Lower Chlorinated Polychlorinated Biphenyls Research Articles

Levels of polychlorinated biphenyls in settled house dust from urban dwellings in China and their neurodevelopmental effects on preschool-aged children

We investigated the levels of polychlorinated biphenyls (PCBs) in settled house dust (SHD) from urban dwellings with resident preschool-aged children in Nanjing, China. The possible neurodevelopmental effects of house-dust PCBs were also explored. SHD was collected from 114 urban houses. The levels of 39 PCB congeners were measured by gas chromatography–tandem mass spectrometry. The Child Behavior Checklist and the Gesell Development Inventory were used to evaluate the child's development. All 39 target congeners measured were detected. The mass percentage of di-PCBs was the highest at 47.8%, followed by tetra- and tri-PCBs at 16.8% and 13.0%, respectively. Spearman's rho correlation showed that di-, tri-, hexa-, hepta-, nona- and total PCBs were positively associated with somatic, thought problem and total problem scores (0.24<r<0.36). After dichotomization at the 75th percentile PCB concentration, we found that the higher PCB3, 6, 12, 25, 44, 71, 174 and 203 might increase the risk of certain behavior problems. Moreover, among the lower-chlorinated PCBs, PCB3 and PCB4 showed some risk of adaptive and gross motor abnormality, respectively. In conclusion, PCBs (especially lower-chlorinated PCBs) are ubiquitous in urban SHD in Nanjing and may carry a risk of certain developmental abnormalities. The potential adverse effects of postnatal exposure to PCBs on the behavior and neurodevelopment of preschool-aged children need to be studied in larger follow-up studies.

Atmospheric concentration characteristics and gas/particle partitioning of PCBs from the North Pacific to the Arctic Ocean

Polychlorinated biphenyls (PCBs) were measured in atmospheric samples collected from the North Pacific to the Arctic Ocean between July and September 2012 to study the atmospheric concentration characteristics of PCBs and their gas/particle partitioning. The mean concentration of 26 PCBs (vapor plus particulate phase) (ΣPCBs) was 19.116 pg/m3 with a standard deviation of 13.833 pg/m3. Three most abundant congeners were CB-28, −52 and −77, accounting for 43.0% to ΣPCBs. The predominance of vapor PCBs (79.0% to ΣPCBs) in the atmosphere was observed. ΣPCBs were negative correlated with the latitudes and inverse of the absolute temperature (1/T). The significant correlation for most congeners was also observed between the logarithm of gas/particle partition coefficient (logKP) and 1/T. Shallower slopes (from −0.15 to −0.46, average −0.27) were measured from the regression of the logarithm of sub-cooled liquid vapor pressures (logpL○) and logKP for all samples. The difference of the slopes and intercepts among samples was insignificant (p>0.1), implying adsorption and/or absorption processes and the aerosol composition did not differ significantly among different samples. By comparing three models, the J-P adsorption model, the octanol/air partition coefficient (KOA) based model and the soot-air model, the gas/particle partitioning of PCBs in the Arctic atmosphere was simulated more precisely by the soot-air model, and the adsorption onto elemental carbon is more sensitive than the absorption into organic matters of aerosols, especially for low-chlorinated PCB congeners.

Historical sediment record and distribution of polychlorinated biphenyls (PCBs) in sediments from tidal flats of Haizhou Bay, China

The spatial and temporal variations and sources of polychlorinated biphenyls (PCBs) in sediment of tidal flat from Haizhou Bay, China were investigated. PCBs concentrations in surface sediments ranged from 1.33 to 6.27ngg−1 dry weight. Low-chlorinated PCBs, dominated by the tri-PCB homologs, were identified as the prevalent contaminate of surface sediments. These results were in agreement with the fact that tri-PCB homologs are the dominant contaminants in China. In surface sediment, the highest level appeared in the estuary, and it decreased with distance from the Linhong River estuary. PCBs concentrations started to rise from the mid-1950s, and reached a maximum in 2005. PCBs in sediment might originate from surface runoff and discharges of local source as well as slight atmospheric deposition, based on PCA. Additionally, the PCBs levels in the sediments were considered to rarely pose hazard to the aquatic and human health, based on Sediment Quality Guidelines (SQGs).

Polychlorinated biphenyl congener distributions in burbot: evidence for a latitude effect.

The authors compared the distributions of the congeners of polychlorinated biphenyls (PCBs) detected in whole-body samples of burbot (Lota lota) from Great Slave Lake and Lake Erie. Total PCB concentrations in Great Slave Lake burbot were about one-sixtieth of the concentrations in Lake Erie burbot. Burbot from Great Slave Lake contained a higher proportion of lower-chlorinated (2-6 chlorines) congeners than did burbot from Lake Erie; the reverse occurred for more highly chlorinated (7-9 chlorines) congeners. Hexachloro congeners, followed by pentachloro congeners, dominated the proportions of total PCBs in burbot from both lakes. There were no differences between sexes in whole-body samples or between gonad and somatic tissues in the proportions of the 39 congeners and 3 sets of coeluters detected in burbot from Great Slave Lake. In contrast, there were distinct sex differences in congener distributions for older burbot from Lake Erie. The results generally supported a prediction of higher proportions of lower-chlorinated PCB homologs in organisms in remote polar areas. However, the latitudinal effect on PCB congener distribution may be more complex than that portrayed in previous studies.

Diurnal Variability of Persistent Organic Pollutants in the Atmosphere over the Remote Southern Atlantic Ocean

A diel (24-h) cycle with daytime atmospheric concentrations higher than nighttime concentrations by a factor of 1.5–3 was observed for several low molecular weight polychlorinated biphenyls (PCBs) and polycyclic aromatic hydrocarbons (PAHs) in remote areas of the tropical South Atlantic during a cruise in October–November 2005. In contrast, high molecular weight PCBs and PAHs did not display diurnal variability. A model which has successfully explained diel variability of persistent organic pollutants (POPs) over land could not reproduce the observed diel cycle by considering variability in temperature, atmospheric OH radical concentrations, atmospheric boundary layer height and wind speed as causal factors. We used the model to conduct two bounding scenarios to explore the possibility that phytoplankton biomass turn-over in the surface ocean drives the observed variability in air concentrations. The model could only qualitatively reproduce the field observations of diel variability for low chlorinated PCB congeners when the ocean acts as a source of pollutants to the atmosphere, and when variability in biomass drives variability in the capacity of the surface ocean.

Polychlorinated biphenyls in glaciers. 2. Model results of deposition and incorporation processes.

In previous work, Alpine glaciers have been identified as a secondary source of persistent organic pollutants (POPs). However, detailed understanding of the processes organic chemicals undergo in a glacial system was missing. Here, we present results from a chemical fate model describing deposition and incorporation of polychlorinated biphenyls (PCBs) into an Alpine glacier (Fiescherhorn, Switzerland) and an Arctic glacier (Lomonosovfonna, Norway). To understand PCB fate and dynamics, we investigate the interaction of deposition, sorption to ice and particles in the atmosphere and within the glacier, revolatilization, diffusion and degradation, and discuss the effects of these processes on the fate of individual PCB congeners. The model is able to reproduce measured absolute concentrations in the two glaciers for most PCB congeners. While the model generally predicts concentration profiles peaking in the 1970s, in the measurements, this behavior can only be seen for higher-chlorinated PCB congeners on Fiescherhorn glacier. We suspect seasonal melt processes are disturbing the concentration profiles of the lower-chlorinated PCB congeners. While a lower-chlorinated PCB congener is mainly deposited by dry deposition and almost completely revolatilized after deposition, a higher-chlorinated PCB congener is predominantly transferred to the glacier surface by wet deposition and then is incorporated into the glacier ice. The incorporated amounts of PCBs are higher on the Alpine glacier than on the Arctic glacier due to the higher precipitation rate and aerosol particle concentration on the former. Future studies should include the effects of seasonal melt processes, calculate the quantities of PCBs incorporated into the entire glacier surface, and estimate the quantity of chemicals released from glaciers to determine the importance of glaciers as a secondary source of organic chemicals to remote aquatic ecosystems.

Study of penetration behavior of PCB-DNAPL in a sand layer by a column experiment

To better understand the infiltration performances of high concentration PCB oils (KC-300 and KC-1000 polychlorinated biphenyl (PCB) mixtures), representative dense non-aqueous phase liquid (DNAPL), under both saturated and unsaturated conditions, we conducted experiments on a sand column filled with Toyoura Standard Sand. When PCB oil with the volume comparable to the total porosity in the column was supplied, the residual PCB concentrations under PCB–water conditions were 4.9×104mgkg−1 in KC-300 and 3.9×104mgkg−1 in KC-1000. Under PCB–air conditions, residual PCB concentrations were 6.0×104mgkg−1 and 2.4×105mgkg−1 in the upper and lower parts for KC-300 and 3.6×104mgkg−1 and 1.5×105mgkg−1 in those for KC-1000, respectively, while the rest of the PCBs were infiltrated. On the other hand, when a small amount of PCB oil with the volume far smaller than the total porosity in the column was supplied, the original PCBs were not transported via water permeation. However, lower-chlorinated PCB congeners—e.g., di- or tri-chlorinated biphenyls—preferentially dissolved and were infiltrated from the bottom of the column. These propensities on PCB oil infiltration can be explained in conjunction with the degree of PCB saturation in the sand column.

Distribution and risk assessment of polychlorinated biphenyls (PCBs) in the remote air and soil of Manipur, India

∑25PCB congeners including dioxin-like compounds were analyzed at three sites of Manipur India to assess the level of polychlorinated biphenyls (PCBs) in air and soil. The ∑25PCBs were higher in urban air (average 2,454 pg/m3), followed by the mountain air (average 2,109 pg/m3) and rural air (average 1,756 pg/m3). PCB levels observed in urban air were higher compared to PCB levels reported in major Indian metropolitan cities especially along the coastal region and were comparable with the pristine sites of India and also with some pockets of China and Europe. The heavier congeners (tetra, penta, tri and hexa) were dominant in both air and soil samples and show significant correlation with the ambient temperature. Emission of PCB congeners was investigated from soil surface. The total organic carbon present in soil shows the significant correlation (r 2 = 0.8; p < 0.05) with the PCBs could indicate that the PCBs originated from the similar sources. Principal component analysis revealed that the sources of higher chlorinated PCB congeners are local emissions while long-range atmospheric transport process is responsible behind elevated levels of lower chlorinated PCBs. Total calculated toxic equivalent (TEQ) levels in soil (37.17–160.5 pg/g) were superior to reported TEQ level of agricultural soil in Delhi, India (0.01–105.40 pg/g). Back trajectory analysis showed that the observed high levels of PCB at Manipur may due to movement of air masses, mostly from the Northern and Southern India and to some extent from Myanmar.

Effects of age, adipose percent, and reproduction on PCB concentrations and profiles in an extreme fasting North Pacific marine mammal.

Persistent organic pollutants, including polychlorinated biphenyls (PCBs), are widely distributed and detectable far from anthropogenic sources. Northern elephant seals (Mirounga angustirostris) biannually travel thousands of kilometers to forage in coastal and open-ocean regions of the northeast Pacific Ocean and then return to land where they fast while breeding and molting. Our study examined potential effects of age, adipose percent, and the difference between the breeding and molting fasts on PCB concentrations and congener profiles in blubber and serum of northern elephant seal females. Between 2005 and 2007, we sampled blubber and blood from 58 seals before and after a foraging trip, which were then analyzed for PCBs. Age did not significantly affect total PCB concentrations; however, the proportion of PCB congeners with different numbers of chlorine atoms was significantly affected by age, especially in the outer blubber. Younger adult females had a significantly greater proportion of low-chlorinated PCBs (tri-, tetra-, and penta-CBs) than older females, with the opposite trend observed for hepta-CBs, indicating that an age-associated process such as parity (birth) may significantly affect congener profiles. The percent of adipose tissue had a significant relationship with inner blubber PCB concentrations, with the highest mean concentrations observed at the end of the molting fast. These results highlight the importance of sampling across the entire blubber layer when assessing contaminant levels in phocid seals and taking into account the adipose stores and reproductive status of an animal when conducting contaminant research.

Serum concentrations of polychlorinated biphenyls (PCBs) in participants of the Anniston Community Health Survey

Serum concentrations of 35 ortho-substituted polychlorinated biphenyl congeners (PCBs) were measured in 765 adults from Anniston, Alabama, where PCBs were manufactured between 1929 and 1971. As part of the Anniston Community Health Survey (ACHS), demographic data, questionnaire information, and blood samples were collected from participants in 2005–2007. Forty-six percent of study participants were African-American, 70% were female, and the median age was 56years. The median concentration of the sum of 35 PCB congeners (ΣPCBs) was 528ng/g lipid, with a 90th percentile of 2600ng/g lipid, minimum of 17.0ng/g lipid, and maximum of 27,337ng/g lipid. The least square geometric mean ΣPCBs was more than 2.5 times higher for African-American participants than for White participants (866ng/g lipid vs. 331ng/g lipid); this difference did not change materially after adjustment for age, sex, body mass index (BMI) and current smoking. In spite of large differences in absolute PCB levels, relative contributions of individual congeners to ΣPCBs were quite similar between race groups. Nevertheless, while percent contributions to ΣPCBs for most of the most abundant penta- to heptachlorobiphenyls were higher among African-Americans, the percentages were higher in Whites for the lower-chlorinated PCBs 28 and 74 and for octa- to decachlorinated PCBs. No major differences were observed in geometric mean ΣPCBs between women and men when adjusted for age, race, BMI and current smoking (516ng/g lipid vs. 526ng/g lipid). Principal component analysis revealed groups of co-varying congeners that appear to be determined by chlorine substitution patterns. These congener groupings were similar between ACHS participants and the National Health and Nutrition Examination Survey (NHANES) 2003–04 sample of the general United States population, despite ACHS participants having serum concentrations of ΣPCBs two to three times higher than those in comparable age and race groups from NHANES.

Levels of persistent organic pollutants in eastern North Atlantic humpback whales

Blubber lipid concentrations of 14 organochlorine compounds and 10 polychlorinated biphenyls (PCB) were measured by gas chromatography with electron-capture detection in eastern North Atlantic humpback whales Megaptera novaeangliae from Cape Verde (n = 20) and Ireland (n = 4). Concentrations were statistically compared to those from 20 samples collected from the Gulf of Maine in the western North Atlantic. Pollutant burdens were compared using males only, in order to circum- vent biases associated with reproductive offloading. Lipid-normalised PCB concentrations were below the estimated threshold toxicity value of 17 000 ng g �1 for blubber in marine mammals. Dichlorodiphenyltrichloroethane (DDT), PCB and chlordane concentrations were an order of mag - nitude lower than those previously reported for Gulf of Maine humpback whales and higher than those reported from the North Pacific Ocean. Higher concentrations of lower-chlorinated PCB con- geners (28, 31 and 52), hexachlorocyclohexanes and hexachlorobenzene in males in eastern North At- lantic sites is consistent with higher latitude feeding grounds. Lower p,p'-DDE (dich loro di phe nyl - dichloroethane):ΣDDT ratios suggest that whales from the eastern North Atlantic harbour more recent inputs of DDT. The ΣDDTs:ΣPCBs ratio was higher for males from Cape Verde (1.69) and Ireland (1.44), indicating proportionately greater sources of agricultural rather than industrial sources of pol- lutants than for the Gulf of Maine whales (0.75). We demonstrate potential for persistent organochlo- rine pollutants (POPs) as tracers to determine foraging ground provenance for samples collected on breeding grounds in the North Atlantic. Low concentrations suggest that POPs are unlikely to be a factor in the poor recovery rate of humpback whales in Cape Verde.

The fate of inhaled 14C-labeled PCB11 and its metabolites in vivo

BackgroundThe production ban of polychlorinated biphenyl (PCB) technical mixtures has left the erroneous impression that PCBs exist only as legacy pollutants. Some lower-chlorinated PCBs are still being produced and contaminate both indoor and ambient air. ObjectivesTo inform PCB risk assessment, we characterized lung uptake, distribution, metabolism and excretion of PCB11 as a signature compound for these airborne non-legacy PCBs. MethodsAfter delivering [14C]PCB11 to the lungs of male rats, radioactivity in 34 major tissues and 5 digestive matter compartments was measured at 12, 25, 50, 100, 200 and 720min postexposure, during which time the excreta and exhaled air were also collected. [14C]PCB11 and metabolites in lung, liver, blood, digestive matter, urine, feces, and adipose tissues were extracted separately to establish the metabolic profile of the disposition. Results[14C]PCB11 was distributed rapidly to all tissues after 99.8% pulmonary uptake and quickly underwent extensive metabolism. The major tissue deposition of [14C]PCB11 and metabolites translocated from liver, blood and muscle to skin and adipose tissue 200min postexposure, while over 50% of administered dose was discharged via urine and feces within 12h. Elimination of the [14C]PCB11 and metabolites consisted of an initial fast phase (t½=9–33min) and a slower clearance phase to low concentrations. Phase II metabolites dominated in liver blood and excreta after 25min postexposure. ConclusionsThis study shows that PCB11 is completely absorbed after inhalation exposure and is rapidly eliminated from most tissues. Phase II metabolites dominated with a slower elimination rate than the PCB11 or phase I metabolites and thus can best serve as urine biomarkers of exposure.

The Effect of Polychlorinated Biphenyls on the Song of Two Passerine Species

Polychlorinated biphenyls (PCBs) are synthetic chemical pollutants with demonstrated detrimental toxic and developmental effects on humans and wildlife. Laboratory studies suggest that PCBs influence behavior due to their effects on endocrine and neurological systems, yet little is known about the behavioral consequences of sublethal PCB exposure in the field. Additionally, specific PCB congener data (in contrast to total PCB load) is necessary to understand the possible effects of PCBs in living organisms since number and position of chlorine substitution in a PCB molecule dictates the toxicity and chemical fate of individual PCB congeners. We non-lethally investigated total PCB loads, congener specific PCB profiles, and songs of black-capped chickadees (Poecile atricapillus) and song sparrows (Melospiza melodia) along a historical PCB gradient at the Hudson River in New York State. Our results indicate that black-capped chickadees and song sparrows have higher total blood PCBs in regions with higher historic PCB contamination. The two bird species varied substantially in their congener-specific PCB profiles; within sites, song sparrows showed a significantly higher proportion of lower chlorinated PCBs, while black-capped chickadees had higher proportions of highly chlorinated PCBs. In areas of PCB pollution, the species-specific identity signal in black-capped chickadee song varied significantly, while variation in song sparrow trill performance was best predicted by the mono-ortho PCB load. Thus, PCBs may affect song production, an important component of communication in birds. In conclusion, we suggest that the ramifications of changes in song quality for bird populations may extend the toxic effects of environmental PCB pollution.

Polychlorinated biphenyls in surface soil in urban and background areas of Mongolia

Polychlorinated biphenyls (PCBs) were measured in soil in some industrial towns (Ulaanbaatar, Suhbaatar, Erdenet, Darhan, Tsetserleg, Hovd, Ulaangom, Altay, Bayanhongor, Arvayheer, Saynshand, Choybalsan) and in background and rural areas of Mongolia. The average sum of all investigated PCB congeners in soil of Mongolia comes to 7.4 ng/g dry weight (DW) and varies from 0.53 ng/g DW till 114 ng/g DW. PCB levels in soil from towns are significantly higher than those in soil from background and rural areas. The PCB homological composition in soil sampled in highly-PCB-polluted sites is similar to the PCB homological pattern in Sovol and Aroclor 1254. Significant correlation between soil organic carbon and low chlorinated PCB both for towns and background sites was found. Significant differences in PCB means in soil in different natural zones were found.

대기 중 PCBs의 PAS에 이용되는 여러 매체의 PCBs 침착 특성

Objective: This study was carried out to determine the depositional characteristics of pine needles, pine tree bark, moss, and soil, which are used as a passive air sampler (PAS) of atmospheric polychlorinated biphenyls (PCBs). Methods: All four media were sampled from the same site. PCB concentrations were analyzed by GC/MSD, and the lipid contents were measured using the gravimetric method. Results: The total PCB concentration (IUPAC No. 28, 52, 101, 138, 153, 180) was the highest in soil (227.97 pg/g dry), followed by pine needles (71.36 pg/g dry), pine tree bark (44.58 pg/g dry), then moss (21.91 pg/g dry). Pine needles contained the highest lipid contents (21.31 mg/g dry), whereas soil (10.01 mg/g dry), pine tree bark (4.85 mg/g dry), and moss (1.92 mg/g dry) contained less. The concentration of lower-chlorinated PCBs was relatively high in pine needles, pine tree bark and moss, but not in soil. The PCB concentrations were proportional to their lipid contents in pine needles, pine tree bark and moss, but a different trend was revealed in soil. Conclusions: The PCBs concentrations in the media were affected by various factors including atmospheric PCB concentrations, lipid contents, and depositional pathways. However, each of these factors had a varying influence depending on the type of medium.

소나무잎을 PAS로 이용하여 지역별 대기 중 PCBs 농도 추정

Objective: This study was carried out in order to estimate atmospheric Polychlorinated Biphenyls (PCBs) concentrations using pine needles as a passive air sampler (PAS) in urban, semi-rural and rural regions. Methods: One-year old pine needles were collected to analyze their PCBs concentrations (Cp, pg/g dry) at the end of December. PCBs concentrations in ambient air (Ca, pg/m 3 ) were calculated with the logKoa-log(Cp/Ca) model. Results: PCBs concentrations in ambient air (Ca) were high in the order of urban, semi-rural and rural regions. The lower-chlorinated PCBs showed a higher concentration in ambient air. However, the distribution of PCBs congeners was similar in all three regions. Correlation between Ca and the population density of the three regions was significant (R 2 =0.9834, p<0.001). Conclusions: It was concluded that although the production and use of PCBs was banned in the1970s, PCBs are currently being produced unintentionally by human activities.

Sulfated Metabolites of Polychlorinated Biphenyls Are High-Affinity Ligands for the Thyroid Hormone Transport Protein Transthyretin

Background: The displacement of l-thyroxine (T4) from binding sites on transthyretin (TTR) is considered a significant contributing mechanism in polychlorinated biphenyl (PCB)-induced thyroid disruption. Previous research has discovered hydroxylated PCB metabolites (OH-PCBs) as high-affinity ligands for TTR, but the binding potential of conjugated PCB metabolites such as PCB sulfates has not been explored.Objectives: We evaluated the binding of five lower-chlorinated PCB sulfates to human TTR and compared their binding characteristics to those determined for their OH-PCB precursors and for T4.Methods: We used fluorescence probe displacement studies and molecular docking simulations to characterize the binding of PCB sulfates to TTR. The stability of PCB sulfates and the reversibility of these interactions were characterized by HPLC analysis of PCB sulfates after their binding to TTR. The ability of OH-PCBs to serve as substrates for human cytosolic sulfotransferase 1A1 (hSULT1A1) was assessed by OH-PCB–dependent formation of adenosine-3´,5´-diphosphate, an end product of the sulfation reaction.Results: All five PCB sulfates were able to bind to the high-affinity binding site of TTR with equilibrium dissociation constants (Kd values) in the low nanomolar range (4.8–16.8 nM), similar to that observed for T4 (4.7 nM). Docking simulations provided corroborating evidence for these binding interactions and indicated multiple high-affinity modes of binding. All OH-PCB precursors for these sulfates were found to be substrates for hSULT1A1.Conclusions: Our findings show that PCB sulfates are high-affinity ligands for human TTR and therefore indicate, for the first time, a potential relevance for these metabolites in PCB-induced thyroid disruption.

PCB 77 dechlorination products modulate pro-inflammatory events in vascular endothelial cells

Persistent organic pollutants such as polychlorinated biphenyls (PCBs) are associated with detrimental health outcomes including cardiovascular diseases. Remediation of these compounds is a critical component of environmental policy. Although remediation efforts aim to completely remove toxicants, little is known about the effects of potential remediation byproducts. We previously published that Fe/Pd nanoparticles effectively dechlorinate PCB 77 to biphenyl, thus eliminating PCB-induced endothelial dysfunction using primary vascular endothelial cells. Herein, we analyzed the toxic effects of PCB congener mixtures (representative mixtures of commercial PCBs based on previous dechlorination data) produced at multiple time points during the dechlorination of PCB 77 to biphenyl. Compared with pure PCB 77, exposing endothelial cells to lower chlorinated PCB byproducts led to improved cellular viability, decreased superoxide production, and decreased nuclear factor kappa B activation based on duration of remediation. Presence of the parent compound, PCB 77, led to significant increases in mRNA and protein inflammatory marker expression. These data implicate that PCB dechlorination reduces biological toxicity to vascular endothelial cells.

Plasma polychlorinated biphenyls in residents of 91 PCB-contaminated and 108 non-contaminated dwellings—An exposure study

In the1950s-1970s polychlorinated biphenyls (PCBs) were used in several countries as plasticizers in elastic sealants in buildings. The primary objective was to study whether residents of PCB-contaminated dwellings had higher plasma levels of PCBs than their neighbours in non-contaminated dwellings. The secondary objective was to study possible associations between concentrations of PCBs in the indoor air and in the plasma of residents. Stratified cross-sectional study of residents of a housing estate with four sections, of which only one section had PCB-containing sealants. The determination of 27 PCB congeners in plasma was performed among 134 exposed and 139 non-exposed residents. Air measurements were conducted in 104 flats. Significant differences in plasma PCBs between exposed versus non-exposed were found for most of the lower chlorinated and many of the higher chlorinated congeners. The median of sum of 27 PCBs was approximately four times higher in exposed compared with non-exposed residents. The elevated PCB concentrations persisted in multivariable analyses controlling for relevant cofactors. We found significant correlations between PCB indoor air concentrations and the PCB concentration in the plasma of the residents for ten of the lower chlorinated congeners. Our study confirms that indoor air exposure to PCBs from PCB containing sealants may result in a considerable internal PCBs exposure of the residents. For the first time we were able to demonstrate that the internal exposure to low chlorinated PCBs is significantly associated with the indoor air concentration of these congeners.

Contamination of indoor dust and air by polychlorinated biphenyls and brominated flame retardants and relevance of non-dietary exposure in Vietnamese informal e-waste recycling sites

This study investigated the occurrence of polychlorinated biphenyls (PCBs), and several additive brominated flame retardants (BFRs) in indoor dust and air from two Vietnamese informal e-waste recycling sites (EWRSs) and an urban site in order to assess the relevance of these media for human exposure. The levels of polybrominated diphenyl ethers (PBDEs), hexabromocyclododecane (HBCD), 1,2-bis-(2,4,6-tribromophenoxy)ethane (BTBPE) and decabromodiphenyl ethane (DBDPE) in settled house dust from the EWRSs (130–12,000, 5.4–400, 5.2–620 and 31–1400ngg−1, respectively) were significantly higher than in urban house dust but the levels of PCBs (4.8–320ngg−1) were not higher. The levels of PCBs and PBDEs in air at e-waste recycling houses (1000–1800 and 620–720pgm−3, respectively), determined using passive sampling, were also higher compared with non-e-waste houses. The composition of BFRs in EWRS samples suggests the influence from high-temperature processes and occurrence of waste materials containing older BFR formulations. Results of daily intake estimation for e-waste recycling workers are in good agreement with the accumulation patterns previously observed in human milk and indicate that dust ingestion contributes a large portion of the PBDE intake (60%–88%), and air inhalation to the low-chlorinated PCB intake (>80% for triCBs) due to their high levels in dust and air, respectively. Further investigation of both indoor dust and air as the exposure media for other e-waste recycling-related contaminants and assessment of health risk associated with exposure to these contaminant mixtures is necessary.