808 nm Near-Infrared Light-Excited UCNPs@mSio2-Ce6-GPC3 Nanocomposites For Photodynamic Therapy In Liver Cancer

被引:27
|
作者
Hu, Jiahe [1 ]
Shi, Jialan [2 ,3 ]
Gao, Yingqian [1 ]
Yang, Wei [1 ]
Liu, Ping [1 ]
Liu, Qinghao [1 ]
He, Fei [4 ]
Wang, Chunxu [2 ]
Li, Tao [2 ]
Xie, Rui [1 ]
Zhu, Jiuxin [5 ]
Yang, Piaoping [4 ]
机构
[1] Harbin Med Univ, Canc Hosp, Dept Digest Internal Med, Harbin 150081, Heilongjiang, Peoples R China
[2] Harbin Med Univ, Affiliated Hosp 1, Dept Hematol, Harbin 150001, Heilongjiang, Peoples R China
[3] Harvard Med Sch, Brigham & Womens Hosp, VA Boston Healthcare Syst, Dept Surg, Boston, MA USA
[4] Harbin Engn Univ, Coll Mat Sci & Chem Engn, Key Lab Superlight Mat & Surface Technol, Minist Educ, Harbin 150001, Heilongjiang, Peoples R China
[5] Harbin Med Univ, Coll Pharm, Key Labs Cardiovasc Med Res, Minist Educ,Dept Pharmacol,State Prov Key Labs Bi, Harbin 150081, Heilongjiang, Peoples R China
来源
基金
黑龙江省自然科学基金; 中国国家自然科学基金;
关键词
liver cancer; photodynamic therapy; upconversion nanoparticles; 808 nm NIR; GPC3; targeted therapy; UP-CONVERSION NANOPARTICLES; HEPATOCELLULAR-CARCINOMA; GLYPICAN-3; LUMINESCENCE; PHOTOSENSITIZERS; NANOPHOSPHORS; EXPRESSION;
D O I
10.2147/IJN.S221496
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Background: It is important to explore effective treatment for liver cancer. Photodynamic therapy (PDT) is a novel technique to treat liver cancer, but its clinical application is obstructed by limited depth of visible light penetration into tissue. The near-infrared (NIR) photosensitizer is a potential solution to the limitations of PDT for deep tumor tissue treatment. Purpose: We aimed to investigate 808 nm NIR light-excited UCNPs@mSiO(2)-Ce6-GPC3 nanocomposites for PDT in liver cancer. Methods: In our study, 808 nm NIR light-excited upconversion nanoparticles (UCNPs) were simultaneously loaded with the photosensitizer chlorin e6 (Ce6) and the antibody glypican-3 (GPC3), which is overexpressed in hepatocellular carcinoma cells. The multi-tasking UCNPs@mSiO(2)-Ce6-GPC3 nanoparticles under 808 nm laser irradiation with enhanced depth of penetration would enable the effective targeting of PDT. Results: We found that the UCNPs@mSiO(2)-Ce6-GPC3 nanoparticles had good biocompatibility, low toxicity, excellent cell imaging in HepG2 cancer cells and high anti-tumor effect in vitro and in vivo. Conclusion: We believe that the utilization of 808 nm NIR excited UCNPs@mSiO(2) -Ce6-GPC3 nanoparticles for PDT is a safe and potential therapeutic option for liver cancer.
引用
收藏
页码:10009 / 10021
页数:13
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