Organophosphorus flame retardants in house dust from the Philippines: occurrence and assessment of human exposure

The use of organophosphorus flame retardants (PFRs) as flame retardants and plasticizers has increased due to the ban on common polybrominated diphenyl ether mixtures. However, only limited information on PFR contamination is available so far from Southeast Asia. In the present study, residual levels of PFRs in house dust and exposure through dust ingestion were investigated in the Philippines. House dust samples (n?=?37) were collected from Malate (residential area) and Payatas (municipal dumping area) in the Philippines and analyzed using ultra-high-performance liquid chromatography coupled with tandem mass spectrometry. Among the targeted seven PFRs, triphenyl phosphate (TPP) was the predominant compound. Median levels of ΣPFRs in Malate (530 ng/g) were two times higher (p?<?0.05) than in Payatas (240 ng/g). The estimated daily intake of PFRs in the Philippines (of areas studied) via house dust ingestion was below the guideline values. House dust may be an important contributor in the overall exposure of humans to TPP even when considering dietary sources. To our knowledge, this is a first report on PFR contamination in house dust from developing country. PFRs were ubiquitously detected in the home environments in the Philippines. Although estimated exposure levels through dust ingestion were below the guideline, it was suggested that toddlers are at higher risk. Therefore, further investigations to understand the behavior of PFRs in house and other microenvironments and overall exposure pathways for the country’s populace to PFRs are necessary.     

Phthalate exposure in pregnant women and their children in central Taiwan

Phthalate exposure was found to be associated with endocrine disruption, respiratory effects, reproductive and developmental toxicity. The intensive use of plastics may be increasing the exposure to phthalates in Taiwanese population, particularly for young children.We studied phthalate metabolites in pregnant women and their newborns in a prospective cohort from a medical center in Central Taiwan. One hundred maternal urine samples and 30 paired cord blood and milk samples were randomly selected from all of participants (430 pregnant women). Eleven phthalate metabolites (MEHP, 5OH-MEHP, 2cx-MEHP, 5cx-MEPP, 5oxo-MEHP, MiBP, MnBP, MBzP, OH-MiNP, oxo-MiNP, and cx-MiNP) representing the exposure to five commonly used phthalates (DEHP, di-isobutyl phthalate (DiBP), DnBP, BBP, DiNP) were measured in urine of pregnant women, cord serum and breast milk after delivery, and in urine of their children. Exposure was estimated with excretion factors and correlation among metabolites of the same parent compound. Thirty and 59 urinary samples from 2 and 5 years-old children were randomly selected from 185 children successfully followed.Total urinary phthalate metabolite concentration (geometric mean, μg L⁻¹) was found to be higher in 2-years-olds (398.6) and 5-years-olds (333.7) than pregnant women (205.2). Metabolites in urine are mainly from DEHP. The proportion of DiNP metabolites was higher in children urine (4.39 and 8.31%, ages 2 and 5) than in adults (0.83%) (p < 0.01). Compared to urinary levels, phthalate metabolite levels are low in cord blood (37.45) and milk (14.90). DEHP metabolite levels in women’s urine and their corresponding cord blood are significantly correlated. Compared to other populations in the world, DEHP derived metabolites in maternal urine were higher, while phthalate metabolite levels in milk and cord blood were similar. The level of phthalate metabolites in milk and cord blood were comparable to those found in other populations. Further studies of health effects related to DEHP and DiNP exposure are necessary for the children.     

The association between maternal nonylphenol exposure and parity on neonatal birth weight: A cohort study in Taiwan

Background

The aim of this study was to explore the association between NP exposure and parity and their effect on neonatal birth weight.

Methods

A cohort of pregnant women was established in a medical center in North Taiwan. Urinary NP concentration was determined by high-performance liquid chromatography coupled with fluorescent detection and adjusted using creatinine. A multivariable regression model was fit to determine the association between the maternal NP level in each trimester and neonatal birth weight. The odds ratios (ORs) of infant birth weight below the 10th, 25th, and 50th percentiles, comparing pregnant women with the different NP exposure levels, was estimated using a logistic regression.

Results

Of the 162 pregnant women in the study, 99 were multiparas and 63 were primiparas. After adjusting for other covariates, the NP level in the second trimester had a significant association with birth weight in the primiparas (β = −182.49 g, p value = 0.02). The OR of low infant birth weight, comparing pregnant women with different NP levels, was increased by decreasing the cutoff percentile for birth weight (OR = 1.18 for the 50th percentile, 2.12 for the 25th percentile, and 7.81 for the 10th percentile). The odds of primiparas with high NP level having a low neonatal birth weight increased to 3.87, 11.77, and 9.40 for the three different percentiles (p value < 0.05).

Conclusion

Maternal NP exposure level is associated with an increased risk of low neonatal weight. Primiparas are especially at risk, and the second trimester of pregnancy may be the critical stage of exposure.     

Association of human cohorts exposed to blood and urinary biomarkers of PAHs with adult asthma in a South Asian metropolitan city

Semi-volatile organic compounds (SVOCs) are a major global problem that causes the greatest impact on urban settings and have been linked to bronchial asthma in both children and adults in Pakistan. The association between exposure of polycyclic aromatic hydrocarbons (PAHs) and asthma in the adult population is less clear. The current study aimed to assess the clinico-chemical parameters and blood levels of naphthalene phenanthrene, pyrene, and 1,2-benzanthracene and urinary levels of 1-OH pyrene and 1-OH phenanthrene as well as asthma-related biomarkers immunoglobulin E (IgE), resistin, and superoxide dismutase (SOD) of oxidative stress and other hematologic parameters in adults and their relationship with bronchial asthma. The GC/MS analysis showed higher mean concentrations of blood PAHs in asthma respondents (4.48 ± 1.34, 3.46 ± 1.04, 0.10 ± 0.03, and 0.29 ± 0.09) (ng/mL) as compared to controls (3.07 ± 0.92, 1.71 ± 0.51, 0.06 ± 0.02, and 0.11 ± 0.03) (ng/mL), with p = .006, p = .001, p = .050, and p = .001. Similarly, urinary levels of 1-OHpyr and 1-OHphe were significantly increased in adults with bronchial asthma (0.54 ± 0.16; 0.13 ± 0.04) (μmol/mol-Cr) than in controls (0.30 ± 0.09; 0.05 ± 0.02) (μmol/mol-Cr), with p = .002 and p = .0001, respectively, with a significant positive correlation to asthma severity. The asthma-related biomarkers IgE, resistin, and SOD were significantly higher (p 0.0001, 0.0001, and 0.0001) in people with asthma than in control persons. The findings showed that higher blood and urine PAHs levels were linked to higher asthma risk in adults and significant interaction with participants who smoked, had allergies, had a family history of asthma, and were exposed to dust. The current study’s findings will be useful to local regulatory agencies in Lahore in terms of managing exposure and advocating efforts to minimize PAH pollution and manage health.

     

Organochlorine contaminants in the hair of Iranian pregnant women

In the present study, the hair of pregnant women was sampled between November 2007 and January 2008 in Ahvaz and Noushahr cities and the countryside of Noushahr, Iran. They were analyzed for organochlorine pesticides (OCPs), such as dichlorodiphenyltrichloroethane (DDT) and its metabolites, hexachlorobenzene (HCB), α-, β-, and γ-hexachlorocyclohexane (HCH) isomers and seven polychlorinated (PCBs) congeners (IUPAC Nos. 28, 52, 101, 118, 138, 153 and 180). Significant differences between the concentrations of investigated pollutants were found between the locations (p < 0.05). For HCHs, the γ-HCH isomer was measured at higher mean concentrations (6 ng g⁻¹ hair) compared to the β-HCH isomer (0.03 ng g⁻¹), which generally is the most prevalent HCH in biological matrices. Very high mean concentrations of p,p′-DDT in countryside of Noushahr (24 ng g⁻¹) combined with lower values (0.6) of ratio p,p′-DDE/p,p′-DDT in the hair samples suggest recent exposure to “fresh” DDT in this region. Significant differences in OCPs and PCBs were found between primiparous and multiparous mothers (p < 0.05). There was no correlation between levels of OCPs and PCBs in the hair of Iranian pregnant women and their age. There was a significant difference (p < 0.05) in the organochlorine levels, including HCHs, between mothers who have eaten fish once a week and those who consumed fish more than once per week in Noushahr.     

Use of an expanded receptor model for personal exposure analysis in schoolchildren with asthma

An expanded receptor model was applied to identify and apportion the PM_2.5 sources that were common to three different environments (personal, indoor: inside school, and outdoor: outside school) resulting in exposure to asthmatic children who attended a school in Denver, CO for children with moderate to severe asthma. Four resolved external sources and three internal sources were resolved from the PM_2.5 data for three different environments. Secondary nitrate and motor vehicle emissions were the two largest external sources in this study. Cooking was the largest internal source. A significant influence of indoor smoking on daily personal exposures to particles was observed for those houses in which smokers reside and the environmental tobacco smoke contribution correlated with urinary cotinine levels in these urban schoolchildren. The influence of the high traffic flow outside the school on the indoor air quality was also observed. The identification and apportionment of these sources will support a subsequent investigation of the potency of air pollution sources on asthma severity in children and provide a better understanding of potential mechanisms of asthma exacerbation.     

Reduction in Residential Chromium Following Site Remediation

ABSTRACT

The purpose of this study was to determine the influence of chromate production waste site remediation on residential Cr concentrations in house dust. Twenty-three homes in Jersey City, NJ, were identified as having had high (>500 u,g/gm, median 739 u,g/gm), medium (100-400 u,g/gm, median 245 u,g/gm), or low (<100 u,g/gm, median 48 u,g/ gm) Cr in house dust during a study conducted in 19921993 prior to site remediation. House dust samples were collected on four visits from each home between November 1996 and February 1998, extracted with HNO₃, and analyzed for Cr with an inductively coupled plasma-mass spectrometer. Homes that had low Cr concentrations in 1992-1993 continued to have low Cr concentrations (median 1 u,g/g). In contrast, substantial declines in Cr concentrations were found in the house dust collected from homes located near the remediated waste sites: previously high-level homes had a median of 50 u,g/g and mid-level homes had a median of 34 u,g/g. Site remediation had a beneficial effect on household loadings of Cr, since no differences in post-remediation house dust Cr concentrations were found among the three groups.     

Selected organochlorine pesticide and polychlorinated biphenyl residues in house dust in Singapore

Although the use of organochlorine pesticides (OCPs) and polychlorinated biphenyls (PCBs) has been prohibited in Singapore since 1980, OCPs and PCBs still can be detected in the environment and represent a potential threat to public health. In this study, OCPs and PCBs were measured in house dust samples collected from 31 homes across the island-state of Singapore. Organochlorine pesticides, such as hexachlorocyclohexanes (HCHs), chlordanes and dichlorodiphenyltrichloroethanes (DDTs) were tested, with a range of 相似文献   

Application of neutral electrolyzed water spray for reducing dust levels in a layer breeding house

Reducing airborne dust is an essential process for improving hen housing environment. Dust reduction effects of neutral electrolyzed water (pH 8.2) spray were investigated in a commercial tunnel-ventilated layer breeding house during production in northern China. A multipoint sampler was used to measure airborne dust concentration to study the dust reduction effects and distribution in the house. Compared with the control treatment (without spray), airborne dust level was reduced 34% in the 3 hr after spraying 216 mL m^?2 neutral electrolyzed water in the breeding house. The dust concentration was significantly higher during the periods of feed distribution (1.13 ± 0.13 mg m^?3) and artificial insemination (0.72 ± 0.13 mg m^?3) compared with after spray (0.47 ± 0.09 mg m^?3) and during lights-off period (0.29 ± 0.08 mg m^?3) in the three consecutive testing days (P < 0.05). The experimental cage area was divided into four zones along the length of the house, with zone 1 nearest to the evaporative cooling pad and zone 4 nearest to the fans. The air temperature, relative humidity, airflow rate, and dust concentration were measured at the sampling points of the four zones in 3 consecutive days and mortality of the birds for the duration of a month were investigated. The results showed that the air temperature, airflow rate, dust concentration, and number of dead birds increase from zone 1 to zone 4 in the tunnel-ventilated layer breeding house.

Implications: It is difficult to effectively reduce hen house airborne dust levels and limited information is available on airborne dust distribution in tunnel-ventilated hen houses. This work investigates (i) the application of neutral electrolyzed water spray for reducing dust in a layer breeding houses; (ii) dust concentration variations in 24-hr house operation; as well as (iii) the effects of location on dust concentrations. It was demonstrated that neutral electrolyzed water spray can be efficiently used for dust reduction in poultry houses. Further, a better understanding of the dust concentration variations in 24-hr house operation and in different spatial zones can contribute to bird housing environment management and poultry house design so as to improve bird health.     

Heavy metals exposure of children from stairway and sidewalk dust in the smelting district,northeast of China

The aim of this work was to study metals accumulation in stairway (inside the residential building) and sidewalk (outside the residential building) dust, and health risk of children due to dust exposure. The investigation included the: (a) spatial distributions of Hg, Pb, Cd, Zn and Cu in stairway and sidewalk dust, (b) source analysis of metals in stairway and sidewalk dust, and (c) assessment of the children health risks due to metals exposure from stairway and sidewalk dust. In the smelting district of Huludao, the maximum Hg, Pb, Cd, Zn and Cu contents in stairway dust were 5.324, 4594, 936.8, 48 253, 1377 mg kg^?1, respectively, and were 144, 213, 8674, 760 and 69.5 times as high, respectively, as the background values in soil. A strong positive relationship was shown between the stairway and sidewalk dust for each metal (p < 0.01). The trends for Hg, Pb, Cd, Zn and Cu in the stairway and sidewalk dust were similar and with higher concentrations trending Huludao Zinc Plant (HZP). Atmospheric deposition due to metal smelting from HZP was the common source of heavy metals in the sidewalk and stairway dust. Vehicular traffic affected the metal accumulation in dust, but their contribution was slight comparing with atmospheric emission from HZP. Almost all hazard indexes (HIs) for metals due to stairway dust exposure in this study were lower than 1. The health risk for children was low if they would not play in the stairway. However, children were also experiencing the potential health risk from Cd and Pb exposure from sidewalk dust outside residential building, especially near HZP.     

Lead,mercury, cadmium,chromium, nickel,copper, zinc,calcium, iron,manganese and chromium (VI) levels in Nigeria and United States of America cement dust

This study was aimed at investigating the relative abundance of heavy metals in cement dust from different cement dust factories in order to predict their possible roles in the severity of cement dust toxicity. The concentrations of total mercury (Hg), copper (Cu), chromium (Cr), cadmium (Cd), nickel (Ni), manganese (Mn), lead (Pb), iron (Fe) and chromium (VI) (Cr (VI)) levels in cement dust and clinker samples from Nigeria and cement dust sample from the United States of America (USA) were determined using graphite furnace atomic absorption (GFAAS), while Zn and Ca were measured by flame atomic absorption spectrophotometry (FAAS), and Cr (VI) by colorimetric method. Total Cu, Ni and Mn were significantly higher in cement dust sample from USA (p < 0.05), also, both total Cr and Cr (VI) were 5.4–26 folds higher in USA cement dust compared with Nigeria cement dust or clinker (p < 0.001). Total Cd was higher in both Nigeria cement dust and clinker (p < 0.05 and p < 0.001), respectively. Mercury was more in both Nigeria cement dust and clinker (p < 0.05), while Pb was only significantly higher in clinker from Nigeria (p < 0.001). These results show that cement dust contain mixture of metals that are known human carcinogens and also have been implicated in other debilitating health conditions. Additionally, it revealed that metal content concentrations are factory dependent. This study appears to indicate the need for additional human studies relating the toxicity of these metals and their health impacts on cement factory workers.     

Brominated flame retardants in dust from UK cars--within-vehicle spatial variability, evidence for degradation and exposure implications

Polybrominated diphenyl ethers (PBDEs), hexabromocyclododecanes (HBCDs), and tetrabromobiphenol-A (TBBP-A) were measured in a preliminary study of dust from passenger cabins and trunks of 14 UK cars. Concentrations in cabin dust of HBCDs, TBBP-A, and BDEs 47, 85, 99, 100, 153, 154, 183, 196, 197, 202, 203, 206, 207, 208, and 209 exceeded significantly (p < 0.05) those in trunk dust. Sampling cabin dust thus appears to provide a more accurate indicator of human exposure via car dust ingestion than trunk dust. Elevated cabin concentrations are consistent with greater in-cabin use of BFRs. In five cars, while no significant differences (p > 0.05) in concentrations of HBCDs and most PBDEs were detected in dust sampled from four different seating areas; concentrations of TBBP-A and of PBDEs 154, 206, 207, 208, and 209 were significantly higher (p < 0.05) in dust sampled in the front seats. Possible photodebromination of BDE-209 was indicated by significantly higher (p < 0.05) concentrations of BDE-202 in cabin dust. In-vehicle exposure via dust ingestion to PBDEs, HBCDs and TBBP-A exceeded that via inhalation. Comparison with overall exposure via diet, dust ingestion, and inhalation shows while in-vehicle exposure is a minor contributor to overall exposure to BDE-99, ΣHBCDs, and TBBP-A, it is a significant pathway for BDE-209.     

Radon exhalation and ultrafine fraction of radon progeny in closed room air

The influence of ²²²Rn exhalation from walls and air exchange (low ventilation rates ν<0.3 h^-1) upon its concentration in room air has been considered. It was found that the radon concentration reachs 84 Bq m^-3 at exhalation and ventilation rates of 66 Bq hm^-2 and 0.28 h^-1, respectively. The radon concentration and the ultrafine fraction f_p of potential α energy concentration as well as the equilibrium factor F of the short-lived radon progeny were also determined in three different completely closed rooms. An electroprecipitation method was applied for determining the ²²²Rn concentration while a single wire-screen technique was used for the determination of ultrafine radon progeny. During the measurements, the radon concentrations were varied between 33 and 134 with a mean value 89 Bq m^-3. A mean ultrafine fraction (f_p) of 0.16 was obtained at a mean aerosol particle concentration (Z) of 1700 cm^-3 and a mean equilibrium factor (F) of 0.33. The obtained mean value of f_p was found to be about five times higher than the value reported in the ICRP publication (f_p=0.03). The attachment rate (X), the deposition rate (q^f) and the deposition velocity (v^f_d) of the ultrafine radionuclide ²¹⁸Po were calculated. A mean value of X was found to be 49 h^-1 at a mean q^f of 46 h^-1 and a mean v^f_d of 4.6 m h^-1. The attachment coefficient β of ²¹⁸Po was found to vary between 0.016 and 0.047 with a mean value 0.028 cm³ h^-1.     

Sorption characteristics of cyromazine and its metabolite melamine in typical agricultural soils of China

A myriad of physical, chemical, and biological processes controls the fate of organic contaminants in soils. The knowledge of bioavailability of a contaminant in soil can be useful to conduct environmental risk assessment. We conducted batch equilibrium experiments to investigate the sorption of cyromazine (CA) and its metabolite melamine (MA) onto five typical soils of China belonging to suborders Ali-Perudic Ferrosols, Udic Argosols, Gleyic-Stagnic Anthrosols, Ustic Cambosols, and Udic Isohumosols. Results showed that sorption of CA and MA onto soils was linear, as indicated by the Freundlich and Langmuir models. Different sorption behaviors of CA and MA were observed on the five agricultural soils, with lgK _f values (Freundlich model) of 1.6505–2.6557 and 1.632–2.549, respectively. Moreover, the K _f values for CA and MA were positively correlated with soil organic matter (r?=?0.989, r?=?0.976) and significantly negatively correlated with pH (r?=??0.938, r?=??0.964). The free energy of sorption of CA and MA ranged from ?20.8 to ?23.0 kJ mol^?1 and ?20.8 to ?22.8 kJ mol^?1, respectively, suggesting that the sorption of CA and MA onto the soils is primarily a physical process.     

Assessing the importance of ab- and adsorption to the gas-particle partitioning of PCDD/Fs

The gas-particle partitioning of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) was examined (i) by re-interpreting results from controlled field experiments and (ii) in diurnal samples taken in the New Jersey (NJ), New York (NY) City region. In the controlled field experiments, aerosol-laden filters were exposed to elevated concentrations of PCDD/Fs. Gas-particle partitioning coefficients, K_p's, were significantly correlated with octanol–air partitioning coefficients, K_oa's. The regression of all individual datapoints resulted in the following best fit (r²=0.74, n=87): log K_p,meas=1.00(±0.13) log(10⁻¹²f_omK_oa/ρ_oct)−0.15(±0.48). We interpret this as showing that the ability of organic matter (OM) to absorb PCDD/Fs is generally well described by the octanol–air partitioning model (f_omK_oa). At the NJ land-based sites, samples were taken and analyzed for organic carbon (OC) and elemental carbon (EC), gaseous and particulate PCDD/Fs. K_p's were significantly correlated with the f_omK_oa approach. Adsorption to the filter and possibly to black carbon (BC), which was estimated based on EC measurements, could have contributed to the observed K_p values. Gas-particle predictions based on BC adsorption and OM absorption, with K_p=f_omK_oa/(10¹²ρ_oct)+f_BCK_BC–air/(10¹²ρ_BC) resulted in K_p predictions that were close to measured values. Adsorption to the filter might have been the major reason for elevated K_p's: The one NJ site with highest K_p's was most prone to the filter adsorption sampling artefact because of relatively low sampling volumes and concentrations of total suspended particulates. In addition, while adsorption to BC would result in better prediction of K_p values, no influence of f_BC or f_BC/f_om ratios was seen, suggesting that it was of lesser importance in our sample set.     

Incense burning at home and the blood lead level of preschoolers in Taiwan

The growth and intellectual development of children less than 6 years old may be affected by exposure to low levels of lead. To further reduce environmental lead exposure, this study examined possible household-related factors that affect the blood lead levels of Taiwanese children. In total, based on a stratified random sampling strategy, 934 kindergarten students were recruited throughout Taiwan from April to October 2011 after their parents signed a statement of consent. A venous blood sample was drawn from each participant and analyzed for lead content using inductively coupled plasma mass spectrometry. Information on the demographics and household environment of the study subjects was collected by administering a questionnaire (Table 1). The geometric mean lead level in the blood samples of the study subjects was 1.84 μg/dL with a geometric standard deviation of 1.55. The blood lead level was negatively correlated with household income and parental educational levels (p?p?p?p?=?0.0022). Because the health effects of low levels of lead exposure have been reported in recent years and because no consensus has been reached regarding a safety threshold for blood lead level in children, any trivial factor is worth investigating to further prevent lead exposure in children. Incense burning at home is a common traditional religious activity in Taiwan; therefore, more study is warranted to further eliminate the lead content in incense and reduce lead exposure for the families who practice this activity.     

Polychlorinated biphenyl levels in the blood of Japanese individuals ranging from infants to over 80 years of age

Individuals’ exposure to various persistent organic pollutants (POPs), including polychlorinated biphenyls (PCBs), and its adverse health effects have been a cause of concern. We measured blood PCB concentrations from samples taken from 507 Japanese individuals ranging from infants to those over 80 years of age. The blood PCB levels increased with age for both male (Spearman’s r?=?0.69, p?<?0.001) and female (Spearman’s r?=?0.70, p?<?0.001) participants. Adult men and nulliparous women showed similar increases with age. However, the PCB levels of multiparous women were lower than those of nulliparous women in their thirties (p?=?0.005), probably because the PCBs were transferred from the mothers to their children during pregnancy and lactation. Among infants (<2 years of age), some had as high levels of accumulated PCB levels as those in adults >30 years of age. In some cases, the PCB levels were over 0.8 ng/g wet weight, similar to levels observed in adults over 50 years of age. In the future, it will be necessary to do research on the health of the children who are exposed by high concentration level of POPs.     

Reduction in residential chromium following site remediation

The purpose of this study was to determine the influence of chromate production waste site remediation on residential Cr concentrations in house dust. Twenty-three homes in Jersey City, NJ, were identified as having had high (> 500 micrograms/gm, median 739 micrograms/gm), medium (100-400 micrograms/gm, median 245 micrograms/gm), or low (< 100 micrograms/gm, median 48 micrograms/gm) Cr in house dust during a study conducted in 1992-1993 prior to site remediation. House dust samples were collected on four visits from each home between November 1996 and February 1998, extracted with HNO3, and analyzed for Cr with an inductively coupled plasma-mass spectrometer. Homes that had low Cr concentrations in 1992-1993 continued to have low Cr concentrations (median 1 microgram/g). In contrast, substantial declines in Cr concentrations were found in the house dust collected from homes located near the remediated waste sites: previously high-level homes had a median of 50 micrograms/g and mid-level homes had a median of 34 micrograms/g. Site remediation had a beneficial effect on household loadings of Cr, since no differences in post-remediation house dust Cr concentrations were found among the three groups.     

Polybrominated diphenyl ethers in house dust in Singapore

The use of polybrominated diphenyl ethers (PBDEs) as flame retardants in Singapore is not strictly regulated; therefore these compounds can be readily found in furniture, electronic devices, and building materials. This study was the first of its kind to be conducted in Singapore to measure concentrations of PBDEs in house dust. Samples were collected from 31 homes in various locations across the island-state of Singapore, and a total eight PBDEs congeners were measured. PBDEs were detected in all 31 dust samples and the number of BDE congener detected per home ranged between 3 and 8. The most abundant BDE congeners found were BDE 47, 99 and 209, with a median value of 20 ng g(-1) dust, 24 ng g(-1) dust and 1000 ng g(-1) dust, respectively. BDE 209 contributed 88% to the median of all the congeners, and BDE 47 and 99 contributed 1.8% and 3.5%, respectively. Different congener profiles were observed between this and studies conducted elsewhere, which is consistent with the use of different commercial PBDE around the world. No significant correlations between PBDE dust levels and residential characteristics (number of TVs and computers, floor area or flooring material) were observed. The daily intake of PBDEs via the inhalation pathway was estimated. House dust may be regarded as the most important exposure route of PBDEs for children.     

Analysis of organochlorine pesticide residues in human and cow’s milk in the towns of Asendabo,Serbo and Jimma in South-Western Ethiopia

The level of some OCPs in human and cow milk collected from Asendabo, Serbo and Jimma in South-West Ethiopia were analyzed using GC–ECD. Results of the analysis indicated that all samples contained detectable quantities of p,p′-DDT and its metabolites, p,p-DDE and p,p-DDD, but none of the other OCPs analyzed. Mean levels of total DDT in the human and cow milk samples in the three areas were 12.68 and 0.389 μg g^?1 respectively. The distributions of p,p-DDT, p,p-DDE and p,p-DDD in the human milk samples from the three locations followed the same trend in which the proportion of p,p-DDT was the highest in all the three cases, comprising 55–71% of total DDT, followed by p,p-DDE, 26–39%, and the least, p,p-DDD of 2–5%. The mean ratio of DDT/DDE concentration for the three areas was calculated to be 2.01. This value was much higher than the values reported from other countries in earlier studies and indicates the existence of a higher quantity of DDT from a fresh input in the three study areas. The mean estimated daily intake of DDT by infants from mother’s milk in the three locations was found to be 62.17 μg kg^?1 body weight, which is about three times higher than the acceptable daily intake set by WHO/FAO for total DDT, 20 μg kg^?1 of body weight. This alarmingly high daily intake value is a cause for concern, since children are highly susceptible to effects from such environmental contaminants. The study has revealed that people in the study areas are facing exposure to DDT from recent use. The observed contamination of mother’s milk and the possible transfer of the contaminant from mother to child is an obvious risk associated with breast-feeding in the study areas and possibly in other parts of the country too.