RESUMO
Anti-inflammatory wound healing involves targeted drug delivery to the wound site using hydrogel materials to prolong drug effectiveness. In this work, hydrogel films were fabricated using carboxymethyl cellulose (CMC) and poly(vinyl alcohol) (PVA) crosslinked with citric acid (CA) and glutaraldehyde (GA) at different concentrations. The crosslinker densities were optimized with various CA (2-10% w/v) and GA (1-5% v/v) concentrations. The optimized crosslink densities in the hydrogel exhibited additional functional group peaks in the FT-IR spectra at 1740 cm-1 for the C=O stretching of the ester linkage in CA and at 1060 cm-1 for the C-O-C stretching of the ether group in GA. Significantly, the internal porous structures of hydrogel composite films improved density, swelling capacities, solubility percentage reduction, and decreased water retention capacities with optimized crosslinker densities. Therefore, these hydrogel composite films were utilized as drug carriers for controlled drug release within 24 h during medical treatment. Moreover, the hydrogel films demonstrated increased triamcinolone acetonide (TAA) absorption with higher crosslinker density, resulting in delayed drug release and improved TAA efficiency in anti-inflammatory activity. As a result, the modified hydrogel showed the capability of being an alternative material with enhanced anti-inflammatory efficiency with hydrogel films.
RESUMO
The present study aimed to extract nanocellulose (NC) from sugarcane bagasse agricultural waste through a chemical method (sulfuric acid hydrolysis and ultrasonication). Subsequently, the nanocellulose product was conjugated with polylysine (NC-PL) and assessed for its efficacy in reducing the toxicity of Fumonisin B1 (FB1), a mycotoxin produced by fungi commonly found in corn, wheat, and other grains. Experimental results confirmed the successful conjugation of NC and PL, as evidenced by FTIR peaks at 1635 and 1625 cm-1 indicating amide I and amide II vibrations in polylysine (PL). SEM analysis revealed a larger size due to PL coating, consistent with DLS results showing the increased size and positive charge (38.0 mV) on the NC-PL surface. Moreover, the effect of FB1 adsorption by NC and NC-PL was evaluated at various concentrations (0-200,000 µg/mL). NC-PL demonstrated the ability to adsorb FB1 at concentrations of 2000, 20,000, and 200,000 µg/mL, with adsorption efficiencies of 94.4-100%. Human hepatocellular carcinoma (HepG2) cells were utilized to assess NC and NC-PL cytotoxic effects. This result is a preliminary step towards standardizing results for future studies on their application as novel FB1 binders in food, food packaging, and functional feeds.
RESUMO
Graphene Quantum dots (GQDs) are used as a surface-enhanced Raman substrate for detecting target molecules with large specific surface areas and more accessible edges to enhance the signal of target molecules. The electrochemical process is used to synthesize GQDs in the solution-based process from which the SERS signals were obtained from GQDs Raman spectra. In this work, GQDs were grown via the electrochemical process with citric acid and potassium chloride (KCl) electrolyte solution to obtain GQDs in a colloidal solution-based format. Then, GQDs were characterized by transmission electron microscope (TEM), Fourier-transform infrared spectroscopy (FTIR), and Raman spectroscopy, respectively. From the results, SERS signals had observed via GQDs spectra through the Raman spectra at D (1326 cm-1) and G (1584 cm-1), in which D intensity is defined as the presence of defects on GQDs and G is the sp2 orbital of carbon signal. The increasing concentration of KCl in the electrolyte solution for 0.15M to 0.60M demonstrated the increment of Raman intensity at the D peak of GQDs up to 100 over the D peak of graphite. This result reveals the potential feasibility of GQDs as SERS applications compared to graphite signals.
RESUMO
Zinc oxide (ZnO) offers a great potential in several applications from sensors to Photovoltaic cells thanks to the material's dependency, to its optical and electrical properties and crystalline structure architypes. Typically, ZnO powder tends to be grown in the form of a wurtzite structure allowing versatility in the phase of material growths; albeit, whereas in this work we introduce an alternative in scalable yet relatively simple 2D hexagonal planed ZnO nanoflakes via the electrochemical deposition of commercially purchased Zn(NO3)2 and KCl salts in an electrochemical process. The resulting grown materials were analyzed and characterized via a series of techniques prior to thermal annealing to increase the grain size and improve the crystal quality. Through observation via scanning electron microscope (SEM) images, we have analyzed the statistics of the grown flakes' hexagonal plane's size showing a non-monotonal strong dependency of the average flake's hexagonal flakes' on the annealing temperature, whereas at 300 °C annealing temperature, average flake size was found to be in the order of 300 µm². The flakes were further analyzed via transmission electron microscopy (TEM) to confirm its hexagonal planes and spectroscopy techniques, such as Raman Spectroscopy and photo luminescence were applied to analyze and confirm the ZnO crystal signatures. The grown materials also underwent further characterization to gain insights on the material, electrical, and optical properties and, hence, verify the quality of the material for Photovoltaic cells' electron collection layer application. The role of KCl in aiding the growth of the less preferable (0001) ZnO is also investigated via various prospects discussed in our work. Our method offers a relatively simple and mass-producible method for synthesizing a high quality 2D form of ZnO that is, otherwise, technically difficult to grow or control.
