IMSaT, University of Dundee , 1 Wurzburg Loan, Dundee DD2 1FD, United Kingdom.
Department of Biology, Università di Pisa , S.S. 12 Abetone e Brennero 4, 56127 Pisa, Italy.
Nano Lett. 2017 Apr 12;17(4):2307-2312. doi: 10.1021/acs.nanolett.6b05052. Epub 2017 Apr 3.
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.
导致恶性肿瘤中血液供应增加的机制之一是血管内皮生长因子(VEGF)的过度表达。已经生产了几种针对 VEGF 的抗体用于成像和治疗。然而,与抗体相比,分子印迹聚合物纳米粒子(nanoMIP)具有显著优势,特别是在提高稳定性、设计速度、成本和功能化控制方面。在本研究中,首次成功生产了针对人 VEGF 的 nanoMIP。将 nanoMIP 与量子点(QDs)偶联用于癌症成像。在斑马鱼胚胎中,复合纳米粒子对过表达 hVEGF 的人黑色素瘤细胞异种移植物表现出特异性归巢。在对照生物中未观察到这种积累的证据。这些结果表明,nanoMIP 是有前途的材料,可以考虑用于推进分子肿瘤学研究,特别是当由于其免疫原性或生产时间长而不太需要抗体时。