Research Article
Fluorescence lifetime imaging microscopy: Pixel-by-pixel analysis of phase-modulation data
Article first published online: 19 JUN 2001
DOI: 10.1002/1361-6374(199409)2:3<139::AID-BIO4>3.0.CO;2-T
Copyright © 1994 IOP Publishing Ltd
Additional Information
How to Cite
Gadella, T. W. J., Clegg, R. M. and Jovin, T. M. (1994), Fluorescence lifetime imaging microscopy: Pixel-by-pixel analysis of phase-modulation data. Bioimaging, 2: 139–159. doi: 10.1002/1361-6374(199409)2:3<139::AID-BIO4>3.0.CO;2-T
Publication History
- Issue published online: 19 JUN 2001
- Article first published online: 19 JUN 2001
- Manuscript Accepted: 26 OCT 1994
- Manuscript Received: 9 AUG 1994
- Abstract
- Cited By
Keywords:
- fluorescence microscopy;
- fluorescence decay;
- frequency domain
Abstract
The novel techniques of fluorescence lifetime imaging (FLI) and FLI-microscopy (FLIM) in the frequency domain enable the mapping of the spatial distribution of fluorescence lifetimes of a specimen. The analysis of FLI(M) data is described. Two computer programs were developed to determine nanosecond fluorescence lifetimes from digitized phase-resolved images produced by the FLI(M) instrument, for single- and double-component systems, respectively. Image processing routines were incorporated for optimal display of the lifetime analysis. The combination of analysis and image processing yields images of the fluorescence lifetimes and of the associated analytical and statistical parameters. The error analysis enables the estimation of the quality of the FLI(M) data at each pixel of the image. The features of the programs are illustrated by simulated and experimental FLIM data, generated in the latter case with commercially available fluorescence microspheres as references for spatial and temporal resolution.

