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Ablation of Hypoxic Tumors with Dose-Equivalent Photothermal but Not Photodynamic Therapy Using a Nanostructured Porphyrin Assembly

机译:使用纳米结构的卟啉组装体用等效剂量的光热疗法而非光动力疗法消融缺氧性肿瘤

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摘要

Tumor hypoxia is increasingly being recognized as a characteristic feature of solid tumors and significantly complicates many treatments based on radio-, chemo-, and phototherapies. While photodynamic therapy (PDT) is based on photosensitizer interactions with diffused oxygen, photothermal therapy (PTT) has emerged as a new phototherapy that is predicted to be independent of oxygen levels within tumors. It has been challenging to meaningfully compare these two modalities due to differences in contrast agents and irradiation parameters, and no comparative in vivo studies have been performed until now. Here, by making use of recently developed nanostructured self-quenched porphysome nanoparticles, we were able to directly compare PDT and PTT using matched light doses and matched porphyrin photosensitizer doses (with the photosensitizer being effective for either PTT or PDT based on the existence of nanostructure or not). Therefore, we demonstrated the nanostructure-driven conversion from the PDT singlet oxygen generating mechanism of porphyrin to a completely thermal mechanism, ideal for PTT enhancement. Using a novel hypoxia tumor model, we determined that nanostructured porphyrin PTT enhancers are advantageous to overcome hypoxic conditions to achieve effective ablation of solid tumors.
机译:肿瘤缺氧越来越多地被认为是实体瘤的特征,并且使基于放射疗法,化学疗法和光疗法的许多治疗变得非常复杂。尽管光动力疗法(PDT)是基于光敏剂与扩散氧的相互作用,但光热疗法(PTT)已作为一种新的光疗法出现,预计将独立于肿瘤中的氧水平。由于造影剂和照射参数的差异,有意义地比较这两种方式是一项挑战,迄今为止,还没有进行过体内比较研究。在这里,通过使用最新开发的纳米结构的自淬灭性卟啉纳米颗粒,我们能够使用匹配的光剂量和匹配的卟啉光敏剂剂量直接比较PDT和PTT(根据纳米结构的存在,光敏剂对PTT或PDT有效)或不)。因此,我们证明了从卟啉的PDT单线态氧生成机理到完全热机理的纳米结构驱动转化,是增强PTT的理想选择。使用新型的缺氧肿瘤模型,我们确定了纳米结构的卟啉PTT增强剂有利于克服缺氧条件,实现实体瘤的有效消融。

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