Human Exposure Research Articles

The Environmental Neuroactive Chemicals List of Prioritized Substances for Human Biomonitoring and Neurotoxicity Testing: A Database and High-Throughput Toxicokinetics Approach

There is a diversity of chemicals to which humans are potentially exposed. Few of these chemicals have linked human biomonitoring data, and most have very limited neurotoxicity testing. Of particular concern are environmental exposures impacting children, who constitute a population of heightened susceptibility due to rapid neural growth and plasticity, yet lack biomonitoring data compared to other age/population subgroups. This study set out to develop a prioritized list of neuroactive substances, titled the Environmental NeuRoactIve CHemicals (ENRICH) list, to be used as a defined screening library in the evaluation of human biological samples, with emphasis on early childhood-relevant environmental exposures. In silico database mining approaches were used to prioritize chemicals based upon likelihood of neuroactivity, human exposure, and feasible detection in biological samples. Evidence of neuroactivity was compiled across in vitro high-throughput screening, animal testing, and/or human epidemiological findings. Chemicals were considered for their likelihood of human exposure and detection presence in biological samples (including metabolites), with additional evidence indicating presence within child-relevant products. The resulting list of 1827 chemicals were ranked using a Chemical Prioritization Index. Manual inclusion/exclusion criteria were employed for the top-ranking chemical candidates to ensure that chemicals were within the study's scope (i.e., environmentally relevant) and, for the purposes of biomonitoring, had properties amenable to mass spectrometry methods. These elements were combined to produce the ENRICH list of 250 top-ranking chemicals, spanning pesticides and those used in home maintenance, personal care, cleaning products, vehicles, arts and crafts, and consumer electronics, among other sources. Chemicals were additionally evaluated for high-throughput toxicokinetics to predict how much of a chemical and/or its metabolite(s) may reach urine, as an example biological matrix for practical use in biomonitoring efforts. This novel study couples databases and in silico-based predictions to prioritize chemicals in the environment with potential neurological impacts for future study.

Prioritising relevant polychlorinated naphthalene (PCN) congeners for human dietary exposure studies.

Following a decline in the production and use of polychlorinated naphthalenes (PCNs) and the restrictions introduced by the Stockholm Convention, dietary intake represents the most significant pathway of human exposure to these dioxin-like contaminants. PCNs occur ubiquitously in foods, originating from the legacy of historical production that is now globally redistributed, as well as from ongoing industrial and domestic combustion sources which have a stronger influence on occurrence patterns in countries where they were not produced. Recent studies have benefited from a wider set of available PCN reference standards, enabling more accurate reporting of a diverse range of congeners. Combining the available information on food occurrence with relative potency (REP) data, an initial selection of twenty PCN congeners are presented here for monitoring of foodstuffs. The selection is expected to provide a good indication of the overall dioxin-like toxic equivalence (TEQ) associated with food occurrence, particularly in industrialised countries and regions where both, historical production and current combustion processes are significant sources. The selection also appears to be representative of the vast majority of PCN TEQ reported in human tissues despite the limited amount of reliable data. Future studies will benefit from the increasing availability of new PCN standards and provide a broader spectrum of occurrence data in foods and human tissues. They will also support toxicological studies on a wider range of congeners and biological effects, enhancing our understanding of PCN-mediated toxicity. Both these information strands will allow refinement and expansion of the proposed selection of congeners, if required.

Bisphenols in indoor dust: A comprehensive review of global distribution, exposure risks, transformation, and biomonitoring.

Bisphenols (BPs) are pervasive environmental contaminants extensively found in indoor environments worldwide. Despite their ubiquitous presence and potential health risks, there remains a notable gap in the comprehensive reviews focusing on BPs in indoor dust. Existing literature often addresses specific aspects such as exposure pathways, transformation products, or biomonitoring techniques, but lacks a consolidated, in-depth review encompassing all these facets. This review provides a comprehensive overview of the global distribution of BPs, emphasizing their prevalence in diverse indoor settings ranging from households and workplaces to public areas. Variations in BP concentrations across these environments are explored, influenced by factors such as industrial activities, consumer product usage patterns, and geographical location. Exposure assessments highlight ingestion, inhalation, and dermal contact as primary pathways for BP exposure, with ingestion being particularly significant for vulnerable groups such as infants and young children. Studies consistently reveal higher concentrations of BPs in urban indoor dust compared to rural settings, reflecting the impact of urbanization and intensive consumer practices. Moreover, BPs from mobile sources like vehicles contribute significantly to overall human exposure, further complicating exposure assessments. The review also delves into the transformation of BPs within indoor environments, emphasizing the diverse roles of physical, chemical, and biological processes in generating various transformation products (TPs). These TPs can exhibit heightened toxicity compared to their parent compounds, necessitating deeper investigations into their environmental fate and potential health implications. Critical examination of biomonitoring techniques for BPs and their metabolites underscores the importance of non-invasive sampling methods, offering ethical advantages and practicality in assessing human exposure levels. The emerging use of bioindicators, encompassing plants, animals, and innovative approaches like spider webs, presents promising avenues for effectively monitoring environmental contamination.

Per- and polyfluoroalkyl substances (PFAS) Accumulation in Fish Occupying Different Trophic Positions from East Canyon Creek, a Seasonally Effluent-Dominated River, Utah, USA

Fish and seafood are considered a major source of human dietary exposure to per- and polyfluoroalkyl substances (PFAS). In this study, we examined levels of 35 PFAS in fish samples of brown trout and mottled sculpin, which occupy different trophic positions, collected in 2014 from East Canyon Creek in Utah, USA. We observed 20 PFAS with ∑20PFAS ranging from 0.46-63.9 ng/g and from <LOQ-52.1 ng/g wet weight in sculpin and brown trout, respectively. Among detected compounds, PFOS was measured at highest levels ranging 3.8 - 46.5 ng/g in sculpin, which occupies a lower trophic level, and 2.5 - 38.4 ng/g in brown trout, which occupies a higher trophic position. The most frequently detected PFAS were PFDA and FOSA, and these contaminants were found in 93% and 81% of fish samples; however, we did not identify appreciable PFAS biomagnification. To evaluate potential risk associated with consumption of fish, we calculated risk-based consumption limits using European Food Safety Authority (EFSA) regulated values of maximum levels (MLs) and total weekly intake for four regulated PFAS: PFOA, PFNA, PFHxS, and PFOS. The levels of regulated PFAS exceeded at least one of the MLs in 74% of sculpin samples and 45% of brown trout samples. Based on calculated weekly intake for the sum of the four regulated PFAS, a typical adult would need to consume 4.2 and 5.6 meals per week of whole body sculpin and brown trout, respectively, to reach the TWI of 4.4 ng/kg body weight per week set by EFSA.

Spatio-temporal variations of air pollutants and human health exposure impacts during 2023 haze through respiratory deposition analysis in Delhi-NCR, India

Spatio-temporal variations of air pollutants and human health exposure impacts during 2023 haze through respiratory deposition analysis in Delhi-NCR, India

Identification, annotation and toxicity estimation of organic pollutants in human serum via non-target analysis.

Environmental organic pollution causes a threat to the ecological environment, constrains social development and can also potentially harm human health. We applied non-target analysis to screen organic pollutants from the serum of 89 individuals, identifying 67 pollutants in the categories of industrial intermediates, plasticizers, surfactants, pharmaceuticals, pesticides, and exogenous pollutant metabolites. The detection rate of chemicals for industrial use (50.3%; 95% CI: 39.7, 60.8) was higher, reflecting the environmental exposure characteristics of the surrounding functional areas. In addition, 1168 potential pollutant features were annotated to 10 superclasses. Exposure levels of identified pollutants were semi-quantified by predicting response factors via machine learning model. Highly exposed pollutants involved various categories, especially pharmaceuticals due to their property of being easily absorbed by human body cross biological barriers. Toxicity of developmental toxicity, bioconcentration, mutagenicity and oral rat median lethal dose (LD50) were predicted with the occurrence rates of 62.7%, 10.4%, 11.9% and 11.9% of the identified pollutants respectively. 4-[3-(Trifluoromethyl)benzyl]piperidine (industrial intermediate), risperidone (pharmaceutical), and aminocarb (insecticide) were predicted to have multiple toxic effects, which deserved attention and further hazard assessment. This study provides a comprehensive pattern of human exposure to organic pollutants, contributing to evaluate the health risks caused by pollutants to the population, thus providing data support for the monitoring and management of pollutants.

High-throughput UPLC-ESI/MSMS method for simultaneous measurement of the urinary metabolites of volatile organic compounds and tobacco alkaloids.

Human exposure to volatile organic compounds (VOCs) poses significant health risks, contributing to cardiovascular disease, pulmonary disease, and cancer. Measurement of VOC metabolites (VOCm) in urine by liquid chromatography-mass spectrometry (LC-MS) is a preferred method for VOCm analysis; however, existing methods encounter challenges related to sensitivity, throughput, and analyte coverage. In addition to VOCm, the measurement of tobacco alkaloids (TAm) is critical to account for tobacco use in population-based studies. A method is needed that is highly sensitive, offers higher throughput, and can analyze VOCm and TAm in a single run. Herein, we present a robust dilute-and-shoot method aimed at overcoming these analytical challenges and expanding the targeted analysis to include 35 urinary VOCm and TAm and their metabolites. By leveraging high-speed polarity switching and optimized chromatographic parameters, our method achieved comprehensive analyte coverage and enhanced sensitivity, enabling reliable individual level VOC exposure assessment. Validation demonstrates robust linearity, sensitivity, accuracy, and precision, with minimal matrix effects. This high-throughput UPLC-MS/MS method significantly enhances VOC exposure assessment by enabling simultaneous measurement of 35 urinary VOC and TAm with high sensitivity and efficiency. Multiple metabolites from single parent xenobiotics are included in one run, expanding biomarker specificity. Our data indicate the method effectively accounts for tobacco consumption as a confounder in population-based studies, ensuring accurate VOC exposure assessment.

Conformation and binding of 12 Microcystin (MC) congeners to PPP1 using molecular dynamics simulations: A potential approach in support of an improved MC risk assessment.

Microcystins (MCs) occur frequently during cyanobacterial blooms worldwide, representing a group of currently about 300 known MC congeners, which are structurally highly similar. Human exposure to MCs via contaminated water, food or dietary supplements can lead to severe intoxications with ensuing high morbidity and in some cases mortality. Currently, one MC congener (MC-LR) is almost exclusively considered for risk assessment (RA) by the WHO. Many MC congeners co-occur during bloom events, of which MC-LR is not the most toxic. Indeed, MC congeners differ dramatically in their inherent toxicity, consequently raising question about the reliability of the WHO RA and the derived guidance values. Molecular dynamics (MD) simulation can aid in understanding differences in toxicity, as experimental validation for all known MC congeners is not feasible. Therefore, we present MD simulations of a total of twelve MC congeners, of which eight MC congeners were simulated for the first time. We show that depending on their structure and toxicity class, MCs adapt to different backbone conformations. These backbone conformations are specific to certain MC congeners and can change or shift to other conformations upon binding to PPP1, affecting the stability of the binding. Analysis of the interactions with PPP1 demonstrated that there are frequently occurring patterns for individual MC congeners, and that published PPP interactions could be reproduced. In addition, common but also unique patterns were found for individual MC congeners, suggesting differences in binding behaviour. The MD simulations presented here therefore enhance our understanding of MC congener-specific differences and demonstrated that congener-specific investigations are prerequisite for allowing characterisation of yet untested or even unknown MC congeners, thereby allowing for a novel potential approach in support of an improved RA of microcystins in humans.

Involvement of mitochondrial dysfunction and oxidative stress in the nephrotoxicity induced by high-fat diet in Sprague-Dawley rats.

The prevalence of obesity-associated kidney injury has increased, yet the precise extent of the injury and its underlying mechanisms remain unclear. This study used a Sprague-Dawley (SD) rat model to simulate human exposure scenarios, with the objective of investigating the involvement of mitochondria in obesity-induced renal toxicity. Biochemical analysis revealed significant increases in serum creatinine, cystatin C, urinary protein, urinary microalbumin, and urinary α1-microglobulin levels in rats fed a high-fat diet, indicating a notable decline in glomerular filtration function. Histopathological examination showed mild to moderate degeneration in renal tubular epithelial cells, slight glomerular enlargement, fusion and disappearance of pedunculated cell, and decreased electron density of mitochondrial matrix and cristae, indicating the impaired filtration function of kidney. Furthermore, the study found reduced mitochondrial membrane potential and superoxide dismutase (SOD) levels, along with increased malondialdehyde (MDA) levels, signifying elevated mitochondrial oxidative stress in the kidneys of high-fat diet-fed rats. Additionally, a decrease in the number of mitochondrial proliferator-activated receptor gamma coactivator 1-alpha (PGC1α) and uncoupling protein-2 (UCP-2)-positive cells, as well as reduced protein expression levels in the mitochondria, suggests a reduced renal mitochondrial resistance to oxidative stress. Collectively, these findings indicate that a high-fat diet triggers abnormalities in both renal filtration and structural functionality in SD rats. The observed reduction in renal mitochondrial density and the elevation in oxidative stress levels could potentially serve as underlying mechanisms.

A biomarkers study of human skin fibroblasts exposition to glyphosate-based herbicide using an untargeted and targeted metabolomics approach.

Metabolomics is a valuable tool to assess glyphosate exposure and its potential impact on human health. However, few studies have used metabolomics to evaluate human exposure to glyphosate or glyphosate-based herbicides (GBHs). In this study, an untargeted and targeted metabolomics approach was applied to human skin fibroblasts exposed to the GBH Roundup (GLYP-R). Cytotoxicity, cell death, and oxidative stress assays were performed to evaluate potential damage caused by GLYP-R in fibroblasts. The herbicide showed a cytotoxic effect at concentrations above 100.0 mg L-1, with IC50 = 164.2 ± 8.7 mg L-1, inducing significant reactive oxygen species (ROS) production and necrosis. A GC×GC/Q-TOFMS method using derivatization with propyl chloroformate/propanol was developed for untargeted analysis, allowing the identification of 400 metabolites of different classes in the samples. The most significant compounds in the discrimination and classification of the samples were fatty acids and amino acids (AA). Based on the relevance of AA in untargeted analysis, a targeted analysis of 21 AA was performed using the same validated GC×GC method. Metabolomic analyses allowed the construction of two biomarker models with performance evaluated by receiver operating characteristic (ROC) curves: an untargeted model formed by four metabolites (methylcysteine, N-acetyl-L-methionine, methyl stearate, and linoleic acid) and a targeted model formed by three AA (L-glutamic acid, L-cysteine, and γ-aminobutyric acid). This study is the first to report the use of metabolomics to evaluate human skin cells exposed to GLYP-R, contributing to the toxicological research on glyphosate.

Revealing mercury species-specific transfer and toxicity mechanisms in placental trophoblasts

Environmental mercury (Hg) follows a biogeochemical cycle resulting in a variety of Hg species. Therefore, human exposure to the three Hg species inorganic Hg via crops and air, methyl Hg through fish consumption and ethyl Hg due to the use as antiseptic agent in medical applications is a rising concern. Especially pregnant women and their developing fetus present a vulnerable population. However, little is known about its transfer and toxicity in placental barrier building cells. Here, Hg species-specific transfer and toxicity in placental trophoblasts, which are the main cell type involved in nutrient transfer, were investigated by using the established BeWo b30 in vitro model. The transfer of inorganic Hg was much lower compared to the organic Hg species and all three species were able to perturb barrier integrity. This was accompanied by a less pronounced cytotoxicity of HgCl2 compared to the two organic species. The energy charge value indicated an increase for inorganic Hg and a decrease for organic Hg compounds. Regarding antioxidative defense, inorganic Hg elevated GSSG levels, while organic Hg decreased GSH. Activity of antioxidative defense related enzymes showed a decrease upon Hg species treatment and all three species induced both apoptotic and necrotic cell death.

Polycyclic Aromatic Compounds in Ambient PM2.5 in the Central Region of Ghana: Molecular Distribution, Origin and Cancer Risk Assessment

The distribution, sources and the cancer risk of human exposure to PM2.5-bound polycyclic aromatic hydrocarbons (PAHs) were investigated in this work. Airborne particulate samples were obtained at the Winneba highway junction (WHJ) and Apam fish-smoking community (AFC) in the Central Region of Ghana from July 2022 to June 2023. PM2.5 particulates were collected using a Gent sampler equipped with a Gast pump and a stacked filter unit. 24-hour sampling was done two times a month using Teflon filters. Dichloromethane and gas chromatography with a mass spectrometer (GC-MS) were used to extract and analyse the samples, respectively, to identify 14 PAH compounds. The study discovered average PAH concentrations of 67.38 ng/m3 at WHJ and 41.59 ng/m3 at AFC. PAH profile was predominated with Phenanthrene, accounting for 25-27 % of total PAHs. The distribution pattern of PAHs was LMW>HMW>MMW at the two research sites. A strong correlation was found among BaA, BkF, BbF and BeP. The diagnostic ratio model revealed that PAHs stemmed from pyrogenic sources. The carcinogenic PAHs (BaP, BaA, Chr, BbF, BkF, BghiP) contributed approximately 90 % to the carcinogenic activity of total PAHs, denoting a high cancer potential of PAHs. The mean levels of BaP were about 8-10 times higher than the permissible limit of 1 ng/m3. The overall cancer risk values for exposure to PAHs via inhalation were more than 10-4, signifying high cancer risks: 11.61×10-4-21.14×10-4 for children and 19.91×10-4-36.24×10-4 for adults. Reducing PM2.5 and its health effects requires the use of clean fuel and the adoption of eco-friendly transportation.

Food supply toxicants and additives alter the gut microbiota and risk of metabolic disease.

Metabolic disease is rising along with both global industrialization and the use of new commercial, agricultural, and industrial chemicals and food additives. Exposure to these compounds may contribute to aspects of metabolic disease such as obesity, diabetes, and fatty liver disease. Ingesting compounds in the food supply is a key route of human exposure, resulting in the interaction between toxicants or additives and the intestinal microbiota. Toxicants can influence the composition and function of the gut microbiota, and these microbes can metabolize and transform toxicants and food additives. Microbe-toxicant interactions in the intestine can alter host mucosal barrier function, immunity, and metabolism, which may contribute to the risk or severity of metabolic disease development. Targeting the connection between toxicants, food, and immunity in the gut using strategies such as fermentable fiber (i.e., inulin) may mitigate some of the effects of these compounds on host metabolism. Understanding causative factors in the microbe-host relationship that promote toxicant-induced dysmetabolism is an important goal. This review highlights the role of common toxicants (i.e. persistent organic pollutants, pesticides, and fungicides) and food additives (emulsifiers and artificial sweeteners) found in our food supply that alter the gut microbiota and promote metabolic disease development.

The Occurrence of Borrelia burgdorferi sensu lato in Ixodes ricinus Ticks Collected from Nature-Educational and Tourist Trails in the Poprad Landscape Park

Throughout Europe, including Poland, Ixodes ricinus ticks are the main vector of numerous pathogenic agents that pose a serious threat to public health. Southern Poland attracts many tourists with its scenic landscapes and abundant recreational opportunities. These areas are ideal habitats for wild fauna, which serve as the main reservoirs and hosts for these pathogens and ticks. The large population and biodiversity of these hosts facilitate the proliferation of ticks. The aim of this study was to determine the potential exposure of humans to ticks and tick-borne pathogens such as Borrelia burgdorferi sensu lato, Anaplasma phagocytophilum, and Babesia spp., along the nature-educational and tourist trails of the Poprad Landscape Park. From 2020 to 2021, ticks were collected using the flagging method on three tourist trails and nature-educational paths within the Poprad Landscape Park. DNA was isolated from 213 I. ricinus ticks using the ammonia method. To detect pathogens in ticks, PCR and nested PCR methods were used. To detect B. burgdorferi s.l. and A. phagocytophilum, two pairs of primers specific to the flaB gene fragment and 16S rRNA gene fragment were used, respectively. For Babesia spp. detection, primers specific to the 18S rRNA gene were used. The amplification products were separated electrophoretically and visualized under ultraviolet light. In total, among the 213 examined ticks, B. burgdorferi s.l. was detected in 31% of the samples. Neither A. phagocytophilum nor Babesia spp. were detected in the studied material. These results indicate a potentially high risk of ticks and tick-borne B. burgdorferi s.l. infections for residents and tourists in the recreational areas of the Poprad Landscape Park.

P-Phenylenediamines and their derived quinones: A review of their environmental fate, human exposure, and biological toxicity.

p-Phenylenediamines (PPDs) are widely used as antioxidants in numerous rubber products to prevent or delay oxidation and corrosion. However, their derived quinones (PPD-Qs), generated through reactions with ozone, are ubiquitous in the environment and raise significant health and toxicity concerns. This review summarizes the current state of knowledge on environmental distribution and fate, human exposure, and biological toxicity of PPDs and PPD-Qs, and makes recommendations for future research directions. Although PPDs and PPD-Qs have been monitored in a variety of environmental matrices, studies on soil, sediment, and organisms remain limited. This shortcoming hinders our understanding of their distribution patterns and migration mechanisms in these specific environments. These contaminants can enter the human body through various exposure routes, but toxicological studies have not yielded sufficient results to derive risk thresholds for the assessment of human health. Most studies examining biological and toxicological effects have focused on acute exposure scenarios, which do not accurately reflect the long-term interactions that occur in natural settings. The toxic effects of PPDs and PPD-Qs on zebrafish, nematodes, and mammals include neurobehavioral changes, reproductive dysfunction, and digestive damage, which are linked to mitochondrial stress, DNA adduct formation, and disrupted lipid metabolism, respectively. However, the underlying toxicological mechanisms remain poorly understood. Future research should prioritize the investigation of the impacts of PPDs and PPD-Qs on various organizational levels within biota to provide a scientific basis for developing effective risk management measures.

An epigenetic memory at the CYP1A gene in cancer-resistant, pollution-adapted killifish

Human exposure to polycyclic aromatic hydrocarbons (PAH) is a significant public health problem that will worsen with a warming climate and increased large-scale wildfires. Here, we characterize an epigenetic memory at the cytochrome P450 1 A (CYP1A) gene in wild Fundulus heteroclitus that have adapted to chronic, extreme PAH pollution. In wild-type fish, CYP1A is highly induced by PAH. In PAH-tolerant fish, CYP1A induction is blunted. Since CYP1A metabolically activates PAH, this memory protects these fish from PAH-mediated cancer. However, PAH-tolerant fish reared in clean water recover CYP1A inducibility, indicating a non-genetic effect. We observed epigenetic control of this reversible memory of generational PAH stress in F1 PAH-tolerant embryos. We detected a bivalent domain in the CYP1A promoter enhancer comprising both activating and repressive histone post-translational modifications. Activating modifications, relative to repressive ones, showed greater increases in response to PAH in sensitive embryos, relative to tolerant, consistent with greater gene activation. PAH-tolerant adult fish showed persistent induction of CYP1A long after exposure cessation, which is consistent with defective CYP1A shutoff. These results indicate that PAH-tolerant fish have epigenetic protection against PAH-induced cancer in early life that degrades in response to continuous gene activation.

A physiologically based pharmacokinetic (PBPK) model describing the kinetics of a commercial mixture α-, β-, and γ-hexabromocyclododecane exposure in mice.

Hexabromocyclododecane (HBCD) is a brominated flame retardant, that is added, but not chemically bonded, to consumer products. HBCD is sold as a commercial-grade HBCD mixture containing three major stereoisomers: alpha (α), beta (β), and gamma (γ), with relative amounts of 12% for α-HBCD, 6% for β-HBCD, and 82% for γ-HBCD. HBCDs are widely measured in the environment and in biological matrices. The toxicological effects of its exposure in humans are not clearly understood. A recent reassessment pointed out potential thyroid disruption as a primary effect. This current work aims to update a physiologically based pharmacokinetic (PBPK) model for γ-HBCD in C57BL/6 mice and incorporate equations and codes for α-HBCD and β-HBCD isomers and simulate them as a mixture. Physiological parameters were taken from the literature, calculated based on the log Kow or optimized with the dataset. The elimination of HBCDs in urine and feces was optimized to reflect the percent dose excreted, as published in the literature. Compared with data from the literature for α-HBCD, β-HBCD, and γ-HBCD in multiple tissues, the model simulations accurately described the pharmacokinetics of HBCDs in the mouse. The utility of the model was demonstrated by predicting blood concentrations from three studies in adult mice evaluating dopaminergic changes in the brain. Although this PBPK model for the mixture explicitly describes α-HBCD, β-HBCD, and γ-HBCD as individual exposures, but also as a mixture, more experimental data with commercial HBCD mixtures is still needed to improve the model.

Current level, sources, and risk of human exposure to PAHs, PBDEs and PCBs in South American outdoor air: A critical review.

This study provides comprehensive overview of the current level, sources and human exposure risk to hazardous polycyclic aromatic hydrocarbons (PAHs), polybrominated diphenyl ethers (PBDEs), and polychlorinated biphenyls (PCBs) in South American outdoor air. Research documents were obtainable for only 6 countries within the target period (2014 - 2024). For all contaminants, urban concentrations exceeded that of rural/remote locations. PAHs were extensively reported with concentration reaching 1100 ∑16PAHs/m3 in Southwest of Buenos Aires province, Argentina. The health risk data also exceeded the threshold level in several locations. The profiles and seasonal fluctuations across all studies were widely influenced by the prevalent local/domestic sources. Biomass combustion (particularly of sugar cane/agricultural wastes and wood/coal for residential heating), vehicular emission, and industrial emission were accounted for most PAH sources. Regulations targeting biomass combustion for improved air quality seem not to currently have significant impacts on current PAH levels. PBDEs were widely reported within 0.3 to 55 pg ∑4-14BDE/m3, albeit high concentrations were documented in Concepción Bay, Chile (maximum = 1100 pg ∑4BDE/m3) and Córdoba, Argentina (maximum = 120 pg ∑4BDE/m3). Most notable source of PBDEs is solid municipal wastes. Similar to other global studies, BDE-47, 99 and 209 dominated the congeners reported. PCBs were reported with the highest concentrations measured in Córdoba, Argentina (maximum = 1700 pg ∑30PCBs/m3), but data remain limited in other important locations such as São Paulo, Brazil. Sources of PCBs were broadly associated with solid wastes, electric transformers, and re-volatilisation from polluted environment. PAHs, PCBs and PBDEs were all within average to top global concentrations. This study underscores potential rise in atmospheric level of the target contaminants without sustainable regulatory structure and the need for continuous monitoring of these contaminants as a measure of policy impacts. We provide sustainable recommendations.

Airborne particulate matter inhalation bioaccessibility: A review of methodological aspects.

Research has consistently linked exposure to particulate matter (PM) with adverse health outcomes, including cardiovascular and pulmonary morbidity and mortality. Understanding the mechanisms by which PM leads to these effects on human health is crucial for developing effective mitigation strategies. One aspect of PM research that has gained increased attention in the past few years is the bioaccessibility of inhaled PM-bound pollutants that have potential to cause adverse health effects. To assess the bioaccessibility of PM-bound pollutants, such as polycyclic aromatic hydrocarbons, phthalate esters, organophosphorus flame retardants and metal(loid)s, simulated lung fluids (SLF) are used as a tool to mimic the conditions in the human respiratory system. In addition to different SLF, various extraction methodologies and experimental conditions (e.g., incubation period, solid to liquid ratio, and pH) have been employed to extract the bioaccessible part of these pollutants, though there is not yet a standardised procedure to do so. This review aims to critically evaluate existing inhalation bioaccessibility methodologies and explore their connection with PM characteristics. More research is needed, and a standardised procedure should be implemented to allow the comparation of data between studies. Better in vitro-in vivo relationships need to be established to enhance the feasibility of in vitro bioaccessibility assays as surrogates in human health exposure assessments. Long-term effects of bioaccessible pollutants and any potential synergetic effects between multiple contaminants should also be explored to assess health repercussions more thoroughly.

Assessing tick attachments to humans with citizen science data: spatio-temporal mapping in Switzerland from 2015 to 2021 using spatialMaxent

BackgroundTicks are the primary vectors of numerous zoonotic pathogens, transmitting more pathogens than any other blood-feeding arthropod. In the northern hemisphere, tick-borne disease cases in humans, such as Lyme borreliosis and tick-borne encephalitis, have risen in recent years, and are a significant burden on public healthcare systems. The spread of these diseases is further reinforced by climate change, which leads to expanding tick habitats. Switzerland is among the countries in which tick-borne diseases are a major public health concern, with increasing incidence rates reported in recent years.MethodsIn response to these challenges, the “Tick Prevention” app was developed by the Zurich University of Applied Sciences and operated by A&K Strategy Ltd. in Switzerland. The app allows for the collection of large amounts of data on tick attachment to humans through a citizen science approach. In this study, citizen science data were utilized to map tick attachment to humans in Switzerland at a 100 m spatial resolution, on a monthly basis, for the years 2015 to 2021. The maps were created using a state-of-the-art modeling approach with the software extension spatialMaxent, which accounts for spatial autocorrelation when creating Maxent models.ResultsOur results consist of 84 maps displaying the risk of tick attachments to humans in Switzerland, with the model showing good overall performance, with median AUCROC values ranging from 0.82 in 2018 to 0.92 in 2017 and 2021 and convincing spatial distribution, verified by tick experts for Switzerland. Our study reveals that tick attachment to humans is particularly high at the edges of settlement areas, especially in sparsely built-up suburban regions with green spaces, while it is lower in densely urbanized areas. Additionally, forested areas near cities also show increased risk levels.ConclusionsThis mapping aims to guide public health interventions to reduce human exposure to ticks and to inform the resource planning of healthcare facilities. Our findings suggest that citizen science data can be valuable for modeling and mapping tick attachment risk, indicating the potential of citizen science data for use in epidemiological surveillance and public healthcare planning.Graphical