Search Results (19,434)

Chronic infected wounds are often characterized by persistent bacterial colonization, biofilm formation, excessive oxidative stress, and prolonged inflammation, which severely impair tissue regeneration. To address these challenges, a multifunctional wound dressing capable of antibacterial activity and microenvironment modulation was developed. In this study, amide-modified hyaluronic acid (HA-ADH) was used as the matrix, and a dynamic coordination network was constructed via Cu²⁺-hydrazide interactions to form an in situ HA-Cu hydrogel. Curcumin-loaded DSPE-PEG2000 micelles were further incorporated to obtain a pH-responsive composite hydrogel (HA-Cu/Cur). The prepared hydrogel exhibited a porous interconnected structure, along with favorable injectability, self-healing capability, tissue adhesiveness, moderate swelling, controllable degradability, and pH-responsive behavior under acidic conditions. In vitro antibacterial assays demonstrated that both HA-Cu and HA-Cu/Cur effectively inhibited the growth and biofilm formation of Escherichia coli and Staphylococcus aureus. The antibacterial activity was associated with disruption of bacterial morphology, depletion of intracellular ATP, and induction of reactive oxygen species, while HA-Cu/Cur showed enhanced performance in antibiofilm activity and oxidative stress-related effects compared with HA-Cu. Cytocompatibility studies revealed that the hydrogel extracts exhibited negligible cytotoxicity toward L929 fibroblasts and RAW 264.7 macrophages, while promoting fibroblast migration and significantly reducing the expression of pro-inflammatory cytokines (TNF-α, IL-6, and IL-1β) in lipopolysaccharide-stimulated RAW 264.7 cells, with HA-Cu/Cur showing a more pronounced anti-inflammatory effect. In summary, the HA-Cu/Cur hydrogel integrates the antibacterial and pro-healing properties of Cu²⁺ with the antioxidant and anti-inflammatory activities of curcumin. The hydrogel effectively inhibited the growth and biofilm formation of both E. coli and S. aureus, reduced the expression of TNF-α, IL-6, and IL-1β in LPS-stimulated macrophages, and promoted fibroblast migration, demonstrating its potential as a multifunctional wound dressing for the management of infected wounds. Full article

Satureja nepeta essential oil (EO) is gaining prominence for its multifaceted pharmacological and biotechnological potential. This study aimed to characterize its volatile profile and evaluate its functional capacity as an antioxidant, antibacterial, and antiproliferative agent. Gas Chromatography Mass Spectrometry (GC–MS) profiling was conducted to identify the volatile constituents of the EO. Antioxidant activity was assessed using DPPH, ABTS, TAC, and FRAP assays. Antibacterial activity was evaluated against Gram-positive and Gram-negative pathogens using disk diffusion and MIC determination. In silico molecular docking against bacterial DNA gyrase B was performed to explore potential mechanisms of action. Antiproliferative activity was assessed on the P3X63Ag8.653 myeloma cell line. Chemical profiling identified nine major constituents, dominated by pulegone (68.63%), menthol (6.64%), and cis-pulegol (2.04%). The EO demonstrated significant free radical-scavenging activity, particularly in the TAC assay (EC₅₀ = 3.747 ± 0.577 µg/mL). Antimicrobial evaluations revealed robust inhibitory effects, with Pseudomonas aeruginosa and Salmonella enterica exhibiting the highest susceptibility. In silico modeling corroborated these findings, identifying menthol as the lead ligand (ΔG = −6.09 kcal/mol), suggesting a synergistic mechanism of action. Notably, the EO displayed potent antiproliferative activity (LC₅₀ = 14.060 ± 1.364 µg/mL), falling well within the high-cytotoxicity threshold. Collectively, these findings underscore the pharmacological significance of S. nepeta EO as a potent reservoir of bioactive monoterpenes with antioxidant, antimicrobial, and anticancer properties, meriting further in vivo validation and mechanistic exploration toward its development as a therapeutic or nutraceutical candidate. Full article

Fluoroquinolones are broad-spectrum, bactericidal antibacterial agents used in both human and veterinary medicine. Some human-approved drugs are used off label in veterinary medicine while veterinary-approved drugs are not used in humans. Veterinary-approved fluoroquinolones are used on both food and companion animals and against a wide range of clinical indications including infections of the urinary tract, respiratory tract, skin and skin structure, mammary gland and others. Not all veterinary-approved fluoroquinolones have the same clinical indication and it is important to understand these important differences. A recently approved for food animals agent called pradofloxacin is characterized as being dual targeting in that it simultaneously inhibits DNA gyrase (topoisomerase II) and Topoisomerase IV—two enzymes critical for DNA replication. Simultaneous targeting of two enzymes is argued to reduce the likelihood for resistance selection. This article reviews veterinary-approved fluoroquinolones including an overview of the drugs, in vitro activity including bactericidal properties, pharmacokinetic/pharmacodynamics, antimicrobial resistance, anti-inflammatory properties and clinical trial results. Appropriate use of this important class of antimicrobial agents is essential for clinical success and long-term viability of these compounds. Full article

Antimicrobial resistance demands intensive research on new nonantibiotics and drug repurposing to expand the arsenal of antimicrobial agents. The present work analysed the combination of diclofenac (DFNAC) and cannabidiol (CBD) and evaluated its potentiation and its biocompatibility. The formulation’s potency has been tested against Staphylococcus epidermidis (S. epidermidis), Staphylococcus aureus (S. aureus), Escherichia coli (E. coli), and P. aeruginosa. The DFNAC-CBD combination showed an evident synergistic effect, a significant decrease in the minimum inhibitory concentration against Staphylococcus epidermidis, and an additive effect against Staphylococcus aureus, indicating the levels of cooperation between the two compounds. All tested treatments exhibited MBC/MIC ratios ≤ 4, indicating bactericidal activity according to accepted interpretative criteria. Overall, the DFNAC-CBD combination accelerated bacterial killing relative to the individual compounds and exhibited a clear time-dependent antibacterial effect. The combination exhibited no antibacterial activity against Gram-negative strains such as E. coli and Pseudomonas aeruginosa. 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) and Lactate Dehydrogenase (LDH) assays demonstrated that the antibacterial concentration (3.906 µg/mL) preserves cell viability and membrane integrity. Live/dead staining confirms cell viability and normal morphology. The results indicate that the DFNAC-CBD combination achieves antimicrobial efficacy through bactericidal rather than merely bacteriostatic activities and without inducing significant cytotoxicity. Therefore, the proposed DFNAC-CBD combination has significant potential as a nonantibiotic formula, which with further profile analysis can develop into formulations that can control the use and dosage of common antibiotics. Full article

ESKAPE pathogens have become a major global health challenge. This study aimed to isolate and characterize LAB from fermented cacao and to evaluate their probiotic properties, preliminary antimicrobial activity against ESKAPE pathogens, safety profiles, and functional bioactivities. Each of P. acidilactici isolates exhibited antibacterial activity against ESKAPE pathogens, with inhibition zone diameters ranging from 10.00 ± 1.00 mm to 23.00 ± 0.00 mm, depending on the isolate and pathogens tested. CR05 was identified as the most promising probiotic candidate, showing the highest survival at pH 2 (69.65 ± 6.66%), strong tolerance to pancreatin (99.95 ± 0.10%), pepsin (89.11 ± 2.38%), bile salts (98.65 ± 0.33%), and favorable adhesion properties, including auto-aggregation, cell surface hydrophobicity, and adhesion to HT-29 intestinal epithelial cells. The safety assessment indicated a notable susceptibility to gentamicin, tetracycline, and chloramphenicol, with resistance to several other tested antibiotics. and showed no hemolytic activity. Three selected isolates were evaluated for minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) against ESKAPE pathogens, with MIC and MBC values ranging from 12.5 to 25 mg/mL and 25 to >50 mg/mL, respectively. The strongest inhibitory activity was observed against A. baumannii, P. aeruginosa, and E. aerogenes, with MIC values of 12.5 mg/mL, particularly for isolates CR05 and CR06. Whole-genome analysis identified genes related to stress response and gastrointestinal tolerance and predicted the enterolysin A gene. No acquired antimicrobial resistance genes were detected. These findings suggest that P. acidilactici isolates from fermented cacao are promising probiotic candidates for further investigation in functional food, probiotic, and postbiotic-related applications. Full article

Skin functionalities are instrumental in four main domains: protection, regulation, sensation, and support. However, excessive exposure to ultraviolet (UV) radiation can compromise skin integrity and, in turn, affect its functions, by generating reactive oxygen species (ROS). Aiming to protect skin from UV radiation, sunscreens incorporate UV filters and antioxidants that absorb/reflect UV rays and neutralise free radicals, respectively. Nevertheless, undesired side and ecological effects of conventional UV filters have spurred the search for safer alternatives. Among synthetic antioxidants, thioethers have attracted attention for their redox power and potential medicinal properties. In this context, a library of aminopyrimidine–arylthioether conjugates was synthesised and evaluated for their antioxidant, enzyme-inhibitory and antibacterial activities, as well as for their cytotoxicity in HaCaT cells and potential photoprotective properties. Among the aminopyrimidine-thioethers studied, compound C5 stood out for its antioxidant potential, exhibiting a value of 566.39 mM FeSO₄ equivalents per mM of the compound, while compound C2 showed the highest anti-enzymatic potential, inhibiting elastase (45.58%) and tyrosinase activities (34.66%). Regarding photoprotective activity, compound C13 reduced by 33.74% the ROS production induced by UV radiation exposure, at 100 μM, a non-cytotoxic concentration. Finally, compound C7 inhibited the growth of Staphylococcus epidermidis, Staphylococcus hominis and Cutibacterium acnes, at 30 μM. These preliminary results demonstrate that aminopyrimidine–arylthioethers constitute a new class of compounds warranting further investigation for skin protection. Compound C5 showed antioxidant activity in the FRAP assay, comparable to that of the positive control, BHT. Full article

ZnO nanopowders were synthesized via a solvent-mediated green route using Mitragyna speciosa Korth. leaf extract as reducing and stabilizing agents. Deionized water and methanol were employed to tailor the phytochemical composition of the extracts. The influence of extract concentration (5–20 mL) and solvent polarity on structural, morphological, and functional properties was systematically investigated. Structural analyses confirmed the formation of Zn-O bonds and a phase-pure hexagonal wurtzite ZnO without secondary phases. Surface morphology revealed solvent-dependent morphological evolution toward spherical shapes and reduced aggregation in the methanol-derived system. For antibacterial activity, green ZnO nanopowders demonstrated enhanced biocidal effects against Gram-negative Escherichia coli and Gram-positive Staphylococcus aureus, comparable to that of commercial ZnO nanoparticles. Enhanced piezo-photocatalytic degradation of rhodamine B was achieved under combined light and ultrasonic irradiation, with superior performance observed for methanol-derived ZnO. This enhancement is attributed to the synergistic interplay of solvent-induced defect states, reduced particle size, and piezoelectric field-driven charge separation. Scavenger analysis confirmed that superoxide radicals (${·\mathrm{O}}_2^{-}$) dominate the degradation pathway by green-synthesized ZnO nanopowders prepared from different solvent extracts. Thus, a correlation between solvent-mediated phytochemical environments and piezo-photocatalytic activity provides new insights for the design of sustainable, high-performance ZnO-based catalysts. Full article

Feline obesity is an increasingly prevalent health concern and is closely associated with metabolic disorders and intestinal dysbiosis. This study aimed to screen feline-derived lactic acid bacteria (LAB) for bile salt hydrolase activity, in vitro cholesterol-removal capacity, and selected probiotic-associated characteristics. Approximately 700 LAB isolates were obtained from fecal samples of healthy domestic cats and evaluated for bile salt hydrolase (BSH) activity, among which 105 isolates were identified as BSH-positive. Further screening was performed based on BSH activity, cholesterol-removal capacity, adhesion-related properties, antioxidant activity, gastrointestinal tolerance, antibacterial activity, organic acid production, hemolytic activity, and antibiotic susceptibility. Three candidate strains were ultimately selected and preliminarily identified by 16S rRNA gene sequencing as Enterococcus hirae C283, Ligilactobacillus animalis C289, and Enterococcus faecium C422. These strains exhibited BSH activity and preliminary in vitro cholesterol-removal phenotypes under the tested culture conditions, together with tolerance to simulated gastrointestinal conditions, antioxidant activity, antibacterial activity, and organic acid production. No hemolytic activity was detected; however, all three strains exhibited resistant or intermediate phenotypes to multiple antibiotics, highlighting the need for further genome-based safety assessment, particularly for the two Enterococcus strains. Overall, these findings identified feline-derived LAB candidates with BSH activity, preliminary in vitro cholesterol-removal phenotypes, and multiple probiotic-associated characteristics. However, these in vitro findings do not demonstrate regulation of host lipid metabolism or blood lipid levels. Comprehensive safety assessment, particularly for the Enterococcus strains, and in vivo validation are required before further application. Full article

Periodontitis, driven by Porphyromonas gingivalis (P. gingivalis) biofilms, is a global health burden with limited treatment options due to antibiotic resistance. Chrysanthemum lavandulifolium is traditionally used in China for clearing heat and reducing swelling, yet its anti-periodontitis potential remains uncharacterized. This study evaluated the antibacterial and therapeutic effects of its essential oil (CLEO) against periodontitis. The minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) of CLEO against P. gingivalis were determined by broth microdilution. Anti-biofilm activity was assessed via XTT assay. Network pharmacology, molecular docking, and 100 ns molecular dynamics simulations were employed to identify active compounds and core targets. Experimental periodontitis was induced in C57BL/6 mice by molar ligation. Mice received topical CLEO at concentrations of 2, 3, and 4 mg/mL, 2% minocycline, or vehicle once daily for 14 days. Periodontal inflammation, alveolar bone loss, collagen organization, osteoclast activity, and serum levels of MMP-9 and COX-2 were evaluated. CLEO exhibited potent anti-P. gingivalis activity, with an MIC of 2 mg/mL and MBC of 4 mg/mL. At the MIC, CLEO disrupted 57.5% of pre-formed P. gingivalis biofilms. Network pharmacology and molecular docking identified α-bisabolol, chamazulene, and 1,8-cineole as key active compounds, with the chamazulene-HSP90AA1 complex showing the strongest binding affinity (−10.0 kcal/mol). The 100 ns MD simulation confirmed the stability of this complex (RMSD < 1 nm). In the mouse periodontitis model, topical application of CLEO at 3 and 4 mg/mL significantly reduced gingival inflammation, alveolar bone resorption, and the number of TRAP-positive osteoclasts compared with the vehicle-treated periodontitis group (all p < 0.05). Furthermore, CLEO treatment dose-dependently lowered serum MMP-9 levels (from 24.15 ± 0.24 pg/mL in the model group to 12.36 ± 0.54 pg/mL in the high-dose group) and COX-2 levels (from 15.38 ± 0.62 pg/mL to 8.99 ± 0.57 pg/mL). The therapeutic efficacy of the high-dose CLEO group was comparable to that of the 2% minocycline group. CLEO exerts anti-P. gingivalis and anti-biofilm effects in vitro and ameliorates periodontitis in vivo through multi-target mechanisms, providing pharmacological evidence for its traditional use in inflammatory conditions. Full article

A series of N’-(4-nitrobenzylidene)propanehydrazides and corresponding bishydrazones, as well as N-(1,3-dioxoisoindolin-2-yl)propanamides and corresponding bis(propanamides), were synthesised. Antioxidant properties were assessed using reducing power, FRAP, DPPH, ABTS radical scavenging, and NBT inhibition assays. Among the tested compounds, phenylaminopropanamide 17 demonstrated the highest activity, showing 1.70-fold higher reducing power and 6.71-fold higher DPPH radical scavenging activity compared to melatonin. Phenylaminopropanehydrazide 9 exhibited the highest activity in the FRAP assay (1.48 times higher than melatonin), while ethoxyphenyl-based bis(propanamide) 24 showed the greatest NBT inhibition (1.58-fold relative to melatonin). Four compounds exhibited moderate antibacterial activity against both Gram-positive and Gram-negative bacteria. Full article

The proliferation of methicillin-resistant Staphylococcus aureus (MRSA) in food processing is an escalating public health issue. This circumstance has intensified the quest for ecological alternatives to impede pathogen proliferation and avert food degradation. This study firstly investigated the chemical compositions of three essential oils (EOs) sourced from Eucalyptus, Rosemary and Lavender plants using GC-MS. Subsequently, the antibacterial and antibiofilm activities of the tested EOs were assessed against MRSA strains. The effects of these EOs on the expression of antibiotic resistance-related (mecA), virulence regulatory (agrA and sarA), and enterotoxin (sea) genes in MRSA strains were also evaluated by real-time PCR. Concerning the composition analyses performed on the EOs, our results revealed a total of 82 compounds, which accounted for 99.20, 98.10 and 92.78% of Eucalyptus, Rosemary and Lavender EOs, respectively. The anti-staphylococcal activity showed that Eucalyptus EO had the greatest effect, with diameter of inhibition exceeding 41 mm. Moreover, the association between Rosemary EO and the antibiotic (cefoxitin) highlighted the enhancement of the antibacterial effect against the MRSA reference strain. Additionally, Eucalyptus EO showed the highest inhibitory effect against both strains, with MIC values ranging from 0.781 to 1.563 mg/mL, followed by the Rosemary and Lavender EOs. All the tested EOs displayed a bactericidal effect against the tested MRSA strains. Regarding the antibiofilm activity, Rosemary and Lavender EOs had varying impacts on the pre-formed biofilms, with percentage reduction values ranging from 36% to 73% and 37% to 68%, respectively. Finally, the mRNA expression of the MRSA gene A mecA and virulence genes agrA, sarA and sea declined following EO treatment compared with the control. The findings of this study highlighted the efficacy of locally tested EOs in reducing MRSA biofilm formation and the expression of virulence factors and suggested their potential use in food safety and culinary applications. Full article

Zanthoxylum bungeanum alkaloids have attracted considerable attention for their potential health benefits, yet systematic investigations into their extraction, purification, and comprehensive bioactivity remain scarce. In this study, an efficient extraction protocol was developed and scaled up, followed by purification using macroporous resin NKA-9 with 70% ethanol as the optimal eluent. Ultra-performance liquid chromatography coupled with ion mobility quadrupole time-of-flight mass spectrometry (UPLC-IM-QTOF/MS) identified 11 major alkaloids in the 70% ethanol eluate fraction. The antioxidant capacity of the 70% ethanol eluate fraction was evaluated through DPPH, ABTS⁺·, and Fe³⁺ reducing power assays, revealing a clear dose-dependent effect, albeit weaker than ascorbic acid. Antibacterial screening against four pathogenic bacteria (Escherichia coli, Bacillus subtilis, Staphylococcus aureus, and Pseudomonas aeruginosa) via the Oxford cup method, macrobroth dilution, and minimum bactericidal concentration (MBC) determination demonstrated strain-selective activity. The strongest effect was observed against E. coli [minimum inhibitory concentration (MIC) = 2 mg/mL, MBC = 8 mg/mL, MBC/MIC = 4, bactericidal], followed by moderate activity against B. subtilis (MIC = 4 mg/mL, MBC = 16 mg/mL), while only bacteriostatic effects were noted against S. aureus and P. aeruginosa within the tested range. These findings provide a robust foundation for further development of Zanthoxylum bungeanum alkaloids as natural functional ingredients or food-compatible bio preservatives. Full article

The escalating global concern regarding bacterial antibiotic resistance in animal production has intensified the search for sustainable and effective alternatives to conventional antimicrobials. In this study, two L. reuteri strains (LBM-Ti195 and LBM-Ti173) are isolated from broiler cecal microbiota that were characterized through an integrated approach, combining phenotypic assays with comparative genomic analysis. Both strains exhibited antibacterial activity against relevant veterinary and foodborne pathogens, including Listeria monocytogenes CECT 934, Staphylococcus aureus CECT 239, Clostridium perfringens Type A, and Campylobacter jejuni CCAMP 162. The inhibitory activity anti-S. aureus increased by more than 10% modifying cultivation conditions, while comparative genomic analysis identified an M23-family metallopeptidase as a potential candidate for pathogen inhibition. Phenotypically, both strains produced folate and metabolized fructooligosaccharides (FOS) and inulin, supporting their potential compatibility with synbiotic formulations. Genome reconstruction reinforces these functional findings by revealing a complete predicted de novo folate biosynthesis pathway. In addition, CAZyme annotation identified higher copy numbers of glycosyltransferases GT2 and GT4 compared with the reference strains, suggesting differences in cell-surface carbohydrate metabolism and exopolysaccharide (EPS)-associated traits. Safety profiling revealed no hemolytic activity or conserved virulence factors under the tested conditions. However, phenotypic tetracycline resistance was detected, and in silico analysis identified an acquired tetW gene in a putative plasmid-associated context, highlighting the importance of an in-depth evaluation of strains with probiotic potential. Collectively, these findings position LBM-Ti195 and LBM-Ti173 as promising avian-derived L. reuteri candidates for next-generation zootechnical probiotic development, while highlighting antimicrobial resistance (AMR) mitigation and further functional validation as essential steps toward safe application. Full article

Uncontrolled hemorrhage remains a major challenge in trauma care and surgical interventions, where rapid hemostasis and wound sealing are essential for improving patient survival. Natural polymer-based hydrogels have emerged as promising hemostatic materials owing to their excellent biocompatibility, biodegradability, and biomimetic properties. However, their clinical translation remains limited by insufficient mechanical robustness, wet adhesion, and functional responsiveness. To address these challenges, considerable progress has been achieved through rational material design and structural engineering strategies. Representative natural polymers, particularly polysaccharides and proteins, exhibit distinct physicochemical and biological characteristics that determine their hemostatic mechanisms and design strategies. Based on these material platforms, molecular modification strategies, including charge regulation, hydrophobic modification, and bioactive functionalization, have been widely employed to modulate interfacial interactions, platelet adhesion, coagulation activation, and tissue adhesion. In parallel, advanced structural architectures, such as porous, particulate, fibrous, multicrosslinked/multinetwork, and nanocomposite systems, have significantly enhanced fluid absorption, mechanical resilience, stress dissipation, and hemorrhage sealing efficiency. Beyond conventional hemostasis, increasing efforts have focused on integrating multifunctional properties, including antibacterial activity, inflammatory regulation, oxidative stress modulation, tissue regeneration, dynamic monitoring, and stimuli-responsive behaviors. This review systematically summarizes recent advances in natural polymer-based hemostatic hydrogels from the perspectives of advanced material modification strategies, structural engineering approaches, and functional integration, with particular emphasis on the relationships among material characteristics, interfacial behavior, structural organization, and hemostatic performance. Finally, current challenges and future perspectives for clinical translation are discussed, aiming to provide valuable insights for the rational design and clinical implementation of next-generation hemostatic biomaterials. Full article

This systematic review aimed to investigate the effect of titanium dioxide (TiO₂) incorporation on the mechanical, physicochemical, and biological properties of conventional glass ionomer cements (GICs). A systematic search was conducted in June 2026 in PubMed, Scopus, Embase, Web of Science and WorldCat databases. Search terms included combinations of glass ionomer AND titanium dioxide OR TiO₂ OR titanium oxide OR titanium nanotubes OR titanium nanoparticles. The study selection process followed the PRISMA guideline and was organized according to the PECO framework. The search yielded the identification of 475 articles, of which 34 met the eligibility criteria. The included studies investigated different TiO₂ forms, concentrations, and commercial GIC formulations. Many studies reported improvements in compressive strength, surface microhardness, fracture toughness, and antibacterial activity following TiO₂ incorporation. However, the findings were heterogeneous. Several studies reported no statistically significant differences or contradictory outcomes, particularly regarding flexural strength, fluoride release, cytocompatibility, and antibacterial performance. Beneficial effects were most frequently observed at TiO₂ concentrations between 3 and 5 wt%, whereas higher concentrations were occasionally associated with nanoparticle agglomeration and reduced material performance. Variability among studies was likely influenced by differences in TiO₂ characteristics, concentration, testing protocols, and GIC formulation. Overall, TiO₂ incorporation appears to be a promising approach for enhancing selected properties of conventional GICs. However, further standardized studies are required to confirm the consistency and clinical relevance of these effects. Full article