Strong Antibacterial Activity Research Articles

Exploring the bioactive potential of Mentha longifolia from Northeast India: an inclusive study on phytochemical composition and biological activities

Mentha longifolia (Lamiaceae) is regarded as highly valuable aromatic medicinal species with wide range of pharmaceutical application. In the present work, leaf essential oil of M. longifolia was applied for the assessment of in vitro pharmacological potentials and compositional analysis. A sum of 15 compounds were detected by GC-FID and GC-MS analysis of M. longifolia essential oil with total area of 99.98% where major compounds were carvone (59.56%), D-limonene (20.81%), eucalyptol (10.08%). The anti-oxidant potency of M. longifolia was estimated using two methods viz., ABTS (2,2-azino-bis-3-ethylbenzothiazoline-6-sulphonic acid) and DPPH (2,2-diphenyl-1-picrylhydrazyl) assay where M. longifolia essential oil showed moderate anti-oxidant potency. M. longifolia essential oil revealed high anti-inflammatory and tyrosinase inhibitory activity with an IC50 value 3.68 μL/mL and 1.22 μL/mL respectively compared to standard sodium diclofenac (5.33 μL/mL) and kojic acid (2.28 μL/mL). The acetylcholinesterase (AchE) inhibitory and genotoxic assay was performed, where M. longifolia essential oil revealed strong anti-acetylcholinesterase and anti-genotoxic activity. Anti-microbial potential of M. longifolia essential oil was also where strong anti-bacterial activity was shown against Salmonella typhimurium, Bacillus cereus, Staphylococcus aureus, Micrococcus luteus. For anti-fungal activity, M. longifolia essential oil showed no zone of inhibition against any used strains except Aspergillus flavus. From the present research it was established that M. longifolia essential oil possesses pharmaceutical potential with strong AchE inhibitory, anti-inflammatory, anti-microbial, anti-tyrosinase, anti-genotoxic and anti-oxidant activity which can be used for plant-based drug development in future endeavor.

Biosynthesis, Antibacterial and Antifungal Activities of Ag Nanoparticles Prepared Using Piper nigrum Fruit Extract

Nanomaterials are promising alternatives to antibiotics with the potential to handle the menace of emerging multidrug resistance in pathogenic microbes. We report a simple biosynthetic approach to prepare Ag nanoparticles (NPs) with strong antibacterial and antifungal actions by using Piper nigrum fruit extract as a bioreducing agent. The biosynthesized material was characterized by SEM, AFM, TEM, HRTEM, XRD and UV–Visible absorption spectroscopy. SEM, AFM and TEM analyses provided evidence that the average diameter of the Ag NPs was 18[Formula: see text]nm, while XRD and HRTEM confirmed the FCC structure of Ag NPs. The biosynthesized Ag NPs demonstrated extremely strong antibacterial activity against Bacillus oceanisediminis and Escherichia coli, and showed extremely strong antifungal action against Schizosaccharomyces pombe, inhibiting their growth at very low concentrations of 3[Formula: see text][Formula: see text]g/mL, 4[Formula: see text][Formula: see text]g/mL and 3[Formula: see text][Formula: see text]g/mL, respectively. The molecular origin of their antibacterial and antifungal activity was studied using various molecular and biochemical assays. The results of these assays revealed a major role for reactive oxygen species (ROS) in the antifungal and antibacterial actions of the biosynthesized Ag NPs. Furthermore, morphological changes in cells and cell wall damage upon Ag NP treatment were observed by scanning electron microscopy. In addition, significant enhancement in protein leakage and fragmentation of DNA was also observed upon treatment of S. pombe, B. oceanisediminis and E. coli with Ag NPs. In conclusion, the observed extremely strong antibacterial and antifungal activities of biosynthesized Ag NPs are due to the oxidative stress triggered by ROS, causing cell wall damage and subsequent protein leakage and DNA fragmentation.

Chemical composition and antibacterial activity of the leaf essential oil of Litsea mekongensis Lecomte growing wild in Lam Dong Province, Vietnam

Litsea mekongensis Lecomte is a native species that originated in Vietnam and Laos. To date, the volatile components and antibacterial activity of the essential oils derived from L. mekongensis leaves have not yet been reported. This study aims to investigate the chemical composition and antibacterial activity of L. mekongensis leaf essential oil. The chemical constituents were analyzed by gas chromatography-mass spectroscopy (GC-MS), and the antibacterial activity was evaluated using the agar well diffusion method. The GC-MS analysis showed that fifty-four volatile components were detected, of which sesquiterpene hydrocarbons accounted for almost 65% of the total, while the proportion of monoterpene hydrocarbons was 19.84%. Germacrene D (16.17%), γ-elemene (7.82%), β-phellandrene (6.76%), α-pinene (6.62%), and δ-cadinene (5.68%) were identified as major components. The essential oil exhibited strong antibacterial activity against Salmonella typhi, Staphylococcus aureus, and Escherichia coli. S. aureus was the most sensitive species, but no inhibitory activity against Pseudomonas aeruginosa was recorded. These findings revealed information on the chemical constituents of the essential oil prepared from L. mekongensis and its potential antibacterial activity against several pathogenic bacteria.

Antimicrobial peptide 2K4L inhibits the inflammatory response in macrophages and Caenorhabditis elegans and protects against LPS-induced septic shock in mice

2K4L is a rationally designed analog of the short α-helical peptide temporin-1CEc, a natural peptide isolated and purified from the skin secretions of the Chinese brown frog Rana chensinensis by substituting amino acid residues. 2K4L displayed improved and broad-spectrum antibacterial activity than temporin-1CEc in vitro. Here, the antibacterial and anti-inflammatory activities of 2K4L in macrophages, C. elegans and mice were investigated. The results demonstrated that 2K4L could enter THP-1 cells to kill a multidrug-resistant Acinetobacter baumannii strain (MRAB 0227) and a sensitive A. baumannii strain (AB 22933), as well as reduce proinflammatory responses induced by MRAB 0227 by inhibiting NF-κB signaling pathway. Similarly, 2K4L exhibited strong bactericidal activity against A. baumannii uptake into C. elegans, extending the lifespan and healthspan of the nematodes. Meanwhile, 2K4L alleviated the oxidative stress response by inhibiting the expression of core genes in the p38 MAPK/PMK-1 signaling pathway and downregulating the phosphorylation level of p38, thereby protecting the nematodes from damage by A. baumannii. Finally, in an LPS-induced septic model, 2K4L enhanced the survival of septic mice and decreased the production of proinflammatory cytokines by inhibiting the signaling protein expression of the MAPK and NF-κB signaling pathways and protecting LPS-induced septic mice from a lethal inflammatory response. In conclusion, 2K4L ameliorated LPS-induced inflammation both in vitro and in vivo.

Nanocellulose-alginate composite beads for improving Ciprofloxacin bioavailability

Nanocellulose is a potential material utilized in numerous biomedical applications. However, its hydrophilic characteristic and uncontrolled encapsulated drug release hinders nanocellulose uses in oral drug administration. Thus, this work developed novel nanocellulose/alginate composite (CNC/Alg) beads for oral delivery and bioavailability enhancement of a model drug, Ciprofloxacin (CIP). CNC was green synthesized employing electrolysis process from sugarcane bagasse. CNC/Alg beads were formulated by dropwise adding CNC-Alg mixture in CaCl2 solution at room temperature. CIP was incorporated into CNC/Alg beads by adsorption technique. X-ray diffractometry and Fourier-transform infrared spectra images showed that the beads were effectively produced with high crystallinity of 75.5 %, and the typical bond of cellulose and alginate. Within 4 h of adsorption, CIP loading efficiency reached 45.27 %, with 87.2 % molecules in the zwitterionic state. The adsorption followed Elovich and pseudo-second-order models, indicating a multi-mechanism including both physical and chemical adsorptions. Importantly, in gastrointestinal tract, the beads could protect CIP from acidic stomach environment while releasing it sustainably in simulated intestinal condition (75.05 %). The beads also showed strong antibacterial activity against both Gram(−) and Gram(+) bacteria, as evidenced by low IC50 and minimum inhibitory concentration values. Finally, CNC/Alg beads could improve CIP bioavailability for effective oral drug delivery route.

Antibacterial potential of extracts and metabolites isolated from the endophytic fungus Chaetomium cochliodes against phytopathogenic bacteria

Summary Five fungal endophytes, Alternaria sp., Aspergillus sp., Chaetomium sp., Rhizopus sp. and Curvularia sp., were isolated from an Egyptian herbaceous plant, Tribulus terrestris, and tested for their antibacterial activity against three phytopathogenic bacteria (Pectobacterium carotovorum subsp. carotovorum, Ralstonia solanacearum, Pseudomonas syringae pv. syringae). Chaetomium sp. showed the highest antibacterial activity. This strain was identified morphologically and molecularly as Chaetomium cochliodes MS03 (MW898133) based on the ITS1-5.8S rRNA-ITS2 genomic region. Chaetomium cochliodes caused 15 and 8 mm inhibition zones of P. carotovorum subsp. carotovorum and R. solanacearum, respectively. Chaetomium cochliodes isolate was fermented and extracted with ethyl acetate. The crude extract of C. cochliodes showed strong antibacterial activity against P. carotovorum subsp. carotovorum (inhibition zone = 27 mm). Bioassay guided isolation of the crude extract using silica gel column chromatography was conducted to isolate bioactive secondary metabolites. Minimum inhibitory concentrations (MICs) were 500, 32 and 4 mg/L for C. cochliodes extract, fraction 14 and fraction 15, respectively, against P. carotovorum subsp. carotovorum. Bioactive fractions were analyzed by GC/MS. The bioactive pure compound was identified as 9,12-octadecadienoic acid (Z,Z) and the chemical structure was confirmed by H1 NMR and C13 NMR spectral analysis. The isolated compound showed a promising antibacterial activity against P. carotovorum subsp. carotovorum with MIC value of 32 mg/L.

Perbandingan Aktivitas Antibakteri Sediaan Gel dan Spray Ekstrak Etanol Biji Pepaya (Carica papaya L.)

Introduction: Acne is a psychological problem that is most frequently experienced from puberty through maturity. The papaya plant (Carica papaya L.), which has antibacterial activities present in the papaya seeds. The bioactive substances found in papaya seeds, including flavonoids, tannins, saponins, proteins, carbohydrates, tocopherols, and carotenoids, are what provide seeds the antibacterial activities Objective: This research compares the effectiveness of papaya seed ethanol extract against Propionibacterium acnes bacteria in gel and spray dose forms. . Methods: This study is an experimental lab experiment that uses 96% ethanol as a solvent and the maceration method of extraction. Results: The concentration of the gel preparation in this study was 5% (F1)with resistance diameter 15.5, namely strong antibacterial activity, 10% (F2)with an inhibitory diameter of 16.5 mm, which has strong antibacterial activity, dan 15% (F3)with an inhibitory diameter of 15.3 mm, namely strong antibacterial activity, positive control with a diameter of 27.5 mm, namely very strong antibacterial activity. On preparationspray has an inhibition zone of 0 mm, positive control 24 mm and negative control 0 mm. The resulting extract was initially tested for phytochemicals using the tube method to guarantee the quality of the extract. Organoleptic testing, homogeneity, pH, spreadability, and adhesion were among the physical qualities of gel and spray preparations that were assessed.Clindamycin served as the positive control in an antibacterial activity test against Propionibacterium acnes utilizing the well diffusion method on Muller Hinton agar (MHA) media. According to the results of the phytochemical screening, the papaya seed ethanol extract included bioactive substances as alkaloids, flavonoids, saponins, and tannins. Physical property evaluation produced results that complied with the criteria for the organoleptic, homogeneity, pH, spreadability, and adhesion tests. Conclusion: Based on this research, it can be concluded that the inhibitory power of EEBP in gel preparations is better than in gel preparation spray because the results in the gel preparation category have a stronger average.

Effectiveness of Citronella Extract (Cymbopogon nardus) Mouthwash From Microwave-Assisted Extraction Method Against Streptococcus mutans

Cymbopogon nardus, or citronella has a distinctive aroma is known as a source of essential oils. Extract of citronella can be use as mouthwash to reduce bad breath and protect teeth from bacteria that cause dental caries. C. nardus contains antibacterial compounds such as flavonoid, essential oils, polyphenols, and saponin which are also act as antioxidant compounds. This research was carried out to formulate mouthwash using citronella extract and determine the antibacterial activity of the citronella mouthwash against S. mutans bacteria using disc diffusion method. The microwave extraction method (MAE) was used to obtain extract using 70 % and 96 % ethanol as a solvents. The mouthwash were made in 3 formulas i.e. formula 1, formula 2, and formula 3 each contain 25 % w/v, 30 % w/v, and 35 % w/v) respectively. The quality of mouthwash includes organoleptic, pH, viscosity and hedonic was evaluated and antibacterial activity was determined by measuring the value of minimum inhibitory concentration (MIC) and diameter of inhibition zone. The MIC value of citronella extract was achieved at concentration 20 %. All mouthwash formula met the requirements for a good mouthwash. Formula 1 was the most preferred formula by the panelists based on the hedonic test. Formula 3 had the strongest antibacterial activity with diameter inhibitory of 17.6 ± 0.52 mm. It was concluded that citronella mothwash has the potential to be developed into an antibacterial mouthwash.

A carrier-free, injectable, and self-assembling hydrogel based on carvacrol and glycyrrhizin exhibits high antibacterial activity and enhances healing of MRSA-infected wounds

Inspired by glycyrrhizin’s strong pharmacological activities and the directed self-assembly into hydrogels, we created a novel carrier-free, injectable hydrogel (CAR@glycygel) by combining glycyrrhizin with carvacrol (CAR), without any other chemical crosslinkers, to promote wound healing on bacteria-infected skin. CAR appeared to readily dissolve and load into CAR@glycygel. CAR@glycygel had a dense, porous, sponge structure and strong antioxidant characteristics. In vitro, it showed better antibacterial ability than free CAR. For methicillin-resistant Staphylococcus aureus (MRSA), Staphylococcus aureus, and Escherichia coli, the diameter of inhibition zone values of CAR@glycygel were 3.80 ± 0.04, 3.31 ± 0.20 and 3.12 ± 0.24 times greater, respectively, than those of free CAR. The MICs for CAR@glycygel was 156.25 μg/mL while it was 1250.00 μg/mL for free CAR to these three bacteria. Its antibacterial mechanism appeared to involve destruction of the integrity of the bacterial cell wall and biomembrane, leading to a leakage of AKP and inhibition of biofilm formation. In vivo, CAR@glycygel effectively stopped bleeding. When applied to skin wounds on rats infected with MRSA, CAR@glycygel had strong bactericidal activity and improved wound healing. The wound healing rates for CAR@glycygel were 49.59 ± 15.78 %, 93.02 ± 3.09 % and 99.02 ± 0.55 % on day 3, day 7, and day 11, respectively, which were much better than blank control and positive control groups. Mechanisms of CAR@glycygel accelerating wound healing involved facilitating epidermis remolding, promoting the growth of hair follicles, stimulating collagen deposition, mitigating inflammation, and promoting angiogenesis. Overall, CAR@glycygel showed great potential as wound dressing for infected skin wounds.

Self-Assembled Borneol-Guanidine-Based Amphiphilic Polymers as an Efficient Antibiofilm Agent.

Biofilm-associated infections remain a tremendous obstacle to the treatment of microbial infections globally. However, the poor penetrability to a dense extracellular polymeric substance matrix of traditional antibacterial agents limits their antibiofilm activity. Here, we show that nanoaggregates formed by self-assembly of amphiphilic borneol-guanidine-based cationic polymers (BGNx-n) possess strong antibacterial activity and can eliminate mature Staphylococcus aureus (S. aureus) biofilms. The introduction of the guanidine moiety improves the hydrophilicity and membrane penetrability of BGNx-n. The self-assembled nanoaggregates with highly localized positive charges are expected to enhance their interaction with negatively charged bacteria and biofilms. Furthermore, nanoaggregates dissociate on the surface of biofilms into smaller BGNx-n polymers, which enhances their ability to penetrate biofilms. BGNx-n nanoaggregates that exhibit superior antibacterial activity have the minimum inhibitory concentration (MIC) of 62.5 μg·mL-1 against S. aureus and eradicate mature biofilms at 4 × MIC with negligible hemolysis. Taken together, this size-variable self-assembly system offers a promising strategy for the development of effective antibiofilm agents.

In vitro activity of the novel antimicrobial peptide WR-286 in combination with vancomycin against methicillin-resistant Staphylococcus aureus

Background: Multidrug resistance bacteria are a serious problem for health specialists and all the people in the world. The main reasons for this problem are the misuse of antibiotics and the limited number of antibiotics as compared to different human diseases. The important antibiotic-resistant bacteria include Methicillin-resistant Staphylococcus aureus (MRSA). Antimicrobial peptides (AMPs) are regarded as promising antimicrobial agents because they satisfy the requirements for the creation of innovative antimicrobial drugs. The aim of the study: To design a novel antimicrobial peptide and study its effect against MRSA when we combined it with vancomycin. Materials and methods: To produce the hexapeptide WR-286, 1-(2, 6-difluorobenzyl)-1H-1, 2, 3-triazole-4-carboxylic acid, tryptophan (W), and arginine (R) were rationally combined. Different bacterial strains were used to test WR-286's antibacterial properties. Investigations of WR-286's hemolytic activity toward human erythrocytes were also conducted. Finally, utilizing the checkerboard approach and the fractional inhibitory index, synergistic tests with vancomycin were carried out. Results: With MIC values as low as 35 μM, WR-286 demonstrated strong antibacterial activity against MRSA. The toxicity of WR-286 to human red blood cells was very low. Additionally, the peptide and vancomycin's activity were improved by the synergistic experiments. Conclusion: According to the current investigation, WR-286 has little hemolytic activity and displays promising antibacterial activity against MRSA. Additionally, when coupled with vancomycin, the peptide has synergistic effect. The novel AMPs described in this work are promising potential candidates for antimicrobial drug development.

Silver nanoparticle-decorated cellulose beads: Eco-friendly catalysts for efficient 4-nitrophenol reduction and antibacterial performance

This study presents an innovative and environmentally friendly method to produce fibrous cellulose beads by mechanically stirring natural fibers in an aqueous medium. Date palm fibers are transformed into uniform beads with a diameter of 1.5 to 2 mm through chemical treatment and mechanical agitation. These beads are then decorated with silver nanoparticles (Ag0 NPs) in a one-step synthesis, giving them catalytic capabilities for the reduction of 4-nitrophenol (4-NP) and antibacterial activities. Characterization techniques such as FTIR, XRD, SEM, EDX, and TGA confirmed the successful synthesis and deposition of Ag0 NPs on the cellulose beads. Tests showed complete conversion of 4-NP to 4-AP in just 7 min, with pseudo-first-order kinetics and a Kapp of 0.590 min-1. Additionally, Ag0@CB demonstrated exceptional recyclability and stability over five cycles, with minimal silver release. The beads also showed strong antibacterial activity against Escherichia coli and Staphylococcus aureus, effectively eradicating bacterial colonies in 30 min. In summary, Ag0@CB exhibits multifunctional capabilities for degrading organic pollutants and biomedical applications, offering promising potential for large-scale production and practical use in water treatment and antibacterial coatings.

Czech Honeydew Honeys-A Potential Source of Local Medical Honey with Strong Antimicrobial Activity.

An increasing resistance of microbes to antibiotics, the emergence of multidrug-resistant and extremely resistant strains, and the long time needed to develop new antibiotics are driving the search for additional sources of antibacterial agents. The aim of the study was to compare the efficacy of Czech honeys with already available pharmaceutical agents containing medicinal honey, and to perform basic biochemical analysis of Czech samples, including detection of undesirable chemical substances. The results showed strong antibacterial activity of Czech honeydew honeys compared to the control group, especially against G+ pathogens, with an average MIC of 9.44% compared to 17.54%, and comparable activity against G- of 16.48% versus 16.66%. In addition to the strong antibacterial activity, this study confirmed the safety and quality of Czech honeys and helped to select the character of a possible source for in vivo testing and subsequent clinical trials.

Antibacterial evaluation of 2-(6-Chloro-2-p-tolylquinazolin-4-ylthio) acetonitrile against pathogenic bacterial isolates with special reference to biofilm formation inhibition and anti-adherence properties

BackgroundEvaluating the effectiveness of a specific quinazoline molecule with antibacterial activity on microorganisms as a potential antibiotic substitution. MethodsA variety of microorganisms were tested with the designated quinazoline molecule. Differences within two groups were analyzed using the two-tailed Student’s t-test,. ResultsSusceptibility tests revealed that the chemical has stronger antibacterial action against S. saprophyticus than other isolates, with just a slight effect on E. coli and M. smegmatis. The bacterial cells were subjected to varying concentrations of a certain molecule, and the results showed that the inhibition of bacterial adhesion was not consistent. This suggests that the effect of the molecule on bacterial adhesion is dependent on its concentration. After 24 h of treatment with varying chemical doses, all of the periodontal bacterial strains examined showed considerable inhibition of biofilm formation. ConclusionsAccording to the findings, the chemical molecule quinazoline could be utilized as an alternative therapeutic approach for microorganism-caused infections.

Introducing the antibacterial and photocatalytic degradation potentials of biosynthesized chitosan, chitosan–ZnO, and chitosan–ZnO/PVP nanoparticles

The development of nanomaterials has been speedily established in recent years, yet nanoparticles synthesized by traditional methods suffer unacceptable toxicity and the sustainability of the procedure for synthesizing such nanoparticles is inadequate. Consequently, green biosynthesis, which employs biopolymers, is gaining attraction as an environmentally sound alternative to less sustainable approaches. Chitosan-encapsulated nanoparticles exhibit exceptional antibacterial properties, offering a wide range of uses. Chitosan, obtained from shrimp shells, aided in the environmentally friendly synthesis of high-purity zinc oxide nanoparticles (ZnO NPs) with desirable features such as the extraction yield (41%), the deacetylation (88%), and the crystallinity index (74.54%). The particle size of ZnO NPs was 12 nm, while that of chitosan–ZnO NPs was 21 nm, and the bandgap energies of these nanomaterials were 3.98 and 3.48, respectively. The strong antibacterial action was demonstrated by ZnO NPs, chitosan–ZnO NPs, and chitosan–ZnO/PVP, particularly against Gram-positive bacteria, making them appropriate for therapeutic use. The photocatalytic degradation abilities were also assessed for all nanoparticles. At a concentration of 6 × 10–5 M, chitosan removed 90.5% of the methylene blue (MB) dye, ZnO NPs removed 97.4%, chitosan-coated ZnO NPs removed 99.6%, while chitosan–ZnO/PVP removed 100%. In the case of toluidine blue (TB), at a concentration of 4 × 10–3 M, the respective efficiencies were 96.8%, 96.8%, 99.5%, and 100%, respectively. Evaluation of radical scavenger activity revealed increased scavenging of ABTS and DPPH radicals by chitosan–ZnO/PVP compared to individual zinc oxide or chitosan–ZnO, where the IC50 results were 0.059, 0.092, 0.079 mg/mL, respectively, in the ABTS test, and 0.095, 0.083, 0.061, and 0.064 mg/mL in the DPPH test, respectively. Moreover, in silico toxicity studies were conducted to predict the organ-specific toxicity through ProTox II software. The obtained results suggest the probable safety and the absence of organ-specific toxicity with all the tested samples.

An In-vitro Antioxidant and Antimicrobial Activity of Vitis vinifera Leaf Extract

Background: Vitis vinifera (Flame red grape) is known for its hepatoprotective, nephroprotective and cardioprotective activity of ethanolic and aqueous extracts of aerial parts has been reported but, due to presence of polyphenols, glycosides, saponins and alkaloid, the antioxidant and antimicrobial activity yet not to evaluated on salad plant and bacteria, respectively. Aim: This research examined grape (V. vinifera flaming red) leaf ethanolic extract (EE) as a bioactive resource. Methods: Ethanolic extract test, primarily to calculate the overall phenolic content by using the Folin-Ciocalteu technique and gallic acid taking as a reference. Similarly, flavonoid content measured using quercetin as a calibration curve. Antioxidant properties was confirmed by getting positive responses from different methods (DPPH, H2O2, FRAP and Phospho-Molybdenum). Antimicrobial activity tested against gram-positive bacteria (Lactobacillus cereus and Staphylococcus aureus) and gramnegative bacteria (Escherichia coli and Staphylococcus enterica ser. Typhimurium) in a broth microdilution test. The ethanolic extract (EE) are rich in antioxidant-rich phenolic compounds show minimum inhibition concentration (MIC) and minimum bactericidal concentration (MBC) for every given bacterium on beetroot and spinach leaves. Results: We investigate this extract’s total phenol, total flavonoid, and antioxidant and antibacterial properties. We also identify its main phenolic components, revealing its phytochemical diversity. We found that the EE had 39.29 gGAkg-1 dw of phenol and 96.05 gQE kg-1 dw of flavonoids. The EE scavenges DPPH, H2O2, FRAP, and PM radicals at 142, 168, 275, and 172 g TE kg-1, respectively. We reveal the complex character of this extract by revealing catechins, flavonoids, tannins, malic acid, enzymes, resveratrol, phenolic acids, flavonols, procyanidins, and anthocyanins. Salmonella enterica subsp. enterica serovar Typhimurium, Escherichia coli, Listeria monocytogenes, and Staphylococcus aureus are all inhibited by EE with a MIC range of 16 to 18 gL-1 (E. coli). The extract affects bacterial growth at different stages. The EE reduces spinach and beetroot leaf total bacterial load by 1.159 to 2.456 log drop when used as a sanitizer at 25 gL-1 (1.156–2.858 log reduction). Conclusion: This research work highlights grape leaf EE as a novel and appealing source of bioactive components with its strong antibacterial and antioxidant activities against common foodborne infectious agents. Our research reveals that leaf ethanolic extract could reduce human pathogenic microorganisms in fresh green vegetables, improving food safety.

Pharmacological and behavioral investigation of putative self-medicative plants in Budongo chimpanzee diets.

Wild chimpanzees consume a variety of plants to meet their dietary needs and maintain wellbeing. While some plants have obvious value, others are nutritionally poor and/or contain bioactive toxins which make ingestion costly. In some cases, these nutrient-poor resources are speculated to be medicinal, thought to help individuals combat illness. In this study, we observed two habituated chimpanzee communities living in the Budongo Forest, Uganda, and collected 17 botanical samples associated with putative self-medication behaviors (e.g., bark feeding, dead wood eating, and pith-stripping) or events (e.g., when consumer had elevated parasite load, abnormal urinalysis, or injury). In total, we selected plant parts from 13 species (nine trees and four herbaceous plants). Three extracts of different polarities were produced from each sample using n-hexane, ethyl acetate, and methanol/water (9/1, v/v) and introduced to antibacterial and anti-inflammatory in vitro models. Extracts were evaluated for growth inhibition against a panel of multidrug-resistant clinical isolates of bacteria, including ESKAPE strains and cyclooxygenase-2 (COX-2) inhibition activity. Pharmacological results suggest that Budongo chimpanzees consume several species with potent medicinal properties. In the antibacterial library screen, 45 out of 53 extracts (88%) exhibited ≥40% inhibition at a concentration of 256 μg/mL. Of these active extracts, 41 (91%) showed activity at ≤256μg/mL in subsequent dose-response antibacterial experiments. The strongest antibacterial activity was achieved by the n-hexane extract of Alstonia boonei dead wood against Staphylococcus aureus (IC50: 16 μg/mL; MIC: 32 μg/mL) and Enterococcus faecium (IC50: 16 μg/mL; MIC: >256 μg/mL) and by the methanol-water extract of Khaya anthotheca bark and resin against E. faecium (IC50: 16 μg/mL; MIC: 32 μg/mL) and pathogenic Escherichia coli (IC50: 16 μg/mL; MIC: 256 μg/mL). We observed ingestion of both these species by highly parasitized individuals. K. anthotheca bark and resin were also targeted by individuals with indicators of infection and injuries. All plant species negatively affected growth of E. coli. In the anti-inflammatory COX-2 inhibition library screen, 17 out of 51 tested extracts (33%) showed ≥50% COX-2 inhibition at a concentration of 5 μg/mL. Several extracts also exhibited anti-inflammatory effects in COX-2 dose-response experiments. The K. anthotheca bark and resin methanol-water extract showed the most potent effects (IC50: 0.55 μg/mL), followed by the fern Christella parasitica methanol-water extract (IC50: 0.81 μg/mL). This fern species was consumed by an injured individual, a feeding behavior documented only once before in this population. These results, integrated with associated observations from eight months of behavioral data, provide further evidence for the presence of self-medicative resources in wild chimpanzee diets. This study addresses the challenge of distinguishing preventative medicinal food consumption from therapeutic self-medication by integrating pharmacological, observational, and health monitoring data-an essential interdisciplinary approach for advancing the field of zoopharmacognosy.

The Diels-Alder Cross-Linked Gelatin/Dextran Nanocomposite Hydrogels with Silver Nanoparticles for Wound Healing Applications: Synthesis, Characterization, and In Vitro Evaluation.

Wound healing involves a sophisticated biological process that relies on ideal conditions to advance through various stages of repair. Modern wound dressings are designed to imitate the natural surroundings around cells and offer properties such as moisture regulation, strength, and antimicrobial defense to boost healing. A recent research project unveiled a new type of gelatin (Gel)/dextran (Dex) hydrogels, linked through Diels-Alder (D-A) reactions, loaded with silver nanoparticles (Ag-NPs) for cutting-edge wound treatment. Gel and Dex were chemically modified to form the hydrogels via the D-A reaction. The hydrogels were enriched with Ag-NPs at varying levels. Thorough analyses of the hydrogels using methods like NMR, FT-IR, and SEM were carried out to assess their structure and nanoparticle integration. Rheological tests displayed that the hydrogels had favorable mechanical attributes, particularly when Ag-NPs were included. The hydrogels demonstrated controlled swelling, responsiveness to pH changes, and were non-toxic. Testing against E. coli showcased the strong antibacterial activity of the nanocomposite hydrogels in a concentration-dependent manner. This investigation showcased the promise of these bioactive nanocomposite hydrogels in promoting speedy wound healing by maintaining a moist environment, offering an antimicrobial shield, and ensuring mechanical support at the wound site.

Anti-MRSA activity of chlorophenyl pyrrolo benzodiazepines compound.

Antibiotic resistant is the major concern in public health to control the infectious diseases. MRSA (Methicillin-resistant Staphylococcus aureus) is a significant concern in healthcare settings due to its resistance to many antibiotics, including methicillin and other beta-lactams. MRSA infection difficult to treat and increases the risk of complications. Here, we have tested a series of highly condensed heterocyclic derivatives of pyrrolo[1,2-a][1,4]benzodiazepines. Compounds were tested against both, Gram-positive bacteria, Staphylococcus aureus and S. epidermidis, and Gram-negative bacteria, Escherichia coli and Pseudomonas aeruginosa, to assess the antimicrobial efficacy. Compared to Gram-negative bacteria, compounds showed much stronger antibacterial activity against Gram-positive bacteria. SM-5 [Ethyl2-(7-(4-chlorophenyl)-4-methoxy-6,7,8,13-tetrahydro-5H-benzo[e]benzo[5,6][1,4]diazepino[2,1-a]isoindol-15-yl)acetate] derivative was selected as best on the basis of higher therapeutic index among the tested compounds, showed MIC value of 7.81 µg. ml-1 against Staphylococcus strains. Molecular docking analysis between cell wall biosynthesis protein of S. aureus and SM-5 revealed that PBP2a showed the highest binding energy (-8.3 Kcal mol-1), followed by beta-lactam-inducible PBP4 (-7.7 Kcal mol-1), and lipoteichoic acid synthase (-7.5 Kcal mol-1) which is comparably higher than methicillin. Ground state energy calculations by DFT analysis revealed that compound SM-5 and SM-6, almost have equal electronegativity 0.11018 au which also satisfy the quality of the compound reactivity. Analysis of their biofilm inhibition in vitro and in silico toxicity analysis demonstrated their substantial potential to be a kind of future lead antibiotic.

Evaluation of antimicrobial and antioxidant effects of silver nanoparticles synthesized with leaves of Lepidium draba L.

Nanoscience is a prominent scientific field with great potential and many novel and cost-effective applications. Numerous green and environmentally friendly synthesis methods have been introduced that use different plant extracts to produce silver, gold, copper, and iron antibacterial nanoparticles. Plant extracts contain rejuvenating compounds which, when exposed to metal salts (in this research, silver nitrate), facilitate their reduction to metal ions. In the present investigation, Lepidium draba was used as a regenerating factor. Silver nanoparticles (AgNPs) containing Azmak leaf extract were synthesized under optimal conditions including silver nitrate concentration, time, temperature, and pH. These nanoparticles were then evaluated for their characteristics using transmission electron microscopy (TEM), Fourier transform infrared (FT-IR) spectroscopy, X-ray diffraction (XRD), dynamic light scattering (DLS), and zeta potential analyses. Subsequently, the antibacterial properties of nanoparticles were assessed using the broth microdilution method. The 2,2-diphenyl-1-picrylhydrazyl (DPPH) method was also employed to examine the antioxidant properties of synthesized nanoparticles. Structural analyses revealed the formation of spherical, stable, and pure AgNPs with a size of 20–35 nm. The synthesized AgNPs exhibited strong antibacterial activity against Gram-negative and Gram-positive bacteria. In addition, investigation of the antioxidant activity of the nanoparticles showed 89% inhibition at a concentration of 250 μg/mL. AgNPs synthesized using the Azmak leaf extract can be employed as low-cost and efficient nanoparticles for environmental and biomedical applications and their dual antimicrobial and antioxidant characteristics could potentially position them as candidates for treating infectious wound.