Chemical Characterization Research Articles

Aqueous Extracts of Rhus trilobata Inhibit the Lipopolysaccharide-Induced Inflammatory Response In Vitro and In Vivo.

Chronic noncommunicable diseases (NCDs) are responsible for approximately 74% of deaths globally. Medicinal plants have traditionally been used to treat NCDs, including diabetes, cancer, and rheumatic diseases, and are a source of anti-inflammatory compounds. This study aimed to evaluate the anti-inflammatory effects of Rhus trilobata (Rt) extracts and fractions in lipopolysaccharide (LPS)-induced inflammation models in vitro and in vivo. The aqueous extract (RtAE) and five fractions (F2 to F6) were obtained via C18 solid-phase separation and tested in murine LPS-induced J774.1 macrophages. Key inflammatory markers, such as IL-1β, IL-6, TNF-α, and COX-2 gene expression were measured using RT-qPCR, and PGE2 production was assessed via HPLC-DAD. The in vivo effects were tested in an LPS-induced paw edema model in Wistar rats. Results showed that RtAE at 15 μg/mL significantly decreased IL-1β and IL-6 gene expression in vitro. Fraction F6 further reduced IL-1β, TNF-α, and IL-6 gene expression, COX-2 expression, and PGE2 production. In vivo, F6 significantly reduced LPS-induced paw edema, inflammatory infiltration, and IL-1β and COX-2 protein expression. Chemical characterization of F6 by UPLC/MS-QTOF revealed at least eight compounds with anti-inflammatory activity. These findings support the anti-inflammatory potential of RtAE and F6, reinforcing the medicinal use of Rt.

Advancing Sustainability: Geraniol-Enhanced Waterborne Acrylic Pressure-Sensitive Adhesives without Chemical Modification.

The escalating global emphasis on sustainability, coupled with stringent regulatory frameworks, has spurred the quest for environmentally viable alternatives to petroleum-derived materials. Within this context, the adhesives industry has been actively seeking renewable options and eco-friendly synthesis pathways. This study introduces geraniol, a monoterpenoid alcohol, in its unmodified form, as a key component in the production of waterborne pressure-sensitive adhesives (PSAs) based on acrylic latex through emulsion polymerization. Multiple formulations were developed at varying reaction times. The adhesives underwent comprehensive chemical characterization employing techniques such as Fourier-transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), Nuclear Magnetic Resonance (NMR), Gel Permeation Chromatography (GPC), and dynamic light scattering (DLS). The viscosities of the formulations were measured between 4000 and 5000 cP. Adhesion tests showed peel strength values of 0.52 N/mm on cardboard and 0.32 N/mm on painted steel for the geraniol-based formulations. The results demonstrate the potential for geraniol-based PSAs to offer a sustainable alternative to petroleum-derived adhesives, with promising thermal and adhesive properties.

Chemical Characterization of Synthesized Nanoparticles from Noni (Morinda citrifolia) Seed

Morinda citrifolia is an herbal medicine that is used for disease treatment as recommended in traditional medicine. The present study aimed to characterize silver nanoparticles from Noni seed. In this experimental study, green synthesis was carried out then the synthesized nanoparticles were characterized using SEM, EDX, TEM and FTIR. Findings showed that SEM images of the AgNPs of different shapes were obtained in the case of different seed extracts being used as reducing and capping agents. Seed extract formed approximately spherical, triangular, and cuboidal AgNPs, respectively. Elemental mapping of AgNPs by SEM-EDX shows the presence of 0.31% Ag and 40% oxides with 39% Carbon and other elements in trace amounts. TEM image demonstrates that the AgNPs were spherical. The image shows agglomerates of small grains and some dispersed nanoparticles, confirming the results obtained by SEM. FTIR result reveals the assignment of functional groups to 19 FTIR bands (690-3833 cm 1). Bands were categorized based on possible functional group classes (alkene, aromatic, alcohol/phenol/ether, amine, etc.). Specific functional groups like alkenes, conjugated alkenes, ketones, aldehydes, nitriles, alkynes, and carboxylic acids were identified based on characteristic wavenumbers. The study presents a green synthesis approach to prepare silver nanoparticles using Noni seed extract. Reduction of silver nitrate with Noni seed extract is a simple, conducted at room temperature, efficient, and clean method to synthesize silver nanostructures.

A multi-disciplinary approach based on chemical characterization of foreshore sediments, ecotoxicity assessment and statistical analyses for environmental monitoring of marine-coastal areas

The present work aims at providing a multi-disciplinary approach for environmental monitoring in marine-coastal areas. A monitoring campaign of 13 months (October 2022–October 2023) was carried out on sandy foreshore sediments (SFSs). The SFSs were analysed for potentially toxic elements (PTEs) and rare earth elements (REEs) content determination. In the investigated area, variable contamination trends were assessed through Friedman and Nemenyi tests. Further results also indicated the usefulness of statistical data elaboration in the identification of potential contamination sources. In fact, from Spearman test, significant positive correlations (between 0.650 and 0.981) were observed among PTEs of possible anthropogenic origin (such as Co, Cr, Cu, Pb, V, and Zn). For REEs, La and Nd showed strong correlations with Ce (0.909 and 0.920, respectively). The study also integrated luminescence inhibition (Aliivibrio fischeri), algal growth inhibition (Phaeodactylum tricornutum), and embryotoxicity assessment (Paracentrotus lividus) on sediment elutriates showing varying degrees of toxicity. Also these data were analysed through statistics in order to highlight possible correlations between contaminants and observed ecotoxicological effects on the involved bioindicators. The results outline an approach useful for more comprehensive monitoring of marine areas quality and identification of suitable environmental restoration strategies.

Inter-laboratory study for extraction testing of medical devices

Biocompatibility evaluation of medical devices often relies on chemical testing according to ISO 10993–18 as a critical component for consideration. However, the precision associated with these non–targeted chemical characterization assessments has not been well established. Therefore, we have conducted a study to characterize intra–laboratory (repeatability) and inter–laboratory (reproducibility) variability associated with chemical testing of extractables from polymeric materials. To accomplish this, this study focused on two polymers, each with nine chemicals that were intentionally compounded into the materials. Eight different laboratories performed extraction testing in two solvents and subsequently characterized the extracts using gas chromatography and liquid chromatography methods. Analysis of the resulting data revealed the central 90 % range for the repeatability and reproducibility relative standard deviations are (0.09, 0.22) and (0.30, 0.85), respectively, for the participating laboratory methods. This finding implies that if the same sample was tested by two different laboratories using the same extraction conditions, there is 95 % confidence for 95 % of systems that the test results could exhibit differences up to 240 %. While the study was not designed to evaluate the relative impact of specific underlying factors that may contribute to variability in quantitation, the data obtained suggest the variability associated with analytical method alone is a substantial contribution to the overall variability. The relatively large reproducibility limits we observed may have significant implications where variability in extraction measurements can impact aspects of biocompatibility risk evaluation, such as exposure dose estimation and chemical equivalence assessments.

Micro-Nanoparticle Characterization: Establishing Underpinnings for Proper Identification and Nanotechnology-Enabled Remediation.

Microplastics (MPLs) and nanoplastics (NPLs) are smaller particles derived from larger plastic material, polymerization, or refuse. In context to environmental health, they are separated into the industrially-created "primary" category or the degradation derivative "secondary" category where the particles exhibit different physiochemical characteristics that attenuate their toxicities. However, some particle types are more well documented in terms of their fate in the environment and potential toxicological effects (secondary) versus their industrial fabrication and chemical characterization (primary). Fourier Transform Infrared Spectroscopy (FTIR/µ-FTIR), Raman/µ-Raman, Proton Nuclear Magnetic Resonance (H-NMR), Curie Point-Gas Chromatography-Mass Spectrometry (CP-gc-MS), Induced Coupled Plasma-Mass Spectrometry (ICP-MS), Nanoparticle Tracking Analysis (NTA), Field Flow Fractionation-Multiple Angle Light Scattering (FFF-MALS), Differential Scanning Calorimetry (DSC), Thermogravimetry (TGA), Differential Mobility Particle [Sizing] (DMPS), Scanning Electron Microscopy (SEM), Transmission Electron Microscopy (TEM), and Scanning Transmission X-ray Microspectroscopy (STXM) are reviewed as part of a suite of characterization methods for physiochemical ascertainment and distinguishment. In addition, Optical-Photothermal Infrared Microspectroscopy (O-PTIR), Z-Stack Confocal Microscopy, Mueller Matrix Polarimetry, and Digital Holography (DH) are touched upon as a suite of cutting-edge modes of characterization. Organizations, like the water treatment or waste management industry, and those in groups that bring awareness to this issue, which are in direct contact with the hydrosphere, can utilize these techniques in order to sense and remediate this plastic polymer pollution. The primary goal of this review paper is to highlight the extent of plastic pollution in the environment as well as introduce its effect on the biodiversity of the planet while underscoring current characterization techniques in this field of research. The secondary goal involves illustrating current and theoretical avenues in which future research needs to address and optimize MPL/NPL remediation, utilizing nanotechnology, before this sleeping giant of a problem awakens.

Exploring Phytochemical profiling, Antioxidant, Enzyme Inhibition, and Antibacterial Potential of Callistemon viminalis (Sol. ex Gaertn.) G.Don ex Loudon)by In vitro and In silico Approaches.

Callistemon viminalis (Sol. ex Gaertn.) G. Don ex Loudon) (Family: Myrtaceae) is used for its medicinal properties in treating various metabolic disorders. We investigated the chemical characterization and biological screening of n-hexane extract of C. viminalis. Total phenolic content was (37.45 ± 7.40 mg GA.E/g D.E ± S.D) and total flavonoid content was (18.43 ± 6.34 mg R.E/g D.E ± S.D). The GC-MS screening of n-hexane extract tentatively identified 70 bioactive phytochemicals. The maximum antioxidant potential (289.99 ± 9.01 mg T.E/g D.E±S.D) was observed by FRAP assay. The enzyme inhibition assays revealed α-glucosidase and α-amylase inhibition (6.9 ± 0.13 and 7.2 ± 0.56 mmol of ACA.E/g D.E±S.D), urease (4.95 ± 0.9 mg of TU.E/g D.E±S.D), acetylcholinesterase (2.9 ± 0.08 mg GALA.E/g D.E±S.D), lipoxygenase (4.93 ± 1.05 mg of Indo.E/g D.E±S.D) and tyrosinase (4.33 ± 0.62 mg of KA.E/g D.E±S.D) inhibition. The extract showed antibacterial potential against Salmonella typhi (53.90±5.05)Bacillus subtilis (68.55±2.70%), Salmonella aureus (71.30±4.44%) and Pseudomonas aeruginosa (57.86±6.02%). The docking studies revealed a good docking interaction of ligands against the studied enzymes while ADME analysis revelaed pharmacokinetic profile of thephytoconstituents.C. viminalispossesses promising therapeutic potential and can be further explored for drug development and drug designing.

Cellulose nanocrystal extraction from tissue paper wastes using different extraction methods and cellulose acetate production

ABSTRACT This paper examines the feasibility of extracting cellulose from tissue paper wastes (TPW’s) using several methods: sonication (SC), subcritical (SU), microwave (MC), and microwave with diluted acid (MA). The chemical characterisation and morphological properties of nanocrystal cellulose were investigated using Fourier-transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), scanning electron microscopy (SEM), and scanning electron microscopy with energy dispersive X-Ray analysis (SEM-EDX). TPW’s have a relatively high crystallinity index (CrI = 61.02%). It was found to be lower than that for cellulose extracted using SU and SC MC, MA methods, where CrI to 65.65%, 68.07%, 69.21% and 73.42%, respectively. The MA method yielded cellulose with the highest CrI and altered surface morphology. This cellulose was selected for cellulose acetate synthesis. After acetylation, the CrI decreased to 61.45%, and the morphological aspect was changed. In conclusion, nanocrystal cellulose was successfully extracted from TPW’s and effectively changed to its esterified form.

Tailoring surgical sutures with chitosan and non-thermal atmospheric plasma: biofunctionalization for antimicrobial efficacy and enhanced wound healing

Surgical sutures serve as medical devices designed to facilitate the closure of wounds by securing opposing tissues. While sutures are an integral part of the surgical healing process, also present favorable surfaces for microbial attachment, increasing surgical site infections (SSIs). In this study, sutures that have antimicrobial and improved wound healing properties are described as novel approaches for minimizing SSIs. The absorbable multifilament suture, poly (glycolic-co-lactic acid) (PGLA), and non-absorbable multifilament suture (silk) are treated with non-thermal atmospheric plasma (NTAP) and subsequently coated with chitosan/chitosan nanoparticles (Ch/ChNp). Suture samples are analyzed in terms of antibacterial properties, in vitro bioactivity, wound healing efficiency, mechanical strength, chemical characterization, and surface morphologies. Bacterial adherence of Staphylococcus aureus and Escherichia coli on both sutures is inhibited effectively due to the surface modification after plasma treatment. The NTAP treatment results in reduced wound healing for silk sutures without a selective effect on PGLA sutures. However, subsequent coating with Ch/ChNp significantly enhances wound healing for both sutures. Although the maximum tensile strength decreases after NTAP treatment, improves following the Ch/ChNp coating. Our findings indicate that the developed sutures demonstrate notable antimicrobial properties, enhance wound healing, and hold promise as a potential material for suturing applications.

Chemical Fingerprinting, PAHs Characterization and Ecological Risks of Carcinogenic PAHs in Surficial Sediments of Egi Crude Oil Producing Communities, Niger-Delta, Nigeria

In order to do PAHs rings analysis, its source identification, extent to which cPAHs present and what kind of ecological risk they pose, the surface sediments from various freshwaters in the Egi crude oil producing cities in the Niger Delta, Nigeria were analyzed. Sediments collected from the research areas for PAHs loadings (in mg/kg dry weight) ranged from 0.020 to 1.790, 0.050 to 1.880, and 0.020 to 1.640, respectively for Obite, Obagi, and Ibewa cluster areas, as measured by gas chromatography-mass spectrometer. In these clusters, the respective average concentration of the three dominant carcinogenic PAHs were Indeno(1,2,3-cd)pyrene (1.170.0mg/kg), Dibenz[a,h]anthrancene (0.870.0 mg/kg), and Dibenz[a,h]anthrancene (1.3670 mg/kg) for Ibewa, Obagi and Obite cluster areas. The findings showed that dominant PAHs rings are of high molecular weight (HMW) PAHs in these sediments are, 5 member rings, which are benzo(b)fluoranthene, Benzo(k)fluoranthene, and Benzo(a)pyrène, and 6-member ring which are, Indeno(1,2,3-cd)pyrene, Dibenz[a,h]anthrancene, and Benzo[ghi] perylene, respectively. Their fingerprints points majorly to pyrogenic sources, combustion of coal, biomass, petroleum, and other related anthropogenic petroleum activities as the primary source of PAHs in the environment. Notably, the RQNCs and RQMPCs for single PAHs molecule are both less than 1, it means the contamination it generates is considered of low ecological risk. Again, the research area experiences frequent flooding, it is believed that this contributes to the low ecological risk of PAHs chemical pollution. Consequently, the area is deemed to be quite safe.

Mechanistic investigation of the suppressed N2O formation during the low-temperature NH3-SCR over the Sb-modified Mn/Ti catalyst

The formation of N2O during the NH3-SCR reaction over the Mn-based is one of the crucial factors limiting the industrial application of Mn-based catalysts. In this work, the Sb-modified Mn/Ti catalyst was prepared by the ultrasonic assistance impregnation method to control the formation of N2O during the NH3-SCR reaction. The preferred Mn3Sb/Ti catalyst had over 80 % NOx conversion at 150–300 °C, and more than 80 % N2selectivity at 150–250 °C, which were higher than that of the Mn/Ti catalyst at the same temperature window. A series of performance experiments showed that the Sb modification inhibited the oxidation of NH3to N2O and suppressed the N2O produced by the E-R mechanism in the NSCR reaction, which is the main pathway for N2O generation. Moreover, the presence of NO inhibited the oxidation of NH3 to generate N2O over the Mn3Sb/Ti catalyst. Based on the physical–chemical characterizations and DFT calculations, it was revealed that the introduced Sb species achieves a trade-off between redox ability and surface acidity over the Mn3Sb/Ti catalyst, which is beneficial to enhance the NH3-SCR performance and simultaneously suppress the over-oxidation of NH3. The high content of Mn3+caused by the electron transfer through the redox cycle of Sb3++Mn4+→Sb5++Mn3+ was beneficial in decreasing the N2O formation.The formation of NH speciesis inhibited on the Mn3Sb/Ti catalyst with a higher energy barrier of the NH2* conversion to NH* species due to the Sb modification. Meanwhile, the energy barrier of NH3*→NH2* is decreased and the energy barrier of NH2*+NO → N2 + H2O is lower than that of NH2*→NH* over the Sb-modified catalyst, indicating that the NH3-SCR reaction is more favorable than the formation of N2O on the Mn3Sb/Ti catalyst.

A readily accessible quaternized cellulose filter paper with high permeability for IgG separation

Anion-exchange chromatography (AEC) is recognized as a highly effective approach for the purification of immunoglobulin G (IgG). This study introduces an innovative strategy that employs waste cellulose filter paper in the production of AEC media. A quaternized cellulose fiber membrane (CFM-QCS) was successfully fabricated that cellulose fibers were as a structural framework, glutaraldehyde (GA) as a crosslinking agent, and quaternary chitosan (QCS) as a modifying agent. Morphological and chemical characterization revealed that GA and QCS were uniformly crosslinked on the surface of the cellulose fibers, resulting in excellent mechanical properties in both dry and wet states. Benefiting from its 3D network scaffold structure, CFM-QCS demonstrated a high adsorption capacity for bovine serum albumin (BSA), with static and dynamic adsorption capacities of 605.15 mg/g and 88.63 mg/ml, respectively. After treated with extreme conditions and 10 cyclic adsorption and elution, the adsorption capacity of CFM-QCS remains almost unchanged, highlighting its excellent stability. Additionally, a CFM-QCS packed chromatography column exhibited high flux of 10.38 L/h at 0.1 MPa, which can efficiently separate IgG from a mixed solution in the presence of BSA and IgG by gravity-driven. This work presents a straightforward approach for preparing high-performance ion-exchange chromatography membranes for IgG separation.

Chemical Characterization of Coal: Quality Control and Applications of Nuclear Analytical Methods Utilizing Neutrons (Thermal and Fast) and Low Energy Protons from Accelerators

Chemical Characterization of Coal: Quality Control and Applications of Nuclear Analytical Methods Utilizing Neutrons (Thermal and Fast) and Low Energy Protons from Accelerators

Crystallization behavior of BOF slag during the cooling process towards leaching for CO2 sequestration

This work addresses the crystallization behavior and microstructure feature of the molten basic oxygen furnace (BOF) slag during a slow cooling process. The aim is to provide a reference for the modification of BOF slag for subsequent leaching of Ca as part of CO2 sequestration. Integrated analysis of XRD, SEM-EDS, and thermodynamic calculations suggest a crystallization behavior of BOF slag during the cooling process. RO phases ((Mg, Fe, Mn) O) was the equilibrium phase at a high temperature of around 1600 °C, followed at lower temperatures by the formation of Ca3SiO5 (C3S) and α-Ca2SiO4 (α-C2S). The Ca2Fe2O5 (C2F) phase forms during the latter stages of melt solidification. On the basis of the combined analysis of the leaching test results and crystallographic analysis, a future direction of modification of BOF slag is suggested that enriches Ca into the C2S and hinders the formation of C2F. However, inhibiting the generation of C2F by adjusting the cooling process alone is difficult since its crystallization rate is fast. The phase of C2F was observed in XRD and SEM even if the BOF slag was quenched from 1600 °C. Furthermore, the chemical characterization and morphological evolution of the crystalline phase of molten BOF slag during the slow cooling process was observed.

Online characterization of primary and secondary emissions of particulate matter and acidic molecules from a modern fleet of city buses

Abstract. The potential impact of transitioning from conventional fossil fuel to a non-fossil-fuel vehicle fleet was investigated by measuring primary emissions via extractive sampling of bus plumes and assessing secondary mass formation using the Gothenburg Potential Aerosol Mass (Go:PAM) reactor from 76 in-use transit buses. Online chemical characterization of gaseous and particulate emissions from these buses was conducted using chemical ionization mass spectrometry (CIMS) with acetate as the reagent ion, coupled with the Filter Inlet for Gases and AEROsols (FIGAERO). Acetate reagent ion chemistry selectively ionizes acidic compounds, including organic and inorganic acids, as well as nitrated and sulfated organics. A significant reduction (48 %–98 %) in fresh particle emissions was observed in buses utilizing compressed natural gas (CNG), biodiesels like rapeseed methyl ester (RME) and hydrotreated vegetable oil (HVO), and hybrid-electric HVO (HVOHEV) compared to diesel (DSL). However, secondary particle formation from photooxidation of emissions was substantial across all the fuel types. The median ratio of particle mass emission factors of aged to fresh emissions increased in the following order: DSL buses at 4.0, HVO buses at 6.7, HVOHEV buses at 10.5, RME buses at 10.8, and CNG buses at 84. Of the compounds that can be identified by CIMS, fresh gaseous emissions from all Euro V/EEV (Enhanced Environmentally friendly Vehicle) buses, regardless of fuel type, were dominated by nitrogen-containing compounds such as nitrous acid (HONO), nitric acid (HNO3), and isocyanic acid (HNCO), alongside small monoacids (C1−C3). Notably, the emission of nitrogen-containing compounds was lower in Euro VI buses equipped with more advanced emission control technologies. Secondary gaseous organic acids correlated strongly with gaseous HNO3 signals (R2=0.85–0.99) in Go:PAM, but their moderate to weak correlations with post-photooxidation secondary particle mass suggest that they are not reliable tracers of secondary organic aerosol formation from bus exhaust. Our study highlights that non-regulated compounds and secondary pollutant formation, not currently addressed in legislation, are crucial considerations in the evaluation of environmental impacts of future fuel and engine technology shifts.

Enhancing hydrogen evolution: Carbon nanotubes as a scaffold for Mo2C deposition via magnetron sputtering and chemical vapor deposition

This study presents an innovative approach to fabricating carbon nanotubes (CNTs) through magnetron sputtering and chemical vapor deposition (CVD). These CNTs serve as a robust structural scaffold for the deposition of molybdenum, which, through thermal annealing, becomes molybdenum carbide (Mo2C), which is highly efficient for hydrogen evolution reaction (HER). Our investigation delves into the physical and chemical attributes of these electrodes, revealing insights into the functionality of Mo2C on CNTs hybrid structures. Chemical characterization confirms the exceptional performance of the electrode. Our Mo2C on CNT hybrid system showcases remarkable electrocatalytic activity, with an onset potential of 103 mV at 1 mA/cm2 and an overpotential of 176 mV at 10 mA/cm2. Further validation comes from tests revealing a Tafel slope of 95 mV/dec, affirming its superiority in facilitating HER. Unparalleled combination of low charge transfer resistance and accelerated reaction kinetics, Mo2C on CNTs hybrid structure is poised to significantly enhance HER activity.

The analytical evaluation threshold for inorganic metal extractables and leachables analysis of medical devices

Chemical characterization of medical devices uses the analytical evaluation threshold (AET) to determine reportable organic extractables, as these chemicals may be of toxicological concern and should be addressed via toxicological risk assessment. The AET is not applicable to metal extractables due to the exclusion of toxicity data on inorganics from the dataset used to derive dose-based threshold (DBT) values. This results in minimal guidance for reporting metal extractables. Herein, an AET for metals, or mAET, is proposed as a reporting threshold for individual metal extractables. The mAET can ensure metals are reported that are at quantities that may present a patient safety risk. This may reduce the number of metals reported in a chemical characterization report, improving the efficiency of the overall biocompatibility evaluation by removing unneeded effort and resource time. Conversely, an analytical method’s ability to report all metals at toxicologically relevant levels can be confirmed by comparing method sensitivity to mAET values. DBTs were developed for 70 metals, permitting mAET values to be determined. These mAET values were then compared to metal reporting limits from 13 previously conducted chemical characterization studies, which used varying extraction designs and analytical methods, to determine the impact of the mAET.

Chemical Characterization and Assessment of Public Health Risk due to Inhalation of PM2.5 in the City of Salamanca, Guanajuato.

In this study, we conducted an analysis of health risks faced by residents of Salamanca, Mexico, who were exposed to fine particulate matter with a diameter of 2.5μm (PM2.5) through inhalation. The characterization and analysis of these particulate matter samples were undertaken. A total of 131 samples were collected from two different sites: 65 from the Red Cross site (RC) and 66 from the Integral Family Development site (DIF) in 2014-2015. These samples were analyzed for a set of chemical components, including metals and ions. Non-cancerous health risk levels associated with PM2.5 exposure through the human respiratory system, as per the WHO benchmark (assigned a value of 1), revealed notable risk values for two elements: Manganese (Mn) with a range of 1.19-2.12 in the adult population and 1.59-2.84 in the child population, and Nickel (Ni) with a uniform risk value of 1.39 for both evaluated population groups. However, concerns arose regarding potential non-cancerous effects as the cumulative risk levels for various assessed elements showed elevated indices. These ranged from 3.81 to 4.4 in adults and 4.48-5.24 in children. This study provided comprehensive data on composition and its potential impact on human health, offering valuable insights for the implementation of mitigation measures aimed at reducing inhalation-related exposure.

Chemical Characterization, Evaluation of Acute Oral Toxicity, and Anti-Diabetic Activity of Aloe sabaea Flowers Extract on Alloxan-Induced Diabetic Rats.

The study aimed to conduct chemical profiling, acute in-vivo toxicity evaluation, and the potential anti-diabetic effect of standardized Aloe sabaea flowers ethanolic extracts (ASFEE) on alloxan-induced diabetic rats. The chemical composition was analyzed using GC-MS and TLC techniques. The oral acute toxicity study was performed according to the WHO 2000 and the OECD 420 guidelines. Furthermore, anti-diabetic activity was investigated using two doses of ASFEE (0.2 and 0.5 g/kg/day BW, p.o.) compared with glibenclamide (5 mg/kg/day, p.o.). A molecular docking investigation of the identified components with the PTPN9 enzyme was performed to figure out the proposed anti-diabetic mechanism. GC-MS analysis displayed the existence of 18 compounds; mostof the compoundswere fatty acids and theiresters, and phytosterols. Total phenolic and flavonoid contents were 42.00±1.26 mg GAE/g DW and 22.21±1.55 mg QE/g DW, respectively. The results of the in-vivo toxicity study revealed the absence of noticeable signs of toxicity or mortality at various doses establishing the safety of the tested extract. The estimated LD50 value was higher than 10 g/kg. Antidiabetic action exhibited a noticeable decline in fasting blood glucose (FBG) levels comparable to glibenclamide with no inducing intense hypoglycemia and considerable excess weight.

A critical review on phytochemicals as antiviral medications for SARS-CoV-2 virus infection.

A pandemic of acute respiratory infection, which was specified as coronavirus disease 2019, was instigated by a different strain of the virulent coronavirus SARS-CoV-2 that first appeared in late 2019. Since viral infections spread fast and there is presently no effective treatment, the use of plants with a long history of use in treating these infections has been explored regularly. The pandemic of coronavirus disease 2019 (COVID-19) has brought to light the dearth of medications with approval to treat acute viral illnesses. Because of this, the illness had a high fatality rate. The mortality rate was initially quite high and varied according to the patient's geographic location. For instance, among Chinese patients, the rate was 3·6%, whereas 1·5% of COVID-19-related deaths were documented outside of China. As of 2020, India has a 1.4% case fatality rate (CFR) of COVID-19 mortality, compared to 2.8% in Brazil and 1.8% in the USA. Many studies are being conducted to create pharmaceutical compounds specifically targeting important SARS-CoV-2 proteins. Several drug discovery initiatives are being undertaken to find powerful inhibitors by combining biochemical assay and computer-aided drug design techniques. Although plant-derived compounds have not had much success in the dominion of antivirals, plants are, however, believed to be a limitless supply of medications for a variety of diseases and clinical conditions. The scientific foundation required for developing novel natural source medications is provided by the chemical characterization and analysis of plant components. Most viral infections treated by ethnobotanical applications and historical literature on ayurveda, and traditional medicine are generally attributed to phytochemicals, which are compounds derived from medicinal plants. In this review, we have described the application of vascular plant-derived chemicals, such as tannins, polyphenols, alkaloids, and flavonoids, as antivirals, especially for managing COVID-19. This article discusses novel bioactive compounds and their molecular structures that target the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) as prospective candidates for anti-coronavirus disease drugs. Moreover, to confirm the effectiveness of the phytochemicals that have demonstrated antiviral activity, clinical trials would need to be conducted in addition to the preclinical research that has already been done. To ensure spectacular findings, more applications of the compound would need to be studied to fully understand the effects of those phytochemicals whose clinical usefulness has already been established.