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首页> 外文期刊>Journal of Photochemistry and Photobiology, B. Biology: Official Journal of the European Society for Photobiology >Bis(3,5-diiodo-2,4,6-trihydroxyphenyl)squaraine: A novel candidate in photodynamic therapy for skin cancer models in vivo
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Bis(3,5-diiodo-2,4,6-trihydroxyphenyl)squaraine: A novel candidate in photodynamic therapy for skin cancer models in vivo

机译:Bis(3,5-diiodo-2,4,6-trihydroxyphenyl)squaraine:体内皮肤癌模型光动力疗法的新型候选药物

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摘要

Photodynamic therapy (PDT) is based on the light-induced activation of a photosensitizer generating highly reactive oxygen species that induce tissue destruction in malignant tissues. The present study was carried out to assess the photosensitizing potential of bis(3,5-diiodo-2,4,6-trihydroxyphenyl)squa-raine in PDT trials in vivo. Male Swiss albino mice were divided into five groups. Skin tumor was induced using 7,12-dimethylbenz(a)anthracene - DMBA in the animals of Groups II, III, IV and V, while animals of Group I served as the control. At the completion of 20 weeks of induction, the tumor bearing mice from Group III, IV and V were given an intraperitoneal injection with the squaraine dye (12.5 mg/kg body weight). After 24 h, in the Group IV and V animals, the tumor area was exposed to visible light from a 1000 W halogen lamp. The mice from groups I to IV were sacrificed two weeks after the PDT treatment and the marker enzymes (myeloperoxidase [MPO], β-D-glucuronidase, rhodanese, lactate dehydrogenase [LDH], hexokinase, sialic acid and caspase) were assayed in tumor and normal tissues. Animals from Group V were sacrificed after 90 days of PDT treatment and the above parameters were recorded. Reduction in tumor volume and reversal of biochemical markers to near normal levels were observed in the treatment groups. The study assumes importance as it is the first report on PDT-a novel modality, using a squaraine dye for skin cancer therapy in vivo. The uniqueness of the mode of treatment lies in the selective uptake of squaraine dye by the cancer cells and their selective destruction using PDT without affecting the neighbouring normal cells, which is much advantageous over radiation therapy now frequently used. Also in skin cancer models, the progression/cure can be visualized by the naked eye which is another point of advantage, while seeking new modalities for the treatment of cancer.
机译:光动力疗法(PDT)基于光敏剂的光诱导活化,该光敏剂会产生高活性氧,从而诱发恶性组织的组织破坏。进行本研究以评估体内PDT试验中双(3,5-二碘-2,4,6-三羟基苯基)squa-raine的光敏潜力。瑞士白化病雄性小鼠分为五组。 II,III,IV和V组的动物使用7,12-二甲基苯并(a)蒽-DMBA诱导皮肤肿瘤,而I组的动物作为对照。诱导20周后,对来自III,IV和V组的荷瘤小鼠进行腹腔注射方酸染料(12.5 mg / kg体重)。 24小时后,在IV和V组动物中,将肿瘤区域暴露于1000 W卤素灯的可见光下。在PDT处理后两周,将I至IV组的小鼠处死,并在肿瘤中检测标记酶(髓过氧化物酶[MPO],β-D-葡萄糖醛酸苷酶,罗丹菌,乳酸脱氢酶[LDH],己糖激酶,唾液酸和胱天蛋白酶)。和正常组织。在PDT处理90天后,处死来自V组的动物,并记录上述参数。在治疗组中观察到肿瘤体积减小和生化标志物逆转至接近正常水平。该研究具有重要意义,因为这是有关PDT的首次报道,PDT是一种新型药物,使用方酸染料在体内进行皮肤癌治疗。治疗方式的独特之处在于癌细胞选择性吸收方酸染料,并使用PDT选择性破坏方酸染料,而不会影响邻近的正常细胞,这比目前常用的放射疗法更具优势。同样在皮肤癌模型中,可以通过肉眼观察进展/治愈,这是另一优点,同时寻求治疗癌症的新方法。

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