| Literature DB >> 29984109 |
Jiheun Ryu1,2, Ungyo Kang3, Jayul Kim1, Hyunjun Kim1, Jue Hyung Kang3, Hyunjin Kim4, Dae Kyung Sohn5, Jae-Heon Jeong1, Hongki Yoo3,6, Bomi Gweon3,7.
Abstract
A fluorescence lifetime imaging microscopy (FLIM) integrated with two-photon excitation technique was developed. A wavelength-tunable femtosecond pulsed laser with nominal pulse repetition rate of 76-MHz was used to acquire FLIM images with a high pixel rate of 3.91 MHz by processing the pulsed two-photon fluorescence signal. Analog mean-delay (AMD) method was adopted to accelerate the lifetime measurement process and to visualize lifetime map in real-time. As a result, rapid tomographic visualization of both structural and chemical properties of the tissues was possible with longer depth penetration and lower photo-damage compared to the conventional single-photon FLIM techniques.Entities:
Keywords: (110.6880) Three-dimensional image acquisition; (170.3650) Lifetime-based sensing; (180.2520) Fluorescence microscopy; (180.4315) Nonlinear microscopy
Year: 2018 PMID: 29984109 PMCID: PMC6033550 DOI: 10.1364/BOE.9.003449
Source DB: PubMed Journal: Biomed Opt Express ISSN: 2156-7085 Impact factor: 3.732