Biodistribution and acute toxicity of naked gold nanoparticles in a rabbit hepatic tumor model

被引:60
作者
Glazer, Evan S. [1 ]
Zhu, Cihui [1 ]
Hamir, Amir N. [2 ]
Borne, Agatha [2 ]
Thompson, Catherine Shea [1 ,4 ]
Curley, Steven A. [1 ,3 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Surg Oncol, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Vet Med & Surg, Houston, TX 77030 USA
[3] Rice Univ, Dept Mech Engn & Mat Sci, Houston, TX 77251 USA
[4] Rice Univ, Dept Biomed Engn, Houston, TX 77251 USA
关键词
Gold nanoparticle; tumor model; biodistribution; acute toxicity; RADIOFREQUENCY FIELD; PARTICLE-SIZE; CANCER-CELLS; PHASE-I; PACLITAXEL; SILVER;
D O I
10.3109/17435390.2010.516026
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
There is a paucity of data regarding the safety of administering solid gold nanoparticles (AuNPs) in large animal tumor models. We assessed the acute toxicity and biodistribution of 5 nm and 25 nm solid AuNPs in New Zealand White rabbits (n = 6 in each) with implanted liver Vx2 tumors 24 h after intravenous injection. Gold concentration was determined by inductively coupled plasma atomic emission spectrometry (ICP) and imaged with transmission electron microscopy (TEM). There was no clinico-pathologic evidence of renal, hepatic, pulmonary, or other organ dysfunction. After 25 nm AuNP administration, the concentration of white blood cells increased after treatment (p = 0.001). Most other blood studies were unchanged. AuNPs were distributed to the spleen, liver, and Vx2 tumors, but not to other tissues. The urinary excretion of AuNPs was bimodal as measured by ICP. 25 nm AuNPs were more evenly distributed throughout tissues and may be better tools for medical therapy.
引用
收藏
页码:459 / 468
页数:10
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