| Literature DB >> 29957804 |
Vladislav I Shcheslavskiy, Marina V Shirmanova, Varvara V Dudenkova, Konstantin A Lukyanov, Alena I Gavrina, Anastasia V Shumilova, Elena Zagaynova, Wolfgang Becker.
Abstract
While laser scanning fluorescence lifetime imaging (FLIM) is a powerful approach for cell biology, its small field of view (typically less than 1 mm) makes it impractical for the imaging of large biological samples that is often required for biomedical applications. Here we present a system that allows performing FLIM on macroscopic samples as large as 18 mm with a lateral resolution of 15 μm. The performance of the system is verified with FLIM of endogenous metabolic cofactor reduced nicotinamide adenine dinucleotide (phosphate), NAD(P)H, and genetically encoded fluorescent protein mKate2 in a mouse tumor in vivo.Entities:
Year: 2018 PMID: 29957804 DOI: 10.1364/OL.43.003152
Source DB: PubMed Journal: Opt Lett ISSN: 0146-9592 Impact factor: 3.776