Inductively Coupled Plasma Optical Emission Spectrometry Research Articles

Advancing circular economy: A study of drinking water sludge for potential uses

The high demand for drinking water has increased the by-products from treatment plants, notably during coagulation-flocculation, leading to substantial sludges' accumulation. This study aims to focus on the characterization of drinking water treatment sludge (DWTS) batches from the three last years and statically studying it's uniformity, as exploring potential repurposing options. The samples were characterized using X-Ray Fluorescence (XRF), X-Ray Diffraction (XRD), Fourier Transform Infrared Spectroscopy (FTIR), Thermogravimetric Analysis (TGA), Inductively Coupled Plasma Optical Emission Spectroscopy (ICP-OES), Loss On Ignition (LOI), and Granulometric analysis. The results evinced that DWTS have a sandy nature, the organic fraction takes third of the DWTS’ chemical composition, the amount of Al2O3 + SiO2 + Fe2O3 is slightly different, with 55.84, 57.47, and 56.14 % for DWTS21, DWTS22, and DWTS23 respectively, as per ANOVA results, which exhibited the consistency sludge composition among the samples, providing valuable insights into repurposing DWTS, and contributing to sustainable and eco-friendly practices in the construction industry especially DWTS21, which presents higher content of CaO with 2.95 %.

Simple Method for Calcium Determination in Crude Oil Emulsion Using Digital Image Colorimetry

A portable device for digital image colorimetry (DIC) is reported for the determination of Ca in crude oil emulsions. ASTM D4807 was used for sample preparation for the isolation of saline species containing Ca. DIC was evaluated based on the complexation reactions with Ca using calcein, murexide, and calcon. Partial least squares (PLS) provided the best determination coefficients (higher than 0.990) for all complexing reagents. Significant interference of Mg was observed for the determination of Ca using calcein. PLS models with the lowest root mean square error of cross validation (RMSECV) values were obtained for murexide and calcon for a concentration of 0.250 mmol L−1 at pH of 13. The best conditions for camera focal length were 11 and 2 mm for murexide and calcon. For light intensity, the optimized conditions for murexide and calcon was 180 lux. Stabilities of color complexes over the time were 30 and 15 min for murexide and calcon, respectively. DIC/murexide provided the lowest root mean square error of prediction (RMSEP) and a linear response was observed from 0.5 to 10 mg L−1 Ca and the relative standard deviation (RSD) was lower than 10%. Significant differences were not observed between the results obtained by DIC/murexide and those obtained by microwave-assisted wet digestion (MAWD) with determination by inductively coupled plasma-optical emission spectrometry (ICP-OES). A limit of quantification of 0.50 mg kg−1 Ca were obtained using DIC/murexide. This approach is an alternative and useful method for the determination of Ca in crude oil samples, with advantages of miniaturization, low cost, and ease of operation.

Investigating UV-Irradiation Parameters in the Green Synthesis of Silver Nanoparticles from Water Hyacinth Leaf Extract: Optimization for Future Sensor Applications.

Silver nanoparticles (AgNPs) can be produced safely and greenly using water hyacinth, an invasive aquatic plant, as a reducing agent. This study aimed to optimize the UV-irradiation parameters for the synthesis of AgNPs from water hyacinth leaf extract. The study varied the reaction time and pH levels and added a stabilizing agent to the mixture. The synthesized AgNPs were characterized using UV-visible spectroscopy (UV-vis), transmission electron microscopy (TEM), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), and inductively coupled plasma optical emission spectroscopy (ICP-OES). The findings revealed that the optimal conditions for synthesizing AgNPs were achieved by adjusting the pH level to 8.5, adding starch as a stabilizing agent, and exposing the mixture to UV-A radiation for one hour. These conditions resulted in the smallest size and highest quantity of AgNPs. Furthermore, the synthesized AgNP colloids remained stable for up to six months. This study highlights the potential of utilizing water hyacinth as a sustainable and cost-effective reducing agent for AgNP synthesis, with potential applications in pharmaceuticals, drug development, catalysis, and sensing detection.

Quality and healthy aspects of Lider cheese at different stages of ripening

Lider cheese is a commercial full- fat semi-hard cheese produced from pasteurized goat`s milk in mountain area of Nikšić, Montenegro. The aim of this paper is to characterize the change of protein and fatty acid profiles, mineral content and antioxidant potential during the period of one month of its ripening. Proteolysis was monitored using electrophoresis of total extracts and water-soluble fractions under reducing conditions. Fatty acid profiles were determined by gas chromatography whereas the mineral content of cheese at different stage of ripening was determined by Inductively coupled plasma - optical emission spectrometry (ICP-OES) for macroelements and Inductively coupled plasma mass spectrometry (ICP-MS) for microelements, respectively. One month of ripening of Lider cheese is characterized by a relatively slow proteolysis which can be attributed to intensive lose of moisture, by the increase in desirable fatty acid content and consequently by the improvement of fatty acid healthy indices. After 30 days of ripening, mainly due to the degradation of αs-CN, the WSN/ TN and TCA/TN contents increased from 4.69 % to 6.06 % and 1.15 % to 1.90 %, respectively. One- month-old cheese had improved indexes of lipid quality as well as improved reducing power and ability to scavenge free radicals. Ripening did not affect mineral content of cheese if it is expressed on dry matter basis. According to obtained results, the optimal ripening period of Lider cheese is 15 days.

VERIFIKASI KUALITAS ANALISIS MANGAN MENGGUNAKAN TEKNIK ICP-OES DALAM SAMPEL AIR MINUM

Drinking water quality, including the levels of dissolved metals, is an important public health consideration. Manganese (Mn) is a naturally occurring metal that can be present in drinking water sources, and excessive intake of Mn can have adverse health effects. The objective of this study was to verify the performance of the analytical method for the determination of manganese (Mn) concentration in drinking water samples using Inductively Coupled Plasma-Optical Emission Spectrometry (ICP-OES) techniques at the PT XYZ Laboratory. The method verification included tests for analyte identity confirmation, linearity, precision, accuracy, as well as the determination of the Method Detection Limit (MDL) and Limit of Quantification (LOQ). The verification results showed that the ICP-OES method met the established performance requirements. The linearity test yielded a correlation coefficient (r) of 0.9998, fulfilling the criteria of r ≥ 0.995. The percent relative standard deviation (% RSD) value in the precision test was 1.41%, meeting the requirement of % RSD ≤ 2/3 % CV Horwitz. The accuracy test provided an average percent recovery of 98.66%, which is within the acceptable range of 85-120%. The determined MDL was 0.0006 mg/L, while the LOQ was 0.002 mg/L, both meeting the criteria of MDL < spiked concentration < 10 MDL and LOQ < environmental quality standard. In conclusion, the method for the determination of Mn concentration in drinking water using ICP-OES has been verified and can be used for routine analysis at the PT. XYZ Laboratory, supporting the monitoring and control of Mn levels in drinking water to ensure public health protection.

Standardization of Pharmaceutical and Analytical Analysis of Chincha Kshara

Acharya Susrutha has narrated Kshara as one of the Upayantras, Anusastras, Agropaharaniya and one of the Upakrama of Vrana. Kshara is considered superior to all surgical and para surgical measures. Kṣharas are more effective than other methods of treatment, because they can be used externally as Pratisaraniya Kshara and internally as Paneeya Kshara. Because of varied applications standardization of the compound formulation is the need of the present era to set standards for maintaining the quality of the products. In the present study work is done on the pharmaceutical and analytical study of Chincha Kshara conducted in the department of Shalya Tantra under the post graduate programme is being presented. Here an attempt has been made to study Chincha Kshara Analytically and to develop fingerprints by organoleptic tests, physico-chemical parameters and Inductively Coupled Plasma - Optical Emission Spectrometry (ICP-OES).

Contamination of trace, non-essential/heavy metals in nutraceuticals/dietary supplements: A chemometric modelling approach and evaluation of human health risk upon dietary exposure

Across the world, nutraceuticals/dietary supplements are commonly consumed without medical supervision, and believing these products are harmless to health. However, these products may contain trace (TMs) and non-essential/heavy metals (nHMs) as contaminants at levels higher than the recommended daily allowance (RDA), which can be hazardous to human health. Consequently, it is crucial to assess the levels of these metals to ensure the safety of these products. This study aimed to analyze the concentration of TMs (Mn, Cu and Zn) and nHMs (Al, Cr, Ni, Cd and Pb) in nutraceuticals/dietary supplements. Metal analysis was conducted using inductively coupled plasma–optical emission spectrometry (ICP-OES). Multivariate and bivariate analysis including principle component analysis (PCA), hierarchical cluster analysis (HCA) and Pearson correlation coefficient (PCC) were applied to understand inter-metal association and sources of these metals. Concentration ranges for TMs were found as, Mn (0.2–4.3 mg/kg), Cu (0.11–2.54 mg/kg), and Zn (0.1–22.66 mg/kg) while the nHMs concentration ranges were: Al (0.046–3.336 mg/kg), Cr (0.11–1.63 mg/kg), Ni (0.18–0.72 mg/kg), Cd (0.04–0.92 mg/kg), and Pb (0.18–1.08 mg/kg). The levels of tolerable dietary intake (TDI) for Cr and Ni, and the provisional tolerable monthly intake (PTMI) limit for Cd, exceeded the values set by the World Health Organization (WHO) and the European Food Safety Authority (EFSA). The estimation of the target hazard quotient (THQ <1), hazard index (HI < 1) and cumulative cancer risk (CCR <1 ✕ 10−3) indicated no significant non-carcinogenic and carcinogenic health risks associated with consuming these products. Therefore, the primary recommendation from this study is to use the nutraceuticals/dietary supplements should be under the supervision of dietitian.

Post‐Synthetic Modification of Mixed‐Metal UiO‐66 Framework for Rapid Neutralization of Chemical Warfare Agent Simulants

AbstractMetal‐organic frameworks (MOFs) are a promising class of materials for catalysis, offering unique opportunities for designing efficient and selective catalysts. In this study, we have focused on the synthesis and catalytic activity of a novel mixed metal MOF, Ce/Zr−UiO‐66@LiOtBu, designed for the rapid hydrolysis of chemical warfare agents simulants: dimethyl 4‐nitrophenyl phosphate (DMNP) and 2‐chloroethyl ethyl sulfide (CEES). This MOF was thoroughly characterized using powder X‐ray diffraction (PXRD), BET surface area, and inductively coupled plasma optical emission spectrometry (ICP‐OES). The catalytic performance of Ce/Zr−UiO‐66@LiOtBu was monitored in the hydrolysis of DMNP and CEES by using 31P NMR and GC‐MS respectively. Remarkably, the MOF demonstrated rapid and efficient catalytic activity, breaking the P−O bond in DMNP with 2 min and the hydrolysis of CEES was observed in less than 45 min The results suggest the potential application of Ce/Zr−UiO‐66@LiOtBu as a robust catalyst in the detoxification of chemical warfare agent simulants. Our findings highlight the novelty of Ce/Zr−UiO‐66@LiOtBu as a catalytically active MOF, showcasing the successful integration of cerium ions and lithium tert‐butoxide to enhance basicity.

Source identification and assessment of heavy metal contamination in different plant species in the alpine ecosystems of Mt. Madra

Heavy metals are among important environmental pollutants due to their environmental persistence, toxicity and ability to accumulate in living organisms. The aim of the present study was to investigate the levels of aluminium (Al), boron (B), cobalt (Co), chromium (Cr), copper (Cu), and molybdenum (Mo) in plants sampled from Mt. Madra, analysed their distribution characteristics and investigated their origins using Positive Matrix Factorization (PMF) modelling. The multi-point sampling technique was used to collect samples of 26 plants from Madra Mountain at altitudes ranging from 177 m to 1347 m. Inductively-coupled plasma optical emission spectroscopy (ICP-OES) was used for the determination of metals. The metal concentrations (all in terms of mg/kg) determined by ICP-OES are the following sequences (mean ± standard deviation): Al (827.97 ± 198.95) > B (38.49 ± 2.50) > Co (0.74 ± 0.15) > Cr (1.90 ± 0.39) > Cu (7.68 ± 0.73) > Mo (0.51 ± 0.06). Based on the results obtained from the plant samples with the highest concentrations, the following metals were identified: Al (Ajuga orientalis, 4643.57 mg/kg), B (Quercus petraea, 69.25 mg/kg), Co (Ajuga orientalis, 4.23 mg/kg), Cr (Teucrium lamiifolium, 8.64 mg/kg), Cu (Ajuga orientalis, 19.75 mg/kg) and Mo (Ajuga orientalis, 1.07 mg/kg). In conclusion, the results of the source identification analysis conducted by PMF indicated that metal concentrations in the alpine zone have a primarily anthropogenic origin.

Heavy Metal Detection and Removal by Composite Carbon Quantum Dots/Ionomer Membranes.

The combination of ion exchange membranes with carbon quantum dots (CQDs) is a promising field that could lead to significant advances in water treatment. Composite membranes formed by sulfonated poly(ether ether ketone) (SPEEK) with embedded CQDs were used for the detection and removal of heavy metal ions, such as lead and cadmium, from water. SPEEK is responsible for the capture of heavy metals based on the cation exchange mechanism, while CQDs detect their contamination by exhibiting changes in fluorescence. Water-insoluble "red" carbon quantum dots (rCQDs) were synthesized from p-phenylenediamine so that their photoluminescence was shifted from that of the polymer matrix. CQDs and the composites were characterized by several techniques: FTIR, Raman, UV/VIS, photoluminescence, XPS spectroscopies, and AFM microscopy. The heavy metal ion concentration was analyzed by inductively coupled plasma-optical emission spectroscopy (ICP-OES). The concentration ranges were 10.8-0.1 mM for Pb2+ and 10.0-0.27 mM for Cd2+. SPEEK/rCQDs showed a more pronounced turn-off effect for lead. The composite achieved 100% removal efficiency for lead and cadmium when the concentration was below a half of the ion exchange capacity of SPEEK. The regeneration of membranes in 1 M NaCl was also studied. A second order law was effective to describe the kinetics of the process.

Appraisal of potentially toxic metals contamination in protein supplements for muscle growth: A chemometric approach and associated human health risks

BackgroundThe use of protein supplements by athletes has risen due to their effectiveness in meeting dietary needs. However, there is a growing concern about the presence of potentially toxic metals (PTMs. Al, Cr, Mn, Ni, Cu, Zn, Cd, and Pb) in these supplements. Consequently, it is crucial to evaluate the levels of these PTMs to ensure the safety of the supplements. MethodsThe objective of the current study was to assess the PTMs concentrations in protein supplements and examine any possible health hazards. Twenty-five samples of protein supplements were purchased from different pharmacies to screen them for metals. Inductively coupled plasma-optical emission spectrometry (ICP-OES) was utilized to analyze metal content. Additionally, chemometric methods such as Pearson’s correlation coefficient (PCC), principal component analysis (PCA), and hierarchical cluster analysis (HCA) were employed to identify possible sources of PTMs contamination in protein supplements. ResultsConcentration ranges for PTMs were found as, Al (0.03–3.05 mg/kg), Cr (0.11–0.89 mg/kg), Mn (1.13–8.40 mg/kg), Ni (0.06–0.71 mg/kg), Cu (1.05–5.51 mg/kg), Zn (2.14–27.10 mg/kg), Cd (0.01–0.78 mg/kg), and Pb (0.06–0.57 mg/kg). The weekly intake of Cd exceeded the level of tolerable weekly intake (TWI) set by the European Food Safety Authority (EFSA). ConclusionAthletes, bodybuilders, fitness enthusiasts, dieters, young adults and adolescents, and health-conscious individuals should be conscious of Cd concentration as it does not compliance the TWI set by EFSA. Target hazard quotient (THQ < 1), hazard index (HI < 1), margin of exposure (MOE ≥ 1), percentile permitted daily exposure (% PDE < 100), and cumulative cancer risk (CCR < 1 × 10−3) analyses revealed that there are no appreciable non-carcinogenic and carcinogenic health risks associated with the use of these products.

Biosorption of copper, nickel, and manganese as well as the production of metal nanoparticles by Bacillus species isolated from soils contaminated with electronic wastes.

Improper electronic waste management in the world especially in developing countries such as Iran has resulted in environmental pollution. Copper, nickel, and manganese are from the most concerned soil contaminating heavy metals which found in many electronic devices that are not properly processed. The aim of this study was to investigate the biological removal of copper, nickel, and manganese by Bacillus species isolated from a landfill of electronic waste (Zainal Pass hills located in Isfahan, Iran) which is the and to produce nanoparticles from the studied metals by the isolated bacteria. The amounts of copper, nickel, and manganese in the soil was measured as 1.9 × 104 mg/kg, 0.011 × 104 mg/kg and 0.013 × 104 mg/kg, respectively based on ICP-OES analysis, which was significantly higher than normal (0.02 mg/kg, 0.05 mg/kg, and 2 mg/kg, respectively. The minimum inhibitory concentration (MIC) and the minimum bactericidal concentration (MBC) of metals on the bacterial isolates was determined. The biosorption of metals by the bacteria was evaluated by inductively coupled plasma optical emission spectroscopy (ICP-OES). The metal nanoparticles were synthetized utilizing the isolates in culture media containing the heavy metals with the concentrations to which the isolates had shown resistance. X ray diffraction (XRD), scanning electron microscopy (SEM), and energy-dispersive X-ray spectroscopy (EDS) were used for the evaluation of the fabrication of the produced metal nanoparticles. Based on the findings of this study, a total of 15 bacterial isolates were obtained from the soil samples. The obtained MICs of copper, nickel, and manganese on the isolates were 40-300 mM, 4-10 mM, and 60-120 mM, respectively. The most resistant isolates to copper were FM1 and FM2 which were able to bio-remove 79.81% and 68.69% of the metal, respectively. FM4 and FM5 were respectively the most resistant isolate to nickel and manganese and were able to bio-remove 86.74% and 91.96% of the metals, respectively. FM1, FM2, FM4, and FM5 was molecularly identified as Bacillus cereus, Bacillus thuringiensis, Bacillus paramycoides, and Bacillus wiedmannii, respectively. The results of XRD, SEM and EDS showed conversion of the copper and manganese into spherical and oval nanoparticles with the approximate sizes of 20-40 nm. Due to the fact that the novel strains in this study showed high resistance to copper, nickel, and manganese and high adsorption of the metals, they can be used in the future, as suitable strains for the bio-removal of these metals from electronic and other industrial wastes.

Investigating the Impact of temperature and storage time on antimony release from polyethylene terephthalate (PET) plastic used for bottled drinking water

In last decade, Prosperity in contemporary Saudi Arabia and the consequent stresses on renewable freshwater resources resulted in the bottled drinking water market. Over the period, sustainable water resources planning (SWRP) has become an essential requirement for the development of places where these resources are highly constrained. To meet this market growth in Saudi Arabia is augmented by increasing demand for bottled water. This drastic increase, leads some countries to develop an alternative sources including desalinated water and treated wastewater for landscaping irrigation, industrial reuse, street cleaning, and aquifer recharge. There are claims on health concerns the possibility of chemicals migration from polyethylene terephthalate (PET) bottles into drinking water. In this paper, inductively coupled plasma -optical emission spectrometry (ICP-OES) was utilized and applied to determine the antimony (Sb) release from PET bottles into mineral water of 8 local brands at different temperature degrees within 8 months storage time.

Assessing cobalt and manganese in foods: A study on determination and health risk using inductively coupled plasma spectrometry

This study aimed to evaluate the concentration and health risk of cobalt (Co) and manganese (Mn) in food using inductively coupled plasma mass spectroscopy (ICP-MS) and ICP optical emission spectroscopy (ICP-OES), respectively. Methods were validated for six food classes based on composition and calorie content. The method limit of quantification (MLOQ) ranged from 0.0766 to 0.2525 μg/kg for Co and 0.0202–0.0832 mg/kg for Mn. Out of 351 food items, Co and Mn were detected above the method limit of detection (MLOD) in 266 and 222 samples, respectively, with highest levels in nuts, seeds, grains, beans, sauces, and seasonings. Pearson correlation analysis showed a significant positive correlation (p < 0.01) between Co and Mn in agricultural (r = 0.390) and processed food (r = 0.543) categories. Exposure to Co and Mn through dietary intake remained within acceptable limits (target hazard quotient (THQ) < 1), suggesting that lifetime consumption is unlikely to elevate potential health risks. In conclusion, this comprehensive study validated methods for Co and Mn analysis and assessed their concentrations and potential health risks across various food categories.

Evaluating Heavy Metals in Human Breast Milk: a Cross-Sectional Study from Mining and Agricultural Areas in Northwestern Iran.

This study aimed to assess the levels of heavy metals in the breast milk of women residing in the mining and agricultural areas of East Azerbaijan province in Iran. This cross-sectional study analyzed 68 lactating mothers from mining (n = 28) and agricultural (n = 40) areas of East Azerbaijan province in Iran between June 2022 and March 2023. The study used an Inductively Coupled Plasma Optical Emission Spectroscopy (ICP-OES) to measure the concentrations of heavy metals, including arsenic (As), chromium (Cr), copper (Cu), and iron (Fe). A semi-quantitative food frequency questionnaire (SQ-FFQ) was used to collect data on the dietary and sociodemographic characteristics of the mothers. Although the concentration of arsenic (As) was below the limit of detection (LOD), the mean concentrations of chromium (Cr), copper (Cu), and iron (Fe) were 1.11, 0.87, and 13.25mg/L in agricultural areas and 0.83, 0.93, and 11.35mg/L in mining areas, respectively. The concentrations of Cr (p < 0.001) and Fe (p = 0.019) were significantly higher in the breast milk of women residing in agricultural areas. However, the concentration of Cu was significantly higher (p = 0.085) in the breast milk of women living in mining areas. Additionally, lactation age had a significant effect on Cu levels (p = 0.015), with a negative coefficient of -0.011. The study indicates that the levels of heavy metals in breast milk can be influenced by the exposure to pesticides, fertilizers, volcanic soil, and disparities in access to post-natal care and iron supplements.

Relevance of using portable X-ray fluorescence to identify gold hyperaccumulator plants

Field Portable X-Ray Fluorescence (FPXRF) was investigated as an alternative analysis tool for the detection and quantification of gold in hyperaccumulator plants in the field. First, synthetic gold standards were prepared with materials chosen to best simulate plant material, using microcrystalline cellulose (mcc) or ash by adding known amounts of gold. Powder samples were obtained containing gold in amounts ranging from 10 to 1000 ppm of gold. They were analysed, as well as blank samples of mcc and ash, using a NITON xl3t GOLDD+ FPXRF spectrometer in AllGeo and Soil modes with an analysis time of 60 s. Results were compared to Inductively Coupled Plasma Optical Emission Spectrometry (ICP-OES) analysis of the synthetic gold standards after digestion in aqua regia. Gold was detected and accurately quantified in synthetic gold standards containing more than 25 ppm of gold in AllGeo mode. At lower concentration, results were much more inaccurate, with no gold being detected at 10 ppm. In Soil mode, similar results to AllGeo mode were obtained with mcc synthetic standards. However, with ash synthetic standard gold quantification was very poor over the whole concentration range and gold was detected in the blank ash sample, which was confirmed as a false positive by the subsequent ICP analysis. Samples of Phyllanthus stipulatus, suspected gold hyperaccumulators, collected on gold-bearing sites in French Guiana were then analysed following the same protocol. The same false positive phenomenon was observed in some of them, with gold being detected by FPXRF in Soil mode but not by ICP analysis. Furthermore, analysis of the FPXRF spectra revealed that none of the characteristic gold emission ray was present. This false positive was attributed to an interference caused by zinc, present in significant amount in the ash of the synthetic standard and the collected plants.

Biogenic synthesis of selenium nanoparticles from Nyctanthes arbor-tristis L. and evaluation of their antimicrobial, antioxidant and photocatalytic efficacy

Biogenic synthesis of nanoparticles has been established as an environmentally benign and sustainable approach. This study emphasizes biosynthesis of selenium nanoparticles (SeNPs) utilizing leaf extract of Nyctanthes arbor-tritis L., well known for its abundant bioactive compounds. Various analytical techniques were employed for characterization of synthesized SeNPs. X-ray diffraction (XRD) spectroscopy confirmed the crystalline structure and revealed the average crystalline size of SeNPs to be 44.57 nm. Additionally, UV–Vis spectroscopy confirmed successful synthesis of SeNPs by validating the surface plasmon resonance (SPR) properties of SeNPs. FTIR analysis data revealed different bonds and their corresponding functional groups responsible for the synthesis and stability of synthesized SeNPs. DLS and zeta analysis revealed that 116.5 nm sized SeNPs were stable in nature. Furthermore, field emission scanning electron microscopy (FE-SEM) validated the spherical morphology of SeNPs with a size range of 60–80 nm. Inductively coupled plasma-optical emission spectroscopy (ICP-OES) determined the concentration of SeNPs in the obtained colloidal solution. Antioxidant activity of synthesized SeNPs was evaluated employing DPPH and H2O2 assay, revealed that the synthesized SeNPs were effective antioxidant agent. Additionally, antimicrobial potential was evaluated against a panel of Gram-positive and Gram-negative bacteria and found to be effective at higher concentration of SeNPs. SeNPs also exhibited strong anti-biofilm activity while evaluated against various biofilm producing bacteria like Escherichia coli,Staphylococcus epidermidis and Klebsiella pneumonia. The cytotoxicity of the bio-synthesized SeNPs was evaluated against HEK 293 cell line, exhibited minimal toxicity even at concentration 100 μg/mL with 65% viable cells. SeNPs has also been evaluated for dye degradation which has indicated excellent photocatalytic activity of synthesized SeNPs. The experimental data obtained altogether demonstrated that synthesized SeNPs exhibited significant antimicrobial and anti-biofilm activity against various pathogens, and also showed significant antioxidant and photocatalytic efficiency.

Elemental, phytochemical analysis and determination of antibacterial, antioxidant, and cytotoxic activities of leaves extracts of eleven Eucalyptus species

The genus Eucalyptus has attracted considerable attention from natural product specialists exploring new phytochemicals for therapeutic purposes due to their possible biological activities. This was stimulated by current findings that Eucalyptus species interrupt the propagation of the recently tormenting COVID-19 virus. Eleven Eucalyptus leaf extracts were subjected to in vitro antimicrobial studies against four bacterial strains: Staphylococcus aureus, Streptococcus pyogenes, Staphylococcus lugdunensis and Staphylococcus epidermis using the broth serial dilution assay. The potential of the extracts to inhibit free radicals 2,2-Diphenyl-1-picrylhydrazyl (DPPH) and 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) was investigated, indicating antioxidant properties. Furthermore, the cytotoxicity test was performed against the human embryonic kidney (HEK293-T) cell line using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. Phytochemicals were identified and characterized using Fourier transform infrared spectroscopy (FTIR) and one-dimensional gas chromatography mass spectrometry (GC–MS). Moreover, the microwave plasma atomic emission spectroscopy (MP-AES) coupled with inductively coupled plasma optical emission spectroscopy (ICP-OES) was used to evaluate the multielemental composition of the extracts. The MP-AES and ICP-OES techniques in this work displayed accuracy and sensitivity for multielement determination by identifying P, B, Ca, Zn, Cu, Mg, Fe, Mn, Na, and K as major constituents in Eucalyptus extracts. The extracts generally had strong antioxidant and antibacterial properties, with E. viminalis (IC50 = 2.91 ± 0.22 µg/mL) demonstrating strong action against the ABTS radical. E. nitens and E. dunnii also showed highest activity against DPPH and ABTS, with IC50 values < 10 µg/mL. Additionally, with IC50 values greater than 20 µg/mL, the extracts demonstrated relative non-toxicity against HEK293-T cells. The existence of the bioactive chemicals found by FTIR and GC–MS may be the cause of the observed biological activity. Because Eucalyptus plant species have the highest antioxidant activity and the most inhibitory action against the majority of Streptococcus bacterial strains, they can be employed as a therapeutic treatment to treat infections caused by Streptococcus.

FDU-12@AGA-Pd: A green, novel, recyclable, and highly versatile mesoporous catalyst for C[sbnd]C coupling reaction and synthesis of tetrazoles

Herein, we present an efficient, novel nanocatalyst through the immobilization of AGA-Pd onto the inside of mesoporous silica FDU-12 channels that were successfully synthesized by a simple procedure. The catalytic activity of FDU-12@AGA-Pd was investigated for the synthesis of 1H-tetrazole derivatives and the Suzuki reaction. The synthesized compounds were identified and confirmed with the help of 1H-NMR. In this research, the nanocatalyst was prepared by the immobilization of palladium into FDU-12 channels coated with 2-amino-5-guanidinovaleric acid (AGA). N2 adsorption-desorption isotherms indicated excellent BET surface area for FDU-12 and FDU-12@AGA-Pd, which is 627.27 and 106.69 (m2 /g), respectively. The physical and chemical properties of raw and modified samples (FDU-12, FDU-12@AGA-Pd) were characterized by Thermogravimetric analysis (TGA), N2 adsorption-desorption analysis, Inductively coupled plasma optical emission spectroscopy (ICP-OES), transmission electron microscopy (TEM), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), Fourier transforms infrared spectroscopy (FT-IR), Mapping, and X-ray diffraction (XRD). The synthesized mesoporous nanocatalyst was recovered and reused in five continuous cycles without considerable change in its catalytic activity.SynopsisOur findings will help researchers and industrial factories to apply a green and sustainable mesoporous catalyst to produce a variety of valuable organic compounds and pharmaceutical products.

A ratiometric and selective fluorescent nanosensor for determining Hg2+ ions based on a novel functionalized metal–organic framework

A new method using fluorescence was developed to detect Hg2+ ions in water. This method relied on the reaction between NH2‐MIL‐53(Al) and 5‐bromo‐2‐hydroxyacetophenone. The method was carefully fine‐tuned for optimal reaction conditions and analytical parameters like pH levels, nanosensor quantity, and detection limits. It showed great linearity in detecting Hg2+ ions in the range of 0.0–3.0 ppm (0.0–1.50 × 10−5 M), with a very low detection limit of 1.65 × 10−2 ppm (8.23 × 10−8 M). We tested how well the method can distinguish between different substances by investigating whether other common substances in water samples would interfere. The results were positive, as the presence of these substances did not significantly affect the accuracy of detecting Hg2+ ions, confirming the method's reliability. In order to confirm its dependability, we conducted a quantitative test to detect Hg2+ ions in water samples. The recovery rates obtained ranged from 97.16% to 103.2%, demonstrating the method's precision and accuracy. A comparison with inductively coupled plasma optical emission spectrometry (ICP‐OES), a well‐known method for analyzing trace metals, produced similar results, further instilling confidence in the 5Br2HA = N‐Al‐MOF nanosensor that was developed. In general, this research emphasizes the exciting potential of the new nanosensor in detecting Hg2+ ions in various water and cosmetic samples. It provides a strong and dependable alternative to traditional detection methods.