Marchesini R, Melloni E, Bottiroli G, Andreola S, Fava G, Mella M, Savi G, Zunino F
Tumori. 1987 Feb 28;73(1):11-7. doi: 10.1177/030089168707300102.
The main side effect in photodynamic therapy is photosensitization of the patient's skin following systemic administration of the photosensitizing agent. In the case of superficial lesions, this problem can be avoided by topically applying the drug: in this way a local treatment can be performed. We tested the photosensitizing properties of a 2% solution of TPPS (tetrasodium-tetraphenylporphinesulfonate) in a vehicle containing a penetration enhancer, Azone, on skin of nude mice. An aliquot of 0.1 ml/cm2 of the solution was painted on the skin overlying an s.c. implanted NMU-1 tumor. Subsequently, animals were sacrificed at different times after application. Fluorescence microscopy revealed that TPPS penetration depth was related to time elapsed after application and to painting modalities. Solution penetration was enhanced by wiping with ether immediately before painting. Irradiation at 80 mW/cm2 for 20 min with a dye laser emitting at 640 nm, 4 h after TPPS application, produced necrosis of the upper skin layers, up to 0.2 mm in depth. These findings suggest that topical TPPS administration, followed by laser irradiation, may be a suitable treatment modality for skin lesions involving epithelial layers, even though several aspects of this metodology need further investigation.
光动力疗法的主要副作用是在全身给予光敏剂后患者皮肤出现光敏反应。对于浅表病变,可通过局部应用药物来避免这一问题:这样就能进行局部治疗。我们在含有渗透促进剂氮酮的载体中测试了2%四苯基卟啉磺酸钠(TPPS)溶液对裸鼠皮肤的光敏特性。将0.1 ml/cm²的该溶液涂覆在皮下植入NMU - 1肿瘤上方的皮肤上。随后,在涂药后的不同时间处死动物。荧光显微镜检查显示,TPPS的渗透深度与涂药后经过的时间以及涂药方式有关。在涂药前立即用乙醚擦拭可增强溶液的渗透。在应用TPPS 4小时后,用发射波长为640 nm的染料激光以80 mW/cm²照射20分钟,可导致上层皮肤坏死,深度达0.2 mm。这些发现表明,局部给予TPPS后再进行激光照射,可能是治疗累及上皮层皮肤病变的一种合适治疗方式,尽管该方法的几个方面还需要进一步研究。