| 1. |
|
|
| 2. |
- Ericson Jogsten, Ingrid, et al.
(author)
-
Perfluorinated chemicals in blood of residents in Catalonia (Spain) in relation to age and gender : a pilot study
- 2007
-
In: Environment International. - : Elsevier BV. - 0160-4120 .- 1873-6750. ; 33:5, s. 616-623
-
Journal article (peer-reviewed)abstract
- Fluorinated organic compounds (FOCs) are a group of chemicals widely used as surfactants, lubricants, polymers, and fire-fighting foams. Recent studies have shown the ubiquitous distribution of FOCs in the environment, wildlife, and humans. We here report the results of a pilot study conducted to provide preliminary data on the levels of 13 FOCs in the blood of 48 residents in Catalonia, Spain, in relation to gender and age (25+/-5 and 55+/-5 years). The highest mean concentration was obtained for perfluorooctane sulfonate (PFOS, 7.64 ng/ml), followed by perfluorohexane sulfonate (PFHxS, 3.56 ng/ml) and perfluorooctanoic acid (PFOA, 1.80 ng/ml). Four other FOCs showed mean levels between 0.30 and 0.44 ng/ml, whereas those of the remaining 6 compounds were below the detection limit. Regarding gender, the blood levels of PFHxS and PFOA were significantly higher (p<0.05) in men than in women, while differences according to age were only noted for PFHxS (p<0.05) and perfluorooctane sulfonamide (PFOSA) (p<0.001), for which the levels were higher in the younger (25+/-5 years) group of subjects. A significant correlation between PFOS levels and those of the remaining detected FOCs (except PFDA) was found. In general terms, the current FOC concentrations were lower than those found in recent studies concerning levels of these chemicals in human blood and serum of subjects from different countries.
|
|
| 3. |
- Hagberg, Jessika, et al.
(author)
-
Chemical and toxicological characterisation of PBDFs from photolytic decomposition of decaBDE in toluene
- 2006
-
In: Environment International. - : Elsevier BV. - 0160-4120 .- 1873-6750. ; 32:7, s. 851-857
-
Journal article (peer-reviewed)abstract
- A substantial formation of PBDF congeners was observed during photolytic decomposition of decaBDE in toluene. The decaBDE degradation was monitored by chemical and toxicological analysis and in all, twenty-seven mono- to hexasubstituted polybrominated dibenzofurans (PBDFs) were detected in toluene solutions of decabromodiphenyl ether (decaBDE) after irradiation with UV-A, UV-AB and UV-ABC. The concentration levels of PBDFs formed after 16 h of UV exposure increased with wider spectra and were determined to be 3.5, 4.2 and 14 microg/ml after UV-A, UV-AB and UV-ABC irradiation, respectively. In accordance, bioassay derived TEQs (bio-TEQs), determined with the DR-CALUX assay, increased with a similar pattern. The PBDFs formed after the three UV exposures accounted for 0.31%, 0.35% and 1.2% of the initial amount of decaBDE (molar basis). The PBDF congener patterns were consistent in all three UV experiments which imply that no alterations were induced in the PBDF formation or degradation processes due to differences in UV irradiation. However, these processes tended to increase with wider spectra and increasing radiation energy most likely due to the strong absorbance of for example decaBDE at shorter wavelengths. After total decaBDE decomposition the PBDF formation increased significantly in the UV-ABC experiment. The tetra to hexasubstituted BDFs constituted the majority of detected compounds in all experiments. In all samples, the estimated chemical TEQ indicate that the bio-TEQs observed are largely explained by the presence of non-2,3,7,8-substituted PBDFs with relatively low toxicological potencies.
|
|
| 4. |
- Jaspers, Veerle L B, et al.
(author)
-
Preen oil as the main source of external contamination with organic pollutants onto feathers of the common magpie (Pica pica).
- 2008
-
In: Environment International. - : Elsevier BV. - 0160-4120 .- 1873-6750. ; 34:6, s. 741-8
-
Journal article (peer-reviewed)abstract
- We investigated the possible sources of contamination with organic pollutants, such as polychlorinated biphenyls (PCBs), /p/,/p/'-dichlorodiphenyltrichloroethane (DDT) and metabolites, and polybrominated diphenyl ethers (PBDEs), in and onto tail feathers of a large songbird, the common magpie (Pica pica). Although feathers are potentially useful as a non-destructive biomonitor for organic pollutants, concentrations may be influenced by external contamination onto the feather surface. In a first approach, a group of magpies was captured after the completion of moult. The third tail feather was pulled out and a blood sample was taken. Most PCBs, DDTs and some PBDEs could be quantified in one single tail feather, indicating that the applicability of feathers goes beyond monitoring with predatory birds, as shown previously. Nevertheless, correlations between levels in serum and feathers were found significant in three cases only (i.e. CB 170, CB 180 and CB 187). This finding may be attributed to different factors, such as varying diet, condition, sample size or external contamination. In a second approach, cadavers of magpies were collected throughout Flanders. The preen gland was removed and the first, third and fifth tail feathers were pulled out at both sides. No significant differences were found among tail feathers within an individual. We compared three washing procedures to remove external contamination with organic pollutants from these feathers: deionised water, acetone and a surfactant/acetone solution. Right feathers were washed and left feathers were kept as control. Concentrations in the resulting washes were found highest in the acetone solutions. Furthermore, feathers washed with acetone or with a surfactant/acetone solution had significantly lower mean concentrations than the control feathers. Highest correlations with levels in preen gland were obtained for the control feathers. Consequently, the source of external contamination with organic pollutants onto feathers seems to be endogenous, originating from the preen gland. This is in great contrast to the extensive airborne pollution that has been reported for most heavy metals. In summary, the results of the current study highlight the usefulness of feathers for non-destructive biomonitoring of organic pollutants.
|
|
| 5. |
- Karlsson, Marie, et al.
(author)
-
Levels of brominated flame retardants in blood in relation to levels in household air and dust
- 2007
-
In: Environment International. - : Elsevier BV. - 0160-4120 .- 1873-6750. ; 33:1, s. 62-69
-
Journal article (peer-reviewed)abstract
- Levels of tri- to decabrominated diphenyl ethers (BDEs), 1,2-bis(2,4,6-tribromophenoxy)ethane (BTBPE) and 1,2-bis(pentabromophenyl)ethane (DeBDethane) were determined in air, sedimentary dust and human plasma from five households in Sweden. The levels of the individual BDEs in the plasma samples were in the same order of magnitude as in other studies of the general population in Scandinavia, and varied between non-detectable (< 0.41 ng g− 1 l.w.) to 17 ng g− 1 (l.w.). BDE#28 and #47 were present in all air samples, with mean values of 0.015 and 0.12 ng m− 3, respectively, except for one sample where the BDE#47 concentration was below the limit of detection (< 0.17 ng m− 3). BDE#209 was found in one of the five air samples at a concentration of 0.26 ng m− 3. DeBDethane was also detected in one sample, in which the BDE#209 level was below LOD (< 0.021 ng m− 3), at a level of 0.023 ng m− 3. All the target compounds were found in the sedimentary dust samples at levels from 0.51 to 1600 ng g− 1, the highest concentration representing BDE#209. The most abundant components in plasma, air and dust were BDE#47, #99 and #209. In the plasma samples BDE#207 and #206 were also present at similar concentrations as BDE#47. In the sedimentary dust samples, DeBDethane was also among the most abundant BFRs. A positive relationship was found for the sumBDE concentrations in dust and plasma, although the relationship was strongly dependent on one of the five observations. BFR levels in dust and air were not dependent on the house characteristics such as living area, floor material or number of electronic devices.
|
|
| 6. |
|
|
| 7. |
- Kärrman, Anna, et al.
(author)
-
Identification and pattern of perfluorooctane sulfonate (PFOS) isomers in human serum and plasma
- 2007
-
In: Environment International. - : Elsevier BV. - 0160-4120 .- 1873-6750. ; 33:6, s. 782-788
-
Journal article (peer-reviewed)abstract
- Human serum and plasma from Sweden (n=17), the United Kingdom (the UK) (n=13) and Australia (n=40) were analyzed by high performance liquid chromatography coupled to mass spectrometry. The objective was to identify different perfluorooctane sulfonate (PFOS) isomers. Similar isomer patterns typical for the electrochemical fluorination (ECF) process were found for all samples. The linear PFOS (L-PFOS) was the major isomer found (58-70%) followed by the monosubstituted PFOS isomers 1/6-CF(3)-PFOS (18-22%) and 3/4/5-CF(3)-PFOS (13-18%). Disubstituted isomers were also detected. The percentage of L-PFOS found in the serum and plasma samples was lower compared to a standard PFOS product (76-79%). The pattern of PFOS isomers in human serum and plasma may be suggestive concerning potential isomeric discrimination since PFOS is only produced by ECF. Possibilities for such isomer discrimination are discussed. Significant higher content of L-PFOS (68%) in Swedish samples compared to Australia and the UK (59%) was also found, which may suggest differences in exposure sources for humans.
|
|
| 8. |
- Kärrman, Anna, et al.
(author)
-
Relationship between dietary exposure and serum perfluorochemical (PFC) levels-A case study
- 2009
-
In: Environment International. - : Elsevier BV. - 0160-4120 .- 1873-6750. ; 35:4, s. 712-717
-
Journal article (peer-reviewed)abstract
- Daily dietary intake of perfluorinated chemicals (PFCs) in relation to serum levels was assessed by determination of nine PFCs including perfluorooctane sulfonate (PFOS) and perfluorooctanoic acid (PFOA) in matched daily diet duplicates and serum samples. Diet and serum were collected in year 2004 from 20 women in Osaka and Miyagi, Japan. Only PFOS and PFOA were detected in the diet samples and no significant difference between cities was seen. After adjusted by water content, diet concentration of PFOA was significantly higher in Osaka. The median daily intake calculated using the measured diet concentrations was 1.47 ng PFOS/kg b.w. and 1.28 ng PFOA/kg b.w. for Osaka, and 1.08 ng PFOS/kg b.w. and 0.72 ng PFOA/kg b.w. for Miyagi. A significant difference between cities was seen for the serum concentrations with median of 31 ng/mL PFOS and PFOA in Osaka, compared to 14 ng/mL PFOS and 4.6 ng/mL PFOA in Miyagi. Carboxylates such as perfluorononanoic acid (PFNA) and perfluoroundecanoic acid (PFUnDA) were also detected in serum at median levels 6.9 ng/mL and 3.2 ng/mL (Osaka), and 2.8 ng/mL and 5.1 ng/mL (Miyagi). Based on one-compartment model under steady state, dietary intake of PFOS and PFOA accounted for only 22.4% and 23.7% of serum levels in Osaka females, and in contrast 92.5% and 110.6% in Miyagi females, respectively. (C) 2009 Elsevier Ltd. All rights reserved.
|
|
| 9. |
- Otte, Jens C., et al.
(author)
-
A bioassay approach to determine the dioxin-like activity in sediment extracts from the Danube River : ethoxyresorufin-O-deethylase induction in gill filaments and liver of three-spined sticklebacks (Gasterosteus aculeatus L.)
- 2008
-
In: Environment International. - Amsterdam : Elsevier. - 0160-4120 .- 1873-6750. ; 34:8, s. 1176-1184
-
Journal article (peer-reviewed)abstract
- Sediment samples from the upper Danube River in Germany have previously been characterized as ecotoxicologically hazardous and contaminants in these sediments may contribute to the observed decline of fish populations in this river section. For the investigation of sediment toxicity there is a need for development, standardization and implementation of in vivo test systems using vertebrates. Therefore, the main objective of this study was to apply and evaluate a recently established fish gill EROD assay as a biomarker in sediment toxicity assessment by using extracts of well characterised sediment samples from the upper Danube River. This to our knowledge is the first application of this novel assay to sediment extracts. Sediments from four different sites along the upper Danube River were Soxhlet-extracted with acetone and dissolved in DMSO. Three-spined sticklebacks (Gasterosteus aculeatus L.) were exposed for 48 h to various concentrations of the extracts, to the positive control β-naphthoflavone or to the solvent. Measurements of EROD activity in gill filaments and liver microsomes followed the exposure. Concentration-dependent induction of EROD in both gill and liver was found for all sediment extracts. The highest EROD-inducing potency was determined for extracts of sediments from the sites “Öpfinger See” and “Sigmaringen” and the EROD activities in gill and liver correlated well. The results from the gill and liver assays were in accordance with in vitro results of previous investigations. The EROD activities measured in the present study corresponded with the concentrations of PAHs, PCBs and PCDD/Fs in the sediment samples derived in a previous study. The sticklebacks in this study were in the reproductive phase and a stronger EROD induction was obtained in the females than in the males. Implementation of the EROD assay in testing of sediment extracts gave highly reliable results which make this assay an ecotoxicologically relevant method for assessment of contamination with Ah receptor agonists in sediments.
|
|
| 10. |
|
|
