Acute Oral, Intramuscular and Intravenous Toxicity Studies of Recombinant Interferon-$\alpha$2a in Sprague-Dawley Rats

  • Lee, Yong-Soon (Department of veterinary Public Health, College of Veterinary Medicine, Seoul National University) ;
  • Park, Jin-Sung (Department of veterinary Public Health, College of Veterinary Medicine, Seoul National University) ;
  • Che, Jeong-Hwan (Department of veterinary Public Health, College of Veterinary Medicine, Seoul National University) ;
  • Li, Guang-Xun (Department of veterinary Public Health, College of Veterinary Medicine, Seoul National University) ;
  • Kim, Tea-Won (Department of veterinary Public Health, College of Veterinary Medicine, Seoul National University) ;
  • Kim, Hyung-Sub (Department of veterinary Public Health, College of Veterinary Medicine, Seoul National University) ;
  • Park, Jie-Eun (Department of veterinary Public Health, College of Veterinary Medicine, Seoul National University) ;
  • Yun, Jun-Won (Department of veterinary Public Health, College of Veterinary Medicine, Seoul National University) ;
  • Kang, Kyung-Sun (Department of veterinary Public Health, College of Veterinary Medicine, Seoul National University)
  • Published : 2000.03.01

Abstract

Acute oral, intramuscluar, and intravenous toxicity studies of recombinant human interferon $\alpha$2$\alpha$(rhIFN $\alpha$2$\alpha$) were performed in Sprague-Dawley (SD) rats. SD rats were administered with doses of 31.25, 62.5, 125, 250 and 500 MIU/kg, respectively, and clinical signs, mortality and body weight changes were observed for 2 weeks. In all animals administered with rhIFN $\alpha$2$\alpha$, there was neither dead animals nor significant changes of body weights. In addition, no differences were found between control and treated groups in clinical signs and autopsy findings. Therefore, $LD_{50}$ of rhIFN $\alpha$2$\alpha$ was considered to be higher than 500 MIU/kg in SD rats.

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