732 resultados para CuO microparticles
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Introduction: One of the most common strategies for pain control during and after surgical procedures is the use of local anesthetics. Prolonged analgesia can be safely achieved with drug delivery systems suitably chosen for each local anesthetic agent.Areas covered: This review considers drug delivery formulations of local anesthetics designed to prolong the anesthetic effect and decrease toxicity. The topics comprise the main drug delivery carrier systems (liposomes, biopolymers, and cyclodextrins) for infiltrative administration of local anesthetics. A chronological review of the literature is presented, including details of formulations as well as the advantages and pitfalls of each carrier system. The review also highlights pharmacokinetic data on such formulations, and gives an overview of the clinical studies published so far concerning pain control in medicine and dentistry.Expert opinion: The design of novel drug delivery systems for local anesthetics must focus on how to achieve higher uploads of the anesthetic into the carrier, and how to sustain its release. This comprehensive review should be useful to provide the reader with the current state-of-art regarding drug delivery formulations for local anesthetics and their possible clinical applications.
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El presente proyecto se llevó a cabo con el fin de contribuir al desarrollo de nuevos materiales para ser implementados en dispositivos para el sensado de glucosa no ezimaticos, en este trabajo se realizaron diversos estudios sobre desarrollo de nanofibras de carbón decoradas con nanoestructuras de ZnO y CuO, en el que según reportes realizados por diversos investigadores tanto el ZnO como el CuO han presentado excelentes resultados para ser implementados en sensores de glucosa no enzimáticos gracias a las propiedades físicas y químicas que estos presentan, además que las nanofibras presentan alta porosidad, buena conducción y pueden funcionalizarse fácilmente por lo que es ampliamente utilizada como sustrato para depósito de nanoestructuras de semiconductores. Las nanofibras de carbón fueron obtenidas mediante la técnica de electrohilado utilizando como materia prima poliacrilonitrilo y posteriormente fueron sometidas a una calcinación en una atmosfera inerte. Las nanofibras de carbón fueron pre-tratadas para el depósito y crecimiento de las nanoestructuras de ZnO y CuO en donde se utilizó síntesis por hidrotermal para crecimiento de los semiconductores. La caracterización morfológica y estructural se lleco a cabo por Microscopia Electrónica de Barrido (SEM), Microcopia Electrónica de Transmisión (TEM), la composición química y cristalográfica de los materiales se determinó por medios de Espectroscopia de Infrarrojo de Transformada de Furier (FTIR), Espectroscopia de Energía Dispersiva de rayos X (EDXS), Difracción de Rayos X (DRX), así mismo se llevó a cabo el Análisis Térmico Diferencial y Análisis Térmico Gravimétrico simultáneamente, finalmente los materiales fueron caracterizados electroquímicamente por Voltamperometría Cíclica (CV) para conocer si este material podría tener potencial aplicación en sensores de glucosa no enzimático. Contribuciones y Conclusiones: Se establecieron las óptimas condiciones para obtención de las NFCs utilizando PAN como precursor mediante la técnica de electrohilado, además se consiguió determinar las condiciones para una carbonización controlada en una atmosfera de airenitrógeno. Así mismo se determinaron las condiciones óptimas para la producción de nanoestructuras de ZnO/CuO mediante el sembrado y crecimiento de nanopartículas sobre las NFCs. La diversidad en la morfología y la cantidad de material en la superficie de las nanofibras son de gran importancia en la eficiencia del material ya que ésta se ve perjudicada cuando se tiene pobres cantidades depositadas. Por otro lado, el ZnO no presenta sensibilidad por sí sólo, ante la presencia de la glucosa, del mismo modo el CuO presentó la misma incapacidad de detección. El uso de CuO como catalizador en el ZnO ha demostrado que el electrodo modificado de NFCs/ZnO-CuO presenta propiedades para oxidar la glucosa, en comparación a los de NFCs/ZnO y NFCs/CuO los cueles no presentaron ninguna actividad de oxidación para esta. Lo que permitió tener una idea que al depositar estos dos materiales depositados en el mismo sustrato, la eficiencia de éstos incrementa, lo cual podría contribuir a investigaciones futuras para estos materiales.
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432 p.
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Copper-based catalysts supported on niobium-doped ceria have been prepared and tested in the preferential oxidation of CO in excess of H2 (PROX) and in total oxidation of toluene. Supports and catalysts have been characterized by several techniques: N2 adsorption, ICP-OES, XRF, XRD, Raman Spectroscopy, SEM, TEM, H2-TPR and XPS, and their catalytic performance has been measured in PROX, with an ideal gas mixture (CO, O2 and H2) with or without CO2 and H2O, and in total oxidation of toluene. The effects of the copper loading and the amount of niobium in the supports have been evaluated. Remarkably, the addition of niobia to the catalysts may improve the catalytic performance in total oxidation of toluene. It allows us to prepare cheaper catalysts (niobia it is far cheaper than ceria) with improved catalytic performance.
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Conspectus: The challenges of the 21st century demand scientific and technological achievements that must be developed under sustainable and environmentally benign practices. In this vein, click chemistry and green chemistry walk hand in hand on a pathway of rigorous principles that help to safeguard the health of our planet against negligent and uncontrolled production. Copper-catalyzed azide–alkyne cycloaddition (CuAAC), the paradigm of a click reaction, is one of the most reliable and widespread synthetic transformations in organic chemistry, with multidisciplinary applications. Nanocatalysis is a green chemistry tool that can increase the inherent effectiveness of CuAAC because of the enhanced catalytic activity of nanostructured metals and their plausible reutilization capability as heterogeneous catalysts. This Account describes our contribution to click chemistry using unsupported and supported copper nanoparticles (CuNPs) as catalysts prepared by chemical reduction. Cu(0)NPs (3.0 ± 1.5 nm) in tetrahydrofuran were found to catalyze the reaction of terminal alkynes and organic azides in the presence of triethylamine at rates comparable to those achieved under microwave heating (10–30 min in most cases). Unfortunately, the CuNPs underwent dissolution under the reaction conditions and consequently could not be recovered. Compelling experimental evidence on the in situ generation of highly reactive copper(I) chloride and the participation of copper(I) acetylides was provided. The supported CuNPs were found to be more robust and efficient catalyst than the unsupported counterpart in the following terms: (a) the multicomponent variant of CuAAC could be applied; (b) the metal loading could be substantially decreased; (c) reactions could be conducted in neat water; and (d) the catalyst could be recovered easily and reutilized. In particular, the catalyst composed of oxidized CuNPs (Cu2O/CuO, 6.0 ± 2.0 nm) supported on carbon (CuNPs/C) was shown to be highly versatile and very effective in the multicomponent and regioselective synthesis of 1,4-disubstituted 1,2,3-triazoles in water from organic halides as azido precursors; magnetically recoverable CuNPs (3.0 ± 0.8 nm) supported on MagSilica could be alternatively used for the same purpose under similar conditions. Incorporation of an aromatic substituent at the 1-position of the triazole could be accomplished using the same CuNPs/C catalytic system starting from aryldiazonium salts or anilines as azido precursors. CuNPs/C in water also catalyzed the regioselective double-click synthesis of β-hydroxy-1,2,3-triazoles from epoxides. Furthermore, alkenes could be also used as azido precursors through a one-pot CuNPs/C-catalyzed azidosulfenylation–CuAAC sequential protocol, providing β-methylsulfanyl-1,2,3-triazoles in a stereo- and regioselective manner. In all types of reaction studied, CuNPs/C exhibited better behavior than some commercial copper catalysts with regard to the metal loading, reaction time, yield, and recyclability. Therefore, the results of this study also highlight the utility of nanosized copper in click chemistry compared with bulk copper sources.
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Purpose: To compare oral bioavailability and pharmacokinetic parameters of different lornoxicam formulations and to assess similarity in plasma level profiles by statistical techniques. Methods: An open-label, two-period crossover trial was followed in 24 healthy Pakistani volunteers (22 males, 2 females). Each participant received a single dose of lornoxicam controlled release (CR) microparticles and two doses (morning and evening) of conventional lornoxicam immediate release (IR) tablet formulation. The microparticles were prepared by spray drying method. The formulations were administered again in an alternate manner after a washout period of one week. Pharmacokinetic parameters were determined by Kinetica 4.0 software using plasma concentration-time data. Moreover, data were statistically analyzed at 90 % confidence interval (CI) and Schuirmann’s two one-sided t-test procedure. Results: Peak plasma concentration (Cmax) was 20.2 % lower for CR formulation compared to IR formulation (270.90 ng/ml vs 339.44 ng/ml, respectively) while time taken to attain Cmax (tmax) was 5.25 and 2.08 h, respectively. Area under the plasma drug level versus time (AUC) curve was comparable for both CR and IR formulations. The 90 % confidence interval (CI) values computed for Cmax, AUC0-24, and AUC0-∞ , after log transformation, were 87.21, 108.51 and 102.74 %, respectively, and were within predefined bioequivalence range (80 - 125 %). Conclusion: The findings suggest that CR formulation of lornoxicam did not change the overall pharmacokinetic properties of lornoxicam in terms of extent and rate of lornoxicam absorption.
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Liver cancer accounts for nearly 10% of all cancers in the US. Intrahepatic Arterial Radiomicrosphere Therapy (RMT), also known as Selective Internal Radiation Treatment (SIRT), is one of the evolving treatment modalities. Successful patient clinical outcomes require suitable treatment planning followed by delivery of the microspheres for therapy. The production and in vitro evaluation of various polymers (PGCD, CHS and CHSg) microspheres for a RMT and RMT planning are described. Microparticles with a 30±10 µm size distribution were prepared by emulsion method. The in vitro half-life of the particles was determined in PBS buffer and porcine plasma and their potential application (treatment or treatment planning) established. Further, the fast degrading microspheres (≤ 48 hours in vitro half-life) were labeled with 68Ga and/or 99mTc as they are suitable for the imaging component of treatment planning, which is the primary emphasis of this dissertation. Labeling kinetics demonstrated that 68Ga-PGCD, 68Ga-CHSg and 68Ga-NOTA-CHSg can be labeled with more than 95% yield in 15 minutes; 99mTc-PGCD and 99mTc-CHSg can also be labeled with high yield within 15-30 minutes. In vitro stability after four hours was more than 90% in saline and PBS buffer for all of them. Experiments in reconstituted hemoglobin lysate were also performed. Two successful imaging (RMT planning) agents were found: 99mTc-CHSg and 68Ga-NOTA-CHSg. For the 99mTc-PGCD a successful perfusion image was obtained after 10 minutes, however the in vivo degradation was very fast (half-life), releasing the 99mTc from the lungs. Slow degrading CHS microparticles (> 21 days half-life) were modified with p-SCN-b-DOTA and labeled with 90Y for production of 90Y-DOTA-CHS. Radiochemical purity was evaluated in vitro and in vivo showing more than 90% stability after 72 and 24 hours respectively. All agents were compared to their respective gold standards (99mTc-MAA for 68Ga-NOTA-CHSg and 99mTc-CHSg; 90Y-SirTEX for 90Y-DOTA-CHS) showing superior in vivo stability. RMT and RMT planning agents (Therapy, PET and SPECT imaging) were designed and successfully evaluated in vitro and in vivo.
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A family of copper oxide catalysts with loadings spanning 1–5 wt% were dispersed on a three dimensional, mesoporous TUD-1 silica through a hydrothermal, surfactant-free route employing tetraethylene glycol as a structure-directing agent. Their bulk and surface properties were characterized by N2 physisorption, XRD, DRUVS, EPR, TEM and Raman spectroscopy, confirming the expected mesoporous wormhole/foam support morphology and presence of well-dispersed CuO nanoparticles (∼5–20 nm). The catalytic performance of Cu/TUD-1 was evaluated as heterogeneous Fenton-like catalysts for Bisphenol A (BPA) oxidative degradation in the presence of H2O2 as a function of [H2O2], and CuO loading. Up to 90.4% of 100 ppm BPA removal was achieved over 2.5 wt% Cu/TUD-1 within 180 min, with negligible Cu leaching into the treated water.
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In a previous work (Nicu et al. 2013), the flocculation efficiency of three chitosans differing by molecular weight and charge density were evaluated for their potential use as wet end additives in papermaking. According to the promising results obtained, chitosan (single system) and its combination with bentonite (dual system) were evaluated as retention aids, and their efficiency was compared with poly(diallyl dimethyl ammonium chloride) (PDADMAC) and polyethylenimine (PEI). In single systems, chitosan was clearly more efficient in drainage rate than PDADMAC and PEI, especially those with the lowest molecular weights; however, retention is considerably lower. This drawback can be overcome by using dual systems with anionic bentonite microparticles, with the optimum ratio of polymer:bentonite being 1:4 (wt./wt.). In dual systems, the differences in retention were almost negligible, and the difference in drainage rate was even higher, together with better floc reversibility. The most efficient chitosan in single systems was Ch.MMW, while Ch.LMW was the most efficient in dual systems. The flocculation mechanism of chitosan was a combination of patch formation, charge neutralization, and partial bridge formation, and the predominant mechanism depended on the molecular weight and charge density of the chitosan.
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El objeto del presente artículo es analizar las políticas de fomento de cooperativas y sociedades laborales durante este periodo de crisis, identificando los principales dispositivos existentes y los de nueva implantación, evaluando su alcance y valorando su nivel de eficacia. Se han distinguido tres grupos de políticas de fomento, las políticas tradicionales de fomento, las políticas de nuevo cuño, incluyendo en estas últimas las medidas urdidas por los gobiernos regionales y la nueva ley de economía social y finalmente las políticas de austeridad. Se concluye, en primer lugar, que las cooperativas y sociedades laborales no constituyen un sector muy subvencionado dado que el alcance de estas políticas ha sido muy reducido. En segundo lugar, contrariamente a lo que cabría esperar en un periodo de crisis, ni los dispositivos tradicionales ni los de nuevo cuño han conocido un mayor despliegue en estos últimos años, al objeto de combatir los problemas de desempleo y de fortalecimiento del sector de la economía social. Al contrario, las políticas de austeridad implantadas han afectado duramente a las políticas de economía social, las cuales han visto reducirse los presupuestos asignados de modo muy acusado.
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IntroducciónLa Asamblea Nacional Constituyente de Guatemala, el día 20 de mayo de 1824, autorizó a la Provincia de Costa Rica a eregir su propia cerca, la Casa de la Moneda. Esta orden tuvo efectos extraordinarios. Costa Rica tenía en sus manos nada menos que la facultad de acuñar moneda, operada por la iniciativa privada a partir de 1825 y por el Poder Civil a partir de 1829. este órgano estatal convirtióse, por la mayor parte, en un centro de espionaje económico. Por ella corrieron las políticas mineralógicas; por medio de ella se sabía quién era el dueño de las pastas o tejos nacionales de oro y plata; ella era tamiz de las importaciones y exportaciones de moneda acuñada y la de rescate. Compárense las acuñaciones llevadas a cabo popr este cuño con respecto a los de Guatemala y Tegucigalpa y podrá concluirse que ellas no fueron bicocas en razón de su cuantía, denominaciones de valores, así como por las habitaciones de moneda nacional y extranjera...
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ResumenEste artículo tiene como objetivo profundizar los estudios concernientes a la interfase entre Bioética y Derechos Humanos, así como contribuir para la solidificación de la interconexión entre los dos campos de saber. Para ello, se investigaron los modos por los cuales la instancia de producción bioéticaque se insiere en el ámbito de la OMS – el Departamento de Ética, Equidad, Comercio y Derechos Humanos – construye la interfase entre Bioética y Derechos Humanos a partir del análisis de los sentidos identificados en los documentos de cuño general producidos por dicha instancia bioética.Para tal fin, se utilizó el abordaje teórico-metodológico que se fundamenta en la acepción de que los sentidos construidos socialmente pueden ser aprehendidos por medio del análisis de las prácticas discursivas. Tal elección metodológica se basó en la percepción de que los documentos producidospor organismos internacionales son prácticas discursivas cuyos sentidos pueden ser identificados mediante el examen de sus repertorios. Como conclusión, se observó que la interconexión entre Bioética y Derechos Humanos se forma de manera compleja, dado que el Departamento de Ética de la OMS al mismo tiempo que se aproxima a la temática, se aleja de ella pues hay elementos que evidencian la incorporación de los principios y normas de los Derechos Humanos en sus documentos y, paradójicamente, se constata la ausencia de la Bioética y sus normativas.Palabras clave: Bioética institucional, derechos humanos, Declaración Universal sobre Bioética y Derechos Humanos, Organización Mundial de la Salud.AbstractThis article aims at intensifying the studies concerning the interface between Bioethics and Human Rights, as well as at contributing to the solidification of the connection between these two fields of knowledge. In order to do so, we investigated the ways through which the instance of bioethics that is part of the scope of the World Health Organization – the Department of Ethics, Equity, Trade and Human Rights – builds the interface between Bioethics and Human Rights by means of the analysis of the meanings identified in the general documents produced by such instance of bioethics. For that end, we used the theoretical-methodological approach that is based on the assumption that the socially constructed meanings can be understood through the analysis of the discourse practices. The choice of such methodology was supported by the perceptionthat the documents elaborated by international organisms are discourse practices whose meanings can be identified through the examination of their repertoires. In sum, it was observed that the interconnection between Bioethics and Human Rights is complex, since the Ethics Department of the WHO deals with this theme by being close to it and far from it, simultaneously, as there are features that constitute evidence of the incorporation of Human Rights norms and principles into the WHO documents, but it is also observed the absence of Bioethics and its norms.Keywords: institutional Bioethics, Human Rights, Universal Declaration on Bioethics and Human Rights,World Health Organization.