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The reduction of average extinction cross section of a localized surface plasmon (LSP) resonance mode under the random orientation condition of Au nanoring (NRI) distribution is first numerically demonstrated. The reduction range depends on the geometry symmetry property of the electron oscillation axis in the LSP resonance mode. Then, by increasing the ring height, an optimized Au NRI geometry is designed to make the resonance wavelengths of its cross-ring dipole mode and axial dipole mode the same. In such an Au NRI, a few higher-order axial LSP modes are discovered. Also, under the condition of random orientation distribution, the ranges of extinction, scattering, and absorption cross section reductions from the corresponding maximum levels of optimized excitations are significantly decreased, when compared with the counterparts of the Au NRIs of a smaller ring height. [ABSTRACT FROM AUTHOR]

Au nanorings (NRIs), which have the localized surface plasmon resonance (LSPR) wavelength around 1058 nm, either with or without linked antibodies, are applied to SAS oral cancer cells for cell inactivation through the LSPR-induced photothermal effect when they are illuminated by a laser of 1065 nm in wavelength. Different incubation times of cells with Au NRIs are considered for observing the variations of cell uptake efficiency of Au NRI and the threshold laser intensity for cell inactivation. In each case of incubation time, the cell sample is washed for evaluating the total Au NRI number per cell adsorbed and internalized by the cells based on inductively coupled plasma mass spectrometry measurement. Also, the Au NRIs remaining on cell membrane are etched with KI/I2 solution to evaluate the internalized Au NRI number per cell. The threshold laser intensities for cell inactivation before washout, after washout, and after KI/I2 etching are calibrated from the circular area sizes of inactivated cells around the illuminated laser spot center with various laser power levels. By using Au NRIs with antibodies, the internalized Au NRI number per cell increases monotonically with incubation time up to 24 h. However, the number of Au NRI remaining on cell membrane reaches a maximum at 12 h in incubation time. The cell uptake behavior of an Au NRI without antibodies is similar to that with antibodies except that the uptake NRI number is significantly smaller and the incubation time for the maximum NRI number remaining on cell membrane is delayed to 20 h. By comparing the threshold laser intensities before and after KI/I2 etching, it is found that the Au NRIs remaining on cell membrane cause more effective cancer cell inactivation, when compared with the internalized Au NRIs. [ABSTRACT FROM AUTHOR]