| Literature DB >> 23187477 |
Heejin Choi1, Dimitrios S Tzeranis, Jae Won Cha, Philippe Clémenceau, Sander J G de Jong, Lambertus K van Geest, Joong Ho Moon, Ioannis V Yannas, Peter T C So.
Abstract
Fluorescence and phosphorescence lifetime imaging are powerful techniques for studying intracellular protein interactions and for diagnosing tissue pathophysiology. While lifetime-resolved microscopy has long been in the repertoire of the biophotonics community, current implementations fall short in terms of simultaneously providing 3D resolution, high throughput, and good tissue penetration. This report describes a new highly efficient lifetime-resolved imaging method that combines temporal focusing wide-field multiphoton excitation and simultaneous acquisition of lifetime information in frequency domain using a nanosecond gated imager from a 3D-resolved plane. This approach is scalable allowing fast volumetric imaging limited only by the available laser peak power. The accuracy and performance of the proposed method is demonstrated in several imaging studies important for understanding peripheral nerve regeneration processes. Most importantly, the parallelism of this approach may enhance the imaging speed of long lifetime processes such as phosphorescence by several orders of magnitude.Mesh:
Year: 2012 PMID: 23187477 PMCID: PMC3601594 DOI: 10.1364/OE.20.026219
Source DB: PubMed Journal: Opt Express ISSN: 1094-4087 Impact factor: 3.894