Search Results (25,156)

Neural regeneration requires an optimal environment, including structural, chemical, mechanical, and electrical properties. Alginate (Alg) and graphene oxide (GO) are promising biomaterials for nerve tissue engineering, as Alg provides biocompatibility and hydrogel formation, while GO enhances mechanical strength and conductivity. For this study, GO was synthesized using the modified Hummer’s method, and Alg–GO scaffolds with varying GO concentrations were developed. FTIR spectroscopy confirmed the successful incorporation of GO into the Alg matrix, while UV–Vis and photoluminescence analyses demonstrated GO-induced modifications of the optical properties. Thermal analysis revealed improved stability with increasing GO content, whereas swelling tests showed enhanced water uptake and retention. Conductivity measurements indicated a clear improvement in electrical conductivity, particularly at moderate GO concentrations. SEM imaging confirmed a homogeneous distribution of GO within the Alg matrix, with structural uniformity across all samples. Cytocompatibility was assessed using SH–SY5Y neuroblastoma cells through MTT, LDH, and LIVE/DEAD assays. All composites supported cell attachment, viability, and proliferation, with GO concentrations up to 6% promoting optimal cell growth without inducing cytotoxicity. In contrast, excessive GO content (9%) resulted in reduced proliferation, although biocompatibility was maintained. These results highlight the potential of Alg–GO scaffolds as promising candidates for neural tissue engineering. The findings demonstrate the potential of Alg–GO scaffolds as advanced biomaterials for regenerative medicine. Future research should focus on in vivo evaluations to confirm their therapeutic applicability. Full article

Postprandial hyperglycemia represents a critical therapeutic target in type 2 diabetes mellitus (T2DM), requiring interventions that simultaneously address glycemic dysregulation and oxidative stress. This study evaluated the anti-hyperglycemic and antioxidant properties of Sclerocarya birrea leaf crude extract (CE) and biosynthesized silver nanoparticles (AgNPs). Phytochemical screening, nanoparticle characterization (UV–Vis, XRD, TEM, SEM, DLS, FTIR), enzyme inhibition assays (α-amylase, α-glucosidase, DPP-IV), glucose dynamics in Caco-2 cells, and antioxidant assays (DPPH, total antioxidant capacity, H₂O₂ cytoprotection) were performed. Phytochemical analysis identified flavonoids, tannins, alkaloids, and terpenoids as major constituents of Sclerocarya birrea leaf extract. AgNPs exhibited spherical morphology (36.8 ± 8.6 nm, n = 100 particles analyzed), face-centered cubic crystallinity (crystallite size: 32.1 nm), and characteristic surface plasmon resonance at 451 nm. Both formulations inhibited α-amylase (CE IC₅₀: 14 µg/mL; AgNPs IC₅₀: 14.07 µg/mL, n = 3) and α-glucosidase (CE IC₅₀: 15.96 µg/mL; AgNPs IC₅₀: 15.82 µg/mL, n = 3), showing substantial inhibition, though less potent than acarbose. Uniquely, AgNPs demonstrated selective DPP-IV inhibition (IC₅₀: 220.5 µg/mL, n = 3, p < 0.001 vs. CE), completely absent in CE. In antioxidant assays, DPPH scavenging potency was comparable between formulations (CE IC₅₀: 23.45 µg/mL; AgNPs IC₅₀: 22.26 µg/mL, n = 3), while CE achieved higher maximal scavenging at the tested concentrations. Conversely, AgNPs provided superior intracellular cytoprotection against H₂O₂-induced oxidative stress in kidney cells (80.2 ± 2.1% viability at 76 µg/mL vs. CE 69.8 ± 3.4% at 190 µg/mL, n = 3, p < 0.001), representing a 2.5-fold dose advantage. Neither formulation significantly altered glucose uptake or SGLT1 expression in intestinal epithelial cells (p > 0.05, two-way ANOVA, n = 3). These findings establish S. birrea-based formulations, particularly AgNPs, as promising multifunctional candidates for managing postprandial hyperglycemia and oxidative complications in T2DM. They also highlight nanotechnology-enhanced phytomedicine as an innovative therapeutic strategy. Full article

This study introduces a novel anticorrosion coating for copper based on an epoxy matrix reinforced with a berberine-loaded graphene oxide (BBR@GO) nanocomposite. The BBR@GO was synthesized via a simple, non-covalent functionalization method, leveraging π-π stacking interactions between the planar berberine molecule and the graphene oxide surface. The successful loading of berberine was confirmed by Fourier-transform infrared (FTIR) spectroscopy, thermogravimetric analysis (TGA), and energy-dispersive X-ray spectroscopy (EDS). The BBR@GO nanocomposite was incorporated into an epoxy resin at 0.1 wt.% loading and applied to a copper substrate. The corrosion protection performance of the BBR@GO/EP coating was systematically evaluated in 3.5 wt.% NaCl solution for 27 days using electrochemical impedance spectroscopy (EIS) and potentiodynamic polarization (PDP). The BBR@GO/EP coating exhibited a total impedance of 5.31 × 10⁸ Ω·cm² after 27 days, which was 17 times higher than the pure epoxy (EP) coating. The corrosion current density (i_corr) was reduced to 2.59 × 10⁻⁸ A·cm⁻², a four-fold decrease compared to the EP coating. Post-immersion analysis confirmed the excellent durability of the BBR@GO/EP coating and the retention of berberine within the matrix. The enhanced performance is attributed to the synergistic effect of the physical barrier provided by the well-dispersed GO nanosheets and the inhibitive action of the retained berberine molecules at the coating–metal interface. Full article

Short-pulse laser machining was employed to transform the flat copper sheet into a microtextured specimen. This specimen was further nanotextured using the nickel wet-plating to build up the IR (InfraRed)-emission metallic device with fractal-like surface. Four-unit cells were designed and fabricated as a micro-/nanotextured specimen by varying the microtextured unit cell structure. The IR-emissivity of these four specimens was measured using the thermographic microscopy with FT-IR (Fourier Transform InfraRed). The bare copper and nickel-nanotextured copper specimens were utilized as a reference. The micro-/nanotextured copper specimen had higher IR-emissivity than 0.8 in the wide wavelength range from 2 μm to 14 μm. Full article

Natural laccases are a widely reported option for pollutant degradation; however, their widespread application is severely restricted by high production costs, limited storage stability, and rapid inactivation at the neutral pH typical of wastewater treatment plants. To overcome these limitations, we rationally designed manganese-based nanozymes (Mn-APTES/1MeIm) that mimic natural metal–histidine coordination within a protective siloxane network. Optimization via Response Surface Methodology produced two variants, Mn-APTES/1MeIm-6 and Mn-APTES/1MeIm-7, revealing distinct synthesis mechanisms: catalytic activity at pH 6 is driven by synthesis temperature, whereas activity at pH 7 is controlled by the APTES:1MeIm molar ratio. TEM and XRD analysis confirmed a delaminated aminoclay architecture composed of electron-transparent nanosheets, while FTIR verified Mn–N coordination through characteristic blue shifts. The optimized nanozymes retained robust activity, exhibiting maximum reaction velocities of 4.331 µM min⁻¹ (Mn-APTES/1MeIm-6) and 1.71 µM min⁻¹ (Mn-APTES/1MeIm-7), whereas Trametes versicolor laccase was practically inactive. Practically, Mn-APTES/1MeIm-6 achieved 75% degradation of oxytetracycline in 120 min without detectable manganese leaching, significantly outperforming the natural enzyme (<13%). These findings present a robust, pH-stable alternative for sustainable environmental remediation. Full article

Biochar is a porous material which can be produced by biomass waste pyrolysis and modified using metal oxide to improve its adsorption performance. Activated biochar (AB) was synthesized from patchouli biomass waste to study the effect of calcination tempera-ture on its potency as a drug pollutant adsorbent. Research processes included the bio-mass pyrolysis with CoCl₂ activator, AB impregnation with FeCl₃, FeCl₃/AB calcination at various temperatures, product characterizations (X-ray diffraction, FTIR spectrometry), and paracetamol adsorption test at various concentrations. The paracetamol concentra-tions were analyzed using UV–Vis spectrophotometry. The adsorption data was treated using Langmuir, Freundlich, and Dubinin–Radushkevich (DR) models. The diffracto-grams indicated the α-Fe₂O₃, γ-Fe₂O₃, FeFe₂O₄, and carbon turbostratic structures. The Fe_xO_y crystallinity increased by increasing temperature. The FTIR spectra significantly indicated the functional group changing at 600 °C. In the adsorption test, the Fe_xO_y/AB-800 compo-site gave the highest adsorption capacity of 53.087 mg/g (Langmuir) with a correlation co-efficient of 0.964 (very high correlation), and the physical adsorption mechanism based on adsorption energy of 530.330 J/mol (DR) and 1/n value of 0.62 (Freundlich) provided the favorable adsorption based on both the RL of 0.457 (Langmuir) and the n constant of 1.579 (Freundlich). Thus, the Fe_xO_y/AB-800 composite has potential as an adsorbent of organic pollutants such as paracetamol. Full article

To address the issue of normal displacement deviation induced by the geometric nonlinearity of cross-spring flexural pivots in pendulum-type interferometers, which leads to modulation attenuation, this study proposes a co-simulation method combining Finite Element Analysis (FEA) and Physical Optics. First, an optomechanical model was established based on the retroreflective property of cube-corner prisms and a double-pendulum differential scanning architecture (where the optical path difference is four times the mechanical displacement). Using the ANSYS Workbench 2022 R1 transient dynamics module with the “Large Deflection” algorithm enabled, the nonlinear motion trajectories of single-pivot and dual-pivot flexural hinges were quantitatively compared. Subsequently, a multi-physics data mapping interface was established to map mechanical motion errors into a physical optics simulation model, where the interference modulation was accurately calculated via electromagnetic field tracing. Results demonstrate that under ambient temperature (25 °C) and a spectral resolution of 1 cm⁻¹, the normal displacement deviation of the single-pivot hinge is only 0.00165 mm, representing a 95.6% reduction compared to the dual-pivot structure (0.03765 mm). Furthermore, the modulation of the single-pivot structure remains above 0.98 throughout the scanning range, significantly outperforming the nonlinear decay characteristic of the dual-pivot structure. These findings provide a theoretical basis for the structural optimization and selection of high-precision portable FTIR spectrometers. Full article

This work examined the development of amylose–lipid complexes in green banana flour (Musa × paradisiaca) incorporated with virgin coconut oil (VCO), focusing on their spectral, thermal, and in vitro digestibility characteristics. Firstly, the native banana flour was analyzed for apparent amylose content using a spectrophotometric assay. To facilitate amylose–lipid complexation, both hot-pressed and cold-pressed VCO were incorporated into the banana flour under controlled thermal conditions, after which amylose–lipid interactions were characterized using Fourier-transform infrared and Raman spectroscopy for spectral features and differential scanning calorimetry for thermal behavior. The banana flour exhibited an AAC of 26.40 ± 0.002%. GCMS analysis of FAME derivatized VCO detected medium- to long-chain fatty acids, including octanoic (C8:0), decanoic (C10:0), dodecanoic (C12:0), tetradecanoic (C14:0), and hexadecanoic acids (C16:0) stearic acid (C18:0) and oleic acid (C18:1). FTIR coupled with multivariate analysis and Raman spectra confirmed lipid incorporation/retention in green banana flour through characteristic O–H, C–H, and C=O bands. While DSC revealed distinct endothermic transitions at 89.56 ± 2.17 °C (ΔHₘ = 0.8587 ± 0.1014 J g⁻¹) for hot-pressed VCO and 89.18 ± 0.98 °C (ΔHₘ = 0.6267 ± 0.0777 J g⁻¹) for cold-pressed VCO, consistent with the melting of V-type amylose–lipid complexes. Morphological analysis revealed that thermal treatment transformed native banana flour from irregular granular structures into an amorphous matrix via starch gelatinization, whereas subsequent incorporation of VCO promoted aggregation. In vitro enzymatic digestion showed a slight reduction in starch hydrolysis in VCO-treated samples. The incorporation of an exogenous lipid, such as VCO, into green banana flour promotes the formation of thermally stable amylose–lipid complexes that reduce enzymatic digestibility. Full article

This study investigates the potential of Quercus robur leaves as a bio-coagulant for the removal of heavy metal ions, including zinc (II), iron (III), copper (II), and chromium (VI), from water. The Quercus robur leaves were used in two forms: Quercus robur powder (QRP) and Quercus robur extract (QRE). The extract was prepared using distilled water to extract the active compounds responsible for coagulation, such as proteins, polysaccharides, and total phenolics. The QRP was characterized by Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), X-ray diffraction (XRD), and zeta potential analysis to identify the active functional groups, surface morphology, crystallinity, and surface charge, all of which are key factors influencing its performance in the coagulation–flocculation process. In this work, the Response Surface Methodology (RSM)-based Central Composite Design (CCD), with two factors (bio-coagulant dosage and initial metal concentration), was used examine the effects of each factor and their interaction, while the responses were zinc (II) removal, iron (III) removal, copper (II) removal, and chromium (VI). The results revealed high removal efficiency for these metal ions, reaching up to 100% for all metal ions treated with QRP and QRE. The quality of the model predictions was evaluated using analysis of variance (ANOVA). For all metal ions, the R² (≥97%), R² adjusted (≥95%), and p-values (<0.05), indicating an excellent model accuracy. These results show that bio-coagulants (QRP and QRE) based a Quercus robur leaves are a promising, effective, and reliable option for removing heavy metal ions from water, and that the models developed can be used to optimize the coagulation-flocculation process. Full article

Composites based on rPE and OPEFB waste are considered sustainable materials. However, their performance is limited by hydrophobic–hydrophilic incompatibility, which weakens interfacial adhesion. This study investigated the atmospheric-pressure air plasma treatment of rPE to enhance its compatibility with OPEFB fibers and evaluated its role as a compatibilizer. Atmospheric plasma treatment for 120 s introduced oxygen-containing groups onto the rPE surface, as evidenced by C-O and OH peaks in the FTIR spectra and the higher O/C ratio in the XPS analysis. Consequently, the water contact angle decreased, reducing the difference in surface tension between rPE and OPEFB from 45.61% to 7.80%. Composites containing 20 wt.% OPEFB were fabricated by varying the proportion of untreated rPE with p-rPE. All p-rPE-based composites exhibited fewer interfacial voids than untreated rPE composites, indicating improved fiber–matrix adhesion. The tensile strength and elastic modulus increased with the p-rPE content, whereas the elongation at break remained higher than that of the untreated composite. Therefore, p-rPE shows potential as a compatibilizer, enabling agricultural and plastic waste value enhancement. Full article

This study investigates the effects of extraction technique, solvent type, and geographical origin on the recovery of bioactive compounds from Arbutus unedo L. leaves collected from two Croatian islands (Vis and Mali Lošinj) and extracted using conventional, Soxhlet, and ultrasound-assisted extraction (UAE) with green solvents (distilled water, 70% ethanol, and ethyl acetate). Extracts were purified and characterized by thin-layer chromatography, column chromatography, and FTIR spectroscopy. Total phenols, hydroxycinnamic acids, flavonols, condensed tannins, and antioxidant capacity were quantified spectrophotometrically. Solvent type had the greatest influence, with 70% ethanol yielding the highest levels of bioactives and antioxidant capacity. Geographical origin significantly affected total phenolics and condensed tannins, with leaves from Vis outperforming those from Mali Lošinj. UAE was slightly more efficient than conventional and Soxhlet methods, particularly for thermolabile phenolics. Machine learning algorithms were applied as exploratory tools, using total phenols as a proxy variable to estimate selected bioactive compounds and antioxidant capacity based on extraction parameters. Decision Tree and Gradient Boosting models showed high goodness of fit within the experimental dataset (R² > 0.91). These results support the potential of green extraction strategies combined with data-driven screening for the valorization of A. unedo leaf extracts, while highlighting the need for further validation prior to industrial application. Full article

Copper-based nanoparticles (Cu-based NPs) represent a major focus in nanomedicine due to their unique physicochemical properties and excellent biocompatibility. In this paper, we present an interdisciplinary study bridging engineering and biomedical sciences by employing a novel synthesis approach to produce highly stable and uniformly dispersed spherical copper nanoparticles (CuNPs), which were subsequently tested for their cytotoxic effects on SKBR3 and MSC human cells. The synthesis of CuNPs was performed in the presence of the complexing agent trisodium citrate (TSC), while starch was used for the chemical reduction step. Characterization of the Cu-based NPs via UV–Vis, FT-IR, Mie theory, DLS and SEM confirmed their nanoscale structure. The obtained CuNPs were subsequently assessed for their biological effects and cytotoxic responses induced in normal and SKBR3 cancer cell lines. The SKBR3 cell line showed a dose-dependent decrease in the cell index and a higher proportion of apoptotic cells compared to normal MSCs, with apoptosis representing the dominant mode of cell death. Although SKBR3 cells appeared to mount an antioxidant response against CuNP oxidative stress, the response was insufficient to counteract the apoptotic progression. In comparison, MSCs showed a greater resilience to CuNP-induced cellular stress. By promoting oxidative stress and disrupting the antioxidant defense system of cancer cells, CuNPs exhibit promising anti-cancer properties. Full article

Thermoplastic starch (TPS) can be a sustainable alternative to petrochemical plastics for flexible packaging, especially in rainforests and tropical regions where native starch sources such as cassava are abundant. However, one problem preventing TPS packaging from widespread use is its susceptibility to moisture. This study evaluated TPS formulations based on Amazonian cassava starch reinforced with plantain leaf fibers, beeswax, and low-density polyethylene (LDPE) particles. The plastic compounds were extruded to obtain pellets and then films at 120–130 °C. The resulting films were then cut and heat-sealed to obtain flexible packaging. Different properties of the TPS packages were evaluated, such as mechanical strength, water vapor transmission (WVTR), color, infrared spectrum (FT-IR), and moisture adsorption. The results showed that the formulation with beeswax (2% w/w), plantain leaves powder (1% w/w), and LDPE powder (2% w/w) had a higher tensile strength (5.99 MPa) and moisture barrier (WVTR = 366.6 g m⁻² d⁻¹) compared to the control formulation only with plasticizers (glycerol and water) but without reinforcements (0.48 MPa and 1486.6 g m⁻² d⁻¹, respectively). Films with only beeswax (4% w/w) and plantain leaves powder (2.5% w/w) had tensile strength = 5.53 MPa and WVTR = 716.8 g m⁻² d⁻¹, with higher moisture adsorption compared to the samples with LDPE. In both cases, homogeneous and heat-sealable bags were obtained. The reinforced TPS films can be used to reduce the environmental impact generated by single-use packaging applications such as food commercialization. Full article

Background: Gefitinib (Gef) is a first-line epidermal growth factor receptor (EGFR) inhibitor for NSCLC, but its clinical application is limited by poor aqueous solubility and low oral bioavailability. Methods: A self-assembled gefitinib nanosuspension (GG-NS) incorporating genistein (Gen) was rapidly developed and optimized via hammer acoustic resonance (HAR) technology. Systematic optimization was conducted using a high-throughput HAR-based process, with particle size, PDI, and zeta potential as key evaluation parameters. Structural and morphological characteristics were analyzed using powder X-ray diffraction (PXRD), thermal analysis, transmission electron microscopy (TEM), and Fourier-transform infrared (FT-IR) spectroscopy. In vitro dissolution behavior and cytotoxicity against A549 lung cancer cells were evaluated. Results: Optimal GG-NS with Z-Ave = 223.50 ± 1.53 nm, PDI = 0.239 ± 0.031 and zeta potential = −24.10 ± 0.47 mV was successfully prepared. The nanosuspension remained physically stable for up to five months at both 4 °C and 25 °C. Compared with the raw drugs, GG-NS enhanced the dissolution of gefitinib and genistein in water by 3.76-fold and 13-fold, respectively. In addition, GG-NS showed significantly enhanced cytotoxicity against A549 cells, with a 33.8% higher inhibition rate than the physical mixture after 72 h. Conclusions: This study demonstrates, for the first time, that HAR technology enables the rapid fabrication of a self-assembled GG-NS with improved dissolution performance, physicochemical stability, and in vitro anticancer activity, highlighting its promise as an efficient and scalable formulation strategy for poorly soluble anticancer drugs. Full article

Background: Myricetin (MYR) is a natural flavonol with antioxidant, neuroprotective, anti-inflammatory, antidiabetic, and cardioprotective activities. Still, its pharmaceutical use is limited by very low aqueous solubility (~16.6 µg/mL) and poor oral bioavailability (<10%). This study aimed to enhance the solubility and potentially improve the bioavailability of MYR by developing an amorphous nanofibrous delivery system. Methods: Electrospinning was applied to fabricate MYR-loaded nanofibers using polyvinylpyrrolidone K30 (PVP30), and the influence of key processing parameters on MYR solubility was evaluated. Nanofibers produced under selected electrospinning conditions were characterized in terms of morphology, encapsulation efficiency, and physicochemical properties. Results: X-ray powder diffraction confirmed complete amorphization of MYR within the BB5 fiber structure (distance: 12 cm, voltage: 25 kV, flow rate: 1.5 mL/h). FTIR analysis indicated hydrogen-bonding interactions between MYR hydroxyl groups and PVP30 carbonyl groups, contributing to stabilization of the amorphous form. SEM images revealed homogeneous, defect-free fibers with diameters below 400 nm, although localized MYR agglomerates were observed. Solubility and release studies demonstrated a characteristic spring-and-parachute effect, enabling rapid MYR release and maintenance of a supersaturated state. Enhanced solubility resulted in significantly improved antioxidant activity in DPPH and CUPRAC assays compared with crystalline MYR. Conclusions: Electrospun PVP30 nanofibers represent a promising platform for improving the solubility, dissolution behavior, and functional activity of poorly soluble bioactive compounds such as myricetin, supporting their potential application in pharmaceutical formulations. Full article