Hyperthermia can be produced by near-infrared laser irradiation of gold nanoparticles present in tumors and thus induce tumor cell killing via a bystander effect. To be clinically relevant, however, several problems still need to be resolved. In particular, selective delivery and physical targeting of gold nanoparticles to tumor cells are necessary to improve therapeutic selectivity. Considerable progress has been made with respect to retargeting adenoviral vectors for cancer gene therapy. We therefore hypothesized that covalent coupling of gold nanoparticles to retargeted adenoviral vectors would allow selective delivery of the nanoparticles to tumor cells, thus feasibilizing hyperthermia and gene therapy as a combinatorial therapeutic approach. For this, sulfo-N-hydroxysuccinimide labeled gold nanoparticles were reacted to adenoviral vectors encoding a luciferase reporter gene driven by the cytomegalovirus promoter (AdCMVLuc). We herein demonstrate that covalent coupling could be achieved, while retaining virus infectivity and ability to retarget tumor-associated antigens. These results indicate the possibility of using adenoviral vectors as carriers for gold nanoparticles.
[Fe49Pt51]88Ag12 nanoparticles were prepared by the simultaneous polyol reduction of platiunum acetylacetonate and silver acetate and the
thermal decomposition of iron pentacarbonyl, giving 3.5 nm diameter FePt particles with Ag atoms substituted in the lattice. The addition of
Ag promoted the fcc to tetragonal phase transition, thereby reducing the temperature required for this transition by some 100 to 150 °C
compared with pure FePt nanoparticles. After heat treatment at 400 °C for 30 min, the coercivity of the films containing [Fe49Pt51]88Ag12
nanoparticles was more than 3400 Oe, while the films containing FePt nanoparticles were superparamagnetic. This decrease in phase
transformation temperature allowed us to decrease the particle coalescence and loss in particle positional order seen when FePt nanoparticles
were transformed at temperatures above 550 °C.
Tailoring the surface of nanoparticles is essential for biological applications of magnetic nanoparticles. FePt nanoparticles are interesting candidates owing to their high magnetic moment. Established procedures to make FePt nanoparticles use oleic acid and oleylamine as the surfactants, which make them dispersed in nonpolar solvents such as hexane. As a model study to demonstrate the modification of the surface chemistry, stable aqueous dispersions of FePt nanoparticles were synthesized after ligand exchange with mercaptoalkanoic acids. This report focuses on understanding the surface chemistry of FePt upon ligand exchange with mercapto compounds by conducting X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared spectroscopy (FTIR) studies. It was found that the mercapto end displaces oleylamine on the Pt atoms and the carboxylic acid end displaces the oleic acid on the Fe atoms, thus exposing carboxylate and thiolate groups on the surface that provide the necessary electrostatic repulsion to form stable aqueous dispersions of FePt nanoparticles.
Summary: Over the last several decades, the process of recycling polymer waste has been attracting the attention of many scientists working on this issue. Polymer recycling is very important for at least two main reasons: firstly, to reduce the ever increasing volumes of polymer waste coming from many sources: from daily life packaging materials and disposables and secondly, to generate value‐added materials from low cost sources by converting them into valuable materials similar, to some extent, to virgin materials. Poly(ethylene terephthalate) (PET) occupies the top of the list of polymers to be recycled due to its easy recycling by different ways, which, in accordance, give variable products that can be introduced as starting ingredients for the synthesis of many other polymers. PET can by recycled by hydrolysis, acidolysis, alkalolysis, aminolysis, alcoholysis and glycolysis. Glycolysis is the breakdown of the ester linkages by a glycol, resulting in oligomers or oligoester diols/polyols with hydroxyl terminal groups. Oligoesters coming from the glycolysis of PET waste have been well known for a number of decades to be utilized as a starting material in the manufacture of polyurethanes, unsaturated polyesters and saturated polyester plasticizers. But, as a current motivation, we are reporting on a new application for these oligoester diols/polyols by converting the hydroxyl terminals into acrylate/methacrylate groups. These new acrylated/methacrylated oligoesters have been tested as UV curable monomers and gave promising results from the point of view of their curability by UV and their mechanical properties. The new motivations open the potential for the market to apply the depolymerization products of PET waste for UV curable coatings, useful for wood surfaces, paints and other applications.Recycling of PET polymer by different chemical routes.magnified imageRecycling of PET polymer by different chemical routes.
Heating of nanoparticles (NPs) using an AC magnetic field depends on several factors, and optimization of these parameters can improve the efficiency of heat generation for effective cancer therapy while administering a low NP treatment dose. This study investigated magnetic field strength and frequency, NP size, NP concentration, and solution viscosity as important parameters that impact the heating efficiency of iron oxide NPs with magnetite (Fe3O4) and maghemite (γ-Fe2O3) crystal structures. Heating efficiencies were determined for each experimental setting, with specific absorption rates (SARs) ranging from 3.7 to 325.9 W/g Fe. Magnetic heating was conducted on iron oxide NPs synthesized in our laboratories (with average core sizes of 8, 11, 13, and 18 nm), as well as commercially-available iron oxides (with average core sizes of 8, 9, and 16 nm). The experimental magnetic coil system made it possible to isolate the effect of magnetic field parameters and independently study the effect on heat generation. The highest SAR values were found for the 18 nm synthesized particles and the maghemite nanopowder. Magnetic field strengths were applied in the range of 15.1 to 47.7 kA/m, with field frequencies ranging from 123 to 430 kHz. The best heating was observed for the highest field strengths and frequencies tested, with results following trends predicted by the Rosensweig equation. An increase in solution viscosity led to lower heating rates in nanoparticle solutions, which can have significant implications for the application of magnetic fluid hyperthermia in vivo.
Fex Co y Pt 100-x-y alloy nanoparticles were prepared by the simultaneous reduction of cobalt acetylacetonate and platinum acetylacetonate and the thermal decomposition of iron pentacarbonyl. The relative amounts of iron, cobalt, and platinum in the particles depended on the amount of iron, cobalt and platinum charged to the reaction. As prepared, the particles were superparamagnetic and had a distorted fcc structure. The average particle diameter was 3.5 nm and the size distribution was very narrow. The particles could be dispersed in hydrocarbon solvents and formed films consisting of hexagonal close-packed particles on carbon-coated copper TEM grids. The films were sputter coated with amorphous carbon and then annealed at temperatures ranging from 550 to 700 °C to transform the particles to the tetragonal (L1 0 ) phase. The coercivity of the annealed films increased with increasing annealing temperature. For films with a similar degree of transformation to the tetragonal phase, increasing the cobalt content decreased the coercivity of the films.
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