23 research outputs found

    Costos académicos de la Beca Presidente de la República

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    Entre los años 2013 y 2014 el Estado peruano a través de PRONABEC ha adjudicado becas para estudiar posgrados en el exterior a 1,004 jóvenes egresados de sus bachilleratos o licenciaturas, todos prometedores por sus notas y comportamiento. De este total de becarios, el 72,8% tiene menos de 30 años: el 53,2% oscila entre los 25 y 29 años y el 19,6% entre 20 y 24 años. El 59% de ellos son varones y el 41% mujeres. Contra lo que podría pensarse, sólo el 31% proviene de Lima y Callao, viniendo el restante 69% de todas las provincias del Perú. La publicación recoge los costos que demandan las becas y los criterios que demandan la selección de instituciones de enseñanza de calidad

    Solid-state properties of pink clay from Jequitinhonha Valley in Brazil for pre-formulation study

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    Clay minerals are still widely used in pharmaceutical products for human health and cosmetic purposes. Pre-formulation studies were conducted to identify solid-state properties of pink clay, a sample from Diamantina, Brazil. Among the solid properties to be analyzed, we have selected type identification, iron phases, crystallinity, powder flow characteristics, thermal behavior, and non-isothermal phase transition kinetics. The pink clay is composed of (1:1) clay type and kaolinite as the main component. The Mössbauer spectrum of pink clay shows Fe3+(α-Fe2O3) hematite, Fe2+, and Fe3+ with large Δ/2ξq of about 2.80 and 2.69 mm.s-1 respectively, related to iron silicates, most likely pyroxene, and a superparamagnetic Fe3+. Pink clay exhibits poor flow properties. The thermal behavior indicates a phase-transition between 400 - 600 ºC associated with the dehydroxylation of the pink clay system requiring ~300 kJ mol-1, being constant until the process reaches a conversion of ~50% when the energy is enhanced to ~530 kJ mol-1, concluding the whole dehydroxylation process (α=80%). Solid-state properties and characteristics found for the pink clay must be considered for the proper design of formulations. This type of clay shows unique pharmaceutical properties that can be favorably exploited by the cosmetic industry

    Heating Capacity and Biocompatibility of Hybrid Nanoparticles for Magnetic Hyperthermia Treatment

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    Cancer is one of the deadliest diseases worldwide and has been responsible for millions of deaths. However, developing a satisfactory smart multifunctional material combining different strategies to kill cancer cells poses a challenge. This work aims at filling this gap by developing a composite material for cancer treatment through hyperthermia and drug release. With this purpose, magnetic nanoparticles were coated with a polymer matrix consisting of poly (L-co-D,L lactic acid-co-trimethylene carbonate) and a poly(ethylene oxide)–poly(propylene oxide)–poly(ethylene oxide) triblock copolymer. High-resolution transmission electron microscopy and selected area electron diffraction confirmed magnetite to be the only iron oxide in the sample. Cytotoxicity and heat release assays on the hybrid nanoparticles were performed here for the first time. The heat induction results indicate that these new magnetic hybrid nanoparticles are capable of increasing the temperature by more than 5 °C, the minimal temperature rise required for being effectively used in hyperthermia treatments. The biocompatibility assays conducted under different concentrations, in the presence and in the absence of an external alternating current magnetic field, did not reveal any cytotoxicity. Therefore, the overall results indicate that the investigated hybrid nanoparticles have a great potential to be used as carrier systems for cancer treatment by hyperthermia

    Preparation of composite with silica-coated nanoparticles of iron oxide spinels for applications based on magnetically induced hyperthermia.

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    It is reported a novel method to prepare magnetic core (iron oxide spinels)–shell (silica) composites containing well-dispersed magnetic nanoparticles in aqueous solution. The synthetic process consists of two steps. In a first step, iron oxide nanoparticles obtained through co-precipitation are dispersed in an aqueous solution containing tetramethylammonium hydroxide; in a second step, particles of this sample are coated with silica, through hydrolyzation of tetraethyl orthosilicate. The intrinsic atomic structure and essential properties of the core–shell system were assessed with powder X-ray diffraction, Fourier transform infrared spectrometry, Mössbauer spectroscopy and transmission electron microscopy. The heat released by this ferrofluid under an AC-generated magnetic field was evaluated by following the temperature evolution under increasingmagnetic field strengths.Results strongly indicate that this ferrofluid based on silica-coated iron oxide spinels is technologically a very promising material to be used in medical practices, in oncology

    Controlled formation of reactive Fe particles dispersed in a carbon matrix active for the oxidation of aqueous contaminants with H2O2

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    In this work, reactive iron nanoparticles dispersed in a carbon matrix were produced by the controlled thermal decomposition of Fe3+ ions in sucrose. During the sucrose decomposition, the Fe3+ ions are reduced to form iron nanometric cores dispersed in a porous carbonaceous matrix. The materials were prepared with iron contents of 1, 4, and 8 wt.% and heated at 400, 600, and 800 °C. Analyses by X-ray diffraction, Mössbauer spectroscopy, magnetization measurements, Raman spectroscopy, termogravimetric analyses, BET surface area, scanning, and transmission electron microscopy showed that at 400 °C, the materials are composed essentially of Fe3O4 particles, while treatments at higher temperatures, i.e., 600 and 800 °C, produced phases such as Fe0 and Fe3C. The composites were tested for the oxidation of methylene blue with H2O2 by a Fenton-type reaction and also H2O2 decomposition, showing better performance for the material containing 8 % of iron heated at 400 and 600 °C. These results are discussed in terms of Fe2+ surface species in the Fe3O4 nanoparticles active for the Fenton reaction

    Structure and magnetic properties of granular NiZn-ferrite - SiO2

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    Granular systems composed by nanostructured magnetic materials embedded in a non-magnetic matrix present unique physical properties that depend crucially on their nanostructure. In this work, we have studied the structural and magnetic properties of NiZn-ferrite nanoparticles embedded in SiO2, a granular system synthesized by sol-gel processing. Samples with ferrite volumetric fraction x ranging from 6% to 78% were prepared, and characterized by X-ray diffraction, Mössbauer spectroscopy and vibrating sample magnetometry. Our results show the formation of pure stoichiometric NiZn-ferrite in the SiO2 matrix for x < 34%. Above these fraction, our samples presented also small amounts of Fe2O3. Mössbauer spectroscopy revealed the superparamagnetic behaviour of the ferrimagnetic NiZn-ferrite nanoparticles. The combination of different ferrite concentration and heat treatments allowed the obtaintion of samples with saturation magnetization between 1.3 and 68 emu/g and coercivity ranging from 0 to 123 Oe, value which is two orders of magnitude higher than the coercivity of bulk NiZn-ferrite

    Facile preparation of carbon coated magnetic Fe3O4 particles by a combined reduction/CVD process.

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    In this work, we report a simple method for the preparation of magnetic carbon coated Fe3O4 particles by a single step combined reduction of Fe2O3 together with a Chemical Vapor Deposition process using methane. The temperature programmed reactionmonitored by Mo¨ ssbauer, X-ray Diffraction and Raman analyses showed that Fe2O3 is directly reduced by methane at temperatures between 600 and 900 8C to produce mainly Fe3O4 particles coated with up to 4 wt% of amorphous carbon. Thesemagneticmaterials can be separated into two fractions by simple dispersion in water, i.e., a settled material composed of large magnetic particles and a suspended material composed of nanoparticles with an average size of 100–200 nm as revealed by Scanning Electron Microscopy and High-resolution Transmission Electron Microscopy. Different uses for these materials, e.g., adsorbents, catalyst supports, rapid coagulation systems, are proposed

    Structure and magnetic properties of granular NiZn-ferrite - SiO2

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    Granular systems composed by nanostructured magnetic materials embedded in a non-magnetic matrix present unique physical properties that depend crucially on their nanostructure. In this work, we have studied the structural and magnetic properties of NiZn-ferrite nanoparticles embedded in SiO2, a granular system synthesized by sol-gel processing. Samples with ferrite volumetric fraction x ranging from 6% to 78% were prepared, and characterized by X-ray diffraction, Mössbauer spectroscopy and vibrating sample magnetometry. Our results show the formation of pure stoichiometric NiZn-ferrite in the SiO2 matrix for x < 34%. Above these fraction, our samples presented also small amounts of Fe2O3. Mössbauer spectroscopy revealed the superparamagnetic behaviour of the ferrimagnetic NiZn-ferrite nanoparticles. The combination of different ferrite concentration and heat treatments allowed the obtaintion of samples with saturation magnetization between 1.3 and 68 emu/g and coercivity ranging from 0 to 123 Oe, value which is two orders of magnitude higher than the coercivity of bulk NiZn-ferrite.235238Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq
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