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Proton-dynamic therapy following photosensitiser activation by accelerated protons demonstrated through fluorescence and singlet oxygen production

机译:通过荧光和单线态氧的产生证明加速光子激活光敏剂后的质子动力疗法

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摘要

We demonstrate excitation of photosensitisers (PSs) by accelerated protons to produce fluorescence and singlet oxygen. Their fluorescence follows a pattern similar to the proton energy loss in matter, while proton-derived fluorescence spectra match the photon-induced spectra. PSs excited in dry gelatin exhibit enhanced phosphorescence, suggesting an efficient PSs triplet state population. Singlet oxygen measurements, both optically at ~1270 nm and through the photoproduct of protoporphyrin IX (PpIX), demonstrate cytotoxic singlet oxygen generation by proton excitation. The singlet oxygen-specific scavenger 1,4-diazabicyclo[2.2.2]octane (DABCO) abrogates the photoproduct formation under proton excitation, but cannot countermand the overall loss of PpIX fluorescence. Furthermore, in two cell lines, M059K and T98G, we observe differential cell death upon the addition of the PS cercosporin, while in U87 cells we see no effect at any proton irradiation dose. Our results pave the way for a novel treatment combining proton therapy and “proton-dynamic therapy” for more efficient tumour eradication.
机译:我们展示了通过加速的质子激发光敏剂(PSs)产生荧光和单线态氧。它们的荧光遵循类似于物质中质子能量损失的模式,而质子衍生的荧光光谱与光子诱导的光谱匹配。在干明胶中激发的PS表现出增强的磷光,表明有效的PSs三重态种群。单线态氧的测量,无论是在〜1270 opticalnm处还是通过原卟啉IX(PpIX)的光产物进行的光学测量,都表明了质子激发产生的细胞毒性单线态氧。单线态氧特异性清除剂1,4-二氮杂双环[2.2.2]辛烷(DABCO)在质子激发下消除了光产物的形成,但不能抵消PpIX荧光的总体损失。此外,在两种细胞系M059K和T98G中,我们观察到添加PS cercosporin后细胞死亡的差异,而在U87细胞中,在任何质子辐照剂量下均无作用。我们的研究结果为结合质子疗法和“质子动力疗法”以更有效地根除肿瘤的新型疗法铺平了道路。

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