Enhancing biological imaging with high-performance probes based on thermally activated delayed fluorescence
Related Experiment Video
Updated: Jan 15, 2026

High-resolution Thermal Micro-imaging Using Europium Chelate Luminescent Coatings
Published on: April 16, 2017
Yunfei Xia1, Meizhu Zheng2, Xue Li1
1School of Life Science, Changchun Normal University, Changchun 130032, China.
Abstract:
Thermally activated delayed fluorescence (TADF) materials have gained significant attention in biological imaging due to their high quantum efficiency and capacity to suppress short-lived background fluorescence. This review comprehensively analyzes recent advancements in organic TADF probes, focusing on their photophysical mechanisms, structural design, and encapsulation strategies to improve biocompatibility and photostability. We highlight their applications in organelle-targeted imaging, dynamic live-cell tracking, and in vivo imaging in model organisms such as zebrafish and mice. Additionally, we discuss current challenges, including oxygen sensitivity and limited long-term stability. The development of high-performance TADF probes promises to enhance imaging quality, facilitate deeper tissue penetration, and support long-term cellular studies, thereby contributing substantially to biomedical research and diagnostic imaging.
More Related Videos
13:47TIRFM and pH-sensitive GFP-probes to Evaluate Neurotransmitter Vesicle Dynamics in SH-SY5Y Neuroblastoma Cells: Cell Imaging and Data Analysis
Published on: January 29, 2015
12:51Simultaneous Multicolor Imaging of Biological Structures with Fluorescence Photoactivation Localization Microscopy
Published on: December 9, 2013
Related Concept Videos
Labeling DNA Probes
Radioisotopes, fluorophores, or small molecule binding partners like biotin or digoxigenin, are the most widely used reporter tags for labeling DNA probes. These labels can be attached to the probe DNA molecule via...
Super-resolution Fluorescence Microscopy
Protein Dynamics in Living Cells
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...