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The clinical significance of benzimidazole-containing drugs has increased in the current study, making them more effective scaffolds. These moieties have attracted strong research interest due to their diverse biological features. To examine their various biological significances, several research synthetic methodologies have recently been established for the synthesis of benzimidazole analogs. The present study aimed to efficiently and quickly synthesize a new series of benzimidazole analogs. Numerous spectroscopic techniques, including 1H-NMR, 13C-NMR, and HREI-MS, were used to confirm the synthesized compounds. To explore the inhibitory activity of the analogs against α-amylase and α-glucosidase, all derivatives (1–17) were assessed for their biological potential. Compared to the reference drug acarbose (IC50 = 8.24 ± 0.08 µM), almost all the derivatives showed promising activity. Among the tested series, analog 2 (IC50 = 1.10 ± 0.10 & 2.10 ± 0.10 µM, respectively) displayed better inhibitory activity. Following a thorough examination of the various substitution effects on the inhibitory capacity of α-amylase and α-glucosidase, the structure-activity relationship (SAR) was determined. We looked at the potential mechanism of how active substances interact with the catalytic cavity of the targeted enzymes in response to the experimental results of the anti-glucosidase and anti-amylase. Molecular docking provided us with information on the interactions that the active substances had with the various amino acid residues of the targeted enzymes for this purpose.

Besides natural sunlight and expensive artificial lights, economical indoor white light can play a significant role in activating a catalyst for photocatalytic removal of organic toxins from contaminated water. In the current effort, CeO2 has been modified with Ni, Cu, and Fe through doping methodology to study the removal of 2-chlorophenol (2-CP) in the illumination of 70 W indoor LED white light. The absence of additional diffractions due to the dopants and few changes such as reduction in peaks’ height, minor peak shift at 2θ (28.525°) and peaks’ broadening in XRD patterns of modified CeO2 verifies the successful doping of CeO2. The solid-state absorption spectra revealed higher absorbance of Cu-doped CeO2 whereas a lower absorption response was observed for Ni-doped CeO2. An interesting observation regarding the lowering of indirect bandgap energy of Fe-doped CeO2 (∼2.7 eV) and an increase in Ni-doped CeO2 (∼3.0 eV) in comparison to pristine CeO2 (∼2.9 eV) was noticed. The process of e-– h+ recombination in the synthesized photocatalysts was also investigated through photoluminescence spectroscopy. The photocatalytic studies revealed the greater photocatalytic activity of Fe-doped CeO2 with a higher rate (∼3.9 × 10−3 min-1) among all other materials. Moreover, kinetic studies also revealed the validation of the Langmuir-Hinshelwood kinetic model (R2 = 0.9839) while removing 2-CP in the exposure of indoor light with a Fe-doped CeO2 photocatalyst. The XPS analysis revealed the existence of Fe3+, Cu2+ and Ni2+ core levels in doped CeO2. Using the agar well-diffusion method, the antifungal activity was assessed against the fungus M. fructicola and F. oxysporum. Compared to CeO2, Ni-doped CeO2, and Cu-doped CeO2 nanoparticles, the Fe-doped CeO2 nanoparticles have outstanding antifungal properties.

Plant Growth Promoting Rhizobacteria (PGPR) has gained immense importance in the last decade due to its in-depth study and the role of the rhizosphere as an ecological unit in the biosphere. A putative PGPR is considered PGPR only when it may have a positive impact on the plant after inoculation. From the various pieces of literature, it has been found that these bacteria improve the growth of plants and their products through their plant growth-promoting activities. A microbial consortium has a positive effect on plant growth-promoting (PGP) activities evident by the literature. In the natural ecosystem, rhizobacteria interact synergistically and antagonistically with each other in the form of a consortium, but in a natural consortium, there are various oscillating environmental conditions that affect the potential mechanism of the consortium. For the sustainable development of our ecological environment, it is our utmost necessity to maintain the stability of the rhizobacterial consortium in fluctuating environmental conditions. In the last decade, various studies have been conducted to design synthetic rhizobacterial consortium that helps to integrate cross-feeding over microbial strains and reveal their social interactions. In this review, the authors have emphasized covering all the studies on designing synthetic rhizobacterial consortiums, their strategies, mechanism, and their application in the field of environmental ecology and biotechnology.

The growth of carbon nanostructures from vegetable oils using a modified conventional approach is a simple and environmentally friendly technology with controllable features. The goal of this study is to develop a simple and environmentally friendly process for making carbon nanoparticles using commercially available, low-cost vegetable oils. The technique involves the controlled burning of “Mustard”, “Olive”, and “Linseed” oils using the traditional clay lamps and collecting the carbon soot on a ceramic plate. The prepared carbon nanoparticles were purified through sonication and subjected to characterization using powder X-ray diffraction, SEM, Fourier transformed infrared, Thermogravimetric and differential scanning calorimetric analyses. The average particle size of carbon nanoparticles as investigated by powder X-Ray Diffraction analyses was found to be 18, 24, and 57 nm for mustard, olive and linseed oils respectively. SEM analyses revealed the surface morphology of these carbon nanostructures as spherical particles. Thermogravimetric analysis (TGA) and Differential Scanning Calorimetry (DSC) providing knowledge about the thermal stability of these carbon nanoparticles. The synthesized carbon nanoparticles were screened for antibacterial activities against different species (e.g., Pseudomonas aeruginosa, Streptococcus haemolyticus, Proteus refrigere and Staphylococcus aureus) and fruitful results have been obtained.

Periodontal disease is a common complication, and conventional periodontal surgery can lead to severe bleeding. Different membranes have been used for periodontal treatment with limitations, such as improper biodegradation, poor mechanical property, and no effective hemostatic property. Guided tissue regeneration (GTR) membranes favoring periodontal regeneration were prepared to overcome these shortcomings. The mucilage of the chia seed was extracted and utilized to prepare the guided tissue regeneration (GTR) membrane. Lignin having antibacterial properties was used to synthesize lignin-mediated ZnO nanoparticles (∼Lignin@ZnO) followed by characterization with analytical techniques like Fourier-transform infrared spectroscopy (FTIR), UV–visible spectroscopy, and scanning electron microscope (SEM). To fabricate the GTR membrane, extracted mucilage, Lignin@ZnO, and polyvinyl alcohol (PVA) were mixed in different ratios to obtain a thin film. The fabricated GTR membrane was evaluated using a dynamic fatigue analyzer for mechanical properties. Appropriate degradation rates were approved by degradability analysis in water for different intervals of time. The fabricated GTR membrane showed excellent antibacterial properties against Staphylococcus aureus (S. aureus) and Escherichia coli (E. coli) bacterial species.

This work includes green synthesis of magnesium oxide nanoparticles (MgO NPs) by using Alstoniascholaris, which is indigenous to many countries such as China, Australia, Sri Lanka, Pakistan, and India. Its pharmacological activities include antidiabetic, antioxidant, anticancer, analgesic, antitussive, and anti-diarrheal activities. In this study, the antioxidant and anti-inflammatory activities of bio-inspired magnesium oxide nanoparticles, MgO NPs, were investigated. MgO NPs were prepared by using the leaf extract of Alstonia scholaris, followed by characterization using EDX, XRD, and SEM techniques. The crystallite size of magnesium oxide nanoparticles was 19.57 nm. XRD analysis confirmed the crystallinity and the purity of MgO NPs. Anti-inflammatory activity was carried out to observe inhibition of protein denaturation. Since the IC50 of MgO nanoparticles was lower than the standard, it was found to be more effective. IC50 values were compared, and results reveal that bioinspired MgO NPs undergo more scavenging of free radicals than standard (ascorbic acid) MgO NPs. These MgO nanoparticles are useful in cosmetics such as scrubs, moisturizers, and an active ingredient in microdermabrasion and in formulating effective drugs for maintaining the protein structure of the body, which will reduce inflammation.

Rapid methyl parathion detection was measured using a fabricated glassy carbon electrode (GCE) sensor designed using the layer-by-layer (LBL) method. Multilayer assemblies were developed on the glassy carbon electrode by alternating depositions of anions and cations in which a Dawson Type Polyoxometalate β-K6[(P2W18O62·H2O)]·14H2O (∼P2W18 POM) and polyethyleneimine (PEI) stabilized silver nanoparticles (∼PEI-AgNPs) acted as anions and cations, respectively. The redox behavior of P2W18 POM within LBL assembly was carried out via cyclic voltammetry. This LBL assembly was thoroughly characterized by UV-Visible, FT-IR, XRD, AFM, and SEM techniques. The fabricate GCE sensor was investigated for the electrocatalytic activity to detect methyl parathion. The results clearly showed that the fabricated GCE sensor was successfully synthesized. More interestingly, the current response for detecting methyl parathion was found to be less than 1 ppm, proving that this fabricated GCE sensor may exhibit potential applications in the detection of targeted pesticide.

In this study, a green synthesis strategy was used to construct CuO-GO-Ag nanocomposites (NCs) by using biological components of Fagonia arabica. Copper Oxide (CuO) nanoparticles and silver (Ag) nanoparticles were fabricated by using a plant extract of Fagonia arabica. Graphene oxide was synthesized by hummer’s method and hydrothermal approach. The characterization techniques used in this work were Energy Dispersive X-ray (EDX), Scanning electron microscopy (SEM), X-ray Diffraction (XRD), and ultra-violet visible spectroscopy (UV-Vis). As an innovative approach graphene oxide (GO) was firstly assorted with green synthesized CuO NPs and then Ag nanoparticles were incorporated to form amalgamated CuO-GO-Ag nanocomposite (NCs). The anti-inflammatory and antioxidant activity of nanocomposite were examined. The anti-inflammatory and antioxidant ability of the nanocomposite were evaluated by UV-Visible spectroscopy. Results reveal that biologically synthesized CuO-GO-Ag NCs have high scavenging and inflammation reduction potential as compared to standards (ascorbic acid, diclofenac sodium). CuO-GO-Ag showed that scavenging efficiency for 0.3 mg/ml is 57.40% and for 0.5 mg/ml is 74.24% while scavenging efficiency for standard (ascorbic acid) is 44.22% for 0.3 mg/ml and 58.42% for 0.5 mg/ml. Likewise, CuO-GO-Ag nanocomposite showed a % inhibition value of 46.59 and 87.80 at 0.1 mg/ml and 0.5 mg/ml while diclofenac sodium showed a % inhibition value of 10.98 and 35.37 a similar concentration. Fagonia arabica seems to be a good source for acclimating the potential of NCs and nanoparticles toward different increased biological activities, according to the findings.

Water is the basic need of human beings with no substitute for it. This research aims to investigate the drinking water quality and dissociated risk calculations of the metropolis area in Pakistan. The present study was based on public awareness toward water quality and the real situation of water quality of filtration plants in Islamabad. A questionnaire was designed with the help of existing literature about public awareness on water quality. In the present study, 450 completed questionnaires were collected and analyzed with the help of statistical tools. To investigate the real situation of water quality in the study area, 32 samples were analyzed from installed filtration plants. The results presented that electrical arsenic, conductivity (EC), and alkalinity were higher, and 26 samples were found to be unsafe for drinking under poor water quality (water quality index >100). The hazard index of arsenic was found to be

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