Desarrollo de nano-agentes magnéticos para aplicación de hipertermia combinada con direccionamiento en el tratamiento selectivo del cáncer

La hipertermia magnética para el tratamiento de tumores es una alternativa terapéutica que se comenzó a estudiar hace ya muchos años, con el fin de encontrar una nueva herramienta para la terapia antitumoral menos agresiva que las ya conocidas. Se sintetizaron nanopartículas magnéticas de magnetita (Fe3O4) de aproximadamente 11 nm de diámetro mediante co-precipitación en medio acuoso. La superficie de las nanopartículas se funcionalizaron con 3aminopropil triethoxisilano (APTS) y ácido fólico (AF) para direccionamiento en células tumorales que sobreexpresen el receptor folato. Estas nanoestructuras tienen una disipación de calor caracterizada por un valor de SpecificAbsorptionRate (SAR) de 7.53 W/gFe para la termoterapia magnética bajo la acción de campos de radiofrecuencia en condiciones clínicas (100 kHz y 5 kA/m). La experimentación in vitro con la célula LM3 (Malignant neoplasms of the mouse mammary gland (NCIt: C21678). https://web.expasy.org/cellosaurus/CVCL_D269)permitió demostrar la disminución de la viabilidad celular un 6-7% luego del contacto con nanopartículas magnéticas durante 24 horas y posterior aplicación de campo magnético, respecto del control no expuesto al campo.Eje: Ciencia e Ingeniería de MaterialesInstituto de Física La Plat

Ascorbic Acid Encapsulation in Hydrophobic Silica Xerogel

Self-assembled hybrid organo-silica sol-gel materials are rapidly expanding for new and novel applications. The microporous solid silica matrix was used as a carrier for the controlled release of ascorbic acid (AA), selected as cargo molecule. One-step synthesis procedure was optimized for the preparation of silica–molecule composites by using tetraethoxysilane and methyltrimethoxysilane as precursors. The hydrophobic silica xerogel matrices were characterized by Fourier transform infrared spectroscopy (FTIR) and X-ray diffraction. Specific surface area and porosity parameters were determined by Brunauer-Emmett-Teller (BET) technique and the matrix surface morphology by scanning electron microscopy (SEM). The observed release pattern could be interesting for the development of AA-fortified food and for use in food packaging.Facultad de Ciencias ExactasCentro de Investigación y Desarrollo en Tecnología de Pintura

Ascorbic Acid Encapsulation in Hydrophobic Silica Xerogel

Self-assembled hybrid organo-silica sol-gel materials are rapidly expanding for new and novel applications. The microporous solid silica matrix was used as a carrier for the controlled release of ascorbic acid (AA), selected as cargo molecule. One-step synthesis procedure was optimized for the preparation of silica–molecule composites by using tetraethoxysilane and methyltrimethoxysilane as precursors. The hydrophobic silica xerogel matrices were characterized by Fourier transform infrared spectroscopy (FTIR) and X-ray diffraction. Specific surface area and porosity parameters were determined by Brunauer-Emmett-Teller (BET) technique and the matrix surface morphology by scanning electron microscopy (SEM). The observed release pattern could be interesting for the development of AA-fortified food and for use in food packaging.Facultad de Ciencias ExactasCentro de Investigación y Desarrollo en Tecnología de Pintura

Stress-induced Gene Expression Sensing Intracellular Heating Triggered by Magnetic Hyperthermia

It is known that alternating magnetic field applications on eukaryotic cells loaded with single domain iron oxide nanoparticles result in high hyperthermic citotoxicity leading to cell dead. Although magnetic hyperthermia therapy for cancer tumours is being developed under this idea, some in vitro assays have shown controversial results indicating that alternating magnetic field triggers large apoptotic effect without significant culture-temperature increase. In agreement with these observations a huge lowering in nanoparticle specific heating rates, when going from the colloidal suspension to cell endosomes, together with cell death, has been reported. Here, we propose a new methodology to determine the occurrence of local heating in cells when alternating magnetic fields in the radiofrequency field range are applied to cell cultures holding very low iron oxide concentrations, being these concentrations insufficient to produce a global cell-culture temperature increase up to therapeutic values. To this end, human lung adenocarcinoma cells (A549 cell line) were transduced with a lentiviral vector encoding the expression of the enhanced green fluorescence protein, EGFP, under the action of the inducible human heat shock protein 70B promoter. This modified A549 cell line was incubated with aqueous suspensions of magnetite core nanoparticles (uncoated or covered with coating agents like citric acid or silicon oxide), and exposed to radiofrequency fields. The application of an alternating magnetic field to cell cultures loaded with nanoparticles resulted in no global temperature increase but EGFP expression. Stress-inducible gene expression scales with uptake and nanoparticle properties like saturation magnetization and heat dissipation efficiency. Our analysis demonstrates that EGFP expression is linked to a localized intracellular temperature increase.Fil: de Sousa, María Elisa. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Física La Plata. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Instituto de Física La Plata; ArgentinaFil: Carrea, Alejandra. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Biotecnológicas. Instituto de Investigaciones Biotecnológicas "Dr. Raúl Alfonsín" (sede Chascomús). Universidad Nacional de San Martín. Instituto de Investigaciones Biotecnológicas. Instituto de Investigaciones Biotecnológicas "Dr. Raúl Alfonsín" (sede Chascomús); ArgentinaFil: Mendoza Zélis, Pedro. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Física La Plata. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Instituto de Física La Plata; ArgentinaFil: Muraca, Diego. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidade Estadual de Campinas; BrasilFil: Mykhaylyk, Olga. Technische Universitat Munchen; AlemaniaFil: Sosa, Yolanda Elena. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Bioquímicas de La Plata "Prof. Dr. Rodolfo R. Brenner". Universidad Nacional de la Plata. Facultad de Ciencias Médicas. Instituto de Investigaciones Bioquímicas de La Plata ; ArgentinaFil: Goya, Rodolfo Gustavo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Bioquímicas de La Plata "Prof. Dr. Rodolfo R. Brenner". Universidad Nacional de la Plata. Facultad de Ciencias Médicas. Instituto de Investigaciones Bioquímicas de La Plata ; ArgentinaFil: Sánchez, Francisco Homero. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Física La Plata. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Instituto de Física La Plata; ArgentinaFil: Dewey, Ricardo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Biotecnológicas. Instituto de Investigaciones Biotecnológicas "Dr. Raúl Alfonsín" (sede Chascomús). Universidad Nacional de San Martín. Instituto de Investigaciones Biotecnológicas. Instituto de Investigaciones Biotecnológicas "Dr. Raúl Alfonsín" (sede Chascomús); ArgentinaFil: Fernández van Raap, Marcela Beatriz. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Física La Plata. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Instituto de Física La Plata; Argentin

Enkapsulacija askorbinske kiseline u hidrofobnom silikagelu

Self-assembled hybrid organo-silica sol-gel materials are rapidly expanding for newand novel applications. The microporous solid silica matrix was used as a carrier for the controlled release of ascorbic acid (AA), selected as cargo molecule. One-step synthesis procedure was optimized for the preparation of silica–molecule composites by using tetraethoxysilane and methyltrimethoxysilane as precursors. The hydrophobic silica xerogel matrices were characterized by Fourier transform infrared spectroscopy (FTIR) and X-ray diffraction. Specific surface area and porosity parameters were determined by Brunauer-Emmett-Teller (BET) technique and the matrix surface morphology by scanning electron microscopy (SEM). The observed release pattern could be interesting for the development of AA-fortified food and for use in food packaging.Hibridni, organsko-silikatni sol-gel materijal sve se više primjenjuje u prehrambenoj industriji. Stoga je kao nosač za kontrolirano otpuštanje askorbinske kiseline upotrijebljen mikroporozni čvrsti silikatni matriks. Optimirana je jednostupanjska sinteza kojom su dobiveni silikatni kompoziti uz pomoć prekurzora: tetraetoksisilana i metiltrimetoksisilana. Matriksi su hidrofobnog silikagela okarakterizirani Fourier transformiranom infracrvenom spektroskopijom (FTIR) i difrakcijom X-zraka. Specifična površina i poroznost matriksa ispitane su Brunaer-Emmett-Teller (BET) metodom, dok su morfološka svojstva površine matriksa određena skenirajućim elektronskim mikroskopom (SEM). Utvrđeno je da se askorbinska kiselina ovako može upotrijebiti za proizvodnju hrane s dodanom vrijednošću, te za pakiranje prehrambenih proizvoda

Enkapsulacija askorbinske kiseline u hidrofobnom silikagelu

Self-assembled hybrid organo-silica sol-gel materials are rapidly expanding for newand novel applications. The microporous solid silica matrix was used as a carrier for the controlled release of ascorbic acid (AA), selected as cargo molecule. One-step synthesis procedure was optimized for the preparation of silica–molecule composites by using tetraethoxysilane and methyltrimethoxysilane as precursors. The hydrophobic silica xerogel matrices were characterized by Fourier transform infrared spectroscopy (FTIR) and X-ray diffraction. Specific surface area and porosity parameters were determined by Brunauer-Emmett-Teller (BET) technique and the matrix surface morphology by scanning electron microscopy (SEM). The observed release pattern could be interesting for the development of AA-fortified food and for use in food packaging.Hibridni, organsko-silikatni sol-gel materijal sve se više primjenjuje u prehrambenoj industriji. Stoga je kao nosač za kontrolirano otpuštanje askorbinske kiseline upotrijebljen mikroporozni čvrsti silikatni matriks. Optimirana je jednostupanjska sinteza kojom su dobiveni silikatni kompoziti uz pomoć prekurzora: tetraetoksisilana i metiltrimetoksisilana. Matriksi su hidrofobnog silikagela okarakterizirani Fourier transformiranom infracrvenom spektroskopijom (FTIR) i difrakcijom X-zraka. Specifična površina i poroznost matriksa ispitane su Brunaer-Emmett-Teller (BET) metodom, dok su morfološka svojstva površine matriksa određena skenirajućim elektronskim mikroskopom (SEM). Utvrđeno je da se askorbinska kiselina ovako može upotrijebiti za proizvodnju hrane s dodanom vrijednošću, te za pakiranje prehrambenih proizvoda

Dipolar interaction and demagnetizing effects in magnetic nanoparticle dispersions: introducing the mean-field interacting superparamagnet model

Aiming to analyze relevant aspects of interacting magnetic nanoparticle systems (frequently called interacting superparamagnets), a model is built from magnetic dipolar interaction and demagnetizing mean-field concepts. By making reasonable simplifying approximations, a simple and useful expression for effective demagnetizing factors is achieved, which allows the analysis of uniform and nonuniform spatial distributions of nanoparticles, in particular the occurrence of clustering. This expression is a function of demagnetizing factors associated with specimen shape and clusters shape, and of the mean distances between near neighbor nanoparticles and between clusters, relative to the characteristic sizes of each of these two types of objects, respectively. The model explains effects of magnetic dipolar interactions, such as the observation of apparent nanoparticle magnetic moments smaller than real ones and approaching to zero as temperature decreases. It is shown that by performing a minimum set of experimental determinations along principal directions of geometrically well-defined specimens, model application allows retrieval of nanoparticle intrinsic properties, like mean volume, magnetic moment, and susceptibility in the absence of interactions. It also permits the estimation of mean interparticle and intercluster relative distances, as well as mean values of demagnetizing factors associated with clusters shape. An expression for average magnetic dipolar energy per nanoparticle is also derived, which is a function of specimen effective demagnetizing factor and magnetization. Experimental test of the model was performed by analysis of results reported in the literature and of original results reported here. The first case corresponds to oleic-acid-coated 8-nm magnetite particles dispersed in PEGDA-600 polymer, and the second one to polyacrilic-acid-coated 13-nm magnetite particles dispersed in PVA solutions from which ferrogels were later produced by a physical cross-linking route. In both cases, several specimens were studied covering a range of nanoparticle volume fractions between 0.002 and 0.046. Magnetic response is clearly different when prism-shaped specimens are measured along different principal directions. These results remark the importance of reporting complete information on measurement geometry when communicating magnetic measurement results of interacting magnetic nanoparticles. Intrinsic nanoparticle properties as well as structural information on particles spatial distribution were retrieved from our analysis in addition to, and in excellent agreement with, analysis previously performed by other authors and/or information obtained from FESEM images. In the studied samples, nanoparticles were found to be in close contact to each other within almost randomly oriented clusters. Intercluster mean distance, relative to cluster size, was found to vary between 2.2 and 7.5, depending on particles volume fraction.Instituto de Física La Plat

On the microstructure and thermal stability of rapidly quenched Fe–B alloys in the intermediate composition range between the crystalline and amorphous states

The structure and the thermal stability of the Fe₀.₈₉B₀.₁₁ rapidly quenched alloy have been investigated. Transmission Mossbauer measurements were carried out as a function of temperature in the range from 148 K to 513 K. Room temperature x-ray diffraction and transmission and conversion-electron Mossbauer experiments, as well as 4.2 K spin-echo nuclear magnetic resonance measurements, were also performed after some selected thermal treatments for one hour between 523 K and 1273 K. Based on these experiments it is suggested that the alloy is inhomogeneous at nanoscopic scale and consists of a fine dispersion of a defective boride phase with an o-Fe₃B-like short-range order, embedded in an α-Fe matrix. This result gives support to the models which indicate phase separation in the amorphous phase with o-Fe3B short-range order prevailing in the hypereutectic iron concentration range. This phase was found to be less stable than the undefective one present in the less boron concentrated alloys. The transformation into the equilibrium phases, analyzed with an Arrhenius-type temperature dependence for the increase of the relative fraction of Fe₂B, led to an activation energy Ea = 1.38 ± 0.68 eV/atom.Facultad de Ciencias Exacta

Size dependent Cu dielectric function for plasmon spectroscopy: Characterization of colloidal suspension generated by fs laser ablation

Copper metal nanoparticles (Nps) have received increasing interest during the last years due to their potential applications in several fields of science and technology. Their optical properties depend on the characteristics of the dielectric function of the metal, their size, and the type of environment. The contribution of free and bound electrons on the dielectric function of copper Nps is analyzed as well as their influence on its plasmonic properties. The contribution of free electrons is corrected for particle size under 10 nm, introducing a term inversely proportional to the particle's radius in the damping constant. For bound electron contribution, interband transitions from the d-band to the conduction band are considered. For particles with sizes below 2 nm, the larger spacing between electronic energy levels must be taken into account by making the electronic density of states in the conduction band size-dependent. Considering these specific modifications, optical parameters and band energy values could be determined by fitting the bulk complex dielectric function. The obtained values were coefficient for bound electron contribution Kbulk = 2 × 1024, gap energy Eg = 1.95 eV, Fermi energy EF = 2.15 eV, and bound electrons damping constant γb = 1.15 × 1014 Hz. Based on the dielectric function determined in this way, experimental extinction spectra of colloid suspensions generated by ultrafast laser ablation of a solid copper target in liquids was fitted using the Drude-interband model and Mie's theory. Depending on the experimental conditions and liquid medium, the particles in the suspension may have nanometric or subnanometric core size and may be capped with a shell of oxide. From the fitting, it was possible to determine the structure and size distribution of spherical bare core and core-shell copper Nps in the nanometer-subnanometer size range. These results were compared with those obtained by standard microscopy techniques such as AFM and HRTEM. There is a very good agreement between the three techniques, showing that optical extinction spectroscopy (OES) is a good complementary technique to standard high resolution electron microscopy and AFM for sizing spherical nanometric-subnanometric Nps. OES has also the advantage of a very good measurement statistics, due to the large number of probed particles across the sample cell. Besides, it avoids coalescence effects since the measurement is made directly on the colloidal suspension.Fil: Santillán, Jesica María José. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Centro de Investigaciones Ópticas. Provincia de Buenos Aires. Gobernación. Comisión de Investigaciones Científicas. Centro de Investigaciones Ópticas. Universidad Nacional de La Plata. Centro de Investigaciones Ópticas; ArgentinaFil: Videla, Fabian Alfredo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Centro de Investigaciones Ópticas. Provincia de Buenos Aires. Gobernación. Comisión de Investigaciones Científicas. Centro de Investigaciones Ópticas. Universidad Nacional de La Plata. Centro de Investigaciones Ópticas; ArgentinaFil: Fernández van Raap, Marcela Beatriz. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Física La Plata. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Instituto de Física La Plata; ArgentinaFil: Schinca, Daniel Carlos. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Centro de Investigaciones Ópticas. Provincia de Buenos Aires. Gobernación. Comisión de Investigaciones Científicas. Centro de Investigaciones Ópticas. Universidad Nacional de La Plata. Centro de Investigaciones Ópticas; ArgentinaFil: Scaffardi, Lucia Beatriz. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Centro de Investigaciones Ópticas. Provincia de Buenos Aires. Gobernación. Comisión de Investigaciones Científicas. Centro de Investigaciones Ópticas. Universidad Nacional de La Plata. Centro de Investigaciones Ópticas; Argentin