Au nanoparticles for SERS: Temperature-controlled nanoparticle morphologies and their Raman enhancing properties.

Quasi-fractal gold nanoparticles can be synthesized via a modified and temperature controlled procedure initially used for the synthesis of star-like gold nanoparticles. The surface features of nanoparticles lead to improved enhancement of Raman scattering intensity of analyte molecules due to the increased number of sharp surface features possessing numerous localized surface plasmon resonances (LSPR). The LSPR is affected by the size and shape of surface features as well as inter-nanoparticle interactions, as these affect the oscillation modes of electrons on the nanoparticle surfaces. The effect of the particle morphologies on the localized surface plasmon resonance (LSPR) and on the surface-enhancing capabilities of these nanoparticles is explored by comparing different nanoparticle morphologies and concentrations. We show that in a fixed nanoparticle concentration regime, quasi-fractal gold nanoparticles (gold nanocaltrop) provide the highest level of surface enhancement, whereas spherical nanoparticles provide the largest enhancement in a fixed gold concentration regime. The presence of highly branched features enables these nanoparticles to couple with a laser wavelength, despite having no strong absorption band and hence no single surface plasmon resonance. This cumulative LSPR may allow these nanoparticles to be used in a variety of applications in which laser wavelength flexibility is beneficial, such as in medical imaging applications where fluorescence at short laser wavelengths may be coupled with non-fluorescing long laser wavelengths for molecular sensing.

Surface-Enhanced Raman Spectroscopy Characterization of Breast Cell Phenotypes: Effect of Nanoparticle Geometry.

The use of surface-enhanced Raman spectroscopy (SERS) to delineate between the breast epithelial cell lines MCF10A, SK-BR-3, and MDA-MB-231 is explored utilizing varied morphologies of gold nanoparticles. The nanoparticles studied had spherical, star-like, and quasi-fractal (nanocaltrop) morphologies and possessed varying degrees of surface inhomogeneity and complexity. The efficacy of Raman enhancement of these nanoparticles was a function of their size, their surface morphology, and the associated density of "hot spots," as well as their cellular uptake. The spherical and star-like nanoparticles provided strong signal enhancement that allowed for the discernment among the three cell phenotypes based solely on the acquired Raman spectra. The presence of overlapping Raman band spectral regions, as well as unique spectral bands, suggests that the underlying biological differences between these cells can be accessed without the need for tagging the nanoparticles or for specific cell targeting, demonstrating the potential ubiquity of this technique in imaging any cancer. This work provides clear evidence for the potential application of SERS as a tool for mapping cancerous lesions, possibly during surgery and under histopathological analysis.