The effects of PEG grafting level and injection dose on gold nanorod biodistribution in the tumor-bearing mice

被引:178
作者
Akiyama, Yasuyuki [1 ]
Mori, Takeshi [1 ,2 ]
Katayama, Yoshiki [1 ,2 ]
Niidome, Takuro [1 ,2 ,3 ]
机构
[1] Kyushu Univ, Fac Engn, Dept Appl Chem, Nishi Ku, Fukuoka 8190395, Japan
[2] Kyushu Univ, Ctr Future Chem, Nishi Ku, Fukuoka 8190395, Japan
[3] Japan Sci & Technol Corp, PRESTO, Kawaguchi, Saitama 3320012, Japan
基金
日本科学技术振兴机构; 日本学术振兴会;
关键词
Biodistribution; EPR effect; Gold nanorods; Photothermal therapy; Polyethylene glycol; IN-VIVO; PARTICLE-SIZE; DRUG-DELIVERY; NANOPARTICLES; SPLEEN;
D O I
10.1016/j.jconrel.2009.06.006
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Gold nanorods have strong absorbance in the near infrared region, which penetrates deeply into tissues, where the absorbed light energy is converted into heat. Therefore, gold nanorods are expected to act as an effective contrast agent for in vivo bioimaging and as a thermal converter for photothermal therapy. We grafted various amounts of polyethylene glycol (PEG) onto the surface of gold nanorods and investigated the effects of grafting level and injection dose on the biodistribution in the tumor-bearing mice after intravenous injection and enhanced permeability and retention (EPR). Higher PEG grafting levels were advantageous for reticuloendothelial system (RES) avoidance and for suppression of aggregation of the gold nanorods in the circulation. Modification with a PEG:gold molar ratio of 1.5 was sufficient to show both prolonged circulation and the EPR effect. When the injection dose was increased above 19.5 mu g of gold, the RES uptake in the liver was saturated and surplus gold nanorods were distributed to other tissues, especially the spleen and the tumor. The results of this study will provide an important basis for the development of cancer therapies mediated by the photothermal effect of gold nanorods. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:81 / 84
页数:4
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