Abstract  Several perfluoroalkyl compounds (PFCs) are ubiquitous environmental contaminants that can biomagnify in species at high trophic levels including wild birds. Perfluorooctane sulfonate (PFOS) and perfluorooctanoic acid (PFOA) have been detected in wild birds and are known to reduce hatching success of laboratory-exposed chicken embryos at environmentally relevant concentrations. Limited toxicity data are available regarding avian exposure to PFCs of chain lengths greater than C(8), which are of increasing environmental relevance following the recent phase-out of PFOS and PFOA. In this study, linear PFOA, perfluoroundecanoic acid (PFUdA) and perfluorodecane sulfonate (PFDS) were injected into the air cell of white leghorn chicken eggs (Gallus gallus domesticus) prior to incubation to determine effects on embryo pipping success. Furthermore, mRNA expression of key genes involved in pathways implicated in PFC toxicity was monitored in liver tissue. PFOA, PFUdA or PFDS had no effect on embryonic pipping success at concentrations up to 10 microg/g. All PFCs accumulated in the liver to concentrations greater than the initial whole-egg concentration as determined by HPLC/MS/MS. Hepatic accumulation was highest for PFOA (4.5 times) compared to PFUdA and PFDS. Cytochrome P450 1A4 and liver fatty acid binding protein mRNA expression increased after exposure to PFUdA but was only statistically significant at 10 microg/g; several orders of magnitude higher than levels found in wild bird eggs. Based on the present results for white leghorn chickens, current environmental concentrations of PFOA, PFUdA and PFDS are unlikely to affect the hatching success of wild birds.

Abstract  Perfluoroalkyl acids (PFAAs) are globally found in various media, including food and especially fishery products. In the present study, the dietary exposure to 15 perfluoroalkyl acids was assessed for 3 French adult populations, namely high seafood consumers, high freshwater fish consumers, and pregnant women. Purified food extracts were analysed by LC-MS/MS and PFBA, PFPA, PFHxA, PFHpA, PFOA, PFNA, PFDA, PFUnA, PFTrDA, PFTeDA, PFBS, PFHxS, PFHpS, PFOS and PFDS were monitored and quantified according to the isotope dilution principle. Under lower bound (LB) hypothesis (i.e. contamination values<LOD considered as 0), high freshwater fish consumers appear as the most exposed to PFOS (7.5ng.kg(-1) bw.d(-1)), PFUnA (1.3ng.kg(-1) bw.d(-1)), PFDA (0.4ng.kg(-1) bw.d(-1)) and PFHpS (0.03ng.kg(-1) bw.d(-1)) while high seafood consumers appear as the most exposed to PFOA (1.2ng.kg(-1) bw.d(-1)), PFNA (0.2ng.kg(-1) bw.d(-1)) and PFHxS (0.06ng.kg(-1) bw.d(-1)). For all considered populations, the major exposure contributors are fish, seafood and water under LB hypothesis, while dairy products, bread and crispbread are the main contributors under upper bound (UB) hypothesis. Besides this food exposure assessment, further studies are needed to assess the more global PFAA exposure, taking into account indoor and outdoor air, dust and cutaneous contact, which could be other important contributors for this particular class of chemicals.

Abstract  Poly(perfluorooctyl-ethylenoxymethylstyrene) (PFDS) and poly(1,1,2,2-tetrahydroperfluorodecyl acrylate) (PFDA) homopolymers as well as poly(styrene)-b-poly(perfluorooctyl-ethylenoxymethylstyrene) (PS-b-PFDS) and poly(styrene)-b-poly(1,1,2,2-tetrahydroperfluorodecyl acrylate) acrylate) (PS-b-PFDA) block copolymers of various chain lengths were synthesized by nitroxide-mediated radical polymerization in the presence of either 2,2,6,6-tetramethyl-1-piperidinyloxy free radical (TEMPO) in the case of FDS monomer or N-tert-butyl-N-(1-diethylphosphono-2,2-dimethylpropyl)-N-oxyl (DEPN) in the case of the FDA monomer. The molar composition of the block copolymers was determined by elemental analysis and proton NMR while the blocky structure was checked by SEC analysis in trifluorotoluene. Block copolymers PS-b-PFDS (3.6K/60K) and PS-b-PFDA (3.7K/43K) were soluble in neat CO2 at moderate pressure and temperature, indicating the formation of micelles. Similar block copolymers with a longer PS block such as PS-b-PFDA (9.5K/49K), corresponding to a lower CO2-philic/CO2-phobic balance, were insoluble in neat CO2 but could be solubilized in the presence of styrene as a cosolvent. Additionally, surface and bulk properties of PS-b-PFDA were investigated, indicating the same surface tension as for the PFDA homopolymer (gamma(LV) = 10.3 mN/m) and a bulk nanostructured morphology. (C) 2004 Wiley Periodicals, Inc.

Abstract  BIOSIS COPYRIGHT: BIOL ABS. Myocardial salvage after reperfusion may be limited by neutrophil-mediated microvascular damage. The effect of the perfluorochemical, Fluosol-DA, and its various components on neutrophil adherence, cytotoxicity, and proteolytic enzyme release was examined on sheep large and small vessel endothelial cells in vitro. Cells were studied under normoxic (N) and anoxic conditions (A). Various concentrations of Fluosol (10%, 25%, and 50%) significantly reduced neutrophil adherence under both experimental conditions (mean 22 | 3.25% versus 7 | 0.8% (N) and 20 | 3.2% versus 7.5 | 0.9% (A); P and lt; 0.01). The perfluorocarbons, perfluorodecalin (PFD), and perfluoro-tripropylamine (PFTP) in a 50 volume/percent concentration exhibited profound effects on adherence, particularly on cells subjected to anoxia (51% and 69% reduction in adherence, respectively; P and lt; 0.01). No effect on adherence was observed with other components including the detergent, pluroinc F68. A 25% reduction (P and

Abstract  HEEP COPYRIGHT: BIOL ABS. As a 1st step in ascertaining the feasibility of using laboratory rats for explosive detection, their sensitivity to vapor-phase concentrations of the explosive ethylene glycol dinitrate (EGDN) and 3 homologous perfluorocarbons, perfluoromethylcyclohexane (PMCH) perfluorodimethylcyclohexane (PDCH) and perfluorodecalin (PFD) was evaluated. These perfluorocarbons are under evaluation by the USA Government as potential explosive taggants, substances added to explosives which identify their source of manufacture or distribution. The mean detection thresholds of these compounds, as determined in an operant discriminaton task using water reinforcement, were as follows: EGDN, 0.05 ppm (range 0.05-0.06); PDCH, 1.4 ppm (0.60-6.50); PMCH, 2.1 ppm (1.85-4.65); and PFD, 1.1 ppm (0.60-1.69). The 1st quantitative data on the olfactory sensitivity of rats to the vapors of explosive/taggant compounds was provided. The detection curves for such odorants may be fundamentally similar to those of other stimuli that were also evaluated.

Abstract  Perfluoroalkyl acids (PFAAs) are highly persistent substances which have been detected in wildlife around the world, including birds. Although bird eggs have often been used to determine and monitor PFAAs levels in the marine environment, this has rarely been done in the terrestrial environment. In the present study we examined the concentrations and composition profile of 12 PFAAs (4 perfluoroalkyl sulfonic acids (PFSAs) and 8 perfluoroalkyl carboxylic acids (PFCAs) in the eggs of great tits (Parus major) collected at a fluorochemical plant and in three other areas, representing a gradient in distance from the pollution source (from 1 to 70 km), in Antwerp, Belgium. The PFSA concentrations measured at the site of the fluorochemical plant were among the highest ever reported in eggs with median concentrations of 10380 ng/g (extrapolated), 99.3 ng/g and 47.7 ng/g for PFOS, PFHxS and PFDS respectively. Furthermore, the median concentration of 19.8 ng/g for PFOA was also among the highest ever reported in bird eggs. Although these concentrations decreased sharply with distance from the fluorochemical plant, levels found in the adjacent sites were still high compared to what has been reported in literature. Moreover, based on what is known in literature, it is likely that these concentrations may cause toxicological effects. PFOS was the dominant contributor to the PFSA and PFAAs (63.4-97.6%) profile at each site, whereas for PFCAs this was PFOA at the plant site and the nearest locations (41.0-52.8%) but PFDoA (37.7%) at the farthest location. Although there is some evidence that PFAAs concentrations close to the plant site are decreasing in comparison with earlier measurements, which may be due to the phase out of PFOS, more research is necessary to understand the extent of the toxicological effects in the vicinity of this PFAAs hotspot.

Abstract  A simple evaporation method was applied to deposit films of hydrophobic organic compounds, either polyethylene (PE) or 1H, 1H, 2H, 2H-perfluorodecyltriethoxysilane (PFDS), on various steel surfaces. The endurance of these films was evaluated after ultrasonic cleaning, ultraviolet (UV) light irradiation and heat treatment, and the corrosion behaviour of the PFDS coated steels was measured in NaCl solutions. The results show that in order to achieve high hydrophobicity on steel, the most suitable deposition conditions are exposure to saturated PE or PFDS vapours for a time of 1.8 ks at 393 K, in the case of PE, and 423 K, in the case of PFDS. The hydrophobicity of the PFDS coated surfaces was significantly more stable than that of the PE coated surfaces under ultrasonic cavitation, UV light irradiation and heating to 373 K. The deposition of a PFDS film on the surfaces of SUS304, SUS316 and SS400 steels improved their corrosion resistance in NaCl solution.

Abstract  Study Title: FYI-01378 I - Consists of three extremely large PDFs in the RAD collection. The attachment is volume 1of 3. The whole file is also in the MF collection. Study Information: Acute/Subacute Toxicity EF

Abstract  PFASs concentrations in dust samples collected from three microenvironments in Cairo ranged from 1.3 to 69 ng g(-1) with FTOHs being dominant. The 8:2 FTOH was detected in all samples. Among the FOSAs and FOSEs the MeFOSE was dominant while among ionic PFASs, PFOS and PFOA were most prominent. The concentrations of PFASs were among the lowest worldwide. Correlations between worldwide concentrations of PFOS + PFOA and country development indexes highlight higher usage and human exposure in more developed countries. Food packaging was analyzed for PFSAs, PFCAs and PAPs. The 6:2 and 8:2 monoPAPs were found to be above the MDL in 18% of the samples. PFOA was detected in 79% of the samples with median concentration of 2.40 ng g(-1). PFOS was detected in 58% of the samples with median concentration of 0.29 ng g(-1) while PFHxS and PFDS were below detection limit. Different human exposure scenarios were estimated.

Abstract  In epidemiological research, it has become increasingly important to assess subjects' exposure to different classes of chemicals in multiple environmental media. It is a common practice to aliquot limited volumes of samples into smaller quantities for specific trace level chemical analyses. A novel method was developed for the determination of 14 perfluorinated alkyl acids (PFAAs) in small volumes (10mL) of drinking water using off-line solid phase extraction (SPE) pre-treatment followed by on-line pre-concentration on a WAX column before analysis on column-switching high performance liquid chromatography tandem mass spectrometry (HPLC-MS/MS). In general, large volumes (100-1000mL) have been used for the analysis of PFAAs in drinking water. The current method requires approximately 10mL of drinking water concentrated by using an SPE cartridge and eluted with methanol. A large volume injection of the extract was introduced on to a column-switching HPLC-MS/MS using a mix-mode SPE column for the trace level analysis of PFAAs in water. The recoveries for most of the analytes in the fortified laboratory blanks ranged from 73±14% to 128±5%. The lowest concentration minimum reporting levels (LCMRL) for the 14 PFAAs ranged from 0.59 to 3.4ng/L. The optimized method was applied to a pilot-scale analysis of a subset of drinking water samples from an epidemiological study. These samples were collected directly from the taps in the households of Ohio and Northern Kentucky, United States and the sources of drinking water samples are both surface water and ground water, and supplied by different water distribution facilities. Only five PFAAs, perfluoro-1-butanesulfonic acid (PFBS), perfluoro-1- -hexanesulfonic acid (PFHxS), perfluoro-1-octanesulfonic acid (PFOS), perfluoro-n-heptanoic acid (PFHpA) and perfluoro-n-octanoic acid (PFOA) are detected above the LCMRL values. The median concentrations of these five PFAAs detected in the samples was ≤4.1ng/L with PFOS at 7.6ng/L and PFOA at 10ng/L. Concentrations of perfluoro-1-decanesulfonic acid, PFDS and other perfluoroalkyl carboxylic acids were below the LCMRL values.

Abstract  This work investigated the bioconcentration of PFASs in juvenile rainbow trout by exposing the fish in separate tanks under flow-through conditions to water continuously spiked with either of the AFFFs FC-203CF light water AFFF 3% (3M) or Niagara 1-3 (Angus Fire); a nonspiked tank served as the control. Three fish in each tank were collected after 1, 3, 6, and 11 days of exposure, and 3, 7, 14, and 25 days of depuration. Liver and carcass homogenate samples were analyzed for 20 PFASs using LC-MS/MS. PFDS, PFOS, PFHxS, and EtFOSAA were detected in fish exposed to the 3M foam, while 6:2 and 8:2 FTSASs, 6:2 and 8:2 FTSAs, 5:3 and 7:3 FTCAs were measured in fish exposed to Angus Fire foam. Bioconcentration factors and rate constants for uptake and depuration were calculated. Total and extractable organofluorine were measured in the fish samples. After fish were exposed to AFFFs, not only known PFASs but also other unknown organofluorines were bioconcentrated. Compared to the control group, significantly greater amounts (at least 10-fold) and proportion of unidentified PFASs were found in both liver and carcass homogenate ranging from ∼50% in 3M foam up to 95% in the Angus Fire foam at the end of exposure.

Abstract  Concentrations of perfluorochemicals (PFCs) including perfluoroalkylsulfonates (PFSAs), and perfluoroalkylcarboxylates (PFCAs) were determined in liver of harbor seals (n=68) collected from the northwest Atlantic between 2000 and 2007. Of ten PFCs measured, perfluorooctane sulfonate (PFOS) concentrations were the highest in liver (8-1388 ng/g, ww), followed by perfluoroundecanoic acid (PFUnDA) (<1-30.7 ng/g, ww). An unusual accumulation profile of long-chain (C7-C12) PFCAs, and the predominance of PFUnDA, followed by PFNA in seal liver suggested that fluorotelomer alcohols (FTOHs) may be a major source of PFCAs in the northwest Atlantic. No gender-related differences in the concentrations of individual PFCs or total PFCs were found. Concentrations of PFOS and PFDS were higher in tissues of the pups than the adults, whereas concentrations of the PFCAs were similar between pups and adults. PFOS concentrations in the pups were 2.6-fold higher than those in the adult females, suggesting the importance of maternal transfer of PFCs. Hepatic PFOS concentrations were strongly, positively correlated with PFOSA, PFDS and individual PFCAs, indicating that harbor seals are exposed simultaneously to these compounds. Temporal comparisons of hepatic PFC concentrations showed a marginal increase of PFOS and PFCAs in the adult seals from 2000 to 2007. Unlike the spatial trend observed for polychlorinated biphenyls (PCBs), no south to north (urban-rural-remote) decreasing trend was observed for PFCs, suggesting the presence of diffuse sources of PFC contamination throughout the northwest Atlantic.

Abstract  The present study documents development and validation of a novel approach for determination of 23 perfluorinated alkylated substances (PFASs) in food of animal origin represented by milk and fish. The list of target analytes comprises four classes of PFASs, both ionic and non-ionic: 11 perfluorocarboxylic acids (PFCAs), 4 perfluorosulphonic acids (PFSAs), 5 perfluorosulphonamides (FOSAs) and 3 perfluorophosphonic acids (PFPAs). Fast sample preparation procedure is based on an extraction of target analytes with acetonitrile (MeCN) and their transfer (supported by inorganic salts and acidification) into the organic phase. Removing of matrix co-extracts by a simple dispersive solid phase extraction (SPE) employing ENVI-Carb and C18 sorbents is followed by an efficient sample pre-concentration performed by acetonitrile evaporation and subsequent dilution of residue in a small volume of methanol (matrix equivalent in the final extracts was 16 and 8 g mL(-1), for milk and fish respectively). Using modern instrumentation consisting of ultra-high performance liquid chromatography (UHPLC) hyphenated with a tandem mass spectrometer (MS/MS), limits of quantification (LOQs) as low as 0.001-0.006 μg kg(-1) for milk and 0.002-0.013 μg kg(-1) for fish can be achieved. Under these conditions, a wide spectrum of PFASs, including minor representatives, can be determined which enables collecting data required for human exposure studies. The pilot study employing the new method for examination of milk and canned fish samples was realized. Whereas in majority of canned fish products a wide spectrum of PFCAs, perfluorooctanesulphonic acid (PFOS) and perfluoro-1-octanesulphonamide (PFOSA) was detected, only in a few milk samples very low concentrations (LOQ levels) of PFOS and perfluorooctansulphonic acid (PFDS) were found.

Abstract  BIOSIS COPYRIGHT: BIOL ABS. Administration of a perfluorodecalin (PFD) emulsion, the liver cytochrome P-450 II B12 inducer, to experimental animals is followed by a two-fold increase of the NADPH oxidation rate in liver microsomes. This phenomenon is caused by the presence in the cytochrome P-450 active center of PFD which uncouples microsomal hydroxylation. The high rate of NADPH oxidation in liver microsomes after administration of the fluorocarbon does not decrease the level of reduced pyridine nucleotides in the liver and does not change the glucose concentration in the plasma. It is suggested that the accelerated weight loss in starved animals following PFD administration is due to the energy dissipation in the fluorocarbon uncoupled monooxygenase reactions in the liver.

Abstract  The stability of self-assembled monolayers (SAMs) at elevated temperatures is of considerable technological importance. The thermal stability of 1-octadecanethiol (ODT), 16-mercaptohexadecanoic acid (MHDA) and 1H, 1H, 2H, 2H-perfluorodecanethiol (PFDT) SAMs on gold surfaces, and of 4-aminobutyltriethoxysilane (ABTES) and 1H, 1H, 2H, 2H-perfluorodecyltriethoxysilane (PFDS) assembled on hydroxylated silicon surfaces, was studied by X-ray photoelectron spectroscopy (XPS). The samples were heated in ultrahigh vacuum to temperatures in excess of that required for SAM degradation. ODT monolayers were stable to ca. 110 degrees C, while MHDA and PFDT SAMs were stable to ca. 145 degrees C. ABTES SAMs were found to be indefinitely stable to 250 degrees C, while PFDS SAMs were stable to 350 degrees C. These studies demonstrate the advantages of using silane monolayers for moderate to high temperature applications and illustrate differences that arise due to the nature of the tail group. To demonstrate the feasibility of silanes for template-directed patterning, a hydroxylated silicon oxide surface containing microcontact-printed PFDS patterns was spin-coated with a mainly hydrophilic block copolymer. Annealing the surface at 90 degrees C for 2 h caused the block copolymer to dewet the hydrophobic PFDS-patterned regions and adsorb exclusively on the unpatterned regions of the surface. (C) 2009 Elsevier B. V. All rights reserved.

Abstract  TiO2 nano-coating with superhydrophobic surface was initially prepared through depositing TiO2 nanopartides on the surface of porous Al2O3 microfiltration membrane by multi-layer assembly technology, then followed by a fluorination surface treatment with 1H,1H,2H,2H-perfluorodecyltriethoxysilane (PFDS). X-ray diffractometer (XRD), fourier transform infrared spectroscope (FTIR), atomic force microscope (AFM), water contact angle measurements (WCA) and scanning electron microscope (SEM) were used for membrane characterization. The crystalline structure of TiO2 nano-coating was analysed. The relationship among TiO2 nanoparticles deposition time, surface roughness and hydrophobicity was discussed. The influence of grafting time on the morphology and hydrophobicity was also researched. The result shows that with TiO2 nano-coating anatase structure is fabricated by annealing at 600 degrees C for 1 h, With the increase of TiO2 nanoparticles deposition time, the surface becomes rougher, and the state of water droplets on it transforms from Wenzel to Cassie contact. When the TiO2 nanoparticles deposition time is 50 min and the TiO2 coating is grafted for three times, an ideal superhydrophobic surface of micro-nanometer morphology is obtained with water contact angle of 174.5 degrees.

Abstract  Municipal waste water effluents (MWWEs) are important sources of chemical contamination for aquatic environments. This study investigated the presence and effects of perfluorinated compounds (PFCs) in environmentally exposed northern pike (Esox lucius) collected upstream and downstream a major municipal waste water treatment plant (WWTP) in the St. Lawrence River, Canada. Twelve PFCs, including the newly detected perfluoroethylcyclohexane sulfonate (PFECHS), were quantified in fish muscle, liver, and plasma. Additionally, the expression of eight genes and the activity of three biomarkers were analyzed in fish tissues at both sites. Mean ∑PFC concentration in fish plasma collected upstream the WWTP was 185ng/g w.w. compared to 545ng/g w.w. downstream the point of release. PFECHS was quantified for the first time in St. Lawrence River fish (mean plasma concentration in MWWE fish: 5.07±4.72ng/g w.w.). Results of transcriptomic responses were tissue-specific and indicated significant up-regulation for metallothionein (MT) in blood and MT, glutathion-S-transferase (GST), superoxide dismutase (SOD), and cytochromes P450 1A1 (CYP1A1) in gill tissue of fish collected in the MWWE suggesting greater stress responses for organisms at this location. Significant relationships were found between vitellogenin (Vtg) gene expression in liver, Vtg activity in plasma and perfluorotridecanoic acid (PFTrA), perfluorotetradecanoic acid (PFTeA), and perfluorodecane sulfonate (PFDS) plasma concentrations. The possible endocrine effects of these PFCs should be further investigated.

Abstract  Aluminum alloy surfaces with micro/nano-structures were fabricated via a simple chemical etching (CE) method. After chemical modification with perfluorodecyltriethoxysilane (PFDS), n-octadecyltriethoxysilane (OTS) and aminopropyltriethoxysilane (APS), surfaces with different wettability were obtained. The morphology and chemical elements of the as-prepared surfaces were investigated by atomic force microscopy (AFM), scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS). In addition, the influence of the surface morphology and chemical modification on the wetting/dewetting properties was investigated. Finally, the anti-corrosion and tribological properties of the as-prepared self-assembled monolayers (SAMs) were characterized using an electrochemical workstation and UMT-3 tribometer. The influence of surface morphology and SAMs on the anti-corrosion and tribological performances is discussed in detail. The results showed that the optimal preparation conditions consisted of a 40% volume fraction of hydrochloric acid with a CE time of 2 min. The corrosion resistance of the surfaces chemically modified with hydrophobic groups was much better than that of those modified with hydrophilic groups. Also, the combination of micro/nano-structures and suitable SAMs on aluminum alloy surfaces could greatly enhance the friction reduction and wear resistance behavior.

Abstract  A novel superhydrophobic Al2O3 microfiltration membrane was prepared by the layer-by-layer assembly of TiO2 coating with subsequent fluorination grafting surface treatment by 1H,1H,2H,2H-perfluorodecyltriethoxysilane. The influence of surface morphology on membrane superhydrophobicity, pore size diameter distributions and pure water permeability of the different membranes were studied. By optimizing the grafting parameters, a needle-like surface of grafted TiO2-coated Al2O3 membrane with a water contact angle of 169.5 degrees was obtained. The pure water permeability of different membranes varied from 100 l m(-2) h(-1) bar(-1) before grafting to 3-5 l m(-2) h(-1) bar(-1) after grafting, and the grafted superhydrophobic membrane showed excellent water repellence. The novel superhydrophobic membrane is shown to be promising for liquid-liquid and gas-liquid separation.

Abstract  Perfluoroundecanoic acid (PFUdA) is one of the most highly detected perfluoroalkyl compounds in wild bird tissues and eggs. Although PFUdA does not affect hatching success, many PFCs are known to impair post-hatch development and survival. Here we use microarrays to survey the transcriptional response of cultured chicken embryonic hepatocytes (CEH) to PFUdA for potential targets of PFUdA action that could lead to developmental deficiencies in exposed birds. At 1 μM and 10 μM PFUdA significantly altered the expression of 346 and 676 transcripts, respectively (fold-change>1.5, p<0.05, false discovery rate-corrected). Using functional, pathway and interactome analysis we identified several potentially important targets of PFUdA exposure, including the suppression of the acute-phase response (APR). We then measured the expression of five APR genes, fibrinogen alpha (fga), fibrinogen gamma (fgg), thrombin (f2), plasminogen (plg), and protein C (proC), in the liver of chicken embryos exposed in ovo to PFUdA. The expression of fga, f2, and proC were down-regulated in embryo livers (100 or 1000 ng/g, p<0.1) as predicted from microarray analysis, whereas fibrinogen gamma (fgg) was up-regulated and plg was not significantly affected. Our results demonstrate the utility of CEH coupled with transcriptome analysis as an in vitro screening tool for identifying novel effects of toxicant exposure. Additionally, we identified APR suppression as a potentially important and environmentally relevant target of PFUdA. These findings suggest in ovo exposure of birds to PFUdA may lead to post-hatch developmental deficiencies, such as impaired inflammatory response.

Abstract  Study Title: FYI-01378 I - Consists of three extremely large PDFs in the RAD collection. The attachment is volume 1of 3. The whole file is also in the MF collection. Study Information: Acute/Subacute Toxicity EF

Abstract  Perfluorinated chemicals (PFCs) are of concern due to their widespread use, persistence in the environment, tendency to accumulate in animal tissues, and growing evidence of toxicity. Between 2006 and 2011 we collected blood plasma from 261 bald eagle nestlings in six study areas from the upper Midwestern United States. Samples were assessed for levels of 16 different PFCs. We used regression analysis in a Bayesian framework to evaluate spatial and temporal trends for these analytes. We found levels as high as 7370 ng/mL for the sum of all 16 PFCs (∑PFCs). Perfluorooctanesulfonate (PFOS) and perfluorodecanesulfonate (PFDS) were the most abundant analytes, making up 67% and 23% of the PFC burden, respectively. Levels of ∑PFC, PFOS, and PFDS were highest in more urban and industrial areas, moderate on Lake Superior, and low on the remote upper St. Croix River watershed. We found evidence of declines in ∑PFCs and seven analytes, including PFOS, PFDS, and perfluorooctanoic acid (PFOA); no trend in two analytes; and increases in two analytes. We argue that PFDS, a long-chained PFC with potential for high bioaccumulation and toxicity, should be considered for future animal and human studies.

Abstract  In this study, we assessed the levels of 18 perfluoroalkyl substances (PFASs) in the most widely consumed foodstuffs in Catalonia, Spain, as well as the total dietary intake of these compounds. Forty food items were analysed. Only perfluoropentanoic acid (PFPeA), perfluorohexadecanoic acid (PFHxDA) and perfluorooctanoicdecanoic acid (PFOcDA) were not detected in any sample. Perfluorooctane sulfonate (PFOS) was the compound found in the highest number of samples (33 out of 80), followed by perfluorooctanoic acid (PFOA), perfluoroheptanoic acid (PFHpA), perfluorohexane sulfonic acid (PFHxS), perfluorodecanoic acid (PFDA) and perfluorodecane sulfonic acid (PFDS). Fish and shellfish was the food group in which more PFASs were detected and where the highest PFAS concentrations were found. The highest dietary intakes corresponded to children, followed by male seniors, with values of 1787 and 1466 ng/day, respectively. For any of the age/gender groups of the population, the Tolerable Daily Intakes (TDIs) recommended by the EFSA were not exceeded. In general terms, PFAS levels found in the current study are lower than the concentrations recently reported in other countries. (C) 2012 Elsevier Ltd. All rights reserved.