Foot-and-mouth disease virus-like particles as integrin-based drug delivery system achieve targeting anti-tumor efficacy
文献类型: 外文期刊
第一作者: Yan, Dan
作者: Yan, Dan;Teng, Zhidong;Sun, Shiqi;Dong, Hu;Gao, Yuan;Wei, Yanquan;Liu, Xiangtao;Yin, Hong;Guo, Huichen;Yan, Dan;Teng, Zhidong;Sun, Shiqi;Dong, Hu;Gao, Yuan;Wei, Yanquan;Liu, Xiangtao;Yin, Hong;Guo, Huichen;Jiang, Shan;Qin, Wenwu
作者机构:
关键词: FMDV VLPs;Integrin receptor;Drug delivery;Dox;Tumor therapy
期刊名称:NANOMEDICINE-NANOTECHNOLOGY BIOLOGY AND MEDICINE ( 影响因子:6.458; 五年影响因子:7.072 )
ISSN: 1549-9634
年卷期: 2017 年 13 卷 3 期
页码:
收录情况: SCI
摘要: The surface of foot-and-mouth disease virus (FMDV)-like particles (VLPs) contains a conserved arginine-glycine-aspartic acid (RGD) motif. Natural FMDV specifically attaches to overexpressed integrin receptors in several cancer cells. The FMDV VLPs produced in Escherichia coli were used for the first time as a delivery system of anti-tumor drug doxorubicin (DOX). The DOX-loaded VLPs exhibited a distinct release profile in different physiological conditions. The effects of FMDV-VLPs-DOX on cellular internalization and viability were evaluated in vitro by cell imaging, MTT assay and apoptosis, respectively. The anti-tumor efficacy in vivo was also determined in a nude mouse xenograft model based on tumor volume/weight and histological changes. The FMDV-VLPs-DOX complex significantly inhibited the proliferation of tumor and improved the pathological damage of DOX to non-targeting tissues. All results supported the potential of FMDV VLPs as a platform for specific targeted delivery of drugs or chemical reagents. (C) 2016 Elsevier Inc. All rights reserved.
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