Hollow sea-urchin gold nanoparticles (HSU-GNPs) were successfully prepared through a novel one-step galvanic replacement strategy, and their corresponding optical properties was studied in detail. During the synthesis process, the sizes of the interior hollows of the HSU-GNPs could be changed by adjusting the amount of silver nitrate added into hydrogen tetrachloroaurate trihydrate solution. The absorption spectra of the HSU-GNPs showed that the localized surface plasmon resonance (LSPR) peaks were red-shifted with increasing size of the interior hollows in the HSU-GNPs. When the added amount of silver nitrate was up to 6 μl, the LSPR peak of the synthesized HSU-GNP reached 726 nm as a maximum red-shift. Furthermore, the absorption spectra of the HSU-GNPs with different morphologies were theoretically simulated by the finite element method, which was consistent with the experimental results and explained the origin of the red-shift of the LSPR peaks. In addition, the surface-enhanced Raman scattering (SERS) of the sea urchin gold nanoparticles were also investigated using 4-mercaptobenzoic acid as a Raman reporter molecule. Both the experimental and calculated results showed that the HSU-GNPs had stronger SERS enhancement than the solid sea-urchin gold nanoparticles. In particular, the HSU-GNPs prepared by adding 6 μl silver nitrate exhibited a maximum SERS enhancement factor, EF = 1.1 × 10(9), due to the LSPR peak at 726 nm which is near to the excitation wavelength, 785 nm. This feature is significant for designing a biosensor with a super-high sensitivity based on the morphology of the HSU-GNPs.

Novel Au@Ag core-shell nanocubes (NCs) were successfully prepared by the controlled epitaxial growth of Ag shells onto Au nanoellipsoids (NEs) in the presence of surfactants. The growth mechanism of the Au@Ag core-shell NCs was systematically investigated by analyzing their morphology, optical properties, and crystallography. The localized surface plasmon resonance (LSPR) characteristics and the electric field distribution of the Au@Ag core-shell NCs were studied using the finite element method (FEM) based on the plasmon hybridization theory. Compared with pure Ag NCs, the absorption spectrum of the Au@Ag core-shell NCs exhibits a red shift and a weak shoulder near 550 nm, and the notable enhancement of electric field occurs around the corners along the long-axis of the Au ellipsoidal core because of plasmonic resonant coupling. Surface-enhanced Raman scattering (SERS) of the Au@Ag core-shell NCs labeled with 4-mercaptobenzoic acid molecules reveals that the bimetallic core-shell NCs possess efficient SERS activity with an enhancement factor EF = 2.27 × 10(6), thus confirming the possibility of using the Au@Ag core-shell NCs as a stable probe for SERS-based biosensing applications.

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A clinical target volume (CTV) to planning target volume (PTV) margin recipes was routinely used to ensure dose was actually delivered to target for all (most) patients. Currently used margin recipes were associated with only translational set-up errors in radiotherapy. However, when set-up errors extended to six-degree (6D) scope (three translational and three rotational set-up errors), margin recipe should be re-evaluated. The purpose of this study was to investigate dosimetric changes of targets (both CTV and PTV) coverage when 6D set-up errors were introduced and testify the practicability of currently used margin recipe in radiotherapy. A total number of 105 cone beam computer tomography scans for ten patients with cervical cancer were derived prior to treatment delivery and 6D set-up errors were acquired with image registration tools. Target coverage was evaluated retrospectively for 6D set-up errors introduced plan with 6 mm CTV to PTV margin. Target coverage of PTV showed significant decreases (3.3 %) in set-up errors introduced plans compared with original plans. But CTV coverage was not susceptible to these set-up errors. A tendency of coverage decrease for PTV along with distance away from treatment was testified, from −0.2 to −6.2 %. However, CTV seems changed less, from −0.2 to −0.8 %. The result indicate that a CTV to PTV margin of 6 mm was sufficient to take into account 6D set-up errors for most patients with cervical cancer. Future research suggests a smaller margin to further improve both tumor coverage and organs at risk sparing.

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