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亚慢性经口暴露后发热性合成无定形二氧化硅(NM-203)的危害识别:一种多靶点方法。

Hazard identification of pyrogenic synthetic amorphous silica (NM-203) after sub-chronic oral exposure in rat: A multitarget approach.

机构信息

Center for Gender-Specific Medicine, Istituto Superiore di Sanità, Rome, Italy.

National Center for Drug Research and Evaluation, Istituto Superiore di Sanità, Rome, Italy.

出版信息

Food Chem Toxicol. 2020 Mar;137:111168. doi: 10.1016/j.fct.2020.111168. Epub 2020 Jan 30.

DOI:10.1016/j.fct.2020.111168
PMID:32007467
Abstract

Food additive E551 consists of synthetic amorphous silica (SAS), comprising agglomerates and aggregates of primary particles in the nanorange (<100 nm), which potential nanospecific risks for humans associated to dietary exposure are not yet completely assessed. In NANoREG project, aim of the study was to identify potential hazards of pyrogenic SAS nanomaterial NM-203 by a 90-day oral toxicity study (OECD test guideline 408). Adult Sprague-Dawley rats of both sexes were orally treated with 0, 2, 5, 10, 20 and 50 mg SAS/kg bw per day; dose levels were selected to be as close as possible to E551 dietary exposure. Several endpoints were investigated, the whole integrative study is presented here along with the results of dispersion characterization, tissue distribution, general toxicity, blood/serum biomarkers, histopathological and immunotoxicity endpoints. No mortality, general toxicity and limited deposition in target tissues were observed. NM-203 affected liver and spleen in both sexes. Proposed NOAEL 5 mg/kg bw per day in male rats for enlarged sinusoids in liver. In female rats, TSH and creatinine levels were affected, proposed LOAEL 2 mg/kg bw per day. Overall, these data provide new insight for a comprehensive risk assessment of SAS exposure by the oral route.

摘要

食品添加剂 E551 由合成无定形二氧化硅 (SAS) 组成,包含初级颗粒的团聚体和聚集体,其纳米范围内(<100nm)的潜在纳米特定风险与饮食暴露相关,尚未得到完全评估。在 NANoREG 项目中,该研究的目的是通过为期 90 天的口服毒性研究(OECD 测试指南 408)来确定热解 SAS 纳米材料 NM-203 的潜在危害。成年 Sprague-Dawley 大鼠雌雄两性分别经口给予 0、2、5、10、20 和 50mg SAS/kg bw/天;剂量水平选择尽可能接近 E551 的饮食暴露量。研究了多个终点,本文介绍了整个综合研究,以及分散特性、组织分布、一般毒性、血液/血清生物标志物、组织病理学和免疫毒性终点的结果。未观察到死亡率、一般毒性和靶组织中的有限沉积。NM-203 影响雌雄两性大鼠的肝脏和脾脏。雄性大鼠中,肝窦扩张的无观察到不良作用水平(NOAEL)为 5mg/kg bw/天。在雌性大鼠中,TSH 和肌酐水平受到影响,建议无观察到不良作用水平(LOAEL)为 2mg/kg bw/天。总体而言,这些数据为经口服途径暴露于 SAS 进行全面风险评估提供了新的见解。

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