Hakli Özgül, Ocakoğlu Kasım, Ayaz Furkan
Department of Chemistry, Faculty of Science, Muğla Sıtkı Koçman University, Muğla, Turkey.
Department of Engineering Fundamental Sciences, Faculty of Engineering, Tarsus University, Mersin, Turkey.
Turk J Chem. 2021 Jun 16;45(6):1752-1760. doi: 10.3906/kim-2104-8. eCollection 2021.
Photodynamic therapy (PDT) applications enable light-controlled activation of drug candidates instead of their constitutive activities to prevent undesired side effects associated with their constant activities. A specific wavelength of light is utilized to enable electron mobility in the chemical structure, which results in differential activities that may alter cell viability and cellular functions. Canonical photodynamic therapy applications mostly focus on cytotoxicity-based antimicrobial and anticancer properties of the PDT agents. In this study, we focused on subtoxic concentrations of three different molecules containing polyoxyethylene group and examined their antiinflammatory activities on stimulated mammalian macrophages. Stimulated macrophages produce proinflammatory cytokines TNF and IL6. In the presence of a light source, our PDT agents were activated for 5 and 10 min during their application to the macrophages. Based on the ELISA results, the compounds had anti-inflammatory PDT activities. Trypan blue staining results suggest that these derivatives exerted their activities without leading to cytotoxicity. Our results suggest noncanonical PDT applications of these derivatives that can alter cellular activities without leading to cell death.
光动力疗法(PDT)的应用能够通过光控激活候选药物,而非其固有活性,以防止与其持续活性相关的不良副作用。利用特定波长的光使化学结构中的电子发生移动,从而产生不同的活性,这可能会改变细胞活力和细胞功能。传统的光动力疗法应用主要集中在基于细胞毒性的光动力疗法药物的抗菌和抗癌特性上。在本研究中,我们关注了三种含有聚氧乙烯基团的不同分子的亚毒性浓度,并研究了它们对受刺激的哺乳动物巨噬细胞的抗炎活性。受刺激的巨噬细胞会产生促炎细胞因子TNF和IL6。在有光源的情况下,我们的光动力疗法药物在应用于巨噬细胞的过程中被激活5分钟和10分钟。基于酶联免疫吸附测定(ELISA)结果,这些化合物具有抗炎光动力疗法活性。台盼蓝染色结果表明,这些衍生物发挥其活性时不会导致细胞毒性。我们的结果表明,这些衍生物的非传统光动力疗法应用能够改变细胞活性而不导致细胞死亡。