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表面改性对纤维素纳米纤维的肺和全身毒性的影响。

Effect of Surface Modification on the Pulmonary and Systemic Toxicity of Cellulose Nanofibrils.

机构信息

Finnish Institute of Occupational Health, P.O. Box 40, 00032 Helsinki, Finland.

Department of Bioproducts and Biosystems, Aalto University, 02150 Espoo, Finland.

出版信息

Biomacromolecules. 2022 Jul 11;23(7):2752-2766. doi: 10.1021/acs.biomac.2c00072. Epub 2022 Jun 9.

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.

摘要

纤维素纳米纤维(CNFs)作为广泛应用的可持续选择已经崭露头角。然而,CNFs 的高纵横比和生物持久性引起了人们对潜在健康影响的关注。在这里,我们评估了未修饰(U-CNF)、羧甲基化(C-CNF)和 TEMPO(2,2,6,6-四甲基-哌啶-1-氧自由基)氧化(T-CNF)CNFs 的体内肺和系统毒性,这些 CNFs 以相同的方式纤丝化,并通过重复(3×)咽部抽吸(14、28 和 56 μg/只/抽吸)施用于小鼠。在最后一次给药后 90 天内评估毒性作用。一些小鼠用添加脂多糖(LPS;0.02-50 ng/只/抽吸)的 T-CNF 样品处理,以评估内毒素污染的作用。CNFs 引起了急性炎症反应,除了 T-CNF 之外,该反应在 90 天内消退。给药后 90 天,暴露于 T-CNF 和 C-CNF 后,支气管肺泡灌洗液和肝细胞中的 DNA 损伤分别增加。此外,LPS 污染剂量依赖性地增加了 T-CNF 的肝遗传毒性作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c73f/9278333/d9c2db3f3cf0/bm2c00072_0002.jpg

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