| Literature DB >> 35680128 |
Kukka Aimonen1, Mira Hartikainen1, Monireh Imani2, Satu Suhonen1, Gerard Vales1, Carlos Moreno3, Hanna Saarelainen1, Kirsi Siivola1, Esa Vanhala1, Henrik Wolff1, Orlando J Rojas2,4, Hannu Norppa1, Julia Catalán1,3.
Abstract
Cellulose nanofibrils (CNFs) have emerged as sustainable options for a wide range of applications. However, the high aspect ratio and biopersistence of CNFs raise concerns about potential health effects. Here, we evaluated the in vivo pulmonary and systemic toxicity of unmodified (U-CNF), carboxymethylated (C-CNF), and TEMPO (2,2,6,6-tetramethyl-piperidin-1-oxyl)-oxidized (T-CNF) CNFs, fibrillated in the same way and administered to mice by repeated (3×) pharyngeal aspiration (14, 28, and 56 μg/mouse/aspiration). Toxic effects were assessed up to 90 days after the last administration. Some mice were treated with T-CNF samples spiked with lipopolysaccharide (LPS; 0.02-50 ng/mouse/aspiration) to assess the role of endotoxin contamination. The CNFs induced an acute inflammatory reaction that subsided within 90 days, except for T-CNF. At 90 days post-administration, an increased DNA damage was observed in bronchoalveolar lavage and hepatic cells after exposure to T-CNF and C-CNF, respectively. Besides, LPS contamination dose-dependently increased the hepatic genotoxic effects of T-CNF.Entities:
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Year: 2022 PMID: 35680128 PMCID: PMC9278333 DOI: 10.1021/acs.biomac.2c00072
Source DB: PubMed Journal: Biomacromolecules ISSN: 1525-7797 Impact factor: 6.978