放射增敏剂
光动力疗法
放射治疗
电离辐射
癌症研究
刘易斯肺癌
光敏剂
医学
垂直波分
癌症
毒性
肉瘤
化学
辐照
内科学
病理
外科
光化学
转移
物理
有机化学
视力
脉络膜新生血管
核物理学
作者
Moshe Schaffer,Pamela Schaffer,Giulio Jori,L. Corti,Guido Sotti,A. Hofstetter,Eckhart Dühmke
标识
DOI:10.1177/030089160208800511
摘要
Ionizing irradiation is a well-established therapeutic modality for cancer. Photodynamic therapy (PDT), especially with 5-ALA and Photofrin, is highly effective in some tumor types. Chemical modifiers, so-called radiosensitizers, are used in order to increase the efficacy of radiotherapy. Most of the known and routinely used radiosensitizers are not tumor selective, so that the normal tissue reaction toxicity is also increased. In the present study we investigated whether a porphyrin derivative that is currently used as a tumor-photosensitizing agent in photodynamic therapy (PDT) may also act as a tumor-specific radiosensitizer.For our investigation we used Balb/c mice implanted with Lewis sarcoma and irradiated with 3 Gy combined with injection of 5-ALA or Photofrin at various concentrations before irradiation.5-ALA had no effect as a radiosensitizer at any of the concentrations examined. Photofrin at a concentration of 5 mg/kg proved to be a chemical modifier of ionizing radiation, delaying tumor growth and reducing the overall tumor volume by about 50% after six days.Photofrin has marked efficacy as a radiosensitizer and can be used in the future as a selective tumor radiosensitizer.
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