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Squaraine - PDT induces oxidative stress in skin tumor of swiss albino mice

机译:Squaraine-PDT诱导瑞士白化病小鼠皮肤肿瘤中的氧化应激

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Photodynamic Therapy (PDT) using a sensitizing drug is recognized as a promising medical technique for cancer treatment. It is a two step process that requires the administration of a photosensitizer followed by light exposure to treat a disease. Following light exposure the photosensitizer is excited to a higher energy state which generates free radicals and singlet oxygen. The present study was carried out to assess the oxidative damage induced by bis (3, 5-diiodo-2,4, 6-trihydroxyphenyl) squaraine in skin tumor tissues of mice with/ without light treatment. Skin tumor was induced using 7, 12-Dimethyl Benz(a)anthracene and croton oil. The tumor bearing mice were given an intraperitoneal injection with the squaraine dye. After 24h, the tumor area of a few animals injected with the dye, were exposed to visible light from a 1000 W halogen lamp and others kept away from light. All the mice were sacrificed one week after the PDT treatment and the oxidative profile was analyzed (TBARS, SOD, catalase, GSH, GPx and GR) in tumor/ skin tissues. The dye induces oxidative stress in the tumor site only on illumination and the oxidative status of the tumor tissue was found to be unaltered in the absence of light. The results of the study clearly shows that the tumor destruction mediated by PDT using bis (3, 5-diiodo-2, 4, 6-trihydroxyphenyl) squaraine as a photosensitizer is due to the generation of reactive oxygen species, produced by the light induced changes in the dye.
机译:使用致敏药物的光动力疗法(PDT)被认为是用于癌症治疗的有前途的医学技术。这是一个两步过程,需要先施用光敏剂,然后进行曝光以治疗疾病。曝光后,光敏剂被激发到更高的能量状态,从而产生自由基和单线态氧。本研究旨在评估双(3,5-二碘-2-4,4,6-三羟苯基)方酸在有/无光治疗的小鼠皮肤肿瘤组织中引起的氧化损伤。用7,12-二甲基苯并蒽油和巴豆油诱导皮肤肿瘤。给荷瘤的小鼠腹腔注射方酸染料。 24小时后,将几只注射了该染料的动物的肿瘤区域暴露于1000 W卤素灯的可见光下,而其他动物则远离光。在PDT处理后一周将所有小鼠处死,并分析肿瘤/皮肤组织中的氧化谱(TBARS,SOD,过氧化氢酶,GSH,GPx和GR)。该染料仅在照明时才在肿瘤部位诱导氧化应激,并且发现在没有光照的情况下肿瘤组织的氧化状态不会改变。研究结果清楚地表明,使用双(3,5-二碘-2-,4,6-三羟基苯基)方酸作为光敏剂的PDT介导的肿瘤破坏是由于光诱导的活性氧的产生染料的变化。

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