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Synthesis and biological evaluation of new chlorin derivatives as potential photosensitizers for photodynamic therapy

机译:新的二氢卟酚衍生物的合成及生物学评价,可作为光动力疗法的潜在光敏剂

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摘要

Three new water-soluble chlorin derivatives 3, 5 and 8 for potential use as photosensitizers in photodynamic therapy (PDT) for cancer were synthesized from photoprotoporphyrin IX dimethyl ester (1). The in vivo biodistribution and clearance of chlorin derivatives 3, 5 and 8 were investigated in tumor-bearing mice. Iminodiacetic acid derivative 8 showed the greatest tumor-selective accumulation among the new chlorin derivatives with maximum accumulation in tumor tissue at 3 h after intravenous injection and rapid clearance from normal tissues within 24 h after injection. The in vivo therapeutic efficacy of PDT using 8 was evaluated by measuring tumor growth rates in tumor-bearing mice with 660 nm light-emitting diode irradiation at 3 h after injection of 8. Tumor growth was significantly inhibited by PDT using 8. These results indicate that iminodiacetic acid derivative 8 is useful as a new photosensitizer to overcome the disadvantages of photosensitizers that are currently in clinical use.
机译:由光原卟啉IX二甲基酯(1)合成了三种新的水溶性二氢二氢卟酚衍生物3、5和8,它们有可能在癌症的光动力疗法(PDT)中用作光敏剂。在荷瘤小鼠中研究了二氢卟酚衍生物3、5和8的体内生物分布和清除。亚氨基二乙酸衍生物8在新的二氢卟酚衍生物中显示出最大的肿瘤选择性积累,在静脉注射后3 h在肿瘤组织中积累最多,在注射后24 h内从正常组织中迅速清除。通过在注射8次后3小时用660 nm发光二极管照射测量荷瘤小鼠的肿瘤生长率,评估使用8对PDT的体内治疗效果。这些结果表明,使用8对PDT可以显着抑制肿瘤生长。亚氨基二乙酸衍生物8可用作新的光敏剂,以克服目前临床上使用的光敏剂的缺点。

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