Journal
FRONTIERS IN BIOENGINEERING AND BIOTECHNOLOGY
Volume 11, Issue -, Pages -Publisher
FRONTIERS MEDIA SA
DOI: 10.3389/fbioe.2023.1248283
Keywords
glioblastoma; iron oxide nanoparticles; photothermal therapy; photodynamic therapy; cancer therapy
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We report the development of chlorin e6 (Ce6)-conjugated iron oxide (Fe3O4-Ce-6) nanoparticles for combinational ablation of glioblastoma cells via photothermal therapy (PTT) and photodynamic therapy (PDT). Under laser irradiation, Fe3O4-Ce-6 nanoparticles exhibited good photothermal stability and produced singlet oxygen to mediate PDT. The combinational effect of PTT and PDT effectively killed glioblastoma cells.
Introduction: The effective treatment of glioblastoma still remains a great challenge. We herein report the development of chlorin e6 (Ce6)-conjugated iron oxide (Fe3O4-Ce-6) nanoparticles for ablation of glioblastoma cells via combining photothermal therapy (PTT) with photodynamic therapy (PDT). Methods: Ce6 was conjugated to the synthesized Fe3O4 nanoparticles to form Fe3O4-Ce-6 nanoparticles displaying the optical property of Ce6. Results and discussion: Under 808 nm laser irradiation, Fe3O4-Ce-6 nanoparticles generated heat and the temperature increase did not have obvious changes after five cycles of laser irradiation, suggesting their good photothermal effect and photothermal stability. In addition, 660 nm laser irradiation of Fe3O4-Ce-6 nanoparticles produced singlet oxygen (1O2) to mediate PDT. The Fe3O4-Ce-6 nanoparticles without laser irradiation showed a low cytotoxicity, but they would obviously kill C6 cancer cells after laser irradiation via the combinational effect of PTT and PDT. Fe3O4-Ce-6 nanoparticles thus could be used as a nanotherapeutic agent for combinational ablation of glioblastoma cells.
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