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A 28-Day Repeated Oral Administration Study of Mechanically Fibrillated Cellulose Nanofibers According to OECD TG407.
Yamashita, Yoshihiro; Tokunaga, Akinori; Aoki, Koji; Ishizuka, Tamotsu; Fujita, Satoshi; Tanoue, Shuichi.
Afiliação
  • Yamashita Y; Research Center for Fibers and Materials, University of Fukui, 3-9-1 Bunkyo, Fukui 910-8507, Japan.
  • Tokunaga A; Life Science Research Laboratory, School of Medical Sciences, University of Fukui, 23-3, Matsuokashimoaizuki, Eiheiji-cho 910-1193, Japan.
  • Aoki K; Department of Pharmacology, Faculty of Medicine, University of Fukui, 23-3, Matsuokashimoaizuki, Eiheiji-cho 910-1193, Japan.
  • Ishizuka T; Department of Respiratory Medicine, Faculty of Medical Sciences, University of Fukui, 23-3, Matsuokashimoaizuki, Eiheiji-cho 910-1193, Japan.
  • Fujita S; Department of Frontier Fiber Technology and Science, Faculty of Engineering, University of Fukui, 3-9-1 Bunkyo, Fukui 910-8507, Japan.
  • Tanoue S; Research Center for Fibers and Materials, University of Fukui, 3-9-1 Bunkyo, Fukui 910-8507, Japan.
Nanomaterials (Basel) ; 14(13)2024 Jun 24.
Article em En | MEDLINE | ID: mdl-38998688
ABSTRACT
The impact of oral administration of mechanically fibrillated cellulose nanofibers (fib-CNF), a commonly used nanofiber, on toxicity and health remains unclear, despite reports of the safety and beneficial effects of chitin-based nanofibers. Thus, evaluating the oral toxicity of fib-CNF in accordance with OECD Test Guideline 407 (TG407) is essential. This study aimed to assess the safety of orally administered fib-CNF through an acute toxicity study in rats, following the OECD TG407 guidelines for 4 weeks. CNF "BiNFi-s" FMa-10005, derived from mechanically fibrillated pulp cellulose, was administered via gavage to male and female CrlCD(SD) rats at doses of 50, 150, 500, and 1000 mg/kg/day for 28 days, with a control group receiving water for injection. The study evaluated the toxic effects of repeated administration, and the rats were monitored for an additional 14 days post-administration to assess recovery from any toxic effects. The results showed no mortality in either sex during the administration period, and no toxicological effects related to the test substance were observed in various assessments, including general condition and behavioral function observations, urinalysis, hematological examination, blood biochemical examination, necropsy findings, organ weights, and histopathological examination. Notably, only female rats treated with 1000 mg/kg/day of CNF exhibited a consistent reduction in body weight during the 14-day recovery period after the end of treatment. They also showed a slight decrease in pituitary and liver weights. However, hematological and blood biochemical tests did not reveal significant differences, suggesting a potential weight-suppressive effect of CNF ingestion.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article