Genotoxicity testing of esterified propoxylated glycerol (EPG)

Regul Toxicol Pharmacol. 2014 Dec:70 Suppl 2:S131-42. doi: 10.1016/j.yrtph.2014.11.013. Epub 2014 Dec 8.

Abstract

Four versions of esterified propoxylated glycerols (EPGs) were evaluated for potential genotoxicity using a range of in vitro and in vivo assays. H-EPG-05 HR/SO 9:1, H-EPG-05 soyate, and H-EPG-14 soyate were non-mutagenic in reverse mutation assays (maximum concentration 1000 μg/plate) using Salmonella typhimurium and Escherichia coli. Heated and unheated H-EPG-05 HR/SO 9:1 and EPG-05 HR/ST 45:55 were likewise non-mutagenic in reverse mutation assays in S. typhimurium strains TA98 and TA100 (maximum concentration 5000 μg/plate). H-EPG-05 HR/SO 9:1, H-EPG-05 soyate, and H-EPG-14 soyate, were devoid of mutagenic activity in a mouse lymphoma assay in L5178Y tk +/- cells (maximum concentration 200 μg/plate for H-EPG-05 HR/SO 9:1; 100 μg/plate for H-EPG-05 soyate and H-EPG-14 soyate), and a chromosomal aberration test using human lymphocytes (maximum concentration 50 μg/plate for H-EPG-05 HR/SO 9:1 and H-EPG-05 soyate; 60 μg/plate for H-EPG-14 soyate). All assays were conducted with and without metabolic activation. Additionally, H-EPG-05 HR/SO 9:1, H-EPG-05 soyate, and H-EPG-14 soyate were non-genotoxic in unscheduled DNA synthesis tests in rats (maximum dose 2000 mg/kg). Based on the results of these assays it was concluded that these versions of EPG were not genotoxic under any of the conditions of the assays performed.

Keywords: EPG; Esterified propoxylated glycerol; Fat substitute; Genotoxicity; Mutagenicity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line, Tumor
  • Cells, Cultured
  • DNA / metabolism
  • Escherichia coli / drug effects
  • Escherichia coli / genetics
  • Fat Substitutes / toxicity*
  • Female
  • Glycerides / toxicity*
  • Hepatocytes / drug effects
  • Hepatocytes / metabolism
  • Humans
  • Lymphocytes / drug effects
  • Male
  • Mice
  • Mutagenicity Tests
  • Mutation
  • Rats, Wistar
  • Salmonella typhimurium / drug effects
  • Salmonella typhimurium / genetics
  • Thymidine Kinase / genetics

Substances

  • Fat Substitutes
  • Glycerides
  • DNA
  • Thymidine Kinase