We report numerical analysis and experimental observation of strongly localized plasmons guided by a triangular metal wedge. Dispersion and dissipation of such wedge plasmons are analyzed using the finite-difference time-domain algorithm. Experimental observation is conducted by the end-fire excitation and near-field detection of the predicted plasmons on a 40° silver nanowedge. Good agreement with the theoretically predicted propagation distances is demonstrated. Differences between the theoretical and experimental field distribution are explained by insufficient resolution of the near-field optical probe.
We report numerical analysis and experimental observation of two-dimensionally localized plasmonic modes guided by a nano-gap in a thin metal film. Dispersion, dissipation and field structure of these modes are analyzed using the finite-difference time-domain algorithm. The experimental observation is conducted by the end-fire excitation of the proposed gap plasmon waveguides and detection of the generated modes using their edge scattering and CCD camera imaging. Physical interpretation of the obtained results is presented and origins of the described modes are discussed.
Nanoparticles are considered to be efficient tools for inducing potent immune responses by an Ag carrier. In this study, we examined the effect of Ag-carrying biodegradable poly(γ-glutamic acid) (γ-PGA) nanoparticles (NPs) on the induction of immune responses in mice. The NPs were efficiently taken up by dendritic cells (DCs) and subsequently localized in the lysosomal compartments. γ-PGA NPs strongly induced cytokine production, up-regulation of costimulatory molecules, and the enhancement of T cell stimulatory capacity in DCs. These maturational changes of DCs involved the MyD88-mediated NF-κB signaling pathway. In vivo, γ-PGA NPs were preferentially internalized by APCs (DCs and macrophages) and induced the production of IL-12p40 and IL-6. The immunization of mice with OVA-carrying NPs induced Ag-specific CTL activity and Ag-specific production of IFN-γ in splenocytes as well as potent production of Ag-specific IgG1 and IgG2a Abs in serum. Furthermore, immunization with NPs carrying a CD8+ T cell epitope peptide of Listeria monocytogenes significantly protected the infected mice from death. These results suggest that Ag-carrying γ-PGA NPs are capable of inducing strong cellular and humoral immune responses and might be potentially useful as effective vaccine adjuvants for the therapy of infectious diseases.
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