Literature DB >> 31344372

Toxicokinetics and bioavailability of sulfolane, a ground water contaminant, following oral and intravenous administration in rodents: A dose, species, and sex comparison.

Suramya Waidyanatha1, Sherry R Black2, Timothy R Fennell2, Scott L Watson2, Purvi R Patel2, Stephen D Cooper2, James Blake2, Veronica Godfrey Robinson3, Reshan A Fernando2, Chad R Blystone3.   

Abstract

Sulfolane is a ground water contaminant near refinery sites. The objective of this work was to investigate the toxicokinetics and bioavailability of sulfolane in male and female Harlan Hsd:Sprague Dawley® SD® rats and B6C3F1/N mice following a single oral administration of 10, 30, or 100 mg/kg. Sulfolane was rapidly absorbed in rats with the maximum plasma concentration, Cmax, reached at ≤1.47 h. Although Cmax increased proportionally to the dose, the half-life of elimination increased with the dose and the area under the concentration versus time curve (AUC) increased more than proportionally to the dose. In male and female rats, plasma elimination half-life increased with the dose from 1.97 to 6.33 h. Absorption of sulfolane in mice following oral administration was more rapid than in rats with Cmax reached at ≤0.55 h. In addition, mice had a shorter half-life (≤ 1.25 h) and a lower AUC than rats. In male and female mice, both Cmax and AUC increased more than proportionally to the dose. Bioavailability of sulfolane was higher in rats (81-83%) than mice (59-63%) at 10 mg/kg; at 30 and 100 mg/kg, bioavailability >100% in both species and sexes suggesting that the saturation of metabolism and clearance processes of sulfolane may begin at a single oral dose of ~30 mg/kg. There was no apparent sex difference in toxicokinetic parameters of sulfolane in rats and mice. These data demonstrate that sulfolane was well-absorbed following oral administration with high bioavailability in rats and mice with some species differences, but no sex difference. Published by Elsevier Inc.

Entities:  

Keywords:  Bioavailability; Rodents; Sulfolane; Toxicokinetics

Mesh:

Substances:

Year:  2019        PMID: 31344372      PMCID: PMC7179091          DOI: 10.1016/j.taap.2019.114690

Source DB:  PubMed          Journal:  Toxicol Appl Pharmacol        ISSN: 0041-008X            Impact factor:   4.219


  9 in total

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3.  Disposition and metabolism of sulfolane in Harlan Sprague Dawley rats and B6C3F1/N mice and in vitro in hepatocytes from rats, mice, and humans.

Authors:  Suramya Waidyanatha; Sherry R Black; Chad R Blystone; Purvi R Patel; Scott L Watson; Rodney W Snyder; Timothy R Fennell
Journal:  Xenobiotica       Date:  2019-07-05       Impact factor: 1.908

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Journal:  Pharm Res       Date:  1993-07       Impact factor: 4.200

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Journal:  J Anal Toxicol       Date:  2019-07-24       Impact factor: 3.367

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  9 in total
  2 in total

1.  Comparison of sulfolane effects in Sprague Dawley rats, B6C3F1/N mice, and Hartley guinea pigs after 28 days of exposure via oral gavage.

Authors:  K A Shipkowski; M C Cora; M F Cesta; V G Robinson; S Waidyanatha; K L Witt; M K Vallant; D M Fallacara; M R Hejtmancik; S A Masten; S D Cooper; R A Fernando; C R Blystone
Journal:  Toxicol Rep       Date:  2021-02-06

2.  Immunotoxicity studies of sulfolane following developmental exposure in Hsd:Sprague Dawley SD rats and adult exposure in B6C3F1/N mice.

Authors:  AtLee T D Watson; Victor J Johnson; Michael I Luster; Gary R Burleson; Dawn M Fallacara; Barney R Sparrow; Mark F Cesta; Michelle C Cora; Keith R Shockley; Matt D Stout; Chad R Blystone; Dori R Germolec
Journal:  J Immunotoxicol       Date:  2021-12       Impact factor: 3.000

  2 in total

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