• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

氧化铈纳米颗粒的安全性评估:在大鼠中进行重复剂量毒性与生殖/发育毒性筛选和生物分布的联合研究。

Safety assessment of cerium oxide nanoparticles: combined repeated-dose toxicity with reproductive/developmental toxicity screening and biodistribution in rats.

机构信息

Developmental and Reproductive Toxicology Research Group, Korea Institute of Toxicology, Daejeon, Republic of Korea.

College of Veterinary Medicine, Chungbuk National University, Cheongju, Republic of Korea.

出版信息

Nanotoxicology. 2020 Jun;14(5):696-710. doi: 10.1080/17435390.2020.1751322. Epub 2020 Apr 17.

DOI:10.1080/17435390.2020.1751322
PMID:32301357
Abstract

Cerium oxide nanoparticles (CeO NPs) are widely used in various commercial applications because of their characteristic properties. People can be easily exposed to CeO NPs in real life, but the safety assessment of CeO NPs has not been fully investigated. Therefore, in this study, we conducted a combined repeated-dose and reproductive/developmental toxicity screening study (OECD testing guideline 422) to investigate the potential hazards on human health, including reproductive/developmental functions, after repeated daily CeO NPs oral gavage administration to both males and females. In addition, tissues from parental animals and their pups were collected to analyze the internal accumulation of cerium. CeO NPs were orally administered to Sprague-Dawley rats at doses of 0, 100, 300 and 1000 mg/kg during their pre-mating, mating, gestation and early lactation periods. In the general systemic and reproductive/developmental examinations, no marked toxicities were observed in any in-life and terminal observation parameters in this study. In the biodistribution analysis, cerium was not detected in either parental or pup tissues (blood, liver, lungs and kidneys). Repeated oral exposure of CeO NPs did not induce marked toxicities affecting general systemic and reproductive/developmental functions up to the dose level of 1000 mg/kg and the CeO NPs were not systemically absorbed in parental animals or their pups. This result could be used in risk assessment for humans, and additional toxicity studies with CeO NPs will be necessary considering various physicochemical properties and exposure probabilities of these nanoparticles.

摘要

氧化铈纳米颗粒(CeO NPs)因其特性而被广泛应用于各种商业应用中。人们在日常生活中很容易接触到 CeO NPs,但对 CeO NPs 的安全性评估尚未进行充分研究。因此,在这项研究中,我们进行了一项联合重复剂量和生殖/发育毒性筛选研究(OECD 测试指南 422),以研究雄性和雌性动物经重复每日口服 CeO NPs 灌胃后对人类健康的潜在危害,包括生殖/发育功能。此外,收集亲代动物及其幼崽的组织,以分析铈的体内蓄积情况。CeO NPs 在亲代动物的交配前、交配期间、妊娠和哺乳期以 0、100、300 和 1000mg/kg 的剂量经口给予 Sprague-Dawley 大鼠。在一般系统和生殖/发育检查中,本研究未观察到任何明显的毒性作用。在生物分布分析中,亲代或幼崽组织(血液、肝脏、肺和肾脏)中均未检测到铈。CeO NPs 的重复口服暴露在高达 1000mg/kg 的剂量水平下未引起明显的毒性作用,影响一般系统和生殖/发育功能,并且 CeO NPs 未在亲代动物或其幼崽中被全身吸收。该结果可用于人类的风险评估,考虑到这些纳米颗粒的各种物理化学性质和暴露概率,需要进行 CeO NPs 的额外毒性研究。

相似文献

1
Safety assessment of cerium oxide nanoparticles: combined repeated-dose toxicity with reproductive/developmental toxicity screening and biodistribution in rats.氧化铈纳米颗粒的安全性评估:在大鼠中进行重复剂量毒性与生殖/发育毒性筛选和生物分布的联合研究。
Nanotoxicology. 2020 Jun;14(5):696-710. doi: 10.1080/17435390.2020.1751322. Epub 2020 Apr 17.
2
Genotoxicity assessment of cerium oxide nanoparticles in female Wistar rats after acute oral exposure.急性经口暴露后雌性Wistar大鼠中氧化铈纳米颗粒的遗传毒性评估
Mutat Res Genet Toxicol Environ Mutagen. 2014 Dec;775-776:7-19. doi: 10.1016/j.mrgentox.2014.09.009. Epub 2014 Oct 2.
3
Genotoxicity analysis of cerium oxide micro and nanoparticles in Wistar rats after 28 days of repeated oral administration.氧化铈微米和纳米颗粒对Wistar大鼠连续28天重复口服给药后的遗传毒性分析。
Mutagenesis. 2014 Nov;29(6):467-79. doi: 10.1093/mutage/geu038. Epub 2014 Sep 10.
4
Safety assessment and gastrointestinal retention of orally administered cerium oxide nanoparticles in rats.口服氧化铈纳米颗粒在大鼠体内的安全性评估及胃肠道滞留研究。
Sci Rep. 2024 Mar 7;14(1):5657. doi: 10.1038/s41598-024-54659-9.
5
SF-1 mediates reproductive toxicity induced by Cerium oxide nanoparticles in male mice.SF-1 介导氧化铈纳米颗粒在雄性小鼠体内引起的生殖毒性。
J Nanobiotechnology. 2019 Mar 21;17(1):41. doi: 10.1186/s12951-019-0474-2.
6
In vivo biodistribution and physiologically based pharmacokinetic modeling of inhaled fresh and aged cerium oxide nanoparticles in rats.大鼠吸入新鲜和老化氧化铈纳米颗粒的体内生物分布及基于生理的药代动力学建模
Part Fibre Toxicol. 2016 Aug 20;13(1):45. doi: 10.1186/s12989-016-0156-2.
7
Combined repeated-dose and reproductive/developmental toxicity screening test of 1-tert-butoxy-4-chlorobenzene in rats.大鼠1-叔丁氧基-4-氯苯的重复剂量联合生殖/发育毒性筛选试验
Drug Chem Toxicol. 2017 Jul;40(3):344-358. doi: 10.1080/01480545.2016.1236265. Epub 2016 Oct 28.
8
Evaluation of the effect of valence state on cerium oxide nanoparticle toxicity following intratracheal instillation in rats.评估价态对大鼠气管内滴注氧化铈纳米颗粒毒性的影响。
Nanotoxicology. 2016 Sep;10(7):992-1000. doi: 10.3109/17435390.2016.1157220. Epub 2016 Mar 17.
9
Evaluation of the reproductive and developmental toxicity of 6:2 fluorotelomer alcohol in rats.评估 6:2 氟代壬基醇在大鼠体内的生殖和发育毒性。
Toxicology. 2014 Mar 20;317:6-16. doi: 10.1016/j.tox.2014.01.002. Epub 2014 Jan 18.
10
The acute pulmonary and thrombotic effects of cerium oxide nanoparticles after intratracheal instillation in mice.二氧化铈纳米颗粒经气管内滴注后对小鼠的急性肺部和血栓形成影响。
Int J Nanomedicine. 2017 Apr 10;12:2913-2922. doi: 10.2147/IJN.S127180. eCollection 2017.

引用本文的文献

1
Exploring the innovative application of cerium oxide nanoparticles for addressing oxidative stress in ovarian tissue regeneration.探索氧化铈纳米颗粒在解决卵巢组织再生中的氧化应激方面的创新应用。
J Ovarian Res. 2024 Dec 5;17(1):241. doi: 10.1186/s13048-024-01566-2.
2
Assessing systemic, developmental, and reproductive toxicity and estrogenicity of Korean red ginseng extract G1899 in juvenile Sprague-Dawley Rats.评估韩国红参提取物G1899对幼年斯普拉格-道利大鼠的全身毒性、发育毒性、生殖毒性及雌激素活性。
J Ginseng Res. 2024 May;48(3):333-340. doi: 10.1016/j.jgr.2024.01.002. Epub 2024 Jan 21.
3
Safety assessment and gastrointestinal retention of orally administered cerium oxide nanoparticles in rats.
口服氧化铈纳米颗粒在大鼠体内的安全性评估及胃肠道滞留研究。
Sci Rep. 2024 Mar 7;14(1):5657. doi: 10.1038/s41598-024-54659-9.
4
Effects of nano-cerium dioxide on intestinal microflora in rats by oral subchronic exposure.经口亚慢性暴露纳米二氧化铈对大鼠肠道菌群的影响。
PLoS One. 2024 Feb 29;19(2):e0298917. doi: 10.1371/journal.pone.0298917. eCollection 2024.
5
Fate and distribution of orally-ingested CeO-nanoparticles based on a mouse model: Implication for human health.基于小鼠模型的口服二氧化铈纳米颗粒的命运和分布:对人类健康的启示。
Soil Environ Health. 2023 Jun;1(2). doi: 10.1016/j.seh.2023.100017. Epub 2023 Apr 17.
6
A Two-Generation Reproductive Toxicity Study of Cerium Nitrate in Sprague-Dawley Rats.硝酸铈致 Sprague-Dawley 大鼠两代生殖毒性研究
Biol Trace Elem Res. 2024 Feb;202(2):597-614. doi: 10.1007/s12011-023-03692-2. Epub 2023 May 6.
7
Exploring the Long-Term Tissue Accumulation and Excretion of 3 nm Cerium Oxide Nanoparticles after Single Dose Administration.单次给药后3纳米氧化铈纳米颗粒的长期组织蓄积与排泄研究
Antioxidants (Basel). 2023 Mar 21;12(3):765. doi: 10.3390/antiox12030765.
8
Delayed Solvent-Nonsolvent Demixing Preparation and Performance of a Highly Permeable Polyethersulfone Ultrafiltration Membrane.高渗透性聚醚砜超滤膜的延迟溶剂-非溶剂相分离制备及其性能
Membranes (Basel). 2022 Dec 28;13(1):39. doi: 10.3390/membranes13010039.
9
Nanoceria: an innovative strategy for cancer treatment.纳诺 Ce 拉:癌症治疗的创新策略。
Cell Mol Life Sci. 2023 Jan 19;80(2):46. doi: 10.1007/s00018-023-04694-y.
10
Foliar Application of Cerium Oxide-Salicylic Acid Nanoparticles (CeO:SA Nanoparticles) Influences the Growth and Physiological Responses of L. under Salinity.氧化铈-水杨酸纳米粒子(CeO:SA 纳米粒子)的叶面喷施影响盐胁迫下 L. 的生长和生理响应。
Int J Mol Sci. 2022 May 3;23(9):5093. doi: 10.3390/ijms23095093.