Stefan Jurga

Star polymers with a cationic core prepared by ATRP for cellular nucleic acids delivery.

Poly(ethylene glycol) (PEG)-based star polymers with a cationic core were prepared by atom transfer radical polymerization (ATRP) for in vitro nucleic acid (NA) delivery. The star polymers were synthesized by ATRP of 2-(dimethylamino)ethyl methacrylate (DMAEMA) and ethylene glycol dimethacrylate (EGDMA). Star polymers were characterized by gel permeation chromatography, zeta potential, and dynamic light scattering. These star polymers were combined with either plasmid DNA (pDNA) or short interfering RNA (siRNA) duplexes to form polyplexes for intracellular delivery. These polyplexes with either siRNA or pDNA were highly effective in NA delivery, particularly at relatively low star polymer weight or molar ratios, highlighting the importance of NA release in efficient delivery systems.

MAS NMR and FTIR spectra of framework aluminosilicates

Abstract In the work, the results of 27 Al MAS NMR studies carried out for structures of different framework aluminosilicates are presented. The spectra of natural clinoptilolite and its sodium and hydrogen forms were measured. The zeolite spectra were obtained before and after incorporation of heavy metal cations (Pb 2+ , Cd 2+ , Ni 2+ and Cr 3+ ) into the zeolite structure. After decomposition of the spectra into component peaks differences caused by ion exchange were observed. Additionally, NMR spectra of kalsilite (framework aluminosilicate, not belonging to zeolite group) and other zeolites (chabazite, heulandite and analcime) were measured. 27 Al MAS NMR spectra of all the samples studied were compared with the FTIR spectra measured in the middle infrared region. Based on the results obtained it has been proved that the interpretation of spectra obtained using these two different techniques can give some information concerning changes occurring in various framework aluminosilicate structures.

Characterization of aged nitrile rubber elastomers by NMR spectroscopy and microimaging

Abstract 1 H spin–lattice and spin–spin NMR relaxation times change markedly during the aging of nitrile rubber elastomers. NMR microimaging reveals heterogeneous changes in the aged samples. Aging proceeds mainly via additional chain cross-linking, and scission of the polymer chains does not appear to contribute. T 1 imaging shows that there is no spatial distribution of spin–lattice relaxation times.

Structural, Spectroscopic, and Magnetic Properties of Eu3+-Doped GdVO4 Nanocrystals Synthesized by a Hydrothermal Method

New interesting aspects of the spectroscopic properties, magnetism, and method of synthesis of gadolinium orthovanadates doped with Eu(3+) ions are discussed. Gd(1-x)Eu(x)VO4 (x = 0, 0.05, 0.2) bifunctional luminescent materials with complex magnetic properties were synthesized by a microwave-assisted hydrothermal method. Products were formed in situ without previous precipitation. The crystal structures and morphologies of the obtained nanomaterials were analyzed by X-ray diffraction and transmission and scanning electron microscopy. Crystallographic data were analyzed using Rietveld refinement. The products obtained were nanocrystalline with average grain sizes of 70-80 nm. The qualitative and quantitative elemental composition as well as mapping of the nanocrystals was proved using energy-dispersive X-ray spectroscopy. The spectroscopic properties of red-emitting nanophosphors were characterized by their excitation and emission spectra and luminescence decays. Magnetic measurements were performed by means of vibrating sample magnetometry. GdVO4 and Gd0.8Eu0.2VO4 exhibited paramagnetic behavior with a weak influence of antiferromagnetic couplings between rare-earth ions. In the substituted sample, an additional magnetic contribution connected with the population of low-lying excited states of europium was observed.

Novel nanostructured hematite–spongin composite developed using an extreme biomimetic approach

The marine sponge Hippospongia communis (Demospongiae: Porifera) is a representative of bath sponges, which possess characteristic mineral-free fibrous skeletons made of a structural protein – spongin. This fibrous skeleton is mechanically robust, resistant to acidic treatment, and thermally stable up to 160 °C. Due to these properties, we decided to use this biological material for the first time for the hydrothermal synthesis of hematite (α-Fe2O3) via catalyzed hydrolysis of FeCl3 to obtain a hematite–spongin composite. The material obtained was studied with Scanning Electron Microscopy (SEM), High-Resolution Transmission Electron Microscopy (HR-TEM), X-ray Photoemission Spectroscopy (XPS) and Raman spectroscopy. The α-Fe2O3–spongin-based composite was tested for its potential application as an anode material in a capacitor. The results indicate that components constructed using this novel composite material have a positive effect on the capacitance of energy storing devices.

Experimental and theoretical studies on the mechanism for chemical oxidation of multiwalled carbon nanotubes

In this study, the oxidation of multiwalled carbon nanotubes (MWCNTs) sonicated and/or refluxed in acids (H2SO4/HNO3) was investigated using a combination of high-resolution transmission electron microscopy, Raman spectroscopy, Fourier transform infrared spectroscopy, and ab initio computational methods. Sonication of the sample has the strongest effect, leading to the highest concentration of defects and carboxyl groups on the walls. Substantial correlations between treatment protocols, CNT size, and the types of chemical moieties are observed. Finally, based on experimental and computational results, we suggest the mechanism of the oxidation process for attaching the functional groups on the sidewalls.

Molecular dynamics in polyethylene and ethylene-1-butene copolymer investigated by NMR methods

H and 13 C NMR spectra and 1 H spin-lattice relaxation times T1 and T1q have been employed to study the structure and molecular dynamics in polyethylene and ethylene-1-butene copolymer in the temperature range from 100 to 370 K. Results are interpreted in terms of a, b and c -relaxation, as well as methyl group rotation. The activation energies for all motions were established. The incorporation of 1-butene into ethylene chain leads to an increase of mobility in amorphous and crystalline phases as well as appearance the 13 C resonance characteristic to the monoclinic structure in addition to the orthorhombic observed in both polymers. The crystallinity degree derived from T1q in studied polymers is close to that determined using DSC method. 2002 Elsevier Science Ltd. All rights reserved.

Peptide-functionalized ZCIS QDs as fluorescent nanoprobe for targeted HER2-positive breast cancer cells imaging

In this paper, the synthesis of alloyed CuInZnxS2+x quantum dots (ZCIS QDs), their transfer into aqueous solution via a polymer coating technique, and the use of these nanocrystals to selectively target HER2-positive cells, are reported. By optimizing first the ZnS shell deposition process onto the CuInS2 core, and next the encapsulation of the dots with the amphiphilic poly(maleic anhydride-alt-1-octadecene) (PMAO) polymer, water-dispersible ZCIS QDs were successfully prepared. The nanocrystals with a photoluminescence quantum yield of 35% were purified via centrifugation and ultracentrifugation and high quality nanoparticles with narrow size distributions and surface charges were obtained. After verifying the biocompatibility of PMO-coated ZCIS QDs, we coupled these nanocrystals with the LTVSPWY peptide and demonstrated via MTT assay that both bare and the peptide-linked QDs exhibit low cytotoxicity. The HER2-mediated delivery of the peptide-linked QDs was confirmed by confocal microscopy. This study indicates that as engineered QDs can efficiently be used as fluorescent nanoprobes for selective labelling of HER2-positive SKBR3 cancer cells.

Lamellar ordering in computer-simulated block copolymer melts by a variety of thermal treatments

A lattice computer simulation of a symmetric A–B–A triblock copolymer melt is reported. This melt is quenched, in simulation, from an athermal state to 39 different temperatures using cooperative motion algorithm. Energy, specific heat, copolymer end-to-end distance, bridging fraction, lamellar spacing, concentration profiles, and microstructure visualizations are reported. The quenching simulation results are compared with those obtained by alternative thermal treatments, that is by slow heating and slow cooling. Quenches yield data consistent with theory and experiment, whereas slow cooling and slow heating results do not capture the expected behavior for the lamellar spacing and the bridging fraction. Finally, at very low temperatures, below the conventional order–disorder transition temperature, an additional ordering is recorded, from a conventional lamellar phase to a lamellar structure showing copolymer junction points condensed into a two-dimensional plane.

Synthesis and characterization of magnetite/silver/antibiotic nanocomposites for targeted antimicrobial therapy

The article is devoted to preparation and characterization of magnetite/silver/antibiotic nanocomposites for targeted antimicrobial therapy. Magnetite nanopowder was produced by thermochemical technique; silver was deposited on the magnetite nanoparticles in the form of silver clusters. Magnetite/silver nanocomposite was investigated by XRD, SEM, TEM, AFM, XPS, EDX techniques. Adsorptivity of magnetite/silver nanocomposite towards seven antibiotics from five different groups was investigated. It was shown that rifampicin, doxycycline, ceftriaxone, cefotaxime and doxycycline may be attached by physical adsorption to magnetite/silver nanocomposite. Electrostatic surfaces of antibiotics were modeled and possible mechanism of antibiotic attachment is considered in this article. Raman spectra of magnetite, magnetite/silver and magnetite/silver/antibiotic were collected. It was found that it is difficult to detect the bands related to antibiotics in the magnetite/silver/antibiotic nanocomposite spectra due to their overlap by the broad carbon bands of magnetite nanopowder. Magnetic measurements revealed that magnetic saturation of the magnetite/silver/antibiotic nanocomposites decreased on 6-19 % in comparison with initial magnetite nanopowder. Pilot study of antimicrobial properties of the magnetite/silver/antibiotic nanocomposites were performed towards Bacillus pumilus.