血管内皮生长因子
癌症研究
血管生成
抗体
体内
免疫原性
化学
PLGA公司
黑色素瘤
纳米技术
材料科学
纳米颗粒
生物医学工程
血管内皮生长因子受体
医学
免疫学
生物
生物技术
作者
Alessandra Cecchini,Vittoria Raffa,Francesco Canfarotta,Giovanni Signore,Sergey A. Piletsky,Michael P. MacDonald,A. Cuschieri
出处
期刊:Nano Letters
[American Chemical Society]
日期:2017-03-28
卷期号:17 (4): 2307-2312
被引量:146
标识
DOI:10.1021/acs.nanolett.6b05052
摘要
One of the mechanisms responsible for cancer-induced increased blood supply in malignant neoplasms is the overexpression of vascular endothelial growth factor (VEGF). Several antibodies for VEGF targeting have been produced for both imaging and therapy. Molecularly imprinted polymer nanoparticles, nanoMIPs, however, offer significant advantages over antibodies, in particular in relation to improved stability, speed of design, cost and control over functionalization. In the present study, the successful production of nanoMIPs against human VEGF is reported for the first time. NanoMIPs were coupled with quantum dots (QDs) for cancer imaging. The composite nanoparticles exhibited specific homing toward human melanoma cell xenografts, overexpressing hVEGF, in zebrafish embryos. No evidence of this accumulation was observed in control organisms. These results indicate that nanoMIPs are promising materials which can be considered for advancing molecular oncological research, in particular when antibodies are less desirable due to their immunogenicity or long production time.
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