Related Experiment Video
Updated: Feb 17, 2026

06:01
Fluorescence Lifetime Macro Imager for Biomedical Applications
Published on: April 7, 2023
1.2K
Recent Advances in Fluorescence Lifetime Analytical Microsystems: Contact Optics and CMOS Time-Resolved Electronics
Liping Wei1, Wenrong Yan2, Derek Ho3
1Department of Materials Science and Engineering, City University of Hong Kong, Hong Kong 999077, China. weiliping1988@gmail.com.
Sensors (Basel, Switzerland)
|December 7, 2017
Summary
Portable fluorescence lifetime measurement is now achievable using contact sensing and CMOS technology. These integrated microsystems offer a low-cost, high-performance alternative to bulky lab equipment for diagnostics.
Area of Science:
- Optoelectronics
- Biomedical Engineering
- Spectroscopy
Background:
- Fluorescence spectroscopy is vital for medical diagnostics and bio-imaging but limited by bulky, expensive equipment.
- Current time-resolved fluorescence techniques like TCSPC are complex and costly.
- A need exists for high-performance, portable, and low-cost fluorescence sensors.
Purpose of the Study:
- To explore advances in contact sensing and CMOS technology for integrated fluorescence lifetime measurement.
- To address the limitations of current time-resolved fluorescence analysis systems.
- To enable the development of portable, low-cost diagnostic devices.
Main Methods:
- Investigating contact sensing to simplify optical components.
- Utilizing complementary metal-oxide-semiconductor (CMOS) for on-chip detection and processing.
- Examining recent prototypes of integrated fluorescence lifetime measurement microsystems.
Main Results:
- Contact sensing and CMOS implementation significantly reduce size and power consumption.
- Prototypes demonstrate high performance, mitigating bulkiness and cost issues.
- Integrated microsystems show potential for advanced diagnostic applications.
Conclusions:
- CMOS-based contact sensing microsystems are a promising technology for portable diagnostics.
- These integrated systems offer a viable solution for application-specific, low-cost, time-resolved devices.
- The research paves the way for wider adoption of fluorescence lifetime measurements outside laboratory settings.
Related Concept Videos
Confocal Fluorescence Microscopy
21.3K
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,...
21.3K
Super-resolution Fluorescence Microscopy
14.6K
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...
14.6K
Protein Dynamics in Living Cells
2.8K
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...
2.8K

