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Visible-light Induced Reduction of Graphene Oxide Using Plasmonic Nanoparticle
Published on: September 22, 2015
Near infrared light-mediated enhancement of reactive oxygen species generation through electron transfer from
Yue He1, Andrea Del Valle2, Yu Qian2
1Department of Biomedical Engineering and Environmental Sciences, National Tsing Hua University, Hsinchu, 30013, Taiwan, Republic of China. yufen@mx.nthu.edu.tw and Laboratory of Quality & Safety Risk Assessment for Citrus Products (Chongqing), Ministry of Agriculture, Citrus Research Institute, Southwest University, Chongqing, 400712, China.
Abstract:
Clinical applications of current photodynamic therapy (PDT) agents are often restricted to be activated only by UV and visible light, which have very poor tissue penetration depths. In this study, a new near infrared (NIR)-absorbing nanoagent based on graphene oxide decorated with iron hydroxide/oxide (GO-FeOxH) was developed for light-activated nanomaterial-mediated PDT. This nanocomposite, GO-FeOxH was prepared via the one-step electrooxidation of iron nails in an aqueous GO solution. The as-prepared GO-FeOxH showed a much higher reactive oxygen species (ROS) activity under NIR light irradiation than GO. Through a variety of spectroscopic analyses, the mechanism involved in the enhancement of ROS activity of GO by FeOxH was systematically investigated. We observed that NIR light irradiation promotes electron transfer from GO to the Fe(iii) of FeOxH and accelerates their reaction with O2, forming superoxide anion radicals, which then undergo a disproportionation reaction to produce H2O2. H2O2 then reacts with Fe(ii) in FeOxH to mediate Fenton reactions, producing amplified hydroxyl radicals. Using in vitro studies, we demonstrated that GO-FeOxH can be used as a NIR activatable PDT nanoagent, providing efficient cancer therapy.

