Prodrug-embedded angiogenic vessel-targeting nanoparticle: A positive feedback amplifier in hypoxia-induced chemo-photo therapy

被引:55
作者
Guo, Dongbo [1 ]
Xu, Shuting [1 ]
Wang, Nan [1 ]
Jiang, Huangyong [1 ]
Huang, Yu [1 ]
Jin, Xin [1 ]
Xue, Bai [1 ]
Zhang, Chuan [1 ]
Zhu, Xinyuan [1 ]
机构
[1] Shanghai Jiao Tong Univ, State Key Lab Met Matrix Composites, Sch Chem & Chem Engn, 800 Dongchuan Rd, Shanghai 200240, Peoples R China
基金
中国国家自然科学基金;
关键词
Photodynamic therapy; Vascular endothelial growth factor; Hypoxia; Angiogenic vessel-targeting; Drug delivery; PHOTODYNAMIC THERAPY; IN-VIVO; TUMOR; CANCER; RESISTANCE; CELLS; RADIOTHERAPY; MECHANISMS; PROBE; GX1;
D O I
10.1016/j.biomaterials.2017.08.032
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Photodynamic therapy (PDT) induced hypoxia can significantly upregulate the expression of vascular endothelial growth factor (VEGF) at the tumor-stromal interface, resulting in a promoted angiogenesis. Thus, an angiogenesis vessel-targeting nanoparticle (AVT-NP) consisting of photosensitizer, angiogenic vessel-targeting peptide, and bioreductive prodrug is developed for a chemo-photo synergistic cancer therapy, with which anti-cancer effect is achieved first by PDT and immediately followed with hypoxia-activated cytotoxic free radicals. With targeting capability, the AVT-NPs can effectively accumulate at the tumor site due to the promoted angiogenesis in response to PDT-induced hypoxia. The more nanoparticles delivered to the tumor tissue, the higher efficacy of PDT can be achieved, resulting in a more severe hypoxia and increased angiogenesis. Therefore, the prodrug embedded AVT-NP functions as a positive feedback amplifier in the combinational chemo-photo treatment and indeed achieves an enhanced anti-tumor effect in both in vitro and in vivo studies. (C) 2017 Published by Elsevier Ltd.
引用
收藏
页码:188 / 198
页数:11
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