Department of Medical Biophysics, Faculty of Medicine and Dentistry, Institute of Molecular and Translational Medicine, Palacky University, Olomouc, Czech Republic.
Physiol Res. 2019 Dec 30;68(Suppl 4):S467-S474. doi: 10.33549/physiolres.934374.
Photodynamic therapy (PDT) uses photosensitive substance to provoke a cytotoxic reaction causing a cell damage or cell death. The substances, photosensitizers, are usually derivates of porphyrine or phtalocyanine. Photosensitizers must be activated by light in order to produce reactive oxygen species, mainly singlet oxygen. Sonodynamic therapy (SDT) utilizes ultrasound to enhance a cytotoxic effects of compounds called sonosensitizers. In this study we investigated photodynamic and sonodynamic effect of chloraluminium phtalocyanine disulfonate (ClAlPcS(2)) on HeLa cells. DNA damage, cell viability and reactive oxygen species (ROS) production were assessed to find whether the combination of PDT and SDT inflicts HeLa cells more than PDT alone. We found that the combined therapy increases DNA fragmentation, enhances ROS production and decreases cell survival. Our results indicate that ClAlPcS(2) can act as a sonosentitiser and combined with PDT causes more irreversible changes to the cells resulting in cell death than PDT alone.
光动力疗法(PDT)使用光敏物质引发细胞毒性反应,导致细胞损伤或死亡。这些物质,即光敏剂,通常是卟啉或酞菁的衍生物。为了产生活性氧,主要是单线态氧,光敏剂必须通过光激活。声动力学疗法(SDT)利用超声波增强称为声敏剂的化合物的细胞毒性作用。在这项研究中,我们研究了氯铝酞菁二磺酸钠(ClAlPcS(2))对 HeLa 细胞的光动力和声动力效应。评估 DNA 损伤、细胞活力和活性氧(ROS)的产生,以确定 PDT 和 SDT 的联合治疗是否比单独 PDT 对 HeLa 细胞造成更大的伤害。我们发现联合治疗会增加 DNA 片段化,增强 ROS 的产生,并降低细胞存活率。我们的结果表明,ClAlPcS(2)可以作为声敏剂,与 PDT 联合使用会导致细胞发生比单独 PDT 更不可逆的变化,从而导致细胞死亡。