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靶向血管内皮生长因子165(VEGF165)的分子磁共振探针:制备及体内外评价

Molecular magnetic resonance probe targeting VEGF165: preparation and in vitro and in vivo evaluation.

作者信息

You Xiao-Guang, Tu Rong, Peng Ming-Li, Bai Yu-Jie, Tan Mingqian, Li Han-Jian, Guan Jing, Wen Li-Jun

机构信息

Department of Radiology and Cancer Institute, Hainan Medical College Hospital, Haikou City, Hainan Province, 570102, China.

出版信息

Contrast Media Mol Imaging. 2014 Sep-Oct;9(5):349-54. doi: 10.1002/cmmi.1584. Epub 2014 Apr 14.

Abstract

A new method for imaging the tumor human vascular endothelial growth factor 165 (VEGF 165) is presented. A magnetic resonance imaging (MRI) probe was prepared by crosslinking ultrasmall superparamagnetic iron oxide (USPIO) nanoparticles to the aptamer for tumor vascular endothelial growth factor 165 (VEGF165-aptamer). The molecular probe was evaluated for its in vitro and in vivo activities toward VEGF165. Enzyme-linked immunosorbent assay showed that the VEGF165-aptamer-USPIO nanoparticles conjugate specifically binds to VEGF165 in vitro. A cell proliferation test showed that VEGF165-aptamer-USPIO seems to block the proliferation of human umbilical vein endothelial cells induced by free VEGF165, suggesting that VEGF165 is an effective target of this molecular probe. In xenograft mice carrying liver cancer that expresses VEGF165, T2-weighted imaging of the tumor displayed marked negative enhancement 3 h after the intravenous administration of VEGF165-aptamer-USPIO. The enhancement disappeared 6 h after administration of the probe. These results suggest the targeted imaging effect of VEGF165-aptamer-USPIO probe in vivo for VEGF165-expressing tumors. This is the first report of a targeted MRI molecular probe based on USPIO and VEGF165-aptamer.

摘要

本文介绍了一种对肿瘤人类血管内皮生长因子165(VEGF 165)进行成像的新方法。通过将超小超顺磁性氧化铁(USPIO)纳米颗粒与肿瘤血管内皮生长因子165适配体(VEGF165-适配体)交联制备了一种磁共振成像(MRI)探针。对该分子探针针对VEGF165的体外和体内活性进行了评估。酶联免疫吸附测定表明,VEGF165-适配体-USPIO纳米颗粒缀合物在体外能特异性结合VEGF165。细胞增殖试验表明,VEGF165-适配体-USPIO似乎能阻断游离VEGF165诱导的人脐静脉内皮细胞增殖,这表明VEGF165是该分子探针的有效靶点。在携带表达VEGF165的肝癌的异种移植小鼠中,静脉注射VEGF165-适配体-USPIO后3小时,肿瘤的T2加权成像显示出明显的负增强。注射探针6小时后增强消失。这些结果表明VEGF165-适配体-USPIO探针在体内对表达VEGF165的肿瘤具有靶向成像作用。这是基于USPIO和VEGF165-适配体的靶向MRI分子探针的首次报道。

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