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首页> 外文期刊>ACS nano >Plasmon-Mediated Generation of Reactive Oxygen Species from Near- Infrared Light Excited Gold Nanocages for Photodynamic Therapy in Vitro
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Plasmon-Mediated Generation of Reactive Oxygen Species from Near- Infrared Light Excited Gold Nanocages for Photodynamic Therapy in Vitro

机译:等离子体介导的近红外激发金纳米笼的活性氧物种的体外光动力疗法。

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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 transforminto either ROS or hyperthermia. Electron spin resonance spectroscopy was applied to demonstrate the production of three main radical species, namely, singlet oxygen (~1O_2), superoxide radical anion (O_2~(-?)), and hydroxyl radical (~?OH). 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, comparedwith onephoton 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.
机译:我们已经进行了金纳米笼(AuNCs)作为内在的无机光敏剂的基本分析,该金纳米笼通过近红外(NIR)一/两光子辐射下通过等离激元使能的光化学介导活性氧物种(ROS)的产生。我们公开了近红外光激发的热电子转化为ROS或高温。应用电子自旋共振光谱法证明了三种主要的自由基种类的产生,即单线态氧(〜1O_2),超氧自由基阴离子(O_2〜(-?))和羟基自由基(〜?OH)。通过精心设计的基于三电极系统的光电化学实验,证实了来自辐照过的AuNC的热电子的存在。可以推测,在AuNCs中激发的表面等离激元首先衰减成热电子,然后产生的热电子通过能量和电子转移模式使氧敏感,从而形成ROS。我们还比较了在一个/两个光子辐照下,AuNCs在不同表面化学环境中的ROS产生效率,并验证了与一个光子辐照相比,两个光子辐照可以带来更多的ROS。此外,在体外,在双光子照射下,ROS可以触发线粒体去极化和caspase蛋白上调,从而启动肿瘤细胞凋亡。同时,热疗主要诱导肿瘤细胞坏死。我们的发现表明,可以轻松调节等离激元介导的ROS和热疗,以优化抗癌光疗。

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