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PEG 修饰金纳米粒子的尺寸依赖性组织动力学

Size-dependent tissue kinetics of PEG-coated gold nanoparticles.

机构信息

The University of Edinburgh, Edinburgh, EH16 4TJ, UK.

出版信息

Toxicol Appl Pharmacol. 2010 May 15;245(1):116-23. doi: 10.1016/j.taap.2010.02.013. Epub 2010 Feb 26.

Abstract

Gold nanoparticles (AuNPs) can be used in various biomedical applications, however, very little is known about their size-dependent in vivo kinetics. Here, we performed a kinetic study in mice with different sizes of PEG-coated AuNPs. Small AuNPs (4 or 13nm) showed high levels in blood for 24h and were cleared by 7days, whereas large (100nm) AuNPs were completely cleared by 24h. All AuNPs in blood re-increased at 3months, which correlated with organ levels. Levels of small AuNPs were peaked at 7days in the liver and spleen and at 1month in the mesenteric lymph node, and remained high until 6months, with slow elimination. In contrast, large AuNPs were taken up rapidly ( approximately 30min) into the liver, spleen, and mesenteric lymph nodes with less elimination phase. TEM showed that AuNPs were entrapped in cytoplasmic vesicles and lysosomes of Kupffer cells and macrophages of spleen and mesenteric lymph node. Small AuNPs transiently activated CYP1A1 and 2B, phase I metabolic enzymes, in liver tissues from 24h to 7days, which mirrored with elevated gold levels in the liver. Large AuNPs did not affect the metabolic enzymes. Thus, propensity to accumulate in the reticuloendothelial organs and activation of phase I metabolic enzymes, suggest that extensive further studies are needed for practical in vivo applications.

摘要

金纳米颗粒(AuNPs)可用于各种生物医学应用,然而,关于其尺寸依赖性体内动力学的信息知之甚少。在这里,我们对不同尺寸聚乙二醇(PEG)包覆的 AuNPs 在小鼠体内进行了动力学研究。小尺寸 AuNPs(4 或 13nm)在血液中 24 小时内水平较高,并在 7 天内被清除,而大尺寸(100nm)AuNPs 在 24 小时内被完全清除。所有在血液中的 AuNPs 在 3 个月时重新增加,这与器官水平相关。小尺寸 AuNPs 的水平在肝脏和脾脏中于 7 天达到峰值,在肠系膜淋巴结中于 1 个月达到峰值,并在 6 个月内保持高水平,清除缓慢。相比之下,大尺寸 AuNPs 迅速(约 30 分钟)被摄取到肝脏、脾脏和肠系膜淋巴结中,其消除阶段较少。TEM 显示,AuNPs 被库普弗细胞和脾脏以及肠系膜淋巴结中的巨噬细胞的细胞质小泡和溶酶体所捕获。小尺寸 AuNPs 在肝脏组织中从 24 小时到 7 天短暂地激活了细胞色素 P450 1A1 和 2B 等 I 相代谢酶,这与肝脏中黄金水平的升高相一致。大尺寸 AuNPs 不会影响代谢酶。因此,倾向于在网状内皮器官中积累并激活 I 相代谢酶,这表明需要进行更广泛的进一步研究,以用于实际的体内应用。

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