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In this work, a microfluidic prototype based on polymeric materials was developed to monitor surface processes using surface-enhanced Raman spectroscopy (SERS), keeping the reagents free of environmental contamination. The prototype was fabricated on poly(methyl methacrylic acid) (PMMA). A micrometric membrane of a functional organic polymer (FOP) based on p-terphenyl and bromopyruvic acid monomers was formed on the PMMA surface to promote the formation of metal nanoclusters. Au nanosized film was deposited on the FOP membrane to give rise to the SERS effect. A microchannel was formed on another piece of PMMA using micromachining. A representative 3D model of the prototype layer arrangement was built and simulated in COMSOL Multiphysics® to approximate the electric field distribution and calculate the power enhancement factor as the Au film changes over time. The fabrication process was characterized using UV-visible and Raman spectroscopies and XPS. The prototype was tested using a Raman microscope and liquid solutions of cysteamine and Escherichia coli (E. coli). The simulation results demonstrated that the morphological characteristics of the Au layer give rise to the SERS effect, and the power enhancement factor reaches values as high as 8.8 × 105 on the FOP surface. The characterization results showed the formation of the FOP and the Au film on PMMA and the surface functionalization with amine groups. The Raman spectra of the prototype showed temporal evolution as different compounds were deposited on the upper wall of the microchannel. Characteristic peaks associated with these compounds were detected with continuous monitoring over time. This prototype offers many benefits for applications like monitoring biological processes. Some advantages include timely surface evaluation while avoiding environmental harm, decreased use of reagents and samples, minimal interference with the process by measuring, and detecting microorganisms in just 1 h, as demonstrated with the E. coli sample.
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Escherichia coli , Nanopartículas Metálicas , Microfluídica , Escherichia coli/isolamento & purificação , Ouro/química , Nanopartículas Metálicas/química , Polímeros , Polimetil Metacrilato , Análise Espectral Raman/métodosRESUMO
Zinc ferrite nanoparticles (ZFO NPs) are a promising magneto-crystalline platform for nanomedicine-based cancer theranostics. ZFO NPs synthesized using co-precipitation method are characterized using different techniques. UV-visible spectroscopy exhibits absorption peaks specific for ZFO. Raman spectroscopy identifies Raman active, infrared active, and silent vibrational modes while Fourier transforms infrared spectroscopic (FTIR) spectra display IR active modes that confirm the presence of ZFO. X-ray diffraction pattern (XRD) exhibits the crystalline planes of single-phase ZFO with a face-centered cubic structure that coincides with the selected area electron diffraction pattern (SAED). The average particle size according to high-resolution transmission electron microscopy (HR-TEM) is 5.6 nm. X-ray photoelectron spectroscopy (XPS) signals confirm the chemical states of Fe, Zn, and O. A superconducting quantum interference device (SQUID) displays the magnetic response of ZFO NPs, showing a magnetic moment of 45.5 emu/gm at 70 kOe. These ZFO NPs were then employed for comparative cytotoxicity evaluation using MTT, crystal violet, and LDH assays on breast adenocarcinoma epithelial cell (MCF-7), triple-negative breast cancer lines (MDA-MB 231), and human embryonic kidney cell lines (HEK-293). Flow cytometric analysis of all the three cell lines were performed in various concentrations of ZFO NPs for automated cell counting and sorting based on live cells, cells entering in early or late apoptotic phase, as well as in the necrotic phase. This analysis confirmed that ZFO NPs are more cytotoxic towards triple-negative breast cancer cells (MDA-MB-231) as compared to breast adenocarcinoma cells (MCF-7) and normal cell lines (HEK-293), thus corroborating that ZFO can be exploited for cancer therapeutics.
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Adenocarcinoma , Antineoplásicos , Neoplasias de Mama Triplo Negativas , Humanos , Violeta Genciana , Zinco , Células HEK293 , ApoptoseRESUMO
This work reports on Fe2O3 and ZnO materials for lactate quantification. In the synthesis, the bi-phase γ-/α-Fe2O3 and γ-/α-Fe2O3/ZnO nanoparticles (NPs) were obtained for their application in a lactate colorimetric sensor. The crystalline phases of the NPs were analyzed by XRD and XPS techniques. S/TEM images showed spheres with an 18 nm average and a needle length from 125 to 330 nm and 18 nm in diameter. The γ-/α-Fe2O3 and γ-/α-Fe2O3/ZnO were used to evaluate the catalytic activity of peroxidase with the substrate 3,3,5,5-tetramethylbenzidine (TMB), obtaining a linear range of 50 to 1000 µM for both NPs, and a 4.3 µM and 9.4 µM limit of detection (LOD), respectively. Moreover, γ-/α-Fe2O3 and γ-/α-Fe2O3/ZnO/lactate oxidase with TMB assays in the presence of lactate showed a linear range of 50 to 1000 µM, and both NPs proved to be highly selective in the presence of interferents. Finally, a sample of human serum was also tested, and the results were compared with a commercial lactometer. The use of ZnO with Fe2O3 achieved a greater response toward lactate oxidation reaction, and has implementation in a lactate colorimetric sensor using materials that are economically accessible and easy to synthesize.
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Nanopartículas Metálicas , Óxido de Zinco , Humanos , Colorimetria/métodos , Ácido Láctico , Nanopartículas Metálicas/químicaRESUMO
In this work, unsupported Pd aerogel catalysts were synthesized for the very first time by using microwaves as a heating source followed by a lyophilization drying process and used towards formic acid electro-oxidation in a microfluidic fuel cell. Aerogels were also made by heating in a conventional oven to evaluate the microwave effect during the synthesis process of the unsupported Pd aerogels. The performance of the catalysts obtained by means of microwave heating favored the formic acid electro-oxidation with H2SO4 as the electrolyte. The aerogels' performance as anodic catalysts was carried out in a microfluidic fuel cell, giving power densities of up to 14 mW cm-2 when using mass loads of only 0.1 mg on a 0.019 cm2 electrode surface. The power densities of the aerogels obtained by microwave heating gave a performance superior to the resultant aerogel prepared using conventional heating and even better than a commercial Pd/C catalyst.
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In this work, atomically substituted three-dimensionally ordered macroporous (3DOM) spinels based on Co and Mn (MnCo2O4 and CoMn2O4) were synthetized and used as cathodic electrocatalysts in a primary Zn-air battery. Scanning/transmission electron microscopy images show a 3DOM structure for both materials. Skeleton sizes of 114.4 and 140.8 nm and surface areas of 65.3 and 74.6 m2 g-1 were found for MnCo2O4 and CoMn2O4, respectively. The increase in surface area and higher presence of Mn3+ and Mn4+ species in the CoMn2O4 3DOM material improved battery performance with a maximum power density of 101.6 mW cm-2 and a specific capacity of 1440 mA h g-1, which shows the highest battery performance reported to date using similar spinel materials. The stability performance of the electrocatalyst was evaluated in half-cell and battery cell systems, showing the higher durability of CoMn2O4, which was related to its better capability to perform the electrocatalytic process as adsorption, electron transfer, and desorption. It was found through density functional theory calculations that the CoMn2O4 spinel has a higher density of states in the Fermi level vicinity and better conductivity. Finally, the unique shape of 3DOM spinels promoted a high interaction between electroactive species and catalytic sites, making them suitable for oxygen reduction reaction applications.
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Se realizó un estudio genético cuantitativo para determinar el peso al nacer (PN), peso al destete corregido a 205 d (P205) y peso a los 18 meses corregido a 548 d (P548) en un rebaño Brahman ubicado en el estado Cojedes, Venezuela, bajo un programa genético y ambiental supervisado. Se analizaron los registros de 5137 animales, nacidos durante los años 1996 a 2007. Se estimaron los componentes de (co)variancias, parámetros genéticos y no genéticos, a través de tres modelos animal univariados usando el paquete de programas MTDFREML. Todos los modelos incluyeron los efectos aleatorios: genético aditivo directo, genético aditivo materno y ambiental permanente de la madre y como efecto fijo: grupo de contemporáneos. Los valores de índices de herencia directos fueron 0,45, 0,20 y 0,34, y los índices de herencia maternos 0,02, 0,13 y 0,04 para PN, P205 y P548, respectivamente. Las correlaciones genéticas aditivas directas - maternas fueron positivas. Los estimados para las tendencias fenotípicas anuales fueron de 0,285 kg para PN, 2,045 kg para P205 y 0,503 kg para P548. Las tendencias genéticas anuales aditivas directas fueron 0,075 kg, 0,523 kg y 1,072 kg y las genéticas maternas fueron 0,0002 kg, 0,230 kg y 0,096 kg para PN, P205 y P548, respectivamente. Los resultados indican que existe suficiente variabilidad genética para crecimiento en la población evaluada, lo que favorece el programa de selección por crecimiento.
A quantitative genetic study for birth weight (BW), weaning weight corrected at 205 days (WW205), and weight at 18 months corrected at 548 days (W548), was conducted in a Brahman herd located in the State of Cojedes, Venezuela, under a supervised genetic and environmental program. The records of 5137 animals born from 1996-2007 were analyzed. Components of covariance, genetic and non-genetic parameters were estimated through three univariate animal models, using the MTDFREML set of programs. All models included random effects, such as direct genetic additive, maternal genetic additive, and permanent environmental of the dam; and as a fixed effect, the contemporary group. The direct heritability indexes were 0.45, 0.20, and 0.34; and the maternal heritability indexes were 0.02, 0.13 and 0.04 for BW, WW205 and W548, respectively. All genetic additive direct-maternal correlations were positive. The estimates for the annual phenotypic trends were 0.285 for BW, 2.045 for WW205, and 0.503 for W548; respectively. The direct additive annual trends were 0.075 kg, 0.523 kg, and 1.072 kg for BW, WW205, and W548, respectively. The results of the investigation indicate the existence of enough genetic variability for growth in the evaluated population, which favors the selection program for growth.
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Humanos , Masculino , Feminino , Universidades , Aprendizagem , Universidades , Docentes , Ensino/métodos , Ensino/organização & administração , Ensino/tendênciasRESUMO
El acarbose es un inhibidor competitivo de aglucosidasa que reduce el aumento postprandial de glucosa e insulina. En este estudio doble ciego, cruzado, con distribución de tratamientos al azar, se administró acarbose o placebo a un grupo de pacientes con DMNID crónicamente descontrolados que recibían sulfonilureas. Los pacientes continuaron su tratamiento previo y fueron distribuidos al azar en dos secuencias: en la A recibieron acarbose 100 mg tres veces al día 12 semanas, dos semanas de placebo tres veces al día (periodo de lavado) y finalmente placebo tres veces al día 12 semanas. En la secuencia B el orden fue inverso al anterior (placebo-placebo-acarbose). Se incluyeron 16 pacientes en cada secuencia. Se excluyeron tres de la secuencia A: uno por efectos colaterales, uno por dolor neuropático y uno por cambio de domicilio. De la secuencia B se excluyó uno por no tomar la sulfonilurea. Se observó una disminución discreta pero significativa del peso con acarbose comparado con placebo en ambas secuencias. Se observaron reducciones significativas de glucosa postprandial con el acarbose en ambas secuencias; también se observaron reducciones en los niveles de glucosa de ayunas en algunas visitas. Aunque los valores promedio de HbA1c y triglicéridos fueron menores con acarbose, la diferencia con el placebo no fue estadísticamente significativa. El acarbose fue tolerado bien en general, ya que si bien casi todos los pacientes mostraron efectos colaterales, sólo tuvo que suspenderse en uno. El acarbose es un recurso terapéutico útil en combinación con sulfonilureas en diabéticos no insulinodependiente