Literature DB >> 21054107

Enhancing precision in time-domain fluorescence lifetime imaging.

Ching-Wei Chang1, Mary-Ann Mycek.   

Abstract

In biological applications of fluorescence lifetime imaging, low signals from samples can be a challenge, causing poor lifetime precision. We demonstrate how optimal signal gating (a method applied to the temporal dimension of a lifetime image) and novel total variation denoising models (a method applied to the spatial dimension of a lifetime image) can be used in time-domain fluorescence lifetime imaging microscopy (FLIM) to improve lifetime precision. In time-gated FLIM, notable fourfold precision improvements were observed in a low-light example. This approach can be employed to improve FLIM data while minimizing sample light exposure and increasing imaging speed.

Mesh:

Year:  2010        PMID: 21054107      PMCID: PMC2966491          DOI: 10.1117/1.3494566

Source DB:  PubMed          Journal:  J Biomed Opt        ISSN: 1083-3668            Impact factor:   3.170


  16 in total

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4.  Physiological fluorescence lifetime imaging microscopy improves Förster resonance energy transfer detection in living cells.

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5.  Picosecond-resolution fluorescence lifetime imaging microscopy: a useful tool for sensing molecular interactions in vivo via FRET.

Authors:  Wei Zhong; Mei Wu; Ching-Wei Chang; Karl A Merrick; Sofia D Merajver; Mary-Ann Mycek
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  5 in total

1.  Total variation versus wavelet-based methods for image denoising in fluorescence lifetime imaging microscopy.

Authors:  Ching-Wei Chang; Mary-Ann Mycek
Journal:  J Biophotonics       Date:  2012-03-13       Impact factor: 3.207

Review 2.  FRAP, FLIM, and FRET: Detection and analysis of cellular dynamics on a molecular scale using fluorescence microscopy.

Authors:  Carla De Los Santos; Ching-Wei Chang; Mary-Ann Mycek; Richard A Cardullo
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3.  Time-domain fluorescence lifetime imaging techniques suitable for solid-state imaging sensor arrays.

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Journal:  Sensors (Basel)       Date:  2012-05-02       Impact factor: 3.576

4.  Can we use rapid lifetime determination for fast, fluorescence lifetime based, metabolic imaging? Precision and accuracy of double-exponential decay measurements with low total counts.

Authors:  Susana Figueiredo Silva; José Paulo Domingues; António Miguel Morgado
Journal:  PLoS One       Date:  2019-05-14       Impact factor: 3.240

5.  Rapid global fitting of large fluorescence lifetime imaging microscopy datasets.

Authors:  Sean C Warren; Anca Margineanu; Dominic Alibhai; Douglas J Kelly; Clifford Talbot; Yuriy Alexandrov; Ian Munro; Matilda Katan; Chris Dunsby; Paul M W French
Journal:  PLoS One       Date:  2013-08-05       Impact factor: 3.240

  5 in total

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