2022
DOI: 10.1016/j.envint.2022.107108
|View full text |Cite
|
Sign up to set email alerts
|

Human exposure to F-53B in China and the evaluation of its potential toxicity: An overview

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
5

Citation Types

0
24
0

Year Published

2022
2022
2024
2024

Publication Types

Select...
9

Relationship

0
9

Authors

Journals

citations
Cited by 68 publications
(24 citation statements)
references
References 95 publications
0
24
0
Order By: Relevance
“…Emerging PFASs that are currently receiving much attention include short-chain perfluoroalkyl acids (PFAAs), hexafluoropropylene oxide dimer acid (HFPO-DA), 6:2 fluorotelomer sulfonic acid (6:2 FTS), and 9-chlorohexadecafluoro-3-oxanonane-1-sulfonic acid (6:2 F-53B). Toxicological investigations have shown that 6:2 F-53B has potential bioaccumulation and endocrine disrupting effects, causing liver damage and activating the peroxisome proliferator-activated receptor pathway in the kidney. This alternative was revealed to be even stronger biological toxicity than PFOS. HFPO-DA also exhibited hepatotoxicity comparable to PFOA, while 6:2 FTS showed clear bioaccumulation and moderate hepatotoxic effects. , The high mobility and adverse toxicological implications of short-chain potassium perfluorobutane sulfonic acid (PFBS) could result in important issues for health and the environment. , …”
Section: Introductionmentioning
confidence: 99%
“…Emerging PFASs that are currently receiving much attention include short-chain perfluoroalkyl acids (PFAAs), hexafluoropropylene oxide dimer acid (HFPO-DA), 6:2 fluorotelomer sulfonic acid (6:2 FTS), and 9-chlorohexadecafluoro-3-oxanonane-1-sulfonic acid (6:2 F-53B). Toxicological investigations have shown that 6:2 F-53B has potential bioaccumulation and endocrine disrupting effects, causing liver damage and activating the peroxisome proliferator-activated receptor pathway in the kidney. This alternative was revealed to be even stronger biological toxicity than PFOS. HFPO-DA also exhibited hepatotoxicity comparable to PFOA, while 6:2 FTS showed clear bioaccumulation and moderate hepatotoxic effects. , The high mobility and adverse toxicological implications of short-chain potassium perfluorobutane sulfonic acid (PFBS) could result in important issues for health and the environment. , …”
Section: Introductionmentioning
confidence: 99%
“…Per- and polyfluoroalkyl substances (PFASs) emerged in industrial production in the 1940s . PFASs possess important chemical properties and are used in various consumer products, such as cosmetics, food packaging, textiles, and nonstick cookware, inevitably resulting in ubiquitous environmental contamination and human exposure. , Epidemiological and toxicological studies suggest that PFAS exposure can lead to various adverse health effects, including hepatoxicity, reproductive toxicity, developmental toxicity, cardiovascular risk, and endocrine disruption effects. Due to their remarkable toxicity, persistence, and bioaccumulation, various PFASs have been listed in the Stockholm Convention on Persistent Organic Pollutants (). In recent years, the Chinese government has been making efforts on emerging pollutant control.…”
Section: Introductionmentioning
confidence: 99%
“…4,5 Recent studies have suggested that these substitutes may have similar environmental fate and health effects like the legacy PFAS. 3,6,7 Pregnant women were perhaps vulnerable to exposure to PFAS via drinking water and dietary intake, 3,7 and their wide exposure to PFAS had been reported from different countries and regions, which aroused health concerns. 8−10 While the declining temporal trends of prenatal legacy PFAS exposure were observed in German (1982−2019), 11 Japanese (2003− 2012), 12 and Chinese (1998−2018) population, 13 many PFAS were frequently detected in serum with a half-life of years (e.g., 7.7 years for PFOS and 18.5 years for 6:2 Cl-PFESA).…”
Section: ■ Introductionmentioning
confidence: 99%
“…The main substitutes comprised of short-chain congeners [ e.g. , perfluorobutanoic acid (PFBA) and perfluorohexanoic acid (PFHxA)] and perfluoroalkyl ether substitutes such as 6:2 chlorinated polyfluorinated ether sulfonate (6:2 Cl-PFESA) and 8:2 Cl-PFESA. , Recent studies have suggested that these substitutes may have similar environmental fate and health effects like the legacy PFAS. ,, …”
Section: Introductionmentioning
confidence: 99%