Cargando…

Oral repeated-dose systemic and reproductive toxicity of 6:2 fluorotelomer alcohol in mice

6:2 fluorotelomer alcohol (6:2 FTOH) was evaluated for potential systemic repeated-dose and reproductive toxicity in mice. 6:2 FTOH was administered by oral gavage to CD-1 mice as a suspension in 0.5% aqueous methylcellulose with 0.1% Tween-80 at dosages of 1, 5, 25, or 100 mg/kg/day. The no-observe...

Descripción completa

Detalles Bibliográficos
Autores principales: Mukerji, Pushkor, Rae, Jessica Caverly, Buck, Robert C., O’Connor, John C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5598097/
https://www.ncbi.nlm.nih.gov/pubmed/28962345
http://dx.doi.org/10.1016/j.toxrep.2014.12.002
_version_ 1783263832883331072
author Mukerji, Pushkor
Rae, Jessica Caverly
Buck, Robert C.
O’Connor, John C.
author_facet Mukerji, Pushkor
Rae, Jessica Caverly
Buck, Robert C.
O’Connor, John C.
author_sort Mukerji, Pushkor
collection PubMed
description 6:2 fluorotelomer alcohol (6:2 FTOH) was evaluated for potential systemic repeated-dose and reproductive toxicity in mice. 6:2 FTOH was administered by oral gavage to CD-1 mice as a suspension in 0.5% aqueous methylcellulose with 0.1% Tween-80 at dosages of 1, 5, 25, or 100 mg/kg/day. The no-observed-adverse-effect level (NOAEL) for systemic toxicity was 25 mg/kg/day (males) and 5 mg/kg/day (females), based on effects at higher doses on mortality, clinical observations, body weight, nutritional parameters, hematology (red and white blood cell), clinical chemistry (liver-related), liver weights, and histopathology (liver, teeth, reproductive tract, and mammary gland). However, 6:2 FTOH was not a selective reproductive toxicant. The NOAEL for reproductive toxicity was >100 mg/kg/day; no effects on reproductive outcome were observed at any dosage. The NOAEL for viability and growth of the offspring was 25 mg/kg/day, based on clinical signs of delayed maturation in pups, and reductions in pup survival and pup body weight during lactation at 100 mg/kg/day. While the severity of the effects was generally greater in mice than previously reported in CD rats, the overall NOAELs were identical in both species, 5 mg/kg/day for systemic toxicity and 25 mg/kg/day for offspring viability/growth. 6:2 FTOH was not a selective reproductive toxicant in either species; no effects on reproductive outcome occurred at any dose level, and any effects observed in offspring occurred at dose levels that induced mortality and severe toxicity in maternal animals.
format Online
Article
Text
id pubmed-5598097
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-55980972017-09-28 Oral repeated-dose systemic and reproductive toxicity of 6:2 fluorotelomer alcohol in mice Mukerji, Pushkor Rae, Jessica Caverly Buck, Robert C. O’Connor, John C. Toxicol Rep Article 6:2 fluorotelomer alcohol (6:2 FTOH) was evaluated for potential systemic repeated-dose and reproductive toxicity in mice. 6:2 FTOH was administered by oral gavage to CD-1 mice as a suspension in 0.5% aqueous methylcellulose with 0.1% Tween-80 at dosages of 1, 5, 25, or 100 mg/kg/day. The no-observed-adverse-effect level (NOAEL) for systemic toxicity was 25 mg/kg/day (males) and 5 mg/kg/day (females), based on effects at higher doses on mortality, clinical observations, body weight, nutritional parameters, hematology (red and white blood cell), clinical chemistry (liver-related), liver weights, and histopathology (liver, teeth, reproductive tract, and mammary gland). However, 6:2 FTOH was not a selective reproductive toxicant. The NOAEL for reproductive toxicity was >100 mg/kg/day; no effects on reproductive outcome were observed at any dosage. The NOAEL for viability and growth of the offspring was 25 mg/kg/day, based on clinical signs of delayed maturation in pups, and reductions in pup survival and pup body weight during lactation at 100 mg/kg/day. While the severity of the effects was generally greater in mice than previously reported in CD rats, the overall NOAELs were identical in both species, 5 mg/kg/day for systemic toxicity and 25 mg/kg/day for offspring viability/growth. 6:2 FTOH was not a selective reproductive toxicant in either species; no effects on reproductive outcome occurred at any dose level, and any effects observed in offspring occurred at dose levels that induced mortality and severe toxicity in maternal animals. Elsevier 2014-12-15 /pmc/articles/PMC5598097/ /pubmed/28962345 http://dx.doi.org/10.1016/j.toxrep.2014.12.002 Text en © 2014 The Authors http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/).
spellingShingle Article
Mukerji, Pushkor
Rae, Jessica Caverly
Buck, Robert C.
O’Connor, John C.
Oral repeated-dose systemic and reproductive toxicity of 6:2 fluorotelomer alcohol in mice
title Oral repeated-dose systemic and reproductive toxicity of 6:2 fluorotelomer alcohol in mice
title_full Oral repeated-dose systemic and reproductive toxicity of 6:2 fluorotelomer alcohol in mice
title_fullStr Oral repeated-dose systemic and reproductive toxicity of 6:2 fluorotelomer alcohol in mice
title_full_unstemmed Oral repeated-dose systemic and reproductive toxicity of 6:2 fluorotelomer alcohol in mice
title_short Oral repeated-dose systemic and reproductive toxicity of 6:2 fluorotelomer alcohol in mice
title_sort oral repeated-dose systemic and reproductive toxicity of 6:2 fluorotelomer alcohol in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5598097/
https://www.ncbi.nlm.nih.gov/pubmed/28962345
http://dx.doi.org/10.1016/j.toxrep.2014.12.002
work_keys_str_mv AT mukerjipushkor oralrepeateddosesystemicandreproductivetoxicityof62fluorotelomeralcoholinmice
AT raejessicacaverly oralrepeateddosesystemicandreproductivetoxicityof62fluorotelomeralcoholinmice
AT buckrobertc oralrepeateddosesystemicandreproductivetoxicityof62fluorotelomeralcoholinmice
AT oconnorjohnc oralrepeateddosesystemicandreproductivetoxicityof62fluorotelomeralcoholinmice