A novel fluorescence lifetime imaging system that optimizes photon efficiency

被引:141
作者
Colyer, Ryan A. [1 ]
Lee, Claudia [1 ]
Gratton, Enrico [1 ]
机构
[1] Univ Calif Irvine, Dept Biomed Engn, Irvine, CA 92717 USA
关键词
FLIM; fluorescence lifetime; confocal microscopy; phasor plot;
D O I
10.1002/jemt.20540
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Fluorescence lifetime imaging (FLIM) is a powerful microscopy technique for providing contrast of biological and other systems by differences in molecular species or their environments. However, the cost of equipment and the complexity of data analysis have limited the application of FLIM. We present a mathematical model and physical implementation for a low cost digital frequency domain FLIM (DFD-FLIM) system, which can provide lifetime resolution with quality comparable to time-correlated single photon counting methods. Our implementation provides data natively in the form of phasors. On the basis of the mathematical model, we present an error analysis that shows the precise parameters for maximizing the quality of lifetime acquisition, as well as data to support this conclusion. The hardware and software of the proposed DFD-FLIM method simplifies the process of data acquisition for FLIM, presents a new interface for data display and interpretation, and optimizes the accuracy of lifetime determination.
引用
收藏
页码:201 / 213
页数:13
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