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通过荧光和单线态氧产生证明了通过加速质子敏化剂激活的质子动力疗法。

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

机构信息

Department of Radiation Biology, Institute for Cancer Research, Radium Hospital, Oslo University Hospital, Montebello, 0379, Oslo, Norway.

Department of Physics, University of Oslo, Blinderrn, 0315, Oslo, Norway.

出版信息

Nat Commun. 2019 Sep 4;10(1):3986. doi: 10.1038/s41467-019-12042-7.

Abstract

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.

摘要

我们证明了加速质子可以激发光敏剂(PS)产生荧光和单线态氧。它们的荧光遵循与物质中质子能量损失相似的模式,而质子衍生的荧光光谱与光诱导的光谱相匹配。在干燥明胶中激发的 PS 表现出增强的磷光,表明 PS 的三重态有效产生。单线态氧的测量,包括在 ~1270nm 处的光学测量和通过原卟啉 IX(PpIX)的光产物测量,都证明了质子激发可以产生细胞毒性的单线态氧。单线态氧特异性清除剂 1,4-二氮杂二环[2.2.2]辛烷(DABCO)可以阻断质子激发下的光产物形成,但不能抵消 PpIX 荧光的整体损失。此外,在 M059K 和 T98G 两种细胞系中,我们观察到添加 PS 尾孢菌素后细胞死亡的差异,而在 U87 细胞中,我们在任何质子辐照剂量下都没有观察到效果。我们的结果为一种新的治疗方法铺平了道路,该方法将质子治疗与“质子动力学治疗”相结合,以更有效地消除肿瘤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e72/6726622/3591cd366667/41467_2019_12042_Fig1_HTML.jpg

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