CHARACTERIZATION OF NANOSTRUCTURES:TOOLS AND CHALLENGES

Apart from long-known and applied nanostructures like carbon black for tyres or pigments for coatings nanotechnology has created highly sophisticated structures used for nano/molecular electronics,diagnostics,drug delivery, UV-absorbers etc.Often the main question to be solved analytically is the local determination of tiny amounts of chemicals resulting in an ever increasing need for highly sensitive as well as locally resolved techniques.Applications of techniques like mass spectroscopy,transmission el...     

Theranostic Layer‐by‐Layer Nanoparticles for Simultaneous Tumor Detection and Gene Silencing

Layer‐by‐layer nanoparticles (NPs) are modular drug delivery vehicles that incorporate multiple functional materials through sequential deposition of polyelectrolytes onto charged nanoparticle cores. Herein, we combined the multicomponent features and tumor targeting capabilities of layer‐by‐layer assembly with functional biosensing peptides to create a new class of nanotheranostics. These NPs encapsulate a high weight percentage of siRNA while also carrying a synthetic biosensing peptide on the surface that is cleaved into a urinary reporter upon exposure to specific proteases overexpressed in the tumor microenvironment. Importantly, this biosensor reports back on a molecular signature characteristic to metastatic tumors and associated with poor prognosis, MMP9 protease overexpression. This nanotheranostic mediates noninvasive urinary‐based diagnostics in mouse models of three different cancers with simultaneous gene silencing in flank and metastatic mouse models of ovarian cancer.     

Partial Air Wetting on Solvophobic Surfaces in Polar Liquids

The properties of solvophobic surfaces in polar liquids are studied by sedimentation experiments as well as by force measurements using a scanning force microscope (SFM). Depending on whether the polar liquid contacts the solvophobic surface under normal air pressure or under vacuum the experimental results are different. Sedimentation velocities of vacuum-contacted solvophobic surfaces are similar to those of solvophilic vacuum- or air-contacted ones. However, for the air-contacted solvophobic surfaces there is a slip boundary condition of the hydrodynamic flow causing a change of the sedimentation velocity of about 20%, and a long-range attraction varying with the polarity of the liquid molecule is observed between them. These effects can be explained by an incomplete air dewetting of the solvophobic surface when brought into contact with the polar liquid at normal air pressure. Copyright 1999 Academic Press.     

FLUORESCENCE ENERGY TRANSFER BETWEEN DIMETHYLDIAZAPEROPYRENIUM DICATION AND ETHIDIUM INTERCALATED IN POLY d(A-T)

Dimethyldiazaperopyrenium is one of the largest known DNA intercalators. Fluorescence energy transfer occurred between dimethyldiazaperopyrenium (donor) and ethidium (acceptor) when these dyes were bound to a double-stranded polynucleotide such as poly d(A-T). The addition of increasing amounts of ethidium bromide led to a marked shortening of the fluorescence lifetime of the donor, whereas the excited state of the acceptor was progressively populated via energy transfer from the donor. Critical Förster distance between these two chromophores was calculated to be 3.8 nm. The observed transfer efficiency was lower than that calculated on the basis of this critical distance and a statistical distribution of bound drugs. These results are discussed taking into account the conformational change induced by intercalation of dimethyldiazaperopyrenium in the double-stranded polynucleotide.     

Novel mixed ligand coordination compounds of some rare earth metal cations containing acesulfamato/N,N-diethylnicotinamide

The mixed ligand coordination compounds containing acesulfamato and N,N -diethylnicotinamide biomolecules of some rare earth metal cations (Eu³⁺, Tb³⁺, Ho³⁺, Er³⁺ and Yb³⁺) were synthesized, and their structural properties were investigated. Possible structural formulas have been proposed by determining the chemical composition of molecules (elemental analysis), binding properties (infrared spectroscopy, mass analysis, solid-state UV-vis spectroscopy), thermal degradation properties (TGA / DTA curves). Based on the data collected, it is suggested that rare earth metal cations with a 3+ oxidation state have sextet coordination. The geometries of the structures were thought to be distorted octahedral. The charge balance of the coordination sphere is balanced by a monoanionic acesulfamato located outside the coordination sphere. When the thermal behaviours of the complexes were examined, it was determined that the compounds with Eu³⁺, Tb³⁺, and Yb³⁺ metal cations contained one hydrate water outside the coordination sphere. Hydrate waters do not exist in the Ho³⁺ and Er³⁺ metal cation-centred complexes. At the end of the thermal decomposition analysis of all complex structures, it was determined that they leave the relevant metal oxides in the reaction vessels as final decomposition products.     

THE PREPARATION AND STABILITY OF COLLOIDAL METAL DISPERSIONS PREPARED BY A TWO-PHASE NON-AQUEOUS ROUTE

Stable suspensions of small metal Au, Ru, PI, Pd, Rh, Co and Nl particles dispersed in n-heptane and n-dodecane have been prepared using a novel two-phase system, Involving the formation of the particles In a methanolic phase and subsequent phase transfer of the panicles to the alkane medium. The dispersions consisted of small particles having diameters In the range of 8-30 nm (the gold sols were very polydlsperse having average diameters of ca.34 nm). The phase transfer of the particles and their subsequent colloid stability were effected by the presence of dissolved dispersant in the hydrocarbon phase (either Oloa 1200 or Hypermer LP 8). In the case of Oloa 1200, a widely-used polylsobutylene succinimide automotive engine dispersant, It Is proposed that the amlne groups adsorb strongly to the acidic surface o1 the particles, and the 70-carbon polyisobutylene chains extend Into the hydrocarbon medium sufficiently to maintain the separation of adjacent particles by steric and possibly also by electrical repulsion.     

Structure and reflective properties of Al-Cu-Fe quasicrystalline thin film prepared by laser induced arc method

Al-Cu-Fe thin films were prepared by laser induced arc (laser-arc) method from a single source-Al63Cu25Fe12 alloy, which was proved to consist of quasicrystalline phase together with approximant phase. The composition of the deposited films meets the requirement for formation of icosahedral symmetry phase. Quasicrystalline phase was obtained after annealing the amorphous as-deposit film samples. The optical properties of the samples were investigated. Thin film samples of Al, Cu and Fe deposited under the same condition were employed for comparison. The results showed specific reflective properties of Al-Cu-Fe quasicrystal thin film in some wavelength range. The optical conductivity of the films exhibited a negative peak, centered about 440 nm in range of 190to 800 nm. The Al-Cu-Fe quasicrystal thin films could absorb almost all the ray in the wavelength range from 420nm to 450 nm. The ratio of absorption was greater than 99%.     

On the initial stage of plastic deformation of sulphur-doped gallium phosphide

The overall deformation behaviour between room temperature and 1000 K has been investigated by bending and uniaxial compression at small strains ≦ 0.1%. Ductile-to-brittle transition temperature was found at 44% of the melting point. Dislocations are generated mainly at surface irregularities. Whereas screw dislocations predominate at the beginning 30° and 60° segments become more important after cross slip and interaction of different slip systems.     

Heat capacity of LiInTe2

The heat capacity of LiInTe₂ at constant pressure was measured with an adiabatic vacuum calorimeter in the temperature rangeT=7–300 K. The standard molar enthalpyH _m ⁰ —H _m ⁰ (0) and the standard molar entropyS ⁰ (T) were calculated. From a theoretical analysis, the contribution to the heat capacity due to the lattice anharmonicity was estimated.The increased effect of the lattice anharmonicity in LiInTe₂ is caused by specific properties of the Li-Te bond.

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Zusammenfassung Die Wärmekapazität von LiInTe₂ bei konstantem Druck wurde mit einem adiabatischen Vakuumkalorimeter im Temperaturbereich 7 T 300 K bestimmt. Die molare StandardenthalpieH _m ⁰ — H _m ⁰ (0) und die molare StandardentropieS ⁰ (T) wurden berechnet. Aus einer theoretischen Analys wurde der Anteil der Gitteranharmonizität an der Wärmekapazität abgeschätzt. Der erhöhte Einfluss der Gitteranharmonitität in LiInTe₂ wird durch spezifische Eigenschaften der Li-Te-Bindung verursacht

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7–300 LiInTe₂. H _M ⁰ -H _M ⁰ (0) S ⁰(T). . LiInTe₂ Li-.