Substances In Environment Research Articles

Mitigating effects of selenium and zinc on oxidative stress and biochemical and histopathological changes in lung during prenatal and lactational exposure rats to barium chloride.

Selenium (Se) and zinc (Zn) are essential trace elements with antioxidant properties, and their supplementation has been shown to be protective against the toxicity of various environmental and dietary substances. The aim of this study was to investigate the potential protective effect of selenium and zinc as adjuvants against barium (Ba) toxicity in lactating rats and their offspring. The pregnant rats were divided into six groups: the first as control; group 2 received barium (67ppm) in the drinking water; group 3 had combined Ba + Se (0.5mg/kg) in the diet; group 4 received Zn (50mg/kg bw) by gavage together with Ba; groups 5 and 6, positive controls, were treated with selenium (0.5mg/kg) and zinc (50mg/kg bw), respectively. MDA, H2O2, AOPP, CAT, GPx, and SOD levels were measured and lung histopathology was performed. Our results showed that barium administration caused lung damage as evidenced by an increase in MDA, H2O2, and AOPP levels and a decrease in the activities of CAT, GPx, and SOD in mothers and their offspring. A decrease in lung GSH, NPSH, and MT levels was also observed. Supplementation of Ba-treated rats with Se and/or Zn significantly improved the pulmonary antioxidant status of mothers and their offspring. Histopathological examinations were also consistent with the results of biochemical parameters, suggesting the beneficial role of Se and Zn supplementation, as evidenced by less accumulation of collagen fibers as studied by hematoxylin and eosin (H&E) and Masson's trichrome staining. In conclusion, we demonstrate the adverse effects of maternal barium exposure during pregnancy and on neonatal lung health and the protective effects of selenium and zinc in preventing the adverse effects of barium exposure.

Characterization of Gamma Spectroscopy Setup, Efficiency Calibration of HPGe detector used for Radiological substances

Background: Contamination of radiological substances in environment is one of the most important factors and harmful for living beings if the activity is high enough with long half-life.‘Gamma Spectrometry Setup’ is comparatively better for detection and analysis of gamma radiations in any type of specimens. Initiating the data acquisition setup, it’s essential to calibrate the entire setup for accuracy measurement. Materials and Methods:The main purpose of the research work is to characterize the data acquisition setup using137Cs and 60Co point sources. 137Cs emits γ-rays of 661.66 keV and 60Coemits two different γ-rays; 1173.2 KeV & 1332.5 KeV. Setup standardization is an essential part of any research works. Results: The HPGe detector used with the setup is also good enough for γ-energy detection. Detector efficiency calibration is another major task needed for activity calculation, using gamma energy lines detected in a sample detector efficiency can be calculated. Conclusion: Initiating every research experiment, the setup calibration should be checked for accurate results

Laser Tweezers Raman Spectroscopy and its application in bio-chemical sensing

Laser Tweezers Raman Spectroscopy (LTRS) technology combines Raman spectroscopy and optical tweezers technology, providing a new way to research in single cell analysis and microbial classification. Driven by the development of precision spectroscopy and deep learning techniques, LTRS plays an increasingly important role in biomedical research, clinical diagnosis and environmental research. For example, it can be used to detect cancer cells, analyse bacterial infections, and monitor harmful environmental substances. In this paper, we review the basic principles of LTRS technology through literature reading and case studies, explain how the technology combines the advantages of optical tweezers and Raman spectroscopy in order to provide a non-destructive, label-free and susceptible single-cell analysis method, summarize the latest development of LTRS technology in recent years, as well as its applications in the field of biochemical sensing, and finally discuss the problems it is currently facing and look forward to its future development direction. Finally, the current problems faced by LTRS are discussed, and the direction of its future development is anticipated.

Perfluoroalkyl functionalized-Au nanoparticle sensor: Employing rate of spectrum shifting for highly selective and sensitive detection of per- and polyfluoroalkyl substances (PFASs) in aqueous environments

Per- and polyfluoroalkyl substances (PFASs) are emerging contaminants detected ubiquitously and have negative impacts on human health and ecosystem; thus, developing in-situ sensing technique is important to ensure safety. Herein, we report a novel colorimetric-based sensor with perfluoroalkyl receptor attached to citrate coated gold nanoparticles (Citrate-Au NPs) that can detect several PFASs including perfluorocarboxylates with different chain lengths (PFHxA, PFOA, PFNA, PFDA), perfluorooctanoic sulfonate (PFOS), and perfluorooctanoic phosphonate (PFOPA). The sensor detects PFASs utilizing fluorous interaction between PFASs and the perfluoroalkyl receptor of Citrate-Au NPs in a solution at a fixed salt concentration, inducing changes in nanoparticle dispersity and the solution color. The rate of spectrum shift was linearly dependent on PFASs concentrations. Citrate-Au NPs with size between 29 – 109 nm were synthesized by adjusting citrate/Au molar ratios, and 78 nm showed the best sensitivity to PFOA concentration (with level of detection of 4.96 µM). Citrate-Au NPs only interacted with PFASs with perfluoroalkyl length > 4 and not with non-fluorinated alkyl compound (nonanoic acid). The performance of Citrate-Au NP based sensor was strongly dependent on the chain length of the perfluoroalkyl group and the head functional group; higher sensitivity was observed with longer chain over shorter chain, and with sulfonate functional group over carboxylate and phosphonate. The sensor was tested using real water samples (i.e., tap water, filtered river water), and it was found that the sensor is capable of detecting PFASs in these conditions if calibrated with the corresponding water matrix. While further optimization is needed, this study demonstrated new capability of Citrate-Au NPs based sensor for detection of PFASs in water.

Cellulosimicrobium sp. Strain L1: A Study on the Optimization of the Conditions and Performance of a Combined Biological Trickling Filter for Hydrogen Sulfide Degradation.

Sulfide is a toxic and hazardous substance in the agricultural environment, which can cause damage to humans and livestock when exposed to large amounts of air. In this study, we performed one-factor optimization of the culture conditions and culture fractions of the Cellulosimicrobium sp. strain L1 and combined it with a biological trickling filter cell for the degradation of hydrogen sulfide for 24 consecutive days. The degradation effect of strain L1 and the biological trickling filter (BTF) on hydrogen sulfide was investigated, and the changes in intermediate products in the degradation process were briefly analyzed. The results showed that strain L1 had the highest conversion efficiency when incubated with 3 g/L sucrose as the carbon source and 1 g/L NH4Cl as the nitrogen source at a temperature of 35 °C, an initial pH of 5, and a NaCl concentration of 1%. The concentration of thiosulfate increased and then decreased during the degradation process, and the concentration of sulfate increased continuously. When strain L1 was applied to the biological trickling filter, it could degrade 359.53 mg/m3 of H2S. This study provides a deeper understanding of sulfide degradation in biological trickling filters and helps promote the development of desulfurization technology and the treatment of malodorous gasses produced by the accumulation of large quantities of livestock manure.

Tissue distribution and exposure risk assessment of dioxins, dioxin-like polychlorinated biphenyls and perfluoroalkyl substances in red swamp crayfish

Significant attention has been paid to the adverse effects of dioxins, dioxin-like polychlorobiphenyls (DL-PCBs) and per-and polyfluoroalkyl substances (PFAS) in environment and food on ecosystem and human health. However, limited information exists regarding the occurrence, tissue distribution and exposure risk of these pollutants in crayfish. This study investigated tissue-specific distribution characteristics, influence factors and exposure risk of dioxins, DL-PCBs and PFAS in crayfish. Dioxins, DL-PCBs, and PFAS were detected in crayfish samples, with concentrations ranging from 0.361 to 1.91 pg TEQ g−1 for sum dioxins and DL-PCBs, and 1.54–21.2 ng g−1 for sum PFAS. The highest concentrations of dioxins, DL-PCBs TEQ and total PFAS were found in crayfish viscera and accounting for over 69% of the relative body burden (RBBs) of these pollutants. The specific-tissue distribution of these pollutants linked to tissue fat and protein content and log Kow and molecular weights of homologues. The consumption of crayfish edible tissue posed no health risks from exposure to dioxins and DL-PCBs as well as sum 4 PFAS in adults. However, consumption of crayfish viscera significantly increased exposure risk. This study can provide valuable insights into the tissue-specific distribution and human exposure risks associated with dioxins, DL-PCBs and PFAS in crayfish.

A colorimetric/electrochemical microfluidic biosensor using target-triggered DNA hydrogels for organophosphorus detection

Organophosphorus compounds are widely distributed and highly toxic to the environment and living organisms. The current detection of organophosphorus compounds is based on a single-mode method, which makes it challenging to achieve good portability, accuracy, and sensitivity simultaneously. This study designed a multifunctional microfluidic chip to develop a dual-mode biosensor employing a DNA hydrogel as a carrier and aptamers as recognition probes for the colorimetric/electrochemical detection of malathion, an organophosphorus compound. The biosensor balanced portability and stability by combining a microfluidic chip and target-triggered DNA hydrogel-sensing technologies. Moreover, the biosensor based on target-triggered DNA hydrogel modified microfluidic developed in this study exhibited a dual-mode response to malathion, providing both colorimetric and electrochemical signals. The colorimetric mode enables rapid visualization and qualitative detection and, when combined with a smartphone, allows on-site quantitative analysis with a detection limit of 56 nM. The electrochemical mode offers a broad linear range (0.01–3000 μM) and high sensitivity (a limit of detection of 5 nM). The two modes could validate each other and improve the accuracy of detection. The colorimetric/electrochemical dual-mode biosensor based on target-triggered DNA hydrogel modified microfluidic chip offers a portable, simple, accurate, and sensitive strategy for detecting harmful environmental and food substances.

Evaluating Solid Phase Adsorption Toxin Tracking (SPATT) for passive monitoring of per- and polyfluoroalkyl substances (PFAS) with Ion Mobility Spectrometry-Mass Spectrometry (IMS-MS)

Detection and monitoring of per- and polyfluoroalkyl substances (PFAS) in aquatic environments has become an increasingly higher priority of regulatory agencies as public concern for human intake of these chemicals continues to grow. While many methods utilize active sampling strategies (“grab samples”) for precise PFAS quantitation, here we evaluate the efficacy of low-cost passive sampling devices (Solid Phase Adsorption Toxin Tracking, or SPATTs) for spatial and temporal PFAS assessment of aquatic systems. For this study, passive samplers were initially deployed in North Carolina along the Cape Fear River during the summer and fall of 2016 and 2017. These were originally intended for the detection of microcystins and monitoring potentially harmful algal blooms, though this period also coincided with occurrences of PFAS discharge from a local fluorochemical manufacturer into the river. Additional samplers were then deployed in 2022 to evaluate changes in PFAS fingerprint and abundances. Assessment of PFAS showed legacy compounds were observed across almost all sampling sites over all 3 years (PFHxS, PFOS, PFHxA, etc.), while emerging replacement PFAS (e.g., Nafion byproducts) were predominantly localized downstream from the manufacturer. Furthermore, samplers deployed downstream from the manufacturer in 2022 noted sharp decreases in observed signal for replacement PFAS in comparison to samplers deployed in 2016 and 2017, indicating mitigation and remediation efforts in the area were able to reduce localized fluorochemical contamination.

Preferential adsorption of medium molecular weight proteins in extracellular polymeric substance alleviates toxicity of small-sized microplastics to Skeletonema costatum

Extracellular polymeric substances (EPS) secreted by organisms tend to encapsulate microplastics (MPs), forming an EPS-corona that affects the fate of MPs in marine ecosystems. However, the impact of the EPS-corona on the biotoxicity of MPs to marine organisms remains poorly understood. Herein, the effect of the EPS-corona on the toxicity of polystyrene (PS) MPs of different sizes (0.1 and 1 µm) to Skeletonema costatum (S. costatum) was investigated. The preferential adsorption of medium molecule weight (∼55 kDa) proteins onto PS MPs mainly contributed to the EPS-corona formation, decreasing the surface charge negativity of small-sized PS MPs (0.1 µm) by 72.4 %. Nitrogen (N) and oxygen (O) moieties in polysaccharides and proteins were identified as the preferential adsorption sites in the EPS-PS MPs interaction. Density functional theory (DFT) calculations confirmed the nuclear magnetic resonance spectroscopy (NMR) results, revealing that the binding mode between EPS and PS MPs was mainly hydrogen bonding. In addition, EPS-corona increased the cell density of S. costatum by 35.5–36.0 % when exposed to small-sized PS MPs (0.1 µm, 25–50 mg/L). These findings provide new insights into how EPS-corona affects the environmental fate and ecological risks associated with micro- and nano-sized plastics in marine ecosystems.

Wastewater-based epidemiology to monitor 68 NPS/conventional drug use in Taipei metropolitan area in Taiwan during and after COVID-19 pandemic

Amidst far-reaching COVID-19 effects and social constraints, this study leveraged wastewater-based epidemiology to track 38 conventional drugs and 30 new psychoactive substances (NPS) in northern Taiwan. Analyzing daily samples from four Taipei wastewater plants between September 2021 and January 2024—encompassing club reopenings, holidays, Lunar New Year, an outbreak, and regular periods—thirty-one drugs were detected, including 5 NPS. Tramadol, zolpidem tartrate, CMA, and MDPV were newly detected in Taiwanese sewage with frequency of 1.4 %− 89.0 %. Conventional drug use typically increased post-pandemic, aside from benzodiazepines and methadone. Methamphetamine showed 100 % frequency, indicating ongoing daily consumption despite COVID-19 measures. Methamphetamine and morphine's consumption dipped then rose around club reopening, hinting at limited access. The consumption trend of methadone appeared to compensate for the use of morphine. Ketamine and NPS demonstrated similar patterns throughout the entire period. NPS as party drugs seemed influenced by an unstable supply chain and complexities in implementation. Benzodiazepines, commonly abused alongside synthetic cathinones in Taiwan exhibited an opposing trend to NPS while aligned with acetaminophen, suggesting elevated stress and anxiety levels during the pandemic. No significant differences were observed in drug consumption between weekdays and weekends, potentially indicating that COVID-19 measures blurred the traditional distinctions between these timeframes. Environmental ImplicationNew psychoactive substances refer to chemically modified variants of controlled drugs designed to mimic the effects of the original drugs while evading modern detection methods, categorizing them as hazardous materials. The study presents a sewage monitoring project conducted from 2021 to 2024, collecting samples from four WWTPs to analyze NPS and conventional drug trends during and after the COVID-19 pandemic. The findings uncovered connections between drug consumption patterns and pandemic-related policies. In light of the persistent drug abuse and their environmental presence, the results bear critical importance for both environmental and public health. We provide a thorough assessment of these relationships and prioritize areas for future research.

Potential Effects of Low-Level Toluene Exposure on the Nervous System of Mothers and Infants.

In day-to-day living, individuals are exposed to various environmentally hazardous substances that have been associated with diverse diseases. Exposure to air pollutants can occur during breathing, posing a considerable risk to those with environmental health vulnerabilities. Among vulnerable individuals, maternal exposure can negatively impact the mother and child in utero. The developing fetus is particularly vulnerable to environmentally hazardous substances, with potentially greater implications. Among air pollutants, toluene is neurotoxic, and its effects have been widely explored. However, the impact of low-level toluene exposure in daily life remains unclear. Herein, we evaluated 194 mothers and infants from the Growing children's health and Evaluation of Environment (GREEN) cohort to determine the possible effects of early-life toluene exposure on the nervous system. Using Omics experiments, the effects of toluene were confirmed based on epigenetic changes and altered mRNA expression. Various epigenetic changes were identified, with upregulated expression potentially contributing to diseases such as glioblastoma and Alzheimer's, and downregulated expression being associated with structural neuronal abnormalities. These findings were detected in both maternal and infant groups, suggesting that maternal exposure to environmental hazardous substances can negatively impact the fetus. Our findings will facilitate the establishment of environmental health policies, including the management of environmentally hazardous substances for vulnerable groups.

The Transformation of Per- and Polyfluoroalkyl Substances in the Aquatic Environment of a Fluorochemical Industrial Park

Jiangsu High-Tech Fluorochemical Industrial Park in Changshu City, Jiangsu Province, is the largest fluorochemical industrial park in Asia. The occurrence of per- and polyfluoroalkyl substances (PFASs) in surface water and widespread local plants was investigated in Jiangsu High-Tech Fluorochemical Industrial Park. Thirty-two target PFASs were detected in dissolved-phase, particle-phase and plant samples. The concentrations of total PFASs ranged from 1650 to 8250 ng/L in the dissolved-phase samples, 132 to 6810 ng/g dw in the particle-phase samples and 25.8 to 9460 ng/g dw in different plant tissues. Perfluorohexanoic acid (PFHxA), Perfluorooctanoate acid (PFOA) and 6:2 fluorotelomer carboxylic acid (6:2 FTCA) were predominant PFASs and contributed 80−91% to ΣPFAS in water samples. A total of 67 emerging PFAS were identified in all samples using nontargeted analysis. Typha orientalis showed better accumulation ability, with an average ΣPFAS concentration of 3450 ng/g dw and the highest root concentration factor (RCF) of 171. Typha orientalis, Eichhornia crassipes and Alternanthera sessilis have potential for use in PFAS phytostabilization.

CardioDPi: An explainable deep-learning model for identifying cardiotoxic chemicals targeting hERG, Cav1.2, and Nav1.5 channels

The cardiotoxic effects of various pollutants have been a growing concern in environmental and material science. These effects encompass arrhythmias, myocardial injury, cardiac insufficiency, and pericardial inflammation. Compounds such as organic solvents and air pollutants disrupt the potassium, sodium, and calcium ion channels cardiac cell membranes, leading to the dysregulation of cardiac function. However, current cardiotoxicity models have disadvantages of incomplete data, ion channels, interpretability issues, and inability of toxic structure visualization. Herein, an interpretable deep-learning model known as CardioDPi was developed, which is capable of discriminating cardiotoxicity induced by the human Ether-à-go-go-related gene (hERG) channel, sodium channel (Na_v1.5), and calcium channel (Ca_v1.5) blockade. External validation yielded promising area under the ROC curve (AUC) values of 0.89, 0.89, and 0.94 for the hERG, Na_v1.5, and Ca_v1.5 channels, respectively. The CardioDPi can be freely accessed on the web server CardioDPipredictor (http://cardiodpi.sapredictor.cn/). Furthermore, the structural characteristics of cardiotoxic compounds were analyzed and structural alerts (SAs) can be extracted using the user-friendly CardioDPi-SAdetector web service (http://cardiosa.sapredictor.cn/). CardioDPi is a valuable tool for identifying cardiotoxic chemicals that are environmental and health risks. Moreover, the SA system provides essential insights for mode-of-action studies concerning cardiotoxic compounds.

Safety evaluation of synthesized magnesium carbonate hydrate particles following inhalation exposure

Numerous fine particles or mist from environmental substances significantly contribute to human beings, affecting health issues for both humans and the environment by irritating the respiratory system. To achieve scarcity of information regarding exposure routes and the relationship between substance and health effects needs to be investigated more. Here, we investigated flame retardants (FRs): magnesium carbonate was synthesized, and its inhalation toxicity was examined for the first time by applying it to Sprague-Dawley rats using a mist aerosol-supplying chamber condition. The synthesized magnesium carbonate was fully physiochemically characterized, exhibiting a mesoporous sheet-like morphology, size distribution of 4.971 ± 2.363 μm, the dypingite phase, a surface area of 10.718 m² g−1, and a pore volume of 0.051 cm³ g−1. As a result of the inhalation toxicity study, the 50% lethal concentration (LC50) of magnesium carbonate was determined to be equal to or greater than 1.91 mg m−3. Microscopic examination for assessing pulmonary residue levels of magnesium carbonate reveals the presence of residues in the lungs up to 3 days post-administration. However, over time, there is a gradual decrease of pulmonary residues, and by the 14th day of administration, it is regarded that no residual presence is observable within the pulmonary system.

Accurate Simulation for 2D Lubricating Materials in Realistic Environments: From Classical to Quantum Mechanical Methods.

2D materials such as graphene, MoS2, and hexagonal BN are the most advanced solid lubricating materials with superior friction and anti-wear performance. However, as a typical surface phenomenon, the lubricating properties of 2D materials are largely dependent on the surrounding environment, such as temperature, stress, humidity, oxygen, and other environmental substances. Given the technical challenges in experiment for real-time and in situ detection of microscopic environment-material interaction, recent years have witnessed the acceleration of computational research on the lubrication behavior of 2D materials in realistic environments. This study reviews the up-to-date computational studies for the effect of environmental factors on the lubrication performance of 2D materials, summarizes the theoretical methods in lubrication from classical to quantum-mechanics ones, and emphasizes the importance of quantum method in revealing the lubrication mechanism at atomic and electronic level. An effective simulation method based on ab initio molecular dynamics is also proposed to try to provide more ways to accurately reveal the friction mechanisms and reliably guide the lubricating material design. On the basis of current development, future prospects, and challenges for the simulation and modeling in lubrication with realistic environment areoutlined.

Occurrence, source modeling, influencing factors and exposure assessment of polycyclic aromatic hydrocarbons in water sources: A mega-study from mainland China

This study investigates the composition and distribution of 16 priority polycyclic aromatic hydrocarbons (PAHs) in 70 water samples collected from centralized drinking water sources (CDWSs) across 30 provinces (cities) in mainland China. Additionally, water quality and socio-economic data were collected to determine the influencing factors. The study discovered that the total concentrations of 16 priority PAHs (Σ16PAHs) varied from 0.17 to 176.71 ng/L (mean: 56.49 ± 38.58 ng/L). Lakes and reservoirs had significantly higher concentrations of PAHs than groundwater. The primary pollutants were low-molecular-weight (LMW) PAHs, such as phenanthrene, naphthalene, and fluorene. There was a strong correlation between LMW PAHs and Σ16PAHs (p < 0.05). The mean Σ16PAHs in the seven geo-environmental zones were ranked as follows, under the comprehensive influence of emission density, natural, and social environmental factors: Northwest China (78.42 ± 66.96 ng/L) > Northeast China (73.70 ± 33.23 ng/L) > East China (64.35 ± 45.66 ng/L) > North China (50.95 ± 31.87 ng/L) > Southwest China (44.05 ± 32.56 ng/L) > Central China (41.68 ± 19.44 ng/L) > Southern China (40.99 ± 16.54 ng/L). The source modeling analysis revealed that the majority of PAHs came from chemical production and metal smelting (42.36%), as well as from the combustion of coal, wood, and biomass (34.17%), and other mixed sources. In addition, the study found a strong correlation between water quality and socio-economic factors with concentrations of PAHs, indicating that these factors may contribute to the re-enrichment, transport, and transformation of PAHs in overlying water to varying degrees. The mean incremental lifetime cancer risk (ILCR) was lower than the risk threshold. These findings provide scientific references for managing hazardous substances in the aquatic environment.

Analysis and Assessment of Contamination Degree and Emission Sources of Polycyclic Aromatic Hydrocarbons (PAHs and Me-PAHs) in Surface Sediments from Central Coast of Vietnam

Polycyclic aromatic hydrocarbons (PAHs) and their derivatives are a diverse group of organic pollutants, which are relatively persistent and toxic. Simultaneous determination of unsubstituted PAHs and methylated PAHs (Me-PAHs) is necessary to provide comprehensive insights into contamination levels and sources of these pollutants. In this study, we collected surface sediment samples in Vietnamese central coast to analyze 7 PAHs and 12 Me-PAHs. The sediment samples were extracted by using a focused ultrasonic processor with acetone/hexane (1:1) mixture and toluene. The extract was purified by column chromatography technique with activated silica gel and dichloromethane/hexane (1:3) as elution solvent. PAHs and Me-PAHs were determined by a gas chromatography/mass spectrometry (GC/MS) system operated in electron impact ionization (EI) and selected ion monitoring mode (SIM). Concentrations of total 7 PAHs and 12 Me-PAHs ranged from 30 to 246 (average 92) nanograms per gram sediment (ng/g). These levels were comparable to or lower than those measured in Vietnamese river sediments and marine sediments from some other countries in the world. The accumulation profiles of PAHs and Me-PAHs indicated that their emissions are likely associated with mixed pyrogenic and petrogenic sources. Our results have provided preliminary information about the pollution degree and accumulation characteristics of these substances in Vietnamese marine environments. Additional comprehensive studies should be performed to characterize contamination characterisrics, emission sources, and ecological risks of PAHs and their derivatives in this country.

Bioinorganic metal nanoparticles and their potential applications as antimicrobial, antioxidant and catalytic agents: a review

Abstract This review article covers the biogenic synthesis of metal nanoparticles (MNPs) having definite shape and size while using extract obtained from different biological sources such as bacteria, fungi, algae and plants. These biological materials are composed of chloroplast, thylakoid, different types of enzymes extracted from different biogenic sources, different phytochemicals such as phenols, flavonoids, and citric acid having functional groups such as sulfate, carboxyl, amino, amide and hydroxyl groups. These functional groups and enzymes act as efficient reductants to convert metal ions into metal atoms and alternatively metal atoms combine to form MNPs while long hydrocarbon chains present in these bio-macromolecules act as cage to stabilize them for prolong time. Effect of nature of source extract, different reaction conditions such as extract amount, salt amount and solvent used during MNPs preparation process have been critically discussed here in detail. Use of synthesized bioinorganic NPs in various areas including their effectiveness in fighting against bacteria, viruses, fungi, cancer, inflammation, and their potential role in catalytic reduction of environmental harmful substances into friendly products has also been described in a clear and concise manner along with their future consideration.

Detection of isoflavones and phytoestrogen-rich plant extracts binding to estrogen receptor β using a yeast-based fluorescent assay

Alchemilla vulgaris L., Trifolium pratense L. and Glycyrrhiza glabra L. are important remedies in traditional medicine, known for many usages, including treating gynecological diseases. Despite folkloric use of the plant materials, there is a lack of scientific data to support their therapeutic application. The aims of the present study were to evaluate the relative binding affinities (RBAs) of plant-derived phytoestrogens for estrogen receptor β (ERβ) using fluorescent biosensor in yeast and to apply this assay for the assessment of the potential of plant materials towards ERs and treatment of estrogen-related disorders. Ligand-binding domain of ERβ fused with yellow fluorescent protein (ERβ LBD-YFP) was expressed in S. cerevisiae and fluorescence was detected by fluorimetry and fluorescence microscopy. Structural basis for experimental results was explored by molecular docking. Yeast-based fluorescent assay was successfully optimized and applied for identification of natural phenolic compounds and phytoestrogen-rich plant extracts that interact with ERβ-LBD, making this biosensor a valuable tool for screening estrogenic potential of a variety of plant extracts. This assay can be used for preliminary testing of plant-derived or fungal extracts, but also other sources of environmental substances with ER-modulating activity in order to assess their possible effects on the female reproductive system.

Pengaruh ketahanan korosi logam alumunium terhadap variasi pada larutan asam klorida 0,1 M dan 0,5 M

Background: Corrosion is a decrease in the quality of a material or metal to electrolyte reactions in the environment that affect the life of the material. Corrosion processes occur in acidic environments, sea water, rainwater, and soil are the result of chemical reactions that are also caused by electrochemical processes. The purpose of this study was to determine the corrosion resistance of aluminum metal to variations in 0.1 M and 0.5 M Hydrochloric Acid solution. This research uses an aluminum plate that will be immersed for 5 days with 0.1 M HCl and 0.5 M HCl solution. Methods: The method of data collection is by scanning Scanning Electron Microscopy (SEM) on each aluminum plate specimen that has been given corrosion treatment by heating at a temperature of 60 C HCl solution is one of the factors causing corrosion of metals. Finding: If in the free environment, air, temperature, and acidic substances are most commonly found as a factor causing corrosion. The increased corrosion rate is due to the higher concentration of the cause of corrosion. Conclusion: In this discussion, HCl as a concentration is used, and aluminum as a metal is tested.