SLIM: A new method for molecular imaging

✍ Scribed by A. Rück; CH. Hülshoff; I. Kinzler; W. Becker; R. Steiner

• Publisher: John Wiley and Sons
• Year: 2007
• Tongue: English
• Weight: 429 KB
• Volume: 70
• Category: Article
• ISSN: 1059-910X
• DOI: 10.1002/jemt.20433

✦ Synopsis

Abstract

We used spectrally resolved fluorescence lifetime imaging (SLIM) to investigate the mitochondria staining dye rhodamine 123 and binding of DAPI to RNA and DNA in cells. Moreover, different components of the photosensitizer Photofrin were resolved in cell cultures by SLIM. To record lifetime images (τ‐mapping) with spectral resolution we used a laser scanning microscope equipped with a spectrograph, a 16 channel multianode PMT, and multidimensional time‐correlated single photon counting. A Ti:Saphir laser was used for excitation or alternatively a ps diode laser. With this system the time‐ and spectral‐resolved fluorescence characteristics of different fluorophores were investigated in cell cultures. As an example, the mitochondria staining dye rhodamine I23 could be easily distinguished from DAPI, which binds to nucleic acids. Also different binding sites of DAPI could be discriminated. This was proved by the appearance of different lifetime components within different spectral channels. Moreover, we were able to detect monomeric and aggregated forms of Photofrin in cells. Different lifetimes could be attributed to the various compounds. In addition, a detailed analysis of the autofluorescence by SLIM could explain changes of mitochondrial metabolism during Photofrin‐PDT. Microsc. Res. Tech., 2007. © 2007 Wiley‐Liss, Inc.