RESUMEN
The demand for high-energy-density and safe energy storage devices has spurred increasing interest in high-voltage rechargeable magnesium batteries (RMB). As electrolytes are the bridge connecting the cathode and anode materials, the development of high-voltage electrolytes is the key factor in realizing high-voltage RMBs. This concept presents an overview of three chloride-free electrolyte systems with wide electrochemical windows, together with the degradation mechanisms and modification strategies at the anode/electrolyte interphase. Finally, future directions in stabilizing Mg anodes and realizing high-voltage RMBs are highlighted.
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The detection signal of carbohydrate antigen 125 (CA125) can be quantitatively amplified via the dual metal-organic framework (MOF) sandwich strategy. We propose a versatile method for synthesizing uniform MXene and MIL-101(Fe)-NH2 composites that combine the advantages of both materials to build a base layer with superb performance. MXene exhibits excellent electrical conductivity and high surface area. The mesoporous MIL-101(Fe)-NH2 not only increases the loading capacity of the primary antibody but also possesses the catalytic activity of the metal center (Fe). UiO66 loaded with methylene blue (MB) was fabricated as an electrochemical immunosensor signal tag to enable the detection of CA125. The mixture of MXene and MIL-101(Fe)-NH2 prepared as the substrate was fixed by chitosan rich in amino groups. As the signal amplification sector, UiO66@MB enhanced secondary antibody loading capacity and generated a redox signal enabling the detection of antigenic substances. The proposed electrochemical immunosensor demonstrated high sensitivity with a low limit of detection (LOD) of 0.006 U/mL. Therefore, the dual MOF sandwich-based immunosensor provides a novel method for the early diagnosis of CA125.
Asunto(s)
Biomarcadores de Tumor , Técnicas Biosensibles , Técnicas Biosensibles/métodos , Anticuerpos Inmovilizados , Inmunoensayo/métodos , Anticuerpos , Antígeno Ca-125 , Azul de Metileno/químicaRESUMEN
The excessive utilization of antibiotics has led to significant water contamination and posed severe threats to human well-being. Consequently, the pressing imperative to identify antibiotics in the environment arises. In this study, we have successfully synthesized a hollow PCN-222 MOF distinguished by its substantial surface area and abundant functional groups, particularly the porphyrin cores. To augment the electrical conductivity of the hollow PCN-222 (HPCN-222), gold (Au) particles were incorporated within the porphyrin core using a fundamental hydrothermal method. This modification facilitated the effective immobilization of aptamer strands through π-π stacking and electrostatic interactions. As a result, the Au@HPCN-222 composite demonstrated exceptional efficacy as a substrate for immobilizing the aptamer (Apt) onto the GCE surface. By employing differential pulse voltammetry (DPV) we successfully achieved the detection of chloramphenicol (CAP) with a remarkably low limit of detection of 0.0138 ng mL-1 and the peak DPV currents at 0.18 V (vs. Ag/AgCl) were used for calibration. Furthermore, this aptasensor exhibited high selectivity and reproducibility.
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Cloranfenicol , Porfirinas , Humanos , Reproducibilidad de los Resultados , Antibacterianos , Calibración , OligonucleótidosRESUMEN
A "signal-on" electrochemiluminescence (ECL) immunosensor has been proposed for detecting carbohydrate antigen 153 (CA153) based on the dual MOFs sandwich strategy. The conductive and porous substrate consisting of 1T-MoS2 and two-dimensional conductive metal-organic framework (MOF, Ni-HAB) was anchored onto the glassy carbon electrode (GCE) to label the capture antibody (Ab1), and the luminescence-functionalized MOF (Ru(bpy)32+@UiO-66-NH2) was utilized to immobilize the detection second antibody (Ab2) to construct a "signal-on" responsive sandwich-type electrochemiluminescence immunoassay. Meanwhile, tripropylamine (TPA) acts as the co-reactant and provides a luminescence system for Ru(bpy)32+@UiO-66-NH2. The luminescence-functionalized MOFs showed excellent ECL activity owing to the tunable structure of MOFs. The remarkable enhancement in ECL intensity was obtained by the immunoreaction of antigen and antibody. Under the optimized conditions, the biosensor exhibited a detection limit of 0.0001 U mL-1 (S/N = 3) with a wide range from 0.001 to 50 U mL-1. The proposed ECL immunosensor was applicable for detecting human serum samples with a recovery of 99.83 â¼ 101 % (RSD < 5 %). This work demonstrates that the advantage of multifunctional MOFs could be applied to construct highly selective ECL immunosensor, and it may facilitate the diagnosis of breast cancer in clinics.
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Técnicas Biosensibles , Nanopartículas del Metal , Estructuras Metalorgánicas , Compuestos Organometálicos , Humanos , Molibdeno , Inmunoensayo/métodos , Técnicas Biosensibles/métodos , Estructuras Metalorgánicas/química , Biomarcadores de Tumor , Compuestos Organometálicos/química , Anticuerpos , Mediciones Luminiscentes/métodos , Técnicas Electroquímicas/métodos , Límite de Detección , Nanopartículas del Metal/químicaRESUMEN
This study proposed an electrochemical sensor combining Mxene@Ni3(HITP)2@AuNPs with NiCo@Fc-MWCNTs-LDH for detecting extracellular vesicles (EVs) derived from MCF-7 cells. Mxene exhibits high conductivity and large surface area. Ni3(HITP)2 is a novel conductive metal-organic framework (MOF) with outstanding conductivity, capable of loading more gold nanoparticles (AuNPs) when combined with polyetherimide (PEI). Tetrahedra DNA (TDN) is anchored on the substrate through gold nanoparticles (AuNPs) for the specific capture of EVs, with CD63 aptamers carried at their vertices. In the signal layer, the NiCo@Fc-MWCNTs-LDH loaded with CD63 aptamers was prepared as the electrochemical sensor signal label for EVs detection. This electrochemical sensor exhibits high sensitivity, evidenced by a low limit of detection (LOD) of 13.79 particles/mL and a linear range from 1.6 × 102 to 1.6 × 106 particles/mL, underscoring its potential for early cancer diagnosis.
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BACKGROUND: Nitrated polycyclic aromatic hydrocarbons (nitro-PAHs) are the derivatives of polycyclic aromatic hydrocarbon which are direct mutagens and carcinogens to human. Nitro-PAHs can be produced in the process of food barbecuing/grilling. At present, there are few studies for the determination of nitro-PAHs in food. OBJECTIVE: To assess the effect of barbecued food to human health, we have established a method for the determination of 5 nitro-PAHs in barbecued foods. METHODS: The target nitro-PAHs were extracted with the mixture of methanol/acetone and then purified with an HLB SPE cartridge and finally analyzed by ultra-high-performance liquid chromatography-tandem mass spectrometry. Two pairs of target multiple reaction monitoring (MRM) ion pairs have been successfully identified for the target nitro-PAHs, and confirmed by high-resolution mass spectrometry to explore their formation mechanism. RESULTS: The method had linear ranges of 2.0-500 µg/L (except 1-nitronaphthalene 20-5000 µg/L) with the correlation coefficients greater than 0.995. The extraction recoveries were between 70.1% and 85.6% with the relative standard deviations less than 10.0%. The limits of detection of the method were less than 0.60 µg/L (except 1-nitronaphthalene 6.0 µg/L). CONCLUSIONS: The method has been successfully applied to the analysis of 5 nitro-PAHs in barbecued foods. 1-nitronaphthalene, 1,8-dinitropyrene , 1-nitropyrene were detected in some charcoal grilled samples with the contents of 1.35-12.9 µg/kg. 1,8-Dinitropyrene was detected in some oil-fried samples with the contents of 2.12-5.12 µg/kg. HIGHLIGHTS: This work presents an ultra-high-performance liquid chromatography-tandem mass spectrometry method for the determination of 5 nitro-PAHs in barbecued foods for the first time. The method has been successfully applied to the analysis of 5 nitro-PAHs in various barbecued foods and the nitro-PAHs were detected in some barbecued food samples. The mechanism of mass spectrometric decomposition of nitro-PAHs was investigated as well.
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Alimentos , Hidrocarburos Policíclicos Aromáticos , Carbón Orgánico , Cromatografía Líquida de Alta Presión , Culinaria , Humanos , Hidrocarburos Policíclicos Aromáticos/análisis , Extracción en Fase Sólida , Espectrometría de Masas en TándemRESUMEN
PURPOSE: The aim of this investigation was to study the osteogenesis activation following asymmetric inter-maxillary elastic on the subchondral bone of adult SD rats. METHODS: Twenty SD ten-week old rats were used in this study (eight rats loading 0.39 N elastic force, another eight rats loading 1.18 N elastic force, the other four rats without loading as control group). The extra-joint device was fixed on the right side by surgery. Tetracycline, calcein and xylenol orange were intraperitoneally injected on one day before surgery, one day before device removal and one day before sacrifice. Masson trichrome staining and in vivo fluorescence technique were used to detect the osteogenesis. RESULTS: The results of bone collagen maturation and velocity of osteogenesis were different from the control group after force loading. Bone collagen showed better maturity in force-loading side and light force induced more active osteogenesis. CONCLUSIONS: The results suggest that even in the adult SD individuals, the subchondral bone still shows remodeling ability to adapt the various mechanical environments. Stress increases the maturity of bone collagen while rotation inhibits maturity. Mechanic force promotes the osteogenesis, especially the light force.
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Colágeno , Osteogénesis , Animales , Cóndilo Mandibular , Ratas , Ratas Sprague-DawleyRESUMEN
A rapid and sensitive method based on microchip capillary electrophoresis with condition optimization of genetic algorithm-support vector regression (GA-SVR) was developed and applied to simultaneous analysis of multiplex PCR products of four foodborne pathogenic bacteria. Four pairs of oligonucleotide primers were designed to exclusively amplify the targeted gene of Vibrio parahemolyticus, Salmonella, Escherichia coli (E. coli) O157:H7, Shigella and the quadruplex PCR parameters were optimized. At the same time, GA-SVR was employed to optimize the separation conditions of DNA fragments in microchip capillary electrophoresis. The proposed method was applied to simultaneously detect the multiplex PCR products of four foodborne pathogenic bacteria under the optimal conditions within 8 min. The levels of detection were as low as 1.2 x 10(2) CFU mL(-1) of Vibrio parahemolyticus, 2.9 x 10(2) CFU mL(-1) of Salmonella, 8.7 x 10(1) CFU mL(-1) of E. coli O157:H7 and 5.2 x 10(1) CFU mL(-1) of Shigella, respectively. The relative standard deviation of migration time was in the range of 0.74-2.09%. The results demonstrated that the good resolution and less analytical time were achieved due to the application of the multivariate strategy. This study offers an efficient alternative to routine foodborne pathogenic bacteria detection in a fast, reliable, and sensitive way.
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Algoritmos , Bacterias/aislamiento & purificación , Electroforesis por Microchip/métodos , Microbiología de Alimentos , Reacción en Cadena de la Polimerasa/métodos , Bacterias/genética , Escherichia coli/genética , Escherichia coli/aislamiento & purificación , Reproducibilidad de los Resultados , Salmonella/genética , Salmonella/aislamiento & purificación , Sensibilidad y Especificidad , Shigella/genética , Shigella/aislamiento & purificación , Factores de Tiempo , Vibrio parahaemolyticus/genética , Vibrio parahaemolyticus/aislamiento & purificaciónRESUMEN
OBJECTIVE: The aim of this investigation was to study the expression of collagen type II in the cartilage of mandibular condyle following asymmetric inter-maxillary traction. METHODS: Two hundred and twenty SD rats were used in this study (one hundred and four rats loading 0.39 N elastic force, another one hundred and four rats loading 1.18 N elastic force, while twelve rats for control). The extra-joint device was fixed on the right side by surgery. Half of the experimental group was killed at 3, 7, 14, 28 days. The devices were removed at the 28th day in the rest rats, and the rats were sacrificed at 3, 7, 14, 28 days after removing the device. The type II collagen expression levels of all the joints were measured using immunohistochemical techniques. RESULTS: The positive expression of the type II collagen was mainly observed in the cytoplasm of chondrocyte, especially in maturative and hypertrophic layer. The expression intensity was different in different stages and different sides. Both of the two experimental groups showed the same tendency, while the changes in the light force group were more obviously than the heavy force group. In the right side (force-loading side), the type II collagen expression decreased at the early force-loading period. After the device was removed, the expressions increased immediately but then reach the lowest level. The expression almost recovered to normal level at the end of experiment. In the left side (none force-loading side), the expression remained increasing after force-loading and reached the peak at the 14th day. CONCLUSION: These results suggest that even in the adult individuals, the chondrocyte showed reaction to the mechanical force by altering type II collagen expression patterns and it may be the cause of the cartilage remolding after asymmetric inter-maxillary traction. A forward elastic force showed a depressant effect in matrix synthesis, and heavy force had stronger effect. But the rotation of condyle accelerated the matrix synthesis.
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Colágeno Tipo II , Tracción , Animales , Cartílago , Condrocitos , Cóndilo Mandibular , Ratas , Ratas Sprague-DawleyRESUMEN
A method for monitoring foodborne pathogenic bacteria by multiplex polymerase chain reaction (PCR)--capillary electrophoresis (CE) with a laser induced fluorescence detector was developed. Three sets of primers were designed to amplify the gene segments of uidA gene in E. coli. O157:H7, invA gene in salmonella and ipaH gene in Shigella, individually. The multiple PCR system and the separation conditions of CE were optimized. Using a capillary coated with linear polyacrylamide and sieving buffer of 7.0 g/L methyl cellulose (MC) under 8.3 kV of electric voltage, the proposed method was able to simultaneously detect the PCR products of specific genes existing in the three kinds of pathogenic bacteria within 22 min. The relative standard deviations of migration time for the detected DNA fragments were ranging from 1.47% to 2.07%. In comparison with agarose gel electrophoresis, the proposed method is rapid, sensitive and accurate.