Superior Photodynamic Therapy of Colon Cancer Cells by Selenophene-BODIPY-Loaded Superparamagnetic Iron Oxide Nanoparticles

被引:3
作者
Sertcelik, Kubra Nur Ozvural [1 ]
Karaman, Osman [2 ]
Almammadov, Toghrul [3 ]
Gunbas, Gorkem [2 ]
Kolemen, Safacan [3 ,4 ,5 ,6 ]
Acar, Havva Yagci [1 ,3 ,4 ]
Onbasli, Kubra [3 ]
机构
[1] Koc Univ, Grad Sch Mat Sci & Engn, TR-34450 Istanbul, Turkey
[2] Middle East Tech Univ METU, Dept Chem, TR-06800 Ankara, Turkey
[3] Koc Univ, Dept Chem, TR-34450 Istanbul, Turkey
[4] Koc Univ Surface Sci & Technol Ctr, KUYTAM, TR-34450 Istanbul, Turkey
[5] Koc Univ, Boron & Adv Mat Applicat & Res Ctr, TR-34450 Istanbul, Turkey
[6] Koc Univ, TUPRAS Energy Ctr KUTEM, TR-34450 Istanbul, Turkey
关键词
BODIPY; colon cancer; iron oxide nanoparticles; photodynamic therapy; photosensitizers; superparamagnetism; PHOTOSENSITIZERS;
D O I
10.1002/cptc.202200104
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Development of targeted nanoparticles as carriers to deliver photosensitizers to cancer cells is highly beneficial for ensuring the expected therapeutic outcome of photodynamic therapy. Herein, polyacrylic acid (PAA) coated superparamagnetic iron oxide nanoparticles (SPIONs), conjugated with endothelial growth factor receptor (EGFR) targeting Cetuximab (Cet) were loaded with a BODIPY-based (BOD-Se-I) photosensitizer (Cet-PAA@SPION/BOD-Se-I) to achieve enhanced and selective photodynamic therapy on colon cancer cells. In vitro studies showed that Cet-PAA@SPION/BOD-Se-I improved phototoxicity dramatically compared to free BOD-Se-I on the HT29 cell line due to high uptake of the photosensitizer via endothelial growth factor receptor. Most importantly, the developed nano-agent completely eliminated the phototoxicity of BOD-Se-I on the healthy L929 cell line.
引用
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页数:8
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