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小鼠和大鼠的金纳米颗粒毒性:种属差异

Gold Nanoparticle Toxicity in Mice and Rats: Species Differences.

作者信息

Bahamonde Javiera, Brenseke Bonnie, Chan Matthew Y, Kent Ronald D, Vikesland Peter J, Prater M Renee

机构信息

1 Department of Biomedical Sciences and Pathobiology, Virginia Tech, Blacksburg, Virginia, USA.

2 Instituto de Farmacología y Morfofisiología, Facultad de Ciencias Veterinarias, Universidad Austral de Chile, Valdivia, Chile.

出版信息

Toxicol Pathol. 2018 Jun;46(4):431-443. doi: 10.1177/0192623318770608. Epub 2018 May 9.

Abstract

Nanotoxicity studies are greatly needed to advance nanomedical technologies into clinical practice. We assessed the toxic effects of a single intravenous exposure to commercially available gold nanoparticles (GNPs) in mice and rats. Fifteen-nm GNPs were purchased and independently characterized. Animals were exposed to either 1,000 mg GNPs/kg body weight (GNP group) or phosphate-buffered saline. Subsets of animals were euthanized and samples collected at 1, 7, 14, 21, and 28 days postexposure. Independent characterization demonstrated that the physicochemical properties of the purchased GNPs were in good agreement with the information provided by the supplier. Mice exposed to GNPs developed granulomas in the liver and transiently increased serum levels of the pro-inflammatory cytokine interleukin-18. No such alterations were found in rats. While there was no fatality in mice post-GNP exposure, a number of the rats died within hours of GNP administration. Differences in GNP biodistribution and excretion were also detected between the two species, with rats having a higher relative accumulation of GNPs in spleen and greater fecal excretion. In conclusion, GNPs have the ability to incite a robust macrophage response in mice, and there are important species-specific differences in their biodistribution, excretion, and potential for toxicity.

摘要

为了将纳米医学技术推进到临床实践中,非常需要进行纳米毒性研究。我们评估了单次静脉注射市售金纳米颗粒(GNP)对小鼠和大鼠的毒性作用。购买了15纳米的GNP并进行了独立表征。动物被注射1000毫克GNP/千克体重(GNP组)或磷酸盐缓冲盐水。在暴露后1、7、14、21和28天对部分动物实施安乐死并采集样本。独立表征表明,所购买的GNP的物理化学性质与供应商提供的信息高度一致。暴露于GNP的小鼠肝脏出现肉芽肿,促炎细胞因子白细胞介素-18的血清水平短暂升高。在大鼠中未发现此类变化。虽然GNP暴露后小鼠没有死亡,但一些大鼠在注射GNP后数小时内死亡。在两个物种之间还检测到GNP生物分布和排泄的差异,大鼠脾脏中GNP的相对积累更高,粪便排泄量更大。总之,GNP能够在小鼠中引发强烈的巨噬细胞反应,并且它们在生物分布、排泄和潜在毒性方面存在重要的物种特异性差异。

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