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靶向血管内皮生长因子受体(VEGFR)可显著增强体内氧化石墨烯纳米材料的肿瘤摄取。

VEGFR targeting leads to significantly enhanced tumor uptake of nanographene oxide in vivo.

作者信息

Shi Sixiang, Yang Kai, Hong Hao, Chen Feng, Valdovinos Hector F, Goel Shreya, Barnhart Todd E, Liu Zhuang, Cai Weibo

机构信息

Materials Science Program, University of Wisconsin-Madison, WI, USA.

Jiangsu Key Laboratory for Carbon-Based Functional Materials and Devices, Institute of Functional Nano and Soft Materials Laboratory (FUNSOM), Soochow University, Suzhou, Jiangsu, China.

出版信息

Biomaterials. 2015 Jan;39:39-46. doi: 10.1016/j.biomaterials.2014.10.061. Epub 2014 Nov 15.

Abstract

Although graphene oxide (GO) has recently been considered as a highly attractive nanomaterial for future cancer imaging and therapy, it is still a major challenge to improve its in vivo tumor active targeting efficiency. Here in this full article, we demonstrated the successful and significantly enhanced in vivo tumor vasculature targeting efficacy of well-functionalized GO nanoconjugates by using vascular endothelial growth factor 121 (VEGF121) as the targeting ligand. As-developed GO nanoconjugate exhibits excellent in vivo stability, specific in vitro and in vivo vascular endothelial growth factor receptor (VEGFR) targeting, significantly enhanced tumor accumulation (>8 %ID/g) as well as high tumor-to-muscle contrast, showing great potential for future tumor targeted imaging and therapy.

摘要

尽管氧化石墨烯(GO)最近被认为是一种对未来癌症成像和治疗极具吸引力的纳米材料,但提高其体内肿瘤主动靶向效率仍然是一项重大挑战。在本文中,我们通过使用血管内皮生长因子121(VEGF121)作为靶向配体,证明了功能化良好的GO纳米缀合物在体内对肿瘤血管的靶向效果成功且显著增强。所开发的GO纳米缀合物在体内表现出优异的稳定性、体外和体内对血管内皮生长因子受体(VEGFR)的特异性靶向、显著增强的肿瘤蓄积(>8 %ID/g)以及高肿瘤与肌肉对比度,显示出在未来肿瘤靶向成像和治疗方面的巨大潜力。

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