Class Of Pollutants Research Articles

A Review on Genotoxic Impurities in Pharmaceutical Dosage Forms and Strategies for Identification

Abstract: Genotoxic pollutants can be broadly defined as pollutants that, regardless of the mechanism, cause significant changes in genetic material. People all over the world suffer from various health problems due to genotoxic pollutants. Recent recommendations from drug regulatory agencies in Europe and the United States (USA) require the monitoring of genotoxic and potentially genotoxic contamination in drug formulations at the ppm level. Therefore, this review evaluates several regulatory agency guidelines for monitoring genotoxic contamination, impurity levels, and toxicity in pharmaceutical products. The review also discusses analytical considerations for measuring genotoxic pollutants at trace levels and concludes with several examples of measuring several important classes of genotoxic pollutants. We will also explain our results. The article provides detailed information on genotoxicity studies of waste solutions, metal wastes, and isolated pollutants.

The burden of cancer attributable to dietary dioxins and dioxin-like compounds exposure in China, 2000–2020

Dioxin is a typical class of persistent organic pollutants (POPs) that could cause cancer. In China, the contribution of dietary dioxins to the cancer burden remains underexplored. This study evaluates the cancer risk and burden due to dietary dioxins and dioxin-like compounds among Chinese residents from 2000 to 2020. Based on adjustments in China’s dioxin policies, the study period was divided into three stages with split years of 2007 and 2014 to estimate the toxic equivalent (TEQ) of dioxins. Participants in dietary surveys conducted in 31 provinces were included. Dietary exposure to dioxins was estimated in a probability model and compared with the provisional tolerable monthly intake (PTMI). The risk was assessed using carcinogenic slope factors and expressed as the incremental lifetime cancer risk (ILCR). A two-stage model evaluated the burden of cancer attributable to dietary dioxins and dioxin-like compounds. Among all food categories, the highest concentration of dioxins and dioxin-like compounds was observed in aquatic foods at 0.15 pg TEQ/kg. Median dietary exposure to dioxins among Chinese residents decreased from 12.39 pg TEQ/kg/month to 8.72 pg TEQ/kg/month between 2000 and 2020. Consequently, the ILCR due to dietary dioxins declined from 6.44 × 10-5 to 4.53 × 10-5. The health risks were higher in younger groups and among residents of coastal areas (P < 0.001). The burden of cancer attributable to dietary intake of dioxins and dioxin-like compounds in the Chinese population in 2000–2007, 2008–2014, and 2015–2020 was 2.25 (2.09–2.42) per 100,000, 2.20 (2.06–2.35) per 100,000, and 1.68 (1.60–1.77) per 100,000, respectively. Furthermore, the disease burden was highest for prostate cancer in men and for breast cancer in women. The dioxin management policies has reduced the burden of cancer attributable to dietary exposure to dioxins and dioxin-like compounds in China. However, excess exposure in coastal areas and children remains a priority for attention.

Adsorption Behavior of Methylene Blue Onto Activated Coconut Shells: Kinetic, Thermodynamic, Mechanism and Regeneration of the Adsorbent.

Adsorption techniques are widely used to remove some classes of pollutants from waters, especially those which are not easily biodegradable. The removal of Methylene blue (MB), as a pollutant, from waste waters of textile, paper, printing and other industries has been addressed by the researchers. The aim of this study is to eliminate MB by Activated Coconut Shells (ACS) produced at low cost by adsorption in batch mode. The ACS was characterized by the FTIR spectroscopy and point of zero charge (pHpzc: 5.06). Some examined factors were found to have significant impacts on the MB uptake of ACS like the initial dye concentration Co (40-120mg/L), solution pH (2-8), ACS dose (1-12g/L), agitation speed (50-500 r/min), particles size (1.0-1.2mm) and temperature (298-333K). The best capacity was found at pH 6 with an adsorbent dose 8g/L, an agitation speed 200 r/min and a contact time of 60 min. Modeling Kinetics and Isotherms shows that the pseudo-second-order kinetic model with R 2 (0.935 -0.998) and Langmuir adsorption isotherm model provide better fitness to the experimental data with the maximum adsorption capacity of 30.30mg/g at 25°C. The separation factor RL (0.933-0.541) in the concentration range studied (10-120mg/L) shows a favorable adsorption. The isotherms at different temperatures have been used for the determination of the free energy ΔG° (198-9.72kJ/mol); enthalpy ΔH° (82.082kJ/mol) and entropy ΔSo (245.689J/K mol) to predict the nature of MB adsorption process. The positive values of (ΔGo) and (ΔHo) indicate a non-spontaneous and endothermic MB adsorption with a chemisorption. The adsorbent elaborated from Coconut Shells was found to efficient and suitable for the removal of MB dye from aqueous solutions, due to its availability, low cost preparation and good uptake capacity.

Photodegradation of polychlorinated biphenyls (PCBs) on suspended particles from the Yellow River under sunlight irradiation: QSAR model and mechanism analysis

Polychlorinated biphenyls (PCBs), as a class of hydrophobic organic pollutants, are widely found in river sediments and suspended particles, and the environmental fate of different PCBs can be better understood by investigating their photochemical transformation process. In this study, the quantitative structure-activity relationship (QSAR) model between the photodegradation rate constants of 17 PCBs adsorbed on Yellow River suspended particles in water (as a typical heterogeneous photodegradation system) and the physicochemical parameters of PCBs was constructed by SPSS and machine learning. The model showed that the more hydrophobicity of the molecule, the more positive charge carried by the aromatic C atoms, and the presence of chlorine atoms adjacent to the carbon bridge could all enhance the photochemical activity of PCBs. From the combined analysis of rate constants, quenching experiments and theoretical calculations, it was revealed for the first time that in natural suspended particle containing organic matter, the higher concentration of •O2- and 1O2 in the hydrophobic zone contributed more to the more hydrophobic PCBs, while •OH in the hydrophilic zone played a major role in the degradation of the less hydrophobic PCBs. Findings of this study would deepen the understanding of the degradation mechanism of hydrophobic pollutants by active species in complex environments.

Characterization and ecological risks of microplastics in urban road runoff

Microplastics (MPs) deposited on urban roads are often flushed into water bodies via drainage systems without treatment, and MP concentrations in the initial road runoff may be particularly high. Yet, there is only a limited understanding of the characteristics, dynamics, and impacts of MPs in urban road runoff. In this study, stormwater and rainwater samples were collected from seven different locations in Hong Kong across 11 rainfall events between February 2021 and September 2022. Characteristics of MPs in the collected samples were analyzed in detail, along with the dynamics of MP concentration in rainfall events, possible influencing factors, and ecological risks. The results show that MP concentration in the initial road runoff is particularly high during a rainfall episode. Overall, the median MP abundance in the collected runoff samples (185 particles/L) was 4.6 times higher than that in rainwater (40 particles/L). The most common polymers identified were polyethylene, polypropylene, and polystyrene, with fragments being the dominant shape. Over 60 % of MP sizes were smaller than 300 μm in the runoff samples. Additionally, risk assessments based on the Polymer Risk Index (PRI) classified most road sites in pollution classes II to III (PRI = 13.3–138.0), indicating moderate to high ecological risks. It appears that MP abundance in the initial runoff was significantly influenced by seasonal changes. These findings highlight urban roads as a major source of MP pollution in stormwater runoff and emphasize the importance of addressing the initial runoff in pollution control.

Effects of multiple microplastic types on growth of winter wheat and soil properties vary in different agricultural soils

Societal Impact StatementWinter wheat is one of the most important crops in the world. Microplastics, as an emerging pollutant, are widespread in agricultural soils due to various modern agricultural practices and can have adverse impacts on agricultural soils and plant growth. Herein, we investigated the effects of 10 types of microplastics on the properties of three agricultural soil types and the growth of winter wheat. This study contributes insights toward the conservation of agricultural soils and potential wheat yield responses to microplastic. Understanding the mechanisms that underpin the differences in responses to this pollutant class is of great importance for management recommendations.Summary Microplastics (MPs) (size &lt; 5 mm) are increasingly recognized as anthropogenic contaminants that severely affect terrestrial ecosystems. These particles are always detected as a mixture of various polymer types and shapes. However, we have limited knowledge of the effect of combined MPs on plant–soil systems. To address this, we selected 10 types of MP, applied to three soil types singly and in combination along an increasing gradient of 1, 2, 5, 8, and 10 MP types at a content of 0.4% (w/v). After 8 weeks of pre‐incubation, winter wheat (TOBAK) was grown in each pot for another 8 weeks. Shoot and root biomass, soil aggregation, and carbon and nitrogen content were measured. The effects of the same MP on both soil and plant properties were drastically different (in size and effect direction) in the different soil types. However, no clear patterns were observed along an increasing number of microplastic types, suggesting that knowing the number of microplastic types in a sample, at equity of overall concentration, does not help predict effects. In contrast, our findings reveal the complex effects of multiple MPs on the soil–plant system and highlight that soil properties need to be taken into consideration when studying MP effects on terrestrial systems.

Applying the water quality indices and geographic information system approach to assessing the suitability of groundwater quality for drinking and irrigation purposes in the semi-arid region of Tebessa-Ain Chabro, Northeastern Algeria

Assessing the groundwater quality is important for the efficient exploitation of water resources in semi-arid areas. The study area in northeast Algeria mostly depends on groundwater as its main source of water, and the quality of groundwater is becoming important due to the increasing need for freshwater. The hydrochemical characteristics and water quality of groundwater in the Tebessa-Ain Chabro were assessed using water quality indices, geochemical modeling, and multivariate statistical approaches. The study discovered that the groundwater samples could be classified into four distinct water groups using hierarchical cluster analysis in Q mode (HCA) based on their electrical conductivity. We identified three forms of water: mixed (Ca2+–Mg2+–Cl−), Na+–K+–HCO3−, and Ca2+–Cl−. According to the water quality assessment, only 38% of the samples were deemed suitable for human consumption, while 34% were categorized as poor water, 10% as extremely poor, and 17% as unsafe for drinking. The irrigation water quality index identified four classifications: low, moderate, high, and severe restriction, with corresponding percentages of 31%, 31%, 7%, and 31%. The nitrate pollution index (NPI) showed that 48% of samples fell into the moderate pollution class. Human activity, such as sewage infiltration and waste disposal in open areas, was the cause of this nitrate contamination. The saturation index values showed that groundwater was less saturated in halite and sylvite and more saturated in aragonite, calcite, dolomite, anhydrite, gypsum, and hydroxyapatite. The Tebessa region’s groundwater’s hydrochemical properties and water quality have been assessed using multivariate statistical techniques, geochemical modeling, and water quality indexes. The study’s conclusions can provide a foundation for upcoming research evaluating the region’s groundwater quality.

NiO/AgNPs nanowell enhanced SERS sensor for efficient detection of micro/nanoplastics in beverages

The ubiquity of plastic products has led to an increased exposure to micro and nano plastics across diverse environments, presenting a novel class of pollutants with substantial health implications. Emerging research indicates their capacity to infiltrate human organs, posing risks of tissue damage and carcinogenesis. Given the prevalent consumption of beverages as a primary vector for these plastics' entry into the human system, there is an imperative need for the advancement of precise detection methodologies in liquids. In this study, we introduce a substrate comprising a Nickel Oxide (NiO) nanosheet array decorated with Silver Nanoparticles (AgNPs) for the Surface-Enhanced Raman Spectroscopy (SERS) analysis of micro//nano plastics. This configuration, leveraging a unique nanowell architecture alongside silver plasmonic enhancement, demonstrates unparalleled sensitivity and repeatability in signal, facilitating the accurate quantification of these contaminants. Through the application of a portable Raman apparatus, this study successfully identifies prevalent micro/nano plastics including polystyrene (PS), polyethylene (PE), and polypropylene (PP), achieving detection sensitivities of 5 μg/mL, 25 μg/mL, and 25 μg/mL, respectively. Moreover, the substrate's efficacy extends to the detection of PS within commonly consumed beverages such as water, milk, and liquor with sensitivities of 25 μg/mL, 50 μg/mL, and 50 μg/mL, respectively. These findings highlight the substrate's potential as an expedient and effective sensor for the real-time monitoring of micro/nano plastic pollutants.

Polycyclic aromatic hydrocarbon exposure effects on trajectories of maternal and adolescent mental health

BackgroundParental psychological distress is a well-known risk factor for developmental psychopathology, with longer term parental distress associated with worse youth mental health. Neurotoxicant exposure during pregnancy is a risk factor for both poor maternal and youth mental health. The impact of one class of pollutant, polycyclic aromatic hydrocarbons (PAH), on long-term trajectories of maternal distress and youth self-reported mental health symptoms in adolescence has been understudied.MethodsPAH exposure was measured by DNA adducts in maternal blood sampled during the third trimester of pregnancy. Maternal distress, operationalized as maternal demoralization, was measured at 11 timepoints (prenatal to child age 16). Adolescent mental health symptoms were measured at age 13–15. Follow up analyses examined a subset of measures available at age 15–20 years. Structural equation modeling examined associations between PAH exposure during pregnancy and latent growth metrics of maternal distress, and between maternal distress (intercept and slope) and youth mental health symptoms in a prospective longitudinal birth cohort (N = 564 dyads).ResultsHigher prenatal PAH exposure was associated with higher concurrent maternal distress. Prenatal maternal distress was associated with adolescent’s self-reported anxiety, depression, and externalizing problems. On average, maternal distress declined over time; a slower decline in mother’s distress across the course of the child’s life was associated with greater self-reported anxiety and externalizing problems in youth.ConclusionsOur findings are consistent with an intergenerational framework of environmental effects on mental health: PAH exposure during pregnancy affects maternal mental health, which in turn influences mental health outcomes for youth well into adolescence. Future research is necessary to elucidate the possible social and biological mechanisms (e.g., parenting, epigenetics) underlying the intergenerational transmission of the negative effects of pollution on mental health in caregiver-child dyads.

Microplastics caused embryonic growth retardation and placental dysfunction in pregnant mice by activating GRP78/IRE1α/JNK axis induced apoptosis and endoplasmic reticulum stress

Microplastics (MPs), a brand-new class of worldwide environmental pollutant, have received a lot of attention. MPs are consumed by both humans and animals through water, food chain and other ways, which may cause potential health risks. However, the effects of MPs on embryonic development, especially placental function, and its related mechanisms still need to be further studied. We investigated the impact on fetal development and placental physiological function of pregnant mice by consecutive gavages of MPs at 0, 25, 50, 100 mg/kg body weight during gestational days (GDs 0–14). The results showed that continuous exposure to high concentrations of MP significantly reduced daily weight gain and impaired reproductive performance of pregnant mice. In addition, MPs could significantly induce oxidative stress and placental dysfunction in pregnant mice. On the other hand, MPs exposure significantly decreased placental barrier function and induced placental inflammation. Specifically, MPs treatment significantly reduced the expression of tight junction proteins in placentas, accompanied by inflammatory cell infiltration and increased mRNA levels of pro-inflammatory cytokines and chemokines in placentas. Finally, we found that MPs induced placental apoptosis and endoplasmic reticulum (ER) stress through the GRP78/IRE1α/JNK axis, leading to placental dysfunction and decreased reproductive performance in pregnant mice. We revealed for the first time that the effects of MPs on placental dysfunction in pregnant animals. Blocking the targets of MPs mediated ER stress will provide potential therapeutic ideas for the toxic effects of MPs on maternal pregnancy.

Studies on the characteristics of polycyclic aromatic hydrocarbons accumulation in lipids and the disturbance of lipid metabolism of Ruditapes philippinarum

Polycyclic aromatic hydrocarbons (PAHs) constitute a class of persistent organic pollutants with strong lipophilicity, which readily accumulate within organisms and have the effect to induce disorders in lipid metabolism. The present study aimed to investigate the accumulation localization and pattern of PAHs in Ruditapes philippinarum, and to reveal the association between PAHs and lipids metabolism. The 21-day exposure experiment was conducted using a mixture of phenanthrene, chrysene, and benzo[a]pyrene (the proportion is 1:1:1) at concentrations of 0.4 μg/L, 2 μg/L, and 10 μg/L. The tissue distribution of PAHs indicated that the digestive gland was the primary site of PAHs accumulation. Meanwhile, fluorescence colocalization suggested that PAHs primarily accumulated within the lipid droplets of digestive gland cells. This study further determined the transcriptomic and lipidomic profiles of the digestive gland to analyze the key genes involved in disrupted lipid metabolism and the major lipids affected. Lipidomic analysis identified the key differential metabolites as triglycerides (TGs). Furthermore, TGs were upregulated in the digestive gland had a total carbon atom number of 50–64 and a total number of 3–9 double bonds in the acyl side chains. Biochemical analysis experiments and oil red O stained frozen sections confirmed that the content of TGs steadily increased in various tissues during the experiment, leading to an elevated digestive gland index. Changes of lipid metabolism associated genes expression level also indicated that the synthesis of lipid in digestive gland were up-regulated while the decomposition was down-regulated. This study is the first to demonstrate the cellular localization of PAHs accumulation in bivalves and confirms the pattern of variation in TGs, providing new insights into the mechanisms of PAHs bioaccumulation and lipid metabolism disruption.

Enhancing dechlorination and inhibiting H2 evolution: Surface N-hydroxymethylation of Pd-loaded carbon nitride for photocatalytic elimination of polychlorinated aromatics

Polychlorinated aromatic compounds (PCAs) are a class of persistent organic pollutants (POPs) characterized by their sp2 C-Cl bonds and the aromatic rings. They are commonly found in flue gases from incinerators and other industrial processes, and are very harmful to human and wildlife health. Sunlight-driven photocatalytic reduction is a straightforward approach to eliminating PCAs. Although many photocatalysts have been developed, their activity remains unsatisfactory under visible-light irradiation, and selectivity is also impeded by the side reactions especially H2 evolution. Here, we report a Pd nanoparticles (NPs)-loaded, surface N-hydroxymethylated Polymeric carbon nitride (PCN) photocatalyst, which achieves rapid and complete hydrodechlorination of PCAs under visible-light irradiation in water. Mechanism studies reveal that contacting Pd NPs with N-hydroxymethylated PCN surfaces boosts the transfer of photo-generated electrons from PCN to Pd NPs and the reduction of C-Cl bonds at the Pd NPs’ surfaces. In contrast, the amino groups of pristine PCN render the catalyst less efficient in interfacial electron transfer, while more active in H2 evolution. Our findings highlight the potential of surface engineering to improve the performance of existing photocatalysts towards selective reduction of halogenated pollutants.

A rapid and accurate fluorescent sensor array based on lanthanide metal-organic framework for identification and determination of perfluorinated compounds

Perfluorinated compounds (PFCs), as an important class of environmental pollutants, have chemical and structural similarities that make their detection a great technical challenge. This study synthesized three species of metal-organic frameworks (MOFs) using different lanthanide metal ions or organic ligands, which were integrated into a fluorescent sensor array. This innovative approach offers a straightforward, rapid, and precise detection strategy for PFCs. Different ionization properties and fluorinated hydrophobic tails of PFCs lead to different electrostatic attraction and hydrophobic effects between PFCs and sensing elements, which become the basis for differential sensing. Furthermore, the fluorescence signal is more convenient to collect, making the sensor array simple to complete the identification. Combined with pattern recognition methods, the array successfully identified seven kinds of PFCs and mixtures with a classification accuracy of 100 % and a detection limit as low as 51 nM. Finally, the utility of the sensor array in river water sample analysis was verified. The strategy provides an effective method for identifying and determining PFCs and offers new opportunities for developing sensor arrays based on lanthanide MOFs.

Unravelling the mechanisms of PFAS toxicity to submerged macrophytes and epiphytic biofilms at metabolic and molecular levels

Per- and poly-fluoroalkyl substances (PFAS) are an emerging class of persistent organic pollutants that are widespread in aquatic ecosystems and pose a serious threat to aquatic organisms. It is thus crucial to explore the toxicity mechanisms of PFAS to submerged macrophytes and biofilms. In this study, Vallisneria natans (V. natans) was exposed to environmentally relevant concentrations of perfluorooctanoic acid (PFOA) and perfluorooctane sulphonate (PFOS). Results showed that PFAS induced the excessive production of reactive oxygen species, triggering antioxidant responses. V. natans exhibited an improved stress tolerance by altering the biosynthesis of several plant secondary metabolites and the histidine, arginine, proline pathways in response to PFAS exposure. Moreover, PIP1–1, PIP2–2, SLAH1 and SLAH2 genes were upregulated, indicating the activation of aquaporins and slow-type anion channels. The uptake of PFOA and PFOS by V. natans was 41.74 % and 52.31 %, respectively. Notably, PFAS bound to functional proteins (GSTF10), promoting the detoxification of plants. Exposure to PFAS also altered the structure of biofilms by inducing the synthesis of large amounts of polysaccharides and proteins. The diversity and richness of the microbial community within periphytic biofilms changed significantly. These results provide a comprehensive description of the responses of aquatic plants and periphytic biofilms to PFAS and the removal mechanism of PFAS, contributing to the environmental risk assessments and removal of PFAS in aquatic ecosystems.

Chemically Tailored Metal‐Organic Frameworks for Enhanced Capture of Short‐ and Long‐Chain Per‐ and Polyfluoroalkyl Substances from Water

AbstractPer‐ and polyfluoroalkyl substances (PFAS) are emerging as bioaccumulative and toxic water pollutants, posing a large threat to human and aquatic organisms. This threat is aggravated by their extreme persistence to common degradation methods. Adsorption is regarded as the most conventional method to treat these contaminants, however, existing sorbents present considerable limitations on performance. The development of more efficient PFAS adsorbents is therefore of urgent need. The class of metal‐organic frameworks (MOFs) can hold great promise for these purposes, featuring porous materials with high tailoring potential. Herein, a series of functionalized Zr‐MOFs have been designed with boosted capacities for the adsorption of short‐ and long‐chain perfluorinated carboxylic acids of environmental interest. The approach relies on chemistry‐based concepts to introduce targeted post‐synthetic modifications that promote PFAS···MOF interactions, specifically through coordinative bonding and hydrophobic effects. In particular, the framework TFA‐MOF‐808 (TFA = trifluoroacetic acid) displays the highest capture capacities reported for MOF materials in this pollutant class. Mechanistic studies, assisted by advanced synchrotron characterization techniques and theoretical calculations, support a ligand exchange process occurring during the adsorption phenomena. The results demonstrate the potential of this design approach in developing advanced PFAS sorbents with optimal performance.

Contamination by microplastics and sorbed organic pollutants in the surface waters of the Tietê River, São Paulo-SP, Brazil

Microplastics (MPs) are particles between 1 μm and 5 mm in size, originating mainly from poor solid waste and effluent management, that can reach water bodies from various sources. In freshwater environments, the occurrence, distribution, and characterization of this new class of pollutants are still little explored, especially in Brazil. The aim of this study was to assess the occurrence of MPs, as well as the presence and concentration of polychlorinated biphenyls (PCBs) sorbed to these particles in the surface waters of the Tietê River - SP. Surface water samples were collected in duplicate during the dry and wet seasons. The identification and characterization of the MPs was carried out through visual inspection and the chemical identity of the particles was verified using Fourier transform infrared spectroscopy with attenuated total reflectance (FTIR-ATR). For the analysis of PCBs adsorbed to the MPs, the sample extracts were analyzed by gas chromatography coupled with mass spectrometry (GC-MS). The MPs were found in concentrations ranging from 6.67 to 1530 particles m−3, with a predominance of the polymers polyethylene (PE, with 58.17 %) and polypropylene (PP, with 23.53 %). The main morphological categories identified were fragments (56.63 %), fibers (28.42 %), and transparent films (13.06 %). Higher abundances of PCBs were observed in the lower size range, between 0.106 and 0.35 mm. The total concentrations of PCBs in MPs ranged from 20.53 to 133.12 ng g−1. The results obtained here are relevant for understanding the dynamics and level of contamination of MPs and organic pollutants sorbed to these particles in the Tietê River, as well as helping with mitigation measures for the restoration and preservation of this ecosystem.

Comprehensive review of combustion ion chromatography for the analysis of total, adsorbable, and extractable organic fluorine.

Poly- and perfluoroalkyl substances (PFAS) are a class of persistent organic pollutants whose high stability and appreciable water solubility have led to near-global contamination. PFAS are bioaccumulative toxins that have been linked to a myriad of disorders and have been detected nearly universally in human blood. Liquid chromatography-tandem mass spectrometry is the most frequent method used for quantitation, though this typically only measures a few dozen of the >14000 known PFAS and has been shown to account for a small portion of the total organic fluorine present. Sum parameter methods such as total, extractable, and adsorbable organic fluorine have emerged as alternative measurements for PFAS determination. Combustion ion chromatography has become the preferred method for organofluorine measurement where the sorbent or extract containing PFAS is combusted and the emitted hydrofluoric acid (HF) is a measure of the cumulative organofluorine present. Herein we critically review the types of organofluorine measurement, their separation from the sample matrix, and key parameters of the analytical instrument that affect sensitivity, reproducibility, and recovery with regards to PFAS analysis.

Determination of volatile organic compounds (VOCs) in indoor work environments by solid phase microextraction-gas chromatography-mass spectrometry

Volatile organic compounds (VOCs) are continuously emitted into the atmosphere from natural and anthropogenic sources and rapidly spread from the atmosphere to different environments. A large group of VOCs has been included in the class of air pollutants; therefore, their determination and monitoring using reliable and sensitive analytical methods represents a key aspect of health risk assessment. In this work, an untargeted approach is proposed for the evaluation of the exposure to volatile organic compounds of workers in an engine manufacturing plant by GC–MS measurements, coupled with solid-phase microextraction (SPME). The analytical procedure was optimized in terms of SPME fiber, adsorption time, desorption time, and temperature gradient of the chromatographic run. For the microextraction of VOCs, the SPME fibers were exposed to the air in two different zones of the manufacturing factory, i.e., in the mixing painting chamber and the engine painting area. Moreover, the sampling was carried out with the painting system active and running (system on) and with the painting system switched off (system off). Overall, 212 compounds were identified, but only 17 were always present in both zones (mixing painting chamber and engine painting area), regardless of system conditions (on or off). Finally, a semi-quantitative evaluation was performed considering the peak area value of the potentially most toxic compounds by multivariate data analyses.

Exposure to synthetic steroid hormones and precocious puberty in girls: A case-control study

Synthetic steroid hormones are an emerging class of environmental pollutants, but their influence on pubertal timing remains unclear. This case-control study explored the association between synthetic steroid hormone exposure and precocious puberty. Using ultrahigh performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS), synthetic steroid hormones were detected in urine samples from 229 Chinese girls, aged 6–9 years. Puberty status was assessed using Tanner staging by professional pediatricians. We conducted the least absolute shrinkage and selection operator (LASSO) regression combined with logistic regression. Besides, we evaluated the joint effects of steroid hormone mixture and identified the main contributor using the Weighted quantile sum (WQS) model and Bayesian kernel machine regression (BKMR) model. The logistic regression model reflected an inverse individual association between precocious puberty and halcinonide [OR (95 %CI): 0.20 (0.07, 0.46)], and budesonide [OR (95 %CI): 0.77 (0.62, 0.95)]. In the joint effects utilizing the WQS model, precocious puberty showed a marginal association with steroid hormone mixture, but was not significant [OR (95 %CI): 0.88 (0.75, 1.04)]. Prednisolone (0.31), fluorometholone acetate (0.24), and dexamethasone acetate (0.12) had the highest weight. Consistently, mixture exposure was not associated with precocious puberty in the BKMR model. In conclusion, precocious puberty was associated with halcinonide and budesonide exposure, but not steroid hormone mixture among girls. It highlighted the management of the residual synthetic steroid hormones in the environment and provided a direction for the prevention of precocious puberty.

Atmospheric deposition of microplastics in an urban conglomerate near to the foothills of Indian Himalayas: Investigating the quantity, chemical character, possible sources and transport mechanisms

The global apprehension regarding the ubiquitous presence of microplastics (MPs) and their associated health risks underscore a significant challenge. However, our understanding on the occurrence and characteristics of this emerging class of pollutants in the different environmental compartments remains limited. For instance, despite housing approximately 20–25% of the global population, the evidence of the atmospheric MPs in Indian Subcontinent is exceedingly rare. Hence, we for the first-time present data on the depositional flux, chemical composition, morphological features of the atmospheric MPs collected from the foothills of Indian Himalayas. The total number of MPs for the collected samples ranged from 65 to 752 particles, with an average of 317 ± 171 particles count. The average flux of atmospheric MPs was 2256 ± 1221 particles/m2/day and varied significantly from 462 particles/m2/day to 5346 particles/m2/day. The highest deposition (5346 particles/m2/day) of atmospheric MPs was recorded during the 3rd week of sampling, coinciding with the Diwali festival. Based on the visual characteristics, we determined that the size of MPs ranged from 67 to 2320 μm, with a predominant presence of smaller particles (<1200 μm), primarily composed of fragments and films/sheets. Raman spectroscopy indicated that the analyzed MPs were mainly composed of 4 different polymer types, including PE (46.8 ± 7.2 %), PP (20.9 ± 7.4 %), PS (15.6 ± 3.8 %) and PET (16.7 ± 9.9 %). We further highlighted the extent to which climate variables control the deposition of atmospheric MPs in this urban conglomerate located in the foothills of Himalayas. Our Lagrangian parcel tracking approach showed that the greater frequencies are of local origin and clustered near to the studied region. We also speculate that atmospheric microplastics can be transported along the westerly winds. Though we did not observe any significant relation (p > 0.05) between meteorological parameters and the quantity of atmospheric MPs.