Levels, distributions, and sources of legacy and novel per- and perfluoroalkyl substances (PFAS) in the topsoil of Tianjin, China.

Soil is a major sink for per- and perfluoroalkyl substances (PFAS), wherein PFAS may be transferred through the food chain to predators at upper trophic levels, which poses a threat to human health. Herein, the concentrations and distributions of legacy and novel PFAS in topsoil samples from different functional areas in Tianjin were comprehensively investigated. Seventeen PFAS congeners were identified, with concentrations ranging from 0.21 ng/g to 5.35 ng/g, with a mean concentration of 1.25 ng/g. The main PFAS in the topsoil was perfluorooctanoic acid (PFOA). 6:2 chlorinated polyfluorinated ether sulfonate (6:2 Cl-PFESA; C8) were the major sources (43.4%), followed by food packaging as well as coating materials (25.5%). In addition, Spearman correlation analysis and the structural equation model showed that population density significantly impacted the PFAS distribution in the topsoil of Tianjin.

Determination of oxylipins and their precursors in breast milk by solid phase extraction-ultra high performance liquid chromatography-triple quadrupole tandem mass spectrometry.

Oxylipins and their precursors (long-chain polyunsaturated fatty acids, LCPUFAs) are key intercellular signaling molecules influencing the inflammatory response. Each oxylipin has pro- and/or anti-inflammatory effects, and the relative abundance of different oxylipins can alter the inflammatory balance, making it important to clarify the oxylipin profile of breast milk for optimal infant health. The extraction, identification, and simultaneous quantification of oxylipins in breast milk are challenging due to the structural similarity, limited stability, and the low endogenous concentration of oxylipins and the complex matrix of breast milk. This study aimed to develop a solid phase extraction-ultra high performance liquid chromatography-triple quadrupole tandem mass spectrometry (SPE-UPLC-MS/MS) method for the comprehensive and specific quantification of oxylipins and their precursors in breast milk. The LC conditions (including column, mobile phase, and gradient conditions) and SPE procedure (including SPE cartridges, elution solvent, and elution volume) were optimized to achieve accurate quantification and better analyte recovery. A single 18-minute chromatographic run allows for the quantification of 20 oxylipins and 5 PUFAs. The results showed good linearity (R2 > 0.99) over the concentration range of 2 to 100 ng/mL, with the instrument detection limits ranging from 0.01 to 0.90 ng/mL for oxylipins and 0.02 to 0.59 ng/mL for PUFAs. The method is rapid, sensitive, and reproducible (RSD ≤ 10%) and is suitable for the quantitative analysis of oxylipins and their precursors in infant formula samples.

PFAS-induced lipidomic dysregulations and their associations with developmental toxicity in zebrafish embryos.

Per- and polyfluoroalkyl substances (PFASs) are persistent environmental contaminants, posing developmental toxicity to fish and human. PFAS-induced lipid metabolism disorders were demonstrated using the zebrafish (Danio rerio) embryo model, but the detailed changes of lipid compositions and the influence of these changes on the biological development are still unclear. Herein, lipidomics analysis was performed to reveal the dysregulations of lipid metabolism in zebrafish embryos exposed to perfluorooctanoic acid (PFOA) or perfluorooctane sulfonate (PFOS) through microinjection. Various abnormal phenotypes were observed, including heart bleeding, pericardium edema, spinal curvature and increased heart rate at 72 h after fertilization, especially in the PFOS exposure groups. Lipidomic profiling found downregulated phosphatidylethanolamines in the PFAS-exposed embryos, especially those containing a docosahexaenoyl (DHA) chain, indicating an excessive oxidative damage to the embryos. Glycerolipids were mainly upregulated in the PFOA groups but downregulated in the PFOS groups. These aberrations may reflect oxidative stress, energy metabolism malfunction and proinflammatory signals induced by PFASs. However, supplement of DHA may not be effective in recovering the lipidomic dysregulations and protecting from the developmental toxicity induced by PFASs, showing the complexity of the toxicological mechanisms. This work has revealed the associations between the abnormal phenotypes and dysregulations of lipid metabolism in zebrafish embryos induced by PFASs from the aspect of lipidomics, and discovered the underlying molecular mechanisms of the developmental toxicity of PFASs.

Assessment of perfluorohexane sulfonic acid (PFHxS)-related compounds degradation potential: Computational and experimental approaches.

Perfluorohexane sulfonic acid (PFHxS) and PFHxS-related compounds are listed in Annex A of the Stockholm Convention without specific exemptions. Substances that potentially degrade to PFHxS are considered as their related compounds. Unfortunately, the degradation behavior of PFHxS precursors, an important basis for the corresponding chemical regulation, remains unclear. Herein, based on the hypothesis that bond dissociation enthalpy (BDE) is the determining factor for the degradation of PFHxS precursors, the BDE of PFHxS-related precursors to produceC6F13SO2-groups was calculated. In addition, quantitative structure-activity relationship models based on partial least squares, partial least squares discrimination analysis, and support vector machine algorithms were developed to predict the BDE of 48 PFHxS precursors and distinguish the precursors with different degradation potential. Subsequent photodegradation experiments demonstrated that the order of degradation rates was consistent with that predicted by theoretical models. Importantly, perfluorohexanoic acid (PFHxA) and perfluorobutanoic acid, and not PFHxS, were detected as the degradation products of potential PFHxS precursors. Sulfonamides, phenyl unit, and other radicals in the non-nucleus part of PFHxS precursors were identified as the critical molecular segments that affect their degradation potential. Ultimately, by comparing BDE values, it was theoretically speculated that PFHxS related compounds exhibit a greater potential to generate PFHxA than PFHxS. Results in this study indicated for the first time that not all the compounds containing C6F13SO2- groups were guaranteed to degrade into PFHxS under natural conditions.

Legacy and emerging per- and polyfluoroalkyl substances (PFAS) in sediments from the East China Sea and the Yellow Sea: Occurrence, source apportionment and environmental risk assessment.

The Yellow Sea (YS), the East China Sea (ECS) and their coastal areas have undergone rapid urbanization and industrialization. These areas are important sinks for many persistent organic pollutants. In this study, the concentration of legacy and emerging per- and polyfluoroalkyl substances (PFAS) in marine sediments from the YS and ECS were investigated. Nineteen PFAS were identified, ranging in concentration from 0.21 ng/g to 4.74 ng/g (mean: 1.60 ng/g). Legacy long-chain PFAS [e.g., perfluorooctanoic acid (PFOA), perfluorononanoic acid (PFNA), and perfluorooctane sulfonate (PFOS)] were the dominant contaminants. Alternative PFAS such as 6:2 chlorinated polyfluorinated ether sulfonate (6:2 Cl-PFESA) and 2,3,3,3-tetrafluoro-2-(1,1,2,2,3,3,3-heptafluoropropoxy) propanoic acid (HFPO-DA) were identified within the detection range of 16%-100%. HFPO-DA was measured in all sediments in equivalent levels to PFOS (0.119 ng/g and 0.139 ng/g, respectively). This is the first reported occurrence of perfluoro-1-butanesulfonamide (FBSA) and HFPO-DA in marine sediments, indicating a replacement in the production of PFAS from legacy to emerging ones along with eastern coastal cities of China. The results of the potential source identification demonstrated that metal plating plants, textile treatments, fluoropolymer products, food packaging, and the degradation of volatile precursor substances were the main sources of PFAS in the ECS and YS. The environmental risk assessment based on the risk quotient demonstrated that PFOA and PFOS in the ECS and YS may present a low to medium risk at most sampling points.

Legacy and emerging per- and polyfluoroalkyl substances (PFAS) in the Bohai Sea and its inflow rivers.

In this study, the occurrence, distribution, sources, and risk of 29 legacy and emerging per- and polyfluoroalkyl substances (PFAS) in four kinds of environmental matrices in the Bohai Sea were investigated. The ∑PFAS concentrations were in the range of 0.40 ~ 61.4 ng/g dry weight (dw) in inflow river sediments, 0.48 ~ 61.4 ng/g dw in soil near river inflow, 0.37 ~ 4.18 ng/g dw in sea sediments, and 13.3 ~ 718 ng/L in seawater. PFAS with eight carbons accounted for > 62.2% by mass, in all samples. Perfluorooctanoic acid (PFOA) was the dominant PFAS both by mass and occurrence. Seawater from Laizhou Bay (south of the Bohai Sea) and sediments of Liaodong Bay (northeast of the Bohai Sea) had the highest levels of ∑PFAS. The sediment-water partition coefficient and organic carbon content normalized partition coefficient (log Kd and log Koc) were calculated using measured PFAS concentrations to determine their distribution in seawater and sea sediments. The values of log Kd and log Koc values increased with the increasing CF2 units for perfluoroalkyl carboxylic acids (PFCAs) and perfluoroalkane sulfonic acids (PFSAs). Six primary sources were identified in this region, including aqueous film-forming foams (AFFF), metal plating, food packages, fluorine chemical industry, fluoropolymer manufacture, and domestic pollution. The risk quotient (RQ) values of PFAS were all < 1, indicating that organisms of the Bohai Sea were at low risk of PFAS exposure.

Temporal trends of novel brominated flame retardants in mollusks from the Chinese Bohai Sea (2011-2018).

Novel brominated flame retardants (NBFRs) have emerged as an alternative to traditional brominated flame retardants (BFRs); however, they may pose risks to the environment and human health. To investigate the occurrence, temporal trends, and human exposure of seven typical NBFRs (∑7 NBFRs), seven species of mollusks (n = 329) were collected from coastal cities in the Chinese Bohai Sea area from 2011 to 2018. The ∑7 NBFRs ranged from 1.52 to 154 ng/g dry weight (dw) (mean: 14.9 ± 21.21 ng/g dw), higher than in other areas worldwide. Decabromodiphenylethane (DBDPE) was the main contaminant, contributing to 33% of the NBFRs. Temporal trends indicate that the DBDPE and 2,3-dibromopropyl-2,4,6-tribromophenyl ether (DPTE) concentrations in mollusks increased significantly (P < 0.05) at rates of about 26% and 5.4%, respectively. This suggests that these NBFRs are continuously released into the environment of the Bohai Sea area. The higher NBFR concentrations in the southern sampling sites relative to the northern sampling sites were consistent with the spatial distribution of the NBFR industry in the Bohai Rim Economic Circle. Chlamys farreri possessed the highest ∑7 NBFR concentrations compared with the other species, while the lowest concentrations were found in Neverita didyma and Rapana venosa, suggesting interspecific differences in bioaccumulation. The estimated daily intake of NBFRs was low, and as the main contaminant, DBDPE was unlikely to pose significant human health risks. Overall, this is the first study to comprehensively assess the occurrence, spatial distribution, and temporal trends of NBFRs in mollusks.

Effect of traditional Chinese medicine injections on severe pneumonia: A protocol for systematic review and meta-analysis.

BACKGROUND: Traditional Chinese medicine injections (TCMJ) used in the treatment of severe pneumonia have been widely implemented in clinical practice, but their overall efficacy and safety remain unclear. This paper aims to evaluate the efficacy and safety of TCMJ in the treatment of severe pneumonia. METHODS: PubMed, EMbase, Cochrane Library, Web of Science, China National Knowledge Infrastructure, WanFang, and the Chongqing VIP Chinese Science and Technology Periodical Database were all searched for randomized controlled trials focusing on the administration of TCMJ for severe pneumonia. Two researchers independently screened titles, abstracts, full texts, and extracted relevant data. The RevMan 5.3 software (The Cochrane Collaboration, Software Update, Oxford, UK) and Stata 14 software (STATA Corporation, College Station, TX) were used for statistical analysis. RESULTS: This study summarizes the related randomized controlled trials to assess the effect and safety of TCMJ in the treatment of severe pneumonia. CONCLUSION: This article provides theoretical support for the clinical application of TCMJ in the treatment of severe pneumonia. PROSPERO REGISTRATION NUMBER: CRD42020185072.

Acidianus tengchongensis sp. nov., a new species of acidothermophilic archaeon isolated from an acidothermal spring.

A new thermoacidophilic, obligately chemolithotrophic, facultatively aerobic archaeon Acidianus S5(T), was isolated from a Tengchong acidothermal spring in southwestern China. It is a Gram-negative, nonmotile, irregular coccoid organism with a cell diameter of 1.2 microm. The optimal pH and temperature for growth are 2.5 and 70 degrees C, respectively. Under anaerobic conditions, the organism reduces elemental sulfur with molecular hydrogen, producing hydrogen sulfide. Under aerobic conditions, it oxidizes elemental sulfur and produces sulfuric acid. No growth occurs when it is cultivated in an iron medium, indicating that ferrous iron cannot serve as an energy source. The G+C content is 38% (mol/mol), which is much different from that of other Acidianus species (31%-32.7%). The phylogenetic distances, based on 16S rDNA sequences, to A. brierleyi, A. infernus, and A. ambivalens were 0.2, 2.6, and 2.5%, respectively. DNA-DNA hybridization rates of strain S5(T) to A. brierleyi, A. infernus, and A. ambivalens are 44, 22, and 23%, respectively. Thus, a new name, Acidianus tengchongensis sp. nov., is proposed for this strain S5(T).