Dimethyl Phthalate Research Articles

Application of ComplexGAPI for the green assessment of a deep eutectic solvent-based ferrofluid assisted liquid-liquid microextraction method for detection of dimethyl phthalate in beverage samples.

In the present study, a novel ferrofluid was prepared by combining a menthol/thymol deep eutectic solvent with magnetic nanoparticles (Fe3O4@OA). This composite was first applied in vortex-assisted liquid-liquid microextraction (VA-LLME), followed by high performance liquid chromatography with ultraviolet detection (HPLC-UV) for the determination of dimethyl phthalate (DMP) residues in beverages. The synthesized deep eutectic solvent-based ferrofluid (DES-FF) was characterized by using Fourier transform infrared spectrometry (FTIR), vibrating sample magnetometry (VSM), X-ray diffraction (XRD), scanning electron microscopy (SEM) and thermogravimetric analysis (TGA). Furthermore, the type of carrier, pH of the sample solution, ferrofluid volume, salt amount, vortex time, type and volume of elution solvents and desorption time were statistically optimized for high extraction efficiencies. Under the optimal extraction conditions, the limit of detection (LOD) and limit of quantification (LOQ) were 0.008 μg mL-1 and 0.03 μg mL-1, respectively. Moreover, the mean recoveries for DMP ranged from 85.2% to 99.5%, and intra- and inter-day precisions were less than 5.5% and 7.8%, respectively. The proposed method was successfully applied to the analysis of dimethyl phthalate in real samples, making it a promising analysis technique for beverage samples. The greenness of the entire procedure of our proposed method was assessed by comparing it with other reported methods using ComplexGAPI (Complex Green Analytical Procedure Index). The results show that our proposed method has a better greenness than other reported methods.

Determination of Dimethyl Phthalate in Beverages by Deep Eutectic Solvent-Based Ferrofluid Assisted Liquid-Liquid Microextraction Technique Combined with Acid-Base Induction

Determination of Dimethyl Phthalate in Beverages by Deep Eutectic Solvent-Based Ferrofluid Assisted Liquid-Liquid Microextraction Technique Combined with Acid-Base Induction

DETECTION OF MICROPLASTIC RESIDUES- DEVELOPING A METHOD FOR PHTALATES IN HONEY

In this pilot study, a method for the determination of phthalates in honey was developed. The following phthalates are included: diethyl phthalate, di-isobutyl phthalate, di-n-butyl phthalate, bis (2-Ethylhexyl) phthalate, and di- (n-octyl) phthalate. For the preparation of the samples, the method of liquid-liquid extraction with hexane with an ultrasonic bath was used. The analysis of the prepared samples was performed using gas chromatography and a mass detector. The method is reliable, sensitive, and reproducible with a detection limit of 0.28 - 1.38 ug/kg. This paper presents the results of testing samples of honey stored in glass and plastic packaging for three years in order to determine the migration of phthalates. Dimethyl phthalate was not found in the tested samples. Diethyl phthalate in glass samples from glass packaging was below the LOQ, and it ranged from 2.1 to 4.11 µg / kg in the samples of honey in plastic packaging. The values of di-isobutyl phthalate, di-n-butyl phthalate and bis (2-ethylhexyl) phthalate ranged between 5.32 and 22.60 µg / kg respectively;1.32 – 27.80 µg/kg; 4.45-19.19 µg/kg; di-(n-octyl) phthalate and di-methyl phthalate were < LOQ

Magnetic response Janus emulsions stabilized by Mangeto-surfactant

Magnetic response emulsions, with regulated motion of droplets by magnetic fields, provide opportunities in system design. Research in Janus emulsion is blooming attributed to excellent multiple chambers, diverse interfaces, and advanced structures. Responsive Janus emulsions are prepared, using two immiscible oils of dimethyl phthalate (DMP)/vegetable oil (VO) and small molecules of magneto-surfactants ([H-G-C16]FeCl4) as stabilizer, in batch-scale by traditional vortex mixing. The composition of emulsion, the concentration of surfactant, and the emulsification energy are applied to control the topology of the structured fluid, and more importantly achieve the quantitative regulation of magnetic response. Janus droplets with clear inner interfaces are successfully constructed solely by magneto-surfactant, and the strategy is universal and even extended to Cerberus emulsions composed of three separated compartments. The magnetic response is visualized by directed moving against gravity and saturated magnetization. The responsivity is enhanced about 44.5%-54.5% accompany with VO lobe transformation from “waxing crescent” to “full moon with a hole”. The magnetic response is increased as high as 80.0% by decreasing the droplet size. Delicate calculations reveal that the ordered arrangement of [H-G-C16]FeCl4 at the interfaces, mainly contributes to the magnetic response compared with aggregates in the continuous phase. The adsorption on the VO/aq interface dominates the overall response due to the higher affinity of the surfactant to the VO phase. The findings open an avenue in the production of magneto-responsive multiple emulsions, which would push forward future application in smart microreactors, intelligent fluids, and responsive delivery systems.

Application of a Liquid-Liquid Microextraction Method Based on a Natural Hydrophobic Deep Eutectic Solvent for the Extraction of Plastic Migrants from Kombuchas.

A vortex-assisted liquid-liquid microextraction, based on a natural hydrophobic deep eutectic solvent made from the monoterpene thymol and octanoic fatty acid, was employed for the analysis of 11 phthalate esters and one adipate in kombucha (a tea-based fermented beverage). Separation and determination were performed using an ultra-high performance liquid chromatography (UHPLC) system coupled to a single quadrupole mass spectrometer. Confirmatory analyses were carried out through UHPLC tandem mass spectrometry. The full method was validated in terms of matrix effect, matrix-matched calibration, sensitivity, recovery, limits of detection and quantification and repeatability. Satisfactory determination coefficients for quadratic calibration curves (≥0.9938), recovery values (67–120%) and limits of detection (0.07–5.45 µg/L) were obtained. Analysis of 26 kombucha samples reported concentrations for dibutyl phthalate and dimethyl phthalate in the range between the limit of quantification (LOQ) and 16.18 ± 1.14 µg/L, although these phthalates were also detected under the LOQ in some of the analyzed samples. Only one of the samples bottled in plastic containers (7) did not present residues while only five of the 19 samples in glass bottles contained any plasticizer. However, the highest concentration was found in a kombucha bottled in food-grade glass. This work represents the first application in which phthalates and adipates are analyzed in kombuchas.

Enhanced Ozone Oxidation by a Novel Fe/Mn@γ−Al2O3 Nanocatalyst: The Role of Hydroxyl Radical and Singlet Oxygen

Catalytic ozonation is a potential alternative to address the dye wastewater effluent, and developing an effective catalyst for catalyzing ozone is desired. In this study, a novel Fe/Mn@γ−Al2O3 nanomaterial was prepared and successfully utilized for catalytic ozonation toward dye wastewater effluent components (dimethyl phthalate and 1−naphthol). The synthesized Fe/Mn@γ−Al2O3 exhibited superior activity in catalytic ozonation of dimethyl phthalate and 1−naphthol in contrast to Fe@γ−Al2O3 and Mn@γ−Al2O3. Quench and probe tests indicated that HO° contributed to almost all removal of dimethyl phthalate, whereas O3, HO°, and singlet oxygen participated in the degradation of 1−naphthol in the Fe/Mn@γ−Al2O3/O3 system. The results of XPS, FT−IR, and EPR suggested that HO° and singlet oxygen were generated from the valence variations of Fe(II/III)and Mn(III/IV). Moreover, the Fe/Mn@γ−Al2O3/O3 system could also have excellent efficacy in actual water samples, including dye wastewater effluent. This study presents an efficient ozone catalyst to purify dye wastewater effluent and deepens the comprehension of the role and formation of reactive species involved in the catalytic ozonation system.

The reaction laws and toxicity effects of phthalate acid esters (PAEs) ozonation degradation on the troposphere

Low-molecular-weight (LMW) phthalate acid esters (PAEs) tend to enter the atmosphere, flying for several kilometers, so it is easy to endanger human health. This work is the first to use quantum chemistry calculations (Gaussian 16 program) and computational toxicology (ECOSAR, TEST, and Toxtree software) to comprehensively study the ozonolysis mechanism of six LMW PAEs (dimethyl phthalate (DMP), diethyl phthalate (DEP), dipropyl phthalate (DPP), diisopropyl phthalate (DIP), dibutyl phthalate (DBP), and diisobutyl phthalate (DIBP)) in the atmosphere and the toxicity of DMP (take DMP as an example) in the conversion process. The results show that the electron-donating effect of the ortho position of the LMW PAEs has the most obvious influence on the ozonolysis. We summarized the ozonation reaction law of LMW PAEs at the optimal reaction site. At 298 K, the law of initial ozonolysis total rate constant of the LMW PAEs is kDIP > kDPP > kDIBP > kDMP > kDEP > kDBP, and the range is 9.56 × 10−25 cm3 molecule−1 s−1 — 1.47 × 10−22 cm3 molecule−1 s−1. According to the results of toxicity assessment, the toxicity of products is lower than DMP for aquatic organisms after ozonolysis. But those products have mutagenicity, developmental toxicity, non-genotoxicity, carcinogenicity, and corrosiveness to the skin. The proposed ozonolysis mechanism promotes our understanding of the environmental risks of PAEs and provides new ideas for studying the degradation of PAEs in the tropospheric gas phase.

Dynamic variations of phthalate esters in PM2.5 during a pollution episode

Phthalate esters (PAEs) as hazardous air pollutants can be easily released during the life cycle of plastic products. In this study, a thermal desorption aerosol comprehensive two-dimensional gas chromatography mass spectrometer coupled with a dual-trap was developed and used to measure the hourly-resolved PAEs characteristics in atmospheric PM2.5 at an urban site. Dimethyl phthalate (DMP), diethyl (DEP), dibutyl (DnBP), benzyl butyl (BBP), di(2-ethylhexyl) (DEHP), and di-n-octyl phthalate (DnOP) in PM2.5 were analyzed. The most abundant compounds were DEHP and DMP, followed by DnBP and DEP. The mass concentrations of the detected PAEs are comparable to those at other urban sites measured using offline methods with a lower time resolution. The concentrations of PAEs showed intense change with the variation of PM2.5 mass concentration. The proportion of DEHP increased while that of DMP decreased with the increase in PM2.5 pollution. Positive correlations between PAEs and PM2.5, organic carbon, and elemental carbon were observed, while PAEs had negative correlation with the ambient temperature. Our observation provides evidences on understanding the volatile and semi-volatile PAEs in the ambient aerosols.

Degradation of Dimethyl phthalate through Fe(II)/ Peroxymonosulfate heightened by fulvic acid: efficiency and possible mechanism

Ferrous iron (Fe(II)) reacts with peroxymonosulfate (PMS) to form active oxidants that can degrade refractory organic pollutants. However, the conversion rate of Fe(III) to Fe(II) is slow, which limits its actual application. In the study, the effect of fulvic acid (FA) on the degradation of dimethyl phthalate (DMP) by Fe(II)/PMS was investigated. Moreover, the degradation process of DMP was predicted by the preliminary identification of active free radicals and intermediates. As expected, FA gave rise to a higher concentration of Fe(II) than that in Fe(II)/PMS to enhance the removal of DMP in Fe(II)/PMS system. The precipitate, involved in FA and iron, was an important composite to promote the degradation of DMP in the system. Also, the response surface methodology (RSM) was applied to model and optimize the degradation conditions of DMP. The highest removal efficiency (85.70%) was obtained at pH = 3.86, [PMS] = 0.96 mM, [FA] = 11.44 mg/L and [DMP] = 5 μM. The results of free radical quenching experiments and EPR showed that ·OH and SO4 •- were the main active radicals in this system. The degradation intermediates of DMP were monomethyl phthalate (MMP), phthalic acid, and benzoic acid. Discoveries of this study had raised current understanding of the application of FA keeping the cycles of Fe(II)/Fe(III) for peroxymonosulfate activation, which could afford valuable information for the degradation of organic pollutants by FA/Fe(II)/PMS.

Facile synthesis of hierarchical ZnO structure for photocatalytic degradation of dimethyl phthalate

A facile co-precipitation method was employed to fabricate hierarchical ZnO structure and characterized by various analytical instruments. The images of ZnO from field-emission scanning electron microscopy exhibited spheroidal morphology which composed of numerous layers of nanosheets and formed a hierarchical structure. Energy dispersive X-ray spectrum validated the presence of Zn and O atoms and its purity. X-ray diffraction pattern of ZnO revealed the establishment of hexagonal wurtzite structure. Optical property analysis disclosed that the as-fabricated ZnO had strong absorbance of wavelength from 350-410 nm with an absorption band edge of 367 nm. In this paper, the photocatalytic activity of hierarchical ZnO structure was confirmed by degradation of endocrine disrupting chemical, namely dimethyl phthalate under UV lamp irradiation. The photodegradation of dimethyl phthalate in aqueous solution over as-fabricated ZnO reached 55.9% after 60 min irradiation. The photocatalytic degradation of DMP obeyed the pseudo first-order kinetic reaction with a rate constant of 0.0166 min−1.

Determination of Phthalate Esters in Beverages and Water Samples by Solid Phase Extraction with Resin Based COFs as Filler

Resin based covalent organic framework material was used as filler for solid phase extraction (SPE), and the solid phase extraction effect was compared with that of traditional COF material (TpBD COFs). The enrichment capacity of four phthalate esters (dimethyl phthalate, diethyl phthalate, dibutyl phthalate, dioctyl phthalate) in beverage samples was investigated by SPE. Adsorption experiments showed that the kinetic adsorption behavior of COF materials for phthalate esters (PAEs) was more consistent with the quasi-second-order kinetic adsorption model, and the static adsorption behavior is more in line with the Freundlich isothermal adsorption model. Solid phase extraction experiments proved that the SPE column prepared with two COF materials as adsorbents had good adsorption effects, high recovery (water: 97.99–100.56% and beverage: 97.93–100.23%) and were reusable (50 cycles), which could meet the requirements for trace detection of phthalate ester. It was found that the solid phase extraction effect was better than the four types of commercial SPE columns. The new COF material reduced the cost of monomer use and provided the possibility for its industrial production. Meanwhile, it also provided a new feasible scheme for enriching trace phthalate esters in practical samples.

In situ monitoring of phthalate esters (PAEs) pollution and environmental risk assessment in Poyang Lake Basin by DGT Technology using cyclodextrin polymer as binding phase

Poyang Lake is the first freshwater lake in China, which is an important drinking water source. In recent years, industrial pollution has led to the increased phthalate acid esters (PAEs) in Poyang Lake. PAEs are a class of typical endocrine disruptors that can accumulate in organisms and interfere with their secretion systems. Thus, the accurate determination of PAEs in Poyang Lake is important for health risk prediction and the development of corresponding control means. Monitoring organic pollutants in water using the diffusive gradient in thin films technique (DGT) has attracted much attention due to more accuracy and convenience than the traditional methods. This study used an inexpensive amphiphilic cyclodextrin polymer (PBCD) as the sorbent for the binding gel. This new binding gel has an ultra-high specific surface area and excellent adsorption performance. Diffusion coefficients of the five PAEs were determined, and the performance of DGT such as adsorption capacity and deployment time (1–4 days) was tested using five PAEs as models. The assembled PBCD-DGT was used to examine the performance in a complex simulated water environment. The sampling capability of PBCD-DGT was verified in Yangshan Lake, and a large-scale field application was conducted in Poyang Lake basin. The results of 11 sampling points showed that the concentration ranges of dimethyl phthalate, diethyl phthalate, diallyl phthalate, dipropyl phthalate, and dibutyl phthalate were 434–2594 ng/L, 40–314 ng/L, 80–527 ng/L, 45–308 ng/L, and ND-182 ng/L, respectively. The health risk index (HI) and ecological risk quotient (RQ) values of PAEs in the Poyang Lake watershed were far below 1, indictating a lower health and ecological risk. Considering that PAEs are bioaccumulative and persistent, it is very necessary to continue to pay attention to its pollution status and health and ecological risk changes in Poyang Lake Basin in the future.

Evaluation of the Removal of Selected Phthalic Acid Esters (PAEs) in Municipal Wastewater Treatment Plants Supported by Constructed Wetlands.

Phthalic acid esters (PAEs) have a negative impact on living organisms in the environment, therefore, are among the group of Endocrine Disrupting Compounds (ECDs). Unfortunately, conventional methods used in municipal wastewater treatment plants (MWWTPs) are not designed to eliminate PAEs. For this reason, the development of cheap and simple but very effective techniques for the removal of such residues from wastewater is crucial. The main aim of this study was the evaluation of the removal of six selected PAEs: diethyl phthalate (DEP), di-n-octyl phthalate (DOP), di-n-butyl phthalate (DBP), benzyl butyl phthalate (BBP), bis(2-ethylhexyl) phthalate (DEHP) and dimethyl phthalate (DMP), in real MWWTPs supported by constructed wetlands (MWWTP–CW system). For the first time, the possibility of using three new plants for this purpose, Cyperus papyrus (papyrus), Lysimachia nemorum (yellow pimpernel) and Euonymus europaeus (European spindle), has been presented. For determining the target PAEs in wastewater samples, a method of SPE (Solid-Phase Extraction)–GC–MS(SIM) was developed and validated, and for plant materials, a method of UAE (Ultrasound-Assisted Extraction)–SPE–GC–MS(SIM) was proposed. The obtained data showed that the application of the MWWTP–CW system allows a significant increase in the removal of DEP, DBP, BBP and DEHP from the wastewater stream. Euonymus europaeus was the most effective among the tested plant species for the uptake of analytes (8938 ng × g−1 dry weight), thus, this plant was found to be optimal for supporting conventional MWWTPs.

Food Processing and Phthalate Exposure: The Nutrition and Health Survey in Taiwan (1993-1996 and 2005-2008).

Background: Phthalates esters are widely used commercially and can leach from a food container or food packaging. Few studies have been conducted in Asia regarding food processed to varying levels and human phthalate exposure. This study aimed to evaluate the association between unprocessed and ultra-processed food intake and urinary phthalate metabolite levels in the Taiwanese adult population.Methods: A total of 516 participant data were extracted from the cross-sectional 1993–1996 and 2005–2008 Nutrition and Health Survey in Taiwan of those aged over 18 years, where urinary measures and one 24-h dietary recall were collected. Urinary concentrations of dimethyl phthalate, diethyl phthalate, dibutyl phthalate, butyl benzyl phthalate, and di-(2-ethylhexyl) phthalate metabolites including monomethyl phthalate, monoethyl phthalate (MEP), monobutyl phthalate (MBP), monobenzyl phthalate, mono-(2-ethylhexyl) phthalate, mono-(2-ethyl-5-hydroxyhexyl) phthalate, and mono-(2-ethyl-5-oxohexyl) phthalate were measured in spot urine samples. The NOVA food processing classification system was applied to divide all consumed foods into four mutually exclusive groups including unprocessed or minimally processed, processed culinary ingredients, processed and ultra-processed food. Generalized linear models were employed to examine the associations between the percentage quartiles (Qs) of unprocessed and ultra-processed foods in the total weight of food and the urinary phthalate metabolites.Results: Compared with participants in the lowest quartiles (Q1) of ultra-processed food intake, highest ultra-processed food intake (Q4) had 65.7% (95% confidence interval [CI]: 4.83, 162) higher urinary concentrations of MEP after adjusted for covariates. In contrast, the higher unprocessed food consumption was inversely associated with urinary concentrations of MEP and MBP (P for trend = 0.03). When compared to the lowest unprocessed food consumers (Q1), higher consumers (Q4) presented 38.6% (95% CI: −61.3, −2.59) lower MEP concentrations and 23.1% (95% CI: −38.5, −3.71) lower MBP concentrations.Conclusion: Ultra-processed food consumption was associated with increased concentrations of urinary MEP. Conversely, consuming unprocessed food was associated with lower concentrations of MEP and MBP in the Asian Taiwanese adult population.

Mass balance and kinetics of biodegradation of endocrine disrupting phthalates by Cellulosimicrobium funkei in a continuous stirred tank reactor system

This study investigated the potential ofCellulosimicrobium funkeifor degrading dimethyl phthalate (DMP) and diethyl phthalate (DEP). Effect of different initial concentrations of phthalates on their biodegradation and growth ofC. funkeiwas examined using shake flasks and a continuous stirred tank reactor (CSTR). Complete degradation of both DMP and DEP was achieved in CSTR, even up to 3000 and 2000 mg/L initial concentrations, respectively. Simultaneous degradation of the phthalates in mixture, i.e. more than 80% and 55% biodegradation efficiency were achieved at 1000 and 2000 mg/L initial concentrations of DMP and DEP, respectively, using the CSTR. Mass balance analysis of the degradation results suggested proficient degradation of DMP and DEP with biomass yield values of 0.64 and 0.712, respectively. The high values of inhibition constant Kiestimated using the Tessier and Edward substrate inhibition models indicated very good tolerance ofC. funkeitoward biodegradation of DMP and DEP.

Degradation of dibutyl phthalate by Paenarthrobacter sp. Shss isolated from Saravan landfill, Hyrcanian Forests, Iran

Phthalic acid esters are predominantly used as plasticizers and are industrially produced on the million ton scale per year. They exhibit endocrine-disrupting, carcinogenic, teratogenic, and mutagenic effects on wildlife and humans. For this reason, biodegradation, the major process of phthalic acid ester elimination from the environment, is of global importance. Here, we studied bacterial phthalic acid ester degradation at Saravan landfill in Hyrcanian Forests, Iran, an active disposal site with 800 tons of solid waste input per day. A di-n-butyl phthalate degrading enrichment culture was established from which Paenarthrobacter sp. strain Shss was isolated. This strain efficiently degraded 1 g L–1 di-n-butyl phthalate within 15 h with a doubling time of 5 h. In addition, dimethyl phthalate, diethyl phthalate, mono butyl phthalate, and phthalic acid where degraded to CO2, whereas diethyl hexyl phthalate did not serve as a substrate. During the biodegradation of di-n-butyl phthalate, mono-n-butyl phthalate was identified in culture supernatants by ultra-performance liquid chromatography coupled to electrospray ionization quadrupole time-of-flight mass spectrometry. In vitro assays identified two cellular esterase activities that converted di-n-butyl phthalate to mono-n-butyl phthalate, and the latter to phthalic acid, respectively. Our findings identified Paenarthrobacter sp. Shss amongst the most efficient phthalic acid esters degrading bacteria known, that possibly plays an important role in di-n-butyl phthalate elimination at a highly phthalic acid esters contaminated landfill.

An insightful analysis of dimethyl phthalate degradation by the collaborative process of DBD plasma and Graphene-WO3 nanocomposites

In this paper, the prepared graphene-WO3 nanocomposites (rGO-WO3) were added into a dielectric barrier discharge (DBD) plasma system with spiral discharge electrode to set up a collaborative process to treat the dimethyl phthalate (DMP) in water. Degradation of the DMP under different experimental conditions were studied to illustrate the catalysis of the rGO-WO3 in the DBD plasma system. The obtained results proved that there was the catalysis of the rGO-WO3 for the DMP degradation within the studied DMP concentration, solution initial pH values and conductivities. From the results of the energy utilization efficiency (G50) analysis, the catalysis was more apparent in the case of the oxygen bubbling system than that in the nitrogen or the air bubbling system, which was due to the higher oxygen constitution in the oxygen bubbling system. The reduction of the measured liquid phase ozone concentrations in the DBD/rGO-WO3 system bubbled with air as well as oxygen than those measured in the sole DBD system, which verified the consumption of the ozone by the catalysis of the rGO-WO3. Furthermore, the UV–Vis and the three-dimensional fluorescence spectra analysis were also carried out to state the catalytic effect of the rGO-WO3 for the DMP degradation. Toxicity analysis for the degradation byproducts confirmed the collaborative process could reduce the negative effect of the original DMP on the environment.

Exploring personal chemical exposures in China with wearable air pollutant monitors: A repeated-measure study in healthy older adults in Jinan, China.

The health impact of airborne contaminants has been challenging to assess due to current limitations in measurement technologies. The emergence of wearable passive samplers coupled with high resolution mass spectrometry (HR-MS) chemical analysis has enabled comprehensive characterization of personal exposures. We conducted a repeated-measure study among 84 older adults in Jinan, China, as part of the Biomarkers for Air Pollutants Exposure (China BAPE) study. Study objectives were: 1) to characterize the occurrence, magnitude, and distribution of personal exposure to airborne contaminants; 2) to evaluate the temporal variation of chemical exposures across the study population; and 3) to identify behavioral and environmental factors that influence the observed variance in chemical exposures. The FreshAir wristband was worn by participants for three consecutive days each month from September 2018 to January 2019 and collected with paired time-activity logs. Passive air samplers were also deployed in parallel at a local outdoor air monitoring station. Spearman's Rho trend test and trajectory cluster analysis were used to identify exposure trends and variation patterns, respectively. Out of the 70 airborne compounds of potential concern screened, 26 compounds from 10 chemical classes were found to be above detection thresholds across >70% of the study population. Personal exposures were predominantly characterized by nine polycyclic aromatic hydrocarbons (PAHs), four phthalates, three nitroaromatics, and two volatile organic compounds (VOCs). Phthalate personal exposures were positively correlated with outdoor temperatures while the inverse relationship was observed for certain PAHs (p<0.05). Specifically, dimethyl phthalate (rs=0.31) decreased as temperatures declined, while nitrobenzene (rs=-0.35) and naphthalene (rs=-0.40) increased as temperatures decreased. Compared to levels measured at the outdoor air monitoring site, personal exposure of phthalates was elevated (p<0.05) and hexachlorobutadiene was lower across participants (p<0.01). Personal exposure of these chemicals was further found to be weakly associated with daily duration participants spent outdoors. Individuals formed distinct clusters based on trajectories of chemical exposures across the sampling period (September to January), potentially suggestive of distinct emission sources. In conclusion, we demonstrate the feasibility of characterizing the occurrence and magnitude of personal exposure to airborne chemical contaminants using passive wristband samplers. The temporal variability of these personal exposure profiles was highlighted and with distinct trends identified across different groups of individuals. Future studies will integrate this data with other omics datasets collected from this population of Chinese older adults to investigate associations between exposure profiles and health relevant biomarkers, to provide evidence in feasibility of disease prevention through environmental improvements.

DNA oxidative damage in pregnant women upon exposure to conventional and alternative phthalates.

Exposure to alternative phthalates and related health effects in pregnant women are rarely reported. Nineteen phthalate metabolites and a DNA oxidative damage biomarker 8-hydroxy-2'-deoxyguanosine (8-OHdG) were determined in urine samples of pregnant women recruited in South China. The detection frequencies and concentration of selected alternative phthalates, i.e., diisononyl phthalate (DiNP), diisodecyl phthalate (DiDP) and di-(2-propylheptyl) phthalate (DPHP) were lower than those of conventional phthalates. However, mono-(6-hydroxy-2-propylheptyl) phthalate, a metabolite of DPHP, was detected in 70% of urine samples (median: 0.13ng/mL). The estimated daily intakes of conventional plasticizers, including dimethyl phthalate, di-n-butyl phthalate, diisobutyl phthalate and di-(2-ethylhexyl) phthalate (median range: 1.0-3.0μg/kg_bw/day) were significantly higher than those of DiNP (0.08μg/kg_bw/day) and DPHP (0.03μg/kg_bw/day) (p<0.05). Approximately 24% of pregnant women were at high risk when cumulative risk from exposure to several phthalates was considered. The concentrations of phthalate metabolites and urinary 8-OHdG were significantly correlated with each other (r=0.206-0.772, p<0.01), which were further conformed by multiple linear regression analysis (β=0.168-0.639, p<0.01). In addition, conventional phthalates were more strongly correlated with 8-OHdG than alternative phthalates (i.e., DiNP, DPHP), partly suggesting the relatively smaller health effects of alternatives due to their low exposure doses and toxicities. These findings suggested that alternative phthalates have entered the human body from consumer products in the study area, and exposure-related risk of DNA oxidative stress was comparatively lower.

Association of endocrine disrupting chemicals levels in serum, environmental risk factors, and hepatic function among 5- to 14-year-old children

Endocrine-disrupting chemicals (EDCs) might increase the risk of childhood diseases by disrupting hormone-mediated processes that are critical for growth and development during childhood, however, the association among the exposure level of EDCs such as Nonylphenol (NP), Bisphenol A (BPA), Dimethyl phthalate (DMP) in children and environmental risk factors, as well as hepatic function has not been elaborated. This study aimed to discuss this interesting relationship among NP, BPA, DMP concentrations in serum, environmental risk factors, hepatic function of 5- to 14-year-old children in industrial zone, residential zone and suburb in northern district of Guizhou Province, China. In Zunyi city, 1006 children participated in cross-sectional health assessments from July to August 2018, and their parents completed identical questionnaires on the environmental risk factors of EDCs exposure to mothers and children. Serum NP, BPA and DMP concentrations were measured by high performance liquid chromatography (HPLC). Serum alanine aminotransferase (ALT), aspartate aminotransferase (AST), AST/ALT, total bilirubin (TBIL), direct bilirubin (DBIL) and indirect bilirubin (IBIL) were detected with automatic biochemical analyzer. The median concentrations of serum NP, BPA, and DMP in the participants were 45.85 ng/mL, 26.31 ng/mL and 31.62 ng/mL, respectively, which were higher than the environmental concentration limits of the U.S. National Environmental Protection Agency (EPA). Hair gels used during pregnancy, types of domestic drinking water, nail polish and cosmetics used by children were significantly positive correlated with serum NP concentration (P < 0.05). Gender, feeding pattern, plastic water cup used during pregnancy, hair spray and perfume use for children, duration of children birth, materials for baby bottle or cup and ways to plastic products were significantly positively correlated with serum BPA concentration (P < 0.05). Gender, perms used during pregnancy, hair spray and perfume use for children, using plastic lunch box during pregnancy, duration of children birth, exposure to pesticides, parents’ occupations were significantly positively correlated with serum DMP concentrations (P < 0.05). Serum NP (β = 0.296, P = 0.036) and DMP (β = 0.316, P = 0.026) concentrations and TBIL level were significantly positively correlated. Serum NP concentration and the levels of IBIL (β = 0.382, P = 0.006) are significantly positively correlated. Cosmetics used during pregnancy significantly increased AST level (β = 2.641, P = 0.021). There was a positive correlation between the frequency of hair spray and perfume use for children and the AST (β = 4.241, P = 0.022). NP, BPA and DMP, which were commonly detected in the serum of children aged 5−14 years old in Zunyi City, Northern Guizhou Province, China, were closely related to the environmental risk factors of exposure environment during pregnancy, infancy and school age. Exposure to NP, BPA and DMP would have negative effects on hepatic function, and these effects showed differences in gender and geographical location. Notably,The relationships were more evident in girls than in boys.