High resolution TCSPC lifetime imaging

被引:17
作者
Becker, W [1 ]
Bergmann, A [1 ]
Biskup, C [1 ]
Kelbauskas, L [1 ]
Zimmer, T [1 ]
Klöcker, N [1 ]
Benndorf, K [1 ]
机构
[1] Becker & Hickl GmbH, D-12277 Berlin, Germany
来源
MULTIPHOTON MICROSCOPY IN THE BIOMEDICAL SCIENCES III | 2003年 / 4963卷
关键词
D O I
10.1117/12.472866
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Time-correlated single photon counting (TCSPC) fluorescence lifetime imaging in laser scanning microscopes can be combined with a multi-detector technique that allows to record time-resolved images in several wavelength channels simultaneously. The technique is based on a multi-dimensional histogramming process that records the photon density versus the time within the fluorescence decay function, the x-y coordinates of the scanning area and the detector channel number. It avoids any time gating or wavelength switching and therefore yields a near-ideal counting efficiency. We show an instrument that records dual wavelength lifetime images with up to 512 x 512 pixels, and single wavelength lifetime images with up to 1024 x 1024 pixels. It resolves the components of double-exponential decay functions down to 30 ps, and works at the full scanning speed of a two-photon laser scanning microscope. The performance of the instrument is demonstrated for simultaneous lifetime imaging of the donor and acceptor fluorescence in CFP / YFP FRET systems and for tissue samples stained with several fluorophores.
引用
收藏
页码:175 / 184
页数:10
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