Raza Ahtasham, Archer Stuart A, Fairbanks Simon D, Smitten Kirsty L, Botchway Stanley W, Thomas James A, MacNeil Sheila, Haycock John W
Materials Science & Engineering, University of Sheffield, Mappin St, Sheffield S1 3JD, U.K.
Department of Chemistry, University of Sheffield, Brook Hill, Sheffield, S3 7HF, U.K.
J Am Chem Soc. 2020 Mar 11;142(10):4639-4647. doi: 10.1021/jacs.9b11313. Epub 2020 Feb 25.
The dinuclear photo-oxidizing Ru complex [{Ru(TAP)}(tpphz)] (TAP = 1,4,5,8- tetraazaphenanthrene, tpphz = tetrapyrido[3,2-:2',3'-:3″,2''-:2‴,3'''-]phenazine), , is readily taken up by live cells localizing in mitochondria and nuclei. In this study, the two-photon absorption cross section of is quantified and its use as a two-photon absorbing phototherapeutic is reported. It was confirmed that the complex is readily photoexcited using near-infrared, NIR, and light through two-photon absorption, TPA. In 2-D cell cultures, irradiation with NIR light at low power results in precisely focused phototoxicity effects in which human melanoma cells were killed after 5 min of light exposure. Similar experiments were then carried out in human cancer spheroids that provide a realistic tumor model for the development of therapeutics and phototherapeutics. Using the characteristic emission of the complex as a probe, its uptake into 280 μm spheroids was investigated and confirmed that the spheroid takes up the complex. Notably TPA excitation results in more intense luminescence being observed throughout the depth of the spheroids, although emission intensity still drops off toward the necrotic core. As can directly photo-oxidize DNA without the mediation of singlet oxygen or other reactive oxygen species, phototoxicity within the deeper, hypoxic layers of the spheroids was also investigated. To quantify the penetration of these phototoxic effects, was photoexcited through TPA at a power of 60 mW, which was progressively focused in 10 μm steps throughout the entire -axis of individual spheroids. These experiments revealed that, in irradiated spheroids treated with , acute and rapid photoinduced cell death was observed throughout their depth, including the hypoxic region.
双核光氧化钌配合物[{Ru(TAP)}(tpphz)](TAP = 1,4,5,8 - 四氮杂菲,tpphz = 四吡啶并[3,2 - :2',3'-:3″,2''-:2‴,3'''-]菲嗪)很容易被定位于线粒体和细胞核的活细胞摄取。在本研究中,对该配合物的双光子吸收截面进行了量化,并报道了其作为双光子吸收光疗剂的应用。已证实该配合物通过双光子吸收(TPA)利用近红外(NIR)光很容易被光激发。在二维细胞培养中,低功率的近红外光照射会导致精确聚焦的光毒性效应,其中人类黑色素瘤细胞在光照5分钟后被杀死。然后在人类癌症球体中进行了类似实验,这些球体为治疗学和光治疗学的发展提供了一个现实的肿瘤模型。利用该配合物的特征发射作为探针,研究了其被280μm球体摄取的情况,并证实球体摄取了该配合物。值得注意的是,TPA激发导致在球体的整个深度都观察到更强的发光,尽管发射强度朝着坏死核心仍然会下降。由于该配合物可以在没有单线态氧或其他活性氧物种介导的情况下直接光氧化DNA,因此还研究了球体较深的缺氧层内的光毒性。为了量化这些光毒性效应的穿透深度,通过TPA以60 mW的功率对该配合物进行光激发,该功率在单个球体的整个z轴上以10μm的步长逐渐聚焦。这些实验表明,在用该配合物处理的照射球体中,在其整个深度,包括缺氧区域,都观察到了急性和快速的光诱导细胞死亡。