Related Experiment Video
Updated: Dec 13, 2025

09:45
Fluorescence Lifetime Imaging of Molecular Rotors in Living Cells
Published on: February 9, 2012
25.8K
Macroscopic fluorescence lifetime topography enhanced via spatial frequency domain imaging
Optics Letters
|August 1, 2020
Summary
We developed a machine learning framework for macroscopic fluorescence lifetime imaging (MFLI) to accurately determine the depth of fluorescent inclusions in biological tissues, aiding in applications like image-guided surgery.
Area of Science:
- Biomedical Optics
- Medical Imaging
- Computational Biology
Background:
- Accurate depth localization of fluorescent inclusions in bio-tissues is crucial for applications like optical-guided surgery.
- Existing methods may face challenges in precisely determining the depth of deeply seated fluorescent targets.
Purpose of the Study:
- To develop a computational framework for macroscopic fluorescence lifetime imaging (MFLI) topography.
- To accurately retrieve the depth of fluorescent inclusions within bio-tissues using machine learning.
Main Methods:
- A machine learning-based computational framework utilizing macroscopic fluorescence lifetime imaging (MFLI) topography.
- Integration of spatial frequency domain imaging (SFDI) for in situ optical property retrieval.
- A Siamese network architecture processing optical properties and time-resolved fluorescence decays to simultaneously determine lifetime maps and depth profiles.
Main Results:
- The developed MFLI topography framework accurately retrieves the depth of fluorescent inclusions.
- Coupling depth retrieval with optical property estimation significantly enhances accuracy.
- Validation performed using extensive in silico datasets and phantom experiments confirmed the approach's efficacy.
Conclusions:
- The proposed machine learning-based MFLI topography framework offers a highly accurate method for depth retrieval of fluorescent inclusions.
- This computational approach is expected to be valuable for advancing optical-guided surgery and other biomedical imaging applications.
More Related Videos
Related Concept Videos
Super-resolution Fluorescence Microscopy
12.1K
Super-resolution fluorescence microscopy (SRFM) provides a better resolution than conventional fluorescence microscopy by reducing the point spread function (PSF). PSF is the light intensity distribution from a point that causes it to appear blurred. Due to PSF, each fluorescing point appears bigger than its actual size, and it is the PSF interference of nearby fluorophores that causes the blurred image. Various approaches to achieving higher resolution through SRFM have recently been...
12.1K
Confocal Fluorescence Microscopy
19.6K
Confocal microscopy is an advanced microscopic technique. The prime advantage of the confocal microscope over other microscopy techniques is its ability to block the out-of-focus light from the illuminated samples using pinholes. It is widely used with fluorescence optics to obtain high-resolution, sharp contrast images. Unlike optical microscopes, confocal microscopes use a focused beam of light laser to scan the entire sample surface at different z-planes. These microscopes are, therefore,...
19.6K
Total Internal Reflection Fluorescence Microscopy
10.9K
Total internal reflection fluorescence microscopy or TIRF is an advanced microscopic technique used to visualize fluorophores in samples close to a solid surface with a higher refractive index, such as a glass coverslip. TIRF only allows fluorophores in proximity to the solid surface to be excited. When light from a medium with a lower refractive index (such as air) hits the glass coverslip at a critical angle, the light undergoes total internal reflection stead of passing through the glass.
10.9K
Protein Dynamics in Living Cells
2.5K
Different fluorescence-based techniques are used to study the protein dynamics in living cells. These techniques include FRAP, FRET, and PET.
Fluorescent recovery after photobleaching (FRAP) is a fluorescent-protein-based detection technique used to quantify protein movement rates within the cell. This method exposes a small portion of the cell to an intense laser beam. The laser beam causes permanent photobleaching of the fluorophore-tagged proteins in the exposed region. As the bleached...
Fluorescent recovery after photobleaching (FRAP) is a fluorescent-protein-based detection technique used to quantify protein movement rates within the cell. This method exposes a small portion of the cell to an intense laser beam. The laser beam causes permanent photobleaching of the fluorophore-tagged proteins in the exposed region. As the bleached...
2.5K

