Fluorescent organic nanoparticles with enhanced fluorescence by self-aggregation and their application to cellular
Fu Tang1, Chun Wang, Jinshan Wang
1School of Materials Science and Engineering, University of Science and Technology Beijing , Beijing 100083, People's Republic of China.
Abstract:
We report a simple strategy to prepare organic biocompatible fluorescent nanoparticles with enhanced fluorescence. A significant fluorescence enhancement was realized by designing a fluorescent small molecule, 4,4'-(2,7-bis[4-{1,2,2-triphenylvinyl}phenyl]-9H-fluorene-9,9-diyl)bis(N,N,N-trimethylbutan-1-aminum)bromide (TPEFN), with aggregation-induced emission enhancement (AIEE) effect. Nanoparticles of TPEFN can be formed through molecular self-aggregation by gradually increasing the water fraction in TPEFN mixed solution (methanol/water). Fluorescence enhancement by about 120-fold was observed after nanoparticle formation. By addition of the biomolecule adenosine triphosphate (ATP), larger nanoparticles of TPEFN are formed and further fluorescence enhancement can be achieved, yielding a total fluorescence enhancement of 420-fold compared with the TPEFN molecular solution. Both of these nanoparticles show very good biocompatibility. Ultrabright spots present in the confocal laser scanning microscopy image again proved the formation of nanoparticles. Positively charged side chains of TPEFN endow these nanoparticles cationic surfaces. The size of the prepared TPEFN nanoparticles and their cationic surface allow them to be rapidly internalized into cells. Cell viability assays prove that the TPEFN nanoparticles have high biocompatibility. These organic fluorescent nanoparticles show great promise for applications in cellular imaging or biotechnology.
Related Concept Videos
Super-resolution Fluorescence Microscopy
Photoluminescence: Applications
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...


