The application of luminescent silver nanoparticles as imaging agents for neural stem and rat basophilic leukemia cells was demonstrated. The experimental size dependence of the extinction and emission spectra for silver nanoparticles were also studied. The nanoparticles were functionalized with fluorescent glycine dimers. Spectral position of the resonance extinction and photoluminescence emission for particles with average diameters ranging from 9 to 32 nm were examined. As the particle size increased, the spectral peaks for both extinction and the intrinsic emission of silver nanoparticles shifted to the red end of the spectrum. The intrinsic photoluminescence of the particles was orders of magnitude weaker and was spectrally separated from the photoluminescence of the glycine dimer ligands. The spectral position of the ligand emission was independent of the particle size; however, the quantum yield of the nanoparticle-ligand system was size-dependent. This was attributed to the enhancement of the ligand’s emission caused by the local electric field strength’s dependence on the particle size. The maximum quantum yield determined for the nanoparticle-ligand complex was (5.2 ± 0.1) %. The nanoparticles were able to penetrate cell membranes of rat basophilic leukemia and neural stem cells fixed with paraformaldehyde. Additionally, toxicity studies were performed. It was found that towards rat basophilic leukemia cells, luminescent silver nanoparticles had a toxic effect in the silver atom concentration range of 10–100 μM.
We used a laser-directed fabrication to create silver nanostructures on glass cover slips via photo-reduction. The resulting silver films exhibited plasmonic properties which show promise in application towards surface enhanced Raman spectroscopy (SERS). The enhancement factor calculated for the deposits was approximately ~106 using the standard thiophenol, which is comparable to other SERS-active plasmonic nanostructures fabricated through more complex techniques, such as electron beam lithography. The silver nanostructures were then employed in the enhancement of Raman signals from N-butyryl-L-homoserine lactone, a signaling molecule relevant to bacteria quorum sensing. In particular, the work presented here shows that the laser-deposited plasmonic nanostructures are promising candidates for monitoring concentrations of signaling molecules within biofilms containing quorum sensing bacteria.
Due to their biocompatibility, ease of surface modification, and heating capabilities, gold nanomaterials are considered excellent candidates for the advancement of photothermal therapy techniques and related applications in cancer treatment. Various morphologies of gold nanomaterials have been shown to heat when exposed to high-powered laser irradiation, especially that which is from the near-infrared (NIR) region. While these lasers work well and are effective, light-emitting diodes (LEDs) may offer a safe and low-powered alternative to these high energy lasers. We investigated the heating capability of NIR-dye conjugated gold nanorods when exposed to an 808 nm LED light source using polyethylene glycol (PEG)-coated gold nanorods as the control. In this way, since the rods exhibited a surface plasmon resonance peak between 795 and 825 nm for both the PEG-coated rods and the dye-conjugated rods, which are fairly close to the frequency of the 530 mW, 850 nm LED light source, we were able to reveal the heating effect of the dye modification. While both morphologies heat when irradiated with the LED light, we demonstrated that the addition of an NIR dye increases the rate of heating and cooling, compared to the PEGylated counterpart. To our knowledge, the complementary effect given by the conjugated NIR-dye has not been previously reported in the literature. The targeting abilities of the NIR-dye combined with the increased heating rate of the modified particles used in this proof-of-concept work suggests that these particles may be exceptional candidates for theranostic applications.
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