Highest Zone Of Inhibition Research Articles

Antibacterial and anticancer activities of three novel lectin-conjugated chitosan nanoparticles

To the best of our knowledge, this is the first attempt to synthesize, characterize, and determine the antibacterial and anticancer effects of three novel conjugates of plant lectins: phytohemagglutinin lectin (PHA), soybean agglutinin (SBA), and peanut agglutinin (PNA) with chitosan nanoparticles (CHNPs). The lectin concentration within prepared conjugates was estimated using nannodrop, and the highest concentration was 0.96 mg/ml in PHA-CHNPs. SDS-PAGE showed the molecular weights of conjugates ranged from 26.9 to 63.9 kDa. UV spectrophotometer recorded the absorbance peaks of conjugates somewhere between 200 and 230 nm. Hemagglutination analysis verified the presence of actively binding lectins. The three conjugates showed strong antibacterial activity against Gram-positive and Gram-negative bacteria compared to pure lectins and chitosan nanoparticles. The highest inhibition zone was 55.67 ± 4.04, 38.67 ± 5.51, and 37.33 ± 2.52 for PHA-CHNPs against Enterococcus faecalis, Salmonella typhimurium, and Shigella sonnei, respectively, followed by 36.3 ± 0.15 for PNA-CHNPs against Staphylococcus aureus. The lowest MIC was 1.5 µg/ml for PHA-CHNPs against Enterococcus faecalis, followed by 12 µg/ml for PNA-CHNPs and SBA-CHNPs against Salmonella typhimurium and Enterococcus faecalis, respectively. TEM microphotographs show the conjugation pattern between lectins and chitosan nanoparticles and the morphological differences between control, treated bacteria, and cancer cells. Moreover, 100 μg/ml of PHA-CHNPs affect tongue carcinoma (HNO-97), colorectal cancer (HT-29), and human melanoma (A375) cancer cell lines, reducing cell viability by 38.78 ± 1.85%, 49.88 ± 1.11%, and 66.92 ± 3.60%, respectively. This study develops three innovative conjugates of lectin chitosan nanoparticles that need to be tested as potential antibacterial and anticancer agents for medical and cancer therapy applications.Key points• Lectin-conjugated chitosan nanoparticles exhibit antibacterial activity.• All conjugates are safe for oral epithelial cells and human skin fibroblasts.• The PHA-CHNP conjugates have anticancer activity against HNO-97, HT-29, and A375.

Antimicrobial Susceptibility of Fructophilic Lactic Acid Bacteria on PHZM Gene of Pseudomonas Aeruginosa Isolates from Wounds Infected

Abstract Introduction The study was to isolate and characterize fructophilic lactic acid bacteria (FLAB) species from the honey bee gut. Based on the results of this study, it was found that the FLAB species obtained from honey were gram-positive and catalase-negative, and this identification was confirmed through 16S rRNA gene sequencing. Materials and methods The results indicated that yeast extract was the most effective nitrogen source, while glucose was the preferred carbon source for cell-free supernatant (CFS) production. The optimal pH for CFS production was found to be 5, and the incubation period of 72 hours was determined to be the most suitable for obtaining a high yield of CFS. Another aspect of the study aimed to identify multidrug-resistant P. aeruginosa isolates from burn wound infections. The isolates were identified using the VITEK 2 system, and the phzM gene was detected in all nine strains. Furthermore, the study evaluated the effect of the CFS of the selected strain (E5) on the expression of the phzM gene. Results The study showed a significant down-regulation of phzM gene expression in multidrug-resistant P. aeruginosa isolates following exposure to the CFS, indicating the potential of E. faecium as an effective antimicrobial agent against P. aeruginosa infections that are resistant to multiple drugs. We performed a primary screening to evaluate the effect of the CFS obtained from E. faecium (E5), and it was observed that the CFS showed a high inhibition zone of 23 mm against multidrug-resistant P. aeruginosa, as determined by the agar well diffusion assay. The study also investigated further to determine the optimal conditions for producing CFS. Conclusion Down-regulation and up-regulation in the expression of the genes following exposure to CFS indicate the potential of E. faecium as an effective antimicrobial agent against multi-drug resistant (MDR) P. aeruginosa infections.

Effect of seasonal variations on phytoconstituents and antimicrobial properties of Holoptelea integrifolia, an important medicinal plant from Kangra District in Himachal Pradesh, India: A case study

Medicinal plants have been used for the treatment of many ailments since time immemorial. The pharmacological significance of these plants is attributed to the presence of secondary metabolites which are greatly affected by the changes in the climatic conditions. This study investigates the effect of seasonal variations on the phytochemical constituents and biological activities of Holoptelea integrifolia leaves and bark in Kangra district, Himachal Pradesh, India. The antimicrobial activity and minimum inhibitory concentration of various plant extracts were determined using agar well diffusion and resazurin dye methods. The qualitative and quantitative analysis of phytochemical, besides antioxidant activity, were compared in all samples during different seasons. The experimental results revealed that the chloroform extracts of leaves and bark of plants during winter season were most effective against S. flexneri with highest zone of inhibition (ZOI) of 19.5±0.12mm and 22.6 ±0.32mm at 4 mg/40 μμl, respectively. However, MIC of leaf and bark extracts in case of S. flexneri were 0.3125 mg/100 μl and 0.0781 mg/100 μl, respectively. Phytochemical analysis of H. integrifolia confirmed significant seasonal variation, with phenols, flavonoids and terpenoids highest in the winter season, while alkaloids dominated in autumn season. The chloroform extract of H. integrifolia leaves and bark exhibited highest antioxidant activity in DPPH assay (78.81±0.12% & 81.41±0.24%) followed by H2O2 and phosphomolybdenum at 300μg/ml conc. respectively. The results of the present work revealed that the bark of H. integrifolia during winter season exhibited better antimicrobial activity than the leaves, providing a valuable basis for the future efforts in developing novel herbal drugs.

Antibacterial Activity of Endophytic Fungi Isolate from Bidara Plant (Ziziphus mauritiana Lam.) Against Bacteria That Cause Digestive Infections by Agar Diffusion Method

Isolates of endophytic fungi coded IFAZ-6 derived from bidara plants (Ziziphus mauritiana Lam) has antibacterial abilities. This study determine whether those isolates has antibacterial activity against bacteria Escherichia coli. Isolates of endophytic fungi were purified and fermented for 21 days and the fermentation results were extracted using ethyl acetate solvent. The ethyl acetate extract obtained was carried out with a minimum inhibitory concentration (MIC) and a minimum bactericidal concentration (MBC) as well as activity tests with the agar diffusion method. From the test results, statistical tests were carried out, the highest concentration IFAZ-6 isolate extracts that has highest inhibitory zone was 300,000 ppm in E. coli bacteria but only significantly different to 200.000 ppm.

Studying the Antimicrobial Effects of Silver Nanoparticles Coated with Alginate Biosynthesized by Dulcicalothrix alborzica

Introduction: Nowadays, Cyanobacteria are one of the important candidates in the green biosynthesis of nanoparticles. Considering the detrimental effects of chemically synthesized nanoparticles, the aim of this study was the biosynthesis and antimicrobial activity of nanoparticles by aquatic cyanobacterium. Methods: Silver nanoparticles (AgNPs) were biosynthesized using three different approaches: wet biomass, boiling, and extracellular polysaccharides (EPS). Alginate coating was employed to enhance the nanoparticles' stability. Characterization of the nanoparticles was performed using UV-vis spectroscopy, Fourier transform infrared (FTIR) analysis, scanning electron microscopy (SEM), transmission electron microscopy (TEM), and zeta potential measurements. The antimicrobial properties of the nanoparticles were evaluated against fish pathogenic bacteria and fungi. Statistical analyzes were performed with SPSS version 16 software, and the significant difference between the means was performed with one-way analysis of variance with 95% confidence limits and Tukey's test, and the results were drawn as a graph with Excel software. Results: The UV-vis spectroscopy results confirmed the synthesis of AgNPs in all three methods. FTIR analysis revealed similar spectra for all three methods, indicating comparable purity and production of similar compounds. Electron microscope images showed the sphericity of nanoparticles prepared by boiling method, and the average diameter of uncoated and alginate coated nanoparticles was 38 and 180.04 nm, respectively. Zeta potential analysis indicated a positive surface charge on the nanoparticles. The highest zone of inhibition was observed for AgNPs synthesized by the boiling method and coated with alginate. Similar results were obtained for the antifungal activity, with Saprolegnia exhibiting higher sensitivity to the synthesized nanoparticles compared to the other species studied. Conclusion: The novel strain Dulcicalothrix alborzica demonstrated potential as a potent producer of AgNPs with unique properties and promising applications in microbial biotechnology.

Bioengineering of glucan coated silver nanoparticles as dynamic biomedical compound; in vitro and in vivo studies

The use of silver nanoparticles (AgNPs) gaining importance for the treatment of microbial infections and are in great demand due to their efficient broad antibacterial action but there is only one problem that silver nanoparticles can cause tissue damage. Therefore, the present study evaluated antimicrobial potential and intricacy of glucan coated silver nanoparticles in comparison with free silver nanoparticles. In this study, glucan coated silver nanoparticles (Glucan-AgNPs) by using Pleurotus spps. were characterized for their antimicrobial, minimum inhibitory concentration (MIC), biofilm inhibition, mutagenicity potential, hemolytic activities and histological examination through in vitro and in vivo analysis. The liver, kidney, intestine, and skin tissues were examined to gauge the adverse effects of the treatment method's toxicity by silver deposition. The results of this study have shown that mushroom's glucan extracted from Pleurotus spps. are excellent reducing agent and due to their best capping ability they reduce the toxicity of AgNPs and enhance their antimicrobial activities. The highest zone of inhibition was observed by Glucan-AgNPs from P. ostreatus (24 mm) against S. aureus while least zone of inhibition was resulted from Glucan-AgNPs from P. sapidus (14 mm) against B. subtilis. The results for biofilm inhibition showed excellent biofilm inhibition ability of Glucan-AgNPs. In results, maximum inhibition 95.2 % was observed by Glucan-AgNPs from P. ostreatus against S. aureus, while minimum inhibition 79.2 % by Glucan-AgNPs of P. sapidus against E. coli. Furthermore, Glucan-AgNPs treated mice showed no deposition and damage in the organs. Glucan-AgNPs has a higher efficacy in treating microbial infection.

Green synthesis, characterization and antibacterial evaluation of ZnO and Ag-doped ZnO nanoparticles using Ruta chalepensis leaf extract

ABSTRACT In this study, a facile, green, and eco-friendly approach was followed for the synthesis of zinc oxide (ZnO), Ag-doped ZnO nanoparticles (NPs) using Ruta chalepensis leaf extract. The biosynthesized nanoparticles were characterized by X-ray diffraction (X-RD), Fourier transform infrared spectroscopy (FT-IR), energy dispersive X-ray (EDX), and ultraviolet–visible spectroscopy (UV-Vis). The UV-Vis absorbance peaks for ZnO, 5%, and 7% Ag-doped ZnO NPs were 357, 360, and 364 nm, with band gaps of 3.00, 2.73, and 2.83 eV, respectively. The XRD data showed average crystalline sizes of ZnO, 5% Ag-doped ZnO, and 7% Ag-doped ZnO NPs were 13.82, 27.50, and 25.92 nm, respectively. The presence of a functional group was confirmed by FTIR spectrum. The improved antibacterial activity of Ag-doped ZnO NPs was due to Reactive Oxygen Species (ROS) formation. The higher zone of inhibition was observed in S. aureus and B. cereus (11 ± 1.0 and 12.33 ± 0.57 mm, respectively), by 7% Ag-doped ZnO NPs. Our finding showed that synthesized Ag-doped ZnO NPs possessed good antibacterial activity as compared to pure ZnO NPs. Hence, the designed plant leaf mediated Ag-doped ZnO NPs synthesis has provided avenues for the enhancement of the high efficiency of its antibacterial activity, this makes the study unique.

Arisarum vulgare: Bridging Tradition and Science Through Phytochemical Characterization and Exploring Therapeutic Potential via In vitro, In vivo, and In silico Biological Activities

AbstractArisarum vulgare O. Targ. Tozz. (Araceae), locally known as “Elbgouga,” holds significant traditional importance in Algeria for the treatment of various human ailments, including pain, infections, inflammation, digestive disorders, cancer, skin problems, eczema, wounds, and burns. The aim of this study was to explore for the first time the phytochemical profile, antioxidant, antibacterial, and inhibitory effects on acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) enzymes, DNA protection, and capacity to promote wound healing. Preliminary phytochemical experiments were conducted to evaluate the major classes of bioactive compounds, in addition to the total phenol and flavonoid amounts in AVEE. An LC‐MS/MS analysis was conducted to clarify the phytochemical composition of this particular botanical species. The antioxidant capacity was assessed using DPPH· and ABTS·+ radical scavenging tests. The agar diffusion approach was used to ascertain the antibacterial efficacy against four bacteria (Staphylococcus aureus, Enterococcus faecium, Escherichia coli, and Salmonella typhimurium). Cholinesterase inhibition was evaluated using a colorimetric method that relies on Ellman's reaction. The protective effects of AVEE on pBR322 plasmid DNA damaged by H2O2 and UV treatment were assessed by their DNA‐breaking forms. The in vivo acute dermal toxicity and wound healing potential of the AVEE ointment (1–5% AVEO) were also investigated, and histological analyses were carried out on biological samples. Five protein targets were the subject of an in silico molecular docking investigation (TNFα, TGFBR1, IL‐1ß, GSK‐3ß, and NOS) and ADMET studies of the main components of the extracts were performed. The screening of phytochemicals revealed a significant concentration of phenolic compounds (176.00 ± 1.08 mg of gallic acid equivalents/g of dry extract), mainly flavonoids (81.21 ± 1.24 mg of quercetin equivalents/g of dry extract). Three major compounds were identified by LC‐MS/MS analysis, belonging mainly to the class of flavonoids, with rutin as the most abundant compound (11.85 mg/g extract), followed by hesperidin (4.125 mg/g extract). A conspicuous presence of isoquercitrin (1.327 mg/g extract) was also found. Small amounts of flavonoids and phenolic acids were also detected (catechin, chlorogenic acid, syringic acid, salicylic acid, kaempferol, and luteolin). DPPH assay showed higher antioxidant capacity compared to the ABTS·+ assay (142.60 ± 5.52 µg/mL and 236.10 ± 0.22 µg/mL, respectively). AVEE was effective against all selected bacterial strains; however, the highest zone of inhibition (36.00 ± 0.1 mm) was noted against E. faecium. The extract of the plant significantly inhibited both AChE and BChE (89.98 ± 18.76 µg/mL inhibitory activity against AChE and 98.28 ± 44.68 µg/mL inhibitory activity against BChE, respectively). The ethanolic extract of A. vulgare and quercetin exhibited more significant DNA protection action in form I, with percentages of 90.41 and 94.23%, respectively, compared to form II, where the percentages were 27.91 and 51.92%, respectively. The AVEO formulation may be safely administered by topical application. A statistically significant wound contraction was discovered in the group treated with 5% AVEO compared to the groups that were not treated or treated with petroleum jelly. Furthermore, there was no notable disparity detected between the group treated with 5% AVEO and the group treated with the reference drug. The 5% AVEO‐treated group showed, after the research was complete, the most significant percentage of wound contraction (96.90 ± 0.42%). Moreover, the topical application of the formulation improved histological parameters. In silico study showed that rutin, hesperidin, and isoquercitrin had a high affinity to the five main targets that might contribute to the wound healing potential of A. vulgare ethanolic extract. The impressive biological capabilities of A. vulgare indicate that the plant has the ability to be a valuable source of bioactive chemicals with various medical applications.

Synthesis, characterization, DFT computational studies and biological activity of transition metal complexes derived from 4-(((6-nitrobenzo[d]thiazol-2-yl)imino)methyl)benzene-1,3-diol

A series of Co(II), Ni(II), Cu(II), Zn(II) complexes have been synthesized with a benzothiazole azo dye containing tridentate (NNO) donor ligand 4-(((6-nitrobenzo[d]thiazol-2-yl)imino)methyl)benzene-1,3-diol derived from 2-amino-6-nitrobenzothiazole and 2,4-dihydroxybenzaldehyde. The structures of the novel ligand and metal complexes were identified and confirmed via various spectroscopic techniques (FT-IR,1H NMR,13C NMR, UV-Vis, mass spectrometry), TGA-DTA, powder X-ray diffraction, and DFT calculations. The optimal structural parameters and chemical reactivity of the ligand and metal complexes have been investigated using Density Functional Theory calculations (DFT/B3LYP,6-31G** and LanL2DZ basis sets) to provide insight about their frontier molecular orbitals (FMO) and molecular electrostatic potential (MESP). In vitro DPPH radical scavenging techniques have been used to assess the antioxidant activity of the ligand and complexes, indicating good antioxidant activity. The Ni(II) complex was the most potent with the lowest IC50 values. The in vitro antibacterial activities have been explored by screening against bacteria (Bacillus subtilis) and bacteria (E. coli) exhibiting significant activity against the tested strains of bacteria with Zn(II) complex as most potent with the lowest MIC value against E. coli and B. subtilis) and highest zone of inhibition against E. coli and B. subtilis at 1000 μg/mL concentration). The antifungal activity of complexes against Aspergillus niger and Candida albicans indicate that the Co(II) complex is most active for C. albicans and Zn(II) complex for A. niger .

Physicochemical and phytochemical analysis of three melon fruit (canary melon, watermelon, and muskmelon) peels, and their valorization in biscuits development

IntroductionMelons are highly sought after worldwide due to their exquisite and delectable taste. However, the peels of these fruits, which are rich in phytochemicals and sustainable components for innovative culinary formulations, are often discarded as waste.MethodsThis study explored the phytochemistry and valorization of three melon fruit, i.e., canary melon (Cucumis melo, var. Fonzy), watermelon (Citrullus lanatus, var. Augusta), and muskmelon (Cucumis melo, var. Cantaloupe), peels in food applications by incorporating into wheat flour biscuits. Peels of fruits were separated, dried and powders were extracted with 70% ethanol.Results and discussionComparing the muskmelon fruit peel to the peels of the other two fruits, the muskmelon fruit peel had the significantly (p < 0.05) high ash (8.36%), fiber (12.06%), fat (1.21%), protein (5.02%), mineral contents (Mg 233, Ca 364, K 1605, Fe 49.72, and Zn 2.39 mg/100 g), total phenolic content (167.49 mg GAE/100 g), total flavonoid content (79.16 mg QE/100 g) and total antioxidant activity (56.92 mg Trolox equivalent/100 g). Results of the antimicrobial experiments of three melon peels showed that extracts from all peels showed enough antimicrobial activities, nearly comparable to the reference drugs (ampicillin and nystatin), which still showed the highest inhibition zones. Among three extracts, highest zone of inhibition against three bacterial species, i.e., Bacillus cereus (12.03 mm), Escherichia coli (10.02 mm), and Streptococcus aureus (18.08 mm), and fungal species, i.e., Candida albicans (8.09 mm), Aspergillus niger (7.06 mm), and Mucor meihi (7.02 mm) was exhibited by muskmelon peel extract. Moisture, ash, fat, fiber, minerals, phenolics, flavonoids, and antioxidant activities of biscuits were increased as a result of incorporating peel flours. Correlation showed TPC and TAA were highly correlated in watermelon (10%; 1). Using principal component analysis, adding 5% canary watermelon peel powder to biscuits improved their healthful and active elements while maintaining sensory features. Baking with 10% muskmelon or watermelon peel powder boosted nutrition and antioxidant activity. After the control, biscuits fortified with 5% melon peel powder exhibited significantly (p < 0.05) high sensory scores. These findings highlight the value of melon peels as sustainable ingredients, promoting waste reduction and enhancing the dietary and functional benefits of food products.

Antimicrobial and Antioxidant Activities of 18β-Glycyrrhetinic Acid Biotransformed by Aspergillus niger

The search for novel plant-based antioxidant and antibacterial medication has garnered a lot of attention lately. Glycyrrhiza glabra, known as licorice, is one of the most important medicinal plants. The primary component of Glycyrrhiza glabra is glycyrrhizin, which is biotransformed into 18α- and 18β-glycyrrhetinic acid for a variety of medicinal purposes. The goal of this study was to improve the bioavailability of glycyrrhizin by its biotransformation into glycyrrhetinic acid by Aspergillus niger. The biotransformation process was optimized using response surface methodology. A two-level Plackett–Burman design was employed to identify the factors that had a significant impact on the process of biotransformation. The three main variables were pH, glycerrhizin concentration, and incubation time. These three medium components were further optimized using a 3-level Box–Behnken design, and their optimum levels were pH of 8, an incubation period of 6 days, and a glycyrrhizin concentration of 1%. Using these optimum conditions, the maximum level obtained was 159% greater than in the screening experiment. Regarding the antimicrobial activity of glycyrrhizin extract, Bacillus subtilis emerged as the most sensitive organism with the lowest MIC (60 µg/mL) and the highest zone of inhibition (17 mm). The most resistant organism was Pseudomonas aeruginosa, which had the highest MIC (400 µg/mL) and the smallest zone of inhibition (10 mm). In the case of glycyrrhetinic acid, Bacillus subtilis was the most sensitive organism with the highest zone of inhibition (32 mm) and the lowest MIC (20 µg/mL). Pseudomonas aeruginosa was the most resistant organism, with the lowest zone of inhibition (18 mm), and the highest MIC (140 µg/mL). The antioxidant activity of glycyrrhizin extract increased from 12.81% at a concentration of 63 µg/100 µL to 41.41% at a concentration of 1000 µg/100 µL, while that of glycyrrhetinic acid extract increased from 35.5% at a concentration of 63 µg/100 µL to 76.85% at a concentration of 1000 µg/100 µL. The present study concluded that biotransformation of glycyrrhizin into glycyrrhetinic acid increased its bioavailability and antioxidant and antimicrobial activities. Glycyrrhizin and glycyrrhetinic acid might be used as a natural antimicrobial and antioxidant in pharmaceutical industries

Antimicrobial Properties of Newer Calcium Silicate-Based Pulp-Capping Agents Against Enterococcus Faecalis and Streptococcus Mutans: An In-Vitro Evaluation.

This study aimed to evaluate the antibacterial activity of calcium silicate-based pulp-capping agents against Enterococcus faecalis and Streptococcus mutans using an agar diffusion test. The agar diffusion method was used to evaluate the antibacterial properties of pulp-capping agents. The materials used included Bio-C® Temp (Angelus, Brazil), Dia-Root™ Bio mineral trioxide aggregate (MTA) (Diadent Europe B.V., Almere, Netherlands), Biodentine™ (Septodont, Saint-Maur-des-Fossés, France), and TheraCal LC (Bisco Inc., Schaumburg, IL). Eighteen petri dishes, nine for S. mutans and nine for E. faecalis, were divided into four parts each (one for each agent), for a total sample size of 72. The bacterial suspensions were transferred to the petri dishes using a sterile swab. Four wells with a diameter of 4 mm were then punched in each petri dish. The wells were filled with the pulp-capping agents, which had been mixed according to the manufacturer's instructions, and the petri dishes were incubated. The zone of inhibition was measured at 24 and 48 hours to assess the pulp-capping agents' antimicrobial efficacy against E. faecalis and S. mutans. The readings were tabulated and subjected to statistical analysis. At 24 hours, the highest zone of inhibition was found in the Biodentine™ group (15.83 ± 0.79 mm), followed by Dia-Root™ Bio MTA (14.5 ± 0.88 mm), TheraCal LC® (12.56 ± 0.53 mm), and the shortest in the Bio-C Temp (9.61 ± 0.70 mm) against S. mutans. Analysis of variance (ANOVA) test showed a high statistical significance. After 48 hours, there was no statistically significant difference in the mean zone of inhibition. At 24 hours, the highest zone of inhibition was found in the Biodentine™ group (20.56 ± 0.73 mm), followed by Dia-Root™ Bio MTA (20.06 ± 1.33 mm), TheraCal LC® (18.22 ± 0.97 mm), and the shortest in the Bio-C Temp (14.11 ± 0.78 mm) against E. faecalis. The ANOVA test indicated no statistically significant difference between the Biodentine™ and the Dia-Root™ Bio MTA groups. After 48 hours, there was no statistically significant difference in the mean zone of inhibition. Biodentine™ has higher antibacterial efficacy against S. mutans, while Biodentine™ and Dia-Root™ Bio MTA have comparably high antibacterial activity against S. mutans and E. faecalis at 24 and 48 hours.

Screening of Extract Secondary Metabolites of Bacteria Which Have Symbiosis with Sponges from Central Tapanuli Bakar Island as an Antibacteria

This study aims to determine the presence of antibacterial-producing bacteria from sponges from Bakar Island, Central Tapanuli Regency and to determine the antibacterial activity of methanol extracts from potential bacterial isolates against Staphylococcus aureus and Escherichiacoli. 21 pure isolates were found and it was known that 9 isolates produced antibacterial against S. aureus and 4 isolates against E. coli. Bacterial isolates with the highest inhibition zone against bothS.aureus and E. coli were found in isolates with code SP20 with each large inhibition zone are 14.5 mm and 16.04 mm. Then microscopic observations were carried out, namely gram staining and were obtained 8 isolates were gram positive, and 1 gram was negative. The biochemical test showed that SP20 showed positive results for the Motility, TSIA and Catalase Test but negative for Citrate Test. Bacterial isolates withthe code SP20 had the largest inhibition zone so that these isolates were to be extracted.The resultsof the screening test showed that the secondary metabolitesof the sponge symbiont bacterial extract from Bakar Island were positive for flavonoids and saponins. And then test the activity of secondary metabolites with 3 concentrations, 10%, 20%, and 30%.The results showed that the best concentration of the test bacteria was S. aureus at a concentration of 30% with an inhibition zone of 3.08 mm and E. coli at 5.04 mm.

Silver nanoparticles mediated apoptosis and cell cycle arrest in lung cancer A549.

The present study was aimed to synthesize the silver nanoparticles from Alangium salvifolium Wang. and evaluating its biomedical applications. The leaves of A. salvifolium collected and subjected for the standard procedure of Soxhlet extraction using distilled water as a solvent. With the help of an aqueous extract AgNPs were synthesized from silver nitrate using phyto-reduction method. Further, synthesized AgNPs were characterized using several analytical techniques such as UV, FTIR, SEM-EDX, XRD, particles size and zeta potential. Synthesized AgNPs were tested for antibacterial, antioxidant, anticancer for lung cancer cell line and flowcytometry-based pathway studies. The visual observation confirmed the formation of AgNPs from the aqueous extract by changing yellow to brown colour formation. Further, characterization techniques also confirmed the formation of AgNPs. Antibacterial activity results showed that the tested AgNPs were potent against bacterial pathogens with a higher zone of inhibition. Further, the antioxidant and anticancer activity of AgNPs revealed that the AgNPs have exhibited significant results with a good percentage of inhibition. Further, the flow cytometry studies confirmed that the AgNPs inducing apoptosis and cell cycle arrest in lung cancer. The phytochemicals of A. salvifolium plant have successfully synthesized AgNPs. In the case of performed biological activity, the synthesized silver nanoparticles exhibited potent activity. In future these AgNPs can be taken for molecular and in vivo studies to identify their efficacy using in vivo and molecular models.

Green synthesis of Titanium dioxide nanoparticle using combination of plants and its antimicrobial study with their characterization

Abstract The characteristics and biological qualities of the nanomaterial rely heavily on how it was made. Green nanoparticle production has been developed to minimize pollution, cut expenses, and enhance safety for both human health and the environment by reducing metal ions using plant extracts as opposed to industrial chemical agents. The goal of the current work is to synthesize titanium dioxide nanoparticles in an environmentally friendly manner by using an extract from the combined shells of Stone apples (Aegle marmelos) and Wood apples (Limonia acidissima). Titanium dioxide nanoparticle formation was verified using various characterization techniques. Well diffusion was used to measure the antimicrobial activity. The fungal strains that were employed were Aspergillus Niger, Candida Albicans, and Aspergillus Flavus. All fungul strains were successfully inhibited by both the crudely prepared extract and the biosynthesized titanium dioxide nanoparticles; however, the biosynthesized titanium dioxide nanoparticles exhibited a high zone of inhibition ranging from 25 to 30 mm, while the crudely prepared extract had a low zone of inhibition ranging from 13 to 19 mm. A moderately sized zone of inhibition was observed in both the crude produced extract and the biosynthesized Titanium dioxide nanoparticles at a dilution of 100 μg/ml. Lower dilutions demonstrated less noticeable inhibition. Overall, these results showed that treatment with biosynthesized titanium dioxide nanoparticles significantly slowed the growth of many microorganisms.

Wild chamomile essential oils bioactivity at different locations in sulaimani region, Iraq

This study was conducted to evaluate the bioactivity of wild chamomile (Matricaria chamomile L.), in response to different elevations flower samples at full blooming. The analysis of chamomile flower essential oils (EOs) through GC-MS identified the predominant abundance of terpenoids including Bisabolol oxides, farnesene, and Azulen, constituting 61.765% of the identified compounds across various locations. The highest concentration was 74.554% out of the total components observed at Kanipanka, while it was the minimum (16.414%) at the Qaradagh location. Oppositely the highest concentration of Farnasene was observed at the Qaradagh location, while the lowest concentration occurred with the essential oil of Kanipanka.α-Bisabolol oxide A% dominates, except in the Qara Dagh location. The best antioxidant concentration was found in Sharbazher essential oil. The essential oil in Sharbazher significantly shows the highest inhibition capacity (IC%). The stronger IC50% value was 64.645 µg mL-1, recorded at the Qara Dagh location. The disc diffusion assay revealed that the activity of chamomile essential oil at various locations significantly affected the death of most bacterial strains (Gram-negative and Gram-positive). Chamomile EOs from the Kanipanka location recorded maximum antibacterial activity on Pseudomonas aeruginosaPenjween EOs observed the maximum antibacterial activity against Staphylococcus haemolyticus, while a high level inhibition zone (IZ) against Enterococcus faecalis was observed in Bakrajo. The finding revealed that the highest MIC and MBC against Pseudomonas aeruginosa were achieved with the concentration of 2.5 µg mL-1 of Kanipanka EOs.

Antioxidant, Antibacterial and Immunomodulatory Properties of Algerian Phoenix dactylifera

The aim of the current study is to evaluate the antioxidant, antibacterial, and phagocytic activities of the hydroethanolic extract of Phoenix dactylifera fruit variety Mech degla. The antioxidant activity was determined through DPPH assay, ferrous ions chelating assay, and CUPRAC assay. The antibacterial activity against four bacteria (Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus, and Streptococcus pneumoniae), was evaluated using the disc diffusion method, while the in vivo phagocytic activity was measured using carbon clearance method. The results showed that the extract exhibited good antioxidant activity with the IC50 values of 0.89 ± 0.3 g/l and 0.56 ± 0.24 g/l for DPPH and ferrous ions chelating activities, respectively, and the A0.5 value of 1.45 ± 0.15 g/l in the CUPRAC assay. Moreover, the extract showed notable antibacterial activity against all tested strains with the highest zone of inhibition (23.3 ± 0.3 mm) against S. pneumonia. Besides the extract did not show any significant toxicity, it was able to stimulate the phagocytic activity with a significantly faster carbon clearance rate at the dose of up to 100 mg/kg compared to the control group. Our results suggested that the Phoenix dactylifera fruit represents a promising source for the development of safe and effective immunomodulators as remedies to prevent and treat various microbial and immune-related diseases.

Silver Nanoparticles Loaded with Bark Extract of Sterculia foetida: Their Green Synthesis, Characterization, and Anti-bacterial Activity Evaluation

Sterculia foetida is a subject of interest in many scientific fields as researchers look for novel treatments because of its varied medicinal qualities and chemical richness. Terpenoids are aromatic and aliphatic chemicals with anti-bacterial properties and can prevent free radical damage. They are present in S. foetida extract. Moreover, it possesses immunomodulatory, hepatoprotective, antiviral, antioxidant, anti-inflammatory, and antifungal properties. This work aims to green synthesize, characterize, and evaluate the anti-bacterial activity of Sterculia foetida bark extract-loaded silver nanoparticles. Chemicals like Methanol, Petroleum Ether, and water have been used to extract the phytoconstituents from the plant bark. AgNO3 and Silver have been used to synthesize the nanoparticles. Instruments like ATR-IR Spectrophotometer, UV- spectrophotometer, DLS, and SEM instruments have been used to characterize the nanoparticles. Bacterial strains like Staphylococcus aureus (ATCC-6538), Escherichia coli (ATCC 25922), saline water, AMX30, swab stick, inoculation loop, susceptibility scale have been used for studying the anti-bacterial activity. DLS and zeta potential analysis demonstrated the creation of stable nanoparticles with a particle size of 79 nm. The anti-bacterial activity of AgNPs with the methanolic bark extract showed significant anti-bacterial activity compared to the standard marketed drug AMX30. The highest zone of inhibition was observed against gram-positive bacteria S.aureus (1.68 cm) and gram-negative bacteria E.coli (1.74 cm), respectively, at 500 μg/ml concentration. The study concludes that greenly synthesized S. foetida bark extract containing nanoparticles is a potential anti-bacterial agent, especially against gram-negative bacteria. Further, in vivo studies are needed to establish its potential. Keywords: Sterculia foetida, Green synthesis, Silver Nanoparticles (AgNPs), ATR-IR, DLS, SEM, Zeta-potential, Anti-bacterial.

Phenolic components from carrot (Daucus carota L.) pomace: Optimizing the extraction and assessing its potential antioxidant and antimicrobial activities

Carrot pomace is a significant agricultural byproduct. Obtained during carrot juice processing. This residue is an appropriate reservoir of constituents with bioactive properties that could be investigated in the development of food constituents and nutritional supplements and in improving the quality and safety of foods. For this purpose, the objective of the present investigation was to extract the polyphenols from carrot pomace utilizing maceration and ultrasound-based extraction (UAE) procedures and to evaluate the antioxidant properties of phenolic constituents. To maximize the extraction of carrot pomace, a response surface approach was used. The optimal mixture of extraction time (A, min), ultrasonication power (B, w), and solvent type (C, v/v) for the highest yield of carrot pomace was found using a three-variable composite rotatable design (CRD). In order to assess different functional groups, Fourier transform infrared spectroscopy was utilized to investigate the extract collected under optimal circumstances. The highest polyphenols (26.53 %) were extracted by ethanol 70 % at 10 min with a sonication power of 250 w. The optimized extract also exhibited significant antioxidant and antimicrobial functions. The total phenolic compounds and scavenging of the DPPH radical were 85 mg GAE/gr and EC50: 55 ± 1 μg/mL, respectively. Together with Staphylococcus aureus, the highest zone of inhibition (12 mm) was identified. Our finding revealed that carrot pomace is an appropriate source of bioactive phenolic constituents, exhibiting antioxidant and antibacterial attributes, and could be applied as a natural preserver for promoting safety and quality properties in food products on an industrial scale.

Antibacterial and antibiofilm effect of Zinc Oxide nanoparticles on P. aeruginosa variants isolated from young patients with cystic fibrosis

BackgroundP. aeruginosa, a biofilm-forming bacteria, is the main cause of pulmonary infection in CF patients. We applied ZnO-np as a therapeutic agent for eradicating multi-drug resistance and biofilm-forming P. aeruginosa isolated from young CF patients. MethodsA total of 73 throat and sputum samples taken from young CF patients were inquired. ZnO-np was synthesized and characterized in terms of size, shape, and structure for anti-bacterial activity. The antibiotic susceptibility of isolates before and after the addition of 16 μg/ml of ZnO was evaluated using disc diffusion and microtiter methods, respectively. The gene expression level of QS genes was assessed after treatment with 16 μg/ml ZnO-np. ResultsThe optimum concentration of ZnO-np with a higher inhibitory zone was 16 μg/ml (MIC) and 32 μg/ml (MBC). All isolates were resistant to applied antibiotics, and about 45 % of isolates were strong biofilm-forming bacteria. After treatment with 16 μg/ml ZnO-np, all strains became susceptible to the applied antibiotic except for amikacin, which confers an intermediate pattern. About 63 % and 20 % of isolates were, respectively, non-biofilm and weak biofilm-forming bacteria following the addition of ZnO-np. Relative gene expression of gacA, lasR, and rhlR genes were downregulated significantly (P < 0.001). Although the retS did not have a significant reduction (P = 0.2) ConclusionZnO-np at a concentration of 16 μg/ml could significantly reduce the P. aeruginosa infection by altering the antibiotic susceptibility pattern and inhibiting biofilm formation. Due to their photocatalytic properties and their ability to penetrate the extracellular polysaccharide layer, ZnO nanoparticles can produce ROS, which increases their susceptibility to antibiotics. Nasal delivery of ZnO-np in the form of aerosol can be considered a potential strategy to decrease the mortality rate in CF patients at an early age.