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本文引用的文献

1
Non-toxic dry-coated nanosilver for plasmonic biosensors.用于等离子体生物传感器的无毒干涂层纳米银。
Adv Funct Mater. 2010 Dec 21;20(24):4250-4257. doi: 10.1002/adfm.201000985.
2
Nanoparticle-induced pulmonary toxicity.纳米颗粒诱导的肺毒性。
Exp Biol Med (Maywood). 2010 Sep;235(9):1025-33. doi: 10.1258/ebm.2010.010021. Epub 2010 Aug 18.
3
Development and characterization of a Versatile Engineered Nanomaterial Generation System (VENGES) suitable for toxicological studies.开发和表征一种多功能工程纳米材料生成系统(VENGES),适用于毒理学研究。
Inhal Toxicol. 2010 Dec;22 Suppl 2(0 2):107-16. doi: 10.3109/08958378.2010.499385. Epub 2010 Aug 11.
4
Antibacterial activity of nanosilver ions and particles.纳米银离子和颗粒的抗菌活性。
Environ Sci Technol. 2010 Jul 15;44(14):5649-54. doi: 10.1021/es101072s.
5
Iron from nanocompounds containing iron and zinc is highly bioavailable in rats without tissue accumulation.纳米复合物中所含的铁和锌形式的铁在大鼠体内具有很高的生物利用度,且不会在组织中蓄积。
Nat Nanotechnol. 2010 May;5(5):374-80. doi: 10.1038/nnano.2010.79. Epub 2010 Apr 25.
6
Origin and fate of dietary nanoparticles and microparticles in the gastrointestinal tract.饮食纳米颗粒和微颗粒在胃肠道中的来源和命运。
J Autoimmun. 2010 May;34(3):J226-33. doi: 10.1016/j.jaut.2009.11.006. Epub 2010 Jan 21.
7
Particle length-dependent titanium dioxide nanomaterials toxicity and bioactivity.颗粒长度依赖性二氧化钛纳米材料的毒性和生物活性。
Part Fibre Toxicol. 2009 Dec 31;6:35. doi: 10.1186/1743-8977-6-35.
8
Use of a rapid cytotoxicity screening approach to engineer a safer zinc oxide nanoparticle through iron doping.利用快速细胞毒性筛选方法,通过铁掺杂工程设计更安全的氧化锌纳米颗粒。
ACS Nano. 2010 Jan 26;4(1):15-29. doi: 10.1021/nn901503q.
9
Better safe than sorry: Understanding the toxicological properties of inorganic nanoparticles manufactured for biomedical applications.宁为安全故,勿为后悔忧:理解为生物医药应用而制造的无机纳米颗粒的毒理学特性。
Adv Drug Deliv Rev. 2010 Mar 8;62(3):362-74. doi: 10.1016/j.addr.2009.11.008. Epub 2009 Nov 10.
10
Airway exposure to silica-coated TiO2 nanoparticles induces pulmonary neutrophilia in mice.气道暴露于硅涂层二氧化钛纳米颗粒会导致小鼠肺部嗜中性粒细胞增多。
Toxicol Sci. 2010 Feb;113(2):422-33. doi: 10.1093/toxsci/kfp254. Epub 2009 Oct 29.

一种用于吸入式工程纳米材料的肺和心血管毒理学特征描述的新平台。

A novel platform for pulmonary and cardiovascular toxicological characterization of inhaled engineered nanomaterials.

机构信息

Department of Mechanical and Process Engineering, Particle Technology Laboratory, Institute of Process Engineering, Swiss Federal Institute of Technology Zurich (ETH Zurich), Zurich, Switzerland.

出版信息

Nanotoxicology. 2012 Sep;6(6):680-90. doi: 10.3109/17435390.2011.604439. Epub 2011 Aug 2.

DOI:10.3109/17435390.2011.604439
PMID:21809902
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3641536/
Abstract

A novel method is presented which is suitable for assessing in vivo the link between the physicochemical properties of engineered nanomaterials (ENM) and their biological outcomes. The ability of the technique to generate a variety of industry-relevant, property-controlled ENM exposure atmospheres for inhalation studies was systematically investigated. The primary particle size for Fe(2)O(3), SiO(2), Ag and Ag/SiO(2) was controlled from 4 to 25 nm, while the corresponding agglomerate mobility diameter of the aerosol was also controlled and varied from 40 to 120 nm. The suitability of the technique to characterize the pulmonary and cardiovascular effects of inhaled ENMs in intact animal models is also demonstrated using in vivo chemiluminescence (IVCL). The IVCL technique is a highly sensitive method for identifying cardiopulmonary responses to inhaled ENMs under relatively small doses and acute exposures. It is shown that moderate and acute exposures to inhaled nanostructured Fe(2)O(3) can cause both pulmonary and cardiovascular effects.

摘要

提出了一种新方法,适用于评估工程纳米材料(ENM)的物理化学性质与其生物结果之间的联系。系统研究了该技术产生各种与工业相关的、受控制的 ENM 暴露气氛以进行吸入研究的能力。Fe(2)O(3)、SiO(2)、Ag 和 Ag/SiO(2)的初级粒径从 4 到 25nm 进行控制,而气溶胶的相应团聚体迁移直径也从 40 到 120nm 进行控制和变化。还使用体内化学发光(IVCL)证明了该技术在完整动物模型中表征吸入 ENM 的肺和心血管效应的适用性。IVCL 技术是一种高度灵敏的方法,可在相对较小的剂量和急性暴露下识别吸入 ENM 的心肺反应。结果表明,适度和急性暴露于吸入的纳米结构 Fe(2)O(3)可引起肺部和心血管效应。