RESUMO
Sugar cane bagasse stands as a prevalent and abundant form of solid agricultural waste, making it a prime candidate for innovative utilization. Harnessing its potential, we embarked on a groundbreaking endeavor to evaluate the sustainability of a molasses-based hydrothermal process to produce graphene quantum dots (GQDs). This pioneering initiative promises remarkable environmental benefits and holds immense economic potential. Embedding crystalline GQDs in activated carbon (AC) boost electrochemical efficiency by enhancing charge-transfer and ion migration kinetics. Optical, structural, and morphological evaluations were used to confirm the formation of GQDs. Transmission electron microscopy (TEM) investigation showed the size, shape, and fact that GQDs were monodispersed, and X-ray diffraction and Fourier transform infrared determined the structure of GQDs. The electrodes with negative (AC) and positive (AC@GQDs) polarity demonstrate a considerable specific capacitance of 220 and 265 F g-1, respectively, when measured at 0.5 A g-1. Additionally, these electrodes exhibit high-rate capabilities of 165 and 230 F g-1 when measured at 5 A g-1, as determined by galvanostatic charge-discharge techniques. The supercapacitor device comprising asymmetric AC//AC@GQDs exhibits a specific capacitance of 118 F g-1. Furthermore, the asymmetric device exhibits exceptional cycling behavior, with an impressive 92% capacitance retention even after undergoing 10,000 cycles. This remarkable performance underscores the immense potential of both the negative and positive electrodes for real-world supercapacitor applications. Such findings pave the way for promising advancements in the field and offer exciting prospects for practical utilization.
RESUMO
Naftidrofuryl is a vasodilator medication used for treating cerebral and peripheral vascular diseases. In this study, two spectroscopical techniques, spectrofluorimetric and resonance Rayleigh scattering (RRS), were utilized to quantify naftidrofuryl in its pharmaceutical samples. The developed methodologies in this study rely on a facile process of forming an association complex between erythrosine B reagent and naftidrofuryl under acidic conditions. The fluorimetric assay is based on the ability of naftidrofuryl to quench and decrease the native fluorescence intensity of the reagent when measured at λ emis . = 550 nm ( λ excit . = 526 nm). Under similar reaction conditions, the RRS method relies on the observed amplification in the RRS spectrum of the reagent at a wavelength of 577 nm following its interaction with naftidrofuryl. The methods exhibited linearity within the ranges 0.2-1.6 µg/ml (r2 = 0.999) and 0.1-1.4 µg/ml (r2 = 0.9994), with limit of quantitation values of 0.146 and 0.099 µg/ml, and limit of detection values of 0.048 and 0.032 µg/ml, for the fluorometric and the RRS methods, respectively. Moreover, the quenching between the dye and naftidrofuryl was studied using Stern-Volmer analysis, and the methodologies were experimentally optimized and validated. Additionally, acceptable recoveries were achieved when the procedures were applied to determine naftidrofuryl in pharmaceutical samples.
Assuntos
Eritrosina , Nafronil , Nafronil/análise , Espectrometria de Fluorescência/métodos , Espalhamento de Radiação , Preparações FarmacêuticasRESUMO
In pursuit of environmental safety, a novel and efficient method-dispersive solid-phase extraction based on functionalized mesoporous silica nanotubes (FMSNT nanoadsorbent)-was developed to remove tetrabromobisphenol A (TBBPA) from water samples. Characterization and comprehensive analysis of the FMSNT nanoadsorbent, including maximum adsorption capacity of 815.85 mg g-1 for TBBPA and its water stability, confirmed its potential. Subsequent analysis revealed the impact of multiple factors, for instance pH, concentration, dose, ionic strength, time, and temperature, on the adsorption process. The findings revealed that the adsorption of TBBPA followed the Langmuir and pseudo-second-order kinetics models while primarily driven by hydrogen bond interactions between bromine ions or hydroxyl groups of TBBPA and amino protons around the cavity. The novel FMSNT nanoadsorbent showed high stability and efficiency even after five times of recycling. Moreover, the overall process was identified as chemisorption, endothermic, and spontaneous. Finally, the Box-Behnken design was applied to optimize the results, confirming good reusability even after five cycles.
RESUMO
Netilmicin is an aminoglycoside antibiotic used to treat infections caused by a broad spectrum of Gram-negative and Gram-positive bacteria and is pharmaceutically formulated in ophthalmic dosage forms. In this study, two spectrofluorimetric approaches were designed and developed to switch-on the fluorescence activity of NTC. The first method, or Hantzsch (HNZ) method, was relied on measuring the generated fluorescence intensity upon the condensation of NTC with acetylacetone and formaldehyde (Hantzsch reaction) at λemis=483 nm/λexcit=425.5 nm. While the second fluorometric method (NHD method) was relied on measuring the generated fluorescence intensity upon the condensation of NTC with ninhydrin/phenylacetaldehyde at λemis=482.2 nm/λexcit=385.8 nm. The reaction conditions for the two approaches were well investigated and optimized. The selectivity study for the methods was investigated by determining NTC in the presence of the co-formulated drug (dexamethasone) and pharmaceutical excipients. The validation for two approaches was performed based on ICH guidelines, and ranges of linearity were 0.1-1.2 and 1.5-6.0 µg/mL, while LOD values were 0.039 and 0.207 µg/mL for the HNZ method and the NHD method, respectively. Finally, NTC has been determined in different ophthalmic preparations by the proposed approaches with adequate recovery values.
