Photodynamic therapy in hypoxia: Near-infrared-sensitive, self-supported, oxygen generation nano-platform enabled by upconverting nanoparticles

被引:40
作者
Niu, Na [1 ,2 ]
Zhang, Zhe [1 ]
Gao, Xi [1 ]
Chen, Zhijun [2 ]
Li, Shujun [2 ]
Li, Jian [2 ]
机构
[1] Northeast Forestry Univ, Coll Sci, Harbin 150001, Heilongjiang, Peoples R China
[2] Northeast Forestry Univ, Key Lab Bio Based Mat Sci & Technol, Minist Educ, Harbin 150001, Heilongjiang, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Au2O3; Photodynamic therapy; Hypoxia microenvironment; Upconversion; UP-CONVERSION NANOPARTICLES; MESOPOROUS SILICA NANOPARTICLES; TARGETED DRUG-DELIVERY; IN-VIVO; PHOTOTHERMAL THERAPY; CANCER-CELLS; FLUORESCENT NANOPARTICLES; BIOMEDICAL APPLICATIONS; LIGHT; CHEMOTHERAPY;
D O I
10.1016/j.cej.2018.07.049
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Photodynamic therapy (PDT) shows great potential in anti-cancer therapy. The efficiency of PDT is greatly limited by the hypoxia environment in tumors. However, current methods developed to conquer this problem did not accurately produce oxygen for PDT of a certain amount and in a certain position, which could bring a potential risk to normal cells and tissues. Here, upconverting nanoparticles (UCNPs) and gold oxide (Au2O3) were integrated to prepare an efficient, self-supported, oxygen generation nano-platform in a hypoxia environment. Upon a near-infrared (NIR) laser, Au2O3 could produce oxygen assisted by UCNPs through the fluorescence resonance energy transfer (FRET) effect. This light-controlled, self-supported oxygen generation system effectively provided oxygen for the as-loaded photosensitizer chlorin e6 (Ce6) in PDT upon NIR irradiation, which enhanced the inhibition effect of the tumor cells, in both in vitro and in vivo experiments. The present strategy of light-induced, oxygen-producible promoted PDT may solve the long-standing contradiction between the oxygen-dependent working mechanism of PDT and hypoxia microenvironments in tumor cells.
引用
收藏
页码:818 / 827
页数:10
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