Shea C R, Chen N, Wimberly J, Hasan T
Wellman Laboratories of Photomedicine, Department of Dermatology, Harvard Medical School, Massachusetts General Hospital, Boston 02114.
Cancer Res. 1989 Jul 15;49(14):3961-5.
The phototoxicity in vitro of rhodamine 123 and tetrabromo rhodamine 123 (TBR) was compared, in order to assess their photochemotherapeutic potential. Exposure to 514.5-nm radiation from an argon ion laser caused phototoxicity in MGH-U1 bladder carcinoma cells previously treated with either dye at 10 microM for 30 min. As assessed by colony formation and cellular morphology, TBR was markedly more phototoxic than rhodamine 123, reflecting increased intersystem crossing of TBR to the triplet manifold via spin-orbital coupling induced by the heavy bromine atoms. Photoreactions of TBR very efficiently generated singlet oxygen (1O2) in solution; furthermore, irradiation of TBR-treated cells was significantly more toxic when performed in the presence of deuterium oxide, an enhancer of damage caused by 1O2. Retention of fluorescence in TBR-treated cells was enhanced by irradiation, indicating that a stable photoproduct may be formed in reaction with cellular components.
比较了罗丹明123和四溴罗丹明123(TBR)的体外光毒性,以评估它们的光化学治疗潜力。用氩离子激光的514.5纳米辐射照射先前用10微摩尔任一种染料处理30分钟的MGH-U1膀胱癌细胞会导致光毒性。通过集落形成和细胞形态评估,TBR的光毒性明显高于罗丹明123,这反映了TBR通过重溴原子诱导的自旋-轨道耦合增加了系间窜越到三重态。TBR的光反应在溶液中非常有效地产生单线态氧(1O2);此外,在氧化氘(一种由1O2引起的损伤增强剂)存在下对TBR处理的细胞进行照射时毒性明显更大。照射增强了TBR处理细胞中荧光的保留,表明与细胞成分反应可能形成稳定的光产物。