Search Results (2,648)

Metal ions exemplify one of the most harmful and environmentally detrimental contaminants of water systems. This work describes the creation of an innovative chelated carbon-doped nickel and titanium oxide (C-NiTiO₂) hybrid as an adsorbent for the effective elimination of metal ions. The dominance of the TiO₂ anatase phase with a ≈ 61 nm crystallite size was verified by XRD and Raman investigation. Morphology investigations exposed polygonal nanoparticles consisting of Ti, C, Ni, and O. The nanostructure exhibited a surface area of 17 m²·g⁻¹, a pore diameter of ≈1.5 nm, and a pore volume of 0.0315 cm³·g⁻¹. The nanostructure was evaluated for the elimination of Zn (II) ions from an aqueous solution. The metal ion adsorption onto the hybrid nanomaterial was described and comprehended using adsorption kinetics and equilibrium models. The adsorption data matched well with the pseudo-second-order kinetics and Langmuir adsorption models, indicating a monolayer chemisorption mechanism and achieving a maximum Zn (II) ion elimination of 369 mg·g⁻¹. Mechanistic investigation indicated film diffusion-controlled adsorption through inner-sphere complexation. The nanosorbent could be regenerated and reused for four rounds without appreciable activity loss, thus demonstrating its potential for water cleanup applications. Full article

Due to its amphiphilicity, the natural fibrous structural protein, silk fibroin (SF), can adsorb at the oil/water interface, form protective viscoelastic layers, and stabilize emulsions. Biocompatible SF-stabilized emulsions can be used in different fields of cosmetics, food, drug delivery, and biomedicine. Depending on the silk processing method, various emulsion types can be obtained, such as film-stabilized emulsions stabilized by SF molecules and Pickering emulsions stabilized by nanostructured SF or SF particles. Nanostructured SF and SF particles, with β-sheet dominated secondary structures, can overcome the drawback of SF molecules with unstable conformation transition during application, and thus endow higher emulsion stability than SF molecules. The emulsions stabilized by SF nanoparticles can endure heat and high ionic strength, while the emulsions stabilized by SF nanofibers show superior stability at high temperature, high salinity, and low pH due to the strong interfacial entangled nanofiber networks. In this review, the recent progress in research on SF-stabilized emulsions is summarized and generalized, including a systematic comparison of the stabilization mechanisms for different SF morphologies, and the influences of the emulsion fabrication technique, component type and proportions, and environmental conditions on the microstructures and properties of SF-stabilized emulsions. Understanding the stabilization mechanism and factors influencing the emulsion stability is of great significance for the design, preparation and application of SF-stabilized emulsions. Full article

The growing demand for portable and wireless electronic devices, along with the necessity to reduce reliance on non-renewable energy sources, has driven the need for energy harvesting materials. Nanocomposites, combining a polymeric matrix and a high-performance dielectric ceramic phase, are a promising solution. In such systems, the design of a hybrid matrix–filler interface is critical for achieving desired properties. Here, nanocomposites (NCs) were prepared by adding various amounts of hydrothermally synthesized BaTiO₃ (BT) nanoparticles (NPs) to polydimethysiloxane (PDMS). To investigate hybrid interfaces, NPs were used either bare or surface-functionalized with two silanes, 3-glycidyloxypropyltrimethoxysilane (GPTMS) or 2-[acetoxy(polyethyleneoxy)propyl]triethoxysilane (APEOPTES). NC films (80–100 μm thick) were characterized by scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDXS), and thermogravimetric analysis (TGA). Dielectric properties and breakdown strength (E_BD) were measured, and the theoretical volumetric energy density was calculated as a function of the filler loading and functionalization. The results demonstrate that hybrid interface design is pivotal for enhancing dielectric performance in NCs. APEOPTES-functionalized NPs significantly improved the dielectric response at a low filler loading (3.5%vol.), increasing permittivity from 2.8 to 7.5, E_BD from 33.8 to 42.1 kV/mm and energy density from 30 to >100 mJ/cm³. These findings underscore that designing hybrid interfaces through NP functionalization provides an effective strategy to achieve superior dielectric performance in PDMS-based NCs, retaining the advantages of the elastomeric matrix by reducing the amount of ceramic fillers. Full article

Surface plasmon resonance (SPR) sensors based on photonic crystal fibers (PCFs) hold significant promise for high-precision detection in biochemical and chemical sensing. However, achieving high sensitivity in low-refractive-index (RI) aqueous environments remains a formidable challenge due to weak light-matter interactions. To address this limitation, this paper designs and proposes a novel dual-channel D-shaped PCF-SPR sensor tailored for the refractive index range of 1.34–1.40. The sensor incorporates a dual-layer gold/titanium dioxide film, with gold nanoparticles deposited on the surface to synergistically enhance both propagating and localized surface plasmon resonance effects. Furthermore, a D-shaped polished structure integrated with double-sided microfluidic channels is employed to significantly strengthen the interaction between the guided-mode electric field and the analyte. Finite element method simulations demonstrate that the proposed sensor achieves an average wavelength sensitivity of 5733 nm/RIU and a peak sensitivity of 15,500 nm/RIU at a refractive index of 1.40. Notably, the introduction of gold nanoparticles contributes to an approximately 1.47-fold sensitivity enhancement over conventional structures. This work validates the efficacy of hybrid plasmonic nanostructures and optimized waveguide design in advancing RI sensing performance. Full article

This study investigates the synthesis of silver nanoparticles (AgNPs) using Crassula ovata (Jade plant) leaf extract and their subsequent incorporation into chitosan-based nanocomposite films for enhanced antimicrobial activity against four pathogenic microorganisms: Escherichia coli, Pseudomonas aeruginosa, Staphylococcus epidermidis, and Methicillin-resistant Staphylococcus aureus. Jade AgNPs were chosen for their ease of synthesis, stability, and potent antimicrobial activity. Chitosan encapsulation improved the stability of AgNPs and enhanced their interaction with bacterial cells, leading to improved bactericidal performance. The addition of gentamicin to the nanocomposite further amplified antibacterial activity, reducing the MBC values from 10 to 4 µg/mL for E. coli, 12.5 to 6 µg/mL for P. aeruginosa, 10 to 6 µg/mL for S. epidermidis, and 15 to 8 µg/mL for MRSA, compared to AgNPs alone. Mechanical characterization using dynamic mechanical analysis revealed improved robustness, with storage modulus increasing from approximately 24 MPa for chitosan-AgNPs films to 36 MPa for gentamicin-loaded nanocomposite films, while maintaining elasticity. Overall, these multifunctional nanocomposite films demonstrate strong antimicrobial activity and improved mechanical performance, supporting further evaluation as candidate materials for wound-related antimicrobial applications and localized infection control strategies. Such localized antimicrobial platforms may also contribute to strategies aimed at mitigating antibiotic resistance. Full article

Many commercially available medications are often unapproved or unavailable in suitable dosage forms for specific patient populations, particularly infants and children. This necessitates the use of extemporaneously compounded formulations to deliver individualized doses based on body weight or body surface area, and when a medication is unavailable at an appropriate concentration or contains excipients potentially unsafe for certain patients. Extemporaneous compounding is required for oral liquids when patients are unable to swallow tablets or capsules. It is also needed for topical preparations and sterile dosage forms when commercial products are unavailable. Across regions, practices follow national pharmacopeial standards for both sterile and non-sterile compounding. Stability factors influencing the safety and efficacy of compounded formulations must be carefully considered when assigning appropriate beyond-use dates. While stability information is available for some medications in monographs, peer-reviewed literature, prescribing information, and investigator’s brochures, such data is often lacking for many compounded preparations. Emerging extemporaneous formulations—such as orodispersible films, nanoparticle systems, and 3D-printed compounds—offer potential advantages over traditional compounded formulations but present unique challenges to widespread implementation. Despite the justified clinical need for extemporaneous compounding, significant barriers remain, including limited access to medications, insufficient compounding expertise or resources, gaps in pharmacokinetic and safety data, and regulatory constraints. This review critically appraises the current state of extemporaneous compounding—drawing primarily on the United States of America frameworks—and highlights its continued necessity, associated challenges, and pragmatic solutions for advancing personalized pharmacotherapy across pediatric age groups worldwide. Full article

The development of functional polymer films on porous paper substrates is inherently constrained by substrate-induced defects that hinder film continuity and barrier performance. In this study, process-controlled amylose–Poly(Vinyl alcohol) (PVA) coatings incorporating ZnO nanoparticles (ZnO NPs) were fabricated via aqueous deposition to investigate the process-structure-property relationship governing oxygen barrier behavior on paper. The moisture resistance of the coating was also evaluated. Single-layer coatings exhibited severe barrier failure due to insufficient film formation and pervasive pinhole defects. In contrast, systematic multi-layer deposition enabled the formation of continuous polymer films. A pronounced non-linear reduction in oxygen transmission rate was observed once the dry coating thickness exceeded approximately 5 µm. Under these conditions, the oxygen transmission rate decreased to approximately 15 cc/m²·day·atm at 20 °C and 65% relative humidity. This transition was correlated with the elimination of substrate-induced defects, as confirmed by morphological analysis. In addition to enhanced barrier performance, ZnO NP-loaded coatings demonstrated strong and broad-spectrum antimicrobial activity against both Escherichia coli and Staphylococcus aureus, indicating their multifunctional potential for active packaging applications. Supporting evaluations further indicated adequate mechanical flexibility and high repulpability, highlighting the suitability of the coating for sustainable paper-based packaging. Overall, this work identifies a quantitative critical film thickness that serves as process-specific design guideline for engineering high-performance functional polymer coatings on porous paper substrates. Full article

Silica nanoparticles (SNPs) are pivotal in designing functional optical films, but accurately modeling their properties is hindered by the limitations of classical effective medium theories, which break down for larger particles and complex morphologies. We introduce a robust, effective medium theory that overcomes these limitations by incorporating full Mie scattering solutions, thereby accounting for size-dependent and multipolar effects. Our model is comprehensively developed for unshelled, shelled, mixed, and hollow SNPs randomly dispersed in a host medium. Its accuracy is rigorously benchmarked against 3D finite-element method simulations. This work establishes a practical and reliable framework for predicting the optical response of SNP composites, significantly facilitating the rational design of high-performance coatings, such as anti-glare layers, with minimal computational cost. Full article

In this study, we investigated the effect of annealing ultrathin silver (Ag) films of varying thicknesses (1–6 nm) on both their optical absorption and the performance of poly(3-hexylthiophene-2,5-diyl) (P3HT) and [6,6]-phenyl-C₆₁-butyric acid methyl ester (PCBM) organic solar cells (OSCs). The Ag films were deposited on indium tin oxide (ITO) anodes and annealed at 300 °C for 1–2 h to modify the anodic interface. The optical and electrical properties of the resulting devices were systematically characterized and optimized. The results revealed that a 1 nm AgO layer annealed for 2 h significantly enhanced the device performance, yielding a 6% increase in power conversion efficiency compared to the standard configuration. This improvement is attributed to two main factors: (i) a 25% increase in light absorption of the AgO/P3HT:PCBM film due to localized surface plasmon resonance of Ag nanoparticles and (ii) an 11% reduction in series resistance resulting from the favorable alignment of the Ag work function with the ITO anode and the polymer HOMO, which facilitates efficient hole extraction. These findings highlight the potential of ultrathin, annealed Ag/AgO interfacial layers as an effective strategy to enhance light absorption and charge transport in OSCs. Full article

Transparent conductive oxides (TCOs), such as indium tin oxide (ITO), are essential for flexible electronics; however, conventional vacuum-based deposition is costly and thermally aggressive for polymers. This study investigated the surface functionalization of PET substrates with ITO thin film-based forced hydrolysis as a low-cost, reproducible alternative. $\mathrm{S}\mathrm{n}{\mathrm{O}}_2$ nanoparticles were synthesized by forced hydrolysis at 180 °C for 3 h and 6 h, yielding crystalline nanoparticles with a cassiterite phase and an average crystallite size of 20.34 nm. The process showed high reproducibility, enabling consistent structural properties without complex equipment or high-temperature treatments. The $\mathrm{S}\mathrm{n}{\mathrm{O}}_2$ sample obtained at 3 h was incorporated into commercial ${\mathrm{I}\mathrm{n}}_2{\mathrm{O}}_3$ to form a mixed In–Sn–O oxide, which was subsequently deposited onto PET substrates by spin coating onto UV-activated PET. The resulting 1.1 µm ITO films demonstrated good adhesion (4B according to ASTM D3359), a low resistivity of 1.27 × 10⁻⁶ Ω·m, and an average optical transmittance of 80% in the visible range. Although their resistivity is higher than vacuum-processed films, this route provides a superior balance of mechanical robustness, featuring a hardness of (H) of 3.8 GPa and an elastic modulus (E) of 110 GPa. These results highlight forced hydrolysis as a reproducible route for producing ITO/PET thin films. The thickness was strategically optimized to act as a structural buffer, preventing crack propagation during bending. Forced hydrolysis-driven PET sheet functionalization is an effective route for producing durable ITO/PET electrodes that are suitable for flexible sensors and solar cells. Full article

Herein, we propose a simple and cost-effective method for fabricating moderate-sensitivity surface-enhanced Raman scattering (SERS) substrates using Cu-plasma polymer fluorocarbon (Cu-PPFC) nanocomposite films fabricated through RF sputtering. The use of a composite target composed of carbon nanotube (CNT), Cu, and polytetrafluoroethylene (PTFE) powders (5:60–80:35–15 wt%) offers the advantage of the simple fabrication of moderate-sensitivity SERS substrates with a single cathode compared to co-sputtering. X-ray photoelectron spectroscopy (XPS) revealed that the film surface was partially composed of metallic Cu with Cu-F bonds and Cu–O bonds, confirming the coexistence of the conducting and plasmon-active domains. UV-VIS spectroscopy revealed a distinct absorption peak at approximately 680 nm, indicating the excitation of localized surface plasmon resonances in the Cu nanoclusters embedded in the plasma polymer fluorocarbon (PPFC) matrix. Atomic force microscopy and grazing incidence small-angle X-ray scattering analyses confirmed that the Cu nanoparticles were uniformly distributed with interparticle distances of 20–35 nm. The Cu-PPFC nanocomposite film with the highest Cu content (80 wt%) exhibited a Raman enhancement factor of 2.18 × 10⁴ for rhodamine 6G, demonstrating its potential as a moderate-sensitivity SERS substrate. Finite-difference time-domain (FDTD) simulations confirmed the strong electromagnetic field localization at the Cu-Cu nanogaps separated by the PPFC matrix, corroborating the experimentally observed SERS enhancement. These results suggest that a Cu-PPFC nanocomposite film, easily fabricated using a composite target, provides an efficient and scalable route for fabricating reproducible, inexpensive, and moderate-sensitivity SERS substrates suitable for practical sensing applications. Full article

Wound dressing coverages (WDC) play a key role in protecting skin lesions and preventing infection. Polymeric membranes have been widely explored as WDC due to their ability to incorporate bioactive agents, including antimicrobial nanoparticles and non-steroidal anti-inflammatory drugs (NSAIDs). In this study, polycaprolactone (PCL)-based membranes functionalized with titanium dioxide nanoparticles (TiO₂ NPs) and ibuprofen (IBP) were fabricated using a film manufacturing approach, and their structural and biocompatibility profiles were evaluated. The membranes were characterized by SEM, FTIR and XPS. Bands at 1725 cm⁻¹, 2950 cm⁻¹, 2955 cm⁻¹, 2865 cm⁻¹ and 510 cm⁻¹ proved molecular stability of reagents during manufacture. In SEM, the control shows the flattest surface, while the PCL-IBP and PCL-IBP-TiO₂ NPs groups had increased rugosity. In vitro biocompatibility was evaluated using human fetal osteoblasts (hFOB). On day 3, the cell adhesion response of hFOB seeded in PCL-IBP and PCL-IBP-TiO₂ NPs groups showed the biggest absorbances (p = 0.0014 and p = 0.0491, respectively). On day 7 PCL-IBP group had lower lectin binding than the control (p = 0.007) and the PCL-IBP-TiO₂ NPs (p = 0.015) membranes, but no evidence of cytotoxicity was observed in any group. Furthermore, the Live/Dead test adds more biocompatibility evidence to conveniently discriminate between live and dead cells. The PCL polymeric membrane elaborated in this study may confer antiseptic, analgesic and anti-inflammatory properties, making these membranes ideal for skin lesions. Full article

This study focuses on the development of antibacterial polymer nanocomposites based on biologically synthesized silver nanoparticles (AgNPs) and polyvinyl alcohol (PVA) as the polymer matrix. Silver nanoparticles were produced using an aqueous extract from dried Lavandula angustifolia (lavender) leaves, which proved to be highly effective in reducing silver ions and stabilizing the resulting nanoparticles. The synthesized AgNPs were characterized by FTIR, UV-Vis, TEM, SEM, and DLS analyses. The nanoparticles were predominantly spherical, with more than 70% having diameters below 20 nm. Subsequently, AgNPs were incorporated into the PVA matrix via an ex situ approach to fabricate nanocomposite fibers and thin films. SEM analysis confirmed successful incorporation and uniform distribution of AgNPs within the polymer structures. The nanocomposites exhibited pronounced antibacterial activity against both Gram-positive (Staphylococcus aureus, Staphylococcus haemolyticus, Streptococcus uberis) and Gram-negative (Escherichia coli, Pseudomonas aeruginosa) bacteria, with nanofibers demonstrating superior performance compared to thin films. These findings highlight the potential of lavender-extract-mediated AgNPs as sustainable functional fillers for the fabrication of eco-friendly antibacterial materials applicable in biomedical and food packaging fields. Full article

The transition toward Industry 4.0 requires advanced sensing platforms capable of delivering real-time, high-fidelity data under extreme industrial conditions. Thin-film sensors, leveraging both photonic and functional approaches, are emerging as key enablers of this transformation. By exploiting optical phenomena such as Fabry–Pérot interference, guided-mode resonance, plasmonics, and photonic crystal effects, thin-film photonic devices provide highly sensitive, electromagnetic interference-immune, and remotely interrogated solutions for monitoring temperature, strain, and chemical environments. Complementarily, functional thin films including oxide-based chemiresistors, nanoparticle coatings, and flexible electronic skins extend sensing capabilities to diverse industrial contexts, from hazardous gas detection to structural health monitoring. This review surveys the fundamental optical principles, material platforms, and deposition strategies that underpin thin-film sensors, emphasizing advances in nanostructured oxides, 2D materials, hybrid perovskites, and additive manufacturing methods. Application-focused sections highlight their deployment in temperature and stress monitoring, chemical leakage detection, and industrial safety. Integration into Internet of Things (IoT) networks, cyber-physical systems, and photonic integrated circuits is examined, alongside challenges related to durability, reproducibility, and packaging. Future directions point to AI-driven signal processing, flexible and printable architectures, and autonomous self-calibration. Together, these developments position thin-film sensors as foundational technologies for intelligent, resilient, and adaptive manufacturing in Industry 4.0. Full article

The main goal of this work was to develop nanoparticles of lysozyme (Lys) for biological and biomedical applications. The developed biosystems were based on Lys-loaded calcium alginate 2% and chitosan 1% beads and films with different concentrations of each polymer. Encapsulation efficiency was 100%. The ratio of adsorbed Lys on the films, Lys activity, and the release profile of Lys were measured using water and buffer solution at pH similar to the environment of cancer cells, at a controlled temperature of 37 °C and a constant speed, to assess the efficacy of the encapsulation process. Lys antimicrobial activity was assessed using Micrococcus lysodeikticus. Moreover, the anti-inflammatory and antioxidant properties of the developed biosystems were also evaluated. The anti-inflammatory activity of Lys released from calcium alginate 2%-chitosan 1% beads loaded with Lys was about 99%. These findings highlight the potential of the developed beads and films for biomedical applications, particularly in antimicrobial and anti-inflammatory therapies. Full article