4.8 Article

Plasmon-Mediated Generation of Reactive Oxygen Species from Near-Infrared Light Excited Gold Nanocages for Photodynamic Therapy in Vitro

Journal

ACS NANO
Volume 8, Issue 7, Pages 7260-7271

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/nn502325j

Keywords

gold nanocages; reactive oxygen species; photodynamic therapy; plasmon-enabled photochemistry; hot electrons; two-photon

Funding

  1. National Key Basic Research Program of China [2013CB932703]
  2. Natural Science Foundation of China [21390410, 31271072, 31200751, 81201133, 81101743, 31300827]

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We have performed fundamental assays of gold nanocages (AuNCs) as intrinsic inorganic photosensitizers mediating generation of reactive oxygen species (ROS) by plasmon-enabled photochemistry under near-infrared (NIR) one/two-photon irradiation. We disclosed that NIR light excited hot electrons transform into either ROS or hyperthermia. Electron spin resonance spectroscopy was applied to demonstrate the production of three main radical species, namely, singlet oxygen (O-1(2)), superoxide radical anion (O-2(-center dot)), and hydroxyl radical ((OH)-O-center dot). The existence of hot electrons from irradiated AuNCs was confirmed by a well-designed photoelectrochemical experiment based on a three-electrode system. It could be speculated that surface plasmons excited in AuNCs first decay into hot electrons, and then the generated hot electrons sensitize oxygen to form ROS through energy and electron transfer modes. We also compared AuNCs' ROS generation efficiency in different surface chemical environments under one/two-photon irradiation and verified that, compared with one-photon irradiation, two-photon irradiation could bring about much more ROS. furthermore, in vitro, under two-photon irradiation, ROS can trigger mitochondrial depolarization and caspase protein up-regulation to initiate tumor cell apoptosis. Meanwhile, hyperthermia mainly induces tumor cell necrosis. Our findings suggest that plasmon-mediated ROS and hyperthermia can be facilely regulated for optimized anticancer phototherapy.

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