Associations between serum per- and polyfluoroalkyl substances and thyroid hormones in Chinese adults: A nationally representative cross-sectional study.

Disruption of thyroid homeostasis has been indicated in human studies on the effects of per- and polyfluoroalkyl substances (PFASs). However, limited research exists on this topic within the general Chinese population. Based on a substantial and representative sample of the Chinese adult population, our study provides insight into how PFASs specifically affect thyroid homeostasis. The study included 10 853 participants, aged 18 years and above, sampled from nationally representative data provided by the China National Human Biomonitoring (CNHBM). Weighted multiple linear regression and restricted cubic spline (RCS) models were used to explore the associations between eight individual PFAS concentrations and total thyroxine (T4), total triiodothyronine (T3), and the T4/T3 ratio. Bayesian kernel machine regression (BKMR) and quantile-based g-computation (qgcomp) were employed to explore the joint and independent effects of PFASs on thyroid homeostasis. Both individual PFASs and PFAS mixtures exhibited a significant inverse association with serum T3 and T4 levels, and displayed a positive association with the T4/T3 ratio. Perfluoroundecanoic acid (PFUnDA) [-0.07 (95 % confidence interval (CI): -0.08, -0.05)] exhibited the largest change in T3 level. PFUnDA also exhibited a higher weight compared to other PFAS compounds in qgcomp models. Additionally, a critical exposure threshold for each PFAS was identified based on nonlinear dose-response associations; beyond these thresholds, the decreases in T3 and T4 levels plateaued. Specifically, for perfluoroheptane sulfonic acid (PFHpS) and 6:2 chlorinated polyfluorinated ether sulfonate (6:2 Cl-PFESA), an initial decline in hormone levels was observed, followed by a slight increase when concentrations surpassed 0.7 ng/mL and 2.5 ng/mL, respectively. Sex-specific effects were more pronounced in females, and significant associations were observed predominantly in younger age groups. These insights contribute to our understanding of how PFAS compounds impact thyroid health and emphasize the need for further research and environmental management measures to address these complexities.

Co-occurrence of organophosphate diesters and organophosphate triesters in daily household products: Potential emission and possible human health risk.

Eight paired organophosphate diesters (Di-OPs) and organophosphate triesters (Tri-OPs) were investigated in wipes from analytical instruments and 47 material samples related to household products, including textiles, electrical/electronic devices, building/ decoration materials and children's products. The total concentrations of Di-OPs ranged in 3577-95551 ng/m2 in the wipes and limit of detection-23002 ng/g in the materials. The Tri-OPs concentrations varied significantly in the ranges of 107218-1756892 ng/m2 and 2.13-503149 ng/g, respectively. Four industrial Di-OPs were detected in > 65% of the studied samples suggesting their direct application in the studied materials. Furthermore, we demonstrated for the first time that four non-industrial Di-OPs, e.g., bis(2-chloroethyl) phosphate, bis(1-chloro-2-propyl) phosphate, bis(1,3-dichloro-2-propyl) phosphate, and bis(butoxyethyl) phosphate, identified as degradation products of their respective Tri-OPs were also detected in these studied samples, which might act as important emission sources of Di-OPs in indoor environments. We estimated the burden of Di-OPs and Tri-OPs in a typical residential house and instrumental room, which both exhibited important contributions from furniture, building and decoration materials, and electrical/electronic devices. Limit health risk was posed to local people via air inhalation.

Regional Distribution of Atmospheric Organophosphate Tri-/Diesters in the Pearl River Delta: Possible Emission, Photo-degradation, and Atmospheric Transportation.

The regional characteristics of atmospheric organophosphate triesters (OPEs) and organophosphate diesters (Di-OPs) in the Pearl River Delta (PRD) were investigated by passive air samplers mounting quartz fiber filters. The analytes were found on a regional scale. Atmospheric OPEs, semi-quantified using sampling rates of particulate-bonded PAHs, were in the range of 537-2852 pg/m3 in spring and in the range of 106-2055 pg/m3 in summer, with tris(2-chloroethyl)phosphate (TCEP) and tris(2-chloroisopropyl)phosphate as the main components. While atmospheric Di-OPs were semi-quantified using sampling rates of SO42-, in the range of 22.5-5576 pg/m3 in spring and in the range of 66.9-1019 pg/m3 in summer, with di-n-butyl phosphate and diphenyl phosphate (DPHP) being the main Di-OPs. Our results indicated that OPEs were mainly distributed in the central part of the region, which might be ascribed to the distribution of industry related to OPE-containing products. In contrast, Di-OPs were scattered in the PRD, suggesting local emission from their direct industrial application. Significantly lower levels of TCEP, triphenyl phosphate (TPHP), and DPHP were detected in summer than in spring, implying that these compounds might be partitioned off particles as the temperature increased and due to possible photo-transformation of TPHP and DPHP. The results also suggested the long-distance atmospheric transportation potential of Di-OPs.

Co-occurrence of polycyclic aromatic hydrocarbons and their oxygenated derivatives in indoor dust from various microenvironments in Guangzhou, China: levels, sources, and potential human health risk.

For decades, the presence and potential health risk of polycyclic aromatic hydrocarbons (PAHs) in indoor dust have been extensively investigated while with limited attention to oxygenated PAHs (OPAHs). In this study, we collected 45 indoor dust from four microenvironments in Guangzhou City, China, and then focused on the co-occurrence of 16 PAHs and 8 OPAHs and their potential carcinogenic risk to humans. The ΣPAHs concentrations, dominated by 4-6 ring PAHs, ranged from 1761 to 14,290 ng/g (mean of 6058 ng/g) without significant difference in the different microenvironments (Tukey, p > 0.05). The OPAHs were observed with concentrations from 250 to 5160 ng/g (mean of 1646 ng/g), and anthraquinone (AQ) was identified as the main OPAHs with significantly high levels in the residential environment than in instrumental rooms. Notably, AQ dominated over the other target analytes in dust in this study. Our results indicated that PAHs and OPAHs in indoor dust were from outdoor environments, which mainly originated from vehicular exhaust and biomass/coal combustion. A potential cancer risk of PAHs and OPAHs to local adults and children was observed via inhalation, ingestion, and dermal absorption, with the main contribution from benzo[a]pyrene and dibenz[a,h]anthracene.

Co-occurrence and potential ecological risk of parent and oxygenated polycyclic aromatic hydrocarbons in coastal sediments of the Taiwan Strait.

Thirty-two surface sediment samples, collected from the Taiwan Strait (TWS), were investigated for the occurrence, composition profile, and spatial distribution of polycyclic aromatic hydrocarbons (PAHs) and oxygenated PAHs (OPAHs). PAHs were ubiquity in the TWS with a total concentration (∑PAHs, excluding naphthalene due to its high volatility) ranging from 17.8-213 ng g-1. Benzo[b] fluoranthene, fluoranthene, phenanthrene, and pyrene were the predominant PAHs. Also, eight OPAHs were detected, having a cumulative concentration range (∑OPAHs) of 10.5-118 ng g-1, predominated by anthraquinone and 6H-Benzo[c,d]Pyren-6-one. Higher concentrations of ∑PAHs and ∑OPAHs were detected at sampling sites adjacent to the mainland and in the northwest part of the TWS. The results suggested important continental input, and particle sedimentation under the specific hydrodynamic conditions of the region. Based on the measured concentrations and sediment quality guidelines, PAHs had a limited ecological impact on the area.

Occurrence and spatio-seasonal distribution of organophosphate tri- and di-esters in surface water from Dongting Lake and their potential biological risk.

In this study, 24 surface water samples were collected from Dongting Lake, China, in the wet and dry seasons, then the concentrations, composition profiles and spatio-seasonal variations of nine organophosphate triesters (OPEs) and five organophosphate diesters (Di-OPs) were determined. Significantly higher total OPE concentrations (∑OPEs) were observed in the wet season (49.5-148 ng L-1) than in the dry season (5.00-45.7 ng L-1) suggesting higher input via tributaries discharge as well as wet deposition in the studied region. Whereas lower levels of TnBP and (triphenyl phosphate (TPHP) in wet season reflected their possible degradation under solar irradiation. Comparable levels of total Di-OPs (∑Di-OPs) were found in the wet season (3.41-13.9 ng L-1) and dry season (1.01-12.3 ng L-1). Tri(2-chloroethyl) phosphate and tris(2-chloroisopropyl) phosphate were the main OPE components, while diphenyl phosphate, di-n-butyl phosphate and bis(1,3-dichloro-2-propyl) phosphate were the main Di-OP components. High levels of OPEs and Di-OPs were found in Datong Lake suggesting possible local emissions potentially related to fishery activity in the land-locked lake. Samples at river mouths to the lake also have higher levels of target OPEs and Di-OPs, the results disclosed obvious discharges from tributaries in Hunan Province. Negligible non-carcinogenic and carcinogenic risks were determined based on the measured concentrations in source waters. A limited ecological risk aquatic organisms in the Dongting Lake was identified, with most risk from TPHP.

Occurrence, spatiotemporal distribution and potential ecological risks of antibiotics in Dongting Lake, China.

We investigated the occurrence and distribution of 18 antibiotics in surface water from Dongting Lake, as well as in influents and effluents from a municipal wastewater treatment plant (WWTP) and a swine farm. The total concentrations of target antibiotics in surface water ranged from limit of quantification to 3107 and 5.32-107 ng L-1 in the dry season and wet season, respectively. Among these studied antibiotics, ciprofloxacin (CIP) and lomefloxacin were as the main components in the dry season, while CIP, oxytetracycline, and chlortetracycline were the main components in the wet season. The concentrations of target compounds exhibited obvious temporal-spatial variation characteristic in the studied region, suggesting their different emission sources related to pig breeding, aquaculture, and human activities, as well as possible degradation in the aquatic system. We estimated that the daily total input and output masses of antibiotics in the influent and effluent from the swine farm were 12.1 mg d-1 pig-1 and 7.49 µg d-1 pig-1, while they were 103 µg d-1 inhabitant-1 and 22.9 µg d-1 inhabitant-1 in the WWTP. The risk assessment results indicated that CIP posed a moderate or high risk to algae in most locations in Dongting Lake.

Co-occurrence and distribution of organophosphate tri- and di-esters in indoor dust from different indoor environments in Guangzhou and their potential human health risk.

In this study, 45 indoor dust samples and four particulate samples from air-conditioner filters were collected from four different indoor environments in Guangzhou, China, and the concentration and composition of organophosphate tri-esters (OPEs) and organophosphate di-esters (Di-OPs) were determined. Eight of the 10 target OPEs were detected in indoor dust at different detection frequencies (DFs), with tris(2-chloroisopropyl) phosphate and tris(2-chloroethyl) phosphate being the main components. Seven target Di-OPs were detected at different DFs, with diphenyl phosphate being the dominant compound. The total OPEs (∑8 OPEs) and total Di-OPs (∑7 Di-OPs) concentrations varied from 726 to 39,312 ng/g and 68.8-14,766 ng/g, respectively. The ∑8 OPEs concentrations in instrumental houses were significantly higher (p < 0.001) than in three other indoor environments. The varying strengths of the correlation between Di-OPs and their respective parent OPEs was suggestive of their emission sources (e.g., direct application, impurities in OPE formulas, and OPE degradation). The hazard index (HI) values of individual OPEs in residential house were lower than 1, the results suggested a limited human health risk from individual OPEs. However, the total HI value (∑HIs) of OPEs was approximately 1 based on a high exposure scenario and suggested a low risk for toddlers.

Occurrence and distribution of organophosphorus flame retardants/plasticizers in coastal sediments from the Taiwan Strait in China.

Concentrations and spatial distributions of organophosphate esters (OPEs) in marine sediment samples in the western Taiwan Strait were investigated and analyzed for the first time. The total OPE concentration (∑OPE) in sediments was in the range of 5263-34,232 pg/g (dry weight), with an average value of 12,796 pg/g. Generally, there was a higher abundance of non-halogenated OPEs than halogenated OPEs and aryl OPEs, with tributyl phosphate, tris (2-ethylhexyl) phosphate, and tri-(1-chloro-2-propyl) phosphate being the main components. The ∑OPE concentrations in the western coastal and northern sampling sites were relatively high. The results indicated that OPEs in the study region originated mainly from terrestrial river inputs and local emission sources, as well as exogenous influxes by ocean currents.

Occurrence of organophosphate esters and their diesters degradation products in industrial wastewater treatment plants in China: Implication for the usage and potential degradation during production processing.

Influent, effluent and sludge samples were collected from eight industrial wastewater treatment plants (WWTPs) in the Pearl River Delta, China. Samples were investigated for the occurrence of 10 organophosphate esters (OPEs) and 7 organophosphate diesters (Di-OPs). Most of the 10 OPEs were detected at total concentrations of OPEs (∑OPEs) ranging from 65.8 to 2842 ng L-1 in influent samples and exhibited different composition profiles. The results indicated that OPEs were widely used with different proportions in versatile OPE-containing products. Meanwhile, ∑OPEs in effluent were found in the range of 6.37-2710 ng L-1; these residuals were subsequently transported to municipal WWTPs for further treatment and posed extra pressure on the plants. Seven Di-OPs, possible degradation products of the OPEs, were also detected in influent, effluent and sludge. The results suggested that OPEs underwent degradation during rigorous industrial manufacturing procedures, such as thermal processes, highly alkaline pH, or processes that involved metal/metal oxide. In addition, high levels of dibutyl phosphate, di(2-ethylhexyl) phosphate and diphenyl phosphate were found in influent suggesting their possible industrial application.

A simple analytical method for the simultaneous determination of multiple organic pollutants in sediment samples.

Due to the extensive application of synthetic organic chemicals, the resulting environmental contamination with such chemicals is of great concern. Herein, we describe the development of a simple analytical method to determine several groups of organic compounds in sediment samples. Samples were soxhlet-extracted with dichloromethane, separated, and cleaned-up by passage through a combined column of neutral alumina/silica gel, then identified and determined by GC-MS analysis. Four sediment samples were analyzed to validate the efficiency, and acceptable recoveries and good repeatability were obtained. •Combined chromatographic columns of silica gel and alumina have been used for separation and clean-up.•Five groups of organic compounds have been simultaneously analyzed.•Acceptable recoveries with good reproducibility have been achieved.

Occurrence, distribution and ecological risks of organophosphate esters and synthetic musks in sediments from the Hun River.

The Hun River is an important main tributary of the Liao River system. It is located in northeast China, and provides water resources for agriculture and industry. A man made reservoir (Dahuofang Reservoir, DHF) has been constructed mid-stream in the Hun River, supplying drinking water to surrounding cities. Pollution from organic contaminants is of great concern. In the present study, 40 sediment samples were collected and analyzed for the occurrence and distribution of two groups of emerging organic pollutants; namely, organophosphate esters (OPs) and synthetic musks (SMs). In all samples taken from upstream of the Hun River (UHR), downstream of the Hun River (DHR), and from DHF, the following concentrations were recorded: 0.141-4.39, 1.21-245, and 0.117-0.726 µg/kg galaxolide (HHCB), and 0.098-3.82, 2.79-213, 0.430-0.956 µg/kg tonalide (AHTN), respectively. For OPs, seven target analytes were detected in most of the sediment samples, with chlorinated OPs Tris-(2-chloroethyl) phosphate and Tris(2-chloro-isopropyl) phosphate being the dominant components, at levels varied in the range of LOD-0.810, ND-49.6, and 0.532-3.18 µg/kg, and LOD-0.786, ND-60.1, and 0.352-1.32 µg/kg from UHR, DHR and DHF, respectively. The elevated levels of these target compounds were detected in DHR, including its two main tributaries, Xi River and Pu River, which drain through cities with industrial development and dense populations. Our results indicate that domestic and industrial wastewater contributed to OPs and SMs sediment pollution, posing low to medium ecological risks to sediment dwelling organisms.