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Triggering cell death by nanographene oxide mediated hyperthermia

机译:纳米氧化烯介导的高温触发细胞死亡

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Graphene oxide (GO) has been proposed as an hyperthermia agent for anticancer therapies due to its near-infrared (NIR) optical absorption ability which, with its small two-dimensional size, could have a unique performance when compared to that of any other nanoparticle. Nevertheless, attention should be given to the hyperthermia route and the kind of GO-cell interactions induced in the process. The hyperthermia laser irradiation parameters, such as exposure time and laser power, were investigated to control the temperature rise and consequent damage in the GOs containing cell culture medium. The type of cell damage produced was evaluated as a function of these parameters. The results showed that cell culture temperature (after irradiating cells with internalized GO) increases preferentially with laser power rather than with exposure time. Moreover, when laser power is increased, necrosis is the preferential cell death leading to an increase of cytokine release to the medium.
机译:氧化石墨烯(GO)因其近红外(NIR)光学吸收能力而被提出作为抗癌治疗的高温药物,其二维尺寸小,与任何其他纳米颗粒相比都具有独特的性能。然而,应注意热疗途径以及在此过程中诱导的GO细胞相互作用的种类。研究了高温激光照射参数,例如曝光时间和激光功率,以控制温度升高以及随之而来的含有GOs的细胞培养基的损坏。根据这些参数评估产生的细胞损伤的类型。结果表明,细胞培养温度(用内在的GO照射细胞后)优先随激光功率而不是随曝光时间增加。而且,当增加激光功率时,坏死是导致细胞因子释放到培养基中的增加的优先细胞死亡。

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