Prenatal developmental toxicity study of 2,4-dichlorobenzyl alcohol in rats

Regul Toxicol Pharmacol. 2022 Jul:132:105168. doi: 10.1016/j.yrtph.2022.105168. Epub 2022 Apr 14.

Abstract

Sore throat lozenges, which are over-the-counter drugs, contain 2,4-dichlorobenzyl alcohol (DCBA) as the primary ingredient. However, comprehensive data on the prenatal developmental toxicity of DCBA is limited. Therefore, this study was conducted to determine the effects of DCBA on pregnant rats and prenatal development. Sprague-Dawley rats were administered different doses of DCBA (0, 25, 100, 400, and 800 mg/kg/day) daily via an oral gavage from gestation day (GD) 6-19. Thereafter, all the live dams were sacrificed on GD 20, and caesarean sections were conducted. Live fetuses and their placenta were weighed and then examined for external, visceral, and skeletal malformations and variations. Based on the results obtained, dams at 800 mg/kg/day showed systemic toxicities, including a decrease in body weight and food consumption, and liver changes. Additionally, this treatment induced decreases in fetal and placental weights, as well as the increased incidence of retarded ossifications and full supernumery rib, and the decreased number of ossification centers. Therefore, based on these findings, the no-observed-adverse-effect level of DCBA was determined to be 400 mg/kg/day for dams and prenatal development.

Keywords: 2,4-dichlorobenzyl alcohol; Embryo-fetal development; Pregnant rats; Sore throat lozenges.

MeSH terms

  • Abnormalities, Drug-Induced* / etiology
  • Animals
  • Benzyl Alcohols
  • Body Weight
  • Female
  • No-Observed-Adverse-Effect Level
  • Placenta*
  • Pregnancy
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Benzyl Alcohols
  • dichlorobenzyl alcohol