Studies have shown that per-and polyfluoroalkyl substances(PFASs)may be hepatotoxic in animals or humans.However,data on clinical epidemiology are very limited.In this study,21PFASs were determined in patients with li...Studies have shown that per-and polyfluoroalkyl substances(PFASs)may be hepatotoxic in animals or humans.However,data on clinical epidemiology are very limited.In this study,21PFASs were determined in patients with liver diseases,with the highest median concentrations detected in the serum sample(26.7 ng/mL),followed by blood(10.7 ng/mL)and urine(5.02 ng/mL).Higher total PFAS concentrations were found in hepatocellular carcinoma(HCC)patients compared to non-HCC patients,with significant discrepancies in serum and blood samples.Besides,significant correlations were also found among PFAS concentrations and age,gender,body mass index(BMI),and liver function biomarkers levels.For example,PFAS concentrations are significantly higher in males than in females;Several serum PFASs concentrations increase with age and BMI,while the serum perfluorohexane sulfonic acid(PFHxS)concentrations are negatively correlated with age.In addition,multiple regression models adjusted for age,gender and BMI found that increased serum perfluorobutane sulfonic acid(PFBS),perfluoroheptane sulfonic acid(PFHpS)and perfluorohexylphosphonic acid(PFHxPA)conentrations are correlated with elevated alkaline phosphatase(ALP),aspartate aminotransferase(AST),and alpha-fetoprotein(AFP)(p<0.05).Our results provide epidemiological support for the future study on the potential clinical hepatotoxicity of PFAS.展开更多
Perfluorooctanoic acid(PFOA), its salts, and related compounds were listed as new persistent organic pollutants by the Stockholm Convention in 2019.In this study, the occurrence of residues of PFOA and other per-and p...Perfluorooctanoic acid(PFOA), its salts, and related compounds were listed as new persistent organic pollutants by the Stockholm Convention in 2019.In this study, the occurrence of residues of PFOA and other per-and polyfluoroalkyl substances(PFASs) in raw materials and fluoropolymer products from the Chinese fluoropolymer industries are reported for the first time.The PFOA concentrations in raw materials and fluoropolymer products were in the range of 6.7 to 1.1 × 10^(6) ng/g, and <MDL(method detection limit) to 5.3 × 10^(3) ng/g,respectively.Generally, the levels of PFOA in raw materials were higher than in products,implying that PFOA in the emulsion/dispersion resin could be partly removed during the polymerization or post-processing steps.By tracking a company’s polytetrafluoroethylene(PTFE) production line, it was found that over a 5 year period, the residual levels of PFOA in emulsion samples declined from 1.1 × 10^(6) to 28.4 ng/g, indicating that the contamination of PFOA in fluoropolymer products from production source gradually decreased after its use had been discontinued.High concentrations of HFPO-TrA(2.7 × 10^(5) to 8.2 × 10^(5) ng/g) were detected in some emulsion samples indicating this alternative has been widely applied in fluoropolymer manufacturing in China.展开更多
Microplastics(MPs)are recognized as vectors for the transport of organic contaminants in aquatic environments in addition to their own adverse effects on aquatic organisms.Per-and polyfluoroalkyl substances(PFASs)are ...Microplastics(MPs)are recognized as vectors for the transport of organic contaminants in aquatic environments in addition to their own adverse effects on aquatic organisms.Per-and polyfluoroalkyl substances(PFASs)are widely present in aquatic environments due to their widespread applications,and thus coexist with MPs.Therefore,we focus on the interaction of MPs and PFASs and related combined toxicity in aquatic environments in this work The adsorption of PFASs on MPs is critically reviewed,and new mechanisms such as halogen bonding,π-πinteraction,cation-πinteractions,and micelle formation are proposed.Moreover,the effect of MPs on the transport and transformation of PFASs in aquatic environments is discussed.Based on four typical aquatic organisms(shellfish,Daphnia,algae,and fish),the toxicity of MPs and/or PFASs at the organismal or molecular levels is also evaluated and summarized.Finally,challenges and research perspectives are proposed,and the roles of the shapes and aging process of MPs on PFAS biogeochemical processes and toxicity,especially on PFAS substitutes,are recommended for further investigation.This review provides a better understanding of the interactions and toxic effects of coexisting MPs and PFASs in aquatic environments.展开更多
The passive sampling technique, diffusive gradients in thin films(DGT) has attracted increasing interests as an in-situ sampler for organic contaminants including per-and polyfluoroalkyl substances(PFAS). However, its...The passive sampling technique, diffusive gradients in thin films(DGT) has attracted increasing interests as an in-situ sampler for organic contaminants including per-and polyfluoroalkyl substances(PFAS). However, its effectiveness has been questioned because of the small effective sampling area(3.1 cm^(2)). In this study, we developed a DGT probe for rapid sampling of eight PFAS in waters and applied it to a water-sediment system. It has a much larger sampling area(27 cm^(2)) and as a result lower method quantification limits(0.15 –0.21 ng/L for one-day deployment and 0.02 – 0.03 ng/L for one-week deployment) and much higher(by > 10 factors) sampling rate(100 m L/day) compared to the standard DGT(piston configuration). The sampler could linearly accumulate PFAS from wastewater, was sensitive enough even for a 24 hr deployment with performance comparable to grab sampling(500m L). The DGT probe provided homogeneous sampling performance along the large exposure area. The use of the probe to investigate distributions of dissolved PFAS around the sediment-water interface was demonstrated. This work, for the first time, demonstrated that the DGT probe is a promising monitoring tool for trace levels of PFAS and a research tool for studying their distribution, migration, and fate in aquatic environments including the sediment-water interface.展开更多
Per-and polyfluoroalkyl substances(PFAS)are found ubiquitously in wastewater treatment plants(WWTPs)due to their multiple sources in industry and consumer products.In Australia,limited spatial data are available on PF...Per-and polyfluoroalkyl substances(PFAS)are found ubiquitously in wastewater treatment plants(WWTPs)due to their multiple sources in industry and consumer products.In Australia,limited spatial data are available on PFAS levels inWWTPs influent,while no temporal data have been reported.The aim of this study was to investigate the occurrence and temporal trend of PFAS in the influent of two large WWTPs in Australia(WWTP A and B)over a four-year period.Daily influent samples were collected over one week at different seasons from 2014 to 2017.Eleven perfluoroalkyl acids(PFAA)(i.e.seven perfluoroalkyl carboxylic acids(PFCAs)and four perfluoroalkyl sulfonic acids(PFSA))were detected with mean S11PFAA concentrations of 57±3.3e94±17 ng/L at WWTP A,and 31±6.1e142±73 ng/L at WWTP B.The highest mean concentrations were observed for perfluorohexanoate(PFHxA)(20±2 ng/L)in WWTP A,and perfluorooctane sulfonate(PFOS)(17±13 ng/L)in WWTP B.The precursor 6:2 fluorotelomer sulfonate was detected over five sampling periods from Aug 2016 to Oct 2017,with mean concentrations of 37±18e138±51 ng/L for WWTP A and 8.8±4.5e29±5.1 ng/L for WWTP B.Higher concentration of 6:2 FTS(1.8e11 folds)than those of PFOA and PFOS in WWTP A indicate a likely substitution of C8 PFAA by fluorotelomer-based PFAS in this catchment.Temporal trends(annual and seasonal)in per-capita mass load were observed for some PFAA,increasing for PFPeA,PFHxA,PFHpA,PFNA,and PFHxS,while decreasing for PFBS and PFOS in either WWTPs.Notably,elevated levels of PFOS in October 2017 were observed at both WWTPs with the highest per capita mass load of up to 67 mg/day/inhabitant.For some PFAS release trends,longer sampling periods would be required to achieve acceptable statistical power.展开更多
全氟/多氟化合物(Perfluorinated and Polyfluoroalkyl Substances,PFAS)是食品接触制品中的高风险物质,由它引起的食品安全不容忽视。本文通过分析我国、欧盟和美国对食品接触制品中PFAS的管控法规的差异分析,发现各国对PFAS管控物质...全氟/多氟化合物(Perfluorinated and Polyfluoroalkyl Substances,PFAS)是食品接触制品中的高风险物质,由它引起的食品安全不容忽视。本文通过分析我国、欧盟和美国对食品接触制品中PFAS的管控法规的差异分析,发现各国对PFAS管控物质和适用范围、管控力度的要求不尽相同。我国更强调对全氟辛酸(Perfluorooctanoic Acid,PFOA)和全氟辛烷磺酸(Perfluorooctane Sulphonate,PFOS)两个物质的管控,美国和欧盟更强调对整体物质的管控。我国和欧盟管控范围是适用于PFAS可能涉及的所有行业,美国更侧重食品包装和纺织品等轻工行业。因此,相关企业尤其是食品接触材料制品企业应高度警觉,积极对标国际要求,并主动研发不含氟的PFAS替代品。展开更多
基金supported by the National Natural Science Foundation of China(No.42177408)Guangdong(China)Innovative and Entrepreneurial Research Team Program(No.2016ZT06N258)。
文摘Studies have shown that per-and polyfluoroalkyl substances(PFASs)may be hepatotoxic in animals or humans.However,data on clinical epidemiology are very limited.In this study,21PFASs were determined in patients with liver diseases,with the highest median concentrations detected in the serum sample(26.7 ng/mL),followed by blood(10.7 ng/mL)and urine(5.02 ng/mL).Higher total PFAS concentrations were found in hepatocellular carcinoma(HCC)patients compared to non-HCC patients,with significant discrepancies in serum and blood samples.Besides,significant correlations were also found among PFAS concentrations and age,gender,body mass index(BMI),and liver function biomarkers levels.For example,PFAS concentrations are significantly higher in males than in females;Several serum PFASs concentrations increase with age and BMI,while the serum perfluorohexane sulfonic acid(PFHxS)concentrations are negatively correlated with age.In addition,multiple regression models adjusted for age,gender and BMI found that increased serum perfluorobutane sulfonic acid(PFBS),perfluoroheptane sulfonic acid(PFHpS)and perfluorohexylphosphonic acid(PFHxPA)conentrations are correlated with elevated alkaline phosphatase(ALP),aspartate aminotransferase(AST),and alpha-fetoprotein(AFP)(p<0.05).Our results provide epidemiological support for the future study on the potential clinical hepatotoxicity of PFAS.
基金supported by the National Natural Science Foundation of China (No.21625702)。
文摘Perfluorooctanoic acid(PFOA), its salts, and related compounds were listed as new persistent organic pollutants by the Stockholm Convention in 2019.In this study, the occurrence of residues of PFOA and other per-and polyfluoroalkyl substances(PFASs) in raw materials and fluoropolymer products from the Chinese fluoropolymer industries are reported for the first time.The PFOA concentrations in raw materials and fluoropolymer products were in the range of 6.7 to 1.1 × 10^(6) ng/g, and <MDL(method detection limit) to 5.3 × 10^(3) ng/g,respectively.Generally, the levels of PFOA in raw materials were higher than in products,implying that PFOA in the emulsion/dispersion resin could be partly removed during the polymerization or post-processing steps.By tracking a company’s polytetrafluoroethylene(PTFE) production line, it was found that over a 5 year period, the residual levels of PFOA in emulsion samples declined from 1.1 × 10^(6) to 28.4 ng/g, indicating that the contamination of PFOA in fluoropolymer products from production source gradually decreased after its use had been discontinued.High concentrations of HFPO-TrA(2.7 × 10^(5) to 8.2 × 10^(5) ng/g) were detected in some emulsion samples indicating this alternative has been widely applied in fluoropolymer manufacturing in China.
基金funded by the National Natural Science Foundation of China(Nos.U2106213,41907332,and 42192572)the National Postdoctoral Program for Innovative Talents of China(BX20190306)+2 种基金the Taishan Scholars Program of Shandong Province(China)(tsqn201909051)the Fundamental Research Funds for the Central Universities(China)(202141003)the USDA Hatch Program(USA)(MAS 00549).
文摘Microplastics(MPs)are recognized as vectors for the transport of organic contaminants in aquatic environments in addition to their own adverse effects on aquatic organisms.Per-and polyfluoroalkyl substances(PFASs)are widely present in aquatic environments due to their widespread applications,and thus coexist with MPs.Therefore,we focus on the interaction of MPs and PFASs and related combined toxicity in aquatic environments in this work The adsorption of PFASs on MPs is critically reviewed,and new mechanisms such as halogen bonding,π-πinteraction,cation-πinteractions,and micelle formation are proposed.Moreover,the effect of MPs on the transport and transformation of PFASs in aquatic environments is discussed.Based on four typical aquatic organisms(shellfish,Daphnia,algae,and fish),the toxicity of MPs and/or PFASs at the organismal or molecular levels is also evaluated and summarized.Finally,challenges and research perspectives are proposed,and the roles of the shapes and aging process of MPs on PFAS biogeochemical processes and toxicity,especially on PFAS substitutes,are recommended for further investigation.This review provides a better understanding of the interactions and toxic effects of coexisting MPs and PFASs in aquatic environments.
基金supported by the Key Deployment Project of Centre for Ocean Mega-Research of Science, Chinese Academy of Sciences (No. COMS2019J08)the Guangzhou Municipal Science and Technology Project (No. 201904010291)+1 种基金National Natural Science Foundation of China (No. 21806042)Guangdong Provincial Key Laboratory of Chemical Pollution and Environmental Safety (No. 2019B030301008)。
文摘The passive sampling technique, diffusive gradients in thin films(DGT) has attracted increasing interests as an in-situ sampler for organic contaminants including per-and polyfluoroalkyl substances(PFAS). However, its effectiveness has been questioned because of the small effective sampling area(3.1 cm^(2)). In this study, we developed a DGT probe for rapid sampling of eight PFAS in waters and applied it to a water-sediment system. It has a much larger sampling area(27 cm^(2)) and as a result lower method quantification limits(0.15 –0.21 ng/L for one-day deployment and 0.02 – 0.03 ng/L for one-week deployment) and much higher(by > 10 factors) sampling rate(100 m L/day) compared to the standard DGT(piston configuration). The sampler could linearly accumulate PFAS from wastewater, was sensitive enough even for a 24 hr deployment with performance comparable to grab sampling(500m L). The DGT probe provided homogeneous sampling performance along the large exposure area. The use of the probe to investigate distributions of dissolved PFAS around the sediment-water interface was demonstrated. This work, for the first time, demonstrated that the DGT probe is a promising monitoring tool for trace levels of PFAS and a research tool for studying their distribution, migration, and fate in aquatic environments including the sediment-water interface.
基金The authors would like to thank Sharon Grant,Jake O'Brien,Ben Tscharke and Rachel Mackie for organizing sample collection and providing data.Hue T.Nguyen is also grateful to Christine M.Baduel for LC/MS-MS analytical training.Hue T.Nguyen is supported by an Australian Award Scholarship granted by Australian Department of Foreign Affairs and Trade.Jochen F.Mueller is funded by a UQ Fellowship.
文摘Per-and polyfluoroalkyl substances(PFAS)are found ubiquitously in wastewater treatment plants(WWTPs)due to their multiple sources in industry and consumer products.In Australia,limited spatial data are available on PFAS levels inWWTPs influent,while no temporal data have been reported.The aim of this study was to investigate the occurrence and temporal trend of PFAS in the influent of two large WWTPs in Australia(WWTP A and B)over a four-year period.Daily influent samples were collected over one week at different seasons from 2014 to 2017.Eleven perfluoroalkyl acids(PFAA)(i.e.seven perfluoroalkyl carboxylic acids(PFCAs)and four perfluoroalkyl sulfonic acids(PFSA))were detected with mean S11PFAA concentrations of 57±3.3e94±17 ng/L at WWTP A,and 31±6.1e142±73 ng/L at WWTP B.The highest mean concentrations were observed for perfluorohexanoate(PFHxA)(20±2 ng/L)in WWTP A,and perfluorooctane sulfonate(PFOS)(17±13 ng/L)in WWTP B.The precursor 6:2 fluorotelomer sulfonate was detected over five sampling periods from Aug 2016 to Oct 2017,with mean concentrations of 37±18e138±51 ng/L for WWTP A and 8.8±4.5e29±5.1 ng/L for WWTP B.Higher concentration of 6:2 FTS(1.8e11 folds)than those of PFOA and PFOS in WWTP A indicate a likely substitution of C8 PFAA by fluorotelomer-based PFAS in this catchment.Temporal trends(annual and seasonal)in per-capita mass load were observed for some PFAA,increasing for PFPeA,PFHxA,PFHpA,PFNA,and PFHxS,while decreasing for PFBS and PFOS in either WWTPs.Notably,elevated levels of PFOS in October 2017 were observed at both WWTPs with the highest per capita mass load of up to 67 mg/day/inhabitant.For some PFAS release trends,longer sampling periods would be required to achieve acceptable statistical power.
