Toxicological evaluations of colostrum ultrafiltrate

Regul Toxicol Pharmacol. 2019 Jun:104:39-49. doi: 10.1016/j.yrtph.2019.02.017. Epub 2019 Mar 1.

Abstract

Colostrum has been consumed safely for many years as a food collected directly from cows. More recently, an ultrafiltrated bovine colostrum product has been developed; however, its safety in toxicology studies has not been extensively evaluated. To assess the safety of bovine colostrum ultrafiltrate, in accordance with internationally accepted standards, the genotoxic potential was investigated in a bacterial reverse mutation test, an in vitro chromosomal aberration test, and an in vivo mammalian micronucleus test. No mutagenicity or genotoxic activity was observed in these three tests. A 90-day repeated-dose oral toxicity study in Hsd.Han Wistar rats was conducted at doses of 0, 1050, 2100, and 4200 mg/kg bw/day by gavage. After 90 days of continuous exposure, no mortality or treatment-related adverse effects were observed, and no target organs were identified. The no-observed-adverse-effect level (NOAEL) was determined to be 4200 mg/kg bw/day, the highest dose tested.

Keywords: Colostrum; Mutagenicity; NOAEL; Safety; Toxicity.

MeSH terms

  • Administration, Oral
  • Animals
  • Colostrum / chemistry*
  • Dairy Products / analysis*
  • Dairy Products / toxicity*
  • Female
  • Male
  • Mice
  • No-Observed-Adverse-Effect Level
  • Pregnancy
  • Rats
  • Rats, Wistar
  • Ultrafiltration