posted on 2017-08-24, 00:00authored byYa Yan, Lingyan Meng, Wenqiang Zhang, Yan Zheng, Shuo Wang, Bin Ren, Zhilin Yang, Xiaomei Yan
Metal-enhanced
fluorescence (MEF) based on localized surface plasmon
resonance (LSPR) is an effective strategy to increase the detection
sensitivity in biotechnology and biomedicine. Because plasmonic nanoparticles
are intrinsically heterogeneous, high-throughput single-particle analysis
of MEF in free solution are highly demanded for the mechanistic understanding
and control of this nanoscale process. Here, we report the application
of a laboratory-built high-sensitivity flow cytometer (HSFCM) to investigate
the fluorescence-enhancing effect of individual plasmonic nanoparticles
on nearby fluorophore molecules. Ag@SiO2 core–shell
nanoparticles were used as the model system which comprised a silver
core, a silica shell, and an FITC-doped thin layer of silica shell.
FITC-doped silica nanoparticles of the same particle size but without
silver core were used as the counterparts. Both the side scattering
and fluorescence signals of single nanoparticles in suspension were
measured simultaneously by the HSFCM at a speed of thousands of particles
per minute. The roles of silver core size (40–100 nm) and fluorophore–metal
distance (5–30 nm) were systematically examined. Fluorescence
enhancement factor exceeding 30 was observed at silver core size of
70 nm and silica shell thickness of 5 nm. Compared with ensemble-averaged
spectrofluorometric measurements, our experimental observation at
the single-particle level was well supported by the finite difference
time domain (FDTD) calculation. It allows us to achieve a fundamental
understanding of MEF, which is important to the design and control
of plasmonic nanostructures for efficient fluorescence enhancement.