Diisobutyl Phthalate Research Articles

Temporal trends of plastic additive contents in sediment cores of three French rivers (Loire, Meuse and Moselle) over the last decades

Sediment cores from three major French watersheds (Loire, Meuse and Moselle) have been dated by 137Cs and 210Pbxs from 1910 (Loire), 1947 (Meuse) and 1930 (Moselle) until the present in order to reconstruct trajectories of plastic additive contaminants including nine phthalate esters (PAEs) and seven organophosphate esters (OPEs), measured by gas chromatography–mass spectrometer (GC–MS–MS). Historical levels of ∑PAEs were higher than those of ∑OPEs in the Loire and the Moselle sediments, while ∑PAEs and ∑OPEs contents were of the same order of magnitude in the Meuse sediments. Although increases in concentrations do not evolve linearly, our results clearly indicate an increase in OPEs and PAEs concentrations from the 1950–1970 period onwards, compared with the first half of the 20th century. Our results show that, ∑OPE contents increase gradually over time in the Loire and Meuse rivers but evolve more randomly in the Moselle River. Trajectories of ∑PAEs depend on the river and no generality can be established, suggesting sedimentary reworking and/or local contamination. Data from this study allowed comparisons of contents of ∑OPEs and ∑PAEs between rivers, with ∑OPE concentrations in the Moselle River > Meuse River > Loire River, and concentrations of ∑PAEs in the Loire River > Moselle River > Meuse River. Among all PAEs, di(2-ethylhexyl) phthalate (DEHP) was the most abundant in all sediment samples, followed by diisobutyl phthalate (DiBP). Tris (2-chloroisopropyl) phosphate (TCPP) was the most abundant OPE in sediments of the three rivers. In addition, strong positive Pearson correlations were observed between organic matter (OM) parameters and OPE concentrations, and to a lesser extent, between OM parameters and PAE concentrations. This is particularly true for the Moselle River and for the Loire River, but less so for the Meuse River.

Phthalates: The Main Issue in Quality Control in the Beverage Industry

Phthalate esters (PAEs) are a group of chemicals used to improve the flexibility and durability of plastics. The chemical properties and the resistance to high temperatures promote their degradation and release into the environment. Food and beverages can be contaminated by PAEs through the migration from packaging material because they are not covalently bound to plastic and also via different kinds of environmental sources or during processing. For instance, alcoholic drinks in plastic containers are a particular risk, since the ethanol contained provides a good solubility for PAEs. According to its role as an endocrine disruptor compound and its adverse effects on the liver, kidney, and reproductive and respiratory systems, the International Agency on Research Cancer (IARC) classified di-(2-ethylhexyl) phthalate (DEHP) as a possible human carcinogen. For this reason, to control human exposure to PAEs, many countries prohibited their use in food as non-food substances. For example, in Europe, the Commission Regulation (EU) 2018/2005 restricts the use of DEHP, dibutyl phthalate (DBP), benzyl butyl phthalate (BBP), and diisobutyl phthalate (DiBP) to a concentration equal to or below 0.1 by weight in plasticizers in articles used by consumers or in indoor areas. There are reports from the US Food and Drug Administration (FDA) that some beverages (and food as well), particularly fruit juices, contain high levels of phthalates. In some cases, the deliberate adulteration of soft drinks with phthalate esters has been reported. This paper would like to show the difficulties of performing PAE analysis in beverage matrices, in particular alcoholic beverages, as well as the main solutions provided for quality control in the industrial branches.

Influencing factors and risk assessment of phthalate ester pollution in the agricultural soil on a tropical island

Phthalate esters (PAEs) are widely prevalent in agricultural soil and pose potential risks to crop growth and food safety. However, the current understanding of factors influencing the behavior and fate of PAEs is limited. This study conducted a large-scale investigation (106 sites in 18 counties with 44 crop types) of 16 types of PAEs on a tropical island. Special attention was given to the impacts of land use type, soil environmental conditions, agricultural activity intensity, and urbanization level. The health risks to adults and children from soil PAEs via multiple routes of exposure were also evaluated. The results showed that the mean concentration of PAEs was 451.87 ± 284.08 μg kg−1 in the agricultural soil. Elevated agricultural and urbanization activities contributed to more pronounced contamination by PAEs in the northern and southern regions. Land use type strongly affected the concentration and composition of PAEs in agricultural soils, and the soil PAE concentration decreased in the order of vegetable fields, orchards, paddy fields, and woodlands. In paddy fields, di-isobutyl phthalate and di-n-butyl phthalate made more substantial contributions to the process through which the overlying water inhibited volatilization. Soil microplastic abundance, pesticide usage, crop yield, gross domestic product, and distance to the nearest city were calculated to be the major factors influencing the concentration and distribution of PAEs. Soil pH, organic matter content, microplastic abundance and the fertilizer application rate can affect the adsorption of PAEs by changing the soil environment. A greater risk was detected in the northern region and paddy fields due to the higher soil PAE concentrations and the dietary structure of the population. This study reveals important pathways influencing the sources and fate of PAE pollution in agricultural soils, providing fundamental data for controlling PAE contamination.

Systemic investigation of di-isobutyl phthalate (DIBP) exposure in the risk of cardiovascular via influencing the gut microbiota arachidonic acid metabolism in obese mice model

Phthalate esters (PE), a significant class of organic compounds used in industry, can contaminate humans and animals by entering water and food chains. Recent studies demonstrate the influence of PE on the development and progression of heart diseases, particularly in obese people. Di-isobutyl phthalate (DIBP) was administered orally to normal and diet-induced obese mice in this research to assess cardiovascular risk. The modifications in the microbial composition and metabolites were examined using RNA sequencing and mass spectrometry analysis. Based on the findings, lean group rodents were less susceptible to DIBP exposure than fat mice because of their cardiovascular systems. Histopathology examinations of mice fed a high-fat diet revealed lesions and plagues that suggested a cardiovascular risk. In the chronic DIBP microbial remodeling metagenomics Faecalibaculum rodentium was the predominant genera in obese mice. According to metabolomics data, arachidonic acid (AA) metabolism changes caused by DIBP were linked to unfavorable cardiovascular events. Our research offers new understandings of the cardiovascular damage caused by DIBP exposure in obese people and raises the possibility that arachidonic acid metabolism could be used as a regulator of the gut microbiota to avert related diseases.

Identification and characterisation of moderately thermostable diisobutyl phthalate degrading esterase from a Great Artesian Basin Bacillus velezensis NP05

Phthalate esters are known to be endocrine disrupting chemicals and are documented to pollute environments. Enzymatic degradation of PAEs is a potential bioremedial strategy to manage contamination. Thermostable bioremedial enzymes have advantages in enzyme manufacturing and storage. In this study, we identified, overexpressed, and characterised a moderately thermostable para-nitrobenzyl esterase from whole genome sequencing of a Bacillus velezensis NP05 from the Great Artesian Basin, capable of sequential 2-step hydrolysis of diisobutyl phthalate. The pnbA enzyme has a molecular weight of 55.14 kDa and pI of 5.31. It preferentially degrades para-nitrophenyl butanoate and has an optimal pH of 7–8. The pnbA esterase has an optimal temperature of 55 °C with a half-life of 4 h. Using HPLC we found that pnbA (0.122 U) can hydrolyse 0.83 mM of DIBP within 25 min. Lastly, pnbA is potentially a more economically viable candidate for enzymatic bioremediation of diisobutyl phthalate as a free enzyme.

Personal environmental exposure to plasticizers and organophosphate flame retardants using silicone wristbands and urine: Patterns, comparisons, and correlations

Plasticizers (PLs) and organophosphate flame retardants (OPFRs) are ubiquitous in the environment due to their widespread use and potential for leaching from consumer products. Environmental exposure is a critical aspect of the human exposome, revealing complex interactions between environmental contaminants and potential health effects. Silicone wristbands (SWBs) have emerged as a novel and non-invasive sampling device for assessing personal external exposure. In this study, SWBs were used as a proxy to estimate personal dermal adsorption (EDdermal) to PLs and OPFRs in Belgian participants for one week; four morning urine samples were also collected and analyzed for estimated daily intake (EDI). The results of the SWBs samples showed that all the participants were exposed to these chemicals, and the exposure was found to be highest for the legacy and alternative plasticizers (LP and AP), followed by the legacy and emerging OPFRs (LOPFR and EOPFR). In urine samples, the highest levels were observed for metabolites of diethyl phthalate (DEP), di-isobutyl phthalate (DiBP) and di-n-butyl phthalate (DnBP) among LPs and di(2-ethylhexyl) terephthalate (DEHT) for APs. Outliers among the participants indicated that there were other sources of exposure that were not identified. Results showed a significant correlation between EDdermal and EDI for DiBP, tris (2-butoxyethyl) phosphate (TBOEP) and triphenyl phosphate (TPhP). These correlations indicated their suitability for predicting exposure via SWB monitoring for total chemical exposure. The results of this pilot study advance our understanding of SWB sampling and its relevance for predicting aggregate environmental chemical exposures, while highlighting the potential of SWBs as low-cost, non-invasive personal samplers for future research. This innovative approach has the potential to advance the assessment of environmental exposures and their impact on public health.

Occurrence and Health Risk Assessment of Phthalates in Municipal Drinking Water Supply of a Central Indian City.

In this study, the occurrence of phthalates in the municipal water supply of Nagpur City, India, was studied for the first time. The study aimed to provide insights into the extent of phthalate contamination and identify potential sources of contamination in thecity's tap water. We analyzed fifteen phthalates and the total concentration (∑15phthalates) ranged from 0.27 to 76.36µgL-1. Prominent phthalates identified were di-n-butyl phthalate (DBP), di-isobutyl phthalate (DIBP), benzyl butyl phthalate (BBP), di (2-ethylhexyl) phthalate (DEHP), di-n-octyl phthalate (DNOP), and di-nonyl phthalate (DNP). Out of the fifteen phthalates analyzed, DEHP showed the highest concentration in all the samples with the median concentration of 2.27µgL-1, 1.39µgL-1, 1.83µgL-1, 2.02µgL-1, respectively in Butibori, Gandhibaag, Civil Lines, and Kalmeshwar areas of the city. In 30% of the tap water samples, DEHP was found higher than the EPA maximum contaminant level of 6µgL-1. The average daily intake (ADI) of phthalates via consumption of tap water was higher for adults (median: 0.25µgkg-1day-1) compared to children (median: 0.07µgkg-1day-1). The hazard index (HI) calculated for both adults and children was below the threshold level, indicating no significant health risks from chronic toxic risk. However, the maximum carcinogenic risk (CR) for adults (8.44 × 10-3) and children (7.73 × 10-3) was higher than the threshold level. Knowledge of the sources and distribution of phthalate contamination in municipal drinking water is crucial for effective contamination control and management strategies.

Basin scale monitoring of microplastics and phthalates in sediments from the Persian Gulf and the Gulf of Makran using GIS-based algorithms: Insights towards spatial variation and potential risk assessment

Information on sedimentary microplastics and phthalates has been restricted to the coastal regions of the Persian Gulf and the Gulf of Makran. Our basin-wide study monitored their levels, spatial behaviors, and potential risks using GIS-based techniques. Microplastics and phthalates ranged from 5 to 75 particles/kg d.w and 0.004–1.219 μg g−1 d.w, respectively. Microplastics were in the size category of 100 μm to 3 mm, and black microfibers (< 1 mm) and high-density polymers were dominant. The total number of microplastics was between 356.333 × 1012 and 469.075 × 1012 particles in the surface sediments of the studied regions (confidence interval = 99 %). Diethylhexyl phthalate (DEHP) and Di-isobutyl phthalate contributed 88 % of detected phthalates. Significant correlations among microplastic abundance, total phthalates, and DEHP were distinguished (p < 0.05). Overall, the findings reiterated the widespread presence of microplastics and a potential link between phthalates and microplastics. Semi-variogram, cluster Voronoi polygons, and Trend analysis identified spatial outliers and major deposition sites of microplastics and phthalates and consequently outlined the localities where upcoming studies should be concentrated. A hotspot of potential risks was marked using Fuzzy logic and GIS-based algorithms in the Sea of Makran, covering an area equal to 342. 99 km2.

Distribution Characteristics and Pollution Sources Analysis of Polycyclic Aromatic Hydrocarbons and Phthalate Esters in the Seawater of Land-Based Outlets around Zhanjiang Bay in Spring

This study analyzed the distribution characteristics and sources of pollutants in the coastal estuaries of Zhanjiang Bay (ZJB) to provide theoretical and data support for the scientific prevention and control of bay pollution. Monitoring data from eight rivers and flood drains flowing into ZJB in March 2021 were used to analyze the composition and spatial distribution characteristics of polycyclic aromatic hydrocarbons (PAHs) and phthalate esters (PAEs) in the water bodies of the bay. The dominant components in the eight rivers and flood drains were 3–4-ring PAHs, with Bis (2-ethylhexyl) phthalate (DEHP), Diisobutyl phthalate (DIBP), and Dibutyl-O-phthalate (DBP) being the main PAE compounds. Higher pollutant levels were observed in residential areas, aquaculture zones, and industrial areas. Eigen-ratio analysis and principal component analysis were used to identify pollution sources, including atmospheric inputs (coal, petroleum products, biomass combustion products), offshore petroleum pollution, and plastic pollution sources. The assessment showed that atmospheric inputs contributed to 89.75% of the total PAHs in the bay, with coal and biomass combustion accounting for 62.12% and petroleum fuel combustion accounting for 27.63%. The content of ΣPAEs ranged from 588.43 to 1427.26 ng·L−1, with a mean value of 906.59 ng·L−1, which is at a low to medium level compared to other regions of China and abroad, indicating a medium-low level of pollution risk. The results of this study have important implications for guiding urban development, adjusting energy consumption structures, and planning pollution prevention and control measures in ZJB.

Occurrence of phthalate esters in the yellow and Yangtze rivers of china: Risk assessment and source apportionment

Phthalate esters (PAEs), recognized as endocrine disruptors, are released into the environment during usage, thereby exerting adverse ecological effects. This study investigates the occurrence, sources, and risk assessment of PAEs in surface water obtained from 36 sampling points within the Yellow River and Yangtze River basins. The total concentration of PAEs in the Yellow River spans from 124.5 to 836.5 ng/L, with Dimethyl phthalate (DMP) (75.4 ± 102.7 ng/L) and Diisobutyl phthalate (DiBP) (263.4 ± 103.1 ng/L) emerging as the predominant types. Concentrations exhibit a pattern of upstream (512.9 ± 202.1 ng/L) > midstream (344.5 ± 135.3 ng/L) > downstream (177.8 ± 46.7 ng/L). In the Yangtze River, the total concentration ranges from 81.9 to 441.6 ng/L, with DMP (46.1 ± 23.4 ng/L), Diethyl phthalate (DEP) (93.3 ± 45.2 ng/L), and DiBP (174.2 ± 67.6 ng/L) as the primary components. Concentration levels follow a midstream (324.8 ± 107.3 ng/L) > upstream (200.8 ± 51.8 ng/L) > downstream (165.8 ± 71.6 ng/L) pattern. Attention should be directed towards the moderate ecological risks of DiBP in the upstream of HH, and both the upstream and midstream of CJ need consideration for the moderate ecological risks associated with Di-n-octyl phthalate (DNOP). Conversely, in other regions, the associated risk with PAEs is either low or negligible. The main source of PAEs in Yellow River is attributed to the release of construction land, while in the Yangtze River Basin, it stems from the accumulation of pollutants in lakes and forests discharged into the river. These findings are instrumental for pinpointing sources of PAEs pollution and formulating control strategies in the Yellow and Yangtze Rivers, providing valuable insights for global PAEs research in other major rivers.

Temporal evolution of plastic additive contents over the last decades in two major European rivers (Rhone and Rhine) from sediment cores analyses

Although global plastic distribution is at the heart of 21st century environmental concerns, little information is available concerning how organic plastic additives contaminate freshwater sediments, which are often subject to strong anthropogenic pressure. Here, sediment core samples were collected in the Rhone and the Rhine watersheds (France), dated using 137Cs and 210Pbxs methods and analysed for nine phthalates (PAEs) and seven organophosphate esters (OPEs). The distribution of these organic contaminants was used to establish a chronological archive of plastic additive pollution from 1860 (Rhine) and 1930 (Rhone) until today. Sediment grain size and parameters related to organic matter (OM) were also measured as potential factors that may affect the temporal distribution of OPEs and PAEs in sediments. Our results show that OPE and PAE levels increased continuously in Rhone and Rhine sediments since the first records. In both rivers, ∑PAEs levels (from 9.1 ± 1.7 to 487.3 ± 27.0 ng g−1 dry weight (dw) ± standard deviation and from 4.6 ± 1.3 to 65.2 ± 11.2 ng g−1 dw, for the Rhine and the Rhone rivers, respectively) were higher than ∑OPEs levels (from 0.1 ± 0.1 to 79.1 ± 13.7 ng g−1 dw and from 0.6 ± 0.1 to 17.8 ± 2.3 ng g−1 dw, for Rhine and Rhone rivers, respectively). In both rivers, di(2-ethylhexyl) phthalate (DEHP) was the most abundant PAE, followed by diisobutyl phthalate (DiBP), while tris (2-chloroisopropyl) phosphate (TCPP) was the most abundant OPE. No relationship was found between granulometry and additives concentrations, while organic matter helps explain the vertical distribution of PAEs and OPEs in the sediment cores. This study thus establishes a temporal trajectory of PAEs and OPEs contents over the last decades, leading to a better understanding of historical pollution in these two Western European rivers.

Evaluation and health risk assessment of phthalates in Okpa (cow pea pudding) packaged and cooked with polyethene bags in Nsukka, Enugu state, South-East Nigeria

Environmental toxicants enter the body via ingestion, inhalation or dermal absorption. Food is one of the major ways by which these toxicants get into the body. Food packaging has evolved in so many ways that materials made with plastics and its additives (Phthalates) are now used. Phthalates are compounds used to make plastics to enhance its functionality. Some have been associated with some health hazards such as endocrine dysfunction, reproductive problems, skin irritations and cancer. The current study was performed to evaluate the risk associated with consuming phthalates in okpa (cow pea pudding). The phthalate quantification and health risks were evaluated using gas chromatography mass-spectrometry (GC–MS) and models adopted by environmental protection agency (EPA) respectively. The Phthalate identified in okpa were diethyl phthalate (DEP), di-n-Butyl phthalate (DBP), benzylbutyl phthalate (BBP), di-iso-butyl phthalate (DiBP), and di (2-ethylhexyl)phthalate DEHP. The total concentration of phthalate detected was 0.0653 mg/kg with DEP as the highest (0.0196 ± 0.000 mg/kg) and BBP as the least (0.0077 ± 0.001 mg.kg). The highest THQ evaluated was DiBP for both adults (2.84E−1) and children (1.42E−1). The THI for adults and children was 3.35E−1 and 3.01E−1 respectively. The THQ and THI values obtained for adults and children were all less than 1 implying that it is safe. The carcinogenic risk (CR) evaluated for adults and children were 7.23E−6 and 3.61E−5. These values obtained for the THQ, THI and CR all together were within the safe limits stipulated by USEPA, FAO and WHO. However, it is still pertinent to continuously monitor the level of phthalates that may migrate into okpa because red oil content variations may positively impact on its leaching ability.

Semi-volatile organic compounds and trace metals in air cleaner captured house dust

Semi-volatile organic compounds (SVOCs) and trace metals are found anywhere in indoor environments. This study aimed to characterize phthalates, alternative plasticizers (APs), organophosphate flame retardants (OPFRs), and trace metals in air cleaner-captured house dust (ACCD) and to identify the determinants of contaminant levels in ACCD. In total, 120 ACCD samples were collected from 120 houses in Korea that had used air cleaners for over 1 year. All study participants completed a housing, behavior, and lifestyle-related factors questionnaire. The samples were analyzed for 16 phthalates, five APs, 18 OPFRs, and seven trace metals. There were seven chemicals in phthalates, three in APs, and in OPFRs, with 80 % or more detection rates. None of trace metals were found with the detection rate above 65 %. Among the three chemical groups, phthalates were detected at the highest concentrations (geometric mean [GM] (geometric standard deviation [GSD]): 575 (4.6) μg/g in total), followed by APs (389 (5.3) μg/g in total) and OPFRs (290 (3.6) μg/g in total). Among the trace metals, lead and manganese in the ACCD showed the highest concentrations (GM (GSD): 24.8 (8.1) and 24.2 (7.6) μg/g, respectively) with a detection rate of ∼60 %, followed by arsenic (2.9 (17.7) μg/g). The phthalates and Aps measured in the ACCD were comparable to those found in previous investigations of settled dust collected from houses in Korea. Butylbenzyl phthalate and acetyl tributyl citrate concentrations were significantly higher in homes with diffusers, and di-isobutyl phthalate concentrations were higher in homes with air fresheners(p ≤ 0.05). No other determinants were associated with contaminant levels. As residents are persistently exposed to these ubiquitous contaminants through inhalation, appropriate measures are required to reduce potential exposures.

Co-exposure to phthalates and polycyclic aromatic hydrocarbons and the risk of gestational hypertension in Chinese women

Phthalates (PAEs) and polycyclic aromatic hydrocarbons (PAHs) are frequently detected in females of reproductive age. Many studies have found that environmental PAE and PAH levels are independent risk factors for gestational hypertension. However, exposure to both components is a more realistic scenario. To better assess the health effects of PAEs and PAHs in pregnant women, we explored the associations of exposure to both individual and combined PAEs and PAHs with gestational hypertension. This nested case–control study was a component of a prospective cohort study conducted in Beijing, China. We included 206 women with gestational hypertension and 214 pregnant controls. We used gas chromatography/tandem mass spectrometry (GC–MS/MS) to detect 8 PAEs and 13 PAHs in > 80 % of all collected hair samples. Multiple linear regression models were employed to test the individual associations between each component and gestational hypertension. A quantile-based g-computation (qgcomp) model and a weighted quantile sum (WQS) regression model were used to estimate whether exposure to both PAEs and PAHs increased the risk of gestational hypertension. The individual exposure analyses revealed that diethyl phthalate (DEP), diisobutyl phthalate (DIBP) (both PAEs), benzo(k)fluoranthene (BKF), anthracene, (ANT), and benzo(a)pyrene (BAP) (all PAHs) were positively associated with increased risk of gestational hypertension. In mixed-effect analyses, the qgcomp model indicated that co-exposure to PAEs and PAHs increased the risk of gestational hypertension (odds ratio = 2.01; 95 % confidence interval: 1.02, 3.94); this finding was verified by the WQS regression model. Our findings support earlier evidence that both PAEs and PAHs increase the risk of gestational hypertension, both individually and in combination. This suggests that reductions in exposure to endocrine system-disrupting chemicals such as PAEs and PAHs might reduce the risk of gestational hypertension.

Оценка риска здоровью населения от фталатов из полимерной упаковки питьевой воды

At present, consumption of packaged drinking water is growing worldwide. In this regard, ensuring packaged drinking water safety, which directly depends on the composition and quality of used polymer materials, is becoming especially relevant. Bottles made of polymer materials, i.e. polyethylene terephthalate and polycarbonate, is the most common packaging for drinking water. The aim of this study was to assess population health risks caused by exposure to phthalates migrating from polymer bottles into drinking water. The study was carried out according to the requirements of the Customs Union Technical Regulation… on packaging and Instruction... on sanitary-chemical study of goods. Bottles and model media were analyzed using gas chromatography with mass-spectrometric detection. Risk assessment was performed according to the current guidelines. The study findings allow to report the following phthalate levels in bottle samples: di(2-ethylhexyl)phthalate (DEHP), 1.7–4.2 mg/kg; di-n-butyl phthalate (DnBP), &lt;2.4–31.3 mg/kg; diisobutyl phthalate (DiBP), 2.2–10.2 mg/kg. Phthalate migration into model media occurred from all analyzed samples: DEHP and DiBP migrated from Polyethylene terephthalate in quantities equal to 8.6–71.0 µg/l and from &lt; 2.6 to 19.2 µg/l respectively; DEHP, DnBP, and DiBP migrated from polycarbonate, 31.5–43.5 µg/l, 4.8–6.2 µg/l, and 17.0–54.0 µg/l, respectively. The identified phthalate levels are safe according to the performed assessment of health risks associated with chronic intake of harmful substances with drinking water. The values of the estrogenicity equivalent calculated for the analyzed phthalates in model samples of bottled water were seen at a minimum level in Russian Federation as compared to other countries. The results of this study can be used in safety assessment of polymer bottles for drinking water.

Assessment of public health risks caused by phthalates migrating from polymer material to bottled water

At present, consumption of packaged drinking water is growing worldwide. In this regard, ensuring packaged drinking water safety, which directly depends on the composition and quality of used polymer materials, is becoming especially relevant. Bottles made of polymer materials, i.e. polyethylene terephthalate and polycarbonate, is the most common packaging for drinking water. The aim of this study was to assess population health risks caused by exposure to phthalates migrating from polymer bottles into drinking water. The study was carried out according to the requirements of the Customs Union Technical Regulation… on packaging and Instruction... on sanitary-chemical study of goods. Bottles and model media were analyzed using gas chromatography with mass-spectrometric detection. Risk assessment was performed according to the current guidelines. The study findings allow to report the following phthalate levels in bottle samples: di(2-ethylhexyl)phthalate (DEHP), 1.7–4.2 mg/kg; di-n-butyl phthalate (DnBP), &lt;2.4–31.3 mg/kg; diisobutyl phthalate (DiBP), 2.2–10.2 mg/kg. Phthalate migration into model media occurred from all analyzed samples: DEHP and DiBP migrated from Polyethylene terephthalate in quantities equal to 8.6–71.0 µg/l and from &lt; 2.6 to 19.2 µg/l respectively; DEHP, DnBP, and DiBP migrated from polycarbonate, 31.5–43.5 µg/l, 4.8–6.2 µg/l, and 17.0–54.0 µg/l, respectively. The identified phthalate levels are safe according to the performed assessment of health risks associated with chronic intake of harmful substances with drinking water. The values of the estrogenicity equivalent calculated for the analyzed phthalates in model samples of bottled water were seen at a minimum level in Russian Federation as compared to other countries. The results of this study can be used in safety assessment of polymer bottles for drinking water.

Pollution characteristics, sources, and health risks of phthalate esters in ambient air: A daily continuous monitoring study in the central Chinese city of Nanchang

In recent years, the atmospheric pollution caused by phthalate esters (PAEs) has been increasing due to the widespread use of PAE-containing materials. Existing research on atmospheric PAEs lacks long-term continuous observation and samples from cities in central China. To investigate the pollution characteristics, sources, and health risks of PAEs in the ambient air of a typical city in central China, daily PM2.5 samples were collected in Nanchang from November 2020 to October 2021. In this study, the detection and quantification of six significant PAE contaminants, namely diethyl phthalate (DEP), di-n-butyl phthalate (DnBP), diisobutyl phthalate (DIBP), Di-2-ethylhexyl phthalate (DEHP), di-n-octyl phthalate (DnOP), and diisodecyl phthalate (DIDP), were accomplished using gas chromatography and mass spectrometry. The results revealed that the concentrations of DEP, DnBP, DEHP, and DnOP were relatively high. Higher temperatures promote the volatilization of PAEs, leading to an increase in the gaseous and particulate PAE concentrations in warm seasons and winter pollution scenarios. The results of principal component analysis show that PAEs mainly come from volatile products and polyvinylchloride plastics. Using positive matrix factorization analysis, it is shown that these two sources contribute 67.0% and 33.0% in atmosphere PAEs, respectively. Seasonally, the contribution of volatile products to both gaseous and particulate PAEs substantially increases during warm seasons. The residents in Nanchang exposed to PAEs have a negligible non-cancer risk and a potential low cancer risk. During the warm seasons, more PAEs are emitted into the air, which will increase the toxicity of PAEs and their impact on human health.

Effects of Packaging Material Type, Storage Time and Lipid Content on Phthalate Migration in Smoked Fish Meat

The objective of this study is an investigation of the influence of six different plastic packages (polyethylene terephthalate, high-density polyethylene, biodegradable high-density polyethylene, low-density polyethylene, polypropylene and polyamide polyethylene) on the migration of phthalate residues in smoked carp, trout and salmon stored at −18 °C for three and six months. Six phthalate residues concentrations were determined using the gas chromatography-mass spectrometry method. Diisobutyl phthalate (DIBP) and dibutyl phthalate (DBP) migrated the most into salmon meat from PAPE packaging after six months of storage, reaching 73.77 μg/kg and 78.45 μg/kg, respectively. The highest concentrations of bis(2-ethylhexyl) phthalate (DEHP) after six months of storage were present in salmon meat packed in polyamide polyethylene (253.56 μg/kg) and the lowest in carp meat packages in polypropylene (157.72 μg/kg). Phthalate residues in all the samples showed higher levels after three and six months of storage compared to the control sample. Among the investigated phthalates, polypropylene was the material with the lowest migration into fish meat. A further amount of DEHP migration in the fish was detected with a higher fat content. We acknowledge that levels of phthalates should be monitored, and research in this field should be continued, especially since there are no legal restrictions regarding the maximum level of phthalates in food.

Identification of inhibitors from a functional food-based plant Perillae Folium against hyperuricemia via metabolomics profiling, network pharmacology and all-atom molecular dynamics simulations.

Hyperuricemia (HUA) is a metabolic disorder caused by purine metabolism dysfunction in which the increasing purine levels can be partially attributed to seafood consumption. Perillae Folium (PF), a widely used plant in functional food, has been historically used to mitigate seafood-induced diseases. However, its efficacy against HUA and the underlying mechanism remain unclear. A network pharmacology analysis was performed to identify candidate targets and potential mechanisms involved in PF treating HUA. The candidate targets were determined based on TCMSP, SwissTargetPrediction, Open Targets Platform, GeneCards, Comparative Toxicogenomics Database, and DrugBank. The potential mechanisms were predicted via Gene Ontology (GO) and Kyoto Gene and Genome Encyclopedia (KEGG) analyses. Molecular docking in AutoDock Vina and PyRx were performed to predict the binding affinity and pose between herbal compounds and HUA-related targets. A chemical structure analysis of PF compounds was performed using OSIRIS DataWarrior and ClassyFire. We then conducted virtual pharmacokinetic and toxicity screening to filter potential inhibitors. We further performed verifications of these inhibitors' roles in HUA through molecular dynamics (MD) simulations, text-mining, and untargeted metabolomics analysis. We obtained 8200 predicted binding results between 328 herbal compounds and 25 potential targets, and xanthine dehydrogenase (XDH) exhibited the highest average binding affinity. We screened out five promising ligands (scutellarein, benzyl alpha-D-mannopyranoside, elemol, diisobutyl phthalate, and (3R)-hydroxy-beta-ionone) and performed MD simulations up to 50 ns for XDH complexed to them. The scutellarein-XDH complex exhibited the most satisfactory stability. Furthermore, the text-mining study provided laboratory evidence of scutellarein's function. The metabolomics approach identified 543 compounds and confirmed the presence of scutellarein. Extending MD simulations to 200 ns further indicated the sustained impact of scutellarein on XDH structure. Our study provides a computational and biomedical basis for PF treating HUA and fully elucidates scutellarein's great potential as an XDH inhibitor at the molecular level, holding promise for future drug design and development.

Photocatalytic activation of peroxymonosulfate (PMS) by CNN@NH2-MIL-101(Fe) Z-scheme heterojunction for phthalates degradation under visible light irradiation

Phthalates (PAEs) are known to pose a serious threat to the environment and human health duo to their endocrine disrupting effects, thus a great deal of effort has been made to develop destruction technologies for PAEs treatment in the water environment, such as peroxymonosulfate (PMS)-based advanced oxidation technology. Here we prepared an environmentally friendly visible light catalyzer, a heterojunction of carbonitride nanosheets (CNN) doped with NH2-iron metal organic frameworks (NH2-MIL-101(Fe)), for the activation of PMS to efficaciously remove two representative PAEs—diisobutyl phthalate (DIBP) and diethyl phthalate (DEP)—from the aquatic environment. The CNN@NH2-MIL-101(Fe) photocatalyst possesses an excellent visible light harvesting performance with a narrow band gap (1.66 eV), low recombination ratio of photoinduced carriers, and long charge lifetime. The pore volume and surface area of the composite material was increased compared with any single component. The optimum CNN@NH2-MIL-101(Fe) catalyst manifested the high performance to activate PMS to degrade DIBP and DEP under visible irradiation with maximum removal of 94.5 ± 2.2 % and 83.4 ± 0.9 %, respectively. Four main active species (•OH, O2−•, SO4−•, and h+) were involved in PAEs photodegradation, with h+ and SO4−• playing a key role in the degradation of DIBP, and h+ in the degradation of DEP. The degradation mechanism of DIBP and DEP mainly involved the ester bond cleavage and oxidationby active species. Additionally, the CNN@NH2-MIL-101(Fe) heterojunction exhibited high and stable catalytic performance to activate PMS for PAEs destruction under pH 3 – 9. Therefore, this study provides a new strategy for designing and selecting environment-friendly treatment approach for the effective eradication of PAEs via a PMS-based advanced oxidation process.