred Reavell, Jan Siegel, Klaus Suhling, Paul Tadrous, Richard Benninger, Peter Lanigan, James McGinty, Clifford Talbot, Bebhinn Treanor, Stephen Webb, Ann Sandison, Andrew Wallace, Dan Davis, John Lever, Mark Neil, David Phillips, Gordon Stamp, Paul French.
Abstract
Fluorescence lifetime imaging (FLIM) is a functional imaging methodology that can provide information, not only concerning the localisation of specific fluorophores, but also about the local fluorophore environment. It may be implemented in scanning confocal or multi-photon microscopes, or in wide-field microscopes and endoscopes. When applied to tissue autofluorescence, it reveals intrinsic excellent contrast between different types and states of tissue. This article aims to review our recent progress in developing time-domain FLIM technology for microscopy and endoscopy and applying it to biological tissue.Mesh:
Year: 2004 PMID: 15295637 DOI: 10.1039/b316456j
Source DB: PubMed Journal: Photochem Photobiol Sci ISSN: 1474-905X Impact factor: 3.982