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

被引:430
作者
Arnida [4 ]
Janat-Amsbury, M. M. [3 ,4 ]
Ray, A. [4 ]
Peterson, C. M. [3 ,4 ]
Ghandehari, H. [1 ,2 ,4 ]
机构
[1] Univ Utah, Dept Pharmaceut & Pharmaceut Chem, Nano Inst Utah, Salt Lake City, UT 84108 USA
[2] Univ Utah, Dept Bioengn, Salt Lake City, UT 84108 USA
[3] Univ Utah, Dept Obstet & Gynecol, Salt Lake City, UT 84108 USA
[4] Univ Utah, Ctr Nanomed, Nano Inst Utah, Salt Lake City, UT 84108 USA
基金
美国国家科学基金会;
关键词
Gold nanoparticles; Nanorods; Nanomedicine; Biodistribution; Ovarian tumor; Macrophages; CELLULAR UPTAKE; DRUG; NANORODS; SIZE; PHARMACOKINETICS; PARTICLES; RECEPTORS; RESONANCE; VECTOR; TUMORS;
D O I
10.1016/j.ejpb.2010.11.010
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:417 / 423
页数:7
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