Nanoparticles containing high-Z elements are known to boost the efficacy of radiation therapy. Gadolinium (Gd) is particularly attractive because this element is also a positive contrast agent for MRI, which allows for the simultaneous use of imaging to guide the irradiation and to delineate the tumor. In this study, we used the Gd-based nanoparticles, AGuIX®. After intravenous injection into animals bearing B16F10 tumors, some nanoparticles remained inside the tumor cells for more than 24 hours, indicating that a single administration of nanoparticles might be sufficient for several irradiations. Combining AGuIX® with radiation therapy increases tumor cell death, and improves the life spans of animals bearing multiple brain melanoma metastases. These results provide preclinical proof-of-concept for a phase I clinical trial.

Acoustic vibrations of assemblies of gold nanoparticles were investigated using ultralow frequency micro-Raman scattering and finite element simulations. When exciting the assemblies resonantly with the surface plasmon resonance of electromagnetically coupled nanoparticles, Raman spectra present an ultralow frequency band whose frequency lies below the lowest Raman active Lamb mode of single nanoparticles that was observed. This feature was ascribed to a Raman vibration mode of gold nanoparticle "supermolecules", that is, nanoparticles mechanically coupled by surrounding polymer molecules. Its measured frequency is inversely proportional to the nanoparticle diameter and sensitive to the elastic properties of the interstitial polymer. The latter dependence as well as finite element simulations suggest that this mode corresponds to the out-of-phase semirigid translation (l = 1 Lamb mode) of each nanoparticle of a dimer inside the matrix, activated by the mechanical coupling between the nanoparticles. These observations were permitted only thanks to the resonant excitation with the coupling plasmon excitation, leading to an enhancement up to 10(4) of the scattering by these vibrations. This enhanced ultralow frequency Raman scattering thus opens a new route to probe the local elastic properties of the surrounding medium.

This paper describes a general stepwise strategy combining diazonium salt, surface-initiated atom transfer radical polymerization (SI-ATRP), and click chemistry for an efficient gold surface functionalization by poly(N-isopropylacrylamide) (PNIPAM) brushes and gold nanoparticle assemblies. We designed by this way a new plasmonic device made of gold nanoparticles separated from a gold film through a thermoresponsive polymer layer. This organic layer responds to temperature variations by conformational changes (with a characteristic temperature called the lower critical solution temperature, LCST) and is therefore able to vary the distance between the gold nanoparticles and the gold film. The optical properties of these stimulable substrates were probed by surface-enhanced raman scattering (SERS) using methylene blue (MB) as a molecular probe. We show that an increase of the external temperature reversibly induces a significant enhancement of the MB SERS signal. This was attributed to a stronger interaction between the gold nanoparticles and the gold substrate. The temperature-responsive plasmonic devices developed in this paper thus provide a dynamic SERS platform, with thermally switchable electromagnetic coupling between the gold nanoparticles and the gold surface.