UTN- FRC -Producción Académica de Investigación y Desarrollo

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    Preparation, charactrization and mathematical modeling of keterolac reléase conteined in LP-SBA-15 host.
    (Universidad Tecnológica Nacional Regional Córdoba., 2017) Cussa , Jorgelina; Juárez , Juliana María; Gómez Costa, Marcos Bruno; Anunziata , Oscar Alfredo; Anunziata , Oscar Alfredo; Juárez , Juliana María
    Drug-controlled release systems can keep the level of drugs in precise doses in the body above the optimal level and with low toxicity. We propose the LP-SBA-15 nanomaterial as a promising new host for drug delivery systems because of its high biocompatibility, in vivo biodegradability, and low toxicity. Ketorolac-LP-SBA-15 was prepared and characterized by XRD, FTIR, UV-Vis DRS, TEM, and texture analysis, determining the adsorption capacity and its release, achieving the required therapeutic efficacy. The host shows ordered mesoporous nanochannels with a diameter of 11-12 nm, maintaining the structure with the incorporation of Keto. The mechanism of drug release the LP-SBA-15 host was evaluated. Different mathematical models were used to adjust the experimental data, being the Ritger-Peppas model followed by the Weibull model the best ones. In this work, we show a promising drug storage material for effective encapsulation and controlled release of KETO, achieving the required therapeutic efficacy. Studies indicate that KETO was adsorbed on the channel surface of LP-SBA-15 without affecting the structure or chemical composition of KETO. Controlled drug delivery systems can achieve precise delivery at the time and place of destination, keeping the concentration of the drug at points in the body within the optimal range and below the toxicity threshold. The study also demonstrates the storage capacity and release properties of LP SBA-15 containing KETO. The release of KETO contained in LP-SBA-15 can offer a significant improvement in the controlled release of the drug and the analgesic and anti-inflammatory effects, positively influenced, by the links formed between the host and drug molecules and by diffusion through the host porosity. The promising results we obtained for the release of the drug thoroughly using the new material, reaching a rapid initial release rate, and maintaining a constant rate afterward, allow us to maintain the concentration of the drug in the therapeutic efficacy range, applying it largely to the treatment of diseases that require a rapid response.
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    KETO/LP-SBA-15 Composite as a drug release system.
    (Universidad Tecnológica Nacional Regional Córdoba., 2017) Cussa , Jorgelina; Juárez , Juliana María; Prados, Antonela; Gómez Costa, Marcos Bruno; Anunziata , Oscar Alfredo; Anunziata , Oscar Alfredo; Juárez , Juliana María
    Controlled drug delivery systems can maintain the concentration of drugs in the exact sites of the body within the optimum range and below the toxicity threshold, improving therapeutic efficacy and reducing toxicity. SBA-15 with larger pore sizes material (LP-SBA-15) is a new promising host for drug delivery systems due to high biocompatibility, in vivo biodegradability and low toxicity. Large pore mesoporous silica supports has been applied in studies of ketorolac tromethamine (KETO) adsorption and release. KETO/LP-SBA-15 composite was synthesized. The material synthesis and loading of KETO into LP-SBA-15 pores were successful. We obtained promising results for controlled drug release using the novel LP-SBA-15 material. The ability of KETO/LP-SBA-15 release was measured. The concentration of KETO in HCl solution or buffer in a specific time was determined by UV-Vis. First-order, Higuchi and Ritger-Peppas (or Korsmeyer-Peppas) models were used to fit experimental release data. Figure 1 show the fitting results, where Qt/Q? is the release fraction per unit mass in time t, k represents release rate in all models and n is a measure of desorption intensity in Ritger-Peppas regression. In this work, we have shown a promising drug storage material for the effective encapsulation and controlled release of KETO, achieving the required therapeutic efficacy. KETO was adsorbed into LP-SBA-15 channel surface without affecting the chemical structure or composition of KETO. The study also demonstrates the storage capacity and release properties of LP-SBA-15 containing KETO. The release of KETO contained in LP-SBA-15 can offer significant improve in controlled drug release and enhance a good analgesia effect.
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    Ketorolac-trometamina/mcf: aplicación en sistemas de liberación de fármacos.
    (Universidad Tecnológica Nacional Regional Córdoba., 2018) Cussa , jorgelina; Juárez , Juliana María; Prados, Antonela; Gómez Costa, Marcos Bruno; Anunziata , Oscar Alfredo; Anunziata , Oscar Alfredo; Juárez , Juliana María
    En los últimos años, la atención se ha dirigido significativamente a la nanociencia y la nanotecnología. La administración de fármacos basados en nanomateriales se ha puesto en relieve por los investigadores académicos e industriales. Diversos materiales nanoestructurados se produjeron y se aplican a la administración de fármacos tales como nanopartículas, nanocápsulas, nanotubos, micelas, microemulsiones y liposomas (Wu et al., 2011). Los sistemas de liberación controlada de fármacos pueden lograr la entrega espacial y temporal precisa de agentes terapéuticos al sitio de destino. Generalmente, los sistemas de administración de fármacos controlada pueden mantener la concentración de fármacos en los sitios precisos del cuerpo dentro de la gama óptima y bajo el umbral de toxicidad, mejorar la eficacia terapéutica y reducir la toxicidad (Wang, 2009). Un sistema de administración de fármacos se puede definir como un sistema capaz de liberar un agente bioactivo portador en una ubicación específica a una velocidad específica. El objetivo principal de este tipo de sistema es la de facilitar la dosificación y la duración del efecto del fármaco, minimizando el daño al paciente y mejorar la salud humana, ya que permiten la reducción de la frecuencia de la dosis (Wang, 2009).
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    Composite MCF/KETO. Aplicación en sistemas de liberación de fármacos.
    (Universidad Tecnológica Nacional Regional Córdoba., 2019) Cussa , jorgelina; Juárez , Juliana María; Prados, Antonela; Gómez Costa, Marcos Bruno; Juárez , Juliana María
    La espuma celular mesoestructurada (MCF) es un prometedor material para los sistemas de administración de fármacos dado a la alta biocompatibilidad, biodegradabilidad y baja toxicidad. Sus propiedades incluyen una gran área superficial, poro grande uniforme. En este trabajo, MCF como material de almacenamiento de drogas fue sintetizado con éxito y cargado con la droga ketorolaco-trometamina, obteniendo el composite MCF/ KETO. La síntesis del material y el proceso de carga de ketorolaco-trometamina en los poros de la MCF fueron exitosos tal como se muestra en los análisis de XRD, FTIR, TGA, TEM y texturales. Hemos obtenido resultados prometedores para la liberación controlada de fármacos utilizando el noble material MCF. La aplicación de estos materiales en la liberación de KETO es innovadora, logrando una alta tasa de liberación inicial y manteniendo una tasa constante en los tiempos altos.
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    LP-SBA-15/Ketorolac Nanocomposite: Development, Characterization, and Mathematical Modeling of Controlled Keto Release.
    (Universidad Tecnológica Nacional Regional Córdoba., 2023) Cussa, Jorgelina; Juárez , Juliana María; Gómez Costa, Marcos Bruno; Anunziata , Oscar Alfredo; Anunziata , Oscar Alfredo; Juárez , Juliana María
    Drug-controlled release systems can keep the level of drugs in precise doses in the body above the optimal level and with low toxicity. We propose the nanomaterial LP-SBA-15 as an attractive new host for drug delivery systems due to its high biocompatibility, in vivo biodegradability, and low toxicity. LP-SBA-15/Ketorolac was prepared and characterized by XRD, FTIR, UV-Vis DRS, TEM, and texture analysis, determining the adsorption capacity and its release and achieving the required therapeutic efficacy. The host shows the ordered mesoporous nanochannels with a diameter of 11-12 nm, maintaining the structure with the incorporation of Keto. The mechanism of drug release from the LP-SBA-15 host was evaluated. Different mathematical models were used to adjust the experimental data, the Ritger-Peppas model followed by the Weibull model the best ones. The promising results we obtained for the release of the drug thoroughly using the new material, reaching a rapid initial release rate, and maintaining a constant rate afterward, allow us to maintain the concentration of the drug in the therapeutic efficacy range, applying it largely to the treatment of diseases that require a rapid response
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    Novel preparation of CMK-3 nanostructured material modified with titania applied in hydrogen uptake and storage.
    (Universidad Tecnológica Nacional., 2017) Juárez , Juliana María; Ledesma , Brenda Cecilia; Gómez Costa, Marcos Bruno; Beltramone , Andrea Raquel; Anunziata , Oscar Alfredo; Anunziata , Oscar Alfredo; Beltramone , Andrea Raquel; Ledesma , Brenda Cecilia
    This work deals with the development of a novel procedure to synthesize titania-modified nano structured carbon employing Ti-SBA-15 as hard template. The new mesoporous carbon displays high specific surface area of 1044 m2/g and large pore volume of 0.7 cm3/g. XRD pattern of Ti-CMK-3 indicates that the ordered structure of this material is similar to the CMK-3. XRD, XPS and UVeVis-DRS analysis indicated that Ti is highly dispersed as anatase phase in Ti-CMK-3. The synthesized Ti-CMK-3 exhibited significantly enhanced H2 storage properties (2.6 wt%, equivalent to 13 mmol/g) compared with CMK-3 without Ti (2.2 wt%, 11 mmol/g) at 77 K and 10 bar.
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    Vanadium and titanium oxide supported on mesoporous CMK-3 asnew catalysts for oxidative desulfurization.
    (Universidad Tecnológica Nacional., 2016) Rivoira , Lorena Paola; Juárez , Juliana María; Falcón , Horacio; Gómez Costa, Marcos Bruno; Anunziata , Oscar Alfredo; Beltramone , Andrea Raquel; Beltramone , Andrea Raquel; Anunziata , Oscar Alfredo; Juárez , Juliana María
    Vanadium supported-CMK-3 catalysts with vanadium loading of 1–7 wt.% were studied in the oxidative desulfurization (ODS) of dibenzothiophene as a model sulfur compound. The activity was compared with titanium supported-CMK-3. Structural and textural characterization of the catalysts was performed by means of N2 adsorption, XRD, UV–vis–DRS, Raman spectroscopy, XPS, TEM and TPR. The dispersion and the nature of the vanadium species depend on the V loading, so does the catalyst activity. Vanadium supported-CMK-3 with 7 wt.% of vanadium loading was the most active catalyst for ODS of DBT using hydrogen peroxide (H2O2) as oxidant and acetonitrile as solvent. 100% of DBT elimination was attained at short time in mild conditions. Carbon ordered mesoporous CMK-3 with high surface area and high pore volume promotes a very good anchorage of metallic oxides in the carbons framework reaching high active sites distribution and more stable nanoclusters. The reusability of the catalyst indicates that V-CMK-3 is a potential catalyst for the ODS of dibenzothiophene.
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    Synthesis and characterization of a nanoporous carbon CMK-3 modified with iron for the ODS of DBT.
    (Universidad Tecnológica Nacional., 2017) Juárez , Juliana María; Rivoira , Lorena Paola; Gómez Costa, Marcos Bruno; Anunziata , Oscar Alfredo; Beltramone , Andrea Raquel; Anunziata , Oscar Alfredo; Rivoira , Lorena Paola
    A nanostructured Carbon CMK-3 modified with Fe by using different sources of Fe, were used in the oxidative desulfurization (ODS) of dibenzothiophene as a model sulfur compound. Ordered mesoporous carbon CMK-3 was synthesized via a two-step impregnation of the SBA-15 silica mesonanopores with a solution of sucrose using an incipient wetness method. The sucrose–silica composite was heated at 1173 K for 4 h under nitrogen flow. The silica A nanostructured Carbon CMK-3 modified with Fe by using different sources of Fe, were used in the oxidative desulfurization (ODS) of dibenzothiophene as a model sulfur compound. Ordered mesoporous carbon CMK-3 was synthesized via a two-step impregnation of the SBA-15 silica mesonanopores with a solution of sucrose using an incipient wetness method. The sucrose–silica composite was heated at 1173 K for 4 h under nitrogen flow. The silica The catalytic activity was improved when the nanoporous carbon was modified with Fe. The sample modified with FeCl3.6H2O was the most active catalyst for ODS of DBT, using hydrogen peroxide (H2O2) as oxidant and acetonitrile as solvent. 100% of DBT elimination was attained at a short time in mild conditions.
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    Preparation of carbon nanotubes with hybrids nanostructure materials.
    (Universidad Tecnológica Nacional., 2017) Martínez , María Laura; Juárez , Juliana María; Gómez Costa, Marcos Bruno; Beltramone, Andrea Raquel; Juárez , Juliana María
    Carbon nanotubes (CNT's) are allotropes carbon, like diamond, graphite and fullerenes. There are different types of CNT's, depending on the type of the graphite layers, it can be single wall carbon nanotubes (SWCNT's) and multi wall carbon nanotubes (MWCNT's). These nanomaterials show good physical properties such as their density, strength and thermal conductivity. The controllable synthesis of materials with the desired structure and dimensionality is of great significance in material science. In this work, the hierarchical carbon nanotubes (CNTs) were synthesized via a simple chemical conversion route by using Carbon Substrate/Fe3O4-SBA-15 hybrid (all in one). The synthesis of Carbon Substrate/Fe3O4-SBA-15 hybrid was carried out using Fe3O4- SBA-15 as a hard template and sucrose as carbon precursor. Sucrose was dissolved in a solution of H2SO4 in water and to this solution, Fe3O4-SBA-15 was added. The resulting mixture was dried at 373 K and then heated at 433 K for 6 h. A second impregnation was performed in order to ensure the filling of the template pores with the carbon precursor. To obtain the carbon nanotubes, the sample was placed in muffle at 1173 K under nitrogen flow (20mL/min) for 30 min. In order to remove the silica, the material was placed in an HF solution. The CNTs was filtered, washed and dried at 323 K. In the present work, we report the synthesis and characterization of CNTs materials of hybrid material. The material was characterized by X-ray diffraction (XRD) and the morphologies and structural features of the prepared materials were observed from the SEM and TEM images.
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    Controlled drug release system: cyclophosphamide delivery contained in LP-SBA-15 functionalized with terbutylamine.
    (Univesidsad Tecnológica Nacional., 2023) Cussa, jorgelina; Juárez , Juliana María; Gómez Costa, Marcos Bruno; Anunziata , Oscar Alfredo; Anunziata , Oscar Alfredo; Juárez , Juliana María
    Controlled drug administration systems can keep the level of drugs in specific locations in the organism with low toxicity and above the optimal level. We suggest the LP-SBA15 material as a auspicious new host for drug delivery systems because of its low toxicity high biocompatibility and in vivo biodegradability. LP-SBA-15 materials were synthesized and functionalized using 0-15-30% of tert-butylamine (TBA) and used as effective drug delivery systems. The anticancer drug Cyclophosphamide (CP) is an alkylating compound which is a phosphoramide derivative and is habitually used in autoimmune diseases. Reactive oxygen species production has been related to the mechanism of CP-induced cell death or tumor cell killing. The activated metabolites of CP are released in both healthy and tumor tissues and destroy the cellular DNA and proteins as well as mitochondrial and lysosomal membranes. CP was loaded into the nanomaterial of the transporters and characterized by XRD, FTIR, TGA, TEM and texture, determining the adsorption capacity and its release. The release of the drug was studied for each material by simulating the physiological conditions and submerging the composite, at 37 °C with constant stirring, in a HCl solution (0.1 M) for the first two hours and in Buffer solution pH = 7 the following hours to simulate the conditions of the organism. Release experiment were conducted to determine the requisite efficacy of treatment. The study was performed by UV-Vis spectrophotometry to evaluate the amount of CP released. The mechanism of drug release from the LP-SBA-15 matrix was evaluated by adjusting the experimental data, being the Ritger-Peppas. The promising results we obtained for the controlled release of the drug in a controlled manner using the new material, reaching a quick initial release rate and maintaining a constant rate at high moments, allow us to keep the concentration of the drug in the therapeutic efficacy range, applying it to a great extent to the treatment of diseases that require a rapid response. Lastly, it was suggested that the LP-SBA-15 nanomaterial functionalized with 15% TBA was the most desirable system due to they had adequate amounts of both drug loading and release.