Evaluation Of Antibacterial Activity Research Articles

Fabrication of large surface area/Microrose-shaped Manganese (II) coordination polymer for evaluation of molecular docking, antibacterial and antioxidant Activity

We report the fabrication of Mn (II) chelate or coordination polymer (CPs) via condensation method for antioxidant and antibacterial performances. Tremendous effort has been directed toward design a scaffold multidentate organic ligand framework. One of interesting chelating ligand viz. Sebacoyl bis(2-ethoxybenzamide) (sebebz) was fabricated by condensation of 2-ethoxybenzamide and sebasic acid. Further, the CPs was fabricated by condensation of sebacoyl bis(2-ethoxybenzamide) with metal ions. As-fabricated multidentate ligand was analyzed by several analytical methods for confirm structural backbone in term of chemical bonding, donor atoms and existence of functional groups. Moreover, CPs was analyzed by XRD, FTIR, Raman, EDX, XPS, DRS, BET, SEM, and TEM for authenticate its structure, crystallite size, chemical bonding, elemental existence, porosity, surface area, sizes, and shape. The SEM revealed microrose-shaped structure of CPs with diameter around 20–30 µm, while BET revealed large surface area material (801 m2/g). Due to scaffold structure and effective functional group in CPs, it's molecular docking was evaluated for the purpose of microbial assay. The antimicrobial clinical assay of CPs was assessed against B. subtilis, S. aureus, K. pneumoniae and E. Coli. Also, α, α-diphenyl-β-picrylhydrazyl was used to evaluate antioxidant property of CPs in ethanolic and methanolic solvent.

In vitro and in vivo evaluation of antibacterial activity and mechanism of luteolin from Humulus scandens against Escherichia coli from chicken

Resistance of Escherichia coli (E.coli) to antibiotics has steadily increased over time; hence, there is an urgent need to develop safer alternatives to antibiotics. The present study aimed to evaluate the effect of luteolin (Lut) on E. coli from chicken. The bioactive compound Lut from Humulus scandens was selected by network pharmacology and molecular docking analyses. Scanning electron microscopy (SEM), transmission electron microscopy (TEM), and confocal laser scanning microscopy (CLSM) were used to observe the effects of Lut on the morphology and structure of E. coli cells. The data-independent acquisition (DIA) method was used to analyze protein expression level of E. coli before and after Lut treatment. The in vivo evaluation of the antibacterial, anti-inflammatory, and oxidative effects of Lut on E.coli was conducted using E.coli isolated strains infected the SPF chicken model. The network pharmacology analysis revealed 19 distinctive bioactive compounds such as Lut and β-sitosterol in H. scandens; furthermore, 30 core targets were selected from H. scandens. The KEGG enrichment analysis showed that the PI3K-Akt, TNF, MAPK, IL-17, JAK-STAT, and HIF-1 pathways were related from H. scandens. Based on the results of the network pharmacology analysis, Lut was subjected to screening by molecular docking analysis to determine its antibacterial effect on E. coli and the associated mechanism of action. The minimum inhibitory concentration (MIC) of Lut against E. coli standard strains was 500 µg/mL. SEM, TEM, and CLSM results indicated that Lut damaged the cell wall and cell membrane of E. coli strains and destroyed the cell structure, leading to cell death.The expression level of membrane structure, Phenylalanine metabolism and some other metabolic pathways in E.coli changed after treatment with Lut (P < 0.05). In vivo experiments in the SPF chicken model showed that Lut treatment alleviated the decline in the growth performance of chickens (P < 0.05), prevented pathological changes in the correspond ding organs and suppressed the inflammatory response induced by E. coli infection (P < 0.05), improved the immunity and antioxidant capacity of chickens (P < 0.05), and protected them against infection with E. coli strains. To summarize, Lut from H. scandens can inhibit E. coli growth by damaging the cell membrane structureand affecting the expression level of some metabolic proteins. In vivo experiments also showed that Lut can significantly reduce the damage caused by E. coli isolates on SPF chickens, improve their antioxidant capacity and immunity, and reduce inflammatory responses following E. coli infection.

Evaluation of anti-diabetic, anti-oxidant and anti-bacterial activities of essential oil collected from wildly growing Calotropis gigantea (Linn.) Aiton f. and its therapeutic applications: insights from chemical profiling, in-vitro and in-silico studies

Calotropis gigantea, often known as giant milkweed, the plant is widely known for producing herbal essential oils that are used as traditional and complementary medicine to cure various ailments. The aim of the present study was evaluation of anti-diabetic, anti-oxidant and anti-bacterial activities of essential oil collected from wildly growing Calotropis gigantea and its its therapeutic applications via chemical profiling, in-vitro and in-silico studies. After Calotropis gigantea (CEO) essential oil was extracted by hydro-distillation, its phytochemical, antioxidant, antibacterial, and anti-diabetic properties were assessed. Fingerprint analysis and GC-FID were used to create a chemical profile. Various tests for antioxidants, such as DPPH, nitric oxide radical, and iron chelating activity, were conducted. The disk diffusion approach was used for antibacterial efficacy against Gram-negative (G-) bacteria. The test of α-amylase inhibition was utilized to investigate anti-diabetic efficacy. In-silico analysis was also conducted to find out interaction of some components to α-amylase enzyme. Chemical profiling indicated the presence of phytol (24%), stearic acid (10%), and cyclohexyl ketone (6%), as predominant components. There was notable antioxidant activity ranged from 82 to 97% for various assays. IC50 values for various assays were iron chelating activity: 18.610, DPPH scavenging activity: 28.246, nitric oxide radical scavenging activity: 58.113. CEO showed a zone of inhibition value of 0.5 cm and significant antibacterial activity against Gram-negative (G-) bacteria. CEO blocked α-amylase in dose-dependent way. At a higher amount of 250 µl, CEO inhibition was 63% and mode of inhibition un-competitive. In-silico analysis validated the blocking of α-amylase and interaction of phytocomponents to α-amylase enzyme which were further validated by UV and fluorescent quenching techniques. It was determined that CEO may be extensively used in many different industries, including as food, herbal medicine, cosmetics.

Green synthesis of cerium oxide nanoparticles using Quercus infectoria: Characterization and evaluation of antibacterial and antioxidant activities

Cerium oxide nanoparticles (CNP) have gained attention for their unique physical, chemical, and biological properties. This study aims to synthesize CNPs using Quercus infectoria gall extract, and its active components mainly tannic acid (TA), and gallic acid (GA), and compare them with chemically synthesized CNPs. Green synthesis involved adding gall extract, TA, or GA solution to cerium nitrate hexahydrate, followed by reaction at 70 °C and calcination at 500 °C. Characterization employed various methods, including dynamic light scattering, scanning electron microscopy, X-ray diffraction, UV–Vis spectroscopy, and Fourier-transform infrared spectroscopy to respectively characterize hydrodynamic diameter, morphology, crystallinity and purity, and surface functional groups. Antibacterial and antioxidant properties were evaluated using the broth microdilution and DPPH radical scavenging methods, respectively.It confirmed successful synthesis of crystalline CNPs, with UV spectra exhibiting a peak at 290 nm. Antibacterial tests revealed that pre-calcined TA-synthesized NPs, at 25 mg ml−1, exhibited inhibitory properties against Staphylococcus aureus and Pseudomonas aeruginosa. CNPs synthesized with gall extract at 100 mg ml−1displayed antibacterial activities against Escherichia coli and S. aureus, while gall extract had highest efficacy on S. aureus with MIC of 1.875 mg ml−1. GA, TA, and gall extract demonstrated DPPH scavenging activities of 86 %, 59 %, and 66 % at 50 µg/ml, respectively. Antioxidant potential of CNPs at 1 mg ml−1was 19 %, 20 %, 21 %, and 17 % for GA, TA, gall extract, and chemically synthesized CNPs, respectively.In conclusion, CNPs synthesized in this study can be considered as antioxidants. Further investigation is needed to optimize synthesis methods and achieve desired antibacterial properties, given contradictory findings in prior studies.

Parmelia perlata mediated microwave-assisted one-pot green synthesis of NiO nanoparticles a noble approach: Antibacterial and photocatalytic activity evaluation

This study reports a green-mediated fabrication of NiO nanoparticles (NiO NPs) using Parmelia Perlata lichen extract as a sustainable source. The Physical, chemical, optical, and morphological behavior of the fabricated NiO NPs were analyzed by employing diverse analytical profiles like XRD, FTIR, UV, and SEM. FTIR spectrum demonstrates the involvement of various phytochemicals in the bio-fabrication of NiO NPs. Furthermore, the appearance of a band at 668 cm−1 indicates the successful formation of NiO NPs. The observations of the SEM analysis depicted that the average particle size was in the range of 40–50 nm. The result of the antibacterial study indicates that the NiO NPs significantly reduce the growth of Staphylococcus aureus (19 mm). The result of the photocatalytic research illustrated that the bio-fabricated NiO NPs exhibited superior photocatalytic activity in the degradation of acridine orange dye achieving 84 % degradation efficiency.

Antibacterial activity evaluation of a novel K3-specific phage against Acinetobacter baumannii and evidence for receptor-binding domain transfer across morphologies

Acinetobacter baumannii (A. baumannii) poses a serious public health challenge due to its notorious antimicrobial resistance, particularly carbapenem-resistant A. baumannii (CRAB). In this study, we isolated a virulent phage, named P1068, from medical wastewater capable of lysing CRAB, primarily targeting the K3 capsule type. Basic characterization showed that P1068 infected the A. baumannii ZWAb014 with an optimal MOI of 1, experienced a latent period of 10 ​min and maintained stability over a temperature range of 4–37 ​°C and pH range of 3–10. Phylogenetic and average nucleotide identity analyses indicate that P1068 can be classified as a novel species within the genus Obolenskvirus of the Caudoviricetes class as per the most recent virus classification released by the International Committee on Taxonomy of Viruses (ICTV). Additionally, according to classical morphological classification, P1068 is identified as a T4-like phage (Myoviridae). Interestingly, we found that the tail fiber protein (TFP) of P1068 shares 74% coverage and 88.99% identity with the TFP of a T7-like phage (Podoviridae), AbKT21phiIII (NC_048142.1). This finding suggests that the TFP gene of phages may undergo horizontal transfer across different genera and morphologies. In vitro antimicrobial assays showed that P1068 exhibited antimicrobial activity against A. baumannii in both biofilm and planktonic states. In mouse models of intraperitoneal infection, P1068 phage protected mice from A. baumannii infection and significantly reduced bacterial loads in various tissues such as the brain, blood, lung, spleen, and liver compared to controls. In conclusion, this study demonstrates that phage P1068 might be a potential candidate for the treatment of carbapenem-resistant and biofilm-forming A. baumannii infections, and expands the understanding of horizontal transfer of phage TFP genes.

Synthesis, molecular docking simulation, and antimicrobial activities of novel bis-heterocycles linked to piperazine and vanillin units as novel hybrid molecules via Hantzsch, Biginelli, and Michael’s reactions

Bacterial infections are a global issue, causing sickness and death, mainly in developing nations. Resistance to current medicines is a significant issue in healthcare. Overcoming the resistance problem will necessitate the development of molecules with novel modes of action that do not cross-react with existing medicines. Synthesis of new bis-heterocycles linked to the piperazine core and vanillin unit is disclosed in this regard. The target compounds were produced via the reaction of 4,4′-((piperazine-1,4-diylbis(2-oxoethane-2,1-diyl))bis(oxy))bis(3-methoxybenzaldehyde) with various reagents using the Hantzsch, Biginelli, and Michael’s reactions. All the generated compounds were tested for their antibacterial activity against a variety of bacterial strains. The antibacterial activity evaluations revealed that compound 32 has the most promising activity against Pseudomonas aeruginosa (19.5 ± 0.7 mm) compared to Ofloxacin (17 mm) with minimum inhibitory concentration (MIC) equaled to 625 µg/mL. A molecular docking investigation revealed that compound 32 had the greatest binding affinity for bacterial enoyl reductase (−36.13 ± 0.2 Kcal/mole) when compared to the co-crystallized ligand (−16.8 ± 0 Kcal/mole).

Evaluation of antibacterial activity and susceptibility antibiotics of native lactic acid bacteria from tilapia (Oreochromis niloticus) in Ivory Coast

Lactic Acid Bacteria probiotics play a crucial role in improving aquaculture productivity however, their use required beforehand a rigorous selection. This study appeared as a preliminary research in LAB potential probiotics selection. The aim of study was to select LAB strains potentially probiotic isolated from gut intestine of tilapia (Oreochromis niloticus) based on antibacterial activity and susceptibility antibiotics tests. The antibacterial activity was carried by agar well diffusion method against five pathogen indicators (E. coli ATCC 25922, K. pneumoniae ATCC 43816, P. aeruginosa ATCC 27853, P. mirabilis JCM1669, and S. aureus ATCC 25913). The susceptibility antibiotic test was performed by disc diffusion method by 12 antibiotics use. Seventy-two (72) from 154 LAB isolates completed the antibacterial activity test. With 79.08% inhibition, S. aureus was the pathogen most inhibited, whereas E. coli had the least inhibition, at 61.44%. In terms of antibiotic susceptibility testing, out of the 72 LAB isolates from earlier studies, only 25 LAB isolates demonstrated resistance to ciprofloxacin, gentamycin, and oxacillin and sensitivity to nine out of the twelve antibiotics employed. The 25 LAB isolates seemed suitable candidates for more probiotic tests.

Evaluation of Arabic gum antibacterial and wound healing activities against Staphylococcus aureus isolates obtained from skin infections

Evaluation of Arabic gum antibacterial and wound healing activities against Staphylococcus aureus isolates obtained from skin infections

Physico-Chemical Properties of Copper-Doped Hydroxyapatite Coatings Obtained by Vacuum Deposition Technique.

The hydroxyapatite and copper-doped hydroxyapatite coatings (Ca10-xCux(PO4)6(OH)2; xCu = 0, 0.03; HAp and 3CuHAp) were obtained by the vacuum deposition technique. Then, both coatings were analyzed by the X-ray diffraction (XRD), scanning electron microscopy (SEM), atomic force microscopy (AFM), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FTIR) and water contact angle techniques. Information regarding the in vitro antibacterial activity and biological evaluation were obtained. The XRD studies confirmed that the obtained thin films consist of a single phase associated with hydroxyapatite (HAp). The obtained 2D and 3D SEM images did not show cracks or other types of surface defects. The FTIR studies' results proved the presence of vibrational bands characteristic of the hydroxyapatite structure in the studied coating. Moreover, information regarding the HAp and 3CuHAp surface wettability was obtained by water contact angle measurements. The biocompatibility of the HAp and 3CuHAp coatings was evaluated using the HeLa and MG63 cell lines. The cytotoxicity evaluation of the coatings was performed by assessing the cell viability through the MTT assay after incubation with the HAp and 3CuHAp coatings for 24, 48, and 72 h. The results proved that the 3CuHAp coatings exhibited good biocompatible activity for all the tested intervals. The ability of Pseudomonas aeruginosa 27853 ATCC (P. aeruginosa) cells to adhere to and develop on the surface of the HAp and 3CuHAp coatings was investigated using AFM studies. The AFM studies revealed that the 3CuHAp coatings inhibited the formation of P. aeruginosa biofilms. The AFM data indicated that P. aeruginosa's attachment and development on the 3CuHAp coatings were significantly inhibited within the first 24 h. Both the 2D and 3D topographies showed a rapid decrease in attached bacterial cells over time, with a significant reduction observed after 72 h of exposure. Our studies suggest that 3CuHAp coatings could be suitable candidates for biomedical uses such as the development of new antimicrobial agents.

Fabrication of poly (1,4-phenylene ether ether sulfone) modified with MWCNTs/reduced (GO-oxSWCNTs) NCs for enhanced antimicrobial activities

Poly (1,4-phenylene ether ether sulfone) (PEES) is a commonly used polymer in membrane technology for water treatment applications such as water purification and blood dialyzing in hemodialysis. In this study, PEES was chemically modified by nitration, yielding nitrated Poly (1,4-phenylene ether ether sulfone) (NPEES). Following that, NPEES nanocomposites (NCs) comprise multi-walled carbon nanotubes (MWCNTs), and the process involved the synthesis of reduced graphene oxide-oxidized single-walled carbon nanotubes, abbreviated as reduced (GO-oxSWCNTs). Various characterization techniques were used on the created membranes, such as Fourier-transform infrared spectroscopy (AT-FTIR), X-ray diffraction (XRD), and scanning electron microscopy (SEM) with energy dispersive X-ray (EDX) analysis. All polymer nanocomposites were found to be amorphous, according to the XRD patterns. SEM scans revealed random crater-like features on the surface of NPEES, but MWCNTs and reduced (GO-oxSWCNTs) NCs were distributed evenly on the polymer surface. The primary goal of this study was to evaluate the antimicrobial activity of modified NPEES membranes against two Gram-positive bacteria, Staphylococcus aureus (S. aureus) and Bacillus subtilis (B. subtilis), two Gram-negative bacteria, Pseudomonas aeruginosa (P. aeruginosa) and Escherichia coli (E. coli), and a fungus, Candida albicans (C. albicans). All modified membranes, including NPEES, NPEES/MWCNTs NCs, and NPEES/MWCNTs/reduced (GO-oxSWCNTs) NCs, exhibited antibacterial activity against S. aureus and B. subtilis. Notably, when compared to NPEES/MWCNTs NCs and NPEES/MWCNTs/reduced (GO-oxSWCNTs) NCs, the NPEES membrane had higher antibacterial activity, generating a 12 mm inhibitory zone. Furthermore, molecular docking studies revealed a strong fit of the tested polymer nanocomposites into the DNA gyrase B active site (PDB ID: 4uro), which was consistent with the practical results of their antibacterial activity evaluation.

Utilizing Silk Sericin as a Biomaterial for Drug Encapsulation in a Hydrogel Matrix with Polycaprolactone: Formulation and Evaluation of Antibacterial Activity.

Hydrogels have emerged as a potential tool for enhancing bioavailability and regulating the controlled release of therapeutic agents. Owing to its excellent biocompatibility, silk sericin-based hydrogels have garnered interest in biomedical applications. This study focuses on synthesizing a soft hydrogel by blending silk sericin (SS) and polycaprolactone (PCL) at room temperature. The physicochemical characteristics of the hydrogels have been estimated by different analytical techniques such as UV-visible spectroscopy, Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), and scanning electron microscopy (SEM). The rheological studies demonstrate the non-Newtonian behavior of the hydrogels. Further, the porosity analysis indicates a commendable absorption capacity of the hydrogels. The swelling degree of the hydrogels has been checked in both distilled water and buffer solutions of different pHs (2-10). Moreover, the drug release profile of the hydrogels, using diclofenac sodium (DS) as a model drug, has revealed a substantial release of approximately 67% within the first 130 min with a drug encapsulation efficiency of 60.32%. Moreover, both the empty and the drug-loaded hydrogels have shown antibacterial properties against Gram-positive and Gram-negative bacteria, with the drug-loaded hydrogels displaying enhanced effectiveness. Additionally, the prepared hydrogels are biodegradable, demonstrating their future prospects in biomedical applications.

Synthesis, Characterization and Evaluation of Antibacterial activity of Amine-Boranes

Amine-Boranes (AB) are an elite class of reagent and belongs to the Borane-Lewis family, has found extensive use in chemical synthesis. Interesting aspect of AB reagents are to display chemo selectivity among the functional groups. The present investigation highlights on the innovative, green synthesis and characterization of the three of unique AB complexes, including triethylamine-borane (aliphatic), aniline-borane (aromatic), and (aromatic substituted) N,N-dimethylaniline-borane (DMAB) under an open air condition. The 11B NMR technique was used to characterize the synthesized AB reagents. The chemical shift values obtained were in accordance with the results of previous research studies, and it's interesting to note that there is a difference in 11B-NMR chemical shift values between the borane complexes of aromatic and aliphatic amines. The antibacterial efficacy of three AB reagents has been stated for the first instance by using disc diffusion method against four bacterial strains: Escherichia coli, Salmonella typhimurium, Pseudomonas aeruginosa, and Staphylococcus aureus. When compared to other AB complexes, the DMAB reagent demonstrated significant antibacterial properties against the four different bacterial species.

Formulation of mouth rinse from natural plant\'s leaf extract and evaluation of antibacterial activity

Herbal liquid formulations are the preparation for oral health related issues like toothache, swelling, redness, bacterial or fungal infection in mouth, tooth decay, bleeding gums, weakened gums, etc. Such preparation also improves gums strength, removing bad breath and give fresh feel during good start of the day. Dentists generally use such preparations as antimicrobials before or after oral surgery to sanitize the surface of affected gums and teeth to avoid further contamination. Herbs like Tulsi, Clove, Mint, Ginger etc., are generally used either alone or in combination in herbal mouth-wash preparations which also render antibacterial activities. The other herbs like Eucalyptus and Liquorices have been reported to possess antibacterial, anti-oxidant, aromatic, anti- inflammatory and sweetening properties. In the present work, the research continues with formulation and evaluation of a herbal mouth rinse by using a combination of selected herbal extracts of Tulsi, Bael, Eucalyptus leaves and Liquorices rhizome for their antimicrobial activity against S. aureus using agar well diffusion plate technique. It was found that the formulated herbal mouth rinse or preparations gave satisfactory results in controlling the microorganism. Different physicochemical tests of prepared preparations were performed to figure out their pH, phase separation, homogeneity and scent.,

Structural and computational exploration of zwitterionic and quinoidal forms in Schiff base compound

The stable NH-form of the Schiff base compound, (Z)-6-(((4-chlorobenzyl) amino) methylene)-2-hydroxycyclohexa-2,4-dienone was synthesized and characterized by FTIR, SEM, EDAX anlysis and X-ray crystallographic analysis. Structural analysis was carried out to examine the NH-form of the halogen-based Schiff base compound. Additionally, an analysis of bond lengths, based on previously reported NH-forms of other Schiff bases, was conducted to distinguish between the zwitterion and quinoid structures. Further, Hirshfeld surface analysis was performed to visualize and quantify intermolecular interactions, supported by shape index, 2D fingerprint plots, and Enrichment ratio analyzes, highlighting the importance of these interactions. Energy frameworks were established to deepen the understanding of crystal packing through the computation of intermolecular interaction energies. QTAIM analysis was performed to visualize and quantify intramolecular interactions, while Density Functional Theory (DFT) studies elucidated molecular properties such as the HOMO-LUMO energy gap and its derivatives. Evaluation of antibacterial activity against S. aureus was conducted via the disc diffusion assay supplemented by molecular docking studies. This comprehensive approach provides valuable structural insights into the NH-form, as well as molecular and biological aspects of (Z)-6-(((4-chlorobenzyl) amino) methylene)-2-hydroxycyclohexa-2,4-dienone.

Curcumin Nanoemulgel: Characterization, Optimization, and Evaluation of Photoprotective Efficacy, Anti-Inflammatory Properties, and Antibacterial Activity

Curcumin Nanoemulgel: Characterization, Optimization, and Evaluation of Photoprotective Efficacy, Anti-Inflammatory Properties, and Antibacterial Activity

Spirothiazolidine-Derivative on Silver Nanoparticles and Carbon Nanotubes: Evaluation of Antibacterial, Anti-Fungal, Anti-Inflammatory, Antioxidant and Gastroprotective Activities.

This study aims to develop innovative heterocyclic nanocomposites incorporating silver nanoparticles (SNPs) for potential therapeutic applications targeting infections, gastric ulceration, inflammation, and oxidative damage. By synthesizing new derivatives of spiro-thiazolidine-carbonitrile (Py-ST-X) and incorporating them into Ag nanoparticles (AgNPs) and carbon nanotubes (CNTs), we have prepared Ag@Py-ST-X and Ag@Py-ST-X@CNT nanocomposites, respectively. The physical properties of these materials were studied using XRD, TEM, SEM, and Zeta potential techniques. In our investigation involving rats with gastric ulcers, we observed noteworthy inhibitory effects on gastric acid enzyme activity, specifically H+/K+ATPase, by Ag@Py-ST-NO2 and Ag@Py-ST-Br nanocomposites, demonstrating reductions of 25 and 34%, respectively, compared to untreated ulcers. Nanotubulation of these compounds further improved their inhibitory efficacy to 29 and 45%, respectively. Additionally, these nanoparticles showed the most potent myeloperoxidase (MPO)-inhibitory activity, demonstrating 36 and 49% inhibition, respectively, with nanotubulated versions reaching 44 and 53%. Moreover, Ag@Py-ST-NO2@CNT and Ag@Py-ST-Br@CNT nanotubes showed significant antioxidant activity, reducing thiobarbituric acid reactive substances (TBARS) by 35 and 51%, and hydrogen peroxide (H2O2) levels by 49 and 71%, respectively. These therapeutic effects were confirmed by reductions in gastric surface area (GSA) by 44% and 52%, a decrease in ulcer index (UI) from 80% to 44 and 38%, and an increase in curative index (CI) from 19 to 55 and 62% following administration of Ag@Py-ST-NO2@CNT and Ag@Py-ST-Br@CNT, respectively. Histological studies support these findings, suggesting the potential of these nanocomposites as promising candidates for treating various disorders.

Molecular Docking, Synthesis and Evaluation for Antioxidant and Antibacterial Activity of New Oxazepane and Benzoxazepine Derivatives

يعد الالتحام الجزيئي طريقة في مجال المحاكاة الجزيئية يمكن خلالها تحديد الاتجاه الأمثل والمفضل لارتباط جزيء معين بجزيء آخر عندما يكونان معقد مستقر. و من معرفة الالتحام يمكن التنبؤ بقوة الارتباط أو تقارب الارتباط المفضل بين الجزيئين. في هذه الدراسة ، تم تقييم سلسلة من المركبات المحضرة ومعرفة وضعيات الربط والتفاعلات المحتملة ومواقع الربط المستهدفة. حضرت بعض مشتقات 1، 3-أوكسازيبان و 1،3-بنزوكسازيبين من ثلاثة مركبات لقواعد شيف .(3S-1S) تم تفاعل المركبات مع (3S-1S أنهيدريد السكسينيك و أنهيدريد الفثاليك للحصول على مشتقات 1،3- أوكسازيبان و 1،3-بنزوكسازيبين .(3C-1B) شخصت المركبات المحضرة من خلال طرق تحليل العناصر و الاشعة تحت الحمراء FT-IR و وطيف الرنين النووي المغناطيسي 1H-13CNMR تم تسجيل النشاط المضاد للبكتيريا للمركبات (1 B-3C) ضد بعض البكتيريا المعزولة بما في ذلك البكتيريا سالبة الجرام (المكورات العنقودية الذهبية ) و موجبة الجرام (البكتريا القولونية) مع استخدام الاموكسيلين كدواء مرجع. أظهرت المركبات (1B-3C)قيمًا جيدة مثل فعاليتها من المتوسطة الى المرتفعة ضد سلالات البكتيريا المستخدمة. علاوة على ذلك ، تم تقييم النشاط المضاد للأكسدة للمركبات المصنعة (1B-3C) باستخدام 2،2-.ثنائي فنيل 1-1-بيكريل هدرازين و أظهرت النتائج أن المركبات لها أعلى القيم كقانص جذور حرة .

Evaluation of phytoactive contents and antibacterial activities of green synthesised cerium oxide nanoparticles using Melastoma sp. leaf extract as the capping agent

Simple and green methods of developing nanoparticles (NPs) have attracted the attention of researchers. Literature on utilising leaf extract to prepare cerium oxide (CeO2 NPs) is scarce. The present study synthesised leaf-mediated-CeO2 NPs to produce nanopowders of controllable sizes for further applications. The study is the first to report the optimised parameters (pH 7, 5 g/150 mL concentration of the leaf extract, and 3 h of reaction time) of procuring CeO2 NPs using Melastoma sp. leaf extract as the capping agent with excellent properties. The absorbance of the NPs suspension obtained in this study was recorded at approximately 252 nm with Ultraviolet–Visible (UV–Vis) Spectroscopy. Fourier Transform Infrared Spectroscopy (FTIR), Scanning Electron Microscopy (SEM), X-ray Diffraction (XRD), and Transmission Electron Microscopy (TEM) were also utilised to characterise and confirm the CeO2 NPs prepared. The XRD spectra documented the purity of the NPs at specific diffraction patterns, while TEM revealed the spherical form of the NPs with a particle size of 16 nm. The formation of CeO2 NPs has been confirmed from the FTIR spectra procured, which exhibited a Ce–O peak at 555 nm. Phytochemical screening test and FT-IR analysis of leaf extract revealed the existence of flavonoids, terpenoids, sugars, saponins, quinones, and glycosides. The NPs suspensions of varying concentrations (control, 50, 100, 150, 200, and 250 μg/mL) were prepared and employed for evaluations against Gram-positive and -negative bacteria. Resultantly, CeO2 NPs demonstrated antibacterial activities against both bacteria types. The highest antibacterial activities were recorded against E. coli and K. pneumonia at 1.83 ± 0.137 and 1.83 ± 0.14 mm maximum inhibition zones, respectively, at 250 mg/uL of the NPs.

In vitro and in vivo evaluation of osteogenesis and antibacterial activity of Mg[sbnd]Ga alloys

MgGa alloys are considered highly potential biodegradable materials, owing to its good mechanical properties and appropriate corrosion resistance. However, it is still far from application due to the lack of biological evaluation. In the present study, biocompatibility, osteogenesis and antibacterial activity of extruded Mg–xGa (x = 1 and 5 wt%) alloys were investigated by in vitro cell culture experiments and in vivo implantation. The cell adhesion and proliferation of osteoblast precursor cells (MC3T3-E1) showed the excellent cytocompatibility of Mg–1Ga and poor cytocompatibility of Mg–5Ga. The osteogenic activity was evaluated and revealed that Ga3+ in the Mg–1Ga extract had the ability to enhance osteogenic differentiation through the facilitation of its early stages. In vivo studies in a rat femoral condyle model revealed that both Mg–1Ga and Mg–5Ga significantly promoted new bone formation without causing any adverse effects. Mg–5Ga exhibited a much higher corrosion rate in vivo than Mg–1Ga. Its osteogenic activity was better due to the rapid release of Mg2+ and Ga3+, but this caused premature structural integrity loss. Mg–1Ga and Mg–5Ga released Ga3+ to inhibit E. coli and S. aureus, with antibacterial rate increasing with Ga content. Our studies demonstrate that Mg–Ga alloys have the potential to be used as osteogenic and antibacterial implant materials. Statement of significanceThis study evaluates the biocompatibility, osteogenesis, and antibacterial activity of Mg–Ga alloys, which are promising biodegradable materials for medical applications. The study finds that Mg–1Ga exhibits excellent cytocompatibility and promotes osteogenic differentiation, facilitating the early stages of osteoblast precursor cell development. In vivo studies in a rat femoral condyle model reveal that Mg–1Ga and Mg–5Ga significantly promote new bone formation without causing any adverse effects. The antibacterial activity of both alloys is evaluated against E. coli and S. aureus, with the inhibition rate increasing with Ga content. These findings suggest that Mg–Ga alloys have the potential to serve as osteogenic and antibacterial implant materials, providing significant insights into the development of novel biomedical implants.