Shinya Maenosono

Semiconductor quantum dot/albumin complex is a long-life and highly photostable endosome marker.

For the purpose of selecting the efficient dispersion condition of hydrophilic semiconductor quantum dots (QDs) in biological buffers, the dispersion of the QDs mixed with a serum albumin from 9 different species or an ovalbumin was compared by a fluorescence intensity analysis. The QDs mixed with sheep serum albumin (SSA) showed the highest fluorescence of all when the mixtures were dissolved in Dulbeccos MEM. QD/SSA complexes were accumulated in the endosome/lysosome of Vero cells and the fluorescence could be detected over a 5-day post-incubation period. The photostability of QD/SSA complexes associated with the endosomes was detectable, at least, 30 times as long as that of fluorescein-labeled dextran involved in endosomes. QD/SSA complex, therefore, can be used as a long-life and highly photostable endosome marker.

Theoretical assessment of FePt nanoparticles as heating elements for magnetic hyperthermia

FePt magnetic nanoparticles (MNPs) are expected to be a high-performance nanoheater for magnetic hyperthermia because of their high Curie temperature, high saturation magnetization, and high chemical stability. Here, we present a theoretical performance assessment of chemically disordered fcc-phase FePt MNPs. We calculate heat generation and heat transfer in the tissue when an MNP-loaded tumor is placed on an external alternating magnetic field. For comparison, we estimate the performances of magnetite, maghemite, FeCo, and L10-phase FePt MNPs. We find that an fcc FePt MNP has a superior ability in magnetic hyperthermia

Synthesis of core-shell gold coated magnetic nanoparticles and their interaction with thiolated DNA

Core-shell magnetic nanoparticles have received significant attention recently and are actively investigated owing to their large potential for a variety of applications. Here, the synthesis and characterization of bimetallic nanoparticles containing a magnetic core and a gold shell are discussed. The gold shell facilitates, for example, the conjugation of thiolated biological molecules to the surface of the nanoparticles. The composite nanoparticles were produced by the reduction of a gold salt on the surface of pre-formed cobalt or magnetite nanoparticles. The synthesized nanoparticles were characterized using ultraviolet-visible absorption spectroscopy, transmission electron microscopy, energy dispersion X-ray spectroscopy, X-ray diffraction and super-conducting quantum interference device magnetometry. The spectrographic data revealed the simultaneous presence of cobalt and gold in 5.6±0.8 nm alloy nanoparticles, and demonstrated the presence of distinct magnetite and gold phases in 9.2±1.3 nm core-shell magnetic nanoparticles. The cobalt-gold nanoparticles were of similar size to the cobalt seed, while the magnetite-gold nanoparticles were significantly larger than the magnetic seeds, indicating that different processes are responsible for the addition of the gold shell. The effect on the magnetic properties by adding a layer of gold to the cobalt and magnetite nanoparticles was studied. The functionalization of the magnetic nanoparticles is demonstrated through the conjugation of thiolated DNA to the gold shell.

Overview of Nanoparticle Array Formation by Wet Coating

We give a concise overview of nanoparticle array formation by wet coating techniques including patterned assembly, surface modification of nanoparticles, rheology, assembling dynamics, and function of nanoparticle arrays. For the rapid fabrication of large-area and/or patterned nanoparticle arrays, wet coating techniques, such as spin, dip, spray, gravure, slot, roll, and ink-jet coating, are promising ways for practical use in combination with an evaporation-driven self-assembly technique. We have also referred to the concept of array formation via surface modification.

Role of base in the formation of silver nanoparticles synthesized using sodium acrylate as a dual reducing and encapsulating agent.

The formation mechanism of Ag nanoparticles (NPs) synthesized with a wet-chemical reduction method using sodium acrylate as a dual reducing and capping agent was investigated with various analytical techniques. The time course of the state of the reaction solution was investigated using UV-vis and XAFS spectroscopies which showed that the NP formation rate increased with increasing concentration of sodium hydroxide (NaOH). The detailed kinetic analyses reveal that both the reduction rate of Ag ions and the nucleation rate of Ag NPs are dramatically increased with increasing NaOH concentration. XANES analyses imply that another reaction pathway via alternative Ag(+) species, such as Ag(OH)(x), was developed in the presence of NaOH. Consequently, NaOH is found to play an important role not only in creating specific intermediates in the reduction of Ag(+) to Ag(0), but also in accelerating the reduction and nucleation rates by enhancing the oxidation of sodium acrylate, thereby increasing the rate of formation of the Ag NPs.

Effect of growth conditions on the structure of two-dimensional latex crystals: experiment

Abstract Essential experimental features of the nucleation and growth of a 2D colloidal crystal on a solid substrate are modeled. The crystal, composed of sub-micron-sized latex spheres, is grown by the evaporation of water from the particle suspension in a circular cell. The calculation of the meniscus profile in the cell allows the prediction of the particle volume fraction in the suspension surrounding the crystal as a function of time. This quantity enters into a convective-diffusion model for the crystal growth which calculates the crystal radius as a function of time. Comparison with experimental data for 2D latex particle crystals shows predominant convective growth over a wide range of evaporation rates set by varying the humidity of the air. Microscopic parameters of the particle assembly can also be estimated such as the particle velocity, diffusivity, characteristic time constants, Peclet number, etc. The nucleation is simulated by simultaneously solving the equations of motion for the ensemble of particles trapped in a thin liquid film using the discrete-element method. These equations account for the forces which are physically important in the system: contact particle–particle friction, increased viscous resistance during the particle motion in a wetting film, long-range capillary attraction between two particles screened by the rest of particles. The final result of the simulation is a particle cluster of hexagonal packing, whose structure resembles very much the monolayer nucleus of latex particles observed experimentally. The models proposed by us could also be implemented for the aggregation of species in a variety of practical processes such as coating, texturing, crystal growth from a melt or liquid solution, or a biological array.

Optical Memory Media Based on Excitation-Time Dependent Luminescence from a Thin Film of Semiconductor Nanocrystals

We describe the increase of photoluminescence intensity from densely packed semiconductor nanocrystals (quantum dots) with excitation time, which is clearly observed by the naked eye under ambient conditions. This enabled the invention of the first luminescence-based optical memory media feasible for practical applications. Bright luminescent images are stored and then read out by exciting the medium, a thin film of cadmium selenide nanocrystals, with blue or UV light. The increase in emission intensity is attributed to the trapping and accumulation of photo-generated electrons in the matrix of organic molecules capping the nanocrystals.

Chemical stabilization of gold coated by silver core-shell nanoparticles via electron transfer.

Silver nanoparticles are notoriously susceptible to oxidation, yet gold nanoparticles coated in silver exhibit a unique electronic interaction that occurs at the interface of the two metals, leading to enhanced stability properties for the silver shell. In order to probe the phenomenon, the stability of gold nanoparticles coated by silver was studied in the presence of various chloride-containing electrolytes. It was found that a critical silver shell thickness of approximately 1 nm exists that cannot be oxidatively etched from the particle surface: this is in contrast to the observation of complete oxidative etching for monometallic silver nanoparticles. The results are discussed in terms of particle composition, structure and morphology before and after exposing the particles to the electrolytes. Raman analysis of the reporter molecule 3-amino-1,2,4-triazole-5-thiol adsorbed on the particle surface illustrates the feasibility of using gold coated by silver nanoparticle probes in sensing applications that require the presence of high levels of salt. The results provide insight into the manipulation of the electronic and stability properties for gold- and silver-based nanoparticles.

Aqueous synthesis and characterization of Ag and Ag–Au nanoparticles: addressing challenges in size, monodispersity and structure

In this paper, we demonstrate the synthesis of monodispersed silver nanoparticles (NPs) of controlled size (20.5 ± 3.3 nm) in aqueous phase from a silver hydroxide precursor with sodium acrylate as dual reducing–capping agent. We then coat these NPs in a layer of gold with controllable thickness through a reduction–deposition process. The materials are characterized using several techniques including high-resolution transmission electron microscopy, ultraviolet–visible spectroscopy, X-ray diffraction and X-ray photoelectron spectroscopy. The results show that we were able to synthesize not only monodispersed Ag NPs but also core–shell Ag–Au NPs with a discrete structure, which is significant because of the challenges associated with the creation of such materials, namely the propensity of metallic Ag to be oxidized by the presence of ionic Au. The NPs are of interest for use in a wide range of potential applications, including biomedical diagnostics and biomolecular detection as well as many others.

Charge-transfer-induced suppression of galvanic replacement and synthesis of (Au@Ag)@Au double shell nanoparticles for highly uniform, robust and sensitive bioprobes

The synthesis of double shell (Au@Ag)@Au nanoparticles is accomplished through suppression of the galvanic replacement reaction caused by an electron transfer phenomenon. The resulting nanoparticles are monodisperse with a thin and uniform second Au shell. These particles are ultimately expected to lead to sensitive probes for biomolecular sensing and diagnostics.