Photothermal versus photodynamic treatment for the inactivation of the bacteria Escherichia coli and Bacillus cereus: An in vitro study.

The widespread occurrence of microbial pathogens, including multidrug-resistant (MDR) bacteria, has ignited research efforts to discover alternative strategies to combat infections in patients. Recently, photodynamic therapy (PDT) and photothermal therapy (PTT) have been proposed for the inactivation of pathogens. Although PDT and PTT are very promising antipathogenic tools, further effort is needed to determine their real impact on pathogens apart from the effects of individual elements involved in the photodynamic/photothermal processes, i.e., light, photosensitizers (PSs), and nanoparticles. Accordingly, in the current study, toluidine blue O (TBO) and gold nanoparticles (GNP) were used as generators of reactive oxygen species (ROS) and hyperthermia in the presence of light, respectively. Escherichia coli (E. coli) and Bacillus cereus (B. cereus) bacteria were chosen as examples of gram-negative and gram-positive bacteria, respectively. Before the bactericidal activity of PDT was assessed, the aggregation of TBO and its effect on the growth of both strains of bacteria were studied. Additionally, E. coli and B. cereus were exposed to a range of doses of 633 nm helium-neon laser light to investigate its effect. In a separate set of experiments, the bactericidal activity of PTT was assessed after the effects of GNP and green light (530 nm) had been assessed. The results showed that PDT and PTT should be considered useful tools for bacterial eradication even when the light, PSs, and nanoparticles are each used at doses safe for bacterial growth. Moreover, different photodynamic responses were observed for E. coli and B. cereus, and light from a 633 nm laser and a 530 nm light-emitting diode (LED) showed disparate responses when applied alone to both bacteria.

Anti-proliferative Activities of Metallic Nanoparticles in an in Vitro Breast Cancer Model.

AIMS: To investigate effect of metallic nanoparticles, silver (AgNPs) and gold nanoparticles (AuNPs) as antitumor treatment in vitro against human breast cancer cells (MCF-7) and their associated mechanisms. This could provide new class of engineered nanoparticles with desired physicochemical properties and may present newer approaches for therapeutic modalities to breast cancer in women. MATERIALS AND METHODS: A human breast cancer cell line (MCF-7) was used as a model of cells. Metallic nanoparticles were characterized using UV-visible spectra and transmission electron microscopy (TEM). Cytotoxic effects of metallic nanoparticles on MCF-7 cells were followed by colorimetric SRB cell viability assays, microscopy, and cellular uptake. Nature of cell death was further investigated by DNA analysis and flow cytometry. RESULTS: Treatment of MCF-7 with different concentrations of 5-10nm diameter of AgNPs inhibited cell viability in a dose-dependent manner, with IC50 value of 6.28µM, whereas treatment of MCF-7 with different concentrations of 13-15nm diameter of AuNPs inhibited cell viability in a dose-dependent manner, with IC50 value of 14.48µM. Treatment of cells with a IC50 concentration of AgNPs generated progressive accumulation of cells in the S phase of the cell cycle and prevented entry into the M phase. The treatment of cells with IC50 concentrations of AuNPs similarly generated progressive accumulation of cells in sub-G1 and S phase, and inhibited the entrance of cells into the M phase of the cell cycle. DNA fragmentation, as demonstrated by electrophoresis, indicated induction of apoptosis. CONCLUSIONS: Our engineered silver nanoparticles effectively inhibit the proliferation of human breast carcinoma cell line MCF-7 in vitro at high concentration (1000 µM) through apoptotic mechanisms, and may be a beneficial agent against human carcinoma but further detailed study is still needed.

Spectroscopic characterization of magnetic Fe3O4@Au core shell nanoparticles.

The magnetic nanoparticles iron oxide (Fe3O4) nanoparticles and iron oxide/gold core-shell (Fe3O4/Au) nanoparticles were synthesized and their catalytic photo-degradation activity towards malathion as example of organophosphorus pesticides were reported. Iron oxide (Fe3O4) magnetic nanoparticle was successfully prepared through co-precipitation method by the reduction of ferric chloride (FeCl3) using ascorbic acid. The morphology of the prepared nanoparticles was characterized by the TEM and XRD (X-ray diffraction) techniques. Degradation of 10 ppm of malathion in the presence of these nanoparticles under UV radiation was monitored using (HPLC) and UV-visible spectra. Fe3O4/Au nanoparticles showed higher efficiency in photo-degradation of malathion than Fe3O4 ones.

Structure-directing and high-efficiency photocatalytic hydrogen production by Ag clusters.

H2 production by water splitting is hindered mainly by the lack of low-cost and efficient photocatalysts. Here we show that sub-nanometric silver clusters can catalyze the anisotropic growth of gold nanostructures by preferential adsorption at certain crystal planes of Au seeds, with the result that the final nanostructure can be tuned via the cluster/seed ratio. Such semiconducting Ag clusters are extremely stable and retain their electronic structure even after adsorption at the tips of Au nanorods, enabling various photocatalytic experiments, such as oxygen evolution from basic solutions. In the absence of electron scavengers, UV irradiation generates photoelectrons, which are stored within the nanorods, increasing their Au Fermi level up to the redox pinning limit at 0 V (RHE), where hydrogen evolution occurs with an estimated high efficiency of 10%. This illustrates the considerable potential of very small zerovalent, nonmetallic clusters as novel atomic-level photocatalysts.

Hybrid Au-CdSe and Ag-CdSe nanoflowers and core-shell nanocrystals via one-pot heterogeneous nucleation and growth.

A general approach, based on heterogeneous nucleation and growth of CdSe nanostructures on Au or Ag nanocrystals, for the synthesis of Au-CdSe and Ag-CdSe hybrid nanostructures is developed. The new approach provides a versatile one-pot route for the synthesis of hybrid nanoflowers consisting of a gold or silver core and multipod CdSe rods or an intact CdSe shell with controlled thickness, depending on the nucleation and growth parameters. At lower growth temperatures such as 150 °C, the CdSe clusters are adsorbed on the surface of the metal cores in their surface defects, then multiple arms and branches form, resulting in nanoflower-shaped hybrid structures. Increasing the size of the metal core through the choice of the reducing and capping agents results in an improvement of the interface between the metal and CdSe domains, producing core-shell structures. The growth temperature appears to be the most important factor determining the nature of the interface between the metal and CdSe domains. At relatively high temperatures such as 300 °C, the formation of large, faceted Au cores creates preferential growth sites for the CdSe nanocrystalline shell, thus resulting in well-defined Au-CdSe core-shell structures with large interfaces between the Au and CdSe domains. The present approach is expected to foster systematic studies of the electronic structures and optical properties of the metal-semiconductor hybrid materials for potential applications in photovoltaic and nanoelectronic devices.

Formation mechanisms of gold-zinc oxide hexagonal nanopyramids by heterogeneous nucleation using microwave synthesis.

This work reports the development of a fast and simple "one-pot" route for the synthesis of hybrid Au-ZnO hexagonal nanopyramids by sequential homogeneous-heterogeneous nucleation steps involving both Au and Zn ions using microwave irradiation (MWI). The rapid decomposition of zinc acetate by MWI in the presence of a mixture of oleic acid (OAc) and oleylamine (OAm) results in the formation of hexagonal ZnO nanopyramids. In the presence of Au ions, the initially formed Au nanocrystals act as heterogeneous nuclei for the nucleation and growth of the ZnO nanopyramids. The Au nanoparticles promote the heterogeneous nucleation of ZnO and the formation of the hexagonal base of the ZnO nanopyramids. Using preformed Au nanoparticles instead of Au ions results in a narrow size distribution of uniform Au-ZnO nanopyramids, each consisting of a gold nanoparticle embedded in the center of the hexagonal base of the ZnO nanopyramid. We study the factors that control the nucleation and growth of these complex structures, and provide new insights into the stepwise homogeneous-heterogeneous mechanism and the conventional heterogeneous nucleation on preformed Au nanoparticles. The formation of the hetero nanostructures Au-ZnO nanopyramids is strongly dependent on the molar ratios of OAc to OAm. The presence of OAc with a considerable dipole moment results in strong electrostatic interaction with the polar surfaces of the growing ZnO nanocrystals thus resulting in slowing the growth rate of the polar planes and allowing the formation of well-developed facets. In the absence of Au nanoparticles, a high concentration of zinc acetate and longer MWI times are required for the production of the nanopyramids. The gold nanoparticles could provide the metallic contact points within the hybrid nanopyramids which could facilitate the bottom-up assembly of Au-ZnO devices. Furthermore, the Au-ZnO nanopyramids could have improved performance in solar energy conversion and photocatalysis.

Growth mechanism of anisotropic gold nanocrystals via microwave synthesis: formation of dioleamide by gold nanocatalysis.

A facile and fast one-pot microwave irradiation method has been developed to prepare different shapes of gold nanoparticles capped with a mixture of oleylamine and oleic acid. The size, shape, and morphology of the nanocrystals could be tailored by varying the ratio of oleylamine to oleic acid, the microwave time, and the concentration of the gold ions. These effects are directly reflected in the surface plasmon resonance properties of the resulting nanocrystals in the visible and near-infrared regions. Pure amine leads to the formation of only spherical particles. Introducing oleic acid increases the growth rate and enhances the formation of anisotropic shapes. Experimental evidence and new insights on the reaction mechanism confirm the formation of dioleamide from the reaction of oleic acid and oleylamine catalyzed by the gold nanocrystals. In the absence of gold nanoparticles, the conventional synthesis of dioleamide requires 12 h of reaction time at 120 degrees C. New insights on the reaction mechanism indicate that excess oleic acid enhances the formation of hexagons and more anisotropic shapes of the gold nanocrystals.

Rapid and sensitive microplate assay for screening the effect of silver and gold nanoparticles on bacteria.

BACKGROUND & AIM: Nanomaterials are the leading requirement of the rapidly developing field of nanomedicine and bionanotechnology, and in this respect, nanotoxicology research is gaining great importance. In the field of infections, nanoparticles are being utilized as therapeutic tools against microbes, thus understanding the properties of nanoparticles and their effect on microbes is essential prior to clinical application. The aim of this study was to evaluate a microplate-based assay for monitoring the toxicity of silver and gold nanoparticles on bacteria. METHOD: Escherichia coli, a Gram-negative bacteria, and Staphylococcus capitis, a Gram-positive bacteria, were exposed to different concentrations of gold and silver nanoparticles. RESULTS: Analysis of bacterial growth showed that the toxicity of silver nanospheres is higher than that of gold nanospheres. The toxicity of silver nanoparticles is dependent on their concentration, whereas in the case of gold nanoparticles, there is no significant toxic effect. Therefore, the described microplate assay could be used as a rapid and sensitive method for detection of bacterial growth inhibition.

Synthesis of high quality zinc blende CdSe nanocrystals.

Highly homogeneous and luminescent CdSe colloidal nanocrystals in the less common zinc blende crystal structure have been obtained at high temperature in a noncoordinating organic solvent. The key parameter appears to be the addition of a phosphonic acid to the trioctylphosphine-selenium complex before its injection into the hot cadmium mixture, while the role of temperature is less relevant. Compared to standard (wurtzite) colloidal CdSe preparations, we find that the growth rate is considerably reduced, and the energy gap between the first two absorption bands becomes larger.