Search Results (10,970)

Silver nanoparticles (AgNPs) possess distinct physicochemical characteristics and demonstrate high antibacterial potential that highlights them as promising alternatives against a wide range of pathogens. The immense antibacterial potential of AgNPs is primarily attributed to the release of silver ions that lead to the disruption of bacterial cell membrane, generation of reactive oxygen species (ROS), inhibition of protein synthesis and interference with DNA replication. Variations in AgNPs’ shape, size, and surface characteristics are also considered key factors determining their effectivity as well as specificity. AgNPs are considered potent antibacterial agents, including against antibiotic- and drug-resistant strains. However, inappropriate dosages or unoptimized application of may result in potential toxicity, consisting one of the main drawbacks of the AgNPs’ safer administration. This article reviews the recent literature on the antibacterial potential of AgNPs, focusing on their broad mechanisms of action, applicability, especially in agriculture, biomedical and environmental fields, toxicity and future perspectives. Full article

This study addresses the critical need for advanced biomedical materials that possess both potent antimicrobial properties and high biocompatibility to prevent device-related infections and promote healing. To this end, we demonstrate the successful development and comprehensive characterization of functional composite materials based on a photopolymerizable acrylate resin modified with laser-ablated copper nanoparticles (Cu NPs). The synthesized Cu NPs exhibited a monomodal size distribution with a peak at 47 nm, a high zeta potential of −33 mV, and a spherical morphology. Incorporation of Cu NPs into the polymer matrix via Masked Stereolithography (MSLA) enabled the fabrication of complex structures that maintained high surface quality and optical transparency after polishing. Modification of photopolymer resin with Cu NPs significantly increased the strength of the resulting products and caused dose-dependent formation of reactive oxygen species (ROS). The resulting composite materials exhibited strong antibacterial activity against E. coli. Crucially, despite their potent antimicrobial efficacy, the materials showed no cytotoxicity towards human fibroblast cultures. These results highlight the potential of these composites for a new generation of biomedical applications, such as implantable devices and wound coatings, which combine programmable antimicrobial activity with high biocompatibility. Full article

This study includes a comparative analysis of four graphene-based electrochemical sensors used for the detection of melatonin, an endogenous hormone involved in circadian rhythm regulation and associated with various neurological pathologies. The sensors were based on screen-printed electrodes (SPE) modified with graphene (G), graphene modified with gold nanoparticles (AuNPs/G), graphene oxide (GO), and reduced graphene oxide (rGO). Melatonin was extracted from commercially available pharmaceutical products, purified, and characterized using UV-Vis spectroscopy, FTIR spectrometry, and HPLC. The performance of the electrodes was evaluated via cyclic voltammetry, using potassium ferrocyanide and standard melatonin solutions to determine the kinetic characteristics, while square-wave voltammetry was employed to determine the detection and quantification limits. G/SPE showed the best performance, with a detection limit of 0.3424 μM, followed by AuNPs/G/SPE with an LOD of 1.2768 μM. GO/SPE had the poorest performance (LOD 23.1056 μM), and rGO/SPE had an LOD of 5.8503 μM. Testing of sensors on pharmaceuticals showed accurate quantification of melatonin in a complex environment. The results highlight the potential of G/SPE and AuNPs/G/SPE sensors for use in the rapid and accurate detection of melatonin in pharmaceutical and biomedical applications. Full article

Ascaris lumbricoides is one of the most epidemiologically significant soil-transmitted helminths, and the environmental persistence of its eggs is largely attributed to their robust structural architecture. The search for ovicidal alternatives capable of overcoming this barrier has increasingly focused on metallic nanoparticles obtained through biological synthesis. Scanning electron microscopy (SEM) was employed to evaluate the ultrastructural effects of silver nanoparticles (AgNPs) biosynthesised by the nematophagous fungus Duddingtonia flagrans on A. lumbricoides eggs. Ultraviolet-visible spectroscopy and transmission electron microscopy confirmed the synthesis of AgNPs, revealing predominantly spherical, well-dispersed particles with an average diameter of 9.22 ± 4.9 nm. Cytotoxicity assays indicated an IC₅₀ of 7.7 µg/mL. SEM analyses showed that eggs in the control group maintained intact morphology, with no apparent deformities. In contrast, exposure to AgNPs induced pronounced structural alterations, including marked wrinkling, surface erosion and shell collapse, suggesting disruption of multiple layers. Albendazole alone produced deep linear fissures consistent with internal metabolic failure, though with minimal external erosion. The combined treatment with AgNPs and albendazole resulted in severe degradation. These findings demonstrate that AgNPs exhibit significant ovicidal activity and may serve as effective adjuvants to enhance the action of conventional anthelmintics against highly resistant helminth eggs. Full article

Cutaneous leishmaniasis is a zoonotic disease caused by Leishmania parasites and leads to chronic, non-healing skin lesions. Although current drugs can control the disease, their use is limited by systemic side effects, low efficacy, and inadequate lesion penetration. Therefore, innovative local delivery systems are required to enhance drug penetration and reduce systemic toxicity. To address these challenges, silver nanoparticles (AgNPs) were synthesized using propolis extract through a green synthesis approach, and a tri-layer wound dressing composed of polyvinyl alcohol and gelatin containing synthesized AgNPs and Glucantime was fabricated by electrospinning. Characterization (SEM-EDX, FTIR, TGA) confirmed uniform morphology, chemical structure, and thermal stability; the wound dressing exhibited hydrophilicity, antioxidant activity, and biphasic release. Biological evaluations against Leishmania tropica demonstrated significant antiparasitic activity. Promastigote viability decreased from 76.3% in neat fibers to 31.6% in nanofibers containing AgNPs and 7.9% in tri-layer nanofibers containing both AgNPs and Glucantime. Similarly, the amastigote infection index dropped from 410 in controls to 250 in neat nanofibers, 204 in AgNPs-containing nanofibers, and 22 in tri-layer nanofibers containing AgNPs and Glucantime. The tri-layer nanofibers demonstrated enhanced antileishmanial activity over AgNPs-containing fibers, confirming synergistic efficacy. All nanofibers were biocompatible, supporting their use as a safe platform for cutaneous leishmaniasis treatment. Full article

Silver nanoparticles (AgNPs) are increasingly applied in agriculture and related technologies due to their antimicrobial properties, yet their interactions with soil-associated organisms and microbial communities remain insufficiently characterized. This study examined the effects of AgNP exposure (10.85 mg/L) on trace element accumulation and gut bacterial communities of the earthworm Eisenia fetida under two substrate conditions (horticultural substrate and compost). High-throughput 16S rRNA gene sequencing revealed substrate-dependent shifts in microbial community structure following AgNP exposure. Several bacterial taxa, including Proteobacteria, Gammaproteobacteria, Bacilli, Streptococcus sp., and Staphylococcus sp., exhibited pronounced numerical declines, indicating sensitivity to AgNPs, whereas Actinobacteria and Bacteroidetes showed comparatively higher relative abundances, suggesting greater tolerance. Compost partially mitigated the inhibitory effects of AgNPs on gut microbiota. Concurrently, AgNP exposure altered trace element accumulation patterns in earthworm tissues, highlighting interactions between silver uptake and elemental homeostasis. Collectively, these findings demonstrate that AgNPs can induce taxon- and substrate-specific responses in earthworm-associated microbial communities and metal accumulation, providing insight into potential ecological consequences of nanoparticle use in agricultural systems. Full article

Glioblastoma (GBM) is a highly aggressive brain tumor characterized by invasive growth, intrinsic drug resistance, and the presence of the blood–brain barrier. All of these features make treatment extremely challenging and underscore the need for developing effective combination strategies and advanced drug delivery systems. This study aimed to develop a bovine serum albumin (BSA) nanoparticle (NP)-based delivery system to overcome the poor bioavailability and pharmacokinetic limitations of two potent anti-tumor agents, all-trans retinoic acid (ATRA) and curcumin (CURC), and to evaluate their antitumor activity in U87-MG GBM cells. Drug-free and ATRA/CURC-loaded BSA-NPs were synthesized using an optimized desolvation method and characterized in terms of particle size, polydispersity index, morphology, drug encapsulation efficiency, and release behavior. The cytotoxic, anti-migratory, and pro-apoptotic effects of the NPs on U87-MG GBM cells were assessed using real-time proliferation and migration assays and Annexin V/PI staining followed by flow cytometry. Collectively, the findings indicated that the co-delivery of ATRA and CURC using BSA-NPs showed enhanced antiproliferative, antimigratory, and pro-apoptotic effects. With its controlled release profile, high loading capacity, and favorable nanoscale dimensions, the ATRA-CURC-BSA–NP system represents a promising nanoplatform for GBM therapy that warrants further in vivo investigation. To the best of our knowledge, this is the first study demonstrating the inhibition of glioblastoma cell growth through the co-delivery of all-trans retinoic acid and curcumin using a bovine serum albumin-based nanoparticle system. Full article

In this study, selenium nanoparticles (SeNPs) were synthesized using polysaccharides extracted from blueberry pomace (BP) as a stabilizing agent. BP was characterized as an acidic polysaccharide with a molecular weight of 5.4 × 10⁵ Da. The resulting BP-SeNPs were monodisperse spheres with an average size of 94.33 nm, as confirmed by TEM, DLS, FT-IR, XRD, and EDX analyses. Compared to SeNPs, BP-SeNPs demonstrated superior stability under varying conditions of storage time, temperature, pH, and ionic strength. Furthermore, in vitro evaluation using AAPH-induced rabbit erythrocytes revealed that BP-SeNPs offered enhanced protection against hemolysis. This protective effect was attributed to their ability to significantly bolster antioxidant enzyme activities (SOD, CAT, and GSH-Px) and preserve membrane integrity by maintaining ATPase function and sialic acid content. These results establish BP as an effective stabilizer for SeNPs and suggest the promising potential of BP-SeNPs as antioxidant agents in functional food or nutraceutical applications. Full article

Saccharomyces cerevisiae was cultured under the influence of static magnetic fields (SMFs) to assess their impact on the biosynthesis of silver nanoparticles (AgNPs). Cell-free media derived from SMF-exposed cultures facilitated the formation of AgNPs, with a significant reduction in nanoparticle size observed at an optimal field strength of 7 mT. AgNPs synthesized under SMF conditions exhibited smaller crystalline structures than those produced in control media, as evidenced by dynamic light scattering (DLS) and transmission electron microscopy (TEM) measurements. Over a 75-day period, SMF-exposed AgNPs demonstrated enhanced stability, as determined by DLS and polydispersity index (PDI) assessments. Further analysis through sodium dodecyl-sulfate polyacrylamide gel electrophoresis (SDS-PAGE) and Fourier transform infrared spectroscopy (FTIR) suggested the formation of a protein corona on the AgNPs in SMF-treated samples, which likely inhibits agglomeration and enhances long-term stability. These findings indicate that SMF-induced stress in S. cerevisiae triggers the secretion of specific proteins that contribute to the stabilization of AgNPs, providing a novel approach to controlling nanoparticle synthesis and stability through magnetic field exposure. Full article

As a natural flavonoid compound, quercetin possesses excellent antioxidant, anti-inflammatory and anti-atherosclerotic activities. However, the poor water solubility and sensitivity to the environment severely limit the application of quercetin. Initially, quercetin-loaded zein/carboxymethyl chitosan nanoparticles (ZCQ NPs) were prepared using an anti-solvent precipitation method. The fabricated ZCQ NPs exhibited a small particle size and polydispersity index (PDI). The ZCQ NPs had a negative zeta potential with an absolute value of 41.50 ± 1.76 mV. ZCQ NPs could remain highly stable against light, heat and ion strength. In addition, ZCQ NPs maintained good monodispersity and displayed minimal changes in particle size under long-term storage conditions. Additionally, a superior antioxidant capacity of ZCQ NPs was also observed in the free radical and reactive oxygen species (ROS) scavenging study compared to that of free quercetin. All these results of this study suggest that ZCQ NPs could serve as an effective drug delivery system for encapsulating and delivering quercetin. 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

Background/Objectives: Wound healing represents a pervasive and urgent clinical challenge. Hard-to-heal chronic wounds are frequently complicated by infections, inflammatory responses, and oxidative stress. Currently, wound dressings are broadly categorized into dry and moist types, with moist wound dressings for chronic wounds accounting for approximately 70% of market revenue. Recently, adipose-derived stem cells (ADSCs), which possess self-renewal and multi-lineage differentiation capabilities, have emerged as a promising strategy for promoting tissue regeneration and wound repair. Methods: In this study, we developed a novel luteolin nanoparticle–ADSCs composite hydrogel (GelCA@LUT@ADSCs). This system was constructed by first encapsulating ADSCs within a chitosan/alginate hydrogel (GelCA), followed by coating the hydrogel with luteolin-loaded nanoparticles (LUT@NPs). Results: The sustained release of LUT@NPs from the hydrogel modulates the wound microenvironment, enhancing the pro-healing functions of ADSCs at the wound site. The GelCA hydrogel exhibited excellent biocompatibility. Both in vitro and in vivo results demonstrated that GelCA@LUT@ADSCs treatment effectively reduced inflammation, promoted angiogenesis and collagen deposition, stimulated cell proliferation and migration, and polarized macrophages toward an anti-inflammatory, pro-healing M₂ phenotype, thereby accelerating wound healing. Conclusions: Overall, this innovative therapeutic approach provides a novel strategy for wound management through a synergistic division of labor between pharmaceutical agents and stem cells. Full article

Based on the pressing need to develop efficient desulfurization technologies for fuel oils, this study presents a novel photoresponsive adsorbent for the removal of refractory thiophenic sulfides. Conventional hydrodesulfurization exhibits limited efficiency for such compounds, while adsorption–desorption processes often suffer from high energy consumption during regeneration. Inspired by natural stimuli-responsive systems, we designed a photothermal adsorbent by incorporating silver nanoparticles (Ag NPs) into a porous aromatic framework (PAF) via a green photoreduction method. The resulting materials, denoted as Ag(0)PBPAF-n (n = 1, 2, 3), were thoroughly characterized to confirm successful synthesis and structural integrity. The introduced Ag NPs serve as adsorption sites, enhancing uptake capacity through weak interactions with sulfur atoms in thiophenic molecules. More significantly, under light irradiation, the localized surface plasmon resonance (LSPR) of Ag NPs enables efficient photothermal conversion, triggering rapid desorption without conventional heating. Adsorption–desorption tests demonstrated that up to 48% of adsorbed thiophenic sulfur could be released upon illumination. Fixed-bed experiments further verified that light can effectively stimulate regeneration and improve energy efficiency. This work offers a promising strategy for designing recyclable adsorbents with low-energy regeneration driven by clean solar energy. Full article

The modification of tantalum oxide (Ta₂O₅) nanoparticles (NPs) with biocompatible polymers is crucial for their biomedical use. Such modification can prolong NP circulation in the bloodstream by minimizing salt-induced aggregation and reducing nonspecific protein adsorption onto their surface. Understanding the features of polymer–NP interactions is a key issue in the fabrication of nanostructures with required characteristics. The present work aims to provide a comprehensive comparative study of bovine serum albumin (BSA) adsorption on bare and polydopamine (PDA)-coated Ta₂O₅ NPs. The synthesized NPs were characterized via transmission electron microscopy, Fourier transform infrared spectroscopy, dynamic light scattering, and zeta potential measurements. Fluorescence and circular dichroism spectroscopy were also employed for the first-time investigation of the interactions of Ta₂O₅ NPs and Ta₂O₅@PDA NPs with BSA. The results obtained show that PDA coating significantly enhances the protein-binding affinity. Time-resolved measurements revealed signatures of Förster resonance energy transfer, confirming complex formation between NPs and BSA. Moreover, colloidal stability tests in phosphate-buffered saline indicated that the presence of adsorbed BSA improves the dispersion stability of bare and PDA-coated Ta₂O₅ NPs. These findings advance the understanding of protein–NP interactions and highlight the potential of PDA coatings for designing stable and functional nanostructures for biomedical applications. Full article