Polymer decorated gold nanoparticles in nanomedicine conjugates.

Noble metal, especially gold nanoparticles and their conjugates with biopolymers have immense potential for disease diagnosis and therapy on account of their surface plasmon resonance (SPR) enhanced light scattering and absorption. Conjugation of noble metal nanoparticles to ligands specifically targeted to biomarkers on diseased cells allows molecular-specific imaging and detection of disease. The development of smart gold nanoparticles (AuNPs) that can deliver therapeutics at a sustained rate directly to cancer cells may provide better efficacy and lower toxicity for treating cancer tumors.

Viral nanoparticles, noble metal decorated viruses and their nanoconjugates.

Virus-based nanotechnology has generated interest in a number of applications due to the specificity of virus interaction with inorganic and organic nanoparticles. A well-defined structure of virus due to its multifunctional proteinaceous shell (capsid) surrounding genomic material is a promising approach to obtain nanostructured materials. Viruses hold great promise in assembling and interconnecting novel nanosized components, allowing to develop organized nanoparticle assemblies.

Dispersions based on noble metal nanoparticles-DNA conjugates.

Many biomolecules have specific binding properties in the nanostructure formation; they are attractive materials for nanotechnology. One such promising construction material for growing a well-defined nanostructure is deoxyribonucleic acid, due to its π-electron hydrophobic core and predictable recognition attributed to the specificity of Watson-Crick base-pairing. Hydrogen bonding provides the specificity behind the matching of complementary pairs of single-stranded (ss) DNA to hybridize into a double strand (ds) of helical DNA.

Kinetics of nanoparticle reassembly mediated by UV-photolysis of surfactant.

Real-time reassembly of an ordered nanoparticle monolayer due to UV-photolysis of the surfactant shell of nanoparticles was observed. The technique of grazing-incidence small-angle X-ray scattering provided the possibility to track in situ the nanoparticle pair correlation function of the sample processed in a UV-ozone reactor. The analysis revealed a total shift of approximately 1 nm of the nanoparticle nearest-neighbor distance.

On inverse miniemulsion polymerization of conventional water-soluble monomers.

Inverse monomer miniemulsions can be generated by sonification of the polar monomer, water, stabilizer and costabilizer in organic solvents as the unpolar continuous phase. The inverse miniemulsion obtains its stability by using a combination of effective surfactant and osmotic pressure agent, so called lypophobe, which is practically insoluble in the continuous phase and prevents the minidroplets from Ostwald ripening. Inverse miniemulsions are typically sterically stabilized with a nonionic surfactant blend so as to provide a relatively condensed interface.

Dispersions, novel nanomaterial sensors and nanoconjugates based on carbon nanotubes.

Nanomaterials are structures with dimensions characteristically much below 100 nm. The unique physical properties (e.g.

Control of single-electron charging of metallic nanoparticles onto amorphous silicon surface.

Sequential single-electron charging of iron oxide nanoparticles encapsulated in oleic acid/oleyl amine envelope and deposited by the Langmuir-Blodgett technique onto Pt electrode covered with undoped hydrogenated amorphous silicon film is reported. Single-electron charging (so-called quantized double-layer charging) of nanoparticles is detected by cyclic voltammetry as current peaks and the charging effect can be switched on/off by the electric field in the surface region induced by the excess of negative/positive charged defect states in the amorphous silicon layer. The particular charge states in amorphous silicon are created by the simultaneous application of a suitable bias voltage and illumination before the measurement.

On total internal reflection investigation of nanoparticles by integrated micro-fluidic system.

We report on a novel sensor for characterization of nanoparticles colloidal suspensions. We employ a diffraction grating under total internal reflection for investigation of nanodisperse fluids passing through an integrated microfluidic channel. Dispersions containing polymeric, metallic, and ferromagnetic nanoparticles are studied.

Nature and properties of ionomer assemblies. II.

The principle subject in the current paper is to summarize and characterize the ionomers based on polymers and copolymers such as polystyrene (PSt), polyisoprene (PIP), polybutadiene (PB), poly(styrene-b-isobutylene-b-styrene) (PSt-PIB-PSt), poly(butadiene-styrene) (PB-PSt), poly(ethylene terephthalate) (PET), poly(butylene adipate) (PBA), poly(butylene succinate) (PBSi), poly(dimethylcarbosiloxanes), polyurethane, etc. The self-assembly of ionomers, models concerning ionomer morphologies, physical and rheological properties of ionomer phase and percolation behavior of ionomers were discussed. The ionomer phase materials and dispersions have been characterized by differential scanning calorimetry (DSC), small-angle X-ray catering (SAXS), small-angle neutron scattering (SANS), Fourier transform infrared (FTIR) spectroscopy, transmission electron microscopy (TEM), etc.

Dispersions of polymer ionomers: I.

The principal subject discussed in the current paper is the effect of ionic functional groups in polymers on the formation of nontraditional polymer materials, polymer blends or polymer dispersions. Ionomers are polymers that have a small amount of ionic groups distributed along a nonionic hydrocarbon chain. Specific interactions between components in a polymer blend can induce miscibility of two or more otherwise immiscible polymers.

Degradation of kinetically-stable o/w emulsions.

This article summarizes the studies on the degradation of the thermodynamically unstable o/w (nano)emulsion--a dispersion of one liquid in another, where each liquid is immiscible, or poorly miscible in the other. Emulsions are unstable exhibiting flocculation, coalescence, creaming and degradation. The physical degradation of emulsions is due to the spontaneous trend toward a minimal interfacial area between the dispersed phase and the dispersion medium.

Sterically and electrosterically stabilized emulsion polymerization. Kinetics and preparation.

The principal subject discussed in the current paper is the radical polymerization in the aqueous emulsions of unsaturated monomers (styrene, alkyl (meth)acrylates, etc.) stabilized by non-ionic and ionic/non-ionic emulsifiers. The sterically and electrosterically stabilized emulsion polymerization is a classical method which allows to prepare polymer lattices with large particles and a narrow particle size distribution.

Fate of excited probes in micellar systems.

This article presents studies on the photophysical and photochemical behavior of probes within micellar systems: organized emulsifier/polymer aggregates; the intra- and interpolymer association of amphiphilic polymers; monomer-swollen micelles (microdroplets); and the interfacial layer. Pyrene (Py) as a probe is particularly attractive because of its ability to measure the polarity of its microenvironment. Dipyme yields information on the microviscosity of micellar systems.