Ziółkowski P, Symonowicz K, Osiecka B J, Rabczyński J
Department of Pathology, University Medical School, Wrocław, Poland.
Arch Immunol Ther Exp (Warsz). 1998;46(5):301-4.
We present results of preliminary studies on 5-aminolevulinic acid (5-ALA)-photodynamic therapy (PDT). In order to assess the effectiveness of 5-ALA-PDT we have used BALB/c mice transplanted subcutaneously with mouse colon adenocarcinoma C51. 5-ALA in the dose of 50 mg/kg was given intraperitoneally and 5 h later tumors were exposed to light at total doses from 50 to 75 J/cm2, wavelength 630+/-20 nm and light intensity 200 mW/cm2. Several time points following 5-ALA injections have been used to measure protoporphyrin IX (PpIX) concentration in different tissues from unirradiated mice. PDT effects were evaluated with regard to survival time, tumor response and necrosis depth. The main finding in our tumor model was that the optimum tumor to skin ratio of PpIX occurs within 5 h after sensitizer injection. 5-ALA-PDT resulted in prolongation of survival time of treated mice as compared to control animals and, in some cases, in complete response of tumors. PDT also caused increase in tumor necrosis, while no skin photodamage was observed.
我们展示了关于5-氨基乙酰丙酸(5-ALA)光动力疗法(PDT)的初步研究结果。为了评估5-ALA-PDT的有效性,我们使用了皮下移植小鼠结肠腺癌C51的BALB/c小鼠。以50mg/kg的剂量腹腔注射5-ALA,5小时后,将肿瘤暴露于总剂量为50至75J/cm²、波长630±20nm、光强度200mW/cm²的光线下。在注射5-ALA后的几个时间点,用于测量未照射小鼠不同组织中原卟啉IX(PpIX)的浓度。从生存时间、肿瘤反应和坏死深度方面评估PDT的效果。在我们的肿瘤模型中的主要发现是,致敏剂注射后5小时内,PpIX在肿瘤与皮肤中的比例达到最佳。与对照动物相比,5-ALA-PDT导致治疗小鼠的生存时间延长,并且在某些情况下,肿瘤出现完全缓解。PDT还导致肿瘤坏死增加,同时未观察到皮肤光损伤。