| Literature DB >> 29981460 |
Xue Yang1, Huipeng Li1, Chenggen Qian1, Yuxin Guo1, Chenzi Li1, Fang Gao1, Ying Yang1, Kaikai Wang1, David Oupicky2, Minjie Sun3.
Abstract
Tumor angiogenesis is a key step in the process of tumor development, and antitumor angiogenesis has a profound influence on tumor growth. Herein we report a dual-function drug delivery system comprising a Near-infrared (NIR) dye and an anti-angiogenic drug within liposomes (Lip-IR780-Sunitinib) for enhanced antitumor therapy. The hydrophobic NIR dye IR780 was loaded into the liposome phospholipid bilayer, and the bilayer would be disrupted by laser irradiation so that anti-angiogenic drug sunitinib release would be activated remotely at the tumor site. The released hydrophilic sunitinib could potentially target multiple VEGF receptors on the tumor endothelial cell surface to inhibit angiogenesis. Meanwhile, IR780-loaded liposomes kill the cancer cells by photothermal therapy. Lip-IR780-Sunitinib exhibited enhanced anti-tumor and anti-angiogenic effects in vitro and in vivo. This system facilitates easy and controlled release of cargos to achieve anti-tumor angiogenesis and photothermal therapy.Entities:
Keywords: Anti-angiogenesis; Drug delivery; Near-infrared light; Photothermal therapy
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Year: 2018 PMID: 29981460 DOI: 10.1016/j.nano.2018.06.011
Source DB: PubMed Journal: Nanomedicine ISSN: 1549-9634 Impact factor: 5.307