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本文引用的文献

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Assessment of the In Vivo Toxicity of Gold Nanoparticles.金纳米颗粒的体内毒性评估
Nanoscale Res Lett. 2009 May 8;4(8):858-864. doi: 10.1007/s11671-009-9334-6.
2
Biodistribution of PEG-modified gold nanoparticles following intratracheal instillation and intravenous injection.经气管内滴注和静脉注射后聚乙二醇修饰的金纳米颗粒的生物分布。
Biomaterials. 2010 Sep;31(25):6574-81. doi: 10.1016/j.biomaterials.2010.05.009. Epub 2010 Jun 9.
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Cellular uptake and toxicity of gold nanoparticles in prostate cancer cells: a comparative study of rods and spheres.金纳米棒和金纳米球对前列腺癌细胞的细胞摄取和毒性:比较研究。
J Appl Toxicol. 2010 Apr;30(3):212-7. doi: 10.1002/jat.1486.
4
The effect of the shape of mesoporous silica nanoparticles on cellular uptake and cell function.介孔二氧化硅纳米颗粒的形状对细胞摄取和细胞功能的影响。
Biomaterials. 2010 Jan;31(3):438-48. doi: 10.1016/j.biomaterials.2009.09.060. Epub 2009 Oct 1.
5
The effects of PEG grafting level and injection dose on gold nanorod biodistribution in the tumor-bearing mice.聚乙二醇接枝水平和注射剂量对荷瘤小鼠体内金纳米棒生物分布的影响。
J Control Release. 2009 Oct 1;139(1):81-4. doi: 10.1016/j.jconrel.2009.06.006. Epub 2009 Jun 16.
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Biodistribution of 1.4- and 18-nm gold particles in rats.1.4纳米和18纳米金颗粒在大鼠体内的生物分布。
Small. 2008 Dec;4(12):2108-11. doi: 10.1002/smll.200800922.
7
Multifunctional and stimuli-sensitive pharmaceutical nanocarriers.多功能及刺激敏感型药物纳米载体
Eur J Pharm Biopharm. 2009 Mar;71(3):431-44. doi: 10.1016/j.ejpb.2008.09.026. Epub 2008 Oct 17.
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Shape effects of filaments versus spherical particles in flow and drug delivery.流动和药物递送中长丝与球形颗粒的形状效应
Nat Nanotechnol. 2007 Apr;2(4):249-55. doi: 10.1038/nnano.2007.70. Epub 2007 Mar 25.
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Cellular uptake and cytotoxicity of silica nanotubes.二氧化硅纳米管的细胞摄取与细胞毒性
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10
Shape induced inhibition of phagocytosis of polymer particles.形状诱导的聚合物颗粒吞噬作用抑制
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金纳米粒子的几何形状和表面特性会影响其在巨噬细胞中的生物分布和摄取。

Geometry and surface characteristics of gold nanoparticles influence their biodistribution and uptake by macrophages.

机构信息

Department of Pharmaceutics and Pharmaceutical Chemistry, University of Utah, Salt Lake City, UT 84108, USA.

出版信息

Eur J Pharm Biopharm. 2011 Apr;77(3):417-23. doi: 10.1016/j.ejpb.2010.11.010. Epub 2010 Nov 18.

DOI:10.1016/j.ejpb.2010.11.010
PMID:21093587
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3379889/
Abstract

Spherical and rod-shaped gold nanoparticles with surface poly(ethylene glycol) (PEG) chains were characterized for size, shape, charge, poly dispersity and surface plasmon resonance. The nanoparticles were injected intravenously to 6-8-week-old female nu/nu mice bearing orthotopic ovarian tumors, and their biodistribution in vital organs was compared. Gold nanorods were taken up to a lesser extent by the liver, had longer circulation time in the blood, and higher accumulation in the tumors, compared with their spherical counterparts. The cellular uptake of PEGylated gold nanoparticles by a murine macrophage-like cell line as a function of geometry was examined. Compared to nanospheres, PEGylated gold nanorods were taken up to a lesser extent by macrophages. These studies point to the importance of gold nanoparticle geometry and surface properties on transport across biological barriers.

摘要

球形和棒状的金纳米粒子具有表面聚乙二醇(PEG)链,其大小、形状、电荷、多分散性和表面等离子体共振都得到了表征。将纳米粒子静脉注射到 6-8 周龄的携带原位卵巢肿瘤的雌性无胸腺裸鼠体内,并比较其在重要器官中的分布。与球形纳米粒子相比,金纳米棒在肝脏中的摄取量较小,在血液中的循环时间更长,在肿瘤中的积累量更高。作为几何形状的函数,考察了聚乙二醇化金纳米粒子被鼠源巨噬细胞样细胞系摄取的情况。与纳米球相比,聚乙二醇化金纳米棒被巨噬细胞摄取的量较少。这些研究表明,金纳米粒子的几何形状和表面性质对穿过生物屏障的转运很重要。