Cytotoxicity of novel fluorinated alternatives to long-chain perfluoroalkyl substances to human liver cell line and their binding capacity to human liver fatty acid binding protein.
Arch Toxicol
; 92(1): 359-369, 2018 Jan.
Article
in En
| MEDLINE
| ID: mdl-28864880
ABSTRACT
Although shorter chain homologues and other types of fluorinated chemicals are currently used as alternatives to long-chain perfluoroalkyl substances (PFASs), their safety information remains unclear and urgently needed. Here, the cytotoxicity of several fluorinated alternatives (i.e., 62 fluorotelomer carboxylic acid (62 FTCA), 62 fluorotelomer sulfonic acid (62 FTSA), 62 chlorinated polyfluorinated ether sulfonate (62 Cl-PFESA), and hexafluoropropylene oxide (HFPO) homologues) to human liver HL-7702 cell line were measured and compared with perfluorooctanoic acid (PFOA) and perfluorooctane sulfonate (PFOS). Their binding mode and affinity to human liver fatty acid binding protein (hL-FABP) were also determined. Compared with PFOA and PFOS, 62 Cl-PFESA, HFPO trimer acid (HFPO-TA), HFPO tetramer acid (HFPO-TeA), and 62 FTSA showed greater toxic effects on cell viabilities. At low exposure doses, these alternatives induced cell proliferation with similar mechanism which was different from that of PFOA and PFOS. Furthermore, binding affinity to hL-FABP decreased in the order of 62 FTCA < 62 FTSA < HFPO dimer acid (HFPO-DA) < PFOA < PFOS/62 Cl-PFESA/HFPO-TA. Due to their distinctive structure, 62 Cl-PFESA and HFPO homologues were bound to the hL-FABP inner pocket with unique binding modes and higher binding energy compared with PFOA and PFOS. This research enhances our understanding of the toxicity of PFAS alternatives during usage and provides useful evidence for the development of new alternatives.
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Fatty Acid-Binding Proteins
/
Fluorocarbons
Limits:
Humans
Language:
En
Journal:
Arch Toxicol
Year:
2018
Document type:
Article