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Nanoparticles of gold, which are in the size range of 10 to 100 nm, undergo a plasmon resonance with light. This is a process whereby the electrons of the gold resonate with incoming radiation causing them to both absorb and scatter light. The effect can be harnessed to either destroy tissue by local heating or release payload molecules of therapeutic importance. Gold nanoparticles can also be conjugated with biologically-active moities, providing possibilities for targeting to particular tissues. Here we review progress in the exploitation of this plasmon resonance of gold nanoparticles in photo-thermal therapeutic medicine. IntroductionMetallic gold, either in the form of bulk surfaces or as nanoparticles, is widely used in the emerging and highly interdisciplinary field of nanotechnology [1][2][3]. Many biodiagnostic applications of gold nanoparticles or electrodes have been developed since the 1970s [4][5][6][7][8][9][10]. However, the rational application of gold nanoparticles in therapeutic situations is a largely undeveloped field. Two properties of gold nanoparticles are attractive in this context. Firstly, antibodies and other biological molecules can be readily attached to the surface of gold nanoparticles, and secondly the plasmon resonances of gold nanoparticles of certain shapes cause them to have photon capture cross sections that are four to five orders of magnitude greater than those of photothermal dyes [11]. These attributes provide the possibility of obtaining very localized heating or drug release in a therapeutic application.

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The optical response from metal nanoparticles and nanostructures is dominated by surface plasmon generation and is critically dependent on the local structure and geometry. Electron energy-loss spectroscopy (EELS), combined with recent developments in spectrum imaging and data processing, has been used to observe the energy and distribution of surface plasmons excited by fast electrons. The energy of the plasmon responses is consistent with the optical response and with calculations. For gold and silver rods and ellipsoids, longitudinal, transverse and distinct cluster modes were readily identified and mapped. The spatial resolution of the presented maps is one order of magnitude better than that achievable with scanning near-field optical microscopy (SNOM)-based techniques.

Gold nanorods have significant technological potential and are of broad interest to the nanotechnology community. The discovery of the seeded, wet-chemical synthetic process to produce them may be regarded as a landmark in the control of metal nanoparticle shape. However, the mechanism by which the initial spherical gold seeds acquire anisotropy is a critical, yet poorly understood, factor. Here we examine the very early stages of rod growth using a combination of techniques including cryogenic transmission electron microscopy, optical spectroscopy, and computational modeling. Reconciliation of the available experimental observations can only be achieved by invoking a stochastic, "popcorn"-like mechanism of growth, in which individual seeds lie quiescent for some time before suddenly and rapidly growing into rods. This is quite different from the steady, concurrent growth of nanorods that has been previously generally assumed. Furthermore we propose that the shape is controlled by the ratio of surface energy of rod sides to rod ends, with values of this quantity in the range of 0.3-0.8 indicated for typical growth solutions.

Hybrid nanostructures containing 1D carbon nanotubes and 2D graphene sheets have many promising applications due to their unique physical and chemical properties. In this study, the authors find Prussian blue (dehydrated sodium ferrocyanide) can be converted to N‐doped graphene–carbon nanotube hybrid materials through a simple one‐step pyrolysis process. Through field emission scanning electron microscopy, transmission electron microscopy, X‐ray diffraction, Raman spectra, atomic force microscopy, and isothermal analyses, the authors identify that 2D graphene and 1D carbon nanotubes are bonded seamlessly during the growth stage. When used as the sulfur scaffold for lithium–sulfur batteries, it demonstrates outstanding electrochemical performance, including a high reversible capacity (1221 mA h g−1 at 0.2 C rate), excellent rate capability (458 and 220 mA h g−1 at 5 and 10 C rates, respectively), and excellent cycling stability (321 and 164 mA h g−1 at 5 and 10 C (1 C = 1673 mA g−1) after 1000 cycles). The enhancement of electrochemical performance can be attributed to the 3D architecture of the hybrid material, in which, additionally, the nitrogen doping generates defects and active sites for improved interfacial adsorption. Furthermore, the nitrogen doping enables the effective trapping of lithium polysulfides on electroactive sites within the cathode, leading to a much‐improved cycling performance. Therefore, the hybrid material functions as a redox shuttle to catenate and bind polysulfides, and convert them to insoluble lithium sulfide during reduction. The strategy reported in this paper could open a new avenue for low cost synthesis of N‐doped graphene–carbon nanotube hybrid materials for high performance lithium–sulfur batteries.

ObjectivesGold nanoparticles (AuNPs) of 21 nm have been previously well characterized in vitro for their capacity to target macrophages via active uptake. However, the short-term impact of such AuNPs on physiological systems, in particular resident macrophages located in fat tissue in vivo, is largely unknown. This project investigated the distribution, organ toxicity and changes in inflammatory cytokines within the adipose tissue after mice were exposed to AuNPs.MethodsMale C57BL/6 mice were injected intraperitoneally (IP) with a single dose of AuNPs (7.85 μg AuNPs/g). Body weight and energy intake were recorded daily. Tissues were collected at 1 h, 24 h and 72 h post-injection to test for organ toxicity. AuNP distribution was examined using electron microscopy. Proinflammatory cytokine expression and macrophage number within the abdominal fat pad were determined using real-time PCR.ResultsAt 72 hours post AuNP injection, daily energy intake and body weight were found to be similar between Control and AuNP treated mice. However, fat mass was significantly smaller in AuNP-treated mice. Following IP injection, AuNPs rapidly accumulated within the abdominal fat tissue and some were seen in the liver. A reduction in TNFα and IL-6 mRNA levels in the fat were observed from 1 h to 72 h post AuNP injection, with no observable changes in macrophage number. There was no detectable toxicity to vital organs (liver and kidney).ConclusionOur 21 nm spherical AuNPs caused no measurable organ or cell toxicity in mice, but were correlated with significant fat loss and inhibition of inflammatory effects. With the growing incidence of obesity and obesity-related diseases, our findings offer a new avenue for the potential development of gold nanoparticles as a therapeutic agent in the treatment of such disorders.