| Literature DB >> 28717558 |
Matthias Eibl1, Sebastian Karpf2, Daniel Weng1, Hubertus Hakert1, Tom Pfeiffer1, Jan Philip Kolb1, Robert Huber1.
Abstract
Two-photon-excited fluorescence lifetime imaging microscopy (FLIM) is a chemically specific 3-D sensing modality providing valuable information about the microstructure, composition and function of a sample. However, a more widespread application of this technique is hindered by the need for a sophisticated ultra-short pulse laser source and by speed limitations of current FLIM detection systems. To overcome these limitations, we combined a robust sub-nanosecond fiber laser as the excitation source with high analog bandwidth detection. Due to the long pulse length in our configuration, more fluorescence photons are generated per pulse, which allows us to derive the lifetime with a single excitation pulse only. In this paper, we show high quality FLIM images acquired at a pixel rate of 1 MHz. This approach is a promising candidate for an easy-to-use and benchtop FLIM system to make this technique available to a wider research community.Keywords: (060.2350) Fiber optics imaging; (060.4370) Nonlinear optics, fibers; (140.3510) Lasers, fiber; (170.3650) Lifetime-based sensing; (180.2520) Fluorescence microscopy; (180.4315) Nonlinear microscopy
Year: 2017 PMID: 28717558 PMCID: PMC5508819 DOI: 10.1364/BOE.8.003132
Source DB: PubMed Journal: Biomed Opt Express ISSN: 2156-7085 Impact factor: 3.732