In this study, we report the surface
enhanced fluorescence (SEF)
of a biologically important organic dye, fluorescein (FL), by silver
nanoparticles (Ag NPs) in an aqueous medium and its implications for
human cell imaging. The as-synthesized Ag NPs were characterized by
dynamic light scattering (DLS), zeta potential, transmission electron
microscopy (TEM), and UV–vis absorption spectroscopic studies.
The interaction and aggregation of FL dye with Ag NPs and a cationic
surfactant, namely, cetyltrimethylammonium bromide (CTAB), were explored
by UV–vis absorption and steady-state and time-resolved fluorescence
spectroscopic methods. The distance-dependent fluorescence enhancement
of FL due to Ag NPs in the solution was also theoretically correlated
by three-dimensional finite-difference time-domain (3D-FDTD) simulation.
The plasmonic coupling between neighboring NPs facilitated the augmentation
of the local electric field, thereby producing various “hotspots”
that influence the overall fluorescence of the emitter. J-type aggregates
of FL in the presence of the CTAB micelles and Ag NP mixed solution
were confirmed by electronic spectroscopy. The density functional
theoretical (DFT) study revealed the electronic energy levels associated
with different forms of FL dye in the aqueous solution. Most interestingly,
the Ag NP/FL mixed system used in fluorescence imaging of human lung
fibroblast cells (WI 38 cell line) showed a significantly stronger
green fluorescence signal compared to that of FL after an incubation
period of only 3 h. This study confirms that the Ag NP mediated SEF
phenomenon of the FL dye is also manifested in the intracellular medium
of human cells giving a brighter and more intense fluorescence image.
The cell viability test after exposure to the Ag NP/FL mixed system
was confirmed by the MTT assay method. The proposed study may have
an implication as an alternate approach for human cell imaging with
higher resolution and more contrast.